TIPS for Parenting an Autistic Child

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News Roundup: New and Noteworthy Information

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Women with Down syndrome who experienced early menopause were almost twice as likely to develop dementia at a younger age than those who entered menopause later, according to research in the January Journal of Alzheimer’s Disease. In a prospective longitudinal cohort study of dementia and mortality in women with Down syndrome, researchers followed 85 postmenopausal subjects for an average of 4.3 years and found a significant correlation between the age at menopause onset and age at diagnosis of dementia. Subjects with an earlier onset of menopause had a 1.8-fold increased risk of dementia. In addition, women who experienced menopause earlier had a twofold increased risk of dying younger.

White, elderly cancer survivors have a reduced risk of developing Alzheimer’s disease, as reported in the January 12 Neurology. Conversely, patients with Alzheimer’s disease have a reduced cancer risk, investigators found. In a prospective cohort study of 3,020 subjects ages 65 and older, the presence of Alzheimer’s disease was associated with a reduced risk of cancer hospitalizations, after adjustments for demographic and other factors. Prevalent cancer was also associated with a reduced risk of Alzheimer’s disease among white subjects after the researchers adjusted for demographics, number of apolipoprotein ε4 alleles, hypertension, diabetes, and coronary heart disease. The opposite was found in minorities, although the sample size was considered too small. No significant association was found between cancer and vascular dementia.

Ginkgo biloba did not preserve cognitive function any better than a placebo, per a study in the December 23, 2009, JAMA. In the randomized, double-blind, placebo-controlled Ginkgo Evaluation of Memory study, researchers at six academic medical centers in the US tracked 3,069 community-dwelling subjects ages 72 to 96 years for an average of 6.1 years. Subjects were given either a twice-daily dose of 120 mg extract of Ginkgo biloba or a placebo. Cognition was measured as rates of change over time in the Modified Mini-Mental State Examination, the cognitive subscale of the Alzheimer Disease Assessment Scale (ADAS-Cog), and neuropsychologic domains of memory, attention, visual-spatial construction, language, and executive functions. Investigators found no significant difference in cognitive decline between the herb and placebo.

A decreased ability to smell is common in patients with Alzheimer’s disease and may be a useful early diagnostic tool, researchers reported in the January 13 Journal of Neuroscience. The study linked olfactory dysfunction with an accumulation of amyloid-β protein in Alzheimer’s disease model mice. “The usefulness of olfactory screens to serve as informative indicators of Alzheimer’s is precluded by a lack of knowledge regarding why the disease impacts olfaction,” the study authors stated. The investigators assayed olfactory perception and amyloid-β deposition in the genetically engineered mice and found that amyloid-β pathology first occurred in an area of the brain responsible for smelling. Mice with higher concentrations of amyloid-β also displayed olfactory dysfunction. Researchers noted the “odor cross-habitation test [was] a powerful behavioral assay…[which] may serve to monitor the efficacy of therapies aimed at reducing amyloid-β.”

The Lancet has retracted the 1998 paper by Wakefield et al that suggested a link between autism and the childhood measles, mumps, and rubella (MMR) vaccine. The retraction, published in the February 2 online issue, follows a judgment by the UK General Medical Council’s Fitness to Practice Panel on January 28. “It has become clear that several elements of the 1998 paper by Wakefield et al are incorrect,” the editors wrote. “In particular, the claims in the original paper that children were ‘consecutively referred’ and that investigations were ‘approved’ by the local ethics committee have been proven to be false.” In 2004, 10 of the original authors retracted parts of the study, stating, “in this paper no causal link was established between MMR vaccine and autism as the data were insufficient.”

Advanced maternal age may be linked to an increased risk of autism, researchers reported in the February 8 online Autism Research. In a study of 12,159 cases of autism from a pool of almost 5 million births between 1990 and 1999, the investigators found a monotonic increased risk of autism related to advancing maternal age (40 and older) regardless of paternal age. However, the study authors noted fathers aged 40 and up who mated with women younger than 30 also had an increased risk of autistic offspring, compared with men in their mid- to late-20s. Yet when the mother was older than 30 and the father was 40 or older, the associated autism risk was similar to that of younger men. The investigators also noted that the “recent trend towards delaying childbearing contributed approximately a 4.6% increase in autism diagnoses in California over the decade.”

 

 

Depression and migraine headaches appear to share a common genetic factor, a Dutch study of 2,652 people found. As reported in the January 26 Neurology, researchers compared heritability estimates among members of the Erasmus Rucphen family for migraine with and without depression, and depression rates between migraineurs and controls. Of the total study population, 360 had migraines, 151 of whom experienced migraine aura as well. One-quarter of migraineurs also had depression, compared with 13% of the controls. Odds ratios for depression in patients with migraine were 1.29 for those without aura and 1.70 for those with aura. “There is a bidirectional association between depression and migraine, in particular migraine with aura, which can be explained, at least partly, by shared genetic factors,” the study authors noted.

The FDA has approved Ampyra (dalfampridine) extended-release tablets to improve walking in patients with multiple sclerosis (MS). In clinical trials, patients treated with dalfampridine had faster walking speeds than those treated with a placebo. It is the first report in which a drug for MS improved function that was lost as a result of the disease. The most common side effects reported were urinary tract infection, insomnia, dizziness, headache, nausea, and others. When taken in doses greater than 10 mg twice a day, seizures may occur. It should not be used in patients with moderate to severe kidney disease. Dalfampridine is distributed by Acorda Therapeutics Inc of Hawthorne, New York.

Black patients with multiple sclerosis showed increased tissue damage and higher lesion volumes compared with white patients, according to research in the February 16 Neurology. In a study of 567 patients, 488 of whom were white and 79 were black, investigators compared quantitative MRI evaluations including T1-, T2-, and gadolinium contrast-enhancing lesion volumes and contrast-enhancing number, global and tissue-specific brain atrophy, and magnetization transfer ratios (MTR) in lesions and normal-appearing gray matter (NAGM) and white matter (NAWM). The researchers found that MTR values in lesions and in NAGM and NAWM were significantly lower in black subjects than in whites, and T1- and T2- lesion volumes were greater, both of which indicate a more aggressive clinical disease.

Dopamine agonists can cause or exacerbate compulsive behaviors in patients with Parkinson’s, according to research published in the January 14 Neuron. “A constellation of pathological behaviors, including gambling, shopping, binge eating, and hypersexuality is seen in 17% of patients on dopamine agonists,” the study authors wrote. Because reinforcement learning algorithms allow for computation of prediction error, the researchers used a reinforcement learning model to deconstruct decision-making processes dysregulated by dopamine agonists in patients who are susceptible to compulsive behaviors. The investigators found that the medications increased the rate of learning from gain outcomes and increased striatal prediction error activity, signifying a “better than expected” outcome.

Patients with acute ischemic stroke admitted to the hospital on the weekend are more likely to receive t-PA than those admitted on a weekday, a study in the January Archives of Neurology reported. Researchers analyzed rates of t-PA administration, as well as death rates, among 78,657stroke patients admitted to Virginia hospitals between 1998 and 2006 and found weekend patients (n=20,279) were 20% more likely to receive t-PA than weekday patients (n=58,378). There was no statistically significant difference in patient mortality based on day of admission; however, because a greater percentage of weekend patients received t-PA while death rates remained equal, the study authors noted that those treated with t-PA may be more likely to die in the hospital.

Impaired cognitive function in elderly men may be an independent predictor of subsequent stroke, according to a report in the February 2 Neurology. In a study of 930 elderly men (mean age, 70), Swedish researchers found that taking longer to complete the Trail Making Test B increased stroke risk by as much as 300% for those in the highest quartile, compared with those in the lowest quartile. Each time increase of 1 SD was associated with a 1.48 higher risk of stroke. “Our results extend previous findings of cognitive decline as an independent predictor of stroke and indicate that the risk of brain infarction is increased already in the subclinical phase of cognitive deficit,” the study authors wrote.

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Women with Down syndrome who experienced early menopause were almost twice as likely to develop dementia at a younger age than those who entered menopause later, according to research in the January Journal of Alzheimer’s Disease. In a prospective longitudinal cohort study of dementia and mortality in women with Down syndrome, researchers followed 85 postmenopausal subjects for an average of 4.3 years and found a significant correlation between the age at menopause onset and age at diagnosis of dementia. Subjects with an earlier onset of menopause had a 1.8-fold increased risk of dementia. In addition, women who experienced menopause earlier had a twofold increased risk of dying younger.

White, elderly cancer survivors have a reduced risk of developing Alzheimer’s disease, as reported in the January 12 Neurology. Conversely, patients with Alzheimer’s disease have a reduced cancer risk, investigators found. In a prospective cohort study of 3,020 subjects ages 65 and older, the presence of Alzheimer’s disease was associated with a reduced risk of cancer hospitalizations, after adjustments for demographic and other factors. Prevalent cancer was also associated with a reduced risk of Alzheimer’s disease among white subjects after the researchers adjusted for demographics, number of apolipoprotein ε4 alleles, hypertension, diabetes, and coronary heart disease. The opposite was found in minorities, although the sample size was considered too small. No significant association was found between cancer and vascular dementia.

Ginkgo biloba did not preserve cognitive function any better than a placebo, per a study in the December 23, 2009, JAMA. In the randomized, double-blind, placebo-controlled Ginkgo Evaluation of Memory study, researchers at six academic medical centers in the US tracked 3,069 community-dwelling subjects ages 72 to 96 years for an average of 6.1 years. Subjects were given either a twice-daily dose of 120 mg extract of Ginkgo biloba or a placebo. Cognition was measured as rates of change over time in the Modified Mini-Mental State Examination, the cognitive subscale of the Alzheimer Disease Assessment Scale (ADAS-Cog), and neuropsychologic domains of memory, attention, visual-spatial construction, language, and executive functions. Investigators found no significant difference in cognitive decline between the herb and placebo.

A decreased ability to smell is common in patients with Alzheimer’s disease and may be a useful early diagnostic tool, researchers reported in the January 13 Journal of Neuroscience. The study linked olfactory dysfunction with an accumulation of amyloid-β protein in Alzheimer’s disease model mice. “The usefulness of olfactory screens to serve as informative indicators of Alzheimer’s is precluded by a lack of knowledge regarding why the disease impacts olfaction,” the study authors stated. The investigators assayed olfactory perception and amyloid-β deposition in the genetically engineered mice and found that amyloid-β pathology first occurred in an area of the brain responsible for smelling. Mice with higher concentrations of amyloid-β also displayed olfactory dysfunction. Researchers noted the “odor cross-habitation test [was] a powerful behavioral assay…[which] may serve to monitor the efficacy of therapies aimed at reducing amyloid-β.”

The Lancet has retracted the 1998 paper by Wakefield et al that suggested a link between autism and the childhood measles, mumps, and rubella (MMR) vaccine. The retraction, published in the February 2 online issue, follows a judgment by the UK General Medical Council’s Fitness to Practice Panel on January 28. “It has become clear that several elements of the 1998 paper by Wakefield et al are incorrect,” the editors wrote. “In particular, the claims in the original paper that children were ‘consecutively referred’ and that investigations were ‘approved’ by the local ethics committee have been proven to be false.” In 2004, 10 of the original authors retracted parts of the study, stating, “in this paper no causal link was established between MMR vaccine and autism as the data were insufficient.”

Advanced maternal age may be linked to an increased risk of autism, researchers reported in the February 8 online Autism Research. In a study of 12,159 cases of autism from a pool of almost 5 million births between 1990 and 1999, the investigators found a monotonic increased risk of autism related to advancing maternal age (40 and older) regardless of paternal age. However, the study authors noted fathers aged 40 and up who mated with women younger than 30 also had an increased risk of autistic offspring, compared with men in their mid- to late-20s. Yet when the mother was older than 30 and the father was 40 or older, the associated autism risk was similar to that of younger men. The investigators also noted that the “recent trend towards delaying childbearing contributed approximately a 4.6% increase in autism diagnoses in California over the decade.”

 

 

Depression and migraine headaches appear to share a common genetic factor, a Dutch study of 2,652 people found. As reported in the January 26 Neurology, researchers compared heritability estimates among members of the Erasmus Rucphen family for migraine with and without depression, and depression rates between migraineurs and controls. Of the total study population, 360 had migraines, 151 of whom experienced migraine aura as well. One-quarter of migraineurs also had depression, compared with 13% of the controls. Odds ratios for depression in patients with migraine were 1.29 for those without aura and 1.70 for those with aura. “There is a bidirectional association between depression and migraine, in particular migraine with aura, which can be explained, at least partly, by shared genetic factors,” the study authors noted.

The FDA has approved Ampyra (dalfampridine) extended-release tablets to improve walking in patients with multiple sclerosis (MS). In clinical trials, patients treated with dalfampridine had faster walking speeds than those treated with a placebo. It is the first report in which a drug for MS improved function that was lost as a result of the disease. The most common side effects reported were urinary tract infection, insomnia, dizziness, headache, nausea, and others. When taken in doses greater than 10 mg twice a day, seizures may occur. It should not be used in patients with moderate to severe kidney disease. Dalfampridine is distributed by Acorda Therapeutics Inc of Hawthorne, New York.

Black patients with multiple sclerosis showed increased tissue damage and higher lesion volumes compared with white patients, according to research in the February 16 Neurology. In a study of 567 patients, 488 of whom were white and 79 were black, investigators compared quantitative MRI evaluations including T1-, T2-, and gadolinium contrast-enhancing lesion volumes and contrast-enhancing number, global and tissue-specific brain atrophy, and magnetization transfer ratios (MTR) in lesions and normal-appearing gray matter (NAGM) and white matter (NAWM). The researchers found that MTR values in lesions and in NAGM and NAWM were significantly lower in black subjects than in whites, and T1- and T2- lesion volumes were greater, both of which indicate a more aggressive clinical disease.

Dopamine agonists can cause or exacerbate compulsive behaviors in patients with Parkinson’s, according to research published in the January 14 Neuron. “A constellation of pathological behaviors, including gambling, shopping, binge eating, and hypersexuality is seen in 17% of patients on dopamine agonists,” the study authors wrote. Because reinforcement learning algorithms allow for computation of prediction error, the researchers used a reinforcement learning model to deconstruct decision-making processes dysregulated by dopamine agonists in patients who are susceptible to compulsive behaviors. The investigators found that the medications increased the rate of learning from gain outcomes and increased striatal prediction error activity, signifying a “better than expected” outcome.

Patients with acute ischemic stroke admitted to the hospital on the weekend are more likely to receive t-PA than those admitted on a weekday, a study in the January Archives of Neurology reported. Researchers analyzed rates of t-PA administration, as well as death rates, among 78,657stroke patients admitted to Virginia hospitals between 1998 and 2006 and found weekend patients (n=20,279) were 20% more likely to receive t-PA than weekday patients (n=58,378). There was no statistically significant difference in patient mortality based on day of admission; however, because a greater percentage of weekend patients received t-PA while death rates remained equal, the study authors noted that those treated with t-PA may be more likely to die in the hospital.

Impaired cognitive function in elderly men may be an independent predictor of subsequent stroke, according to a report in the February 2 Neurology. In a study of 930 elderly men (mean age, 70), Swedish researchers found that taking longer to complete the Trail Making Test B increased stroke risk by as much as 300% for those in the highest quartile, compared with those in the lowest quartile. Each time increase of 1 SD was associated with a 1.48 higher risk of stroke. “Our results extend previous findings of cognitive decline as an independent predictor of stroke and indicate that the risk of brain infarction is increased already in the subclinical phase of cognitive deficit,” the study authors wrote.

Women with Down syndrome who experienced early menopause were almost twice as likely to develop dementia at a younger age than those who entered menopause later, according to research in the January Journal of Alzheimer’s Disease. In a prospective longitudinal cohort study of dementia and mortality in women with Down syndrome, researchers followed 85 postmenopausal subjects for an average of 4.3 years and found a significant correlation between the age at menopause onset and age at diagnosis of dementia. Subjects with an earlier onset of menopause had a 1.8-fold increased risk of dementia. In addition, women who experienced menopause earlier had a twofold increased risk of dying younger.

White, elderly cancer survivors have a reduced risk of developing Alzheimer’s disease, as reported in the January 12 Neurology. Conversely, patients with Alzheimer’s disease have a reduced cancer risk, investigators found. In a prospective cohort study of 3,020 subjects ages 65 and older, the presence of Alzheimer’s disease was associated with a reduced risk of cancer hospitalizations, after adjustments for demographic and other factors. Prevalent cancer was also associated with a reduced risk of Alzheimer’s disease among white subjects after the researchers adjusted for demographics, number of apolipoprotein ε4 alleles, hypertension, diabetes, and coronary heart disease. The opposite was found in minorities, although the sample size was considered too small. No significant association was found between cancer and vascular dementia.

Ginkgo biloba did not preserve cognitive function any better than a placebo, per a study in the December 23, 2009, JAMA. In the randomized, double-blind, placebo-controlled Ginkgo Evaluation of Memory study, researchers at six academic medical centers in the US tracked 3,069 community-dwelling subjects ages 72 to 96 years for an average of 6.1 years. Subjects were given either a twice-daily dose of 120 mg extract of Ginkgo biloba or a placebo. Cognition was measured as rates of change over time in the Modified Mini-Mental State Examination, the cognitive subscale of the Alzheimer Disease Assessment Scale (ADAS-Cog), and neuropsychologic domains of memory, attention, visual-spatial construction, language, and executive functions. Investigators found no significant difference in cognitive decline between the herb and placebo.

A decreased ability to smell is common in patients with Alzheimer’s disease and may be a useful early diagnostic tool, researchers reported in the January 13 Journal of Neuroscience. The study linked olfactory dysfunction with an accumulation of amyloid-β protein in Alzheimer’s disease model mice. “The usefulness of olfactory screens to serve as informative indicators of Alzheimer’s is precluded by a lack of knowledge regarding why the disease impacts olfaction,” the study authors stated. The investigators assayed olfactory perception and amyloid-β deposition in the genetically engineered mice and found that amyloid-β pathology first occurred in an area of the brain responsible for smelling. Mice with higher concentrations of amyloid-β also displayed olfactory dysfunction. Researchers noted the “odor cross-habitation test [was] a powerful behavioral assay…[which] may serve to monitor the efficacy of therapies aimed at reducing amyloid-β.”

The Lancet has retracted the 1998 paper by Wakefield et al that suggested a link between autism and the childhood measles, mumps, and rubella (MMR) vaccine. The retraction, published in the February 2 online issue, follows a judgment by the UK General Medical Council’s Fitness to Practice Panel on January 28. “It has become clear that several elements of the 1998 paper by Wakefield et al are incorrect,” the editors wrote. “In particular, the claims in the original paper that children were ‘consecutively referred’ and that investigations were ‘approved’ by the local ethics committee have been proven to be false.” In 2004, 10 of the original authors retracted parts of the study, stating, “in this paper no causal link was established between MMR vaccine and autism as the data were insufficient.”

Advanced maternal age may be linked to an increased risk of autism, researchers reported in the February 8 online Autism Research. In a study of 12,159 cases of autism from a pool of almost 5 million births between 1990 and 1999, the investigators found a monotonic increased risk of autism related to advancing maternal age (40 and older) regardless of paternal age. However, the study authors noted fathers aged 40 and up who mated with women younger than 30 also had an increased risk of autistic offspring, compared with men in their mid- to late-20s. Yet when the mother was older than 30 and the father was 40 or older, the associated autism risk was similar to that of younger men. The investigators also noted that the “recent trend towards delaying childbearing contributed approximately a 4.6% increase in autism diagnoses in California over the decade.”

 

 

Depression and migraine headaches appear to share a common genetic factor, a Dutch study of 2,652 people found. As reported in the January 26 Neurology, researchers compared heritability estimates among members of the Erasmus Rucphen family for migraine with and without depression, and depression rates between migraineurs and controls. Of the total study population, 360 had migraines, 151 of whom experienced migraine aura as well. One-quarter of migraineurs also had depression, compared with 13% of the controls. Odds ratios for depression in patients with migraine were 1.29 for those without aura and 1.70 for those with aura. “There is a bidirectional association between depression and migraine, in particular migraine with aura, which can be explained, at least partly, by shared genetic factors,” the study authors noted.

The FDA has approved Ampyra (dalfampridine) extended-release tablets to improve walking in patients with multiple sclerosis (MS). In clinical trials, patients treated with dalfampridine had faster walking speeds than those treated with a placebo. It is the first report in which a drug for MS improved function that was lost as a result of the disease. The most common side effects reported were urinary tract infection, insomnia, dizziness, headache, nausea, and others. When taken in doses greater than 10 mg twice a day, seizures may occur. It should not be used in patients with moderate to severe kidney disease. Dalfampridine is distributed by Acorda Therapeutics Inc of Hawthorne, New York.

Black patients with multiple sclerosis showed increased tissue damage and higher lesion volumes compared with white patients, according to research in the February 16 Neurology. In a study of 567 patients, 488 of whom were white and 79 were black, investigators compared quantitative MRI evaluations including T1-, T2-, and gadolinium contrast-enhancing lesion volumes and contrast-enhancing number, global and tissue-specific brain atrophy, and magnetization transfer ratios (MTR) in lesions and normal-appearing gray matter (NAGM) and white matter (NAWM). The researchers found that MTR values in lesions and in NAGM and NAWM were significantly lower in black subjects than in whites, and T1- and T2- lesion volumes were greater, both of which indicate a more aggressive clinical disease.

Dopamine agonists can cause or exacerbate compulsive behaviors in patients with Parkinson’s, according to research published in the January 14 Neuron. “A constellation of pathological behaviors, including gambling, shopping, binge eating, and hypersexuality is seen in 17% of patients on dopamine agonists,” the study authors wrote. Because reinforcement learning algorithms allow for computation of prediction error, the researchers used a reinforcement learning model to deconstruct decision-making processes dysregulated by dopamine agonists in patients who are susceptible to compulsive behaviors. The investigators found that the medications increased the rate of learning from gain outcomes and increased striatal prediction error activity, signifying a “better than expected” outcome.

Patients with acute ischemic stroke admitted to the hospital on the weekend are more likely to receive t-PA than those admitted on a weekday, a study in the January Archives of Neurology reported. Researchers analyzed rates of t-PA administration, as well as death rates, among 78,657stroke patients admitted to Virginia hospitals between 1998 and 2006 and found weekend patients (n=20,279) were 20% more likely to receive t-PA than weekday patients (n=58,378). There was no statistically significant difference in patient mortality based on day of admission; however, because a greater percentage of weekend patients received t-PA while death rates remained equal, the study authors noted that those treated with t-PA may be more likely to die in the hospital.

Impaired cognitive function in elderly men may be an independent predictor of subsequent stroke, according to a report in the February 2 Neurology. In a study of 930 elderly men (mean age, 70), Swedish researchers found that taking longer to complete the Trail Making Test B increased stroke risk by as much as 300% for those in the highest quartile, compared with those in the lowest quartile. Each time increase of 1 SD was associated with a 1.48 higher risk of stroke. “Our results extend previous findings of cognitive decline as an independent predictor of stroke and indicate that the risk of brain infarction is increased already in the subclinical phase of cognitive deficit,” the study authors wrote.

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Grand Rounds: Girl, 6, With Rapid Heart Rate

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A 6-year-old girl was brought by her parents to the emergency department (ED) with an elevated heart rate. According to the parents, the girl was carrying her younger sister when they both fell, landing on their buttocks. The child told them that her heart was beating fast, and the parents said she appeared to be on the verge of fainting.

They stated that their daughter was healthy and active; they denied previous episodes of shortness of breath, headache, weakness, tachycardia, syncope, or fatigue with exercise. Her caffeine intake, they claimed, was limited to one small cup of soda they allowed her each week.

Initial evaluation in the ED revealed an anxious child with tachycardia and shortness of breath. She presented with a temperature of 98.3°F (36.8°C); pulse, 210 beats/min; respirations, 33 breaths/min; blood pressure, 100/72 mm Hg; weight, 78 lb; height, 45 in; and BMI, 27.1. ECG revealed a heart rate exceeding 210 beats/min, and a pediatric cardiologist made a diagnosis of supraventricular tachycardia (SVT).

The pediatric cardiologist prescribed an adenosine IV drip, which successfully stabilized the child’s heart to sinus rhythm. After three hours in the ED, the patient was discharged with a stable heart rate of 100 beats/min. (It is well known that heart rate regulation changes significantly during development; this is most obvious in higher basal rates in infants and children, compared with adults.1)

The parents were advised to administer atenolol 12.5 mg (one tablet) twice daily and to make a follow-up appointment with a pediatric electrophysiologist. (Although atenolol is not currently FDA approved for this use, a multicenter prospective randomized controlled trial comparing digoxin with beta-blockers for the treatment of SVT in children is presently under way.2)

At that appointment, the pediatric electrophysiologist provided information to the parents regarding the therapeutic options for SVT. The parents continued to administer atenolol to the child, as was deemed necessary until any accessory electrical pathway could be identified and, if so, an ablation procedure could be performed. They were uncertain how to proceed so long as their daughter experienced no recurrent episodes of SVT while receiving pharmacologic therapy.

However, six months after the initial episode, the child (then age 7) presented to the ED once again with recurrent SVT. The pediatric cardiologist ordered an adenosine IV drip, which resulted in successful conversion to sinus rhythm. The parents were instructed to increase the child’s atenolol dosage to 25 mg twice a day.

Six months later, after extensive research and consultation, the parents agreed to an ablation procedure in order to prevent further episodes of SVT. Upon their informed consent, the child was sent to a cardiac catheterization laboratory for an electrophysiology study (EPS), which confirmed the presence of an accessory pathway, as well as the diagnosis of atrioventricular reciprocating tachycardia (AVRT). The procedure was followed by radiofrequency catheter ablation to correct the 7-year-old patient’s accessory pathway–mediated reentry tachycardia.

Discussion
SVT, also known as paroxysmal supraventricular tachycardia (PSVT), is one of the most common symptomatic pediatric arrhythmias, affecting between one in 25,000 and one in 250 children.3 It is defined as rapid heart rhythm (140 to 240 beats/min) that is caused by the presence of additional electrical connections and/or congenital muscle fibers between the atrium and the ventricle or within the atrioventricular (AV) node that did not, for unknown reasons, separate completely during development.4 SVT can be triggered by physical or psychological stress automaticity.3

Approximately 50% of children with SVT present with a first episode before age 1. SVT usually occurs in early childhood, between ages 6 and 9.4 Almost 90% of pediatric patients with SVT are diagnosed with a reentry mechanism.3 The symptoms experienced may be resolved pharmacologically or by means of an invasive therapy. Serious sequelae associated with SVT include heart failure and cardiac arrest.

For children with rare and mildly symptomatic episodes in whom SVT is easily terminated, the SVT may not warrant treatment. However, it may be advisable to offer medical therapy or transcatheter ablation as therapeutic options for children with episodes that are difficult to terminate, occur frequently, or occur during participation in athletics.4

Pathophysiology
SVT generally presents as one of three types: AVRT, which is also known as Wolff-Parkinson-White syndrome; atrioventricular nodal reentry tachycardia (AVNRT); and automatic tachycardia (AT).

AVRT, the most common type of SVT, comprises about 90% of pediatric cases. It is defined by the presence of one or more accessory conduction pathways that are anatomically separated from the normal cardiac conduction system.5 AVRT may be orthodromic (that is, the arrhythmia circuit proceeds down the AV node and retrograde up the accessory conduction pathway) or antedromic (ie, proceeding down the accessory pathway and up the AV node5; see figure.6,7)

 

 

AVNRT, considered the second most common type of SVT in children, accounts for about 10% of pediatric cases. AVNRT is caused by an interaction between the two types of pathways within the AV node—one with a fast conduction time and a short refractory period, and the other with a slow conduction time and a long refractory period. AVNRT occurs when the antegrade conduction block in the fast pathway results in conduction over the slow pathway and back up the fast pathway, forming a microreentrant circuit.5

AT is the result of rapid depolarization from an automatic focus originating within the atria but outside the sinus node.3

Patient Presentation and History
The typical presentation of AVRT in children of school age includes palpitations, chest pain or tightness, dizziness, anxiety, decrease in exercise tolerance, easy fatigability, and/or shortness of breath.3 Onset is described as abrupt, while termination of SVT is described as slower because the catecholamine levels are typically elevated.4

The frequency and duration of SVT can vary greatly, from a few minutes to a few hours; it can occur as regularly as daily or as uncommonly as once or twice per year.4 Additionally, SVT symptoms can go unrecognized until a cardiac dysfunction develops. As for the patient in the case study, no apparent factor in her history was identified that may have induced SVT.

The differential diagnosis for SVT is broad, including sinus tachycardia, multifocal atrial tachycardia, and SVT with aberrancy.8 Additional considerations include stress, anxiety, hyperthyroidism, electrolyte abnormalities, and dehydration—any of which can present with a tachycardia response.4 Furthermore, clinicians are often unlikely to diagnose a child with any cardiac problem because chest pain is more commonly a presenting symptom of a pulmonary or musculoskeletal condition than a cardiac problem.3

Physical Examination
SVT can be diagnosed based on medical history and physical examination. During the physical examination, providers will assess the patient’s blood pressure and pulse, auscultate heart and lung sounds, assess the veins in the patient’s neck for different types of pulsations, and conduct cardiac maneuvers, including the Valsalva maneuver and carotid sinus massage.9,10

Laboratory Work-up and Diagnosis
Three specific tests help clinicians monitor and evaluate a patient’s conduction system. ECG is important to assess the heart rhythm both at baseline and when symptoms are occurring, if possible.3 Ambulatory ECG (ie, Holter monitoring, event recorders) record the patient’s heart rhythm on a continuous basis.

An EPS, which is performed to classify the mechanism of SVT, is conducted by inserting one or more electrocatheters into the heart by way of the femoral vein or other peripheral vessel.3 Pacing and sensing electrodes at the ends of the catheters record local intracardiac electrical activity and timing information, providing a detailed analysis of the heart’s electrical activity. The EPS is critical to determine the presence of one or more extra electrical pathways within the heart and to localize it by region.3,11 An ablation procedure may follow.

Management Options
SVT can be treated pharmacologically or nonpharmacologically. First-line pharmacologic options include certain beta-blockers (including atenolol and propranolol), digoxin, and calcium channel blockers. Second-line pharmacologic treatments include amiodarone, flecainide, and sotalol,4 all of which are contraindicated in children younger than 1 year because of these patients’ hemodynamic dependency on the heart and inability to generate stroke volume.3 Pharmacologic treatment of SVT is associated with a 68% success rate in children4 (see Table 14).

For children in whom pharmacologic treatment is ineffective, an ablation procedure may be performed. Radiofrequency catheter ablation is currently considered first-line therapy for AVRT and AVNRT.12 In this invasive procedure, intracardiac electrical mapping is performed and the initiating focus of the arrhythmia or the accessory electrical pathway that has been identified within the heart is destroyed by radiofrequency energy, delivered by electrocatheter. Ablations performed during the acute phase of SVT have a 95% success rate.3,13

Cryoablation is a relatively new treatment in which liquid nitrous oxide is used to cool the catheter to subfreezing temperatures, enabling it to destroy the myocardial tissue by freezing.3,14 The advantage of cryoablation is the option of reversible cooling, which allows the electrophysiologist to test the area first, confirming the accuracy of the apparent location accessory pathway.15

Noninvasive, nonpharmacologic interventions that increase the refractoriness of the AV node may be successful in terminating the tachyarrhythmia during episodes of SVT (see Table 23,9,13,16). They are used to terminate and diagnose tachydysrhythmias, increase parasympathetic tone, and slow conduction through the AV node.3

Patient Education
It is very important for health care providers to relieve parents’ and caregivers’ stress, anxiety, and uncertainty by educating them about the child’s cardiac condition of SVT. Information to convey include an understanding of what SVT is, what may cause it, what triggers the patient should avoid, what treatments are available and appropriate (including the maneuvers shown in Table 2), and what outcomes may be expected. An excellent patient/family education handout from the Children’s Hospitals and Clinics of Minnesota17 is available at www.childrensmn.org/Manuals/PFS/Condill/018303.pdf.

 

 

Follow-Up
Primary care providers must emphasize the importance of monitoring the patient’s progress, based on the severity of his or her SVT symptoms. The provider may choose to monitor the patient for a few weeks or a few months, assessing the frequency of arrhythmia recurrence and the heart rate, to adjust or substitute medications based on repeat ECG or Holter evaluations, and to plan further therapy, should the condition worsen.5

The Case Patient
One month after undergoing radiofrequency catheter ablation, the child presented to the pediatric cardiologist for follow-up. Since the procedure, she had been without any symptoms referable to the cardiovascular system. She denied experiencing any fast heart rate, palpitations, chest pain, shortness of breath, or dizziness. ECG demonstrated normal sinus rhythm.

Two years after undergoing radiofrequency ablation, the child is functioning at a normal activity level with no recurrence of SVT episodes.

Conclusion
The purpose of this case study is to improve primary care providers’ understanding of SVT in children and to convey the importance of identifying the condition in a timely manner and referring patients to a pediatric cardiologist or electrophysiologist. For most children affected by SVT, a regimen of pharmacologic and/or nonpharmacologic treatment—supported by detailed education for their parents and caregivers—can allow them to live a healthy, normal life.

References

1. Kudielka BM, Buske-Kirschbaum A, Hellhammer DH, Kirschbaum C. Differential heart rate reactivity and recovery after psychosocial stress (TSST) in healthy children, younger adults, and elderly adults: the impact of age and gender. Int J Behav Med. 2004;11(2):116-121.

 2. Multicenter Study of Antiarrhythmic Medications for Treatment of Infants With Supraventricular Tachycardia. www.clinicaltrials.gov/ct2/results?term=NCT00390546. Accessed January 26, 2010.

3. Schlechte EA, Boramanand N, Funk M. Supraventricular tachycardia in the pediatric primary care setting: age-related presentation, diagnosis, and management. J Pediatr Health Care. 2008;22(5): 289-299.

4. Salerno JC, Seslar SP. Supraventricular tachycardia. Arch Pediatr Adolesc Med. 2009;163(3): 268-274.

5. Doniger SJ, Sharieff GQ. Pediatric dysrhythmias. Pediatr Clin North Am. 2006;53(1):85-105, vi.

6. Mavroudis C, Deal BJ, Backer CL, Tsao S. Arrhythmia surgery in patients with and without congenital heart disease. Ann Thorac Surg. 2008;86(3):857-868. 

7. Wang PJ, Estes NAM III. Supraventricular tachycardia. Circulation. 2002;106(25):e206-e208.

8. Buttaro TM, Trybulski J, Bailey PP, Sandberg-Cook J. Primary Care: A Collaborative Practice. 3rd ed. St. Louis, MO: Mosby Elsevier; 2008.

9. Wen ZC, Chen SA, Tai CT, et al. Electrophysiological mechanisms and determinants of vagal maneuvers for termination of paroxysmal supraventricular tachycardia. Circulation.1998;98(24):2716-2723.

10. Julian MR. Treatment of paroxysmal supraventricular tachycardia using instrument-assisted manipulation of the fourth rib: a 6-year case study. J Manipulative Physiol Ther. 2008;31(5):389-391.

11. Calkins H, Kumar VKA, Francis J. Radiofrequency catheter ablation of supraventricular tachycardia. Indian Pacing Electrophysiol J. 2002;2(2):45-49.

12. Nakagawa H, Jackman WM. Catheter ablation of paroxysmal supraventricular tachycardia. Circulation. 2007;116(21):2465-2478.

13. Kugler JD, Danford DA, Houston K, Felix G; Pediatric Radiofrequency Ablation Registry of the Pediatric Electrophysiology Society. Pediatric radiofrequency catheter ablation registry success, fluoroscopy time, and complication rate for supraventricular tachycardia: comparison of early and recent eras. J Cardiovasc Electrophysiol. 2002;13(4):336-341.

14. Chun TU, Van Hare GF. Advances in the approach to treatment of supraventricular tachycardia in the pediatric population. Curr Cardiol Rep. 2004; 6(5):322-326.

15. Friedman PL, Dubuc M, Green MS, et al. Catheter cryoablation of supraventricular tachycardia: results of the multicenter prospective “frosty” trial. Heart Rhythm. 2004;1(2):129-138.

16. Bosen DM. Atrio-ventricular nodal reentry tachycardia in children. Dimens Crit Care Nurs. 2002; 21(4):134-139.

17. Children’s Hospitals and Clinics of Minnesota. Patient and family education: supraventricular tachycardia (2009). www.childrensmn.org/Manuals/PFS/Condill/018303.pdf. Accessed January 26, 2010.

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Michele Bednarzyk, DNP, FNP-BC, Nancy Snober, BA, BSN, FNP-S

A 6-year-old girl was brought by her parents to the emergency department (ED) with an elevated heart rate. According to the parents, the girl was carrying her younger sister when they both fell, landing on their buttocks. The child told them that her heart was beating fast, and the parents said she appeared to be on the verge of fainting.

They stated that their daughter was healthy and active; they denied previous episodes of shortness of breath, headache, weakness, tachycardia, syncope, or fatigue with exercise. Her caffeine intake, they claimed, was limited to one small cup of soda they allowed her each week.

Initial evaluation in the ED revealed an anxious child with tachycardia and shortness of breath. She presented with a temperature of 98.3°F (36.8°C); pulse, 210 beats/min; respirations, 33 breaths/min; blood pressure, 100/72 mm Hg; weight, 78 lb; height, 45 in; and BMI, 27.1. ECG revealed a heart rate exceeding 210 beats/min, and a pediatric cardiologist made a diagnosis of supraventricular tachycardia (SVT).

The pediatric cardiologist prescribed an adenosine IV drip, which successfully stabilized the child’s heart to sinus rhythm. After three hours in the ED, the patient was discharged with a stable heart rate of 100 beats/min. (It is well known that heart rate regulation changes significantly during development; this is most obvious in higher basal rates in infants and children, compared with adults.1)

The parents were advised to administer atenolol 12.5 mg (one tablet) twice daily and to make a follow-up appointment with a pediatric electrophysiologist. (Although atenolol is not currently FDA approved for this use, a multicenter prospective randomized controlled trial comparing digoxin with beta-blockers for the treatment of SVT in children is presently under way.2)

At that appointment, the pediatric electrophysiologist provided information to the parents regarding the therapeutic options for SVT. The parents continued to administer atenolol to the child, as was deemed necessary until any accessory electrical pathway could be identified and, if so, an ablation procedure could be performed. They were uncertain how to proceed so long as their daughter experienced no recurrent episodes of SVT while receiving pharmacologic therapy.

However, six months after the initial episode, the child (then age 7) presented to the ED once again with recurrent SVT. The pediatric cardiologist ordered an adenosine IV drip, which resulted in successful conversion to sinus rhythm. The parents were instructed to increase the child’s atenolol dosage to 25 mg twice a day.

Six months later, after extensive research and consultation, the parents agreed to an ablation procedure in order to prevent further episodes of SVT. Upon their informed consent, the child was sent to a cardiac catheterization laboratory for an electrophysiology study (EPS), which confirmed the presence of an accessory pathway, as well as the diagnosis of atrioventricular reciprocating tachycardia (AVRT). The procedure was followed by radiofrequency catheter ablation to correct the 7-year-old patient’s accessory pathway–mediated reentry tachycardia.

Discussion
SVT, also known as paroxysmal supraventricular tachycardia (PSVT), is one of the most common symptomatic pediatric arrhythmias, affecting between one in 25,000 and one in 250 children.3 It is defined as rapid heart rhythm (140 to 240 beats/min) that is caused by the presence of additional electrical connections and/or congenital muscle fibers between the atrium and the ventricle or within the atrioventricular (AV) node that did not, for unknown reasons, separate completely during development.4 SVT can be triggered by physical or psychological stress automaticity.3

Approximately 50% of children with SVT present with a first episode before age 1. SVT usually occurs in early childhood, between ages 6 and 9.4 Almost 90% of pediatric patients with SVT are diagnosed with a reentry mechanism.3 The symptoms experienced may be resolved pharmacologically or by means of an invasive therapy. Serious sequelae associated with SVT include heart failure and cardiac arrest.

For children with rare and mildly symptomatic episodes in whom SVT is easily terminated, the SVT may not warrant treatment. However, it may be advisable to offer medical therapy or transcatheter ablation as therapeutic options for children with episodes that are difficult to terminate, occur frequently, or occur during participation in athletics.4

Pathophysiology
SVT generally presents as one of three types: AVRT, which is also known as Wolff-Parkinson-White syndrome; atrioventricular nodal reentry tachycardia (AVNRT); and automatic tachycardia (AT).

AVRT, the most common type of SVT, comprises about 90% of pediatric cases. It is defined by the presence of one or more accessory conduction pathways that are anatomically separated from the normal cardiac conduction system.5 AVRT may be orthodromic (that is, the arrhythmia circuit proceeds down the AV node and retrograde up the accessory conduction pathway) or antedromic (ie, proceeding down the accessory pathway and up the AV node5; see figure.6,7)

 

 

AVNRT, considered the second most common type of SVT in children, accounts for about 10% of pediatric cases. AVNRT is caused by an interaction between the two types of pathways within the AV node—one with a fast conduction time and a short refractory period, and the other with a slow conduction time and a long refractory period. AVNRT occurs when the antegrade conduction block in the fast pathway results in conduction over the slow pathway and back up the fast pathway, forming a microreentrant circuit.5

AT is the result of rapid depolarization from an automatic focus originating within the atria but outside the sinus node.3

Patient Presentation and History
The typical presentation of AVRT in children of school age includes palpitations, chest pain or tightness, dizziness, anxiety, decrease in exercise tolerance, easy fatigability, and/or shortness of breath.3 Onset is described as abrupt, while termination of SVT is described as slower because the catecholamine levels are typically elevated.4

The frequency and duration of SVT can vary greatly, from a few minutes to a few hours; it can occur as regularly as daily or as uncommonly as once or twice per year.4 Additionally, SVT symptoms can go unrecognized until a cardiac dysfunction develops. As for the patient in the case study, no apparent factor in her history was identified that may have induced SVT.

The differential diagnosis for SVT is broad, including sinus tachycardia, multifocal atrial tachycardia, and SVT with aberrancy.8 Additional considerations include stress, anxiety, hyperthyroidism, electrolyte abnormalities, and dehydration—any of which can present with a tachycardia response.4 Furthermore, clinicians are often unlikely to diagnose a child with any cardiac problem because chest pain is more commonly a presenting symptom of a pulmonary or musculoskeletal condition than a cardiac problem.3

Physical Examination
SVT can be diagnosed based on medical history and physical examination. During the physical examination, providers will assess the patient’s blood pressure and pulse, auscultate heart and lung sounds, assess the veins in the patient’s neck for different types of pulsations, and conduct cardiac maneuvers, including the Valsalva maneuver and carotid sinus massage.9,10

Laboratory Work-up and Diagnosis
Three specific tests help clinicians monitor and evaluate a patient’s conduction system. ECG is important to assess the heart rhythm both at baseline and when symptoms are occurring, if possible.3 Ambulatory ECG (ie, Holter monitoring, event recorders) record the patient’s heart rhythm on a continuous basis.

An EPS, which is performed to classify the mechanism of SVT, is conducted by inserting one or more electrocatheters into the heart by way of the femoral vein or other peripheral vessel.3 Pacing and sensing electrodes at the ends of the catheters record local intracardiac electrical activity and timing information, providing a detailed analysis of the heart’s electrical activity. The EPS is critical to determine the presence of one or more extra electrical pathways within the heart and to localize it by region.3,11 An ablation procedure may follow.

Management Options
SVT can be treated pharmacologically or nonpharmacologically. First-line pharmacologic options include certain beta-blockers (including atenolol and propranolol), digoxin, and calcium channel blockers. Second-line pharmacologic treatments include amiodarone, flecainide, and sotalol,4 all of which are contraindicated in children younger than 1 year because of these patients’ hemodynamic dependency on the heart and inability to generate stroke volume.3 Pharmacologic treatment of SVT is associated with a 68% success rate in children4 (see Table 14).

For children in whom pharmacologic treatment is ineffective, an ablation procedure may be performed. Radiofrequency catheter ablation is currently considered first-line therapy for AVRT and AVNRT.12 In this invasive procedure, intracardiac electrical mapping is performed and the initiating focus of the arrhythmia or the accessory electrical pathway that has been identified within the heart is destroyed by radiofrequency energy, delivered by electrocatheter. Ablations performed during the acute phase of SVT have a 95% success rate.3,13

Cryoablation is a relatively new treatment in which liquid nitrous oxide is used to cool the catheter to subfreezing temperatures, enabling it to destroy the myocardial tissue by freezing.3,14 The advantage of cryoablation is the option of reversible cooling, which allows the electrophysiologist to test the area first, confirming the accuracy of the apparent location accessory pathway.15

Noninvasive, nonpharmacologic interventions that increase the refractoriness of the AV node may be successful in terminating the tachyarrhythmia during episodes of SVT (see Table 23,9,13,16). They are used to terminate and diagnose tachydysrhythmias, increase parasympathetic tone, and slow conduction through the AV node.3

Patient Education
It is very important for health care providers to relieve parents’ and caregivers’ stress, anxiety, and uncertainty by educating them about the child’s cardiac condition of SVT. Information to convey include an understanding of what SVT is, what may cause it, what triggers the patient should avoid, what treatments are available and appropriate (including the maneuvers shown in Table 2), and what outcomes may be expected. An excellent patient/family education handout from the Children’s Hospitals and Clinics of Minnesota17 is available at www.childrensmn.org/Manuals/PFS/Condill/018303.pdf.

 

 

Follow-Up
Primary care providers must emphasize the importance of monitoring the patient’s progress, based on the severity of his or her SVT symptoms. The provider may choose to monitor the patient for a few weeks or a few months, assessing the frequency of arrhythmia recurrence and the heart rate, to adjust or substitute medications based on repeat ECG or Holter evaluations, and to plan further therapy, should the condition worsen.5

The Case Patient
One month after undergoing radiofrequency catheter ablation, the child presented to the pediatric cardiologist for follow-up. Since the procedure, she had been without any symptoms referable to the cardiovascular system. She denied experiencing any fast heart rate, palpitations, chest pain, shortness of breath, or dizziness. ECG demonstrated normal sinus rhythm.

Two years after undergoing radiofrequency ablation, the child is functioning at a normal activity level with no recurrence of SVT episodes.

Conclusion
The purpose of this case study is to improve primary care providers’ understanding of SVT in children and to convey the importance of identifying the condition in a timely manner and referring patients to a pediatric cardiologist or electrophysiologist. For most children affected by SVT, a regimen of pharmacologic and/or nonpharmacologic treatment—supported by detailed education for their parents and caregivers—can allow them to live a healthy, normal life.

A 6-year-old girl was brought by her parents to the emergency department (ED) with an elevated heart rate. According to the parents, the girl was carrying her younger sister when they both fell, landing on their buttocks. The child told them that her heart was beating fast, and the parents said she appeared to be on the verge of fainting.

They stated that their daughter was healthy and active; they denied previous episodes of shortness of breath, headache, weakness, tachycardia, syncope, or fatigue with exercise. Her caffeine intake, they claimed, was limited to one small cup of soda they allowed her each week.

Initial evaluation in the ED revealed an anxious child with tachycardia and shortness of breath. She presented with a temperature of 98.3°F (36.8°C); pulse, 210 beats/min; respirations, 33 breaths/min; blood pressure, 100/72 mm Hg; weight, 78 lb; height, 45 in; and BMI, 27.1. ECG revealed a heart rate exceeding 210 beats/min, and a pediatric cardiologist made a diagnosis of supraventricular tachycardia (SVT).

The pediatric cardiologist prescribed an adenosine IV drip, which successfully stabilized the child’s heart to sinus rhythm. After three hours in the ED, the patient was discharged with a stable heart rate of 100 beats/min. (It is well known that heart rate regulation changes significantly during development; this is most obvious in higher basal rates in infants and children, compared with adults.1)

The parents were advised to administer atenolol 12.5 mg (one tablet) twice daily and to make a follow-up appointment with a pediatric electrophysiologist. (Although atenolol is not currently FDA approved for this use, a multicenter prospective randomized controlled trial comparing digoxin with beta-blockers for the treatment of SVT in children is presently under way.2)

At that appointment, the pediatric electrophysiologist provided information to the parents regarding the therapeutic options for SVT. The parents continued to administer atenolol to the child, as was deemed necessary until any accessory electrical pathway could be identified and, if so, an ablation procedure could be performed. They were uncertain how to proceed so long as their daughter experienced no recurrent episodes of SVT while receiving pharmacologic therapy.

However, six months after the initial episode, the child (then age 7) presented to the ED once again with recurrent SVT. The pediatric cardiologist ordered an adenosine IV drip, which resulted in successful conversion to sinus rhythm. The parents were instructed to increase the child’s atenolol dosage to 25 mg twice a day.

Six months later, after extensive research and consultation, the parents agreed to an ablation procedure in order to prevent further episodes of SVT. Upon their informed consent, the child was sent to a cardiac catheterization laboratory for an electrophysiology study (EPS), which confirmed the presence of an accessory pathway, as well as the diagnosis of atrioventricular reciprocating tachycardia (AVRT). The procedure was followed by radiofrequency catheter ablation to correct the 7-year-old patient’s accessory pathway–mediated reentry tachycardia.

Discussion
SVT, also known as paroxysmal supraventricular tachycardia (PSVT), is one of the most common symptomatic pediatric arrhythmias, affecting between one in 25,000 and one in 250 children.3 It is defined as rapid heart rhythm (140 to 240 beats/min) that is caused by the presence of additional electrical connections and/or congenital muscle fibers between the atrium and the ventricle or within the atrioventricular (AV) node that did not, for unknown reasons, separate completely during development.4 SVT can be triggered by physical or psychological stress automaticity.3

Approximately 50% of children with SVT present with a first episode before age 1. SVT usually occurs in early childhood, between ages 6 and 9.4 Almost 90% of pediatric patients with SVT are diagnosed with a reentry mechanism.3 The symptoms experienced may be resolved pharmacologically or by means of an invasive therapy. Serious sequelae associated with SVT include heart failure and cardiac arrest.

For children with rare and mildly symptomatic episodes in whom SVT is easily terminated, the SVT may not warrant treatment. However, it may be advisable to offer medical therapy or transcatheter ablation as therapeutic options for children with episodes that are difficult to terminate, occur frequently, or occur during participation in athletics.4

Pathophysiology
SVT generally presents as one of three types: AVRT, which is also known as Wolff-Parkinson-White syndrome; atrioventricular nodal reentry tachycardia (AVNRT); and automatic tachycardia (AT).

AVRT, the most common type of SVT, comprises about 90% of pediatric cases. It is defined by the presence of one or more accessory conduction pathways that are anatomically separated from the normal cardiac conduction system.5 AVRT may be orthodromic (that is, the arrhythmia circuit proceeds down the AV node and retrograde up the accessory conduction pathway) or antedromic (ie, proceeding down the accessory pathway and up the AV node5; see figure.6,7)

 

 

AVNRT, considered the second most common type of SVT in children, accounts for about 10% of pediatric cases. AVNRT is caused by an interaction between the two types of pathways within the AV node—one with a fast conduction time and a short refractory period, and the other with a slow conduction time and a long refractory period. AVNRT occurs when the antegrade conduction block in the fast pathway results in conduction over the slow pathway and back up the fast pathway, forming a microreentrant circuit.5

AT is the result of rapid depolarization from an automatic focus originating within the atria but outside the sinus node.3

Patient Presentation and History
The typical presentation of AVRT in children of school age includes palpitations, chest pain or tightness, dizziness, anxiety, decrease in exercise tolerance, easy fatigability, and/or shortness of breath.3 Onset is described as abrupt, while termination of SVT is described as slower because the catecholamine levels are typically elevated.4

The frequency and duration of SVT can vary greatly, from a few minutes to a few hours; it can occur as regularly as daily or as uncommonly as once or twice per year.4 Additionally, SVT symptoms can go unrecognized until a cardiac dysfunction develops. As for the patient in the case study, no apparent factor in her history was identified that may have induced SVT.

The differential diagnosis for SVT is broad, including sinus tachycardia, multifocal atrial tachycardia, and SVT with aberrancy.8 Additional considerations include stress, anxiety, hyperthyroidism, electrolyte abnormalities, and dehydration—any of which can present with a tachycardia response.4 Furthermore, clinicians are often unlikely to diagnose a child with any cardiac problem because chest pain is more commonly a presenting symptom of a pulmonary or musculoskeletal condition than a cardiac problem.3

Physical Examination
SVT can be diagnosed based on medical history and physical examination. During the physical examination, providers will assess the patient’s blood pressure and pulse, auscultate heart and lung sounds, assess the veins in the patient’s neck for different types of pulsations, and conduct cardiac maneuvers, including the Valsalva maneuver and carotid sinus massage.9,10

Laboratory Work-up and Diagnosis
Three specific tests help clinicians monitor and evaluate a patient’s conduction system. ECG is important to assess the heart rhythm both at baseline and when symptoms are occurring, if possible.3 Ambulatory ECG (ie, Holter monitoring, event recorders) record the patient’s heart rhythm on a continuous basis.

An EPS, which is performed to classify the mechanism of SVT, is conducted by inserting one or more electrocatheters into the heart by way of the femoral vein or other peripheral vessel.3 Pacing and sensing electrodes at the ends of the catheters record local intracardiac electrical activity and timing information, providing a detailed analysis of the heart’s electrical activity. The EPS is critical to determine the presence of one or more extra electrical pathways within the heart and to localize it by region.3,11 An ablation procedure may follow.

Management Options
SVT can be treated pharmacologically or nonpharmacologically. First-line pharmacologic options include certain beta-blockers (including atenolol and propranolol), digoxin, and calcium channel blockers. Second-line pharmacologic treatments include amiodarone, flecainide, and sotalol,4 all of which are contraindicated in children younger than 1 year because of these patients’ hemodynamic dependency on the heart and inability to generate stroke volume.3 Pharmacologic treatment of SVT is associated with a 68% success rate in children4 (see Table 14).

For children in whom pharmacologic treatment is ineffective, an ablation procedure may be performed. Radiofrequency catheter ablation is currently considered first-line therapy for AVRT and AVNRT.12 In this invasive procedure, intracardiac electrical mapping is performed and the initiating focus of the arrhythmia or the accessory electrical pathway that has been identified within the heart is destroyed by radiofrequency energy, delivered by electrocatheter. Ablations performed during the acute phase of SVT have a 95% success rate.3,13

Cryoablation is a relatively new treatment in which liquid nitrous oxide is used to cool the catheter to subfreezing temperatures, enabling it to destroy the myocardial tissue by freezing.3,14 The advantage of cryoablation is the option of reversible cooling, which allows the electrophysiologist to test the area first, confirming the accuracy of the apparent location accessory pathway.15

Noninvasive, nonpharmacologic interventions that increase the refractoriness of the AV node may be successful in terminating the tachyarrhythmia during episodes of SVT (see Table 23,9,13,16). They are used to terminate and diagnose tachydysrhythmias, increase parasympathetic tone, and slow conduction through the AV node.3

Patient Education
It is very important for health care providers to relieve parents’ and caregivers’ stress, anxiety, and uncertainty by educating them about the child’s cardiac condition of SVT. Information to convey include an understanding of what SVT is, what may cause it, what triggers the patient should avoid, what treatments are available and appropriate (including the maneuvers shown in Table 2), and what outcomes may be expected. An excellent patient/family education handout from the Children’s Hospitals and Clinics of Minnesota17 is available at www.childrensmn.org/Manuals/PFS/Condill/018303.pdf.

 

 

Follow-Up
Primary care providers must emphasize the importance of monitoring the patient’s progress, based on the severity of his or her SVT symptoms. The provider may choose to monitor the patient for a few weeks or a few months, assessing the frequency of arrhythmia recurrence and the heart rate, to adjust or substitute medications based on repeat ECG or Holter evaluations, and to plan further therapy, should the condition worsen.5

The Case Patient
One month after undergoing radiofrequency catheter ablation, the child presented to the pediatric cardiologist for follow-up. Since the procedure, she had been without any symptoms referable to the cardiovascular system. She denied experiencing any fast heart rate, palpitations, chest pain, shortness of breath, or dizziness. ECG demonstrated normal sinus rhythm.

Two years after undergoing radiofrequency ablation, the child is functioning at a normal activity level with no recurrence of SVT episodes.

Conclusion
The purpose of this case study is to improve primary care providers’ understanding of SVT in children and to convey the importance of identifying the condition in a timely manner and referring patients to a pediatric cardiologist or electrophysiologist. For most children affected by SVT, a regimen of pharmacologic and/or nonpharmacologic treatment—supported by detailed education for their parents and caregivers—can allow them to live a healthy, normal life.

References

1. Kudielka BM, Buske-Kirschbaum A, Hellhammer DH, Kirschbaum C. Differential heart rate reactivity and recovery after psychosocial stress (TSST) in healthy children, younger adults, and elderly adults: the impact of age and gender. Int J Behav Med. 2004;11(2):116-121.

 2. Multicenter Study of Antiarrhythmic Medications for Treatment of Infants With Supraventricular Tachycardia. www.clinicaltrials.gov/ct2/results?term=NCT00390546. Accessed January 26, 2010.

3. Schlechte EA, Boramanand N, Funk M. Supraventricular tachycardia in the pediatric primary care setting: age-related presentation, diagnosis, and management. J Pediatr Health Care. 2008;22(5): 289-299.

4. Salerno JC, Seslar SP. Supraventricular tachycardia. Arch Pediatr Adolesc Med. 2009;163(3): 268-274.

5. Doniger SJ, Sharieff GQ. Pediatric dysrhythmias. Pediatr Clin North Am. 2006;53(1):85-105, vi.

6. Mavroudis C, Deal BJ, Backer CL, Tsao S. Arrhythmia surgery in patients with and without congenital heart disease. Ann Thorac Surg. 2008;86(3):857-868. 

7. Wang PJ, Estes NAM III. Supraventricular tachycardia. Circulation. 2002;106(25):e206-e208.

8. Buttaro TM, Trybulski J, Bailey PP, Sandberg-Cook J. Primary Care: A Collaborative Practice. 3rd ed. St. Louis, MO: Mosby Elsevier; 2008.

9. Wen ZC, Chen SA, Tai CT, et al. Electrophysiological mechanisms and determinants of vagal maneuvers for termination of paroxysmal supraventricular tachycardia. Circulation.1998;98(24):2716-2723.

10. Julian MR. Treatment of paroxysmal supraventricular tachycardia using instrument-assisted manipulation of the fourth rib: a 6-year case study. J Manipulative Physiol Ther. 2008;31(5):389-391.

11. Calkins H, Kumar VKA, Francis J. Radiofrequency catheter ablation of supraventricular tachycardia. Indian Pacing Electrophysiol J. 2002;2(2):45-49.

12. Nakagawa H, Jackman WM. Catheter ablation of paroxysmal supraventricular tachycardia. Circulation. 2007;116(21):2465-2478.

13. Kugler JD, Danford DA, Houston K, Felix G; Pediatric Radiofrequency Ablation Registry of the Pediatric Electrophysiology Society. Pediatric radiofrequency catheter ablation registry success, fluoroscopy time, and complication rate for supraventricular tachycardia: comparison of early and recent eras. J Cardiovasc Electrophysiol. 2002;13(4):336-341.

14. Chun TU, Van Hare GF. Advances in the approach to treatment of supraventricular tachycardia in the pediatric population. Curr Cardiol Rep. 2004; 6(5):322-326.

15. Friedman PL, Dubuc M, Green MS, et al. Catheter cryoablation of supraventricular tachycardia: results of the multicenter prospective “frosty” trial. Heart Rhythm. 2004;1(2):129-138.

16. Bosen DM. Atrio-ventricular nodal reentry tachycardia in children. Dimens Crit Care Nurs. 2002; 21(4):134-139.

17. Children’s Hospitals and Clinics of Minnesota. Patient and family education: supraventricular tachycardia (2009). www.childrensmn.org/Manuals/PFS/Condill/018303.pdf. Accessed January 26, 2010.

References

1. Kudielka BM, Buske-Kirschbaum A, Hellhammer DH, Kirschbaum C. Differential heart rate reactivity and recovery after psychosocial stress (TSST) in healthy children, younger adults, and elderly adults: the impact of age and gender. Int J Behav Med. 2004;11(2):116-121.

 2. Multicenter Study of Antiarrhythmic Medications for Treatment of Infants With Supraventricular Tachycardia. www.clinicaltrials.gov/ct2/results?term=NCT00390546. Accessed January 26, 2010.

3. Schlechte EA, Boramanand N, Funk M. Supraventricular tachycardia in the pediatric primary care setting: age-related presentation, diagnosis, and management. J Pediatr Health Care. 2008;22(5): 289-299.

4. Salerno JC, Seslar SP. Supraventricular tachycardia. Arch Pediatr Adolesc Med. 2009;163(3): 268-274.

5. Doniger SJ, Sharieff GQ. Pediatric dysrhythmias. Pediatr Clin North Am. 2006;53(1):85-105, vi.

6. Mavroudis C, Deal BJ, Backer CL, Tsao S. Arrhythmia surgery in patients with and without congenital heart disease. Ann Thorac Surg. 2008;86(3):857-868. 

7. Wang PJ, Estes NAM III. Supraventricular tachycardia. Circulation. 2002;106(25):e206-e208.

8. Buttaro TM, Trybulski J, Bailey PP, Sandberg-Cook J. Primary Care: A Collaborative Practice. 3rd ed. St. Louis, MO: Mosby Elsevier; 2008.

9. Wen ZC, Chen SA, Tai CT, et al. Electrophysiological mechanisms and determinants of vagal maneuvers for termination of paroxysmal supraventricular tachycardia. Circulation.1998;98(24):2716-2723.

10. Julian MR. Treatment of paroxysmal supraventricular tachycardia using instrument-assisted manipulation of the fourth rib: a 6-year case study. J Manipulative Physiol Ther. 2008;31(5):389-391.

11. Calkins H, Kumar VKA, Francis J. Radiofrequency catheter ablation of supraventricular tachycardia. Indian Pacing Electrophysiol J. 2002;2(2):45-49.

12. Nakagawa H, Jackman WM. Catheter ablation of paroxysmal supraventricular tachycardia. Circulation. 2007;116(21):2465-2478.

13. Kugler JD, Danford DA, Houston K, Felix G; Pediatric Radiofrequency Ablation Registry of the Pediatric Electrophysiology Society. Pediatric radiofrequency catheter ablation registry success, fluoroscopy time, and complication rate for supraventricular tachycardia: comparison of early and recent eras. J Cardiovasc Electrophysiol. 2002;13(4):336-341.

14. Chun TU, Van Hare GF. Advances in the approach to treatment of supraventricular tachycardia in the pediatric population. Curr Cardiol Rep. 2004; 6(5):322-326.

15. Friedman PL, Dubuc M, Green MS, et al. Catheter cryoablation of supraventricular tachycardia: results of the multicenter prospective “frosty” trial. Heart Rhythm. 2004;1(2):129-138.

16. Bosen DM. Atrio-ventricular nodal reentry tachycardia in children. Dimens Crit Care Nurs. 2002; 21(4):134-139.

17. Children’s Hospitals and Clinics of Minnesota. Patient and family education: supraventricular tachycardia (2009). www.childrensmn.org/Manuals/PFS/Condill/018303.pdf. Accessed January 26, 2010.

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Impetigo Update: New Challenges in the Era of Methicillin Resistance

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When a screening mammogram isn't enough...Undiagnosed heart condition leads to brain injury...more

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When a screening mammogram isn’t enough

A LUMP IN THE BREAST was discovered by a woman in her mid-40s. She underwent a screening (rather than a diagnostic) mammogram; no abnormalities were reported. An ultrasound ordered when the woman returned to her physician the following year noted problems. However, the report that was faxed to the physician never reached him, and no follow-up was done.

A year later, the patient made a follow-up appointment on her own initiative. A diagnostic mammogram and surgical biopsy revealed advanced cancer of the left breast. Vacuum-assisted core biopsy and clip localization performed shortly thereafter identified infiltrating ductal carcinoma.

The patient underwent neoadjuvant chemotherapy, resulting in complications and hospitalization. She subsequently had additional chemotherapy and radiation treatment.

PLAINTIFF’S CLAIM Immediate treatment would have improved the patient’s chances of cure.

THE DEFENSE No information about the defense is available.

VERDICT $575,000 settlement in South Carolina under the Federal Tort Claims Act, plus a $5,000 settlement with a hospital.

COMMENT A couple of lessons from this unfortunate case: Make sure a diagnostic (not screening) mammogram is ordered when evaluating a breast mass, and maintain a tickler file for critical lab and imaging results.

Insurance denied, appeal delayed, treatment of appendicitis deferred

ABDOMINAL PAIN SEVERE ENOUGH TO AWAKEN HER prompted a 48-year-old woman to contact her physician, who saw her 2 days later. The doctor performed an ultrasound examination, which ruled out gallstones, and ordered a computed tomography (CT) scan of the pelvis for the following day.

After the patient was injected with contrast medium for the scan, it was learned that her insurer had refused to approve the test. The patient’s pain persisted, and her doctor prescribed a pain reliever for a presumed pulled muscle. A week later, the doctor appealed the insurer’s denial of the CT scan in writing. The insurer responded that the scan would be approved if a fecal blood test proved negative.

Test results were submitted 4 days later; the CT scan was approved and performed a little more than 3 weeks after the initial order. The patient was diagnosed with appendicitis and underwent emergency surgery, including removal of part of her colon and bowel. Eight days in the hospital and a lengthy recovery followed.

PLAINTIFF’S CLAIM The physician was negligent in failing to follow up promptly on the insurer’s denial of approval for the CT scan.

DOCTOR’S DEFENSE The physician claimed that he had ordered the proper test in a timely manner; denial of approval by the insurer delayed treatment.

VERDICT $1.3 million Kentucky verdict against the physician after the plaintiff settled with the insurer.

COMMENT Ouch! This outcome is one we all fear—the insurer denying approval for a test and the physician bearing the brunt of a malpractice claim. When in doubt, get the test done and sort out the paperwork later.

Undiagnosed heart condition leads to brain injury

A 14-YEAR-OLD BOY collapsed while participating in a rodeo branding event. He was revived and taken to an emergency room (ER), where a physician evaluated him and admitted him to the hospital for overnight monitoring. The heart monitor recorded QT intervals suggesting long QT syndrome, a rare congenital condition that can lead to fainting and, occasionally, death from cardiac arrhythmias. The condition wasn’t diagnosed at the time.

A year and a half later, the patient collapsed again, this time during school wrestling practice. This more severe event resulted in anoxic brain injury, which left the patient disabled and in need of assistance with activities of daily living.

PLAINTIFF’S CLAIM The ER physician failed to diagnose congenital long QT syndrome. Proper diagnosis and treatment after the first incident could have prevented the second incident.

THE DEFENSE No information about the defense is available.

VERDICT Confidential Wyoming settlement, which included a provision that the defendant’s insurer provide inservice training on sudden arrhythmias and long QT syndrome for local doctors and other health care providers.

COMMENT Remember the zebras, as well as the horses, particularly when evaluating a patient for an unusual and potentially life-altering problem. Although syncope may be common in elders, such events in teenagers should prompt a comprehensive and meticulous evaluation.

 

 

Suicide follows antidepressant use

A 58-YEAR-OLD MAN with unexplained weight loss, diminished appetite, increased stress, edginess, and decreased libido sought care from his physician. The doctor diagnosed depression and prescribed escitalopram, 10 mg per day. He gave the patient a 5-week supply of sample medication with no warning literature or product information. Twenty days later, the patient hanged himself at home.

PLAINTIFF’S CLAIM The physician wrongly diagnosed depression; he shouldn’t have given the patient escitalopram because the US Food and Drug Administration (FDA) has issued an advisory concerning increased risk of suicide for adults treated with antidepressants. Neither the patient nor his family was informed about the possible side effects of escitalopram.

THE DEFENSE The diagnosis of depression was proper; nothing the defendants did or failed to do contributed to the patient’s death.

VERDICT Ohio defense verdict.

COMMENT Given the FDA’s black-box warning, it is imperative that we counsel and document concerning the risk of suicide when initiating therapy for depression.

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When a screening mammogram isn’t enough

A LUMP IN THE BREAST was discovered by a woman in her mid-40s. She underwent a screening (rather than a diagnostic) mammogram; no abnormalities were reported. An ultrasound ordered when the woman returned to her physician the following year noted problems. However, the report that was faxed to the physician never reached him, and no follow-up was done.

A year later, the patient made a follow-up appointment on her own initiative. A diagnostic mammogram and surgical biopsy revealed advanced cancer of the left breast. Vacuum-assisted core biopsy and clip localization performed shortly thereafter identified infiltrating ductal carcinoma.

The patient underwent neoadjuvant chemotherapy, resulting in complications and hospitalization. She subsequently had additional chemotherapy and radiation treatment.

PLAINTIFF’S CLAIM Immediate treatment would have improved the patient’s chances of cure.

THE DEFENSE No information about the defense is available.

VERDICT $575,000 settlement in South Carolina under the Federal Tort Claims Act, plus a $5,000 settlement with a hospital.

COMMENT A couple of lessons from this unfortunate case: Make sure a diagnostic (not screening) mammogram is ordered when evaluating a breast mass, and maintain a tickler file for critical lab and imaging results.

Insurance denied, appeal delayed, treatment of appendicitis deferred

ABDOMINAL PAIN SEVERE ENOUGH TO AWAKEN HER prompted a 48-year-old woman to contact her physician, who saw her 2 days later. The doctor performed an ultrasound examination, which ruled out gallstones, and ordered a computed tomography (CT) scan of the pelvis for the following day.

After the patient was injected with contrast medium for the scan, it was learned that her insurer had refused to approve the test. The patient’s pain persisted, and her doctor prescribed a pain reliever for a presumed pulled muscle. A week later, the doctor appealed the insurer’s denial of the CT scan in writing. The insurer responded that the scan would be approved if a fecal blood test proved negative.

Test results were submitted 4 days later; the CT scan was approved and performed a little more than 3 weeks after the initial order. The patient was diagnosed with appendicitis and underwent emergency surgery, including removal of part of her colon and bowel. Eight days in the hospital and a lengthy recovery followed.

PLAINTIFF’S CLAIM The physician was negligent in failing to follow up promptly on the insurer’s denial of approval for the CT scan.

DOCTOR’S DEFENSE The physician claimed that he had ordered the proper test in a timely manner; denial of approval by the insurer delayed treatment.

VERDICT $1.3 million Kentucky verdict against the physician after the plaintiff settled with the insurer.

COMMENT Ouch! This outcome is one we all fear—the insurer denying approval for a test and the physician bearing the brunt of a malpractice claim. When in doubt, get the test done and sort out the paperwork later.

Undiagnosed heart condition leads to brain injury

A 14-YEAR-OLD BOY collapsed while participating in a rodeo branding event. He was revived and taken to an emergency room (ER), where a physician evaluated him and admitted him to the hospital for overnight monitoring. The heart monitor recorded QT intervals suggesting long QT syndrome, a rare congenital condition that can lead to fainting and, occasionally, death from cardiac arrhythmias. The condition wasn’t diagnosed at the time.

A year and a half later, the patient collapsed again, this time during school wrestling practice. This more severe event resulted in anoxic brain injury, which left the patient disabled and in need of assistance with activities of daily living.

PLAINTIFF’S CLAIM The ER physician failed to diagnose congenital long QT syndrome. Proper diagnosis and treatment after the first incident could have prevented the second incident.

THE DEFENSE No information about the defense is available.

VERDICT Confidential Wyoming settlement, which included a provision that the defendant’s insurer provide inservice training on sudden arrhythmias and long QT syndrome for local doctors and other health care providers.

COMMENT Remember the zebras, as well as the horses, particularly when evaluating a patient for an unusual and potentially life-altering problem. Although syncope may be common in elders, such events in teenagers should prompt a comprehensive and meticulous evaluation.

 

 

Suicide follows antidepressant use

A 58-YEAR-OLD MAN with unexplained weight loss, diminished appetite, increased stress, edginess, and decreased libido sought care from his physician. The doctor diagnosed depression and prescribed escitalopram, 10 mg per day. He gave the patient a 5-week supply of sample medication with no warning literature or product information. Twenty days later, the patient hanged himself at home.

PLAINTIFF’S CLAIM The physician wrongly diagnosed depression; he shouldn’t have given the patient escitalopram because the US Food and Drug Administration (FDA) has issued an advisory concerning increased risk of suicide for adults treated with antidepressants. Neither the patient nor his family was informed about the possible side effects of escitalopram.

THE DEFENSE The diagnosis of depression was proper; nothing the defendants did or failed to do contributed to the patient’s death.

VERDICT Ohio defense verdict.

COMMENT Given the FDA’s black-box warning, it is imperative that we counsel and document concerning the risk of suicide when initiating therapy for depression.

When a screening mammogram isn’t enough

A LUMP IN THE BREAST was discovered by a woman in her mid-40s. She underwent a screening (rather than a diagnostic) mammogram; no abnormalities were reported. An ultrasound ordered when the woman returned to her physician the following year noted problems. However, the report that was faxed to the physician never reached him, and no follow-up was done.

A year later, the patient made a follow-up appointment on her own initiative. A diagnostic mammogram and surgical biopsy revealed advanced cancer of the left breast. Vacuum-assisted core biopsy and clip localization performed shortly thereafter identified infiltrating ductal carcinoma.

The patient underwent neoadjuvant chemotherapy, resulting in complications and hospitalization. She subsequently had additional chemotherapy and radiation treatment.

PLAINTIFF’S CLAIM Immediate treatment would have improved the patient’s chances of cure.

THE DEFENSE No information about the defense is available.

VERDICT $575,000 settlement in South Carolina under the Federal Tort Claims Act, plus a $5,000 settlement with a hospital.

COMMENT A couple of lessons from this unfortunate case: Make sure a diagnostic (not screening) mammogram is ordered when evaluating a breast mass, and maintain a tickler file for critical lab and imaging results.

Insurance denied, appeal delayed, treatment of appendicitis deferred

ABDOMINAL PAIN SEVERE ENOUGH TO AWAKEN HER prompted a 48-year-old woman to contact her physician, who saw her 2 days later. The doctor performed an ultrasound examination, which ruled out gallstones, and ordered a computed tomography (CT) scan of the pelvis for the following day.

After the patient was injected with contrast medium for the scan, it was learned that her insurer had refused to approve the test. The patient’s pain persisted, and her doctor prescribed a pain reliever for a presumed pulled muscle. A week later, the doctor appealed the insurer’s denial of the CT scan in writing. The insurer responded that the scan would be approved if a fecal blood test proved negative.

Test results were submitted 4 days later; the CT scan was approved and performed a little more than 3 weeks after the initial order. The patient was diagnosed with appendicitis and underwent emergency surgery, including removal of part of her colon and bowel. Eight days in the hospital and a lengthy recovery followed.

PLAINTIFF’S CLAIM The physician was negligent in failing to follow up promptly on the insurer’s denial of approval for the CT scan.

DOCTOR’S DEFENSE The physician claimed that he had ordered the proper test in a timely manner; denial of approval by the insurer delayed treatment.

VERDICT $1.3 million Kentucky verdict against the physician after the plaintiff settled with the insurer.

COMMENT Ouch! This outcome is one we all fear—the insurer denying approval for a test and the physician bearing the brunt of a malpractice claim. When in doubt, get the test done and sort out the paperwork later.

Undiagnosed heart condition leads to brain injury

A 14-YEAR-OLD BOY collapsed while participating in a rodeo branding event. He was revived and taken to an emergency room (ER), where a physician evaluated him and admitted him to the hospital for overnight monitoring. The heart monitor recorded QT intervals suggesting long QT syndrome, a rare congenital condition that can lead to fainting and, occasionally, death from cardiac arrhythmias. The condition wasn’t diagnosed at the time.

A year and a half later, the patient collapsed again, this time during school wrestling practice. This more severe event resulted in anoxic brain injury, which left the patient disabled and in need of assistance with activities of daily living.

PLAINTIFF’S CLAIM The ER physician failed to diagnose congenital long QT syndrome. Proper diagnosis and treatment after the first incident could have prevented the second incident.

THE DEFENSE No information about the defense is available.

VERDICT Confidential Wyoming settlement, which included a provision that the defendant’s insurer provide inservice training on sudden arrhythmias and long QT syndrome for local doctors and other health care providers.

COMMENT Remember the zebras, as well as the horses, particularly when evaluating a patient for an unusual and potentially life-altering problem. Although syncope may be common in elders, such events in teenagers should prompt a comprehensive and meticulous evaluation.

 

 

Suicide follows antidepressant use

A 58-YEAR-OLD MAN with unexplained weight loss, diminished appetite, increased stress, edginess, and decreased libido sought care from his physician. The doctor diagnosed depression and prescribed escitalopram, 10 mg per day. He gave the patient a 5-week supply of sample medication with no warning literature or product information. Twenty days later, the patient hanged himself at home.

PLAINTIFF’S CLAIM The physician wrongly diagnosed depression; he shouldn’t have given the patient escitalopram because the US Food and Drug Administration (FDA) has issued an advisory concerning increased risk of suicide for adults treated with antidepressants. Neither the patient nor his family was informed about the possible side effects of escitalopram.

THE DEFENSE The diagnosis of depression was proper; nothing the defendants did or failed to do contributed to the patient’s death.

VERDICT Ohio defense verdict.

COMMENT Given the FDA’s black-box warning, it is imperative that we counsel and document concerning the risk of suicide when initiating therapy for depression.

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The Child With Persistent Hives

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[email protected]

Persistent hives, or chronic urticaria, can be challenging to diagnose, treat, and manage. This condition is also somewhat common—I see it often at Miami Children's Hospital.

Persistent hives are distinctive from an acute presentation because they typically last 6 weeks or longer. They are not only frustrating for physicians—the etiology is identified in only a minority of affected children, but this disease can significantly impair quality of life for patients and their families.

Infections are a common cause of persistent hives. Other conditions to consider in your differential diagnosis include drug and food allergies, physical urticaria (caused by exposure to heat or cold), autoimmune disease, erythema multiforme minor, and dermatographism. Dermatographism is a condition in which stroking or scratching the skin with a dull instrument causes a raised welt, or wheal, to appear because of increased mast cell activation. The skin generally appears pale in the center with a red flare on either side. A physical allergy causes this type of urticaria.

In conjunction with the physical examination, review all medications taken in the last 6 weeks, including but not limited to new agents. Also ask the patient and parents about the type of foods the child consumed within the last several weeks with regularity.

A long-acting antihistamine, with 24-hour coverage, can be helpful. For some children with persistent hives, you may need to think outside the box and prescribe both a short-acting and long-acting antihistamine. The short-acting agent can be used to control an acute presentation while the long-acting drug provides maintenance.

If the condition improves with antihistamines and the hives are not interfering with quality of life or sleep, then you should feel comfortable treating the child.

If antihistamine therapy is not helpful, the lesions are interfering with lifestyle or sleep, or the patient complains of swelling, it is appropriate to refer the child to a specialist for additional work-up. Swelling is often a presenting sign with chronic urticaria, and typically it is generalized or affects the hands or face. The swelling often makes the patient and family uncomfortable.

If you decide to order laboratory testing prior to a specialist referral, a complete blood count, an erythrocyte sedimentation rate assay, a liver function test, and thyroid studies can be useful. But you also can simply refer the patient to an allergist or immunologist, and we can order the testing.

In contrast, a food-specific immunoglobulin G test is not helpful for the assessment of a child with persistent hives. This laboratory assay should not be ordered because it only adds to the cost of the diagnosis without aiding in the clinical diagnosis.

If you are fortunate and can identify the cause of the chronic urticaria—which only occurs in 5%-20% of cases—it calls for strict avoidance. This is another aspect where persistent hives differ from an acute presentation, because the etiology of an acute condition is more frequently found and subsequently may be avoided by the child.

Also educate the patient that persistent hives can be daily or episodic. Again, if the patient is lucky, the lesions resolve in less than 1 year. However, inform the patient that—in some cases—the hives can persist for several years.

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[email protected]

Persistent hives, or chronic urticaria, can be challenging to diagnose, treat, and manage. This condition is also somewhat common—I see it often at Miami Children's Hospital.

Persistent hives are distinctive from an acute presentation because they typically last 6 weeks or longer. They are not only frustrating for physicians—the etiology is identified in only a minority of affected children, but this disease can significantly impair quality of life for patients and their families.

Infections are a common cause of persistent hives. Other conditions to consider in your differential diagnosis include drug and food allergies, physical urticaria (caused by exposure to heat or cold), autoimmune disease, erythema multiforme minor, and dermatographism. Dermatographism is a condition in which stroking or scratching the skin with a dull instrument causes a raised welt, or wheal, to appear because of increased mast cell activation. The skin generally appears pale in the center with a red flare on either side. A physical allergy causes this type of urticaria.

In conjunction with the physical examination, review all medications taken in the last 6 weeks, including but not limited to new agents. Also ask the patient and parents about the type of foods the child consumed within the last several weeks with regularity.

A long-acting antihistamine, with 24-hour coverage, can be helpful. For some children with persistent hives, you may need to think outside the box and prescribe both a short-acting and long-acting antihistamine. The short-acting agent can be used to control an acute presentation while the long-acting drug provides maintenance.

If the condition improves with antihistamines and the hives are not interfering with quality of life or sleep, then you should feel comfortable treating the child.

If antihistamine therapy is not helpful, the lesions are interfering with lifestyle or sleep, or the patient complains of swelling, it is appropriate to refer the child to a specialist for additional work-up. Swelling is often a presenting sign with chronic urticaria, and typically it is generalized or affects the hands or face. The swelling often makes the patient and family uncomfortable.

If you decide to order laboratory testing prior to a specialist referral, a complete blood count, an erythrocyte sedimentation rate assay, a liver function test, and thyroid studies can be useful. But you also can simply refer the patient to an allergist or immunologist, and we can order the testing.

In contrast, a food-specific immunoglobulin G test is not helpful for the assessment of a child with persistent hives. This laboratory assay should not be ordered because it only adds to the cost of the diagnosis without aiding in the clinical diagnosis.

If you are fortunate and can identify the cause of the chronic urticaria—which only occurs in 5%-20% of cases—it calls for strict avoidance. This is another aspect where persistent hives differ from an acute presentation, because the etiology of an acute condition is more frequently found and subsequently may be avoided by the child.

Also educate the patient that persistent hives can be daily or episodic. Again, if the patient is lucky, the lesions resolve in less than 1 year. However, inform the patient that—in some cases—the hives can persist for several years.

[email protected]

Persistent hives, or chronic urticaria, can be challenging to diagnose, treat, and manage. This condition is also somewhat common—I see it often at Miami Children's Hospital.

Persistent hives are distinctive from an acute presentation because they typically last 6 weeks or longer. They are not only frustrating for physicians—the etiology is identified in only a minority of affected children, but this disease can significantly impair quality of life for patients and their families.

Infections are a common cause of persistent hives. Other conditions to consider in your differential diagnosis include drug and food allergies, physical urticaria (caused by exposure to heat or cold), autoimmune disease, erythema multiforme minor, and dermatographism. Dermatographism is a condition in which stroking or scratching the skin with a dull instrument causes a raised welt, or wheal, to appear because of increased mast cell activation. The skin generally appears pale in the center with a red flare on either side. A physical allergy causes this type of urticaria.

In conjunction with the physical examination, review all medications taken in the last 6 weeks, including but not limited to new agents. Also ask the patient and parents about the type of foods the child consumed within the last several weeks with regularity.

A long-acting antihistamine, with 24-hour coverage, can be helpful. For some children with persistent hives, you may need to think outside the box and prescribe both a short-acting and long-acting antihistamine. The short-acting agent can be used to control an acute presentation while the long-acting drug provides maintenance.

If the condition improves with antihistamines and the hives are not interfering with quality of life or sleep, then you should feel comfortable treating the child.

If antihistamine therapy is not helpful, the lesions are interfering with lifestyle or sleep, or the patient complains of swelling, it is appropriate to refer the child to a specialist for additional work-up. Swelling is often a presenting sign with chronic urticaria, and typically it is generalized or affects the hands or face. The swelling often makes the patient and family uncomfortable.

If you decide to order laboratory testing prior to a specialist referral, a complete blood count, an erythrocyte sedimentation rate assay, a liver function test, and thyroid studies can be useful. But you also can simply refer the patient to an allergist or immunologist, and we can order the testing.

In contrast, a food-specific immunoglobulin G test is not helpful for the assessment of a child with persistent hives. This laboratory assay should not be ordered because it only adds to the cost of the diagnosis without aiding in the clinical diagnosis.

If you are fortunate and can identify the cause of the chronic urticaria—which only occurs in 5%-20% of cases—it calls for strict avoidance. This is another aspect where persistent hives differ from an acute presentation, because the etiology of an acute condition is more frequently found and subsequently may be avoided by the child.

Also educate the patient that persistent hives can be daily or episodic. Again, if the patient is lucky, the lesions resolve in less than 1 year. However, inform the patient that—in some cases—the hives can persist for several years.

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Pediatric VTE Surge Draws Skeptical Response

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In the wake of a study that showed a 70% spike in the rate of VTE in pediatric hospitals, pediatric hospitalists and others are calling for a deeper analysis of the data.

The seven-year, multicenter study measured 11,337 hospitalized patients under the age of 18. Researchers found the annual rate of VTE increased by 70%, to 58 cases from 34 cases per 10,000 (P<0.001) (Pediatrics 2009;124(4):1001-1008). Several pediatricians note that the increase looks outsized because there has been little research on the topic over the past decade. Those interviewed say they expect more research in the future to define the breadth of the problem and potential solutions.

“I don’t think we think there’s been a seven-fold increase,” says Janna Journeycake, MD, MSCS, director of the Hemophilia and Thrombosis Program at Children's Medical Center, University of Texas Southwestern Medical Center at Dallas. “It was there all along. We just didn’t know how to recognize it.”

Mark Shen, MD, medical director of hospital medicine at Dell Children’s Medical Center in Austin, Texas, and The Hospitalist's pediatric editor, attributes a large part of the study’s findings to more awareness of VTE in the pediatric community and increases in serious bone and joint infections that lead to more central lines, a risk factor for VTE. Dr. Shen also points out that as physicians learn more about pediatric VTE, it is expected that the rate of its incidence will increase. “Before, we wouldn’t look for signs of a clot unless there were physical signs of swelling, discomfort, or shortness of breath,” he adds. “Now we are much quicker to go and do an ultrasound or look for some kind of thromboembolism.”

Dr. Journeycake sees pediatric hospitalists as the vanguard in moving forward, as long as they stay vigilant to recognize the warning signs. “The job of the hospitalist is to recognize the certain medical conditions in which VTE are most likely,” she says. “They are going to be the most critically ill kids, the ones with deep-seated infection, such as osteomyelitis, mastoiditis. … Those are going to be children with central venous catheters. Hospitalists need to realize this complication exists.”

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In the wake of a study that showed a 70% spike in the rate of VTE in pediatric hospitals, pediatric hospitalists and others are calling for a deeper analysis of the data.

The seven-year, multicenter study measured 11,337 hospitalized patients under the age of 18. Researchers found the annual rate of VTE increased by 70%, to 58 cases from 34 cases per 10,000 (P<0.001) (Pediatrics 2009;124(4):1001-1008). Several pediatricians note that the increase looks outsized because there has been little research on the topic over the past decade. Those interviewed say they expect more research in the future to define the breadth of the problem and potential solutions.

“I don’t think we think there’s been a seven-fold increase,” says Janna Journeycake, MD, MSCS, director of the Hemophilia and Thrombosis Program at Children's Medical Center, University of Texas Southwestern Medical Center at Dallas. “It was there all along. We just didn’t know how to recognize it.”

Mark Shen, MD, medical director of hospital medicine at Dell Children’s Medical Center in Austin, Texas, and The Hospitalist's pediatric editor, attributes a large part of the study’s findings to more awareness of VTE in the pediatric community and increases in serious bone and joint infections that lead to more central lines, a risk factor for VTE. Dr. Shen also points out that as physicians learn more about pediatric VTE, it is expected that the rate of its incidence will increase. “Before, we wouldn’t look for signs of a clot unless there were physical signs of swelling, discomfort, or shortness of breath,” he adds. “Now we are much quicker to go and do an ultrasound or look for some kind of thromboembolism.”

Dr. Journeycake sees pediatric hospitalists as the vanguard in moving forward, as long as they stay vigilant to recognize the warning signs. “The job of the hospitalist is to recognize the certain medical conditions in which VTE are most likely,” she says. “They are going to be the most critically ill kids, the ones with deep-seated infection, such as osteomyelitis, mastoiditis. … Those are going to be children with central venous catheters. Hospitalists need to realize this complication exists.”

In the wake of a study that showed a 70% spike in the rate of VTE in pediatric hospitals, pediatric hospitalists and others are calling for a deeper analysis of the data.

The seven-year, multicenter study measured 11,337 hospitalized patients under the age of 18. Researchers found the annual rate of VTE increased by 70%, to 58 cases from 34 cases per 10,000 (P<0.001) (Pediatrics 2009;124(4):1001-1008). Several pediatricians note that the increase looks outsized because there has been little research on the topic over the past decade. Those interviewed say they expect more research in the future to define the breadth of the problem and potential solutions.

“I don’t think we think there’s been a seven-fold increase,” says Janna Journeycake, MD, MSCS, director of the Hemophilia and Thrombosis Program at Children's Medical Center, University of Texas Southwestern Medical Center at Dallas. “It was there all along. We just didn’t know how to recognize it.”

Mark Shen, MD, medical director of hospital medicine at Dell Children’s Medical Center in Austin, Texas, and The Hospitalist's pediatric editor, attributes a large part of the study’s findings to more awareness of VTE in the pediatric community and increases in serious bone and joint infections that lead to more central lines, a risk factor for VTE. Dr. Shen also points out that as physicians learn more about pediatric VTE, it is expected that the rate of its incidence will increase. “Before, we wouldn’t look for signs of a clot unless there were physical signs of swelling, discomfort, or shortness of breath,” he adds. “Now we are much quicker to go and do an ultrasound or look for some kind of thromboembolism.”

Dr. Journeycake sees pediatric hospitalists as the vanguard in moving forward, as long as they stay vigilant to recognize the warning signs. “The job of the hospitalist is to recognize the certain medical conditions in which VTE are most likely,” she says. “They are going to be the most critically ill kids, the ones with deep-seated infection, such as osteomyelitis, mastoiditis. … Those are going to be children with central venous catheters. Hospitalists need to realize this complication exists.”

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Prevention Prowess

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Three medical centers have been nationally recognized for innovative approaches to preventing DVT and its potentially fatal complications. Central to each of the prevention strategies is a risk assessment tool that is easy to use, built directly into routine care, and linked directly to guideline-recommended choices for prophylaxis.

The North American Thrombosis Forum (NATF), in coordination with the pharmaceutical company Eisai Inc., recognized the following centers with the first DVTeamCare Hospital Award:

  • The University of California at San Diego Medical Center was awarded as a representative of medical centers with more than 200 beds. The hospital embedded its VTE prevention protocol into admission, transfer, and perioperative order sets across all medical and surgical services, says Gregory A. Maynard, MD, chief of the division of hospital medicine. The protocol flags three levels of DVT risk, notes possible contraindications for a particular kind of patient, and presents a set of options for guideline-recommended prophylaxis. The protocol can be paper- or computer-based.
  •  

  • The Johns Hopkins Hospital in Baltimore, also awarded as a representative for medical centers with more than 200 beds, developed a mandatory computer-based decision support system to facilitate specialty-specific risk factor assessment and the application of risk-appropriate VTE prophylaxis.
  •  

  • The Washington, D.C., Veterans Affairs Medical Center won in the category representing medical centers with fewer than 200 beds. The hospital designed a seven-step process that walks providers through an evidence-based risk-factor assessment to determine appropriate thromboprophylactic therapy. 

 

The DVTeamCare Hospital Award reflects NATF's goal of enhancing thrombosis education, prevention, diagnosis, and treatment to improve patient outcomes, says NATF Executive Director Ilene Sussman, PhD.

Dr. Maynard and his UCSD colleagues have made their DVT prophylaxis toolkit available to other hospitalists wanting to lead similar efforts in their own hospital. The toolkit is posted both on the AHRQ and SHM Web sites.

"SHM and AHRQ should feel proud about this because we were one of the first places to do this successfully at such a high level," Dr. Maynard says. "We partnered with others and with SHM to build similar toolkits. SHM built VTE prevention collaboratives that enroll hospitalist leaders and mentor them through the process of VTE prevention performance improvement, tracking results longitudinally. Divya Shroff and her group in Washington, D.C., were enrolled in that VTE prevention collaborative. Their team won an award in VTE prevention by following the road map and by coming up with a good order set for DVT prevention that could be used in their VA hospital and in many other VAs across the country. I think that speaks to the strength of the concepts that we're using."

Each of the award-winning protocols will be presented at an NATF-sponsored program April 9 at Harvard Medical School in Boston. After the presentation, the winning protocols and implementation plans will be available at www.DVTeamCareAward.com to help other hospitals enhance their efforts to prevent DVT.

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Three medical centers have been nationally recognized for innovative approaches to preventing DVT and its potentially fatal complications. Central to each of the prevention strategies is a risk assessment tool that is easy to use, built directly into routine care, and linked directly to guideline-recommended choices for prophylaxis.

The North American Thrombosis Forum (NATF), in coordination with the pharmaceutical company Eisai Inc., recognized the following centers with the first DVTeamCare Hospital Award:

  • The University of California at San Diego Medical Center was awarded as a representative of medical centers with more than 200 beds. The hospital embedded its VTE prevention protocol into admission, transfer, and perioperative order sets across all medical and surgical services, says Gregory A. Maynard, MD, chief of the division of hospital medicine. The protocol flags three levels of DVT risk, notes possible contraindications for a particular kind of patient, and presents a set of options for guideline-recommended prophylaxis. The protocol can be paper- or computer-based.
  •  

  • The Johns Hopkins Hospital in Baltimore, also awarded as a representative for medical centers with more than 200 beds, developed a mandatory computer-based decision support system to facilitate specialty-specific risk factor assessment and the application of risk-appropriate VTE prophylaxis.
  •  

  • The Washington, D.C., Veterans Affairs Medical Center won in the category representing medical centers with fewer than 200 beds. The hospital designed a seven-step process that walks providers through an evidence-based risk-factor assessment to determine appropriate thromboprophylactic therapy. 

 

The DVTeamCare Hospital Award reflects NATF's goal of enhancing thrombosis education, prevention, diagnosis, and treatment to improve patient outcomes, says NATF Executive Director Ilene Sussman, PhD.

Dr. Maynard and his UCSD colleagues have made their DVT prophylaxis toolkit available to other hospitalists wanting to lead similar efforts in their own hospital. The toolkit is posted both on the AHRQ and SHM Web sites.

"SHM and AHRQ should feel proud about this because we were one of the first places to do this successfully at such a high level," Dr. Maynard says. "We partnered with others and with SHM to build similar toolkits. SHM built VTE prevention collaboratives that enroll hospitalist leaders and mentor them through the process of VTE prevention performance improvement, tracking results longitudinally. Divya Shroff and her group in Washington, D.C., were enrolled in that VTE prevention collaborative. Their team won an award in VTE prevention by following the road map and by coming up with a good order set for DVT prevention that could be used in their VA hospital and in many other VAs across the country. I think that speaks to the strength of the concepts that we're using."

Each of the award-winning protocols will be presented at an NATF-sponsored program April 9 at Harvard Medical School in Boston. After the presentation, the winning protocols and implementation plans will be available at www.DVTeamCareAward.com to help other hospitals enhance their efforts to prevent DVT.

Three medical centers have been nationally recognized for innovative approaches to preventing DVT and its potentially fatal complications. Central to each of the prevention strategies is a risk assessment tool that is easy to use, built directly into routine care, and linked directly to guideline-recommended choices for prophylaxis.

The North American Thrombosis Forum (NATF), in coordination with the pharmaceutical company Eisai Inc., recognized the following centers with the first DVTeamCare Hospital Award:

  • The University of California at San Diego Medical Center was awarded as a representative of medical centers with more than 200 beds. The hospital embedded its VTE prevention protocol into admission, transfer, and perioperative order sets across all medical and surgical services, says Gregory A. Maynard, MD, chief of the division of hospital medicine. The protocol flags three levels of DVT risk, notes possible contraindications for a particular kind of patient, and presents a set of options for guideline-recommended prophylaxis. The protocol can be paper- or computer-based.
  •  

  • The Johns Hopkins Hospital in Baltimore, also awarded as a representative for medical centers with more than 200 beds, developed a mandatory computer-based decision support system to facilitate specialty-specific risk factor assessment and the application of risk-appropriate VTE prophylaxis.
  •  

  • The Washington, D.C., Veterans Affairs Medical Center won in the category representing medical centers with fewer than 200 beds. The hospital designed a seven-step process that walks providers through an evidence-based risk-factor assessment to determine appropriate thromboprophylactic therapy. 

 

The DVTeamCare Hospital Award reflects NATF's goal of enhancing thrombosis education, prevention, diagnosis, and treatment to improve patient outcomes, says NATF Executive Director Ilene Sussman, PhD.

Dr. Maynard and his UCSD colleagues have made their DVT prophylaxis toolkit available to other hospitalists wanting to lead similar efforts in their own hospital. The toolkit is posted both on the AHRQ and SHM Web sites.

"SHM and AHRQ should feel proud about this because we were one of the first places to do this successfully at such a high level," Dr. Maynard says. "We partnered with others and with SHM to build similar toolkits. SHM built VTE prevention collaboratives that enroll hospitalist leaders and mentor them through the process of VTE prevention performance improvement, tracking results longitudinally. Divya Shroff and her group in Washington, D.C., were enrolled in that VTE prevention collaborative. Their team won an award in VTE prevention by following the road map and by coming up with a good order set for DVT prevention that could be used in their VA hospital and in many other VAs across the country. I think that speaks to the strength of the concepts that we're using."

Each of the award-winning protocols will be presented at an NATF-sponsored program April 9 at Harvard Medical School in Boston. After the presentation, the winning protocols and implementation plans will be available at www.DVTeamCareAward.com to help other hospitals enhance their efforts to prevent DVT.

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Injury Predictors After Inpatient Falls

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Predictors of serious injury among hospitalized patients evaluated for falls

An estimated 2% to 15% of all hospitalized patients experience at least one fall.1 Approximately 30% of such falls result in injury and up to 6% may be serious in nature.1, 2 These injuries can result in pain, functional impairment, disability, or even death, and can contribute to longer lengths of stay, increased health care costs, and nursing home placement.25 As a result, inpatient falls have become a major priority for hospital quality assurance programs, and hospital risk management departments have begun to target inpatient falls as a source of legal liability.13, 6, 7 Recently, the Centers for Medicare and Medicaid Services announced that it will no longer pay for preventable complications of hospitalizations, including falls and fall‐related injury.8

Much of the literature on falls comes from community and long‐term care settings, and only a few studies have investigated falls during acute care hospitalization.3, 9, 10 From these studies, risk factors for inpatient falls have been identified and various models have been developed to predict an individual patient's risk of falling. However, unlike in the community setting, interventions to prevent falls in the acute care setting have not proven to be beneficial.11, 12 Commonly used approaches including restraints, alarms, bracelets, or having a volunteer sit with high‐risk patients have not been found to be effective.13, 14 Only 1 study found a multicomponent care plan that targeted specific risk factors in older inpatients to be associated with a reduced relative risk of recorded falls.15 Given this dearth of consistent evidence for the prevention of falls in hospitalized inpatients, the American Geriatrics Society has identified this as a gap area for future research.16

There are also limited data regarding predictors of injury after inpatient falls. A few small studies have identified potential risk factors for sustaining an injury after a fall in acute care, such as age >75 years, altered mental status, increased comorbidities, visual impairment, falls in the bathroom, and admission to a geriatric psychiatry floor.2, 5, 17 However, to our knowledge, there are no studies that have identified potential characteristics of inpatients found immediately after a fall that predict an injury. Providers who assess inpatients who have fallen need guidance on how to identify those in need of further evaluation and testing. This study sought to quantify the types and severity of injuries resulting from inpatient falls and to identify predictors of injury after a fall among a cohort of patients who fell at an urban academic medical center.

Patients and Methods

Patient Population

The study population included all inpatients on 13 medical and surgical units who experienced a fall between January 1, 2006 and December 31, 2006, while hospitalized at an 1171‐bed urban academic medical center. Telemetry, intensive care, pediatric, psychiatric, rehabilitation, and obstetrics or gynecology units were excluded from this analysis; the patients on these units are special populations that are qualitatively different than other acute care patients and have a different set of risk factor for falls and predictors of fall‐related injury. The study was approved by the institutional review board of the Mount Sinai School of Medicine.

Data Collection

Inpatient falls were identified retrospectively by review of hospital incident reports, which are most often completed by the unit nurses. In our institution, all falls generate an incident report. Using a standardized abstraction form, patient characteristics, circumstances surrounding falls, and fall‐related injuries were collected from the reports.

Laboratory data for anemia (hemoglobin < 12.0 g/dL), low albumin (<3.5 g/dL), elevated creatinine (>1.5 mg/dL), prolonged partial thromboplastin time (>35 seconds), and elevated international normalized ratio (INR > 1.3), were extracted from the patient's computerized medical record, if available. Number of days from admission to the fall, length of stay to the nearest hundredth of a day, and discharge disposition were also recorded for each patient.

Results of all radiographic studies, including x‐ray, ultrasound, computed tomography (CT), and magnetic resonance imaging (MRI), performed within 2 weeks after the fall were obtained. The indication for the imaging study was assessed from the order given to the radiology department and from the patient's medical record. A positive finding on an imaging study was defined as evidence of intracranial hemorrhage, fracture, joint effusion, soft‐tissue swelling, or any other injury potentially caused by trauma. Fall‐related injury was defined as positive findings on any of these imaging studies that were performed as a result of the fall. Evaluation of fall‐related injuries was conducted by a reviewer blinded to the baseline patient characteristics and laboratory data.

Statistical Analyses

Baseline characteristics and risk factors of patients with and without fall‐related injuries were compared using the chi square test or Student t test as appropriate. Univariate and multivariate logistic regression were used to calculate adjusted odds ratios (ORs) for injury after an inpatient fall. The multivariate model was developed using a manual forward method. Prior research shows that patients with recurrent falls do so in the same manner and for the same reasons.2, 3, 17 Thus, analyses were performed including only the first fall episode as the outcome of interest. Analyses were performed with SPSS statistical software (SPSS Inc., Chicago, IL) using 2‐sided P values.

Results

During the study period, 513 inpatients sustained 636 falls at the Mount Sinai Medical Center. There were 54,257 admissions to the hospital with 322,670 total patient days during this time. Therefore the fall incidence rate was 1.97 falls per 1,000 patient days. Characteristics of inpatients who fell are shown in Table 1. Most patients had 1 fall episode; however, 95 patients (19%) fell multiple times (range, 2‐6 events). There were no significant differences between recurrent fallers and those who fell once with respect to baseline characteristics, injuries sustained, or discharge disposition.

Demographic Characteristics of Patients Who Sustained a Fall
CharacteristicNumber of Patients (n = 513) [number (%)]
  • NOTE: All values are given as number (%) except age, which is median (range).

Age (years)70 (21‐104)
Age >75 years202 (39)
Male gender255 (50)
Assessed at risk of falling
Yes378 (74)
No2 (5)
Unknown110 (21)
Number of falls
1418 (82)
278 (15)
310 (2)
44 (1)
52 (0.4)
61 (0.2)
Multiple falls95 (19)

Fall Circumstances

The majority of patients who fell (74%) had been assessed by the nursing staff as being at risk for falling prior to the event. Overall, most falls (73%) occurred on medical rather than surgical units. The units with the most falls were geriatrics, neurology, and general medicine. Details about circumstances surrounding the falls are shown in Table 2. In most instances (71%) patients were found on the floor after the fall while less than 8% of falls were witnessed. Approximately 12% of patients received sedatives within 4 hours of falling (40% opioids, 30% benzodiazepines, 16% zolpidem, and 14% other). Laboratory values at the time of fall revealed that 70% of patients who fell were anemic, 62% had low albumin, and 19% had an elevated creatinine. Almost 20% of the patients had a prolonged partial thromboplastin time (PTT) and 18% had an elevated INR.

Circumstances of First Inpatient Fall
CharacteristicNumber of Falls (n = 513) [number (%)]*
  • Abbreviation: benzos, benzodiazepines.

  • Percentages were rounded to nearest whole number and may not add exactly to 100%.

Location
Medical unit374 (73)
Surgical unit139 (27)
Time
Day shift (7:00 AM to 6:59 PM)225 (44)
Night shift (7:00 PM to 6:59 AM)282 (56)
Character of fall
Assisted to floor15 (3)
Fall alleged92 (18)
Fall witnessed39 (8)
Found on Floor363 (71)
Unknown4 (<1)
Fall‐related activity
Ambulation164 (32)
Bathroom122 (24)
Bed21 (4)
Chair19 (4)
Other/unknown187 (36)
Mental status
Oriented274 (53)
Confused151 (29)
Unknown88 (17)
Activity level ordered
Ambulatory246 (48)
Nonambulatory135 (26)
Unknown132 (26)
Siderails
Complete15 (3)
Partial352 (69)
None15 (3)
Unknown126 (25)
Environmental obstacle
None355 (69)
Wet20 (4)
Debris2 (<1)
Unknown136 (27)
Restraints
Yes3 (<1)
No374 (73)
Unknown136 (27)
Sedative use
Total64 (12)
Opioids28 (6)
Benzos21 (4)
Antipsychotics7 (1)
Other8 (2)
Evidence of trauma
Yes25 (5)
No285 (56)
Unknown203 (40)

The median number of days from patient admission until they fell was 4 days (range, 0‐134), with 70% of patients falling within the first week of admission. In general, there was no difference in fall rate by time of day, though slightly more falls (56%) occurred during the night shift (7 PM to 7 AM).

Fall‐related Outcomes

Twenty‐five patients (5%) had evidence of trauma on physical exam after the fall, including lacerations, swelling, and ecchymoses, as documented by the evaluating nurse. A total of 120 imaging procedures were ordered following the first fall; when all inpatient falls were included, 145 imaging procedures were ordered. Most imaging studies (87%) did not show significant findings. Among studies with positive findings, the most common abnormality was fracture, including 3 hip, 1 humeral, 1 vertebral, 1 nasal, and 1 rib fracture. Other injuries found on imaging studies included 1 subdural hematoma, 1 acute cerebral infarct, 2 soft‐tissue hematomas, and 2 knee effusions. The acute cerebral infarct was not considered to be a result of the fall. Additionally, 3 patients had soft‐tissue swelling noted on head CT and 1 had Foley catheter‐related trauma.

The average length of stay for the 513 inpatients who fell was 20 days (range, 7‐444) compared to 6 days for all patients admitted to the hospital during the same period. Among inpatients who fell, there was no statistical difference in length of stay between those who did and those who did not have a fall‐related injury found on imaging. More than one‐half (53%) of the patients who fell were discharged to home, 21% to rehabilitation facilities, 12% to nursing homes, and 9% died during the hospitalization.

Results of Univariate Analysis

Univariate predictors of injury after a fall are shown in Table 3. Patients having evidence of trauma indicated by the evaluating nurse after a fall had an increased risk for having an abnormal imaging study (OR = 14.7, P < 0.001). Having an activity level of ambulatory ordered by the provider (OR = 2.5, P = 0.09), falling during the night shift (OR = 2.5, P = 0.11), having ambulation as the fall‐related activity (OR = 2.2, P = 0.12), and older age (P = 0.19) all showed a trend toward higher rates of injury being found after a fall. There was no significant association between fall‐related injury and being an elderly patient (age > 75 years), sedative use, falling in the bathroom, or having an elevated PTT or INR.

Univariate Analysis of Predictors of Injury Being Found on Imaging Studies After Inpatient Falls
VariablePatients without injury (n = 497) [number (%)]Patients with injury (n = 16) [number (%)]ORP Value
  • Abbreviations: INR, international normalized ratio; OR, odds ratio; PTT, partial thromboplastin time.

Elderly195 (39)7 (44)1.20.72
Gender male245 (49)10 (63)1.70.30
Location surgical unit142 (29)6 (38)1.50.44
At risk of falling prior to event365 (73)13 (8)1.60.49
Protocol in place338 (68)11 (69)1.00.95
Activity level ambulatory235 (47)11 (69)2.50.09
Occurrence on night shift270 (54)12 (75)2.50.11
Restraint use3 (1)0 (0)  
Sedative within 4 hours61 (12)3 (19)1.60.44
Fall related to ambulation156 (31)8 (50)2.20.12
Evidence of trauma19 (4)6 (38)14.7<0.001
Prolonged PTT93 (19)5 (31)1.90.29
Elevated INR90 (18)3 (19)1.00.96
Anemia351 (71)9 (56)0.60.32
Elevated creatinine97 (20)2 (13)0.70.60
Low albumin309 (62)8 (50)1.60.58

Multivariate Predictors of Injury

In multivariate analysis, after adjusting for age and sex, evidence of trauma after a fall (OR = 24.6, P < 0.001) and having an activity level of ambulatory ordered by the provider (OR = 7.3, P = 0.01) were independent predictors of injury being found on imaging studies (Table 4). Analyses limited to the 120 patients who had imaging found that the association between evidence of trauma (OR = 6.22, P = 0.02) and having an activity level of ambulatory ordered (OR = 5.53, P = 0.04) remained statistically significant.

Multivariate Analysis of Predictors of Injury Being Found on Imaging Studies After Inpatient Fall
VariableAll Patients (n = 513)Patients with Imaging (n = 120)*
ORP ValueORP Value
  • Abbreviation: OR, odds ratio.

  • Since not every patient who fell had imaging, the analysis was repeated only including those patients who did have imaging studies.

Age1.030.171.0160.52
Gender3.190.112.8430.17
Evidence of trauma24.63<0.0016.220.02
Activity level ambulatory7.330.015.530.04

Discussion

Inpatient falls are common and result in significant patient morbidity and increased healthcare costs. Falls in the acute care setting have also proven to be difficult to prevent and as a result have become a priority for patient safety and hospital quality.

Our study confirms that a high percentage of patients with an initial fall will have recurrent falls.1 Additionally, the majority of patients in this cohort fell despite having been assessed as at risk for falling prior to the event. The types of injuries sustained after inpatient falls (eg, subdural hematoma, multiple fractures, joint effusions, other hematomas, and soft‐tissue swelling) are similar to those found by other authors.2, 3, 17, 18

In this study, inpatient falls were associated with an almost 2‐week increase in length of stay. Though we cannot say that this was directly due to falls, and an increased length of stay may just be a marker of severity of illness, this association warrants further study, perhaps with a matched control group of patients who did not fall, and has implications for healthcare cost containment.

We found that having evidence of trauma after a fall and having an activity level of ambulatory ordered by the provider were independent predictors of injury being found after an inpatient fall. It seems intuitive that patients who have physical evidence of trauma, such as lacerations or bruising, would be more likely to have an underlying injury. Clinically, this confirms that providers should have a high index of suspicion for injury being found on imaging studies in such patients. Similar findings have been noted in the emergency medicine literature that further support the validity of our findings.19

Less clear are the reasons for the observed association between having an activity level of ambulatory ordered and higher risk of injury after an inpatient fall. Prior studies have found that ambulatory inpatients are less likely to use assistive devices that they use at home while hospitalized and are less likely to call for help; these factors may contribute to falls.2, 3 However, the interpretation of this finding is limited by the fact that 26% of the patients who fell had an unknown activity level ordered.

Altered mental status, comorbidity, age > 75 years, visual impairment, falling in the bathroom, and being on a geriatric psychiatry floor have previously been found to be risk factors for sustaining an injury after an inpatient fall.2, 5, 17 Conversely, this study did not find altered mental status to be a significant predictor of injury. One reason may be that this was subjectively determined by the evaluating nurse and not by a standardized measure of cognitive impairment. Patients who are oriented may also be more likely to report unwitnessed falls and injuries than patients with altered mental status.3

There was also no association between age and fall‐related injury in our cohort. On univariate analysis, patients who were older in age were more likely to have an injury found after an inpatient fall but this was not statistically significant. Previous authors have suggested that today's inpatients are increasingly ill and may have risk factors for falls and injuries that are independent of age, such as multiple comorbid conditions or deconditioning.3

We hypothesized that patients who are anticoagulated and had an elevated INR or PTT would be more likely to sustain an injury. Anemic inpatients have also been found to be at increased risk of falls.20 We found no significant association between fall‐related injury being found on imaging studies and anemia, low albumin, elevated creatinine, prolonged PTT, or elevated INR. Not every patient who fell had these laboratory values available. However, even when only inpatients who fell and had laboratory tests were included in the analysis, there was still no association with fall‐related injury.

This study has several limitations. First, a low number of serious injuries was found on imaging studies after inpatient falls in this cohort; this limited the power of the study to identify predictors of fall‐related injury.

Second, fall‐related injury was defined as a positive finding on imaging studies within 2 weeks of an inpatient fall. Thus, some fall‐related injuries may have been missed in patients who did not have imaging. However, any patient who had a serious injury after a fall and remained hospitalized would likely have had symptoms such as pain or altered mental status that would have led to an imaging study. Moreover, the analysis was repeated including only inpatients who fell and had imaging, and the association between having evidence of trauma and having an activity level of ambulatory ordered and sustaining a fall‐related injury remained significant.

Third, we relied on hospital incident reports to identify inpatient falls. These reports yield a limited amount of information and may be inaccurate or incomplete. A recent study also raised concern that incident reports significantly underreport actual fall incidence.21 However, previous studies have found no indication that falls are underreported and suggest that incident reports are an established custom in hospital culture.1, 22 Medical staff are aware that administrators want to keep track of hospital fall rates for both quality improvement and documentation for risk management.1, 22 It is unlikely that severe falls or falls leading to serious injury are not reported. A different source of underreporting may actually be failure of patients to tell the medical team about an unwitnessed fall. Older patients may be concerned they will be placed in nursing homes and those with memory loss may forget to report a minor fall. Education of patients and family members could improve reporting of inpatient falls and further our understanding of contributing factors.

Finally, although the evaluation of fall‐related injuries was conducted by a blinded reviewer, the potential for bias does exist among even the best‐intentioned reviewers. Additionally, there may be some degree of variability within the reviewer's data abstraction.

This study adds valuable information about the epidemiology of inpatient falls at large, urban, tertiary‐care academic medical centers, including characteristics of patients who fell, circumstances surrounding falls, injuries sustained, and predictors of fall‐related injury found on imaging. Although additional research is essential to identify methods to effectively prevent inpatient falls, this study contributes to the limited data in this area, can guide providers who are evaluating inpatients who have fallen, and may be used to design future investigations. It is imperative that measures are identified to avoid the frequent adverse outcomes that result from inpatient falls. Insurance companies, hospital administrators, patients, and providers will be demanding that a safe environment be a key component of quality of care measures.

This study draws attention to the scope of the problem at our institution that is common to hospitals across the country. In our study, our academic medical center had a fall rate consistent with published reports, but new efforts have been focused on quality improvement in this area. An interdisciplinary fall prevention committee has been formed that includes physicians, nurses, patient care assistants, physical therapists, pharmacists, and representatives from information technology (IT). Currently, a program of a fall risk‐factor assessment with targeted interventions to reduce those risk factors is being developed for all high‐risk patients and will be piloted on inpatient units.

Acknowledgements

The authors thank Susan Emro, BS, Department of Health Policy, Susan Davis, MS, MPH, RN, CNAA, Department of Nursing, and Albert Siu, MD, MSPH, Brookdale Department of Geriatrics and Adult Development, for their review of this article. Author contributions were as followsconception and design: S.M.B, R.K., and T.M.; collection and assembly of data: S.M.B.; analysis and interpretation of the data: S.M.B, R.K., and J.W.; drafting of the article: S.M.B.; critical revision of the article for important intellectual content: R.K. and J.W.; final approval of the article: S.M.B, R.K., and J.W.; statistical expertise: J.W.; obtaining of funding: S.M.B.

References
  1. Halfon P,Eggli Y,Van Melle G,Vagnair A.Risk of falls for hospitalized patients: a predictive model based on routinely available data.J Clin Epidemiol.2001;54(12):12581266.
  2. Krauss MJ,Evanoff B,Hitcho E, et al.A case‐control study of patient, medication, and care‐related risk factors for inpatient falls.J Gen Intern Med.2005;20(2):116122.
  3. Hitcho EB,Krauss MJ,Birge S, et al.Characteristics and circumstances of falls in a hospital setting: a prospective analysis.J Gen Intern Med.2004;19(7):732739.
  4. Schwendimann R,Buhler H,De Geest S,Milisen K.Falls and consequent injuries in hospitalized patients: effects of an interdisciplinary falls prevention program.BMC Health Serv Res.2006;6:69.
  5. Bates DW,Pruess K,Souney P,Platt R.Serious falls in hospitalized patients: correlates and resource utilization.Am J Med.1995;99(2):137143.
  6. Gowdy M,Godfrey S.Using tools to assess and prevent inpatient falls.Jt Comm J Qual Saf.2003;29(7):363368.
  7. Nakai A,Akeda M,Kawabata I.Incidence and risk factors for inpatient falls in an academic acute‐care hospital.J Nippon Med Sch.2006;73(5):265270.
  8. Rosenthal MB.Nonpayment for performance? Medicare's new reimbursement rule.N Engl J Med.2007;357(16):15731575.
  9. Tinetti ME.Clinical practice. preventing falls in elderly persons.N Engl J Med.2003;348(1):4249.
  10. Capezuti E.Building the science of falls‐prevention research.J Am Geriatr Soc.2004;52(3):461462.
  11. Coussement J,De Paepe L,Schwendimann R,Denhaerynck K,Dejaeger E,Milisen K.Interventions for preventing falls in acute‐ and chronic‐care hospitals: a systematic review and meta‐analysis.J Am Geriatr Soc.2008;56(1):2936.
  12. Chang JT,Morton SC,Rubenstein LZ, et al.Interventions for the prevention of falls in older adults: systematic review and meta‐analysis of randomised clinical trials.BMJ.2004;328(7441):680.
  13. Vassallo M,Stockdale R,Wilkinson C, et al.Acceptability of fall prevention measures for hospital inpatients.Age Ageing.2004;33(4):400401.
  14. Giles LC,Bolch D,Rouvray R, et al.Can volunteer companions prevent falls among inpatients? A feasibility study using a pre‐post comparative design.BMC Geriatr.2006;6:11.
  15. Healey F,Monro A,Cockram A,Adams V,Heseltine D.Using targeted risk factor reduction to prevent falls in older in‐patients: a randomised controlled trial.Age Ageing.2004;33(4):390395.
  16. Oliver D.Prevention of falls in hospital inpatients: agendas for research and practice.Age Ageing.2004;33(4):328330.
  17. Fischer ID,Krauss MJ,Dunagan WC, et al.Patterns and predictors of inpatient falls and fall‐related injuries in a large academic hospital.Infect Control Hosp Epidemiol.2005;26(10):822827.
  18. Vassallo M,Vignaraja R,Sharma JC,Briggs R,Allen S.The relationship of falls to injury among hospital in‐patients.Int J Clin Pract.2005;59(1):1720.
  19. Haydel MJ,Preston CA,Mills TJ,Luber S,Blaudeau E,DeBlieux PM.Indications for computed tomography in patients with minor head injury.N Engl J Med.2000;343(2):100105.
  20. Dharmarajan TS,Avula S,Norkus EP.Anemia increases risk for falls in hospitalized older adults: an evaluation of falls in 362 hospitalized, ambulatory, long‐term care, and community patients.J Am Med Dir Assoc.2006;7(5):287293.
  21. Shorr RI,Mion LC,Chandler AM,Rosenblatt LC,Lynch D,Kessler LA.Improving the capture of fall events in hospitals: combining a service for evaluating inpatient falls with an incident report system.J Am Geriatr Soc.2008;56(4):701704.
  22. Evans SM,Berry JG,Smith BJ, et al.Attitudes and barriers to incident reporting: a collaborative hospital study.Qual Saf Health Care.2006;15(1):3943.
Article PDF
Issue
Journal of Hospital Medicine - 5(2)
Page Number
63-68
Legacy Keywords
fall prevention, injury, inpatient falls
Sections
Article PDF
Article PDF

An estimated 2% to 15% of all hospitalized patients experience at least one fall.1 Approximately 30% of such falls result in injury and up to 6% may be serious in nature.1, 2 These injuries can result in pain, functional impairment, disability, or even death, and can contribute to longer lengths of stay, increased health care costs, and nursing home placement.25 As a result, inpatient falls have become a major priority for hospital quality assurance programs, and hospital risk management departments have begun to target inpatient falls as a source of legal liability.13, 6, 7 Recently, the Centers for Medicare and Medicaid Services announced that it will no longer pay for preventable complications of hospitalizations, including falls and fall‐related injury.8

Much of the literature on falls comes from community and long‐term care settings, and only a few studies have investigated falls during acute care hospitalization.3, 9, 10 From these studies, risk factors for inpatient falls have been identified and various models have been developed to predict an individual patient's risk of falling. However, unlike in the community setting, interventions to prevent falls in the acute care setting have not proven to be beneficial.11, 12 Commonly used approaches including restraints, alarms, bracelets, or having a volunteer sit with high‐risk patients have not been found to be effective.13, 14 Only 1 study found a multicomponent care plan that targeted specific risk factors in older inpatients to be associated with a reduced relative risk of recorded falls.15 Given this dearth of consistent evidence for the prevention of falls in hospitalized inpatients, the American Geriatrics Society has identified this as a gap area for future research.16

There are also limited data regarding predictors of injury after inpatient falls. A few small studies have identified potential risk factors for sustaining an injury after a fall in acute care, such as age >75 years, altered mental status, increased comorbidities, visual impairment, falls in the bathroom, and admission to a geriatric psychiatry floor.2, 5, 17 However, to our knowledge, there are no studies that have identified potential characteristics of inpatients found immediately after a fall that predict an injury. Providers who assess inpatients who have fallen need guidance on how to identify those in need of further evaluation and testing. This study sought to quantify the types and severity of injuries resulting from inpatient falls and to identify predictors of injury after a fall among a cohort of patients who fell at an urban academic medical center.

Patients and Methods

Patient Population

The study population included all inpatients on 13 medical and surgical units who experienced a fall between January 1, 2006 and December 31, 2006, while hospitalized at an 1171‐bed urban academic medical center. Telemetry, intensive care, pediatric, psychiatric, rehabilitation, and obstetrics or gynecology units were excluded from this analysis; the patients on these units are special populations that are qualitatively different than other acute care patients and have a different set of risk factor for falls and predictors of fall‐related injury. The study was approved by the institutional review board of the Mount Sinai School of Medicine.

Data Collection

Inpatient falls were identified retrospectively by review of hospital incident reports, which are most often completed by the unit nurses. In our institution, all falls generate an incident report. Using a standardized abstraction form, patient characteristics, circumstances surrounding falls, and fall‐related injuries were collected from the reports.

Laboratory data for anemia (hemoglobin < 12.0 g/dL), low albumin (<3.5 g/dL), elevated creatinine (>1.5 mg/dL), prolonged partial thromboplastin time (>35 seconds), and elevated international normalized ratio (INR > 1.3), were extracted from the patient's computerized medical record, if available. Number of days from admission to the fall, length of stay to the nearest hundredth of a day, and discharge disposition were also recorded for each patient.

Results of all radiographic studies, including x‐ray, ultrasound, computed tomography (CT), and magnetic resonance imaging (MRI), performed within 2 weeks after the fall were obtained. The indication for the imaging study was assessed from the order given to the radiology department and from the patient's medical record. A positive finding on an imaging study was defined as evidence of intracranial hemorrhage, fracture, joint effusion, soft‐tissue swelling, or any other injury potentially caused by trauma. Fall‐related injury was defined as positive findings on any of these imaging studies that were performed as a result of the fall. Evaluation of fall‐related injuries was conducted by a reviewer blinded to the baseline patient characteristics and laboratory data.

Statistical Analyses

Baseline characteristics and risk factors of patients with and without fall‐related injuries were compared using the chi square test or Student t test as appropriate. Univariate and multivariate logistic regression were used to calculate adjusted odds ratios (ORs) for injury after an inpatient fall. The multivariate model was developed using a manual forward method. Prior research shows that patients with recurrent falls do so in the same manner and for the same reasons.2, 3, 17 Thus, analyses were performed including only the first fall episode as the outcome of interest. Analyses were performed with SPSS statistical software (SPSS Inc., Chicago, IL) using 2‐sided P values.

Results

During the study period, 513 inpatients sustained 636 falls at the Mount Sinai Medical Center. There were 54,257 admissions to the hospital with 322,670 total patient days during this time. Therefore the fall incidence rate was 1.97 falls per 1,000 patient days. Characteristics of inpatients who fell are shown in Table 1. Most patients had 1 fall episode; however, 95 patients (19%) fell multiple times (range, 2‐6 events). There were no significant differences between recurrent fallers and those who fell once with respect to baseline characteristics, injuries sustained, or discharge disposition.

Demographic Characteristics of Patients Who Sustained a Fall
CharacteristicNumber of Patients (n = 513) [number (%)]
  • NOTE: All values are given as number (%) except age, which is median (range).

Age (years)70 (21‐104)
Age >75 years202 (39)
Male gender255 (50)
Assessed at risk of falling
Yes378 (74)
No2 (5)
Unknown110 (21)
Number of falls
1418 (82)
278 (15)
310 (2)
44 (1)
52 (0.4)
61 (0.2)
Multiple falls95 (19)

Fall Circumstances

The majority of patients who fell (74%) had been assessed by the nursing staff as being at risk for falling prior to the event. Overall, most falls (73%) occurred on medical rather than surgical units. The units with the most falls were geriatrics, neurology, and general medicine. Details about circumstances surrounding the falls are shown in Table 2. In most instances (71%) patients were found on the floor after the fall while less than 8% of falls were witnessed. Approximately 12% of patients received sedatives within 4 hours of falling (40% opioids, 30% benzodiazepines, 16% zolpidem, and 14% other). Laboratory values at the time of fall revealed that 70% of patients who fell were anemic, 62% had low albumin, and 19% had an elevated creatinine. Almost 20% of the patients had a prolonged partial thromboplastin time (PTT) and 18% had an elevated INR.

Circumstances of First Inpatient Fall
CharacteristicNumber of Falls (n = 513) [number (%)]*
  • Abbreviation: benzos, benzodiazepines.

  • Percentages were rounded to nearest whole number and may not add exactly to 100%.

Location
Medical unit374 (73)
Surgical unit139 (27)
Time
Day shift (7:00 AM to 6:59 PM)225 (44)
Night shift (7:00 PM to 6:59 AM)282 (56)
Character of fall
Assisted to floor15 (3)
Fall alleged92 (18)
Fall witnessed39 (8)
Found on Floor363 (71)
Unknown4 (<1)
Fall‐related activity
Ambulation164 (32)
Bathroom122 (24)
Bed21 (4)
Chair19 (4)
Other/unknown187 (36)
Mental status
Oriented274 (53)
Confused151 (29)
Unknown88 (17)
Activity level ordered
Ambulatory246 (48)
Nonambulatory135 (26)
Unknown132 (26)
Siderails
Complete15 (3)
Partial352 (69)
None15 (3)
Unknown126 (25)
Environmental obstacle
None355 (69)
Wet20 (4)
Debris2 (<1)
Unknown136 (27)
Restraints
Yes3 (<1)
No374 (73)
Unknown136 (27)
Sedative use
Total64 (12)
Opioids28 (6)
Benzos21 (4)
Antipsychotics7 (1)
Other8 (2)
Evidence of trauma
Yes25 (5)
No285 (56)
Unknown203 (40)

The median number of days from patient admission until they fell was 4 days (range, 0‐134), with 70% of patients falling within the first week of admission. In general, there was no difference in fall rate by time of day, though slightly more falls (56%) occurred during the night shift (7 PM to 7 AM).

Fall‐related Outcomes

Twenty‐five patients (5%) had evidence of trauma on physical exam after the fall, including lacerations, swelling, and ecchymoses, as documented by the evaluating nurse. A total of 120 imaging procedures were ordered following the first fall; when all inpatient falls were included, 145 imaging procedures were ordered. Most imaging studies (87%) did not show significant findings. Among studies with positive findings, the most common abnormality was fracture, including 3 hip, 1 humeral, 1 vertebral, 1 nasal, and 1 rib fracture. Other injuries found on imaging studies included 1 subdural hematoma, 1 acute cerebral infarct, 2 soft‐tissue hematomas, and 2 knee effusions. The acute cerebral infarct was not considered to be a result of the fall. Additionally, 3 patients had soft‐tissue swelling noted on head CT and 1 had Foley catheter‐related trauma.

The average length of stay for the 513 inpatients who fell was 20 days (range, 7‐444) compared to 6 days for all patients admitted to the hospital during the same period. Among inpatients who fell, there was no statistical difference in length of stay between those who did and those who did not have a fall‐related injury found on imaging. More than one‐half (53%) of the patients who fell were discharged to home, 21% to rehabilitation facilities, 12% to nursing homes, and 9% died during the hospitalization.

Results of Univariate Analysis

Univariate predictors of injury after a fall are shown in Table 3. Patients having evidence of trauma indicated by the evaluating nurse after a fall had an increased risk for having an abnormal imaging study (OR = 14.7, P < 0.001). Having an activity level of ambulatory ordered by the provider (OR = 2.5, P = 0.09), falling during the night shift (OR = 2.5, P = 0.11), having ambulation as the fall‐related activity (OR = 2.2, P = 0.12), and older age (P = 0.19) all showed a trend toward higher rates of injury being found after a fall. There was no significant association between fall‐related injury and being an elderly patient (age > 75 years), sedative use, falling in the bathroom, or having an elevated PTT or INR.

Univariate Analysis of Predictors of Injury Being Found on Imaging Studies After Inpatient Falls
VariablePatients without injury (n = 497) [number (%)]Patients with injury (n = 16) [number (%)]ORP Value
  • Abbreviations: INR, international normalized ratio; OR, odds ratio; PTT, partial thromboplastin time.

Elderly195 (39)7 (44)1.20.72
Gender male245 (49)10 (63)1.70.30
Location surgical unit142 (29)6 (38)1.50.44
At risk of falling prior to event365 (73)13 (8)1.60.49
Protocol in place338 (68)11 (69)1.00.95
Activity level ambulatory235 (47)11 (69)2.50.09
Occurrence on night shift270 (54)12 (75)2.50.11
Restraint use3 (1)0 (0)  
Sedative within 4 hours61 (12)3 (19)1.60.44
Fall related to ambulation156 (31)8 (50)2.20.12
Evidence of trauma19 (4)6 (38)14.7<0.001
Prolonged PTT93 (19)5 (31)1.90.29
Elevated INR90 (18)3 (19)1.00.96
Anemia351 (71)9 (56)0.60.32
Elevated creatinine97 (20)2 (13)0.70.60
Low albumin309 (62)8 (50)1.60.58

Multivariate Predictors of Injury

In multivariate analysis, after adjusting for age and sex, evidence of trauma after a fall (OR = 24.6, P < 0.001) and having an activity level of ambulatory ordered by the provider (OR = 7.3, P = 0.01) were independent predictors of injury being found on imaging studies (Table 4). Analyses limited to the 120 patients who had imaging found that the association between evidence of trauma (OR = 6.22, P = 0.02) and having an activity level of ambulatory ordered (OR = 5.53, P = 0.04) remained statistically significant.

Multivariate Analysis of Predictors of Injury Being Found on Imaging Studies After Inpatient Fall
VariableAll Patients (n = 513)Patients with Imaging (n = 120)*
ORP ValueORP Value
  • Abbreviation: OR, odds ratio.

  • Since not every patient who fell had imaging, the analysis was repeated only including those patients who did have imaging studies.

Age1.030.171.0160.52
Gender3.190.112.8430.17
Evidence of trauma24.63<0.0016.220.02
Activity level ambulatory7.330.015.530.04

Discussion

Inpatient falls are common and result in significant patient morbidity and increased healthcare costs. Falls in the acute care setting have also proven to be difficult to prevent and as a result have become a priority for patient safety and hospital quality.

Our study confirms that a high percentage of patients with an initial fall will have recurrent falls.1 Additionally, the majority of patients in this cohort fell despite having been assessed as at risk for falling prior to the event. The types of injuries sustained after inpatient falls (eg, subdural hematoma, multiple fractures, joint effusions, other hematomas, and soft‐tissue swelling) are similar to those found by other authors.2, 3, 17, 18

In this study, inpatient falls were associated with an almost 2‐week increase in length of stay. Though we cannot say that this was directly due to falls, and an increased length of stay may just be a marker of severity of illness, this association warrants further study, perhaps with a matched control group of patients who did not fall, and has implications for healthcare cost containment.

We found that having evidence of trauma after a fall and having an activity level of ambulatory ordered by the provider were independent predictors of injury being found after an inpatient fall. It seems intuitive that patients who have physical evidence of trauma, such as lacerations or bruising, would be more likely to have an underlying injury. Clinically, this confirms that providers should have a high index of suspicion for injury being found on imaging studies in such patients. Similar findings have been noted in the emergency medicine literature that further support the validity of our findings.19

Less clear are the reasons for the observed association between having an activity level of ambulatory ordered and higher risk of injury after an inpatient fall. Prior studies have found that ambulatory inpatients are less likely to use assistive devices that they use at home while hospitalized and are less likely to call for help; these factors may contribute to falls.2, 3 However, the interpretation of this finding is limited by the fact that 26% of the patients who fell had an unknown activity level ordered.

Altered mental status, comorbidity, age > 75 years, visual impairment, falling in the bathroom, and being on a geriatric psychiatry floor have previously been found to be risk factors for sustaining an injury after an inpatient fall.2, 5, 17 Conversely, this study did not find altered mental status to be a significant predictor of injury. One reason may be that this was subjectively determined by the evaluating nurse and not by a standardized measure of cognitive impairment. Patients who are oriented may also be more likely to report unwitnessed falls and injuries than patients with altered mental status.3

There was also no association between age and fall‐related injury in our cohort. On univariate analysis, patients who were older in age were more likely to have an injury found after an inpatient fall but this was not statistically significant. Previous authors have suggested that today's inpatients are increasingly ill and may have risk factors for falls and injuries that are independent of age, such as multiple comorbid conditions or deconditioning.3

We hypothesized that patients who are anticoagulated and had an elevated INR or PTT would be more likely to sustain an injury. Anemic inpatients have also been found to be at increased risk of falls.20 We found no significant association between fall‐related injury being found on imaging studies and anemia, low albumin, elevated creatinine, prolonged PTT, or elevated INR. Not every patient who fell had these laboratory values available. However, even when only inpatients who fell and had laboratory tests were included in the analysis, there was still no association with fall‐related injury.

This study has several limitations. First, a low number of serious injuries was found on imaging studies after inpatient falls in this cohort; this limited the power of the study to identify predictors of fall‐related injury.

Second, fall‐related injury was defined as a positive finding on imaging studies within 2 weeks of an inpatient fall. Thus, some fall‐related injuries may have been missed in patients who did not have imaging. However, any patient who had a serious injury after a fall and remained hospitalized would likely have had symptoms such as pain or altered mental status that would have led to an imaging study. Moreover, the analysis was repeated including only inpatients who fell and had imaging, and the association between having evidence of trauma and having an activity level of ambulatory ordered and sustaining a fall‐related injury remained significant.

Third, we relied on hospital incident reports to identify inpatient falls. These reports yield a limited amount of information and may be inaccurate or incomplete. A recent study also raised concern that incident reports significantly underreport actual fall incidence.21 However, previous studies have found no indication that falls are underreported and suggest that incident reports are an established custom in hospital culture.1, 22 Medical staff are aware that administrators want to keep track of hospital fall rates for both quality improvement and documentation for risk management.1, 22 It is unlikely that severe falls or falls leading to serious injury are not reported. A different source of underreporting may actually be failure of patients to tell the medical team about an unwitnessed fall. Older patients may be concerned they will be placed in nursing homes and those with memory loss may forget to report a minor fall. Education of patients and family members could improve reporting of inpatient falls and further our understanding of contributing factors.

Finally, although the evaluation of fall‐related injuries was conducted by a blinded reviewer, the potential for bias does exist among even the best‐intentioned reviewers. Additionally, there may be some degree of variability within the reviewer's data abstraction.

This study adds valuable information about the epidemiology of inpatient falls at large, urban, tertiary‐care academic medical centers, including characteristics of patients who fell, circumstances surrounding falls, injuries sustained, and predictors of fall‐related injury found on imaging. Although additional research is essential to identify methods to effectively prevent inpatient falls, this study contributes to the limited data in this area, can guide providers who are evaluating inpatients who have fallen, and may be used to design future investigations. It is imperative that measures are identified to avoid the frequent adverse outcomes that result from inpatient falls. Insurance companies, hospital administrators, patients, and providers will be demanding that a safe environment be a key component of quality of care measures.

This study draws attention to the scope of the problem at our institution that is common to hospitals across the country. In our study, our academic medical center had a fall rate consistent with published reports, but new efforts have been focused on quality improvement in this area. An interdisciplinary fall prevention committee has been formed that includes physicians, nurses, patient care assistants, physical therapists, pharmacists, and representatives from information technology (IT). Currently, a program of a fall risk‐factor assessment with targeted interventions to reduce those risk factors is being developed for all high‐risk patients and will be piloted on inpatient units.

Acknowledgements

The authors thank Susan Emro, BS, Department of Health Policy, Susan Davis, MS, MPH, RN, CNAA, Department of Nursing, and Albert Siu, MD, MSPH, Brookdale Department of Geriatrics and Adult Development, for their review of this article. Author contributions were as followsconception and design: S.M.B, R.K., and T.M.; collection and assembly of data: S.M.B.; analysis and interpretation of the data: S.M.B, R.K., and J.W.; drafting of the article: S.M.B.; critical revision of the article for important intellectual content: R.K. and J.W.; final approval of the article: S.M.B, R.K., and J.W.; statistical expertise: J.W.; obtaining of funding: S.M.B.

An estimated 2% to 15% of all hospitalized patients experience at least one fall.1 Approximately 30% of such falls result in injury and up to 6% may be serious in nature.1, 2 These injuries can result in pain, functional impairment, disability, or even death, and can contribute to longer lengths of stay, increased health care costs, and nursing home placement.25 As a result, inpatient falls have become a major priority for hospital quality assurance programs, and hospital risk management departments have begun to target inpatient falls as a source of legal liability.13, 6, 7 Recently, the Centers for Medicare and Medicaid Services announced that it will no longer pay for preventable complications of hospitalizations, including falls and fall‐related injury.8

Much of the literature on falls comes from community and long‐term care settings, and only a few studies have investigated falls during acute care hospitalization.3, 9, 10 From these studies, risk factors for inpatient falls have been identified and various models have been developed to predict an individual patient's risk of falling. However, unlike in the community setting, interventions to prevent falls in the acute care setting have not proven to be beneficial.11, 12 Commonly used approaches including restraints, alarms, bracelets, or having a volunteer sit with high‐risk patients have not been found to be effective.13, 14 Only 1 study found a multicomponent care plan that targeted specific risk factors in older inpatients to be associated with a reduced relative risk of recorded falls.15 Given this dearth of consistent evidence for the prevention of falls in hospitalized inpatients, the American Geriatrics Society has identified this as a gap area for future research.16

There are also limited data regarding predictors of injury after inpatient falls. A few small studies have identified potential risk factors for sustaining an injury after a fall in acute care, such as age >75 years, altered mental status, increased comorbidities, visual impairment, falls in the bathroom, and admission to a geriatric psychiatry floor.2, 5, 17 However, to our knowledge, there are no studies that have identified potential characteristics of inpatients found immediately after a fall that predict an injury. Providers who assess inpatients who have fallen need guidance on how to identify those in need of further evaluation and testing. This study sought to quantify the types and severity of injuries resulting from inpatient falls and to identify predictors of injury after a fall among a cohort of patients who fell at an urban academic medical center.

Patients and Methods

Patient Population

The study population included all inpatients on 13 medical and surgical units who experienced a fall between January 1, 2006 and December 31, 2006, while hospitalized at an 1171‐bed urban academic medical center. Telemetry, intensive care, pediatric, psychiatric, rehabilitation, and obstetrics or gynecology units were excluded from this analysis; the patients on these units are special populations that are qualitatively different than other acute care patients and have a different set of risk factor for falls and predictors of fall‐related injury. The study was approved by the institutional review board of the Mount Sinai School of Medicine.

Data Collection

Inpatient falls were identified retrospectively by review of hospital incident reports, which are most often completed by the unit nurses. In our institution, all falls generate an incident report. Using a standardized abstraction form, patient characteristics, circumstances surrounding falls, and fall‐related injuries were collected from the reports.

Laboratory data for anemia (hemoglobin < 12.0 g/dL), low albumin (<3.5 g/dL), elevated creatinine (>1.5 mg/dL), prolonged partial thromboplastin time (>35 seconds), and elevated international normalized ratio (INR > 1.3), were extracted from the patient's computerized medical record, if available. Number of days from admission to the fall, length of stay to the nearest hundredth of a day, and discharge disposition were also recorded for each patient.

Results of all radiographic studies, including x‐ray, ultrasound, computed tomography (CT), and magnetic resonance imaging (MRI), performed within 2 weeks after the fall were obtained. The indication for the imaging study was assessed from the order given to the radiology department and from the patient's medical record. A positive finding on an imaging study was defined as evidence of intracranial hemorrhage, fracture, joint effusion, soft‐tissue swelling, or any other injury potentially caused by trauma. Fall‐related injury was defined as positive findings on any of these imaging studies that were performed as a result of the fall. Evaluation of fall‐related injuries was conducted by a reviewer blinded to the baseline patient characteristics and laboratory data.

Statistical Analyses

Baseline characteristics and risk factors of patients with and without fall‐related injuries were compared using the chi square test or Student t test as appropriate. Univariate and multivariate logistic regression were used to calculate adjusted odds ratios (ORs) for injury after an inpatient fall. The multivariate model was developed using a manual forward method. Prior research shows that patients with recurrent falls do so in the same manner and for the same reasons.2, 3, 17 Thus, analyses were performed including only the first fall episode as the outcome of interest. Analyses were performed with SPSS statistical software (SPSS Inc., Chicago, IL) using 2‐sided P values.

Results

During the study period, 513 inpatients sustained 636 falls at the Mount Sinai Medical Center. There were 54,257 admissions to the hospital with 322,670 total patient days during this time. Therefore the fall incidence rate was 1.97 falls per 1,000 patient days. Characteristics of inpatients who fell are shown in Table 1. Most patients had 1 fall episode; however, 95 patients (19%) fell multiple times (range, 2‐6 events). There were no significant differences between recurrent fallers and those who fell once with respect to baseline characteristics, injuries sustained, or discharge disposition.

Demographic Characteristics of Patients Who Sustained a Fall
CharacteristicNumber of Patients (n = 513) [number (%)]
  • NOTE: All values are given as number (%) except age, which is median (range).

Age (years)70 (21‐104)
Age >75 years202 (39)
Male gender255 (50)
Assessed at risk of falling
Yes378 (74)
No2 (5)
Unknown110 (21)
Number of falls
1418 (82)
278 (15)
310 (2)
44 (1)
52 (0.4)
61 (0.2)
Multiple falls95 (19)

Fall Circumstances

The majority of patients who fell (74%) had been assessed by the nursing staff as being at risk for falling prior to the event. Overall, most falls (73%) occurred on medical rather than surgical units. The units with the most falls were geriatrics, neurology, and general medicine. Details about circumstances surrounding the falls are shown in Table 2. In most instances (71%) patients were found on the floor after the fall while less than 8% of falls were witnessed. Approximately 12% of patients received sedatives within 4 hours of falling (40% opioids, 30% benzodiazepines, 16% zolpidem, and 14% other). Laboratory values at the time of fall revealed that 70% of patients who fell were anemic, 62% had low albumin, and 19% had an elevated creatinine. Almost 20% of the patients had a prolonged partial thromboplastin time (PTT) and 18% had an elevated INR.

Circumstances of First Inpatient Fall
CharacteristicNumber of Falls (n = 513) [number (%)]*
  • Abbreviation: benzos, benzodiazepines.

  • Percentages were rounded to nearest whole number and may not add exactly to 100%.

Location
Medical unit374 (73)
Surgical unit139 (27)
Time
Day shift (7:00 AM to 6:59 PM)225 (44)
Night shift (7:00 PM to 6:59 AM)282 (56)
Character of fall
Assisted to floor15 (3)
Fall alleged92 (18)
Fall witnessed39 (8)
Found on Floor363 (71)
Unknown4 (<1)
Fall‐related activity
Ambulation164 (32)
Bathroom122 (24)
Bed21 (4)
Chair19 (4)
Other/unknown187 (36)
Mental status
Oriented274 (53)
Confused151 (29)
Unknown88 (17)
Activity level ordered
Ambulatory246 (48)
Nonambulatory135 (26)
Unknown132 (26)
Siderails
Complete15 (3)
Partial352 (69)
None15 (3)
Unknown126 (25)
Environmental obstacle
None355 (69)
Wet20 (4)
Debris2 (<1)
Unknown136 (27)
Restraints
Yes3 (<1)
No374 (73)
Unknown136 (27)
Sedative use
Total64 (12)
Opioids28 (6)
Benzos21 (4)
Antipsychotics7 (1)
Other8 (2)
Evidence of trauma
Yes25 (5)
No285 (56)
Unknown203 (40)

The median number of days from patient admission until they fell was 4 days (range, 0‐134), with 70% of patients falling within the first week of admission. In general, there was no difference in fall rate by time of day, though slightly more falls (56%) occurred during the night shift (7 PM to 7 AM).

Fall‐related Outcomes

Twenty‐five patients (5%) had evidence of trauma on physical exam after the fall, including lacerations, swelling, and ecchymoses, as documented by the evaluating nurse. A total of 120 imaging procedures were ordered following the first fall; when all inpatient falls were included, 145 imaging procedures were ordered. Most imaging studies (87%) did not show significant findings. Among studies with positive findings, the most common abnormality was fracture, including 3 hip, 1 humeral, 1 vertebral, 1 nasal, and 1 rib fracture. Other injuries found on imaging studies included 1 subdural hematoma, 1 acute cerebral infarct, 2 soft‐tissue hematomas, and 2 knee effusions. The acute cerebral infarct was not considered to be a result of the fall. Additionally, 3 patients had soft‐tissue swelling noted on head CT and 1 had Foley catheter‐related trauma.

The average length of stay for the 513 inpatients who fell was 20 days (range, 7‐444) compared to 6 days for all patients admitted to the hospital during the same period. Among inpatients who fell, there was no statistical difference in length of stay between those who did and those who did not have a fall‐related injury found on imaging. More than one‐half (53%) of the patients who fell were discharged to home, 21% to rehabilitation facilities, 12% to nursing homes, and 9% died during the hospitalization.

Results of Univariate Analysis

Univariate predictors of injury after a fall are shown in Table 3. Patients having evidence of trauma indicated by the evaluating nurse after a fall had an increased risk for having an abnormal imaging study (OR = 14.7, P < 0.001). Having an activity level of ambulatory ordered by the provider (OR = 2.5, P = 0.09), falling during the night shift (OR = 2.5, P = 0.11), having ambulation as the fall‐related activity (OR = 2.2, P = 0.12), and older age (P = 0.19) all showed a trend toward higher rates of injury being found after a fall. There was no significant association between fall‐related injury and being an elderly patient (age > 75 years), sedative use, falling in the bathroom, or having an elevated PTT or INR.

Univariate Analysis of Predictors of Injury Being Found on Imaging Studies After Inpatient Falls
VariablePatients without injury (n = 497) [number (%)]Patients with injury (n = 16) [number (%)]ORP Value
  • Abbreviations: INR, international normalized ratio; OR, odds ratio; PTT, partial thromboplastin time.

Elderly195 (39)7 (44)1.20.72
Gender male245 (49)10 (63)1.70.30
Location surgical unit142 (29)6 (38)1.50.44
At risk of falling prior to event365 (73)13 (8)1.60.49
Protocol in place338 (68)11 (69)1.00.95
Activity level ambulatory235 (47)11 (69)2.50.09
Occurrence on night shift270 (54)12 (75)2.50.11
Restraint use3 (1)0 (0)  
Sedative within 4 hours61 (12)3 (19)1.60.44
Fall related to ambulation156 (31)8 (50)2.20.12
Evidence of trauma19 (4)6 (38)14.7<0.001
Prolonged PTT93 (19)5 (31)1.90.29
Elevated INR90 (18)3 (19)1.00.96
Anemia351 (71)9 (56)0.60.32
Elevated creatinine97 (20)2 (13)0.70.60
Low albumin309 (62)8 (50)1.60.58

Multivariate Predictors of Injury

In multivariate analysis, after adjusting for age and sex, evidence of trauma after a fall (OR = 24.6, P < 0.001) and having an activity level of ambulatory ordered by the provider (OR = 7.3, P = 0.01) were independent predictors of injury being found on imaging studies (Table 4). Analyses limited to the 120 patients who had imaging found that the association between evidence of trauma (OR = 6.22, P = 0.02) and having an activity level of ambulatory ordered (OR = 5.53, P = 0.04) remained statistically significant.

Multivariate Analysis of Predictors of Injury Being Found on Imaging Studies After Inpatient Fall
VariableAll Patients (n = 513)Patients with Imaging (n = 120)*
ORP ValueORP Value
  • Abbreviation: OR, odds ratio.

  • Since not every patient who fell had imaging, the analysis was repeated only including those patients who did have imaging studies.

Age1.030.171.0160.52
Gender3.190.112.8430.17
Evidence of trauma24.63<0.0016.220.02
Activity level ambulatory7.330.015.530.04

Discussion

Inpatient falls are common and result in significant patient morbidity and increased healthcare costs. Falls in the acute care setting have also proven to be difficult to prevent and as a result have become a priority for patient safety and hospital quality.

Our study confirms that a high percentage of patients with an initial fall will have recurrent falls.1 Additionally, the majority of patients in this cohort fell despite having been assessed as at risk for falling prior to the event. The types of injuries sustained after inpatient falls (eg, subdural hematoma, multiple fractures, joint effusions, other hematomas, and soft‐tissue swelling) are similar to those found by other authors.2, 3, 17, 18

In this study, inpatient falls were associated with an almost 2‐week increase in length of stay. Though we cannot say that this was directly due to falls, and an increased length of stay may just be a marker of severity of illness, this association warrants further study, perhaps with a matched control group of patients who did not fall, and has implications for healthcare cost containment.

We found that having evidence of trauma after a fall and having an activity level of ambulatory ordered by the provider were independent predictors of injury being found after an inpatient fall. It seems intuitive that patients who have physical evidence of trauma, such as lacerations or bruising, would be more likely to have an underlying injury. Clinically, this confirms that providers should have a high index of suspicion for injury being found on imaging studies in such patients. Similar findings have been noted in the emergency medicine literature that further support the validity of our findings.19

Less clear are the reasons for the observed association between having an activity level of ambulatory ordered and higher risk of injury after an inpatient fall. Prior studies have found that ambulatory inpatients are less likely to use assistive devices that they use at home while hospitalized and are less likely to call for help; these factors may contribute to falls.2, 3 However, the interpretation of this finding is limited by the fact that 26% of the patients who fell had an unknown activity level ordered.

Altered mental status, comorbidity, age > 75 years, visual impairment, falling in the bathroom, and being on a geriatric psychiatry floor have previously been found to be risk factors for sustaining an injury after an inpatient fall.2, 5, 17 Conversely, this study did not find altered mental status to be a significant predictor of injury. One reason may be that this was subjectively determined by the evaluating nurse and not by a standardized measure of cognitive impairment. Patients who are oriented may also be more likely to report unwitnessed falls and injuries than patients with altered mental status.3

There was also no association between age and fall‐related injury in our cohort. On univariate analysis, patients who were older in age were more likely to have an injury found after an inpatient fall but this was not statistically significant. Previous authors have suggested that today's inpatients are increasingly ill and may have risk factors for falls and injuries that are independent of age, such as multiple comorbid conditions or deconditioning.3

We hypothesized that patients who are anticoagulated and had an elevated INR or PTT would be more likely to sustain an injury. Anemic inpatients have also been found to be at increased risk of falls.20 We found no significant association between fall‐related injury being found on imaging studies and anemia, low albumin, elevated creatinine, prolonged PTT, or elevated INR. Not every patient who fell had these laboratory values available. However, even when only inpatients who fell and had laboratory tests were included in the analysis, there was still no association with fall‐related injury.

This study has several limitations. First, a low number of serious injuries was found on imaging studies after inpatient falls in this cohort; this limited the power of the study to identify predictors of fall‐related injury.

Second, fall‐related injury was defined as a positive finding on imaging studies within 2 weeks of an inpatient fall. Thus, some fall‐related injuries may have been missed in patients who did not have imaging. However, any patient who had a serious injury after a fall and remained hospitalized would likely have had symptoms such as pain or altered mental status that would have led to an imaging study. Moreover, the analysis was repeated including only inpatients who fell and had imaging, and the association between having evidence of trauma and having an activity level of ambulatory ordered and sustaining a fall‐related injury remained significant.

Third, we relied on hospital incident reports to identify inpatient falls. These reports yield a limited amount of information and may be inaccurate or incomplete. A recent study also raised concern that incident reports significantly underreport actual fall incidence.21 However, previous studies have found no indication that falls are underreported and suggest that incident reports are an established custom in hospital culture.1, 22 Medical staff are aware that administrators want to keep track of hospital fall rates for both quality improvement and documentation for risk management.1, 22 It is unlikely that severe falls or falls leading to serious injury are not reported. A different source of underreporting may actually be failure of patients to tell the medical team about an unwitnessed fall. Older patients may be concerned they will be placed in nursing homes and those with memory loss may forget to report a minor fall. Education of patients and family members could improve reporting of inpatient falls and further our understanding of contributing factors.

Finally, although the evaluation of fall‐related injuries was conducted by a blinded reviewer, the potential for bias does exist among even the best‐intentioned reviewers. Additionally, there may be some degree of variability within the reviewer's data abstraction.

This study adds valuable information about the epidemiology of inpatient falls at large, urban, tertiary‐care academic medical centers, including characteristics of patients who fell, circumstances surrounding falls, injuries sustained, and predictors of fall‐related injury found on imaging. Although additional research is essential to identify methods to effectively prevent inpatient falls, this study contributes to the limited data in this area, can guide providers who are evaluating inpatients who have fallen, and may be used to design future investigations. It is imperative that measures are identified to avoid the frequent adverse outcomes that result from inpatient falls. Insurance companies, hospital administrators, patients, and providers will be demanding that a safe environment be a key component of quality of care measures.

This study draws attention to the scope of the problem at our institution that is common to hospitals across the country. In our study, our academic medical center had a fall rate consistent with published reports, but new efforts have been focused on quality improvement in this area. An interdisciplinary fall prevention committee has been formed that includes physicians, nurses, patient care assistants, physical therapists, pharmacists, and representatives from information technology (IT). Currently, a program of a fall risk‐factor assessment with targeted interventions to reduce those risk factors is being developed for all high‐risk patients and will be piloted on inpatient units.

Acknowledgements

The authors thank Susan Emro, BS, Department of Health Policy, Susan Davis, MS, MPH, RN, CNAA, Department of Nursing, and Albert Siu, MD, MSPH, Brookdale Department of Geriatrics and Adult Development, for their review of this article. Author contributions were as followsconception and design: S.M.B, R.K., and T.M.; collection and assembly of data: S.M.B.; analysis and interpretation of the data: S.M.B, R.K., and J.W.; drafting of the article: S.M.B.; critical revision of the article for important intellectual content: R.K. and J.W.; final approval of the article: S.M.B, R.K., and J.W.; statistical expertise: J.W.; obtaining of funding: S.M.B.

References
  1. Halfon P,Eggli Y,Van Melle G,Vagnair A.Risk of falls for hospitalized patients: a predictive model based on routinely available data.J Clin Epidemiol.2001;54(12):12581266.
  2. Krauss MJ,Evanoff B,Hitcho E, et al.A case‐control study of patient, medication, and care‐related risk factors for inpatient falls.J Gen Intern Med.2005;20(2):116122.
  3. Hitcho EB,Krauss MJ,Birge S, et al.Characteristics and circumstances of falls in a hospital setting: a prospective analysis.J Gen Intern Med.2004;19(7):732739.
  4. Schwendimann R,Buhler H,De Geest S,Milisen K.Falls and consequent injuries in hospitalized patients: effects of an interdisciplinary falls prevention program.BMC Health Serv Res.2006;6:69.
  5. Bates DW,Pruess K,Souney P,Platt R.Serious falls in hospitalized patients: correlates and resource utilization.Am J Med.1995;99(2):137143.
  6. Gowdy M,Godfrey S.Using tools to assess and prevent inpatient falls.Jt Comm J Qual Saf.2003;29(7):363368.
  7. Nakai A,Akeda M,Kawabata I.Incidence and risk factors for inpatient falls in an academic acute‐care hospital.J Nippon Med Sch.2006;73(5):265270.
  8. Rosenthal MB.Nonpayment for performance? Medicare's new reimbursement rule.N Engl J Med.2007;357(16):15731575.
  9. Tinetti ME.Clinical practice. preventing falls in elderly persons.N Engl J Med.2003;348(1):4249.
  10. Capezuti E.Building the science of falls‐prevention research.J Am Geriatr Soc.2004;52(3):461462.
  11. Coussement J,De Paepe L,Schwendimann R,Denhaerynck K,Dejaeger E,Milisen K.Interventions for preventing falls in acute‐ and chronic‐care hospitals: a systematic review and meta‐analysis.J Am Geriatr Soc.2008;56(1):2936.
  12. Chang JT,Morton SC,Rubenstein LZ, et al.Interventions for the prevention of falls in older adults: systematic review and meta‐analysis of randomised clinical trials.BMJ.2004;328(7441):680.
  13. Vassallo M,Stockdale R,Wilkinson C, et al.Acceptability of fall prevention measures for hospital inpatients.Age Ageing.2004;33(4):400401.
  14. Giles LC,Bolch D,Rouvray R, et al.Can volunteer companions prevent falls among inpatients? A feasibility study using a pre‐post comparative design.BMC Geriatr.2006;6:11.
  15. Healey F,Monro A,Cockram A,Adams V,Heseltine D.Using targeted risk factor reduction to prevent falls in older in‐patients: a randomised controlled trial.Age Ageing.2004;33(4):390395.
  16. Oliver D.Prevention of falls in hospital inpatients: agendas for research and practice.Age Ageing.2004;33(4):328330.
  17. Fischer ID,Krauss MJ,Dunagan WC, et al.Patterns and predictors of inpatient falls and fall‐related injuries in a large academic hospital.Infect Control Hosp Epidemiol.2005;26(10):822827.
  18. Vassallo M,Vignaraja R,Sharma JC,Briggs R,Allen S.The relationship of falls to injury among hospital in‐patients.Int J Clin Pract.2005;59(1):1720.
  19. Haydel MJ,Preston CA,Mills TJ,Luber S,Blaudeau E,DeBlieux PM.Indications for computed tomography in patients with minor head injury.N Engl J Med.2000;343(2):100105.
  20. Dharmarajan TS,Avula S,Norkus EP.Anemia increases risk for falls in hospitalized older adults: an evaluation of falls in 362 hospitalized, ambulatory, long‐term care, and community patients.J Am Med Dir Assoc.2006;7(5):287293.
  21. Shorr RI,Mion LC,Chandler AM,Rosenblatt LC,Lynch D,Kessler LA.Improving the capture of fall events in hospitals: combining a service for evaluating inpatient falls with an incident report system.J Am Geriatr Soc.2008;56(4):701704.
  22. Evans SM,Berry JG,Smith BJ, et al.Attitudes and barriers to incident reporting: a collaborative hospital study.Qual Saf Health Care.2006;15(1):3943.
References
  1. Halfon P,Eggli Y,Van Melle G,Vagnair A.Risk of falls for hospitalized patients: a predictive model based on routinely available data.J Clin Epidemiol.2001;54(12):12581266.
  2. Krauss MJ,Evanoff B,Hitcho E, et al.A case‐control study of patient, medication, and care‐related risk factors for inpatient falls.J Gen Intern Med.2005;20(2):116122.
  3. Hitcho EB,Krauss MJ,Birge S, et al.Characteristics and circumstances of falls in a hospital setting: a prospective analysis.J Gen Intern Med.2004;19(7):732739.
  4. Schwendimann R,Buhler H,De Geest S,Milisen K.Falls and consequent injuries in hospitalized patients: effects of an interdisciplinary falls prevention program.BMC Health Serv Res.2006;6:69.
  5. Bates DW,Pruess K,Souney P,Platt R.Serious falls in hospitalized patients: correlates and resource utilization.Am J Med.1995;99(2):137143.
  6. Gowdy M,Godfrey S.Using tools to assess and prevent inpatient falls.Jt Comm J Qual Saf.2003;29(7):363368.
  7. Nakai A,Akeda M,Kawabata I.Incidence and risk factors for inpatient falls in an academic acute‐care hospital.J Nippon Med Sch.2006;73(5):265270.
  8. Rosenthal MB.Nonpayment for performance? Medicare's new reimbursement rule.N Engl J Med.2007;357(16):15731575.
  9. Tinetti ME.Clinical practice. preventing falls in elderly persons.N Engl J Med.2003;348(1):4249.
  10. Capezuti E.Building the science of falls‐prevention research.J Am Geriatr Soc.2004;52(3):461462.
  11. Coussement J,De Paepe L,Schwendimann R,Denhaerynck K,Dejaeger E,Milisen K.Interventions for preventing falls in acute‐ and chronic‐care hospitals: a systematic review and meta‐analysis.J Am Geriatr Soc.2008;56(1):2936.
  12. Chang JT,Morton SC,Rubenstein LZ, et al.Interventions for the prevention of falls in older adults: systematic review and meta‐analysis of randomised clinical trials.BMJ.2004;328(7441):680.
  13. Vassallo M,Stockdale R,Wilkinson C, et al.Acceptability of fall prevention measures for hospital inpatients.Age Ageing.2004;33(4):400401.
  14. Giles LC,Bolch D,Rouvray R, et al.Can volunteer companions prevent falls among inpatients? A feasibility study using a pre‐post comparative design.BMC Geriatr.2006;6:11.
  15. Healey F,Monro A,Cockram A,Adams V,Heseltine D.Using targeted risk factor reduction to prevent falls in older in‐patients: a randomised controlled trial.Age Ageing.2004;33(4):390395.
  16. Oliver D.Prevention of falls in hospital inpatients: agendas for research and practice.Age Ageing.2004;33(4):328330.
  17. Fischer ID,Krauss MJ,Dunagan WC, et al.Patterns and predictors of inpatient falls and fall‐related injuries in a large academic hospital.Infect Control Hosp Epidemiol.2005;26(10):822827.
  18. Vassallo M,Vignaraja R,Sharma JC,Briggs R,Allen S.The relationship of falls to injury among hospital in‐patients.Int J Clin Pract.2005;59(1):1720.
  19. Haydel MJ,Preston CA,Mills TJ,Luber S,Blaudeau E,DeBlieux PM.Indications for computed tomography in patients with minor head injury.N Engl J Med.2000;343(2):100105.
  20. Dharmarajan TS,Avula S,Norkus EP.Anemia increases risk for falls in hospitalized older adults: an evaluation of falls in 362 hospitalized, ambulatory, long‐term care, and community patients.J Am Med Dir Assoc.2006;7(5):287293.
  21. Shorr RI,Mion LC,Chandler AM,Rosenblatt LC,Lynch D,Kessler LA.Improving the capture of fall events in hospitals: combining a service for evaluating inpatient falls with an incident report system.J Am Geriatr Soc.2008;56(4):701704.
  22. Evans SM,Berry JG,Smith BJ, et al.Attitudes and barriers to incident reporting: a collaborative hospital study.Qual Saf Health Care.2006;15(1):3943.
Issue
Journal of Hospital Medicine - 5(2)
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Journal of Hospital Medicine - 5(2)
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Predictors of serious injury among hospitalized patients evaluated for falls
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Predictors of serious injury among hospitalized patients evaluated for falls
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fall prevention, injury, inpatient falls
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fall prevention, injury, inpatient falls
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Brookdale Department of Geriatrics and Adult Development, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1070, New York, NY 10029
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AMI Treatment for PAC/LTC Residents

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Examining guideline‐concordant care for acute myocardial infarction (AMI): The case of hospitalized post‐acute and long‐term care (PAC/LTC) residents

The American College of Cardiology (ACC) and the American Heart Association (AHA) recommend early intervention for older persons with acute coronary syndrome (ACS) to improve prognosis. However, numerous studies demonstrate that elderly patients with acute myocardial infarction (AMI) are less likely than their younger counterparts to receive guideline‐recommended therapies.13 No prior studies specifically demonstrate that adherence to AMI guidelines is effective in patients admitted from post‐acute or long‐term care (PAC/LTC) settings such as nursing homes, intermediate care facilities, and LTC hospitals. Recognizing that the barriers to guideline‐adherent care among the elderly may also be present for clinically‐complex PAC/LTC patients, we examined whether hospitalized patients with AMI admitted from PAC/LTC settings were less likely to receive guideline‐recommended therapies and if guideline‐concordant treatment was associated with short‐term (30‐day) survival in this relatively vulnerable subgroup of patients.

Medical decision making, including applicability of guidelines, is not exclusively based on empirical evidence but is also related to morally complex issues such as patient age, social status, and other unknown factors. However, lack of outcome expectancy may limit adherence for AMI care in PAC/LTC populations.4 In particular, treating physicians may not expect that desired outcomes will result when guidelines are followed in the PAC/LTC group compared to community‐based patients. This notion is supported by other research indicating that physicians caring for nursing home residents' chronic health conditions often tailor the care approach according to the patients' functional and cognitive status rather than adhering to recommended guidelines.5 In a study that used hypothetical scenarios, nursing home patients with a better physical condition, a more obvious social role, and a lower age were more likely to be treated with life‐sustaining treatments than were other patients.6 For AMI care, some physicians provide care that is not guideline‐adherent due to concerns that reduced renal function is an absolute rather than relative contraindication to angiography.7, 8 And, because the clinical trials that informed practice guidelines for AMI care did not explicitly include individuals with the chronic complex medical problems prevalent among the PAC/LTC population, treating clinicians may be reluctant to apply acute care guidelines to this subgroup.9 However, we know of no prior research demonstrating that guideline‐adherent care for either chronic or acute conditions results in differential outcomes for PAC/LTC patients cared for in the hospital setting.

For the present study, we examined whether admission source was an independent predictor of AMI treatment and whether guideline‐concordant care was related to mortality for those admitted from PAC/LTC and community settings. We hypothesized that rates of guideline‐concordant care would be higher for patients admitted from community settings vs. PAC/LTC and that differences between the groups would be greater for more intensive interventions such as reperfusion compared to aspirin. The data included detailed clinical eligibility information for treatments based on contemporary ACC/AHA guidelines,10 along with numerous other patient demographic and clinical characteristics, thus allowing us to address the presumptive concern that PAC/LTC patients were sicker or otherwise less‐suited for treatment than other patients.

Methods

This retrospective cohort study relied on existing observational data. The primary data source for this research was the Cooperative Cardiovascular Project (CCP) national baseline data. The CCP was sponsored by the Centers for Medicare & Medicaid Services (CMS) to measure the quality of care provided to a national cohort of Medicare patients hospitalized with AMI. The national data collection and reporting effort was administered through the 53 Medicare Quality Improvement Organization (QIO) contracts established to serve each State, the District of Columbia, Puerto Rico, and the U.S. Virgin Islands. Hospital medical records were requested under QIO authority and then abstracted by centrally‐contracted Clinical Data Abstraction Centers (CDACs). Data quality monitoring involved random reabstraction of records with double entry of the information to ensure consistency across personnel, and data were found to be very reliable. Detailed data collection procedures and main findings from these data have been reported elsewhere.1126

The CCP baseline data included an initial sample of 234,754 records abstracted from inpatient medical charts for fee‐for‐services Medicare beneficiaries hospitalized in 1 of 6684 hospitals located in any of the 50 states, the District of Columbia, Puerto Rico, the U.S. Virgin Islands, American Samoa, Guam, and the Northern Mariana Islands between February 1994 and July 1995. Although the data analyzed for this research relate to hospitalizations for AMI in 1994‐1995, the 2008 ACC/AHA report regarding AMI performance measures retains recommendations for both early aspirin and reperfusion treatments.27 Even though the data are not derived from recent years, the CCP baseline data represent a unique dataset to address questions related to both clinical eligibility and guideline compliance for both community and PAC/LTC patients. The inclusion of PAC/LTC admissions and detailed information regarding clinical eligibility for treatment are particularly important to adequately address the research aim; the CCP baseline data are the single extant U.S. data source we identified that has both features.

AMI cases were identified through inpatient hospital claims using an International Classification of Diseases, 9th Revision, Clinical Modification (ICD‐9‐CM) principal discharge diagnosis of 410 (ACS) for extended chart review to verify AMI and determine clinical eligibility for treatments. CCP records were subsequently linked with the Medicare Denominator File, Area Resource File (ARF), and Medicare PPS cost reports for hospitals (PPS) to obtain additional information regarding patients, local health resources, and admitting hospital.

For the present study, we excluded cases without a confirmed AMI diagnosis; cases with missing geographic information to allow us to control for local practice variation including all cases from outside the Continental U.S.; cases admitted to nonacute facilities or with inadequate information to link with provider data; and cases that originated in states selected for the CCP pilot study due to differences in record abstraction timing and some of the measures. Clinical eligibility for treatments relied on the standardized criteria established by the CCP advisory panel and used in other research.10, 14, 2831

To test whether admission from a LTC setting was negatively associated with guideline adherence and if the relationship varied according to the intensity of the treatment, we examined 2 guidelines related to early interventions care during the hospital stay: (1) administration of aspirin; and (2) reperfusion through either thrombolytic drugs or percutaneous intervention (PTCA). We chose these measures because they range from a simple and readily‐available medical intervention (aspirin), to a clinically complex and costly intervention for a more clinically‐select group of patients (reperfusion). The hypothesis that more intensive acute treatment would be less likely for patients admitted from PAC/LTC settings was empirically tested by examining the differences in overall probabilities and adjusted probabilities of receiving each of these interventions. We then modeled the odds ratios (ORs) for survival based on receiving these treatments.

Guideline adherence and clinical eligibility indicators for the CCP data have been presented elsewhere.10, 20, 23, 29, 32 Using these criteria, we divided patients into clinical eligibility groups, including ideal candidates, eligible candidates, and candidates for whom the care was not indicated. For the present research, all eligible patients were included in the sample; with ideal eligibility included as a covariate in the regression models. All patients in the study sample were at least minimally eligible to receive aspirin during their hospital stay. Ideal candidates for aspirin did not have: a gastrointestinal (GI) ulcer, same day admission/discharge, history of bleeding disorder, risk of bleeding, anemia, allergy to aspirin, warfarin, or terminal illness. Eligible candidates for reperfusion via PTCA or thrombolysis were not transferred from another hospital or emergency department. Ideal eligibility for reperfusion required, in addition, that the patient: was under age 80 years; arrived at the hospital within 6 hours of symptom onset; showed evidence of a transmural (Q‐wave) MI or ST elevation in 2 contiguous leads on arrival electrocardiogram (ECG); was not taking warfarin; did not have cardiac arrest requiring cardiopulmonary resuscitation (CPR), cardioversion, defibrillation, or chemical cardioversion in the 6 hours prior; did not refuse a thrombolytic; did not have cardiac catheterization without PTCA within 12 hours of arrival; had no evidence of hepatic failure or cirrhosis; had no history of active ulcer disease, internal bleeding, trauma, or injury in the month prior to arrival; and had no bleeding risk, cerebral vascular accident, or surgery/biopsy within 2 months of admission.

Prearrival setting was of particular interest for the present study; this information was derived from the patient's medical chart using a standardized chart abstraction process for the CCP. From the original admission source categories, we created a single dichotomous variable that indicated PAC/LTC vs. community setting prior to arrival. We defined PAC/LTC settings to include patients admitted from either a skilled nursing facility (SNF) or intermediate care facility (ICF), chronic hospital, or other residential care facility. Three categories of admission source were used to identify the comparison sample: home, noninstitutional setting, and outpatient setting.

Because differences in care according to admission source could result from observable causes, multiple regression analysis was incorporated to control for observed factors previously shown to be associated with guideline adherence. These included: ideal eligibility for treatment; age; Caucasian (vs. other) ethnicity; gender; limitation of aggressive treatment orders (eg, do not resuscitate, do not intubate, chemical code only, no cardiac monitoring, no invasive procedures, no vasopressor, no antiarrhythmic therapy, no feeding tube, palliative care measures only); Charlson comorbidity index and Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision) (APACHE III) score, body mass index (BMI), rural hospital location, hospital teaching status, and number of full‐time equivalent cardiologists on staff at the treating hospital. The regression methods also included adjustment for clustering of patients within health services area to account for geographic variation in practice patterns.33

In developing the regression model, we predicted whether the patient received care in accord with guidelines and 30‐day mortality. We also tested whether the regression errors terms (unobserved variables) for these equations were significantly related to error terms in a regression to predict source of admission, which would indicate rejecting the hypothesis that admission source and treatments were determined independently of each other. In particular, admission source may be a proxy for underlying health status (severity of illness), care preferences, or other unobserved factors that differ systematically between patients admitted from the community vs. those admitted from PAC/LTC. In testing the models, we found that the error terms for both treatments (aspirin and reperfusion) and admission source models were significantly negatively correlated (rho or chi‐square P value <0.001), indicating the need to adjust regression estimates to account for unobserved variables related to both admission source and guideline concordant treatment. Because we rejected the hypothesis that admission source was exogenous to treatments, a seemingly‐unrelated regressions (SUR) bivariate probit model was deemed appropriate, as this methodology corrects for correlation between unobserved variables that are related to both admission source and treatment decisions (eg, residual confounding).34 And, since coefficients from SUR bivariate probit models are not directly interpretable as either ORs or relative risks with respect to the outcome variables, we converted the coefficients to reflect marginal probabilities. The correlation in error terms for models predicting 30‐day mortality and admission source was not substantively or statistically significant. As such, we utilized standard logistic regression methods for assessing mortality. Mortality models were predicted separately according to admission source and treatment to allow presentation of ORs associated with each treatment for each group.

Analyses used the Stata statistical package (version 10.1 SE).35 Approval for this use of the CCP data was received from the CMS. Approval for the data analysis protocol was received from the authors' institutional review board.

Results

Of the 128,183 patients in the analytic sample, 7.6% (n = 8151) were admitted from PAC/LTC (Table 1). The members of the PAC/LTC cohort were older on average than the community‐dwelling cohort (83 vs. 76 years, P < 0.001) and more likely to be female (69% vs. 48%, P < 0.001). Limitation of aggressive treatment orders (LAT/DNR) were in place for 55% of the PAC/LTC cohort compared to only 16% of the community‐dwelling cohort (P < 0.001). Severity of illness scores were higher among the PAC/LTC cohort with APACHE III scores of 50.8 in the PAC/LTC cohort vs. 36.8 in the community‐dwelling cohort (P < 0.001). The PAC/LTC cohort also had lower BMI (P < 0.001). Mortality at 30 days and 1 year was 39.5% and 65.4%, respectively, in the PAC/LTC cohort vs. 17.6% and 33.4%, respectively, in the community‐dwelling cohort. These differences across groups were significant at both time points (P < 0.001). PAC/LTC admissions were significantly more likely to be admitted to a hospital located in a rural area (P < 0.001), though the numbers of full‐time equivalent residents and presence of cardiologists in the treating hospitals were similar across groups.

Characteristics of Sample Admitted for Acute Myocardial Infarction from PAC/LTC and the Community
Sample CharacteristicsOverallPAC/LTCCommunityP Value (2‐sided test)
  • NOTE: Source: CCP Baseline data. Sample inclusive from February 1994 to July 1995.

  • Abbreviations: APACHE III, Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision); BMI, body mass index; CCP, Cooperative Cardiovascular Project; FTE, full‐time equivalents employed by the treating hospital; LAT/DNR, limitation of aggressive treatment/do‐not‐resuscitate; PAC/LTC, post‐acute/long‐term care; SD, standard deviation.

  • P 0.05.

  • P 0.01.

  • P 0.001.

Number of cases128,1838,151120,032 
Percentage of sample1006.493.6 
Average age, years (mean SD)76.7 7.482.6 7.676.3 7.2<0.001
Female (%)49.669.148.3<0.001
Non‐White (%)9.79.19.70.09
Length of stay, days (mean SD)7.3 7.27.4 7.17.3 7.20.33
With LAT/DNR order in place (%)18.155.415.6<0.001
APACHE III score (mean SD)37.7 17.550.8 21.036.8 16.8<0.001
Charlson comorbidity index (mean SD)2.2 1.22.7 1.32.2 1.2<0.001
BMI (mean SD)26.2 5.224.2 5.926.2 5.2<0.001
Hospital residents, FTE (mean SD)29.3 78.429.0 78.729.3 78.30.75
Hospital cardiologists, FTE (mean SD)11.3 13.511.0 13.911.3 13.50.03*
Admitted to rural hospital (%)20.122.320.0<0.001
Number of secondary diagnosis codes (0‐8) (mean SD)5.1 2.35.8 2.15.0 2.26<0.001
30‐day mortality (%)18.9 0.3939.5 0.4917.6 0.38<0.001
1‐year mortality (%)33.5 0.4765.4 0.4831.4 0.46<0.001

Table 2 provides overall unadjusted data comparing eligibility and treatment information for PAC/LTC and community admissions. Rates of guideline adherence were uniformly higher for patients admitted from the community. Guideline adherence rates were higher for aspirin compared to reperfusion, and followed the predicted pattern that more resource‐intensive treatments would be less common for both groups and that PAC/LTC admissions would be less likely to receive treatments compared to patients admitted from community settings. Though all 8151 PAC/LTC patients were eligible to receive aspirin, only 4370 were ideally eligible and 3015 (69%) received acetylsalicylic acid (ASA). There were 1418 PAC/LTC patients (17% of the PAC/LTC sample) meeting at least minimal eligibility requirements for reperfusion. Among the 214 PAC/LTC cases that were ideally eligible for reperfusion, 65 (30%) received the treatment; 12 patients received PTCA and 53 received thrombolytic agents. Eligibility and treatment rates for reperfusion were substantially higher for the community sample, with almost 27% meeting minimum eligibility requirements and 60% of the ideally‐eligible group receiving the treatment.

Unadjusted Guideline Adherence by Admission Source
 Aspirin (ASA) [n (% received)]Reperfusion (PTCA or thrombolysis) [n (% received)]
  • NOTE: Source: CCP Baseline data. Sample inclusive from February 1994 to July 1995.

  • Abbreviations: ASA, acetylsalicylic acid; CCP, Cooperative Cardiovascular Project; PAC/LTC, post‐acute/long‐term care; PTCA, percutaneous intervention.

  • P < 0.0001 for all 2‐sided t tests of mean difference in treatment % (PAC/LTC vs. community).

Eligible sample*  
PAC/LTC8151 (60)1418 (13)
Community120,032 (79)34,501 (45)
Ideal sample*  
PAC/LTC4370 (69)214 (30)
Community78,973 (86)16,557 (60)

Table 3 presents the adjusted probability of treatment based upon the SUR bivariate probit regression model. As with the unadjusted results presented in Table 2, PAC/LTC patients had a lower probability of treatment even after controlling for important patient and hospital characteristics. Compared to the unadjusted results, the adjusted probabilities calculated with the SUR bivariate probit model indicated a relatively higher predicted probability of treatment for the PAC/LTC patients and a relatively lower predicted probability of treatment among the community patients. In other words, the probability of treatment becomes more similar across groups once the adjustments for both observed and unobserved differences in patient characteristics are considered. Nonetheless, a difference in probability of treatment remains across the 2 groups.

Adjusted Guideline Adherence Probability by Admission Source
 Aspirin (ASA)Reperfusion
  • NOTE: Bivariate probit regression model predicting treatment among all eligible patients and nursing home admission sources, adjusting for: ideal eligibility, gender, age, race, smoking status, body mass index, LAT/DNR status, APACHE III score, Charlson score, transfer status, hospital teaching status, rural vs. urban hospital location, and number of cardiologists on staff at the treating hospital. Models were adjusted to reflect clustering of patients within Health Service Areas (ie, geographic variation in local practice patterns).

  • Abbreviations: APACHE III, Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision); ASA, acetylsalicylic acid; COPD, chronic obstructive pulmonary disease; LAT/DNR, limitation of aggressive treatment/do‐not‐resuscitate; PAC/LTC, post‐acute/long‐term care.

  • The equation predicting admission source was predicted simultaneously and adjusted for a similar list of covariates, but was identified using specific diagnoses of cancer, diabetes, dementia, heart failure, renal failure, hypertension, and COPD rather than the summary measures of health status (APACHE III and Charlson). The Rho statistic reflects the correlation between the error terms for the 2 equations, with significance detected using a chi‐square test.

PAC/LTC (%)6412
Community (%)7723
Rho (P value)*0.069 (<0.001)0.17 (<0.001)

To determine whether there was survival difference associated with treatment in these data, we conducted a logistic regression analyses to predict 30‐day mortality for both groups (Tables 4 and 5). Table 4 presents results (ORs) of our models emphasizing the relationship between aspirin and 30‐day mortality, while Table 5 presents the models with reperfusion. Model discrimination was tested using a C‐statistic and was at least 0.70 for all models, indicating good predictive validity. However, for the reperfusion models (Table 5) there were relatively few PAC/LTC patients ideally eligible for treatment, which limited statistical power. There was an association between aspirin provision and improved survival for both the PAC/LTC and community admissions (95% confidence intervals [CIs] were less than 1.0) for all eligible patients. For the eligible samples, we did not find the anticipated relationship between reperfusion and 30‐day survival. The ORs and CIs for community admissions were significantly greater than 1.0. However, we noted lower ORs of mortality for the subgroups of ideally eligible patients, with 95% CIs under 1.0 for both PAC/LTC and community admissions, indicating better survival among those who were ideally eligible for reperfusion treatment. The unadjusted data indicated that PAC/LTC patients were much more likely than their community counterparts to die within 30 days of AMI (Table 1). The multiple logistic regression results indicates PAC/LTC patients had similar ORs for mortality compared to community patients when aspirin was given to eligible patients and when reperfusion was given to ideally eligible patients (Tables 4 and 5). Based on the logistic regression results, we calculated that the adjusted probability of 30‐day mortality among eligible PAC/LTC patients who received aspirin was 0.14 compared to 0.32 for those who did not, which is a difference in probability of 0.18. For eligible community admissions, the adjusted probability of mortality with aspirin was 0.09 with aspirin treatment compared to 0.26 without. For reperfusion, the adjusted probability of 30‐day mortality for ideally eligible PAC/LTC admissions falls from 0.27 to 0.15 if treatment is given, representing a difference in probability of 0.12. Similarly, the adjusted probability difference for community admissions who were ideally eligible and received reperfusion was approximately 0.08 (P = 0.16 without treatment and P = 0.08 with treatment).

Logistic Regression Predicting 30‐day Mortality Related to Aspirin for PAC/LTC and Community Admissions
Explanatory VariablesPAC/LTC AdmissionsCommunity Admissions
OR95% CIOR95% CI
  • NOTE: Source: CCP Baseline data. Sample inclusive from February 1994 to July 1995. Bold values indicate statistically significant ORs.

  • Abbreviations: APACHE III, the Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision); ASA, acetylsalicylic acid; BMI, body mass index; CCP, Cooperative Cardiovascular Project; CI, confidence interval; FTE, full‐time equivalents employed by the treating hospital; LAT/DNR, limitation of aggressive treatment/do‐not‐resuscitate; OR, odds ratio.

  • *CIs were adjusted to reflect robust standard errors.

  • ORs are presented at the mean value of continuous variables.

Aspirin (ASA) given during hospital stay0.500.43‐0.580.570.54‐0.60
Ideal eligibility for ASA0.880.76‐1.010.700.67‐0.73
Female (vs. Male)0.850.73‐0.990.940.90‐0.98
Patient age, 5‐year increments0.990.94‐1.041.041.02‐1.05
Non‐white Ethnicity (vs. White)0.980.76‐1.280.950.89‐1.03
Current Smoker (vs. non‐smoker)0.930.71‐1.220.970.91‐1.03
Body mass index0.990.97‐1.000.990.99‐1.00
LAT/DNR Order4.093.53‐4.737.837.46‐8.21
APACHE 3 Score, 5 point increments1.101.08‐1.121.131.12‐1.13
Charlson Index, 3 point increments0.870.74‐1.031.061.00‐1.11
Patient received in transfer0.990.65‐1.511.180.95‐1.46
Number of hospital residents, 5 FTE increments1.001.00‐1.001.001.00‐1.00
Hospital located in rural area1.100.92‐1.311.091.03‐1.15
Number of cardiologists on staff, 5 FTE increments0.970.94‐1.001.001.00‐1.02
C‐statistic0.76 0.79 
Number of observations4,559 92,004 
Logistic Regression Predicting 30‐day Mortality Related to Reperfusion for PAC/LTC and Community Admissions
Explanatory VariablesPAC/LTC AdmissionsCommunity Admissions
OR95% CI*OR95% CI*
  • NOTE: Source: CCP Baseline data. Sample inclusive from February 1994 to July 1995. Bold text indicates statistically significant ORs.

  • Abbreviations: APACHE III, Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision); BMI, body mass index; CCP, Cooperative Cardiovascular Project; CI, confidence interval; FTE, full‐time equivalents employed by the treating hospital; LAT/DNR, limitation of aggressive treatment/do‐not‐resuscitate; OR, odds ratio; PAC/LTC, post‐acute/long‐term care; PTCA, percutaneous intervention.

  • CIs were adjusted to reflect robust standard errors.

  • ORs are presented as the mean value of continuous variables.

Reperfusion via thrombolytics or PTCA1.330.85‐.101.241.13‐1.35
Ideal eligibility for reperfusion0.580.35‐0.950.740.68‐0.81
Female (vs. male)0.920.66‐1.291.050.97‐1.14
Patient age, 5‐year increments0.970.85‐1.101.030.99‐1.06
Non‐White ethnicity (vs. White)1.110.59‐2.101.100.95‐1.28
Current smoker (vs. nonsmoker)1.130.66‐1.940.870.78‐0.98
BMI1.010.98‐1.041.000.99‐1.01
LAT/DNR order3.412.48‐4.708.267.52‐9.06
APACHE III score, 5‐point increments1.131.07‐1.191.151.14‐1.17
Charlson comorbidity index, 3‐point increments0.840.58‐1.221.301.17‐1.44
Patient received in transfer1.080.27‐4.431.490.85‐2.60
Number of hospital residents, 5‐FTE increments0.990.98‐1.011.001.00‐1.00
Hospital located in rural area0.900.61‐1.341.121.01‐1.25
Number of cardiologists on staff, 5‐FTE increments0.970.90‐1.051.000.98‐1.01
C‐statistic0.71 0.78 
Number of observations856 26,720 

Discussion

This investigation has important implications. The results suggest systematic differences in care for PAC/LTC compared to community‐based patients hospitalized with AMI. It is possible that short‐term mortality was impacted by guideline adherence differences according to admission source. The analytic methods accounted for clinical eligibility, tested for residual confounding and used econometric methods (SUR bivariate probit) to correct it where found, and excluded patients who refused treatments. Therefore, poor eligibility and treatment refusal are inadequate explanations for the observed differences in treatment according to admission source from a PAC/LTC facility.

Providers may not to follow AMI treatment guidelines because the perceived risks for patients transferred from PAC/LTC were too great or due to a limited clinical evidence base. Even though PAC/LTC patients were not included in clinical trials for AMI care, studies that carefully use observational data may help guide applicability of clinical recommendations for acute care to subgroups of clinically complex patients. This study offers observational evidence and information to guide additional studies regarding of the clinical benefit of treating a particularly vulnerable subgroup of patients.

Other research has noted that adherence to clinical practice guidelines in PAC/LTC facilities is low.36, 37 LTC practitioners have been reluctant to apply clinical practice guidelines to residents with chronic illnesses because these regimens often do not take into consideration individuals with the multiple chronic diseases prevalent among PAC/LTC patients9 and the complexity of the PAC/LTC environment.38, 39 Rather than dismiss the utility of clinical practice guidelines in the PAC/LTC population, this study is one of the first to demonstrate that use of acute care clinical practice guidelines, particularly aspirin, was associated with improved acute care outcomes among PAC/LTC patients transferred to acute care hospitals with AMI. Thus, guidelines for acute inpatient care may be more readily applied to the PAC/LTC population than studies aimed at treating chronic illnesses.9, 38, 40 Our results indicate that reperfusion might not be indicated for the preponderance of PAC/LTC patients, but many would agree that treatments such as aspirin would be a low‐burden intervention for most PAC/LTC patients. This investigation supports considering AMI treatment guidelines even for frail subpopulations such as those transferred from PAC/LTC. Further, the findings suggest there may be important information obtained by including PAC/LTC patients in future clinical trials.

This study has several limitations. First, the data were collected during 1995, and may not adequately reflect the current state of the art for AMI treatment or other changes in the organization, financing, and delivery of care for AMI. Nevertheless, care guidelines for AMI have not changed in ways that we anticipate altering the patterns of care examined in this study. For example, in the 2004 National Healthcare Disparities Report,41 receipt of aspirin among elderly individuals ranged from 79.6% to 86%, which closely resembles our results. Despite overall care improvements from 1990 to 2006, women, minorities, and patients ages 75 years and older remain significantly less likely to receive revascularization or discharge lipid‐lowering therapy relative to their counterparts indicating that differences in care persist today.42 While the data used in these analyses existed before recommendations included specific guidance regarding the care of older adults, other researchers examined data collected from January 1, 2005 to June 30, 2006 and demonstrated that elderly individuals remained less likely to receive indicated therapies.43 Further, this is the only dataset we identified that included an adequate presence of both PAC/LTC and community admission sources and sufficient data to assess guideline adherence and other covariates for our models. Second, The SUR bivariate probit models that account for correlation of error terms in models predicting both admission source and treatment were included to minimize issues related to residual confounding, but may not completely eliminate all systematic variation related to the underlying health status of community vs. PAC/LTC residents. Third, limitation of aggressive treatments was not recorded as to specific type of directives but research has shown that orders to forego treatments other than CPR are written for fewer than 8 % of nursing home residents.44, 45 Furthermore, all of these patients were transferred to a hospital; these transfers almost certainly occurred with an expectation that acute treatment would be offered. Fourth, we were unable to distinguish PAC vs. LTC based on admission source categories provided in the original data source. Finally, PTCA and thrombolysis were considered as a single variable because separating the 2 procedures would result in inadequate sample size to detect statistical differences between the 2 groups.

Conclusions

Patients admitted from PAC/LTC settings were less likely to receive early guideline‐recommended treatment for AMI compared to community‐dwelling patients. Our study finds evidence that following the aspirin guideline may improve survival for most patients, but that reperfusion improved survival only for a clinically‐select subgroup of patients. As such, a possible recommendation for further clinical study is that low‐burden treatments such as aspirin should be offered to most patients with AMI, including those from PAC/LTC. Higher‐burden treatments with have greater associated risks, such as reperfusion, also require more study to inform situations applicable to PAC/LTC patients. Clinical trials data would be indicated to strengthen evidence regarding which AMI treatment guidelines should be followed in frail populations from PAC/LTC settings; we identified no randomized trials that specifically demonstrate efficacy of AMI guidelines for this subgroup of vulnerable patients.

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Article PDF
Issue
Journal of Hospital Medicine - 5(2)
Page Number
E3-E10
Legacy Keywords
acute myocardial infarction, clinical practice guidelines, geriatrics, long‐term care, nursing home, post‐acute care
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Article PDF

The American College of Cardiology (ACC) and the American Heart Association (AHA) recommend early intervention for older persons with acute coronary syndrome (ACS) to improve prognosis. However, numerous studies demonstrate that elderly patients with acute myocardial infarction (AMI) are less likely than their younger counterparts to receive guideline‐recommended therapies.13 No prior studies specifically demonstrate that adherence to AMI guidelines is effective in patients admitted from post‐acute or long‐term care (PAC/LTC) settings such as nursing homes, intermediate care facilities, and LTC hospitals. Recognizing that the barriers to guideline‐adherent care among the elderly may also be present for clinically‐complex PAC/LTC patients, we examined whether hospitalized patients with AMI admitted from PAC/LTC settings were less likely to receive guideline‐recommended therapies and if guideline‐concordant treatment was associated with short‐term (30‐day) survival in this relatively vulnerable subgroup of patients.

Medical decision making, including applicability of guidelines, is not exclusively based on empirical evidence but is also related to morally complex issues such as patient age, social status, and other unknown factors. However, lack of outcome expectancy may limit adherence for AMI care in PAC/LTC populations.4 In particular, treating physicians may not expect that desired outcomes will result when guidelines are followed in the PAC/LTC group compared to community‐based patients. This notion is supported by other research indicating that physicians caring for nursing home residents' chronic health conditions often tailor the care approach according to the patients' functional and cognitive status rather than adhering to recommended guidelines.5 In a study that used hypothetical scenarios, nursing home patients with a better physical condition, a more obvious social role, and a lower age were more likely to be treated with life‐sustaining treatments than were other patients.6 For AMI care, some physicians provide care that is not guideline‐adherent due to concerns that reduced renal function is an absolute rather than relative contraindication to angiography.7, 8 And, because the clinical trials that informed practice guidelines for AMI care did not explicitly include individuals with the chronic complex medical problems prevalent among the PAC/LTC population, treating clinicians may be reluctant to apply acute care guidelines to this subgroup.9 However, we know of no prior research demonstrating that guideline‐adherent care for either chronic or acute conditions results in differential outcomes for PAC/LTC patients cared for in the hospital setting.

For the present study, we examined whether admission source was an independent predictor of AMI treatment and whether guideline‐concordant care was related to mortality for those admitted from PAC/LTC and community settings. We hypothesized that rates of guideline‐concordant care would be higher for patients admitted from community settings vs. PAC/LTC and that differences between the groups would be greater for more intensive interventions such as reperfusion compared to aspirin. The data included detailed clinical eligibility information for treatments based on contemporary ACC/AHA guidelines,10 along with numerous other patient demographic and clinical characteristics, thus allowing us to address the presumptive concern that PAC/LTC patients were sicker or otherwise less‐suited for treatment than other patients.

Methods

This retrospective cohort study relied on existing observational data. The primary data source for this research was the Cooperative Cardiovascular Project (CCP) national baseline data. The CCP was sponsored by the Centers for Medicare & Medicaid Services (CMS) to measure the quality of care provided to a national cohort of Medicare patients hospitalized with AMI. The national data collection and reporting effort was administered through the 53 Medicare Quality Improvement Organization (QIO) contracts established to serve each State, the District of Columbia, Puerto Rico, and the U.S. Virgin Islands. Hospital medical records were requested under QIO authority and then abstracted by centrally‐contracted Clinical Data Abstraction Centers (CDACs). Data quality monitoring involved random reabstraction of records with double entry of the information to ensure consistency across personnel, and data were found to be very reliable. Detailed data collection procedures and main findings from these data have been reported elsewhere.1126

The CCP baseline data included an initial sample of 234,754 records abstracted from inpatient medical charts for fee‐for‐services Medicare beneficiaries hospitalized in 1 of 6684 hospitals located in any of the 50 states, the District of Columbia, Puerto Rico, the U.S. Virgin Islands, American Samoa, Guam, and the Northern Mariana Islands between February 1994 and July 1995. Although the data analyzed for this research relate to hospitalizations for AMI in 1994‐1995, the 2008 ACC/AHA report regarding AMI performance measures retains recommendations for both early aspirin and reperfusion treatments.27 Even though the data are not derived from recent years, the CCP baseline data represent a unique dataset to address questions related to both clinical eligibility and guideline compliance for both community and PAC/LTC patients. The inclusion of PAC/LTC admissions and detailed information regarding clinical eligibility for treatment are particularly important to adequately address the research aim; the CCP baseline data are the single extant U.S. data source we identified that has both features.

AMI cases were identified through inpatient hospital claims using an International Classification of Diseases, 9th Revision, Clinical Modification (ICD‐9‐CM) principal discharge diagnosis of 410 (ACS) for extended chart review to verify AMI and determine clinical eligibility for treatments. CCP records were subsequently linked with the Medicare Denominator File, Area Resource File (ARF), and Medicare PPS cost reports for hospitals (PPS) to obtain additional information regarding patients, local health resources, and admitting hospital.

For the present study, we excluded cases without a confirmed AMI diagnosis; cases with missing geographic information to allow us to control for local practice variation including all cases from outside the Continental U.S.; cases admitted to nonacute facilities or with inadequate information to link with provider data; and cases that originated in states selected for the CCP pilot study due to differences in record abstraction timing and some of the measures. Clinical eligibility for treatments relied on the standardized criteria established by the CCP advisory panel and used in other research.10, 14, 2831

To test whether admission from a LTC setting was negatively associated with guideline adherence and if the relationship varied according to the intensity of the treatment, we examined 2 guidelines related to early interventions care during the hospital stay: (1) administration of aspirin; and (2) reperfusion through either thrombolytic drugs or percutaneous intervention (PTCA). We chose these measures because they range from a simple and readily‐available medical intervention (aspirin), to a clinically complex and costly intervention for a more clinically‐select group of patients (reperfusion). The hypothesis that more intensive acute treatment would be less likely for patients admitted from PAC/LTC settings was empirically tested by examining the differences in overall probabilities and adjusted probabilities of receiving each of these interventions. We then modeled the odds ratios (ORs) for survival based on receiving these treatments.

Guideline adherence and clinical eligibility indicators for the CCP data have been presented elsewhere.10, 20, 23, 29, 32 Using these criteria, we divided patients into clinical eligibility groups, including ideal candidates, eligible candidates, and candidates for whom the care was not indicated. For the present research, all eligible patients were included in the sample; with ideal eligibility included as a covariate in the regression models. All patients in the study sample were at least minimally eligible to receive aspirin during their hospital stay. Ideal candidates for aspirin did not have: a gastrointestinal (GI) ulcer, same day admission/discharge, history of bleeding disorder, risk of bleeding, anemia, allergy to aspirin, warfarin, or terminal illness. Eligible candidates for reperfusion via PTCA or thrombolysis were not transferred from another hospital or emergency department. Ideal eligibility for reperfusion required, in addition, that the patient: was under age 80 years; arrived at the hospital within 6 hours of symptom onset; showed evidence of a transmural (Q‐wave) MI or ST elevation in 2 contiguous leads on arrival electrocardiogram (ECG); was not taking warfarin; did not have cardiac arrest requiring cardiopulmonary resuscitation (CPR), cardioversion, defibrillation, or chemical cardioversion in the 6 hours prior; did not refuse a thrombolytic; did not have cardiac catheterization without PTCA within 12 hours of arrival; had no evidence of hepatic failure or cirrhosis; had no history of active ulcer disease, internal bleeding, trauma, or injury in the month prior to arrival; and had no bleeding risk, cerebral vascular accident, or surgery/biopsy within 2 months of admission.

Prearrival setting was of particular interest for the present study; this information was derived from the patient's medical chart using a standardized chart abstraction process for the CCP. From the original admission source categories, we created a single dichotomous variable that indicated PAC/LTC vs. community setting prior to arrival. We defined PAC/LTC settings to include patients admitted from either a skilled nursing facility (SNF) or intermediate care facility (ICF), chronic hospital, or other residential care facility. Three categories of admission source were used to identify the comparison sample: home, noninstitutional setting, and outpatient setting.

Because differences in care according to admission source could result from observable causes, multiple regression analysis was incorporated to control for observed factors previously shown to be associated with guideline adherence. These included: ideal eligibility for treatment; age; Caucasian (vs. other) ethnicity; gender; limitation of aggressive treatment orders (eg, do not resuscitate, do not intubate, chemical code only, no cardiac monitoring, no invasive procedures, no vasopressor, no antiarrhythmic therapy, no feeding tube, palliative care measures only); Charlson comorbidity index and Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision) (APACHE III) score, body mass index (BMI), rural hospital location, hospital teaching status, and number of full‐time equivalent cardiologists on staff at the treating hospital. The regression methods also included adjustment for clustering of patients within health services area to account for geographic variation in practice patterns.33

In developing the regression model, we predicted whether the patient received care in accord with guidelines and 30‐day mortality. We also tested whether the regression errors terms (unobserved variables) for these equations were significantly related to error terms in a regression to predict source of admission, which would indicate rejecting the hypothesis that admission source and treatments were determined independently of each other. In particular, admission source may be a proxy for underlying health status (severity of illness), care preferences, or other unobserved factors that differ systematically between patients admitted from the community vs. those admitted from PAC/LTC. In testing the models, we found that the error terms for both treatments (aspirin and reperfusion) and admission source models were significantly negatively correlated (rho or chi‐square P value <0.001), indicating the need to adjust regression estimates to account for unobserved variables related to both admission source and guideline concordant treatment. Because we rejected the hypothesis that admission source was exogenous to treatments, a seemingly‐unrelated regressions (SUR) bivariate probit model was deemed appropriate, as this methodology corrects for correlation between unobserved variables that are related to both admission source and treatment decisions (eg, residual confounding).34 And, since coefficients from SUR bivariate probit models are not directly interpretable as either ORs or relative risks with respect to the outcome variables, we converted the coefficients to reflect marginal probabilities. The correlation in error terms for models predicting 30‐day mortality and admission source was not substantively or statistically significant. As such, we utilized standard logistic regression methods for assessing mortality. Mortality models were predicted separately according to admission source and treatment to allow presentation of ORs associated with each treatment for each group.

Analyses used the Stata statistical package (version 10.1 SE).35 Approval for this use of the CCP data was received from the CMS. Approval for the data analysis protocol was received from the authors' institutional review board.

Results

Of the 128,183 patients in the analytic sample, 7.6% (n = 8151) were admitted from PAC/LTC (Table 1). The members of the PAC/LTC cohort were older on average than the community‐dwelling cohort (83 vs. 76 years, P < 0.001) and more likely to be female (69% vs. 48%, P < 0.001). Limitation of aggressive treatment orders (LAT/DNR) were in place for 55% of the PAC/LTC cohort compared to only 16% of the community‐dwelling cohort (P < 0.001). Severity of illness scores were higher among the PAC/LTC cohort with APACHE III scores of 50.8 in the PAC/LTC cohort vs. 36.8 in the community‐dwelling cohort (P < 0.001). The PAC/LTC cohort also had lower BMI (P < 0.001). Mortality at 30 days and 1 year was 39.5% and 65.4%, respectively, in the PAC/LTC cohort vs. 17.6% and 33.4%, respectively, in the community‐dwelling cohort. These differences across groups were significant at both time points (P < 0.001). PAC/LTC admissions were significantly more likely to be admitted to a hospital located in a rural area (P < 0.001), though the numbers of full‐time equivalent residents and presence of cardiologists in the treating hospitals were similar across groups.

Characteristics of Sample Admitted for Acute Myocardial Infarction from PAC/LTC and the Community
Sample CharacteristicsOverallPAC/LTCCommunityP Value (2‐sided test)
  • NOTE: Source: CCP Baseline data. Sample inclusive from February 1994 to July 1995.

  • Abbreviations: APACHE III, Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision); BMI, body mass index; CCP, Cooperative Cardiovascular Project; FTE, full‐time equivalents employed by the treating hospital; LAT/DNR, limitation of aggressive treatment/do‐not‐resuscitate; PAC/LTC, post‐acute/long‐term care; SD, standard deviation.

  • P 0.05.

  • P 0.01.

  • P 0.001.

Number of cases128,1838,151120,032 
Percentage of sample1006.493.6 
Average age, years (mean SD)76.7 7.482.6 7.676.3 7.2<0.001
Female (%)49.669.148.3<0.001
Non‐White (%)9.79.19.70.09
Length of stay, days (mean SD)7.3 7.27.4 7.17.3 7.20.33
With LAT/DNR order in place (%)18.155.415.6<0.001
APACHE III score (mean SD)37.7 17.550.8 21.036.8 16.8<0.001
Charlson comorbidity index (mean SD)2.2 1.22.7 1.32.2 1.2<0.001
BMI (mean SD)26.2 5.224.2 5.926.2 5.2<0.001
Hospital residents, FTE (mean SD)29.3 78.429.0 78.729.3 78.30.75
Hospital cardiologists, FTE (mean SD)11.3 13.511.0 13.911.3 13.50.03*
Admitted to rural hospital (%)20.122.320.0<0.001
Number of secondary diagnosis codes (0‐8) (mean SD)5.1 2.35.8 2.15.0 2.26<0.001
30‐day mortality (%)18.9 0.3939.5 0.4917.6 0.38<0.001
1‐year mortality (%)33.5 0.4765.4 0.4831.4 0.46<0.001

Table 2 provides overall unadjusted data comparing eligibility and treatment information for PAC/LTC and community admissions. Rates of guideline adherence were uniformly higher for patients admitted from the community. Guideline adherence rates were higher for aspirin compared to reperfusion, and followed the predicted pattern that more resource‐intensive treatments would be less common for both groups and that PAC/LTC admissions would be less likely to receive treatments compared to patients admitted from community settings. Though all 8151 PAC/LTC patients were eligible to receive aspirin, only 4370 were ideally eligible and 3015 (69%) received acetylsalicylic acid (ASA). There were 1418 PAC/LTC patients (17% of the PAC/LTC sample) meeting at least minimal eligibility requirements for reperfusion. Among the 214 PAC/LTC cases that were ideally eligible for reperfusion, 65 (30%) received the treatment; 12 patients received PTCA and 53 received thrombolytic agents. Eligibility and treatment rates for reperfusion were substantially higher for the community sample, with almost 27% meeting minimum eligibility requirements and 60% of the ideally‐eligible group receiving the treatment.

Unadjusted Guideline Adherence by Admission Source
 Aspirin (ASA) [n (% received)]Reperfusion (PTCA or thrombolysis) [n (% received)]
  • NOTE: Source: CCP Baseline data. Sample inclusive from February 1994 to July 1995.

  • Abbreviations: ASA, acetylsalicylic acid; CCP, Cooperative Cardiovascular Project; PAC/LTC, post‐acute/long‐term care; PTCA, percutaneous intervention.

  • P < 0.0001 for all 2‐sided t tests of mean difference in treatment % (PAC/LTC vs. community).

Eligible sample*  
PAC/LTC8151 (60)1418 (13)
Community120,032 (79)34,501 (45)
Ideal sample*  
PAC/LTC4370 (69)214 (30)
Community78,973 (86)16,557 (60)

Table 3 presents the adjusted probability of treatment based upon the SUR bivariate probit regression model. As with the unadjusted results presented in Table 2, PAC/LTC patients had a lower probability of treatment even after controlling for important patient and hospital characteristics. Compared to the unadjusted results, the adjusted probabilities calculated with the SUR bivariate probit model indicated a relatively higher predicted probability of treatment for the PAC/LTC patients and a relatively lower predicted probability of treatment among the community patients. In other words, the probability of treatment becomes more similar across groups once the adjustments for both observed and unobserved differences in patient characteristics are considered. Nonetheless, a difference in probability of treatment remains across the 2 groups.

Adjusted Guideline Adherence Probability by Admission Source
 Aspirin (ASA)Reperfusion
  • NOTE: Bivariate probit regression model predicting treatment among all eligible patients and nursing home admission sources, adjusting for: ideal eligibility, gender, age, race, smoking status, body mass index, LAT/DNR status, APACHE III score, Charlson score, transfer status, hospital teaching status, rural vs. urban hospital location, and number of cardiologists on staff at the treating hospital. Models were adjusted to reflect clustering of patients within Health Service Areas (ie, geographic variation in local practice patterns).

  • Abbreviations: APACHE III, Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision); ASA, acetylsalicylic acid; COPD, chronic obstructive pulmonary disease; LAT/DNR, limitation of aggressive treatment/do‐not‐resuscitate; PAC/LTC, post‐acute/long‐term care.

  • The equation predicting admission source was predicted simultaneously and adjusted for a similar list of covariates, but was identified using specific diagnoses of cancer, diabetes, dementia, heart failure, renal failure, hypertension, and COPD rather than the summary measures of health status (APACHE III and Charlson). The Rho statistic reflects the correlation between the error terms for the 2 equations, with significance detected using a chi‐square test.

PAC/LTC (%)6412
Community (%)7723
Rho (P value)*0.069 (<0.001)0.17 (<0.001)

To determine whether there was survival difference associated with treatment in these data, we conducted a logistic regression analyses to predict 30‐day mortality for both groups (Tables 4 and 5). Table 4 presents results (ORs) of our models emphasizing the relationship between aspirin and 30‐day mortality, while Table 5 presents the models with reperfusion. Model discrimination was tested using a C‐statistic and was at least 0.70 for all models, indicating good predictive validity. However, for the reperfusion models (Table 5) there were relatively few PAC/LTC patients ideally eligible for treatment, which limited statistical power. There was an association between aspirin provision and improved survival for both the PAC/LTC and community admissions (95% confidence intervals [CIs] were less than 1.0) for all eligible patients. For the eligible samples, we did not find the anticipated relationship between reperfusion and 30‐day survival. The ORs and CIs for community admissions were significantly greater than 1.0. However, we noted lower ORs of mortality for the subgroups of ideally eligible patients, with 95% CIs under 1.0 for both PAC/LTC and community admissions, indicating better survival among those who were ideally eligible for reperfusion treatment. The unadjusted data indicated that PAC/LTC patients were much more likely than their community counterparts to die within 30 days of AMI (Table 1). The multiple logistic regression results indicates PAC/LTC patients had similar ORs for mortality compared to community patients when aspirin was given to eligible patients and when reperfusion was given to ideally eligible patients (Tables 4 and 5). Based on the logistic regression results, we calculated that the adjusted probability of 30‐day mortality among eligible PAC/LTC patients who received aspirin was 0.14 compared to 0.32 for those who did not, which is a difference in probability of 0.18. For eligible community admissions, the adjusted probability of mortality with aspirin was 0.09 with aspirin treatment compared to 0.26 without. For reperfusion, the adjusted probability of 30‐day mortality for ideally eligible PAC/LTC admissions falls from 0.27 to 0.15 if treatment is given, representing a difference in probability of 0.12. Similarly, the adjusted probability difference for community admissions who were ideally eligible and received reperfusion was approximately 0.08 (P = 0.16 without treatment and P = 0.08 with treatment).

Logistic Regression Predicting 30‐day Mortality Related to Aspirin for PAC/LTC and Community Admissions
Explanatory VariablesPAC/LTC AdmissionsCommunity Admissions
OR95% CIOR95% CI
  • NOTE: Source: CCP Baseline data. Sample inclusive from February 1994 to July 1995. Bold values indicate statistically significant ORs.

  • Abbreviations: APACHE III, the Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision); ASA, acetylsalicylic acid; BMI, body mass index; CCP, Cooperative Cardiovascular Project; CI, confidence interval; FTE, full‐time equivalents employed by the treating hospital; LAT/DNR, limitation of aggressive treatment/do‐not‐resuscitate; OR, odds ratio.

  • *CIs were adjusted to reflect robust standard errors.

  • ORs are presented at the mean value of continuous variables.

Aspirin (ASA) given during hospital stay0.500.43‐0.580.570.54‐0.60
Ideal eligibility for ASA0.880.76‐1.010.700.67‐0.73
Female (vs. Male)0.850.73‐0.990.940.90‐0.98
Patient age, 5‐year increments0.990.94‐1.041.041.02‐1.05
Non‐white Ethnicity (vs. White)0.980.76‐1.280.950.89‐1.03
Current Smoker (vs. non‐smoker)0.930.71‐1.220.970.91‐1.03
Body mass index0.990.97‐1.000.990.99‐1.00
LAT/DNR Order4.093.53‐4.737.837.46‐8.21
APACHE 3 Score, 5 point increments1.101.08‐1.121.131.12‐1.13
Charlson Index, 3 point increments0.870.74‐1.031.061.00‐1.11
Patient received in transfer0.990.65‐1.511.180.95‐1.46
Number of hospital residents, 5 FTE increments1.001.00‐1.001.001.00‐1.00
Hospital located in rural area1.100.92‐1.311.091.03‐1.15
Number of cardiologists on staff, 5 FTE increments0.970.94‐1.001.001.00‐1.02
C‐statistic0.76 0.79 
Number of observations4,559 92,004 
Logistic Regression Predicting 30‐day Mortality Related to Reperfusion for PAC/LTC and Community Admissions
Explanatory VariablesPAC/LTC AdmissionsCommunity Admissions
OR95% CI*OR95% CI*
  • NOTE: Source: CCP Baseline data. Sample inclusive from February 1994 to July 1995. Bold text indicates statistically significant ORs.

  • Abbreviations: APACHE III, Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision); BMI, body mass index; CCP, Cooperative Cardiovascular Project; CI, confidence interval; FTE, full‐time equivalents employed by the treating hospital; LAT/DNR, limitation of aggressive treatment/do‐not‐resuscitate; OR, odds ratio; PAC/LTC, post‐acute/long‐term care; PTCA, percutaneous intervention.

  • CIs were adjusted to reflect robust standard errors.

  • ORs are presented as the mean value of continuous variables.

Reperfusion via thrombolytics or PTCA1.330.85‐.101.241.13‐1.35
Ideal eligibility for reperfusion0.580.35‐0.950.740.68‐0.81
Female (vs. male)0.920.66‐1.291.050.97‐1.14
Patient age, 5‐year increments0.970.85‐1.101.030.99‐1.06
Non‐White ethnicity (vs. White)1.110.59‐2.101.100.95‐1.28
Current smoker (vs. nonsmoker)1.130.66‐1.940.870.78‐0.98
BMI1.010.98‐1.041.000.99‐1.01
LAT/DNR order3.412.48‐4.708.267.52‐9.06
APACHE III score, 5‐point increments1.131.07‐1.191.151.14‐1.17
Charlson comorbidity index, 3‐point increments0.840.58‐1.221.301.17‐1.44
Patient received in transfer1.080.27‐4.431.490.85‐2.60
Number of hospital residents, 5‐FTE increments0.990.98‐1.011.001.00‐1.00
Hospital located in rural area0.900.61‐1.341.121.01‐1.25
Number of cardiologists on staff, 5‐FTE increments0.970.90‐1.051.000.98‐1.01
C‐statistic0.71 0.78 
Number of observations856 26,720 

Discussion

This investigation has important implications. The results suggest systematic differences in care for PAC/LTC compared to community‐based patients hospitalized with AMI. It is possible that short‐term mortality was impacted by guideline adherence differences according to admission source. The analytic methods accounted for clinical eligibility, tested for residual confounding and used econometric methods (SUR bivariate probit) to correct it where found, and excluded patients who refused treatments. Therefore, poor eligibility and treatment refusal are inadequate explanations for the observed differences in treatment according to admission source from a PAC/LTC facility.

Providers may not to follow AMI treatment guidelines because the perceived risks for patients transferred from PAC/LTC were too great or due to a limited clinical evidence base. Even though PAC/LTC patients were not included in clinical trials for AMI care, studies that carefully use observational data may help guide applicability of clinical recommendations for acute care to subgroups of clinically complex patients. This study offers observational evidence and information to guide additional studies regarding of the clinical benefit of treating a particularly vulnerable subgroup of patients.

Other research has noted that adherence to clinical practice guidelines in PAC/LTC facilities is low.36, 37 LTC practitioners have been reluctant to apply clinical practice guidelines to residents with chronic illnesses because these regimens often do not take into consideration individuals with the multiple chronic diseases prevalent among PAC/LTC patients9 and the complexity of the PAC/LTC environment.38, 39 Rather than dismiss the utility of clinical practice guidelines in the PAC/LTC population, this study is one of the first to demonstrate that use of acute care clinical practice guidelines, particularly aspirin, was associated with improved acute care outcomes among PAC/LTC patients transferred to acute care hospitals with AMI. Thus, guidelines for acute inpatient care may be more readily applied to the PAC/LTC population than studies aimed at treating chronic illnesses.9, 38, 40 Our results indicate that reperfusion might not be indicated for the preponderance of PAC/LTC patients, but many would agree that treatments such as aspirin would be a low‐burden intervention for most PAC/LTC patients. This investigation supports considering AMI treatment guidelines even for frail subpopulations such as those transferred from PAC/LTC. Further, the findings suggest there may be important information obtained by including PAC/LTC patients in future clinical trials.

This study has several limitations. First, the data were collected during 1995, and may not adequately reflect the current state of the art for AMI treatment or other changes in the organization, financing, and delivery of care for AMI. Nevertheless, care guidelines for AMI have not changed in ways that we anticipate altering the patterns of care examined in this study. For example, in the 2004 National Healthcare Disparities Report,41 receipt of aspirin among elderly individuals ranged from 79.6% to 86%, which closely resembles our results. Despite overall care improvements from 1990 to 2006, women, minorities, and patients ages 75 years and older remain significantly less likely to receive revascularization or discharge lipid‐lowering therapy relative to their counterparts indicating that differences in care persist today.42 While the data used in these analyses existed before recommendations included specific guidance regarding the care of older adults, other researchers examined data collected from January 1, 2005 to June 30, 2006 and demonstrated that elderly individuals remained less likely to receive indicated therapies.43 Further, this is the only dataset we identified that included an adequate presence of both PAC/LTC and community admission sources and sufficient data to assess guideline adherence and other covariates for our models. Second, The SUR bivariate probit models that account for correlation of error terms in models predicting both admission source and treatment were included to minimize issues related to residual confounding, but may not completely eliminate all systematic variation related to the underlying health status of community vs. PAC/LTC residents. Third, limitation of aggressive treatments was not recorded as to specific type of directives but research has shown that orders to forego treatments other than CPR are written for fewer than 8 % of nursing home residents.44, 45 Furthermore, all of these patients were transferred to a hospital; these transfers almost certainly occurred with an expectation that acute treatment would be offered. Fourth, we were unable to distinguish PAC vs. LTC based on admission source categories provided in the original data source. Finally, PTCA and thrombolysis were considered as a single variable because separating the 2 procedures would result in inadequate sample size to detect statistical differences between the 2 groups.

Conclusions

Patients admitted from PAC/LTC settings were less likely to receive early guideline‐recommended treatment for AMI compared to community‐dwelling patients. Our study finds evidence that following the aspirin guideline may improve survival for most patients, but that reperfusion improved survival only for a clinically‐select subgroup of patients. As such, a possible recommendation for further clinical study is that low‐burden treatments such as aspirin should be offered to most patients with AMI, including those from PAC/LTC. Higher‐burden treatments with have greater associated risks, such as reperfusion, also require more study to inform situations applicable to PAC/LTC patients. Clinical trials data would be indicated to strengthen evidence regarding which AMI treatment guidelines should be followed in frail populations from PAC/LTC settings; we identified no randomized trials that specifically demonstrate efficacy of AMI guidelines for this subgroup of vulnerable patients.

The American College of Cardiology (ACC) and the American Heart Association (AHA) recommend early intervention for older persons with acute coronary syndrome (ACS) to improve prognosis. However, numerous studies demonstrate that elderly patients with acute myocardial infarction (AMI) are less likely than their younger counterparts to receive guideline‐recommended therapies.13 No prior studies specifically demonstrate that adherence to AMI guidelines is effective in patients admitted from post‐acute or long‐term care (PAC/LTC) settings such as nursing homes, intermediate care facilities, and LTC hospitals. Recognizing that the barriers to guideline‐adherent care among the elderly may also be present for clinically‐complex PAC/LTC patients, we examined whether hospitalized patients with AMI admitted from PAC/LTC settings were less likely to receive guideline‐recommended therapies and if guideline‐concordant treatment was associated with short‐term (30‐day) survival in this relatively vulnerable subgroup of patients.

Medical decision making, including applicability of guidelines, is not exclusively based on empirical evidence but is also related to morally complex issues such as patient age, social status, and other unknown factors. However, lack of outcome expectancy may limit adherence for AMI care in PAC/LTC populations.4 In particular, treating physicians may not expect that desired outcomes will result when guidelines are followed in the PAC/LTC group compared to community‐based patients. This notion is supported by other research indicating that physicians caring for nursing home residents' chronic health conditions often tailor the care approach according to the patients' functional and cognitive status rather than adhering to recommended guidelines.5 In a study that used hypothetical scenarios, nursing home patients with a better physical condition, a more obvious social role, and a lower age were more likely to be treated with life‐sustaining treatments than were other patients.6 For AMI care, some physicians provide care that is not guideline‐adherent due to concerns that reduced renal function is an absolute rather than relative contraindication to angiography.7, 8 And, because the clinical trials that informed practice guidelines for AMI care did not explicitly include individuals with the chronic complex medical problems prevalent among the PAC/LTC population, treating clinicians may be reluctant to apply acute care guidelines to this subgroup.9 However, we know of no prior research demonstrating that guideline‐adherent care for either chronic or acute conditions results in differential outcomes for PAC/LTC patients cared for in the hospital setting.

For the present study, we examined whether admission source was an independent predictor of AMI treatment and whether guideline‐concordant care was related to mortality for those admitted from PAC/LTC and community settings. We hypothesized that rates of guideline‐concordant care would be higher for patients admitted from community settings vs. PAC/LTC and that differences between the groups would be greater for more intensive interventions such as reperfusion compared to aspirin. The data included detailed clinical eligibility information for treatments based on contemporary ACC/AHA guidelines,10 along with numerous other patient demographic and clinical characteristics, thus allowing us to address the presumptive concern that PAC/LTC patients were sicker or otherwise less‐suited for treatment than other patients.

Methods

This retrospective cohort study relied on existing observational data. The primary data source for this research was the Cooperative Cardiovascular Project (CCP) national baseline data. The CCP was sponsored by the Centers for Medicare & Medicaid Services (CMS) to measure the quality of care provided to a national cohort of Medicare patients hospitalized with AMI. The national data collection and reporting effort was administered through the 53 Medicare Quality Improvement Organization (QIO) contracts established to serve each State, the District of Columbia, Puerto Rico, and the U.S. Virgin Islands. Hospital medical records were requested under QIO authority and then abstracted by centrally‐contracted Clinical Data Abstraction Centers (CDACs). Data quality monitoring involved random reabstraction of records with double entry of the information to ensure consistency across personnel, and data were found to be very reliable. Detailed data collection procedures and main findings from these data have been reported elsewhere.1126

The CCP baseline data included an initial sample of 234,754 records abstracted from inpatient medical charts for fee‐for‐services Medicare beneficiaries hospitalized in 1 of 6684 hospitals located in any of the 50 states, the District of Columbia, Puerto Rico, the U.S. Virgin Islands, American Samoa, Guam, and the Northern Mariana Islands between February 1994 and July 1995. Although the data analyzed for this research relate to hospitalizations for AMI in 1994‐1995, the 2008 ACC/AHA report regarding AMI performance measures retains recommendations for both early aspirin and reperfusion treatments.27 Even though the data are not derived from recent years, the CCP baseline data represent a unique dataset to address questions related to both clinical eligibility and guideline compliance for both community and PAC/LTC patients. The inclusion of PAC/LTC admissions and detailed information regarding clinical eligibility for treatment are particularly important to adequately address the research aim; the CCP baseline data are the single extant U.S. data source we identified that has both features.

AMI cases were identified through inpatient hospital claims using an International Classification of Diseases, 9th Revision, Clinical Modification (ICD‐9‐CM) principal discharge diagnosis of 410 (ACS) for extended chart review to verify AMI and determine clinical eligibility for treatments. CCP records were subsequently linked with the Medicare Denominator File, Area Resource File (ARF), and Medicare PPS cost reports for hospitals (PPS) to obtain additional information regarding patients, local health resources, and admitting hospital.

For the present study, we excluded cases without a confirmed AMI diagnosis; cases with missing geographic information to allow us to control for local practice variation including all cases from outside the Continental U.S.; cases admitted to nonacute facilities or with inadequate information to link with provider data; and cases that originated in states selected for the CCP pilot study due to differences in record abstraction timing and some of the measures. Clinical eligibility for treatments relied on the standardized criteria established by the CCP advisory panel and used in other research.10, 14, 2831

To test whether admission from a LTC setting was negatively associated with guideline adherence and if the relationship varied according to the intensity of the treatment, we examined 2 guidelines related to early interventions care during the hospital stay: (1) administration of aspirin; and (2) reperfusion through either thrombolytic drugs or percutaneous intervention (PTCA). We chose these measures because they range from a simple and readily‐available medical intervention (aspirin), to a clinically complex and costly intervention for a more clinically‐select group of patients (reperfusion). The hypothesis that more intensive acute treatment would be less likely for patients admitted from PAC/LTC settings was empirically tested by examining the differences in overall probabilities and adjusted probabilities of receiving each of these interventions. We then modeled the odds ratios (ORs) for survival based on receiving these treatments.

Guideline adherence and clinical eligibility indicators for the CCP data have been presented elsewhere.10, 20, 23, 29, 32 Using these criteria, we divided patients into clinical eligibility groups, including ideal candidates, eligible candidates, and candidates for whom the care was not indicated. For the present research, all eligible patients were included in the sample; with ideal eligibility included as a covariate in the regression models. All patients in the study sample were at least minimally eligible to receive aspirin during their hospital stay. Ideal candidates for aspirin did not have: a gastrointestinal (GI) ulcer, same day admission/discharge, history of bleeding disorder, risk of bleeding, anemia, allergy to aspirin, warfarin, or terminal illness. Eligible candidates for reperfusion via PTCA or thrombolysis were not transferred from another hospital or emergency department. Ideal eligibility for reperfusion required, in addition, that the patient: was under age 80 years; arrived at the hospital within 6 hours of symptom onset; showed evidence of a transmural (Q‐wave) MI or ST elevation in 2 contiguous leads on arrival electrocardiogram (ECG); was not taking warfarin; did not have cardiac arrest requiring cardiopulmonary resuscitation (CPR), cardioversion, defibrillation, or chemical cardioversion in the 6 hours prior; did not refuse a thrombolytic; did not have cardiac catheterization without PTCA within 12 hours of arrival; had no evidence of hepatic failure or cirrhosis; had no history of active ulcer disease, internal bleeding, trauma, or injury in the month prior to arrival; and had no bleeding risk, cerebral vascular accident, or surgery/biopsy within 2 months of admission.

Prearrival setting was of particular interest for the present study; this information was derived from the patient's medical chart using a standardized chart abstraction process for the CCP. From the original admission source categories, we created a single dichotomous variable that indicated PAC/LTC vs. community setting prior to arrival. We defined PAC/LTC settings to include patients admitted from either a skilled nursing facility (SNF) or intermediate care facility (ICF), chronic hospital, or other residential care facility. Three categories of admission source were used to identify the comparison sample: home, noninstitutional setting, and outpatient setting.

Because differences in care according to admission source could result from observable causes, multiple regression analysis was incorporated to control for observed factors previously shown to be associated with guideline adherence. These included: ideal eligibility for treatment; age; Caucasian (vs. other) ethnicity; gender; limitation of aggressive treatment orders (eg, do not resuscitate, do not intubate, chemical code only, no cardiac monitoring, no invasive procedures, no vasopressor, no antiarrhythmic therapy, no feeding tube, palliative care measures only); Charlson comorbidity index and Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision) (APACHE III) score, body mass index (BMI), rural hospital location, hospital teaching status, and number of full‐time equivalent cardiologists on staff at the treating hospital. The regression methods also included adjustment for clustering of patients within health services area to account for geographic variation in practice patterns.33

In developing the regression model, we predicted whether the patient received care in accord with guidelines and 30‐day mortality. We also tested whether the regression errors terms (unobserved variables) for these equations were significantly related to error terms in a regression to predict source of admission, which would indicate rejecting the hypothesis that admission source and treatments were determined independently of each other. In particular, admission source may be a proxy for underlying health status (severity of illness), care preferences, or other unobserved factors that differ systematically between patients admitted from the community vs. those admitted from PAC/LTC. In testing the models, we found that the error terms for both treatments (aspirin and reperfusion) and admission source models were significantly negatively correlated (rho or chi‐square P value <0.001), indicating the need to adjust regression estimates to account for unobserved variables related to both admission source and guideline concordant treatment. Because we rejected the hypothesis that admission source was exogenous to treatments, a seemingly‐unrelated regressions (SUR) bivariate probit model was deemed appropriate, as this methodology corrects for correlation between unobserved variables that are related to both admission source and treatment decisions (eg, residual confounding).34 And, since coefficients from SUR bivariate probit models are not directly interpretable as either ORs or relative risks with respect to the outcome variables, we converted the coefficients to reflect marginal probabilities. The correlation in error terms for models predicting 30‐day mortality and admission source was not substantively or statistically significant. As such, we utilized standard logistic regression methods for assessing mortality. Mortality models were predicted separately according to admission source and treatment to allow presentation of ORs associated with each treatment for each group.

Analyses used the Stata statistical package (version 10.1 SE).35 Approval for this use of the CCP data was received from the CMS. Approval for the data analysis protocol was received from the authors' institutional review board.

Results

Of the 128,183 patients in the analytic sample, 7.6% (n = 8151) were admitted from PAC/LTC (Table 1). The members of the PAC/LTC cohort were older on average than the community‐dwelling cohort (83 vs. 76 years, P < 0.001) and more likely to be female (69% vs. 48%, P < 0.001). Limitation of aggressive treatment orders (LAT/DNR) were in place for 55% of the PAC/LTC cohort compared to only 16% of the community‐dwelling cohort (P < 0.001). Severity of illness scores were higher among the PAC/LTC cohort with APACHE III scores of 50.8 in the PAC/LTC cohort vs. 36.8 in the community‐dwelling cohort (P < 0.001). The PAC/LTC cohort also had lower BMI (P < 0.001). Mortality at 30 days and 1 year was 39.5% and 65.4%, respectively, in the PAC/LTC cohort vs. 17.6% and 33.4%, respectively, in the community‐dwelling cohort. These differences across groups were significant at both time points (P < 0.001). PAC/LTC admissions were significantly more likely to be admitted to a hospital located in a rural area (P < 0.001), though the numbers of full‐time equivalent residents and presence of cardiologists in the treating hospitals were similar across groups.

Characteristics of Sample Admitted for Acute Myocardial Infarction from PAC/LTC and the Community
Sample CharacteristicsOverallPAC/LTCCommunityP Value (2‐sided test)
  • NOTE: Source: CCP Baseline data. Sample inclusive from February 1994 to July 1995.

  • Abbreviations: APACHE III, Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision); BMI, body mass index; CCP, Cooperative Cardiovascular Project; FTE, full‐time equivalents employed by the treating hospital; LAT/DNR, limitation of aggressive treatment/do‐not‐resuscitate; PAC/LTC, post‐acute/long‐term care; SD, standard deviation.

  • P 0.05.

  • P 0.01.

  • P 0.001.

Number of cases128,1838,151120,032 
Percentage of sample1006.493.6 
Average age, years (mean SD)76.7 7.482.6 7.676.3 7.2<0.001
Female (%)49.669.148.3<0.001
Non‐White (%)9.79.19.70.09
Length of stay, days (mean SD)7.3 7.27.4 7.17.3 7.20.33
With LAT/DNR order in place (%)18.155.415.6<0.001
APACHE III score (mean SD)37.7 17.550.8 21.036.8 16.8<0.001
Charlson comorbidity index (mean SD)2.2 1.22.7 1.32.2 1.2<0.001
BMI (mean SD)26.2 5.224.2 5.926.2 5.2<0.001
Hospital residents, FTE (mean SD)29.3 78.429.0 78.729.3 78.30.75
Hospital cardiologists, FTE (mean SD)11.3 13.511.0 13.911.3 13.50.03*
Admitted to rural hospital (%)20.122.320.0<0.001
Number of secondary diagnosis codes (0‐8) (mean SD)5.1 2.35.8 2.15.0 2.26<0.001
30‐day mortality (%)18.9 0.3939.5 0.4917.6 0.38<0.001
1‐year mortality (%)33.5 0.4765.4 0.4831.4 0.46<0.001

Table 2 provides overall unadjusted data comparing eligibility and treatment information for PAC/LTC and community admissions. Rates of guideline adherence were uniformly higher for patients admitted from the community. Guideline adherence rates were higher for aspirin compared to reperfusion, and followed the predicted pattern that more resource‐intensive treatments would be less common for both groups and that PAC/LTC admissions would be less likely to receive treatments compared to patients admitted from community settings. Though all 8151 PAC/LTC patients were eligible to receive aspirin, only 4370 were ideally eligible and 3015 (69%) received acetylsalicylic acid (ASA). There were 1418 PAC/LTC patients (17% of the PAC/LTC sample) meeting at least minimal eligibility requirements for reperfusion. Among the 214 PAC/LTC cases that were ideally eligible for reperfusion, 65 (30%) received the treatment; 12 patients received PTCA and 53 received thrombolytic agents. Eligibility and treatment rates for reperfusion were substantially higher for the community sample, with almost 27% meeting minimum eligibility requirements and 60% of the ideally‐eligible group receiving the treatment.

Unadjusted Guideline Adherence by Admission Source
 Aspirin (ASA) [n (% received)]Reperfusion (PTCA or thrombolysis) [n (% received)]
  • NOTE: Source: CCP Baseline data. Sample inclusive from February 1994 to July 1995.

  • Abbreviations: ASA, acetylsalicylic acid; CCP, Cooperative Cardiovascular Project; PAC/LTC, post‐acute/long‐term care; PTCA, percutaneous intervention.

  • P < 0.0001 for all 2‐sided t tests of mean difference in treatment % (PAC/LTC vs. community).

Eligible sample*  
PAC/LTC8151 (60)1418 (13)
Community120,032 (79)34,501 (45)
Ideal sample*  
PAC/LTC4370 (69)214 (30)
Community78,973 (86)16,557 (60)

Table 3 presents the adjusted probability of treatment based upon the SUR bivariate probit regression model. As with the unadjusted results presented in Table 2, PAC/LTC patients had a lower probability of treatment even after controlling for important patient and hospital characteristics. Compared to the unadjusted results, the adjusted probabilities calculated with the SUR bivariate probit model indicated a relatively higher predicted probability of treatment for the PAC/LTC patients and a relatively lower predicted probability of treatment among the community patients. In other words, the probability of treatment becomes more similar across groups once the adjustments for both observed and unobserved differences in patient characteristics are considered. Nonetheless, a difference in probability of treatment remains across the 2 groups.

Adjusted Guideline Adherence Probability by Admission Source
 Aspirin (ASA)Reperfusion
  • NOTE: Bivariate probit regression model predicting treatment among all eligible patients and nursing home admission sources, adjusting for: ideal eligibility, gender, age, race, smoking status, body mass index, LAT/DNR status, APACHE III score, Charlson score, transfer status, hospital teaching status, rural vs. urban hospital location, and number of cardiologists on staff at the treating hospital. Models were adjusted to reflect clustering of patients within Health Service Areas (ie, geographic variation in local practice patterns).

  • Abbreviations: APACHE III, Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision); ASA, acetylsalicylic acid; COPD, chronic obstructive pulmonary disease; LAT/DNR, limitation of aggressive treatment/do‐not‐resuscitate; PAC/LTC, post‐acute/long‐term care.

  • The equation predicting admission source was predicted simultaneously and adjusted for a similar list of covariates, but was identified using specific diagnoses of cancer, diabetes, dementia, heart failure, renal failure, hypertension, and COPD rather than the summary measures of health status (APACHE III and Charlson). The Rho statistic reflects the correlation between the error terms for the 2 equations, with significance detected using a chi‐square test.

PAC/LTC (%)6412
Community (%)7723
Rho (P value)*0.069 (<0.001)0.17 (<0.001)

To determine whether there was survival difference associated with treatment in these data, we conducted a logistic regression analyses to predict 30‐day mortality for both groups (Tables 4 and 5). Table 4 presents results (ORs) of our models emphasizing the relationship between aspirin and 30‐day mortality, while Table 5 presents the models with reperfusion. Model discrimination was tested using a C‐statistic and was at least 0.70 for all models, indicating good predictive validity. However, for the reperfusion models (Table 5) there were relatively few PAC/LTC patients ideally eligible for treatment, which limited statistical power. There was an association between aspirin provision and improved survival for both the PAC/LTC and community admissions (95% confidence intervals [CIs] were less than 1.0) for all eligible patients. For the eligible samples, we did not find the anticipated relationship between reperfusion and 30‐day survival. The ORs and CIs for community admissions were significantly greater than 1.0. However, we noted lower ORs of mortality for the subgroups of ideally eligible patients, with 95% CIs under 1.0 for both PAC/LTC and community admissions, indicating better survival among those who were ideally eligible for reperfusion treatment. The unadjusted data indicated that PAC/LTC patients were much more likely than their community counterparts to die within 30 days of AMI (Table 1). The multiple logistic regression results indicates PAC/LTC patients had similar ORs for mortality compared to community patients when aspirin was given to eligible patients and when reperfusion was given to ideally eligible patients (Tables 4 and 5). Based on the logistic regression results, we calculated that the adjusted probability of 30‐day mortality among eligible PAC/LTC patients who received aspirin was 0.14 compared to 0.32 for those who did not, which is a difference in probability of 0.18. For eligible community admissions, the adjusted probability of mortality with aspirin was 0.09 with aspirin treatment compared to 0.26 without. For reperfusion, the adjusted probability of 30‐day mortality for ideally eligible PAC/LTC admissions falls from 0.27 to 0.15 if treatment is given, representing a difference in probability of 0.12. Similarly, the adjusted probability difference for community admissions who were ideally eligible and received reperfusion was approximately 0.08 (P = 0.16 without treatment and P = 0.08 with treatment).

Logistic Regression Predicting 30‐day Mortality Related to Aspirin for PAC/LTC and Community Admissions
Explanatory VariablesPAC/LTC AdmissionsCommunity Admissions
OR95% CIOR95% CI
  • NOTE: Source: CCP Baseline data. Sample inclusive from February 1994 to July 1995. Bold values indicate statistically significant ORs.

  • Abbreviations: APACHE III, the Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision); ASA, acetylsalicylic acid; BMI, body mass index; CCP, Cooperative Cardiovascular Project; CI, confidence interval; FTE, full‐time equivalents employed by the treating hospital; LAT/DNR, limitation of aggressive treatment/do‐not‐resuscitate; OR, odds ratio.

  • *CIs were adjusted to reflect robust standard errors.

  • ORs are presented at the mean value of continuous variables.

Aspirin (ASA) given during hospital stay0.500.43‐0.580.570.54‐0.60
Ideal eligibility for ASA0.880.76‐1.010.700.67‐0.73
Female (vs. Male)0.850.73‐0.990.940.90‐0.98
Patient age, 5‐year increments0.990.94‐1.041.041.02‐1.05
Non‐white Ethnicity (vs. White)0.980.76‐1.280.950.89‐1.03
Current Smoker (vs. non‐smoker)0.930.71‐1.220.970.91‐1.03
Body mass index0.990.97‐1.000.990.99‐1.00
LAT/DNR Order4.093.53‐4.737.837.46‐8.21
APACHE 3 Score, 5 point increments1.101.08‐1.121.131.12‐1.13
Charlson Index, 3 point increments0.870.74‐1.031.061.00‐1.11
Patient received in transfer0.990.65‐1.511.180.95‐1.46
Number of hospital residents, 5 FTE increments1.001.00‐1.001.001.00‐1.00
Hospital located in rural area1.100.92‐1.311.091.03‐1.15
Number of cardiologists on staff, 5 FTE increments0.970.94‐1.001.001.00‐1.02
C‐statistic0.76 0.79 
Number of observations4,559 92,004 
Logistic Regression Predicting 30‐day Mortality Related to Reperfusion for PAC/LTC and Community Admissions
Explanatory VariablesPAC/LTC AdmissionsCommunity Admissions
OR95% CI*OR95% CI*
  • NOTE: Source: CCP Baseline data. Sample inclusive from February 1994 to July 1995. Bold text indicates statistically significant ORs.

  • Abbreviations: APACHE III, Acute Physiology, Age, Chronic Health Evaluation assessment (3rd revision); BMI, body mass index; CCP, Cooperative Cardiovascular Project; CI, confidence interval; FTE, full‐time equivalents employed by the treating hospital; LAT/DNR, limitation of aggressive treatment/do‐not‐resuscitate; OR, odds ratio; PAC/LTC, post‐acute/long‐term care; PTCA, percutaneous intervention.

  • CIs were adjusted to reflect robust standard errors.

  • ORs are presented as the mean value of continuous variables.

Reperfusion via thrombolytics or PTCA1.330.85‐.101.241.13‐1.35
Ideal eligibility for reperfusion0.580.35‐0.950.740.68‐0.81
Female (vs. male)0.920.66‐1.291.050.97‐1.14
Patient age, 5‐year increments0.970.85‐1.101.030.99‐1.06
Non‐White ethnicity (vs. White)1.110.59‐2.101.100.95‐1.28
Current smoker (vs. nonsmoker)1.130.66‐1.940.870.78‐0.98
BMI1.010.98‐1.041.000.99‐1.01
LAT/DNR order3.412.48‐4.708.267.52‐9.06
APACHE III score, 5‐point increments1.131.07‐1.191.151.14‐1.17
Charlson comorbidity index, 3‐point increments0.840.58‐1.221.301.17‐1.44
Patient received in transfer1.080.27‐4.431.490.85‐2.60
Number of hospital residents, 5‐FTE increments0.990.98‐1.011.001.00‐1.00
Hospital located in rural area0.900.61‐1.341.121.01‐1.25
Number of cardiologists on staff, 5‐FTE increments0.970.90‐1.051.000.98‐1.01
C‐statistic0.71 0.78 
Number of observations856 26,720 

Discussion

This investigation has important implications. The results suggest systematic differences in care for PAC/LTC compared to community‐based patients hospitalized with AMI. It is possible that short‐term mortality was impacted by guideline adherence differences according to admission source. The analytic methods accounted for clinical eligibility, tested for residual confounding and used econometric methods (SUR bivariate probit) to correct it where found, and excluded patients who refused treatments. Therefore, poor eligibility and treatment refusal are inadequate explanations for the observed differences in treatment according to admission source from a PAC/LTC facility.

Providers may not to follow AMI treatment guidelines because the perceived risks for patients transferred from PAC/LTC were too great or due to a limited clinical evidence base. Even though PAC/LTC patients were not included in clinical trials for AMI care, studies that carefully use observational data may help guide applicability of clinical recommendations for acute care to subgroups of clinically complex patients. This study offers observational evidence and information to guide additional studies regarding of the clinical benefit of treating a particularly vulnerable subgroup of patients.

Other research has noted that adherence to clinical practice guidelines in PAC/LTC facilities is low.36, 37 LTC practitioners have been reluctant to apply clinical practice guidelines to residents with chronic illnesses because these regimens often do not take into consideration individuals with the multiple chronic diseases prevalent among PAC/LTC patients9 and the complexity of the PAC/LTC environment.38, 39 Rather than dismiss the utility of clinical practice guidelines in the PAC/LTC population, this study is one of the first to demonstrate that use of acute care clinical practice guidelines, particularly aspirin, was associated with improved acute care outcomes among PAC/LTC patients transferred to acute care hospitals with AMI. Thus, guidelines for acute inpatient care may be more readily applied to the PAC/LTC population than studies aimed at treating chronic illnesses.9, 38, 40 Our results indicate that reperfusion might not be indicated for the preponderance of PAC/LTC patients, but many would agree that treatments such as aspirin would be a low‐burden intervention for most PAC/LTC patients. This investigation supports considering AMI treatment guidelines even for frail subpopulations such as those transferred from PAC/LTC. Further, the findings suggest there may be important information obtained by including PAC/LTC patients in future clinical trials.

This study has several limitations. First, the data were collected during 1995, and may not adequately reflect the current state of the art for AMI treatment or other changes in the organization, financing, and delivery of care for AMI. Nevertheless, care guidelines for AMI have not changed in ways that we anticipate altering the patterns of care examined in this study. For example, in the 2004 National Healthcare Disparities Report,41 receipt of aspirin among elderly individuals ranged from 79.6% to 86%, which closely resembles our results. Despite overall care improvements from 1990 to 2006, women, minorities, and patients ages 75 years and older remain significantly less likely to receive revascularization or discharge lipid‐lowering therapy relative to their counterparts indicating that differences in care persist today.42 While the data used in these analyses existed before recommendations included specific guidance regarding the care of older adults, other researchers examined data collected from January 1, 2005 to June 30, 2006 and demonstrated that elderly individuals remained less likely to receive indicated therapies.43 Further, this is the only dataset we identified that included an adequate presence of both PAC/LTC and community admission sources and sufficient data to assess guideline adherence and other covariates for our models. Second, The SUR bivariate probit models that account for correlation of error terms in models predicting both admission source and treatment were included to minimize issues related to residual confounding, but may not completely eliminate all systematic variation related to the underlying health status of community vs. PAC/LTC residents. Third, limitation of aggressive treatments was not recorded as to specific type of directives but research has shown that orders to forego treatments other than CPR are written for fewer than 8 % of nursing home residents.44, 45 Furthermore, all of these patients were transferred to a hospital; these transfers almost certainly occurred with an expectation that acute treatment would be offered. Fourth, we were unable to distinguish PAC vs. LTC based on admission source categories provided in the original data source. Finally, PTCA and thrombolysis were considered as a single variable because separating the 2 procedures would result in inadequate sample size to detect statistical differences between the 2 groups.

Conclusions

Patients admitted from PAC/LTC settings were less likely to receive early guideline‐recommended treatment for AMI compared to community‐dwelling patients. Our study finds evidence that following the aspirin guideline may improve survival for most patients, but that reperfusion improved survival only for a clinically‐select subgroup of patients. As such, a possible recommendation for further clinical study is that low‐burden treatments such as aspirin should be offered to most patients with AMI, including those from PAC/LTC. Higher‐burden treatments with have greater associated risks, such as reperfusion, also require more study to inform situations applicable to PAC/LTC patients. Clinical trials data would be indicated to strengthen evidence regarding which AMI treatment guidelines should be followed in frail populations from PAC/LTC settings; we identified no randomized trials that specifically demonstrate efficacy of AMI guidelines for this subgroup of vulnerable patients.

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  38. Hutt E,Reznickova N,Morgenstern N,Frederickson E,Kramer AM.Improving care for nursing home‐acquired pneumonia in a managed care environment.Am J Manag Care.2004;10(10):681686.
  39. Colon‐Emeric CS,Lekan D,Utley‐Smith Q, et al.Barriers to and facilitators of clinical practice guideline use in nursing homes.J Am Geriatr Soc.2007;55(9):14041409.
  40. Tinetti ME,Bogardus ST,Agostini JV.Potential pitfalls of disease‐specific guidelines for patients with multiple conditions.N Engl J Med.2004;351(27):28702874.
  41. Holmes JS,Arispe IE,Moy E.Heart disease and prevention: race and age differences in heart disease prevention, treatment, and mortality.Med Care.2005;43(3 suppl):I33I41.
  42. Peterson ED,Shah BR,Parsons L, et al.Trends in quality of care for patients with acute myocardial infarction in the National Registry of Myocardial Infarction from 1990 to 2006.Am Heart J.2008;156(6):10451055.
  43. Alexander KP,Roe MT,Chen AY, et al.Evolution in cardiovascular care for elderly patients with non‐ST‐segment elevation acute coronary syndromes: results from the CRUSADE National Quality Improvement Initiative.J Am Coll Cardiol.2005;46(8):14791487.
  44. Bradley EH,Peiris V,Wetle T.Discussions about end‐of‐life care in nursing homes.J Am Geriatr Soc.1998;46:12351241.
  45. Teno J,Branco K,Mor C, et al.Changes in advance care planning in nursing homes before and after the Patient Self‐Determination Act: report of a 10‐state survey.J Am Geriatr Soc.1997;45(8):939944.
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  37. Resnick B,Quinn C,Baxter S.Testing the feasibility of implementation of clinical practice guidelines in long‐term care facilities.J Am Med Dir Assoc.2004;5(1):18.
  38. Hutt E,Reznickova N,Morgenstern N,Frederickson E,Kramer AM.Improving care for nursing home‐acquired pneumonia in a managed care environment.Am J Manag Care.2004;10(10):681686.
  39. Colon‐Emeric CS,Lekan D,Utley‐Smith Q, et al.Barriers to and facilitators of clinical practice guideline use in nursing homes.J Am Geriatr Soc.2007;55(9):14041409.
  40. Tinetti ME,Bogardus ST,Agostini JV.Potential pitfalls of disease‐specific guidelines for patients with multiple conditions.N Engl J Med.2004;351(27):28702874.
  41. Holmes JS,Arispe IE,Moy E.Heart disease and prevention: race and age differences in heart disease prevention, treatment, and mortality.Med Care.2005;43(3 suppl):I33I41.
  42. Peterson ED,Shah BR,Parsons L, et al.Trends in quality of care for patients with acute myocardial infarction in the National Registry of Myocardial Infarction from 1990 to 2006.Am Heart J.2008;156(6):10451055.
  43. Alexander KP,Roe MT,Chen AY, et al.Evolution in cardiovascular care for elderly patients with non‐ST‐segment elevation acute coronary syndromes: results from the CRUSADE National Quality Improvement Initiative.J Am Coll Cardiol.2005;46(8):14791487.
  44. Bradley EH,Peiris V,Wetle T.Discussions about end‐of‐life care in nursing homes.J Am Geriatr Soc.1998;46:12351241.
  45. Teno J,Branco K,Mor C, et al.Changes in advance care planning in nursing homes before and after the Patient Self‐Determination Act: report of a 10‐state survey.J Am Geriatr Soc.1997;45(8):939944.
Issue
Journal of Hospital Medicine - 5(2)
Issue
Journal of Hospital Medicine - 5(2)
Page Number
E3-E10
Page Number
E3-E10
Article Type
Display Headline
Examining guideline‐concordant care for acute myocardial infarction (AMI): The case of hospitalized post‐acute and long‐term care (PAC/LTC) residents
Display Headline
Examining guideline‐concordant care for acute myocardial infarction (AMI): The case of hospitalized post‐acute and long‐term care (PAC/LTC) residents
Legacy Keywords
acute myocardial infarction, clinical practice guidelines, geriatrics, long‐term care, nursing home, post‐acute care
Legacy Keywords
acute myocardial infarction, clinical practice guidelines, geriatrics, long‐term care, nursing home, post‐acute care
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