ACE inhibitors are better than diuretics for treatment of hypertension in the elderly

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ACE inhibitors are better than diuretics for treatment of hypertension in the elderly
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Despite similar reductions in blood pressure, angiotensin-converting enzyme (ACE) inhibitors demonstrate lower combined rates of cardiovascular events or all-cause mortality in elderly hypertensive patients compared with diuretics. This benefit is most evident in men.

These results may differ from those of the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack (ALLHAT) trial because that study included younger patients, had a greater representation of patients with African ancestry, used different brands of medication, and had a slightly different primary outcome. Despite these differences, both treatments offer an inexpensive means for reducing blood pressure and preventing hypertension-related complications.

 
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Wing LM, Reid CM, Ryan P, et al. A comparison of outcomes with angiotensin-converting-enzyme inhibitors and diuretics for hypertension in the elderly. N Engl J Med 2003; 348:583–592.

Jenny M. Frazier, MD
Kevin Y. Kane, MD MSPH
Department of Family Practice, University of Missouri–Columbia. E-mail: [email protected].

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Wing LM, Reid CM, Ryan P, et al. A comparison of outcomes with angiotensin-converting-enzyme inhibitors and diuretics for hypertension in the elderly. N Engl J Med 2003; 348:583–592.

Jenny M. Frazier, MD
Kevin Y. Kane, MD MSPH
Department of Family Practice, University of Missouri–Columbia. E-mail: [email protected].

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Wing LM, Reid CM, Ryan P, et al. A comparison of outcomes with angiotensin-converting-enzyme inhibitors and diuretics for hypertension in the elderly. N Engl J Med 2003; 348:583–592.

Jenny M. Frazier, MD
Kevin Y. Kane, MD MSPH
Department of Family Practice, University of Missouri–Columbia. E-mail: [email protected].

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PRACTICE RECOMMENDATIONS

Despite similar reductions in blood pressure, angiotensin-converting enzyme (ACE) inhibitors demonstrate lower combined rates of cardiovascular events or all-cause mortality in elderly hypertensive patients compared with diuretics. This benefit is most evident in men.

These results may differ from those of the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack (ALLHAT) trial because that study included younger patients, had a greater representation of patients with African ancestry, used different brands of medication, and had a slightly different primary outcome. Despite these differences, both treatments offer an inexpensive means for reducing blood pressure and preventing hypertension-related complications.

 
PRACTICE RECOMMENDATIONS

Despite similar reductions in blood pressure, angiotensin-converting enzyme (ACE) inhibitors demonstrate lower combined rates of cardiovascular events or all-cause mortality in elderly hypertensive patients compared with diuretics. This benefit is most evident in men.

These results may differ from those of the Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack (ALLHAT) trial because that study included younger patients, had a greater representation of patients with African ancestry, used different brands of medication, and had a slightly different primary outcome. Despite these differences, both treatments offer an inexpensive means for reducing blood pressure and preventing hypertension-related complications.

 
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Analgesics do not interfere with diagnosing abdominal pain

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Analgesics do not interfere with diagnosing abdominal pain
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Despite the limitations in this review, it seems appropriate to administer analgesics to patients with generalized abdominal pain, even before a surgical evaluation. Surgeons can be assured that they will not be misled as a result of analgesia.

 
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Thomas SH, Silen W. Effect on diagnostic efficiency of analgesia for undifferentiated abdominal pain. Br J Surg 2003; 90:5–9.

Brian T. Easton, MD
Department of Family Medicine, University of Virginia, Highlands Family Medicine, Lebanon, Va. E-mail: [email protected].

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Thomas SH, Silen W. Effect on diagnostic efficiency of analgesia for undifferentiated abdominal pain. Br J Surg 2003; 90:5–9.

Brian T. Easton, MD
Department of Family Medicine, University of Virginia, Highlands Family Medicine, Lebanon, Va. E-mail: [email protected].

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Thomas SH, Silen W. Effect on diagnostic efficiency of analgesia for undifferentiated abdominal pain. Br J Surg 2003; 90:5–9.

Brian T. Easton, MD
Department of Family Medicine, University of Virginia, Highlands Family Medicine, Lebanon, Va. E-mail: [email protected].

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PRACTICE RECOMMENDATIONS

Despite the limitations in this review, it seems appropriate to administer analgesics to patients with generalized abdominal pain, even before a surgical evaluation. Surgeons can be assured that they will not be misled as a result of analgesia.

 
PRACTICE RECOMMENDATIONS

Despite the limitations in this review, it seems appropriate to administer analgesics to patients with generalized abdominal pain, even before a surgical evaluation. Surgeons can be assured that they will not be misled as a result of analgesia.

 
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12-hour protocol safe for cocaine-associated chest pain

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12-hour protocol safe for cocaine-associated chest pain
PRACTICE RECOMMENDATIONS

A 12-hour emergency department observation period is safe for patients with cocaine-associated chest pain, provided they have symptoms consistent with low-to-intermediate likelihood of unstable angina according to the Braunwald classification, and normal serial troponin I levels and cardiogram.

Patients with traditional cardiac risk factors should undergo cardiac stress testing within 2 weeks following the chest pain event, as atherosclerosis enhances the vasoconstrictive effects of cocaine. All patients should be referred for substance abuse counseling, as recurrent cocaine use was associated with subsequent nonfatal myocardial infarction (MI).

 
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Weber JE, Shofer FS, Larkin GL, et al. Validation of a brief observation period for patients with cocaine-associated chest pain. N Engl J Med 2003; 348:510–517.

Christy L. Arthur, MD
Mark H. Greenawald, MD
Carilion Family Practice Residency, Roanoke, Va. E-mail: [email protected].

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Weber JE, Shofer FS, Larkin GL, et al. Validation of a brief observation period for patients with cocaine-associated chest pain. N Engl J Med 2003; 348:510–517.

Christy L. Arthur, MD
Mark H. Greenawald, MD
Carilion Family Practice Residency, Roanoke, Va. E-mail: [email protected].

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Weber JE, Shofer FS, Larkin GL, et al. Validation of a brief observation period for patients with cocaine-associated chest pain. N Engl J Med 2003; 348:510–517.

Christy L. Arthur, MD
Mark H. Greenawald, MD
Carilion Family Practice Residency, Roanoke, Va. E-mail: [email protected].

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Article PDF
PRACTICE RECOMMENDATIONS

A 12-hour emergency department observation period is safe for patients with cocaine-associated chest pain, provided they have symptoms consistent with low-to-intermediate likelihood of unstable angina according to the Braunwald classification, and normal serial troponin I levels and cardiogram.

Patients with traditional cardiac risk factors should undergo cardiac stress testing within 2 weeks following the chest pain event, as atherosclerosis enhances the vasoconstrictive effects of cocaine. All patients should be referred for substance abuse counseling, as recurrent cocaine use was associated with subsequent nonfatal myocardial infarction (MI).

 
PRACTICE RECOMMENDATIONS

A 12-hour emergency department observation period is safe for patients with cocaine-associated chest pain, provided they have symptoms consistent with low-to-intermediate likelihood of unstable angina according to the Braunwald classification, and normal serial troponin I levels and cardiogram.

Patients with traditional cardiac risk factors should undergo cardiac stress testing within 2 weeks following the chest pain event, as atherosclerosis enhances the vasoconstrictive effects of cocaine. All patients should be referred for substance abuse counseling, as recurrent cocaine use was associated with subsequent nonfatal myocardial infarction (MI).

 
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Transdermal progesterone ineffective for menopausal symptoms

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Transdermal progesterone ineffective for menopausal symptoms
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Transdermal progesterone cream, at the dose used in this study, did not improve menopausal symptoms compared with placebo. The study, however, might not have been large enough to detect a difference if one really exists.

In light of recent safety concerns over the use of other types of hormone replacement therapy, treatment of menopausal symptoms with transdermal progesterone should not be used unless better information supporting its benefit becomes available.

 
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Wren BG, Champion SM, Willetts K, Manga RZ, Eden JA. Transdermal progesterone and its effect on vasomotor symptoms, blood lipid levels, bone metabolic markers, moods, and quality of life for postmenopausal women. Menopause 2003; 10:13–18.

Deborah Sturpe, PharmD, BCPS
Department of Pharmacy Practice and Science University of Maryland School of Pharmacy, Baltimore

[email protected]

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Wren BG, Champion SM, Willetts K, Manga RZ, Eden JA. Transdermal progesterone and its effect on vasomotor symptoms, blood lipid levels, bone metabolic markers, moods, and quality of life for postmenopausal women. Menopause 2003; 10:13–18.

Deborah Sturpe, PharmD, BCPS
Department of Pharmacy Practice and Science University of Maryland School of Pharmacy, Baltimore

[email protected]

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Wren BG, Champion SM, Willetts K, Manga RZ, Eden JA. Transdermal progesterone and its effect on vasomotor symptoms, blood lipid levels, bone metabolic markers, moods, and quality of life for postmenopausal women. Menopause 2003; 10:13–18.

Deborah Sturpe, PharmD, BCPS
Department of Pharmacy Practice and Science University of Maryland School of Pharmacy, Baltimore

[email protected]

Article PDF
Article PDF
PRACTICE RECOMMENDATIONS

Transdermal progesterone cream, at the dose used in this study, did not improve menopausal symptoms compared with placebo. The study, however, might not have been large enough to detect a difference if one really exists.

In light of recent safety concerns over the use of other types of hormone replacement therapy, treatment of menopausal symptoms with transdermal progesterone should not be used unless better information supporting its benefit becomes available.

 
PRACTICE RECOMMENDATIONS

Transdermal progesterone cream, at the dose used in this study, did not improve menopausal symptoms compared with placebo. The study, however, might not have been large enough to detect a difference if one really exists.

In light of recent safety concerns over the use of other types of hormone replacement therapy, treatment of menopausal symptoms with transdermal progesterone should not be used unless better information supporting its benefit becomes available.

 
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Optimal digoxin range for men is 0.5 to 0.8 ng/mL

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PRACTICE RECOMMENDATIONS

The optimal serum drug concentration for digoxin among men in sinus rhythm with stable heart failure is 0.5 to 0.8 ng/mL. This range is associated with decreased risk of hospitalization and mortality compared with placebo. Higher levels are associated with either no reduction, or an increased risk of hospitalization and mortality compared with placebo.

 
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Rathore SS, Curtis JP, Wang Y, Bristow MR, Krumholz, HM. Association of serum digoxin concentration and outcomes in patients with heart failure. JAMA 2003; 289:871–878.

Jeffrey Rosenberg, MD
Carol Federiuk, MD, PhD
Department of Family Medicine, Thomas Jefferson University, Philadelphia, Pa

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Rathore SS, Curtis JP, Wang Y, Bristow MR, Krumholz, HM. Association of serum digoxin concentration and outcomes in patients with heart failure. JAMA 2003; 289:871–878.

Jeffrey Rosenberg, MD
Carol Federiuk, MD, PhD
Department of Family Medicine, Thomas Jefferson University, Philadelphia, Pa

[email protected]

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Rathore SS, Curtis JP, Wang Y, Bristow MR, Krumholz, HM. Association of serum digoxin concentration and outcomes in patients with heart failure. JAMA 2003; 289:871–878.

Jeffrey Rosenberg, MD
Carol Federiuk, MD, PhD
Department of Family Medicine, Thomas Jefferson University, Philadelphia, Pa

[email protected]

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Article PDF
PRACTICE RECOMMENDATIONS

The optimal serum drug concentration for digoxin among men in sinus rhythm with stable heart failure is 0.5 to 0.8 ng/mL. This range is associated with decreased risk of hospitalization and mortality compared with placebo. Higher levels are associated with either no reduction, or an increased risk of hospitalization and mortality compared with placebo.

 
PRACTICE RECOMMENDATIONS

The optimal serum drug concentration for digoxin among men in sinus rhythm with stable heart failure is 0.5 to 0.8 ng/mL. This range is associated with decreased risk of hospitalization and mortality compared with placebo. Higher levels are associated with either no reduction, or an increased risk of hospitalization and mortality compared with placebo.

 
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Nebulized 3% saline effective for viral bronchiolitis

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Nebulized 3% saline effective for viral bronchiolitis
PRACTICE RECOMMENDATIONS

This small, poorly described study suggests that nebulized 3% hypertonic saline improves outcomes for nonhospitalized infants with bronchiolitis more than the use of normal saline.

While this study has significant flaws, the intervention appears safe. It would be reasonable to use nebulized 3% saline while waiting for larger, better studies.

 
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Sarrell EM, Tal G, Witzling M, et al. Nebulized 3% hypertonic saline solution treatment in ambulatory children with viral bronchiolitis decreases symptoms. Chest 2002; 122:2015–2020.

Andrea D. Tribastone, MD
University of Virginia, Stoney Creek Family Practice Nellysford, Va

[email protected]

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Sarrell EM, Tal G, Witzling M, et al. Nebulized 3% hypertonic saline solution treatment in ambulatory children with viral bronchiolitis decreases symptoms. Chest 2002; 122:2015–2020.

Andrea D. Tribastone, MD
University of Virginia, Stoney Creek Family Practice Nellysford, Va

[email protected]

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Sarrell EM, Tal G, Witzling M, et al. Nebulized 3% hypertonic saline solution treatment in ambulatory children with viral bronchiolitis decreases symptoms. Chest 2002; 122:2015–2020.

Andrea D. Tribastone, MD
University of Virginia, Stoney Creek Family Practice Nellysford, Va

[email protected]

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Article PDF
PRACTICE RECOMMENDATIONS

This small, poorly described study suggests that nebulized 3% hypertonic saline improves outcomes for nonhospitalized infants with bronchiolitis more than the use of normal saline.

While this study has significant flaws, the intervention appears safe. It would be reasonable to use nebulized 3% saline while waiting for larger, better studies.

 
PRACTICE RECOMMENDATIONS

This small, poorly described study suggests that nebulized 3% hypertonic saline improves outcomes for nonhospitalized infants with bronchiolitis more than the use of normal saline.

While this study has significant flaws, the intervention appears safe. It would be reasonable to use nebulized 3% saline while waiting for larger, better studies.

 
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What is a reasonable interval for retinopathy screening in patients with diabetes?

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What is a reasonable interval for retinopathy screening in patients with diabetes?
PRACTICE RECOMMENDATIONS

Assuming that a given patient is reliable for follow-up and that a clinical system is in place to handle a more individualized screening protocol, the investigators suggest the following approach: 3-year intervals for patients with no retinopathy and no risk factors (risk factors being diabetes for longer than 20 years or use of insulin); annual screening for patients with no retinopathy and 1 or both risk factors or for patients with background retinopathy; and 4-month intervals for patients with mild preproliferative retinopathy.

These intervals provide at least a 95% probability of remaining free of sight-threatening diabetic retinopathy between screenings.

 
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Younis N, Broadbent DM, Vora JP, Harding SP. Incidence of sight-threatening retinopathy in patients with type 2 diabetes in the Liverpool Diabetic Eye Study: a cohort study. Lancet 2003; 361:195–200.

Seth Miller, MD
Erik J. Lindbloom, MD, MSPH
Department of Family and Community Medicine, University of Missouri–Columbia

[email protected]

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Younis N, Broadbent DM, Vora JP, Harding SP. Incidence of sight-threatening retinopathy in patients with type 2 diabetes in the Liverpool Diabetic Eye Study: a cohort study. Lancet 2003; 361:195–200.

Seth Miller, MD
Erik J. Lindbloom, MD, MSPH
Department of Family and Community Medicine, University of Missouri–Columbia

[email protected]

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Younis N, Broadbent DM, Vora JP, Harding SP. Incidence of sight-threatening retinopathy in patients with type 2 diabetes in the Liverpool Diabetic Eye Study: a cohort study. Lancet 2003; 361:195–200.

Seth Miller, MD
Erik J. Lindbloom, MD, MSPH
Department of Family and Community Medicine, University of Missouri–Columbia

[email protected]

Article PDF
Article PDF
PRACTICE RECOMMENDATIONS

Assuming that a given patient is reliable for follow-up and that a clinical system is in place to handle a more individualized screening protocol, the investigators suggest the following approach: 3-year intervals for patients with no retinopathy and no risk factors (risk factors being diabetes for longer than 20 years or use of insulin); annual screening for patients with no retinopathy and 1 or both risk factors or for patients with background retinopathy; and 4-month intervals for patients with mild preproliferative retinopathy.

These intervals provide at least a 95% probability of remaining free of sight-threatening diabetic retinopathy between screenings.

 
PRACTICE RECOMMENDATIONS

Assuming that a given patient is reliable for follow-up and that a clinical system is in place to handle a more individualized screening protocol, the investigators suggest the following approach: 3-year intervals for patients with no retinopathy and no risk factors (risk factors being diabetes for longer than 20 years or use of insulin); annual screening for patients with no retinopathy and 1 or both risk factors or for patients with background retinopathy; and 4-month intervals for patients with mild preproliferative retinopathy.

These intervals provide at least a 95% probability of remaining free of sight-threatening diabetic retinopathy between screenings.

 
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Low-dose tricyclics effective for depression

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Low-dose tricyclics effective for depression
PRACTICE RECOMMENDATIONS

Minimum effective dosage and ranges for antidepressants have not been established. While studies suggest that lower-dose tricyclic antidepressants (TCAs) may be as effective as higherdose TCAs, dose comparison studies with other antidepressants have not been conducted.

Low-dose TCAs may not be as effective as standard doses, but they do have fewer treatment dropouts due to side effects, and thus patients may have better long-term compliance. Regular monitoring of patient rate of reduction in severity of depression should be used to help determine optimal individual dosing.

 
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Furukawa TA, McGuire H, Barbui C. Meta-analysis of effects and side effects of low dosage tricyclic antidepressants in depression: systematic review. BMJ 2002; 325:991–995.

Eugene R. Bailey, MD
Kenneth M. Johnson, III,, MD
Center for Evidence-Based Practice, Department of Family Medicine, SUNY Upstate Medical University, Syracuse, NY

[email protected]

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Furukawa TA, McGuire H, Barbui C. Meta-analysis of effects and side effects of low dosage tricyclic antidepressants in depression: systematic review. BMJ 2002; 325:991–995.

Eugene R. Bailey, MD
Kenneth M. Johnson, III,, MD
Center for Evidence-Based Practice, Department of Family Medicine, SUNY Upstate Medical University, Syracuse, NY

[email protected]

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Furukawa TA, McGuire H, Barbui C. Meta-analysis of effects and side effects of low dosage tricyclic antidepressants in depression: systematic review. BMJ 2002; 325:991–995.

Eugene R. Bailey, MD
Kenneth M. Johnson, III,, MD
Center for Evidence-Based Practice, Department of Family Medicine, SUNY Upstate Medical University, Syracuse, NY

[email protected]

Article PDF
Article PDF
PRACTICE RECOMMENDATIONS

Minimum effective dosage and ranges for antidepressants have not been established. While studies suggest that lower-dose tricyclic antidepressants (TCAs) may be as effective as higherdose TCAs, dose comparison studies with other antidepressants have not been conducted.

Low-dose TCAs may not be as effective as standard doses, but they do have fewer treatment dropouts due to side effects, and thus patients may have better long-term compliance. Regular monitoring of patient rate of reduction in severity of depression should be used to help determine optimal individual dosing.

 
PRACTICE RECOMMENDATIONS

Minimum effective dosage and ranges for antidepressants have not been established. While studies suggest that lower-dose tricyclic antidepressants (TCAs) may be as effective as higherdose TCAs, dose comparison studies with other antidepressants have not been conducted.

Low-dose TCAs may not be as effective as standard doses, but they do have fewer treatment dropouts due to side effects, and thus patients may have better long-term compliance. Regular monitoring of patient rate of reduction in severity of depression should be used to help determine optimal individual dosing.

 
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Ultrasonography helpful in diagnosing developmental hip dysplasia

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Ultrasonography helpful in diagnosing developmental hip dysplasia
PRACTICE RECOMMENDATIONS

Ultrasonography for diagnosis and management of possible hip instability may lead to less splinting and surgery in the first 2 years of life, with no significant difference in radiographic abnormalities. Cost-effectiveness, long-term hip mobility, and consistency of ultrasound interpretation is not proven.

 
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Elbourne D, Dezateux C, Arthur R, et al. Ultrasonography in the diagnosis and management of developmental hip dysplasia (UK Hip Trial): clinical and economic results of a multicentre randomised controlled trial. Lancet 2002; 360:2009–2017.

Jennifer Bowe, MD
Erik J. Lindbloom, MD, MSPH
Department of Family and Community Medicine, University of Missouri–Columbia

[email protected]

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Elbourne D, Dezateux C, Arthur R, et al. Ultrasonography in the diagnosis and management of developmental hip dysplasia (UK Hip Trial): clinical and economic results of a multicentre randomised controlled trial. Lancet 2002; 360:2009–2017.

Jennifer Bowe, MD
Erik J. Lindbloom, MD, MSPH
Department of Family and Community Medicine, University of Missouri–Columbia

[email protected]

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Elbourne D, Dezateux C, Arthur R, et al. Ultrasonography in the diagnosis and management of developmental hip dysplasia (UK Hip Trial): clinical and economic results of a multicentre randomised controlled trial. Lancet 2002; 360:2009–2017.

Jennifer Bowe, MD
Erik J. Lindbloom, MD, MSPH
Department of Family and Community Medicine, University of Missouri–Columbia

[email protected]

Article PDF
Article PDF
PRACTICE RECOMMENDATIONS

Ultrasonography for diagnosis and management of possible hip instability may lead to less splinting and surgery in the first 2 years of life, with no significant difference in radiographic abnormalities. Cost-effectiveness, long-term hip mobility, and consistency of ultrasound interpretation is not proven.

 
PRACTICE RECOMMENDATIONS

Ultrasonography for diagnosis and management of possible hip instability may lead to less splinting and surgery in the first 2 years of life, with no significant difference in radiographic abnormalities. Cost-effectiveness, long-term hip mobility, and consistency of ultrasound interpretation is not proven.

 
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Use of sputum eosinophil count decreases asthma exacerbations

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Use of sputum eosinophil count decreases asthma exacerbations
PRACTICE RECOMMENDATIONS

The use of regular sputum eosinophil counts to initiate and follow treatment in patients with asthma produced a small decrease in the number of hospitalizations and asthma exacerbations in compliant, moderate-to-severe asthmatics.

The definition of asthma exacerbation used in this study (a 30% decrease in morning peak expiratory flow on 2 consecutive days or initiation of oral corticosteroids) may not be clinically relevant.

 
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Green RH, Brightling CE, McKenna S, et al. Asthma exacerbations and sputum eosinophil counts: a randomized controlled trial. Lancet 2002; 360:1715–1721.

Heather Bittner Fagan, MD
Marc Harwood, MD
Thomas Jefferson University Family Practice Philadelphia, Pa

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Green RH, Brightling CE, McKenna S, et al. Asthma exacerbations and sputum eosinophil counts: a randomized controlled trial. Lancet 2002; 360:1715–1721.

Heather Bittner Fagan, MD
Marc Harwood, MD
Thomas Jefferson University Family Practice Philadelphia, Pa

[email protected]

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Green RH, Brightling CE, McKenna S, et al. Asthma exacerbations and sputum eosinophil counts: a randomized controlled trial. Lancet 2002; 360:1715–1721.

Heather Bittner Fagan, MD
Marc Harwood, MD
Thomas Jefferson University Family Practice Philadelphia, Pa

[email protected]

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PRACTICE RECOMMENDATIONS

The use of regular sputum eosinophil counts to initiate and follow treatment in patients with asthma produced a small decrease in the number of hospitalizations and asthma exacerbations in compliant, moderate-to-severe asthmatics.

The definition of asthma exacerbation used in this study (a 30% decrease in morning peak expiratory flow on 2 consecutive days or initiation of oral corticosteroids) may not be clinically relevant.

 
PRACTICE RECOMMENDATIONS

The use of regular sputum eosinophil counts to initiate and follow treatment in patients with asthma produced a small decrease in the number of hospitalizations and asthma exacerbations in compliant, moderate-to-severe asthmatics.

The definition of asthma exacerbation used in this study (a 30% decrease in morning peak expiratory flow on 2 consecutive days or initiation of oral corticosteroids) may not be clinically relevant.

 
Issue
The Journal of Family Practice - 52(5)
Issue
The Journal of Family Practice - 52(5)
Page Number
349-364
Page Number
349-364
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Use of sputum eosinophil count decreases asthma exacerbations
Display Headline
Use of sputum eosinophil count decreases asthma exacerbations
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