What Keeps You Awake at Night?

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What Keeps You Awake at Night?

"The greatest enemy of knowledge is the illusion of knowledge." – Stephen Hawking

In my fellowship, I had a challenging RA case. This woman was in her 50s, and usually she was quite dynamic, personable, and spunky. But the disease was wearing her down. She developed methotrexate pneumonitis. Leflunomide gave her severe diarrhea. She got frequent upper respiratory tract infections from etanercept. We could not get her prednisone dose lower than 15 mg/day. Whenever we saw her in clinic and she had encountered a new glitch in her treatment, my preceptor would say to her "you keep me up at night." Disturbed to hear this, I wondered how insecure I would be as a newly minted rheumatologist if my preceptor, with her decades of practice, still had uncertainties.

I feel like in these, the first 3 years of practice after training, I have an inordinate number of patients who keep me up at night. They come in all shapes and sizes. Even cases that I think are straightforward frequently end up being anything but.

I like treating patients with polymyalgia rheumatica, for example, because the relief they get from a little prednisone is so dramatic and immediate. Seems straightforward, no? But I get anxious about the diagnosis sometimes – what if I’m missing a paraneoplastic syndrome? Not infrequently there are patients who absolutely refuse to go on prednisone, and I worry about them, too. Or I get anxious about tapering, because I’ve had it happen often enough that their symptoms recur at 3 mg of prednisone and I need to put them on a DMARD, none of which have any conclusive evidence of efficacy.

Rheumatoid arthritis is not always easy, either. I have had my share of refractory cases, which, in this age of different varieties of biologics, is even more frustrating. (Although, for the life of me, I cannot imagine what it must have been like to practice before the age of biologics!) It’s even worse for refractory psoriatic arthritis, for which there are fewer drug options available.

And what about scleroderma? I watched a patient’s hands progress from being simply puffy at presentation to being contracted, with severe skin tightening and skin ulcerations over the PIP joints, in just 2 years. We are lucky to be close enough to Boston that I could send the patient to a medical center there to receive an investigational therapy, which seemed to lessen the patient’s symptoms somewhat. Unfortunately, she developed urinary bladder cancer and is now ineligible to receive the experimental anti-TGF-beta in an open label extension.

But perhaps my most insomnia-inducing patient is a lovely 70-year-old man with a new diagnosis of dermatomyositis. His antinuclear antibody was negative, and he had no myositis-specific antibodies. We knew we should be looking for a malignancy, but a CT of the chest, abdomen, and pelvis was negative. A colonoscopy was next, but if that did not turn anything up, what would be next? Do we keep searching? How do we know where to look?

Worse, the pulse of methylprednisolone did not work completely, and he ended up needing a percutaneous endoscopic gastrostomy tube because he failed his swallow evaluation miserably. I was really saddened by all this. It made me feel small and insignificant in the face of such a terrible disease.

In that process of placing a PEG tube, we serendipitously found, on biopsy, adenocarcinoma at the gastroesophageal junction. Though this was, indeed, terrible news, it was a source of comfort for me that we had found the malignancy and would at least have a target for treatment.

I know he will not be my last dermatomyositis patient, and there are no prescribed guidelines for searching for a malignancy. How can we possibly find something if we have no idea what it is or where it might be?

I can think of so many more lupus, spondyloarthritis, temporal arteritis, even mechanical back pain patients who worry me, to say nothing of the not-insignificant number of patients for whom the diagnosis is uncertain. True, my learning curve has been steep in these first 3 years, but the more patients I see, the more striking the large number of phenotypes of our diseases. It’s quite humbling and has kept me up more nights than I expected.

Dr. Chan practices rheumatology in Pawtucket, R.I. E-mail her at [email protected].

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"The greatest enemy of knowledge is the illusion of knowledge." – Stephen Hawking

In my fellowship, I had a challenging RA case. This woman was in her 50s, and usually she was quite dynamic, personable, and spunky. But the disease was wearing her down. She developed methotrexate pneumonitis. Leflunomide gave her severe diarrhea. She got frequent upper respiratory tract infections from etanercept. We could not get her prednisone dose lower than 15 mg/day. Whenever we saw her in clinic and she had encountered a new glitch in her treatment, my preceptor would say to her "you keep me up at night." Disturbed to hear this, I wondered how insecure I would be as a newly minted rheumatologist if my preceptor, with her decades of practice, still had uncertainties.

I feel like in these, the first 3 years of practice after training, I have an inordinate number of patients who keep me up at night. They come in all shapes and sizes. Even cases that I think are straightforward frequently end up being anything but.

I like treating patients with polymyalgia rheumatica, for example, because the relief they get from a little prednisone is so dramatic and immediate. Seems straightforward, no? But I get anxious about the diagnosis sometimes – what if I’m missing a paraneoplastic syndrome? Not infrequently there are patients who absolutely refuse to go on prednisone, and I worry about them, too. Or I get anxious about tapering, because I’ve had it happen often enough that their symptoms recur at 3 mg of prednisone and I need to put them on a DMARD, none of which have any conclusive evidence of efficacy.

Rheumatoid arthritis is not always easy, either. I have had my share of refractory cases, which, in this age of different varieties of biologics, is even more frustrating. (Although, for the life of me, I cannot imagine what it must have been like to practice before the age of biologics!) It’s even worse for refractory psoriatic arthritis, for which there are fewer drug options available.

And what about scleroderma? I watched a patient’s hands progress from being simply puffy at presentation to being contracted, with severe skin tightening and skin ulcerations over the PIP joints, in just 2 years. We are lucky to be close enough to Boston that I could send the patient to a medical center there to receive an investigational therapy, which seemed to lessen the patient’s symptoms somewhat. Unfortunately, she developed urinary bladder cancer and is now ineligible to receive the experimental anti-TGF-beta in an open label extension.

But perhaps my most insomnia-inducing patient is a lovely 70-year-old man with a new diagnosis of dermatomyositis. His antinuclear antibody was negative, and he had no myositis-specific antibodies. We knew we should be looking for a malignancy, but a CT of the chest, abdomen, and pelvis was negative. A colonoscopy was next, but if that did not turn anything up, what would be next? Do we keep searching? How do we know where to look?

Worse, the pulse of methylprednisolone did not work completely, and he ended up needing a percutaneous endoscopic gastrostomy tube because he failed his swallow evaluation miserably. I was really saddened by all this. It made me feel small and insignificant in the face of such a terrible disease.

In that process of placing a PEG tube, we serendipitously found, on biopsy, adenocarcinoma at the gastroesophageal junction. Though this was, indeed, terrible news, it was a source of comfort for me that we had found the malignancy and would at least have a target for treatment.

I know he will not be my last dermatomyositis patient, and there are no prescribed guidelines for searching for a malignancy. How can we possibly find something if we have no idea what it is or where it might be?

I can think of so many more lupus, spondyloarthritis, temporal arteritis, even mechanical back pain patients who worry me, to say nothing of the not-insignificant number of patients for whom the diagnosis is uncertain. True, my learning curve has been steep in these first 3 years, but the more patients I see, the more striking the large number of phenotypes of our diseases. It’s quite humbling and has kept me up more nights than I expected.

Dr. Chan practices rheumatology in Pawtucket, R.I. E-mail her at [email protected].

"The greatest enemy of knowledge is the illusion of knowledge." – Stephen Hawking

In my fellowship, I had a challenging RA case. This woman was in her 50s, and usually she was quite dynamic, personable, and spunky. But the disease was wearing her down. She developed methotrexate pneumonitis. Leflunomide gave her severe diarrhea. She got frequent upper respiratory tract infections from etanercept. We could not get her prednisone dose lower than 15 mg/day. Whenever we saw her in clinic and she had encountered a new glitch in her treatment, my preceptor would say to her "you keep me up at night." Disturbed to hear this, I wondered how insecure I would be as a newly minted rheumatologist if my preceptor, with her decades of practice, still had uncertainties.

I feel like in these, the first 3 years of practice after training, I have an inordinate number of patients who keep me up at night. They come in all shapes and sizes. Even cases that I think are straightforward frequently end up being anything but.

I like treating patients with polymyalgia rheumatica, for example, because the relief they get from a little prednisone is so dramatic and immediate. Seems straightforward, no? But I get anxious about the diagnosis sometimes – what if I’m missing a paraneoplastic syndrome? Not infrequently there are patients who absolutely refuse to go on prednisone, and I worry about them, too. Or I get anxious about tapering, because I’ve had it happen often enough that their symptoms recur at 3 mg of prednisone and I need to put them on a DMARD, none of which have any conclusive evidence of efficacy.

Rheumatoid arthritis is not always easy, either. I have had my share of refractory cases, which, in this age of different varieties of biologics, is even more frustrating. (Although, for the life of me, I cannot imagine what it must have been like to practice before the age of biologics!) It’s even worse for refractory psoriatic arthritis, for which there are fewer drug options available.

And what about scleroderma? I watched a patient’s hands progress from being simply puffy at presentation to being contracted, with severe skin tightening and skin ulcerations over the PIP joints, in just 2 years. We are lucky to be close enough to Boston that I could send the patient to a medical center there to receive an investigational therapy, which seemed to lessen the patient’s symptoms somewhat. Unfortunately, she developed urinary bladder cancer and is now ineligible to receive the experimental anti-TGF-beta in an open label extension.

But perhaps my most insomnia-inducing patient is a lovely 70-year-old man with a new diagnosis of dermatomyositis. His antinuclear antibody was negative, and he had no myositis-specific antibodies. We knew we should be looking for a malignancy, but a CT of the chest, abdomen, and pelvis was negative. A colonoscopy was next, but if that did not turn anything up, what would be next? Do we keep searching? How do we know where to look?

Worse, the pulse of methylprednisolone did not work completely, and he ended up needing a percutaneous endoscopic gastrostomy tube because he failed his swallow evaluation miserably. I was really saddened by all this. It made me feel small and insignificant in the face of such a terrible disease.

In that process of placing a PEG tube, we serendipitously found, on biopsy, adenocarcinoma at the gastroesophageal junction. Though this was, indeed, terrible news, it was a source of comfort for me that we had found the malignancy and would at least have a target for treatment.

I know he will not be my last dermatomyositis patient, and there are no prescribed guidelines for searching for a malignancy. How can we possibly find something if we have no idea what it is or where it might be?

I can think of so many more lupus, spondyloarthritis, temporal arteritis, even mechanical back pain patients who worry me, to say nothing of the not-insignificant number of patients for whom the diagnosis is uncertain. True, my learning curve has been steep in these first 3 years, but the more patients I see, the more striking the large number of phenotypes of our diseases. It’s quite humbling and has kept me up more nights than I expected.

Dr. Chan practices rheumatology in Pawtucket, R.I. E-mail her at [email protected].

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Communicating Discharge Instructions

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Communicating discharge instructions to patients: A survey of nurse, intern, and hospitalist practices

Discharge from the hospital is a vulnerable time for patients. Nearly 1 in 5 patients experiences an adverse event during this transition, with a third of these being likely preventable.1, 2 Comprehensive discharge instructions are necessary to ensure a smooth transition from hospital to home, as the responsibility for care shifts from providers to the patient and caregivers. Unfortunately, patients often go home without understanding critical information about their hospital stay, such as their discharge diagnosis or medication changes,3, 4 leaving them both dissatisfied with their discharge instructions5 and at risk for hospital readmission.

Efforts to improve discharge education have focused on increasing communication between care provider and patient. The use of designated discharge coordinators,6, 7 implementation of teach‐back techniques to assess and confirm understanding,8 and adoption of patient‐centered educational materials all offer tools to improve communication with patients. However, guidelines for communication between providers and their shared role in patient discharge education, particularly between nurses and physicians, are scarce. Daily interdisciplinary rounds9 and shared electronic health records are potential ways to foster such communication, but the methods and frequency with which providers communicate about discharge instructions with each other is poorly understood. Furthermore, despite a common set of goals for discharge instructions,10, 11 it is unclear where the responsibility to provide these elements lies: with nurses, physicians, neither, or both.

Understanding perceptions and communication practices of providers in their delivery of discharge instructions is an important first step in defining responsibilities and improving accountability for discharge education. In this study, we surveyed nurses and physicians about their discharge education practices to better understand how each group sees their own role in discharge teaching, and how these findings may generate recommendations to improve future practices.

METHODS

Setting and Subjects

University of California, San Francisco Medical Center (UCSFMC) is a 600‐bed tertiary care academic teaching hospital. We surveyed interns, hospitalists on a teaching service, and day‐shift nurses from the inpatient medical service, based on care they provided at UCSFMC from July 2010 to February 2011. The 3 groups are the primary providers at our institution who deliver discharge education. The study was approved by our Institutional Review Board (IRB), the Committee on Human Research.

Survey Development

We developed a survey tool based on a literature review and expert input from local institutional leaders in nursing, residency training, and hospital medicine. The aims of the survey tool were to: 1) assess perceptions and practice of the nurse and physician role in patient discharge education; 2) describe the current practice of physiciannurse communication at discharge; and 3) assess openness to new communication tools.

Specific elements of discharge education assessed in the survey were established from the existing literature,10, 11 and our local best practices (see Supporting Information, Text Box, in the online version of this article). Prior to survey administration, we conducted informal focus groups of interns, hospitalists, and day‐shift nurses, and piloted the survey to assure clarity in the questions and proposed responses.

The survey asked respondents to assign responsibility for the discharge education elements to the physician, nurse, both, or neither, and then to describe their current practice in patient education and in physiciannurse communication. The frequency that respondents provide discharge education to patients and the frequency of nursephysician communication around the elements of discharge education were assessed using Likert scales (1 = never, 2 = rarely, 3 = sometimes, 4 = often, 5 = always). Finally, the survey asked respondents about their interest in tools to improve provider communication at discharge.

Survey Administration

Surveys were administered on paper and electronically, the latter using a commercial online survey tool. Paper surveys were circulated at nurse staff meetings on the 2 units in January and February 2011, with links to an electronic survey sent by e‐mail for those unable to attend. Electronic surveys were distributed via e‐mail to all interns and hospitalists in January 2011. The mid‐year time period was selected to ensure that all interns had provided clinical care at this hospital site. Two reminder e‐mails were sent to non‐respondents.

Data Analysis

Paper‐based surveys were subsequently entered into the online survey tool. Student t tests were used to compare Likert scale means between 2 provider groups, while analysis of variance (ANOVA) was used to compare differences between nurses, interns, and hospitalists. Chi‐squared analysis was used to compare dichotomous variables of agreement and disagreement.

Likert scales of education to patients were dichotomized into frequent education (that provided often or always) versus infrequent education (that provided never, rarely, or sometimes). Likert scales of communication between nurses were similarly dichotomized. Correlation between frequent education to patients (often or always) and the frequency of communication between nurses and physicians (often or always) was assessed using Pearson's r.

RESULTS

One hundred twenty‐nine providers responded to the survey with an overall survey response rate of 129/184 (70%). Forty‐five (64%) nurses, 56 (71%) interns, and 28 (78%) hospitalists participated. We organized the results into 4 sections based on the survey's question domains. First, we analyzed providers' (defined as nurses, interns, and hospitalists) perceived responsibility for the elements of patient discharge education (see Supporting Information, Text Box, in the online version of this article). Second, we examined how providers' responsibility compared to their reported practice. Third, we looked at the communication between nurses and physicians on the care team around these shared elements of discharge education. Lastly, we looked at providers' willingness to adopt tools to improve nursephysician communication around the time of discharge.

Perceived Responsibility for Discharge Education

Providers felt that most elements of discharge education were a shared responsibility, accounting for 58% of the responses to all the questions. Nurses, however, were the most likely to respond that the elements of discharge education were a shared responsibility, with 64% of all nursing responses indicating that the discharge education elements were a shared responsibility, compared to 54% of intern's responses and 55% of hospitalist's responses (P < 0.005). Correspondingly, nurses also responded least often that items were primarily a nursing responsibility (10% of all responses), compared to interns (12% of all responses) and hospitalists (18% of all responses) (nurses vs hospitalists, P < 0.001). No single elements were responsible for these differences, instead Table 1 demonstrates this trend across most elements. Hospitalists, despite their increased experience in discharging patients, were less likely than interns to respond that elements of discharge education were a physician's responsibility (21% vs 32% of all responses, P < 0.001).

Perceived Responsibility for Discharge Education by Provider
 Nursing Responsibility (%)Combined (%)Physician Responsibility (%)
 Nurse N = 45Intern N = 56Hospitalist N = 28Nurse N = 45Intern N = 56Hospitalist N = 28Nurse N = 45Intern N = 56Hospitalist N = 28
  • NOTE: Bolded items represent the majority answer for each provider.

  • Abbreviations: CT, computed tomography; SOB, shortness of breath.

Medication teaching and schedule332933555852000
Contact information for postdischarge questions2845336044591294
Instructions for self‐care (eg, diet, activity, wound care)233043776257070
Follow‐up appointment dates and times92046868250500
Signs and symptoms that may develop and when to seek care (eg, call physician, 911)18111982677002011
Symptom management at home (eg, pain, SOB, nausea)112218969750294
Home health services ordered592179655414220
Reason for follow‐up appointments2411776768202921
Changes to medication regimen made during hospitalization224665379304318
Discharge medical diagnoses000605661404539
Explanation of diagnosis in lay terms000694564315536
Summary of hospital findings and treatments (eg, CT scan results, response to antibiotics)000181118828871
Pending results from studies during hospitalization020122729886668

The majority of providers were in agreement that 9 of the 13 elements were a shared nursephysician responsibility, with varying degrees of consensus. All groups also agreed that 2 of the elements, summary of hospital findings and pending results from studies during hospitalization, should be primarily the physician's responsibility. However, there was disagreement on the remaining 2 items. The majority of interns viewed the explanation of the diagnosis in lay terms as a physician responsibility (55%), compared to a minority of nurses (31%) and hospitalists (36%) (P < 0.05). Interns were also more likely than others to view providing contact information for questions after discharge as a uniquely nursing responsibility (45%), compared to nurses (28%) and hospitalists (33%) who viewed this as shared responsibility; this difference was not statistically significant.

Discharge Education by Providers on the Care Team

Despite nurses' reluctance to claim sole responsibility for elements of discharge education, nurses on the whole reported providing discharge education more often than either interns or hospitalists (P < 0.05). Figure 1 illustrates each group's reported practice of communicating specific discharge education on a Likert scale. For the 9 elements viewed as a shared responsibility and the 2 elements where there was disagreement, nurses reported communicating most items significantly more often than both interns and hospitalists (P < 0.001 for all elements except reason for follow‐up appointments, explanation of diagnosis in lay terms, and changes to medication regimen made during hospitalization). Items that were reported to be a physician responsibility were communicated more often by interns and hospitalists than nurses (P < 0.005), but were the items least often communicated by any care provider. Hospitalists did not report communicating any items significantly more than interns.

Figure 1
Self‐reported perceptions of discharge education. *Significantly more often performed by nurse (P < 0.001). **Significantly more often performed by hospitalists and interns (P < 0.005).

Communication Between Nurses and Physicians

Overall, communication between nurses and physicians was infrequent, with the 64% of nurses, 64% of interns, and 70% of hospitalists reporting that they never or rarely communicate with the other around any discharge education elements. Hospitalists were not more likely than interns to report communicating with nurses on any items, instead reported communicating with nurses around follow‐up appointments and home health services significantly less often (P < 0.05). There was a statistically significant increase in communication by all providers around items of shared responsibility, compared to items viewed as the responsibility of the physicians (14% vs 5.0% increase in communicated often or always; P < 0.001). Elements on which nurses and physicians communicated often or always were also discharge education elements reported as more often provided to patients (r = 0.577).

Potential Solutions for Sharing Discharge Information

Overall, both nurses, interns, and hospitalists were very open to proposed methods of enhancing their communication at discharge. Compared to interns and hospitalists, nurses were more likely to support communication tools, and significantly more in favor of verbal communication, discharge summary availability at the time of discharge, and access to a physician handoff tool. Only 1 solution, a standardized checklist, was favored more by interns and hospitalists, but the difference was not statistically significant. Verbal communication with the other group on the day of discharge was supported most strongly, with 100% of nurses, and 81% of interns and hospitalists reporting being likely or very likely to use this strategy. The least supported item by all groups was using white boards to communicate discharge information (Table 2).

Potential Solutions to Improve NursePhysician Communication
 Likelihood of Using the Proposed Strategies
 NurseInternHospitalistP (ANOVA)
  • NOTE: All responses on a Likert scale of likelihood of using these solutions (1, very unlikely; 2, unlikely; 3, somewhat; 4, likely; 5, very likely).

Verbal communication between providers on day of discharge4.84.24.1<0.001
Discharge summary available at time of discharge4.73.84.4<0.001
Discharge information in physician sign‐out tool4.33.83.2<0.001
Nurse participation in daily physician rounds on the floor4.24.14.60.057
Standardized checklist for discharges3.64.04.20.122
Discharge information on white boards3.43.03.30.259

DISCUSSION

Our study demonstrated that nurses, interns, and hospitalists all feel that they play a pivotal role in discharge education. Compared to both interns and hospitalists, nurses were more likely to view discharge education as a shared responsibility, but nurses also reported providing more discharge education to patients. The elements of discharge education deemed a physician responsibility were reported as the least often provided to patients. Despite the majority of responses indicating that discharge education is a shared nursephysician responsibility, reported provider communication about discharge education was infrequent. Arguing for more communication, elements for which nurses and physicians perceived communicating more frequently were also more often reportedly conveyed to patients. The summative findings suggest that inconsistent discharge education and communication between providers may be leading to patients who are not regularly receiving complete discharge information. Nurses, interns, and hospitalists, however, were all very engaged in potential solutions to improve discharge communication, providing opportunities for immediate impact.

The question becomes where to start. Poor discharge instructions are associated with increased hospital readmission,10 and comprehensive discharge education is a suggested strategy to reduce preventable readmissions.12 Academic hospitalists, despite likely having witnessed the negative impact of poor discharge education, were not more likely than interns to report educating patients, nor did they report communicating more often with nurses. In teaching institutions, specifically, discharge education is being provided by multiple physicians: interns, residents, and hospitalists who may not have clearly defined roles in providing discharge education.13 Thus, providing comprehensive discharge instructions may require a hardwired system to ensure all elements of discharge education are addressed.

Further, our increasing dependence on technology may paradoxically necessitate more formal structures for in‐person communication, as the ability to enter discharge orders remotely leads to less frequent direct communication. Fortunately, as institutions move to computerized systems for discharge orders and instructions, there are increasing opportunities for a standardized approach to the elements of discharge education. While these results may suggest that one individual should be solely responsible for discharge education, trials using teams of nurse practitioners to facilitate transitions of care found no difference in patient length of stay or 30‐day readmission rates.14, 15

Formal systems that increase communication in high‐risk circumstances remain a focus in patient safety, and have been implemented successfully in procedural settings and with handoffs in patient care.1618 A prominent example is operating room time‐outs, which implemented a structured tool and shared process to increase nursephysician communication and reduce mortality.19 Since elements of discharge education with more frequent communication between nurses and physicians were more often conveyed to patients, our results suggest that a discharge time‐out might offer similar benefit. Fortunately, nurses and physicians rated verbal communication as the most desirable solution to share discharge education information. While not formally evaluated, one solution may be adoption of the previously described critical conversation, a structured format and a consistent time for communication that ensures both nurses and physicians understand what education needs to be provided to patients and by whom.20 The 13 discharge elements outlined in our study now provide a starting point for defining specific discussion points at discharge, delineation of who should communicate each element, and the basis for developing an operational discharge time‐out.

There are several limitations to our study. First, the survey instrument was not previously used or validated. However, we did seek formal and structured input while developing our survey, and conducted pilot testing to ensure clarity and comprehension with representatives of all study groups. Second, the 13 discharge education elements we included do not represent a comprehensive list, and were chosen based on our literature review and best practices at our institution. Third, our cross‐sectional study only captures perceptions and practices during a single time point, and may not adequately capture the greater continuum of true practice. Finally, our results may not be generalizable outside UCSFMC or other academic medical centers, particularly if other institutions have employed specific structures for discharge, such as a dedicated discharge coordinator.

CONCLUSION

Discharging patients is a complex process and one in which multiple providers and poor systems contribute to the redesign challenges. Providing high‐quality discharge education instructions to patients is an important step in making a complex process safer. Poor communication between nurses and physicians, complicated by ambiguous perceptions of responsibility for specific information, offers an opportunity for improvement efforts. We should not let well thought out treatment plans fail due to poor patient education on discharge. Our findings argue for a more systematic approach to the discharge education provided by nurses, interns, and hospitalists.

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References
  1. Forster AJ,Murff HJ,Peterson JF,Gandhi TK,Bates DW.The incidence and severity of adverse events affecting patients after discharge from the hospital.Ann Intern Med.2003;138(3):161167.
  2. Forster AJ,Clark HD,Menard A, et al.Adverse events among medical patients after discharge from hospital.Can Med Assoc J.2004;170(3):345349.
  3. Makaryus AN,Friedman EA.Patients' understanding of their treatment plans and diagnosis at discharge.Mayo Clin Proc.2005;80(8):991994.
  4. Maniaci MJ,Heckman MG,Dawson NL.Functional health literacy and understanding of medications at discharge.Mayo Clin Proc.2008;83(5):554558.
  5. Jha AK,Orav EJ,Zheng J,Epstein AM.Patients' perception of hospital care in the United States.N Engl J Med.2008;359(18):19211931.
  6. Naylor MD,Brooten D,Campbell R, et al.Comprehensive discharge planning and home follow‐up of hospitalized elders: a randomized clinical trial.JAMA.1999;281(7):613620.
  7. Jack BW,Chetty VK,Anthony D, et al.A reengineered hospital discharge program to decrease rehospitalization: a randomized trial.Ann Intern Med.2009;150(3):178187.
  8. Schillinger D,Piette J,Grumbach K, et al.Closing the loop: physician communication with diabetic patients who have low health literacy.Arch Intern Med.2003;163(1):8390.
  9. O'Leary KJ,Buck R,Fligiel HM, et al.Structured interdisciplinary rounds in a medical teaching unit: improving patient safety.Arch Intern Med.2011;171(7):678684.
  10. Halasyamani L,Kripalani S,Coleman E, et al.Transition of care for hospitalized elderly patients—development of a discharge checklist for hospitalists.J Hosp Med.2006;1(6):354360.
  11. Kripalani S,Jackson AT,Schnipper JL,Coleman EA.Promoting effective transitions of care at hospital discharge: a review of key issues for hospitalists.J Hosp Med.2007;2(5):314323.
  12. Allaudeen N,Vidyarthi A,Maselli J,Auerbach A.Redefining readmission risk factors for general medicine patients.J Hosp Med.2011;6(2):5460.
  13. Greysen SR,Schiliro D,Horwitz LI,Curry L,Bradley EH.“Out of sight, out of mind”: housestaff perceptions of quality‐limiting factors in discharge care at teaching hospitals.J Hosp Med.2012;7:376381.
  14. Ornstein K,Smith KL,Foer DH,Lopez‐Cantor MT,Soriano T.To the hospital and back home again: a nurse practitioner‐based transitional care program for hospitalized homebound people.J Am Geriatr Soc.2011;59(3):544551.
  15. Finn KM,Heffner R,Chang Y, et al.Improving the discharge process by embedding a discharge facilitator in a resident team.J Hosp Med.2011;6(9):494500.
  16. Risser DT,Rice MM,Salisbury ML,Simon R,Jay GD,Berns SD.The potential for improved teamwork to reduce medical errors in the emergency department. The MedTeams Research Consortium.Ann Emerg Med.1999;34(3):373383.
  17. Baggs JG,Schmitt MH,Mushlin AI, et al.Association between nurse‐physician collaboration and patient outcomes in three intensive care units.Crit Care Med.1999;27(9):19911998.
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Discharge from the hospital is a vulnerable time for patients. Nearly 1 in 5 patients experiences an adverse event during this transition, with a third of these being likely preventable.1, 2 Comprehensive discharge instructions are necessary to ensure a smooth transition from hospital to home, as the responsibility for care shifts from providers to the patient and caregivers. Unfortunately, patients often go home without understanding critical information about their hospital stay, such as their discharge diagnosis or medication changes,3, 4 leaving them both dissatisfied with their discharge instructions5 and at risk for hospital readmission.

Efforts to improve discharge education have focused on increasing communication between care provider and patient. The use of designated discharge coordinators,6, 7 implementation of teach‐back techniques to assess and confirm understanding,8 and adoption of patient‐centered educational materials all offer tools to improve communication with patients. However, guidelines for communication between providers and their shared role in patient discharge education, particularly between nurses and physicians, are scarce. Daily interdisciplinary rounds9 and shared electronic health records are potential ways to foster such communication, but the methods and frequency with which providers communicate about discharge instructions with each other is poorly understood. Furthermore, despite a common set of goals for discharge instructions,10, 11 it is unclear where the responsibility to provide these elements lies: with nurses, physicians, neither, or both.

Understanding perceptions and communication practices of providers in their delivery of discharge instructions is an important first step in defining responsibilities and improving accountability for discharge education. In this study, we surveyed nurses and physicians about their discharge education practices to better understand how each group sees their own role in discharge teaching, and how these findings may generate recommendations to improve future practices.

METHODS

Setting and Subjects

University of California, San Francisco Medical Center (UCSFMC) is a 600‐bed tertiary care academic teaching hospital. We surveyed interns, hospitalists on a teaching service, and day‐shift nurses from the inpatient medical service, based on care they provided at UCSFMC from July 2010 to February 2011. The 3 groups are the primary providers at our institution who deliver discharge education. The study was approved by our Institutional Review Board (IRB), the Committee on Human Research.

Survey Development

We developed a survey tool based on a literature review and expert input from local institutional leaders in nursing, residency training, and hospital medicine. The aims of the survey tool were to: 1) assess perceptions and practice of the nurse and physician role in patient discharge education; 2) describe the current practice of physiciannurse communication at discharge; and 3) assess openness to new communication tools.

Specific elements of discharge education assessed in the survey were established from the existing literature,10, 11 and our local best practices (see Supporting Information, Text Box, in the online version of this article). Prior to survey administration, we conducted informal focus groups of interns, hospitalists, and day‐shift nurses, and piloted the survey to assure clarity in the questions and proposed responses.

The survey asked respondents to assign responsibility for the discharge education elements to the physician, nurse, both, or neither, and then to describe their current practice in patient education and in physiciannurse communication. The frequency that respondents provide discharge education to patients and the frequency of nursephysician communication around the elements of discharge education were assessed using Likert scales (1 = never, 2 = rarely, 3 = sometimes, 4 = often, 5 = always). Finally, the survey asked respondents about their interest in tools to improve provider communication at discharge.

Survey Administration

Surveys were administered on paper and electronically, the latter using a commercial online survey tool. Paper surveys were circulated at nurse staff meetings on the 2 units in January and February 2011, with links to an electronic survey sent by e‐mail for those unable to attend. Electronic surveys were distributed via e‐mail to all interns and hospitalists in January 2011. The mid‐year time period was selected to ensure that all interns had provided clinical care at this hospital site. Two reminder e‐mails were sent to non‐respondents.

Data Analysis

Paper‐based surveys were subsequently entered into the online survey tool. Student t tests were used to compare Likert scale means between 2 provider groups, while analysis of variance (ANOVA) was used to compare differences between nurses, interns, and hospitalists. Chi‐squared analysis was used to compare dichotomous variables of agreement and disagreement.

Likert scales of education to patients were dichotomized into frequent education (that provided often or always) versus infrequent education (that provided never, rarely, or sometimes). Likert scales of communication between nurses were similarly dichotomized. Correlation between frequent education to patients (often or always) and the frequency of communication between nurses and physicians (often or always) was assessed using Pearson's r.

RESULTS

One hundred twenty‐nine providers responded to the survey with an overall survey response rate of 129/184 (70%). Forty‐five (64%) nurses, 56 (71%) interns, and 28 (78%) hospitalists participated. We organized the results into 4 sections based on the survey's question domains. First, we analyzed providers' (defined as nurses, interns, and hospitalists) perceived responsibility for the elements of patient discharge education (see Supporting Information, Text Box, in the online version of this article). Second, we examined how providers' responsibility compared to their reported practice. Third, we looked at the communication between nurses and physicians on the care team around these shared elements of discharge education. Lastly, we looked at providers' willingness to adopt tools to improve nursephysician communication around the time of discharge.

Perceived Responsibility for Discharge Education

Providers felt that most elements of discharge education were a shared responsibility, accounting for 58% of the responses to all the questions. Nurses, however, were the most likely to respond that the elements of discharge education were a shared responsibility, with 64% of all nursing responses indicating that the discharge education elements were a shared responsibility, compared to 54% of intern's responses and 55% of hospitalist's responses (P < 0.005). Correspondingly, nurses also responded least often that items were primarily a nursing responsibility (10% of all responses), compared to interns (12% of all responses) and hospitalists (18% of all responses) (nurses vs hospitalists, P < 0.001). No single elements were responsible for these differences, instead Table 1 demonstrates this trend across most elements. Hospitalists, despite their increased experience in discharging patients, were less likely than interns to respond that elements of discharge education were a physician's responsibility (21% vs 32% of all responses, P < 0.001).

Perceived Responsibility for Discharge Education by Provider
 Nursing Responsibility (%)Combined (%)Physician Responsibility (%)
 Nurse N = 45Intern N = 56Hospitalist N = 28Nurse N = 45Intern N = 56Hospitalist N = 28Nurse N = 45Intern N = 56Hospitalist N = 28
  • NOTE: Bolded items represent the majority answer for each provider.

  • Abbreviations: CT, computed tomography; SOB, shortness of breath.

Medication teaching and schedule332933555852000
Contact information for postdischarge questions2845336044591294
Instructions for self‐care (eg, diet, activity, wound care)233043776257070
Follow‐up appointment dates and times92046868250500
Signs and symptoms that may develop and when to seek care (eg, call physician, 911)18111982677002011
Symptom management at home (eg, pain, SOB, nausea)112218969750294
Home health services ordered592179655414220
Reason for follow‐up appointments2411776768202921
Changes to medication regimen made during hospitalization224665379304318
Discharge medical diagnoses000605661404539
Explanation of diagnosis in lay terms000694564315536
Summary of hospital findings and treatments (eg, CT scan results, response to antibiotics)000181118828871
Pending results from studies during hospitalization020122729886668

The majority of providers were in agreement that 9 of the 13 elements were a shared nursephysician responsibility, with varying degrees of consensus. All groups also agreed that 2 of the elements, summary of hospital findings and pending results from studies during hospitalization, should be primarily the physician's responsibility. However, there was disagreement on the remaining 2 items. The majority of interns viewed the explanation of the diagnosis in lay terms as a physician responsibility (55%), compared to a minority of nurses (31%) and hospitalists (36%) (P < 0.05). Interns were also more likely than others to view providing contact information for questions after discharge as a uniquely nursing responsibility (45%), compared to nurses (28%) and hospitalists (33%) who viewed this as shared responsibility; this difference was not statistically significant.

Discharge Education by Providers on the Care Team

Despite nurses' reluctance to claim sole responsibility for elements of discharge education, nurses on the whole reported providing discharge education more often than either interns or hospitalists (P < 0.05). Figure 1 illustrates each group's reported practice of communicating specific discharge education on a Likert scale. For the 9 elements viewed as a shared responsibility and the 2 elements where there was disagreement, nurses reported communicating most items significantly more often than both interns and hospitalists (P < 0.001 for all elements except reason for follow‐up appointments, explanation of diagnosis in lay terms, and changes to medication regimen made during hospitalization). Items that were reported to be a physician responsibility were communicated more often by interns and hospitalists than nurses (P < 0.005), but were the items least often communicated by any care provider. Hospitalists did not report communicating any items significantly more than interns.

Figure 1
Self‐reported perceptions of discharge education. *Significantly more often performed by nurse (P < 0.001). **Significantly more often performed by hospitalists and interns (P < 0.005).

Communication Between Nurses and Physicians

Overall, communication between nurses and physicians was infrequent, with the 64% of nurses, 64% of interns, and 70% of hospitalists reporting that they never or rarely communicate with the other around any discharge education elements. Hospitalists were not more likely than interns to report communicating with nurses on any items, instead reported communicating with nurses around follow‐up appointments and home health services significantly less often (P < 0.05). There was a statistically significant increase in communication by all providers around items of shared responsibility, compared to items viewed as the responsibility of the physicians (14% vs 5.0% increase in communicated often or always; P < 0.001). Elements on which nurses and physicians communicated often or always were also discharge education elements reported as more often provided to patients (r = 0.577).

Potential Solutions for Sharing Discharge Information

Overall, both nurses, interns, and hospitalists were very open to proposed methods of enhancing their communication at discharge. Compared to interns and hospitalists, nurses were more likely to support communication tools, and significantly more in favor of verbal communication, discharge summary availability at the time of discharge, and access to a physician handoff tool. Only 1 solution, a standardized checklist, was favored more by interns and hospitalists, but the difference was not statistically significant. Verbal communication with the other group on the day of discharge was supported most strongly, with 100% of nurses, and 81% of interns and hospitalists reporting being likely or very likely to use this strategy. The least supported item by all groups was using white boards to communicate discharge information (Table 2).

Potential Solutions to Improve NursePhysician Communication
 Likelihood of Using the Proposed Strategies
 NurseInternHospitalistP (ANOVA)
  • NOTE: All responses on a Likert scale of likelihood of using these solutions (1, very unlikely; 2, unlikely; 3, somewhat; 4, likely; 5, very likely).

Verbal communication between providers on day of discharge4.84.24.1<0.001
Discharge summary available at time of discharge4.73.84.4<0.001
Discharge information in physician sign‐out tool4.33.83.2<0.001
Nurse participation in daily physician rounds on the floor4.24.14.60.057
Standardized checklist for discharges3.64.04.20.122
Discharge information on white boards3.43.03.30.259

DISCUSSION

Our study demonstrated that nurses, interns, and hospitalists all feel that they play a pivotal role in discharge education. Compared to both interns and hospitalists, nurses were more likely to view discharge education as a shared responsibility, but nurses also reported providing more discharge education to patients. The elements of discharge education deemed a physician responsibility were reported as the least often provided to patients. Despite the majority of responses indicating that discharge education is a shared nursephysician responsibility, reported provider communication about discharge education was infrequent. Arguing for more communication, elements for which nurses and physicians perceived communicating more frequently were also more often reportedly conveyed to patients. The summative findings suggest that inconsistent discharge education and communication between providers may be leading to patients who are not regularly receiving complete discharge information. Nurses, interns, and hospitalists, however, were all very engaged in potential solutions to improve discharge communication, providing opportunities for immediate impact.

The question becomes where to start. Poor discharge instructions are associated with increased hospital readmission,10 and comprehensive discharge education is a suggested strategy to reduce preventable readmissions.12 Academic hospitalists, despite likely having witnessed the negative impact of poor discharge education, were not more likely than interns to report educating patients, nor did they report communicating more often with nurses. In teaching institutions, specifically, discharge education is being provided by multiple physicians: interns, residents, and hospitalists who may not have clearly defined roles in providing discharge education.13 Thus, providing comprehensive discharge instructions may require a hardwired system to ensure all elements of discharge education are addressed.

Further, our increasing dependence on technology may paradoxically necessitate more formal structures for in‐person communication, as the ability to enter discharge orders remotely leads to less frequent direct communication. Fortunately, as institutions move to computerized systems for discharge orders and instructions, there are increasing opportunities for a standardized approach to the elements of discharge education. While these results may suggest that one individual should be solely responsible for discharge education, trials using teams of nurse practitioners to facilitate transitions of care found no difference in patient length of stay or 30‐day readmission rates.14, 15

Formal systems that increase communication in high‐risk circumstances remain a focus in patient safety, and have been implemented successfully in procedural settings and with handoffs in patient care.1618 A prominent example is operating room time‐outs, which implemented a structured tool and shared process to increase nursephysician communication and reduce mortality.19 Since elements of discharge education with more frequent communication between nurses and physicians were more often conveyed to patients, our results suggest that a discharge time‐out might offer similar benefit. Fortunately, nurses and physicians rated verbal communication as the most desirable solution to share discharge education information. While not formally evaluated, one solution may be adoption of the previously described critical conversation, a structured format and a consistent time for communication that ensures both nurses and physicians understand what education needs to be provided to patients and by whom.20 The 13 discharge elements outlined in our study now provide a starting point for defining specific discussion points at discharge, delineation of who should communicate each element, and the basis for developing an operational discharge time‐out.

There are several limitations to our study. First, the survey instrument was not previously used or validated. However, we did seek formal and structured input while developing our survey, and conducted pilot testing to ensure clarity and comprehension with representatives of all study groups. Second, the 13 discharge education elements we included do not represent a comprehensive list, and were chosen based on our literature review and best practices at our institution. Third, our cross‐sectional study only captures perceptions and practices during a single time point, and may not adequately capture the greater continuum of true practice. Finally, our results may not be generalizable outside UCSFMC or other academic medical centers, particularly if other institutions have employed specific structures for discharge, such as a dedicated discharge coordinator.

CONCLUSION

Discharging patients is a complex process and one in which multiple providers and poor systems contribute to the redesign challenges. Providing high‐quality discharge education instructions to patients is an important step in making a complex process safer. Poor communication between nurses and physicians, complicated by ambiguous perceptions of responsibility for specific information, offers an opportunity for improvement efforts. We should not let well thought out treatment plans fail due to poor patient education on discharge. Our findings argue for a more systematic approach to the discharge education provided by nurses, interns, and hospitalists.

Discharge from the hospital is a vulnerable time for patients. Nearly 1 in 5 patients experiences an adverse event during this transition, with a third of these being likely preventable.1, 2 Comprehensive discharge instructions are necessary to ensure a smooth transition from hospital to home, as the responsibility for care shifts from providers to the patient and caregivers. Unfortunately, patients often go home without understanding critical information about their hospital stay, such as their discharge diagnosis or medication changes,3, 4 leaving them both dissatisfied with their discharge instructions5 and at risk for hospital readmission.

Efforts to improve discharge education have focused on increasing communication between care provider and patient. The use of designated discharge coordinators,6, 7 implementation of teach‐back techniques to assess and confirm understanding,8 and adoption of patient‐centered educational materials all offer tools to improve communication with patients. However, guidelines for communication between providers and their shared role in patient discharge education, particularly between nurses and physicians, are scarce. Daily interdisciplinary rounds9 and shared electronic health records are potential ways to foster such communication, but the methods and frequency with which providers communicate about discharge instructions with each other is poorly understood. Furthermore, despite a common set of goals for discharge instructions,10, 11 it is unclear where the responsibility to provide these elements lies: with nurses, physicians, neither, or both.

Understanding perceptions and communication practices of providers in their delivery of discharge instructions is an important first step in defining responsibilities and improving accountability for discharge education. In this study, we surveyed nurses and physicians about their discharge education practices to better understand how each group sees their own role in discharge teaching, and how these findings may generate recommendations to improve future practices.

METHODS

Setting and Subjects

University of California, San Francisco Medical Center (UCSFMC) is a 600‐bed tertiary care academic teaching hospital. We surveyed interns, hospitalists on a teaching service, and day‐shift nurses from the inpatient medical service, based on care they provided at UCSFMC from July 2010 to February 2011. The 3 groups are the primary providers at our institution who deliver discharge education. The study was approved by our Institutional Review Board (IRB), the Committee on Human Research.

Survey Development

We developed a survey tool based on a literature review and expert input from local institutional leaders in nursing, residency training, and hospital medicine. The aims of the survey tool were to: 1) assess perceptions and practice of the nurse and physician role in patient discharge education; 2) describe the current practice of physiciannurse communication at discharge; and 3) assess openness to new communication tools.

Specific elements of discharge education assessed in the survey were established from the existing literature,10, 11 and our local best practices (see Supporting Information, Text Box, in the online version of this article). Prior to survey administration, we conducted informal focus groups of interns, hospitalists, and day‐shift nurses, and piloted the survey to assure clarity in the questions and proposed responses.

The survey asked respondents to assign responsibility for the discharge education elements to the physician, nurse, both, or neither, and then to describe their current practice in patient education and in physiciannurse communication. The frequency that respondents provide discharge education to patients and the frequency of nursephysician communication around the elements of discharge education were assessed using Likert scales (1 = never, 2 = rarely, 3 = sometimes, 4 = often, 5 = always). Finally, the survey asked respondents about their interest in tools to improve provider communication at discharge.

Survey Administration

Surveys were administered on paper and electronically, the latter using a commercial online survey tool. Paper surveys were circulated at nurse staff meetings on the 2 units in January and February 2011, with links to an electronic survey sent by e‐mail for those unable to attend. Electronic surveys were distributed via e‐mail to all interns and hospitalists in January 2011. The mid‐year time period was selected to ensure that all interns had provided clinical care at this hospital site. Two reminder e‐mails were sent to non‐respondents.

Data Analysis

Paper‐based surveys were subsequently entered into the online survey tool. Student t tests were used to compare Likert scale means between 2 provider groups, while analysis of variance (ANOVA) was used to compare differences between nurses, interns, and hospitalists. Chi‐squared analysis was used to compare dichotomous variables of agreement and disagreement.

Likert scales of education to patients were dichotomized into frequent education (that provided often or always) versus infrequent education (that provided never, rarely, or sometimes). Likert scales of communication between nurses were similarly dichotomized. Correlation between frequent education to patients (often or always) and the frequency of communication between nurses and physicians (often or always) was assessed using Pearson's r.

RESULTS

One hundred twenty‐nine providers responded to the survey with an overall survey response rate of 129/184 (70%). Forty‐five (64%) nurses, 56 (71%) interns, and 28 (78%) hospitalists participated. We organized the results into 4 sections based on the survey's question domains. First, we analyzed providers' (defined as nurses, interns, and hospitalists) perceived responsibility for the elements of patient discharge education (see Supporting Information, Text Box, in the online version of this article). Second, we examined how providers' responsibility compared to their reported practice. Third, we looked at the communication between nurses and physicians on the care team around these shared elements of discharge education. Lastly, we looked at providers' willingness to adopt tools to improve nursephysician communication around the time of discharge.

Perceived Responsibility for Discharge Education

Providers felt that most elements of discharge education were a shared responsibility, accounting for 58% of the responses to all the questions. Nurses, however, were the most likely to respond that the elements of discharge education were a shared responsibility, with 64% of all nursing responses indicating that the discharge education elements were a shared responsibility, compared to 54% of intern's responses and 55% of hospitalist's responses (P < 0.005). Correspondingly, nurses also responded least often that items were primarily a nursing responsibility (10% of all responses), compared to interns (12% of all responses) and hospitalists (18% of all responses) (nurses vs hospitalists, P < 0.001). No single elements were responsible for these differences, instead Table 1 demonstrates this trend across most elements. Hospitalists, despite their increased experience in discharging patients, were less likely than interns to respond that elements of discharge education were a physician's responsibility (21% vs 32% of all responses, P < 0.001).

Perceived Responsibility for Discharge Education by Provider
 Nursing Responsibility (%)Combined (%)Physician Responsibility (%)
 Nurse N = 45Intern N = 56Hospitalist N = 28Nurse N = 45Intern N = 56Hospitalist N = 28Nurse N = 45Intern N = 56Hospitalist N = 28
  • NOTE: Bolded items represent the majority answer for each provider.

  • Abbreviations: CT, computed tomography; SOB, shortness of breath.

Medication teaching and schedule332933555852000
Contact information for postdischarge questions2845336044591294
Instructions for self‐care (eg, diet, activity, wound care)233043776257070
Follow‐up appointment dates and times92046868250500
Signs and symptoms that may develop and when to seek care (eg, call physician, 911)18111982677002011
Symptom management at home (eg, pain, SOB, nausea)112218969750294
Home health services ordered592179655414220
Reason for follow‐up appointments2411776768202921
Changes to medication regimen made during hospitalization224665379304318
Discharge medical diagnoses000605661404539
Explanation of diagnosis in lay terms000694564315536
Summary of hospital findings and treatments (eg, CT scan results, response to antibiotics)000181118828871
Pending results from studies during hospitalization020122729886668

The majority of providers were in agreement that 9 of the 13 elements were a shared nursephysician responsibility, with varying degrees of consensus. All groups also agreed that 2 of the elements, summary of hospital findings and pending results from studies during hospitalization, should be primarily the physician's responsibility. However, there was disagreement on the remaining 2 items. The majority of interns viewed the explanation of the diagnosis in lay terms as a physician responsibility (55%), compared to a minority of nurses (31%) and hospitalists (36%) (P < 0.05). Interns were also more likely than others to view providing contact information for questions after discharge as a uniquely nursing responsibility (45%), compared to nurses (28%) and hospitalists (33%) who viewed this as shared responsibility; this difference was not statistically significant.

Discharge Education by Providers on the Care Team

Despite nurses' reluctance to claim sole responsibility for elements of discharge education, nurses on the whole reported providing discharge education more often than either interns or hospitalists (P < 0.05). Figure 1 illustrates each group's reported practice of communicating specific discharge education on a Likert scale. For the 9 elements viewed as a shared responsibility and the 2 elements where there was disagreement, nurses reported communicating most items significantly more often than both interns and hospitalists (P < 0.001 for all elements except reason for follow‐up appointments, explanation of diagnosis in lay terms, and changes to medication regimen made during hospitalization). Items that were reported to be a physician responsibility were communicated more often by interns and hospitalists than nurses (P < 0.005), but were the items least often communicated by any care provider. Hospitalists did not report communicating any items significantly more than interns.

Figure 1
Self‐reported perceptions of discharge education. *Significantly more often performed by nurse (P < 0.001). **Significantly more often performed by hospitalists and interns (P < 0.005).

Communication Between Nurses and Physicians

Overall, communication between nurses and physicians was infrequent, with the 64% of nurses, 64% of interns, and 70% of hospitalists reporting that they never or rarely communicate with the other around any discharge education elements. Hospitalists were not more likely than interns to report communicating with nurses on any items, instead reported communicating with nurses around follow‐up appointments and home health services significantly less often (P < 0.05). There was a statistically significant increase in communication by all providers around items of shared responsibility, compared to items viewed as the responsibility of the physicians (14% vs 5.0% increase in communicated often or always; P < 0.001). Elements on which nurses and physicians communicated often or always were also discharge education elements reported as more often provided to patients (r = 0.577).

Potential Solutions for Sharing Discharge Information

Overall, both nurses, interns, and hospitalists were very open to proposed methods of enhancing their communication at discharge. Compared to interns and hospitalists, nurses were more likely to support communication tools, and significantly more in favor of verbal communication, discharge summary availability at the time of discharge, and access to a physician handoff tool. Only 1 solution, a standardized checklist, was favored more by interns and hospitalists, but the difference was not statistically significant. Verbal communication with the other group on the day of discharge was supported most strongly, with 100% of nurses, and 81% of interns and hospitalists reporting being likely or very likely to use this strategy. The least supported item by all groups was using white boards to communicate discharge information (Table 2).

Potential Solutions to Improve NursePhysician Communication
 Likelihood of Using the Proposed Strategies
 NurseInternHospitalistP (ANOVA)
  • NOTE: All responses on a Likert scale of likelihood of using these solutions (1, very unlikely; 2, unlikely; 3, somewhat; 4, likely; 5, very likely).

Verbal communication between providers on day of discharge4.84.24.1<0.001
Discharge summary available at time of discharge4.73.84.4<0.001
Discharge information in physician sign‐out tool4.33.83.2<0.001
Nurse participation in daily physician rounds on the floor4.24.14.60.057
Standardized checklist for discharges3.64.04.20.122
Discharge information on white boards3.43.03.30.259

DISCUSSION

Our study demonstrated that nurses, interns, and hospitalists all feel that they play a pivotal role in discharge education. Compared to both interns and hospitalists, nurses were more likely to view discharge education as a shared responsibility, but nurses also reported providing more discharge education to patients. The elements of discharge education deemed a physician responsibility were reported as the least often provided to patients. Despite the majority of responses indicating that discharge education is a shared nursephysician responsibility, reported provider communication about discharge education was infrequent. Arguing for more communication, elements for which nurses and physicians perceived communicating more frequently were also more often reportedly conveyed to patients. The summative findings suggest that inconsistent discharge education and communication between providers may be leading to patients who are not regularly receiving complete discharge information. Nurses, interns, and hospitalists, however, were all very engaged in potential solutions to improve discharge communication, providing opportunities for immediate impact.

The question becomes where to start. Poor discharge instructions are associated with increased hospital readmission,10 and comprehensive discharge education is a suggested strategy to reduce preventable readmissions.12 Academic hospitalists, despite likely having witnessed the negative impact of poor discharge education, were not more likely than interns to report educating patients, nor did they report communicating more often with nurses. In teaching institutions, specifically, discharge education is being provided by multiple physicians: interns, residents, and hospitalists who may not have clearly defined roles in providing discharge education.13 Thus, providing comprehensive discharge instructions may require a hardwired system to ensure all elements of discharge education are addressed.

Further, our increasing dependence on technology may paradoxically necessitate more formal structures for in‐person communication, as the ability to enter discharge orders remotely leads to less frequent direct communication. Fortunately, as institutions move to computerized systems for discharge orders and instructions, there are increasing opportunities for a standardized approach to the elements of discharge education. While these results may suggest that one individual should be solely responsible for discharge education, trials using teams of nurse practitioners to facilitate transitions of care found no difference in patient length of stay or 30‐day readmission rates.14, 15

Formal systems that increase communication in high‐risk circumstances remain a focus in patient safety, and have been implemented successfully in procedural settings and with handoffs in patient care.1618 A prominent example is operating room time‐outs, which implemented a structured tool and shared process to increase nursephysician communication and reduce mortality.19 Since elements of discharge education with more frequent communication between nurses and physicians were more often conveyed to patients, our results suggest that a discharge time‐out might offer similar benefit. Fortunately, nurses and physicians rated verbal communication as the most desirable solution to share discharge education information. While not formally evaluated, one solution may be adoption of the previously described critical conversation, a structured format and a consistent time for communication that ensures both nurses and physicians understand what education needs to be provided to patients and by whom.20 The 13 discharge elements outlined in our study now provide a starting point for defining specific discussion points at discharge, delineation of who should communicate each element, and the basis for developing an operational discharge time‐out.

There are several limitations to our study. First, the survey instrument was not previously used or validated. However, we did seek formal and structured input while developing our survey, and conducted pilot testing to ensure clarity and comprehension with representatives of all study groups. Second, the 13 discharge education elements we included do not represent a comprehensive list, and were chosen based on our literature review and best practices at our institution. Third, our cross‐sectional study only captures perceptions and practices during a single time point, and may not adequately capture the greater continuum of true practice. Finally, our results may not be generalizable outside UCSFMC or other academic medical centers, particularly if other institutions have employed specific structures for discharge, such as a dedicated discharge coordinator.

CONCLUSION

Discharging patients is a complex process and one in which multiple providers and poor systems contribute to the redesign challenges. Providing high‐quality discharge education instructions to patients is an important step in making a complex process safer. Poor communication between nurses and physicians, complicated by ambiguous perceptions of responsibility for specific information, offers an opportunity for improvement efforts. We should not let well thought out treatment plans fail due to poor patient education on discharge. Our findings argue for a more systematic approach to the discharge education provided by nurses, interns, and hospitalists.

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  16. Risser DT,Rice MM,Salisbury ML,Simon R,Jay GD,Berns SD.The potential for improved teamwork to reduce medical errors in the emergency department. The MedTeams Research Consortium.Ann Emerg Med.1999;34(3):373383.
  17. Baggs JG,Schmitt MH,Mushlin AI, et al.Association between nurse‐physician collaboration and patient outcomes in three intensive care units.Crit Care Med.1999;27(9):19911998.
  18. Davenport DL,Henderson WG,Mosca CL,Khuri SF,Mentzer RM.Risk‐adjusted morbidity in teaching hospitals correlates with reported levels of communication and collaboration on surgical teams but not with scale measures of teamwork climate, safety climate, or working conditions.J Am Coll Surg.2007;205(6):778784.
  19. Haynes AB,Weiser TG,Berry WR, et al.A surgical safety checklist to reduce morbidity and mortality in a global population.N Engl J Med.2009;360(5):491499.
  20. Sehgal NL,Fox M,Sharpe BA,Vidyarthi AR,Blegen M,Wachter RM.Critical conversations: a call for a nonprocedural “time out.”J Hosp Med.2011;6(4):225230.
References
  1. Forster AJ,Murff HJ,Peterson JF,Gandhi TK,Bates DW.The incidence and severity of adverse events affecting patients after discharge from the hospital.Ann Intern Med.2003;138(3):161167.
  2. Forster AJ,Clark HD,Menard A, et al.Adverse events among medical patients after discharge from hospital.Can Med Assoc J.2004;170(3):345349.
  3. Makaryus AN,Friedman EA.Patients' understanding of their treatment plans and diagnosis at discharge.Mayo Clin Proc.2005;80(8):991994.
  4. Maniaci MJ,Heckman MG,Dawson NL.Functional health literacy and understanding of medications at discharge.Mayo Clin Proc.2008;83(5):554558.
  5. Jha AK,Orav EJ,Zheng J,Epstein AM.Patients' perception of hospital care in the United States.N Engl J Med.2008;359(18):19211931.
  6. Naylor MD,Brooten D,Campbell R, et al.Comprehensive discharge planning and home follow‐up of hospitalized elders: a randomized clinical trial.JAMA.1999;281(7):613620.
  7. Jack BW,Chetty VK,Anthony D, et al.A reengineered hospital discharge program to decrease rehospitalization: a randomized trial.Ann Intern Med.2009;150(3):178187.
  8. Schillinger D,Piette J,Grumbach K, et al.Closing the loop: physician communication with diabetic patients who have low health literacy.Arch Intern Med.2003;163(1):8390.
  9. O'Leary KJ,Buck R,Fligiel HM, et al.Structured interdisciplinary rounds in a medical teaching unit: improving patient safety.Arch Intern Med.2011;171(7):678684.
  10. Halasyamani L,Kripalani S,Coleman E, et al.Transition of care for hospitalized elderly patients—development of a discharge checklist for hospitalists.J Hosp Med.2006;1(6):354360.
  11. Kripalani S,Jackson AT,Schnipper JL,Coleman EA.Promoting effective transitions of care at hospital discharge: a review of key issues for hospitalists.J Hosp Med.2007;2(5):314323.
  12. Allaudeen N,Vidyarthi A,Maselli J,Auerbach A.Redefining readmission risk factors for general medicine patients.J Hosp Med.2011;6(2):5460.
  13. Greysen SR,Schiliro D,Horwitz LI,Curry L,Bradley EH.“Out of sight, out of mind”: housestaff perceptions of quality‐limiting factors in discharge care at teaching hospitals.J Hosp Med.2012;7:376381.
  14. Ornstein K,Smith KL,Foer DH,Lopez‐Cantor MT,Soriano T.To the hospital and back home again: a nurse practitioner‐based transitional care program for hospitalized homebound people.J Am Geriatr Soc.2011;59(3):544551.
  15. Finn KM,Heffner R,Chang Y, et al.Improving the discharge process by embedding a discharge facilitator in a resident team.J Hosp Med.2011;6(9):494500.
  16. Risser DT,Rice MM,Salisbury ML,Simon R,Jay GD,Berns SD.The potential for improved teamwork to reduce medical errors in the emergency department. The MedTeams Research Consortium.Ann Emerg Med.1999;34(3):373383.
  17. Baggs JG,Schmitt MH,Mushlin AI, et al.Association between nurse‐physician collaboration and patient outcomes in three intensive care units.Crit Care Med.1999;27(9):19911998.
  18. Davenport DL,Henderson WG,Mosca CL,Khuri SF,Mentzer RM.Risk‐adjusted morbidity in teaching hospitals correlates with reported levels of communication and collaboration on surgical teams but not with scale measures of teamwork climate, safety climate, or working conditions.J Am Coll Surg.2007;205(6):778784.
  19. Haynes AB,Weiser TG,Berry WR, et al.A surgical safety checklist to reduce morbidity and mortality in a global population.N Engl J Med.2009;360(5):491499.
  20. Sehgal NL,Fox M,Sharpe BA,Vidyarthi AR,Blegen M,Wachter RM.Critical conversations: a call for a nonprocedural “time out.”J Hosp Med.2011;6(4):225230.
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Journal of Hospital Medicine - 8(1)
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Communicating discharge instructions to patients: A survey of nurse, intern, and hospitalist practices
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Communicating discharge instructions to patients: A survey of nurse, intern, and hospitalist practices
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Nutrition in the hospitalized patient

Malnutrition is present in 20% to 50% of hospitalized patients.1, 2 Despite simple, validated screening tools, malnutrition tends to be underdiagnosed.3, 4 Over 90% of elderly patients transitioning from an acute care hospital to a subacute care facility are either malnourished or at risk of malnutrition.5 Malnutrition has been associated with increased risk of nosocomial infections,6 worsened discharge functional status,7 and higher mortality,8 as well as longer lengths of stay7, 8 and higher hospital costs.2

Malnutrition describes either overnutrition or undernutrition that causes a change in body composition and decreased function.9 Malnutrition in hospitalized patients is typically related to undernutrition due to either reduced intake or increased metabolic rate. Reasons for reduced intake include poor appetite, reduced ability to chew or swallow, and nil per os (NPO) status. Patients with acute or chronic illnesses may either be malnourished on admission, or develop malnutrition within a few days of hospital admission, due to the effects of the inflammatory state on metabolism. Given that malnutrition is potentially modifiable, it is important to screen for malnutrition and, when present, develop, implement, and monitor a nutrition care plan10 (Figure 1).

Figure 1
Algorithm for nutrition care (adapted from Ukleja et al. Standard for nutrition support: adult hospitalized patients. Nutr Clin Pract. 2010;24(4):403–414; copyright 2010 by American Society of Parenteral and Enteral Nutrition. Reprinted by permission of SAGE Publications).

The purpose of this review is to provide the hospitalist with an overview of screening, assessment, and development and implementation of a nutrition care plan in the acutely ill hospitalized patient.

PATIENT SCREENING

Nutrition screening identifies patients with nutritional deficits who may benefit from further detailed nutrition assessment and intervention.11 The Joint Commission requires that all patients admitted to acute care hospitals be screened for risk of malnutrition within 24 hours.12 Those considered at risk for malnutrition have significant weight changes, chronic disease or an acute inflammatory process, or have been unable to ingest adequate calories for 7 days.13

Those not at risk should be regularly rescreened throughout their hospital stay. The American Society of Parenteral and Enteral Nutrition (ASPEN) recommends that institutions create and approve a screening process according to the patient population served.10 There are several tools validated for use in the acute care setting.14 Many institutions trigger an automatic nutrition consult when certain screening criteria are met.

PATIENT ASSESSMENT

Nutrition assessment should be performed by a dietitian or nutrition consult provider in patients who screen at risk for malnutrition to characterize and determine the cause of nutritional deficits.10 The nutrition assessment identifies history and physical examination elements to diagnose malnutrition. An ASPEN consensus statement recommends the diagnosis of malnutrition if 2 or more of the following are present: insufficient energy intake, weight loss, loss of muscle mass, loss of subcutaneous fat, localized or generalized fluid accumulation, and decreased functional status measured by hand‐grip strength.9 The nutrition assessment should also consider how long the patient has been without adequate nutrition, document baseline nutrition parameters,15 and estimate caloric requirements to determine nutrition support therapy needs.10 Nutrition assessment typically includes the following components.

History

A careful history elicits the majority of information needed to determine the cause and severity of malnutrition.16 Patients should be questioned about a typical day's oral intake prior to hospitalization, and about factors that affect their intake such as sensory deficits, fine motor dysfunction, or chewing and swallowing difficulties, which often decline in chronically ill and elderly patients. Nutrition may be affected by financial difficulties or limited social support, and access to food should be assessed.

Physical Findings

Weight loss is the best physical exam predictor of malnutrition risk, although nutritional depletion can occur in a very short time in acutely ill or injured patients before substantial weight loss has occurred. The likelihood of malnutrition is increased if a patient has: a body mass index (BMI) <18.5 kg/m2; unintentional loss of >2.3 kg (5 lb) or 5% of body weight over 1 month; and unintentional loss of >4.5 kg (10 lb) or 10% of body weight over 6 months.17 Weight loss may be masked by fluid retention from chronic conditions, such as heart failure, or from volume resuscitation in the acutely ill patient.9, 16

Body mass index can be misleading, as age‐related height loss may artificially increase BMI, and height may be difficult to accurately measure in a kyphotic, unsteady, or bedridden patient. The clinician may find evidence of loss of subcutaneous fat or muscle mass in patients with chronic illness, but these findings may not be evident in the acutely ill patient.9 Other physical exam assessments of malnutrition, such as arm span, skinfold thickness, and arm circumference are not reliable.16

Laboratory Tests

Biochemical markers, including transferrin, albumin, and prealbumin, have not been proven as accurate predictors of nutrition status because they may change as a result of other factors not related to nutrition.15, 18 Serum albumin, for example, may be more reflective of the degree of metabolic stress.19 Prealbumin has a serum half‐life much shorter than albumin or transferrin (approximately 2448 hours) and is perhaps the most useful protein marker to assess the adequacy of nutritional replacement after the inflammatory state is resolved.18

Calculating Caloric Requirements

Energy expenditure measurement is considered the gold standard to determine patients' caloric needs. Actual measurement by methods such as indirect calorimetry, which measures oxygen consumption and carbon dioxide production, and calculates energy expenditure, is challenging in everyday clinical settings. Predictive equations often are used as alternative methods to estimate patients' caloric requirements.20 There is no consensus among the 3 North American societies' guidelines (the Canadian Clinical Practice Guidelines; the American Dietetics Association's evidence‐based guideline for critical illness; and the Society of Critical Care Medicine and American Society of Parenteral and Enteral Nutrition's joint guideline) as to the best method.21

In the simplest equation, caloric needs are estimated by calories per kilogram.22 In obese patients, using actual body weight will overestimate needs, but using ideal body weight may cause underfeeding. A small study comparing predictive equations in obese hospitalized patients found the Harris‐Benedict equations (H‐BE) using adjusted body weight and a stress factor to be most accurate, but only in 50% of patients.23 Most clinicians are familiar with the H‐BE, but alternatives such as calories per kilogram or the Mifflin St.‐Jeor equation24 are often used (S. Brantley (May 5, 2012), S. Lundy (May 23, 2012), personal communication).

Indications for Nutritional Intervention

In adults without preexisting malnutrition, inadequate nutritional intake for approximately 714 days should prompt nutritional intervention.25, 26 This timeline should be shorter (37 days) in those with lower energy reserves (eg, underweight or recent weight loss) or significant catabolic stress (eg, acutely ill patients).27, 28 Other patient populations shown to benefit from nutritional intervention include: postoperative patients who are anticipated to be NPO for more than 7 days or to be taking less than 60% of estimated caloric needs by postoperative day 10; preoperative patients with severe malnutrition29; those with gastrointestinal cancer undergoing elective surgery30; and stroke patients with persistent dysphagia for more than 7 days.31

DEVELOPMENT OF A NUTRITION CARE PLAN

The formal nutrition assessment of the at‐risk patient derives the information needed for the development of a nutrition care plan. This plan guides the provision of nutrition therapy, the intervention, the monitoring protocols, evaluation, and reassessment of nutrition goals or termination of specialized nutrition support.10 Assessments for adequacy of nutritional repletion are best done by repeated screening and physical examinations.18

IMPLEMENTATION OF NUTRITION CARE PLAN

Nutritional interventions include dietary modifications, enteral nutrition, and parenteral nutrition.

Dietary Modifications

The purpose of the diet is to provide the necessary nutrients to the body in a well‐tolerated form. Diets can be modified to provide for individual requirements, personal eating patterns and food preferences, and disease process and digestive capacity. Dietary adjustments include change in consistency of foods (eg, pureed, mechanical soft), increase or decrease in energy value, increase or decrease in the type of food or nutrient consumed (eg, sodium restriction, fiber enhancement), elimination of specific foods (eg, gluten‐free diet), adjustment in protein, fat, and carbohydrate content (eg, ketogenic diet, renal diet, cholesterol‐lowering diet), and adjustment of the number and frequency of meals.32

Dietary supplementation (eg, Boost, Ensure) is common practice in persons diagnosed with such conditions as cancer, diabetes, and cardiovascular disease. Supplements enhance the diet by increasing the total daily intake of a vitamin, a mineral, an amino acid, an herb or other botanical33, and should not be used as a meal substitute.34 These supplements are varied in content of calories, protein, vitamins, and minerals. Various flavors and consistencies are also available. Several oral supplements are reviewed in Table 1.

Nutritional Content of Oral Supplements
Oral Supplement* (Serving Size; mL) Kcal/svg Protein (g/svg) Fat (g/svg) CHO (g/svg) Na (mg/svg) K (mg/svg) Ca (mg/svg) Phos (mg/svg) Mg (mg/svg)
  • Abbreviations: Ca, calcium; CHO, carbohydrate; g, gram; K, potassium; Kcal, kilocalories; Mg, magnesium; mg, milligram; Na, sodium; Phos, phosphorus; svg, serving. *All information provided for vanilla‐flavored supplement, unless otherwise noted.

Boost Original (237) 240 10 4 41 150 460 300 300 100
Ensure Nutrition Shake (237) 250 9 6 40 200 370 300 250 100
Carnation Instant Breakfast Ready to Drink (325) 250 14 5 34 180 330 500 500 120
Resource Breeze (fruit‐flavored) clear liquid (237) 250 9 0 54 80 10 10 150 1
Glucerna 1.0 Ready to Drink low‐CHO (237) 240 10 13 23 220 370 170 170 67
Re/Gen low K and Phos (180) 375 12 17 47 180 23 15 68 3

Enteral Nutrition

Enteral nutrition (EN) support should be provided to patients who have functioning gastrointestinal (GI) tracts but are unable to take adequate calories orally. Compared to parenteral nutrition (PN), EN is associated with favorable improvements in inflammatory cytokines, acute phase proteins, hyperglycemia, insulin resistance, nosocomial infections, mortality, and cost.35 Enteral feeds are more physiologic than parenteral feeds, maintain GI structure and integrity, and avoid intravenous (IV) access complications. Patients with normal nutritional status on admission who require EN should be receiving over 50% of their caloric needs within the first week of hospital stay.25 Malnourished patients should reach this minimum goal within 35 days of admission.27, 28 EN is not contraindicated in the absence of bowel sounds or in the presence of increased gastric residuals.35 Withholding enteral feedings for gastric residual volumes <250 mL36, 37 or reduced bowel sounds can result in inadequate caloric intake or inappropriate use of PN.27

Gastric feedings are more physiologic than small bowel feedings, can be given by bolus or continuous infusion, and can be given by tubes that are easy to place at the bedside. Post‐pyloric feedings (nasoduodenal or nasojejunal) may be associated with a lower risk of pneumonia, and should be considered in high‐risk patients such as those receiving continuous sedatives or neuromuscular blockers.36 Post‐pyloric tube placement usually requires endoscopy, fluoroscopy, or electromagnetic guidance. Percutaneous feeding tubes (gastrostomy or jejunostomy) should be considered in those who require tube feedings for longer than 30 days.38

Assessment of patient requirements and disease state, as well as extensive knowledge of available formulas, is important in the selection of the appropriate enteral formula.39 Standardized formulas are used for most patients. The provision of adequate water must be considered with these formulas, particularly in the long‐term care and home settings.40 Many specialized formulas are designed for a particular disease state or condition, some of which are further reviewed in Table 2.

Nutritional Content of Tube Feed Formulas
Formula Kcal/mL Protein (g/L) Fat (g/L) CHO (g/L) Osmolality (mOsm/kg H2O) Na (mEq/L) K (mEq/L) Ca (mg/L) Mg (mg/L) Phos (mg/L)
  • Abbreviations: Ca, calcium; CHO, carbohydrate; g, gram; H2O, water; K, potassium; Kcal, kilocalories; kg, kilogram; L, liter; mEq, milliequivalent; Mg, magnesium; mL, milliliter; mOsm, milliosmoles; Na, sodium; Phos, phosphorus; RTF, ready to feed.

Nutren 1.0‐low residue 1 40 38 127 315 38 32 668 268 668
Osmolite 1.0 Cal low residue 1 44.3 34.7 143.9 300 40.4 40.2 760 305 1760
Replete high protein, low residue 1 62.4 34 112 300 38.1 38.5 1000 400 1000
Replete Fiber high protein with fiber 1 62.4 34 112 310 38.1 38.5 1000 400 1000
Osmolite 1.5 low residue, calorically dense 1.5 62.7 49.1 203.6 525 60.9 46 1000 400 1000
Two Cal calorie and protein dense 2 83.5 91 219 725 64 63 1050 425 1050
Vivonex RTF‐elemental 1 50 11.6 176 630 30.4 31 668 268 668
Nepro with Carb Steady‐for electrolyte, fluid restriction (eg, dialysis) 1.8 81 96 161 745 46 27 1060 210 720
Nutren Glytrol low CHO 1 45.2 47.6 100 280 32.2 35.9 720 286 720
NutriHep‐for hepatic disease 1.5 40 21.2 290 790 160 33.9 956 376 1000

If concerned about formula tolerance, one solution is to initiate the formula at a low rate and increase to the goal rate over 2448 hours. Dilution of enteral formulas is not necessary to assure optimal tolerance. Continuous feedings are recommended for most patients initially and after tolerance has been established, bolus feedings can be attempted if the feeding tube terminates in the stomach. Bolus feedings, where 240480 mL of formula are delivered through a syringe over 1015 minutes, may be more physiological for patients. This regimen can be repeated 46 times daily to meet nutrition goals.41

Parenteral Nutrition

PN provides macronutrients such as carbohydrates, protein, and fat; micronutrients such as vitamins, minerals, electrolytes, and trace elements are added in appropriate concentrations. PN may also provide the patient's daily fluid needs. The timing of PN initiation depends upon the patient's initial nutritional status. ASPEN does not recommend PN during the first 7 days of hospitalization in critically ill patients with normal nutritional status. If the patient is not receiving 100% of caloric needs from EN after 7 days, supplemental PN should be considered. However, if on admission a patient is already malnourished and EN is not feasible, PN should be initiated and continued until the patient is receiving at least 60% of caloric needs by enteral route.42 This includes patients with intestinal obstruction, ileus, peritonitis, malabsorption, high output enterocutaneous fistulae, intestinal ischemia, intractable vomiting and diarrhea, severe shock, and fulminant sepsis.10, 43

Standardized commercial PN products are available and reduce the number of steps required between ordering and administration, as compared to customized PN, which is compounded for a particular patient. However, despite improved efficiency and lower cost, there is no evidence that standardized preparations are safer to patients than customized solutions. Institutions utilizing standardized PN must also have a mechanism to customize formulas for those with complex needs.44

Creating a customized parenteral solution involves several basic steps. Total caloric requirement may be estimated using a predictive formula, as previously discussed; calories/kg of ideal body weight is the simplest method. Most hospitalized patients require 2030 calories/kg/d. Daily fluid requirement may be based on kilocalories (kcal) delivered, or by ideal body weight (eg, 1 mL/kcal or 3040 mL/kg). More fluid may be needed in patients with significant sensible or insensible losses; those with renal failure or heart failure should receive less fluid.

Protein needs are calculated by multiplying ideal body weight (kg) by estimated protein needs in g/kg/d (1.22 g/kg/d for catabolic patients). Protein should provide approximately 20% of total calories. Protein restriction is not required in renal impairment; acutely ill patients on renal replacement therapy should receive 1.51.8 g/kg/d. In hepatic failure patients, protein should be restricted only if hepatic encephalopathy fails to improve with other measures.

Knowing the protein, kcal, and fluid needs of the patient, the practitioner divides the remaining non‐protein calories between carbohydrates and fat. Approximately 70%85% of non‐protein calories should be provided as carbohydrates (dextrose), up to 7 g/kg/d. The other 15%30% are as fat, in lipid solutions, providing a maximum of 2.5 g/kg/d. Lipid solutions are provided as either 10% (1.1 kcal/mL) or 20% (2.2 kcal/mL) concentrations.43, 44 Propofol's contribution to fat intake complicates estimating total fat intake in critically ill patients.45

Standardized parenteral multivitamin preparations are available; the clinician must determine if preparations containing vitamin K are appropriate. Of the trace elements, copper and manganese should be restricted in hepatobiliary disease.44

Acutely ill patients receive PN as a 24‐hour infusion, to minimize its impact on volume status and energy expenditure,46 providing 50% of needs on infusion day one and reaching goal within 4872 hours, rather than cyclic infusions over shorter intervals. Daily assessments of vital signs, intake and output, and weight are necessary to monitor volume status.

Once a patient is taking at least 60% of caloric needs either by mouth or by EN, PN can be discontinued. Tapering the infusion is not required, as abrupt discontinuation has not been demonstrated to cause symptomatic hypoglycemia.47, 48

PATIENT MONITORING

Laboratory monitoring with nutrition support should include baseline electrolytes, glucose, renal function, coagulation studies, triglycerides, magnesium, phosphorus, cholesterol, platelet count, and hepatobiliary enzymes. Electrolytes, calcium, magnesium, and phosphorus should be checked daily for 3 days and, if normal, should then be checked biweekly. Capillary glucose should be monitored several times a day until stable. Weekly triglycerides, albumin, cholesterol, coagulation studies, and liver enzymes should also be checked in patients while on parenteral nutrition.25 Patients at risk for refeeding syndrome should have potassium, phosphate, calcium, and magnesium measured daily for 7 days, with repletion as necessary. These electrolytes should be monitored 3 times the following week if stable.49

Patients should be monitored clinically for gastrointestinal tolerance of enteral nutrition. All 3 North American guidelines recommend monitoring gastric residual volumes (GRV); however, there is no consensus on the volume considered to require intervention. Motility agents are recommended as first line treatment of high GRV.36, 37, 42 If high GRV continues, tube feeding should be held, and tube placement, medications, and metabolic assessment should be reviewed. Placement of a transpyloric feeding tube may be indicated.50

Adverse Effects and Complications of Nutrition Support

Regarding EN, complications include those related to tube placement and maintenance, infections, and medical complications of the feeds themselves. Some of the adverse effects of the enteral formulas may be attenuated. Diarrhea, which occurs in up to 20% of patients, may be avoided with slow feed advancement, use of low‐osmotic formulas, or fiber additives.51 Gastric distention and abdominal pain may improve with slow feed advancement and continuous (rather than bolus) feeds. Small‐bore tubes and acid‐reducing medications may decrease gastroesophageal reflux, and aspiration pneumonia may be avoided by semi‐recumbent positioning and post‐pyloric feeding.52

Complications of PN may be grouped as mechanical, infectious, and metabolic. The mechanical complications of central line placement include pneumothorax, arterial puncture, hematoma, air embolism, and line malpositioning. Catheter‐related deep venous thrombosis may occur. Patients on PN through a central line are at risk for central line‐associated bloodstream infections.25 The metabolic complications such as hyperglycemia, electrolyte disorders, hepatic steatosis, and volume overload may have severe consequences, such as heart failure or neuromuscular dysfunction, thus they require close attention.53

A complication of nutrition support that may occur regardless of route is the refeeding syndrome. Refeeding syndrome describes fluid shifts and electrolyte abnormalities that occur after initiation of oral, enteral, or parenteral nutrition in a malnourished or starved patient.54, 55 There are no formal criteria for diagnosing refeeding syndrome.

In the starved state, the body switches from carbohydrate to protein and fat metabolism. Reintroduction of carbohydrates stimulates insulin release with glycogen, fat, and protein synthesis. Associated uptake of glucose, potassium, magnesium, phosphate, and water into cells causes electrolyte and fluid abnormalities. Although hypophosphatemia is the hallmark of refeeding syndrome, it is not pathognomonic. Additional disturbances include hypokalemia, hyperglycemia, hypomagnesemia, thiamine deficiency, and fluid imbalance.49 Patients at risk of refeeding should have serum electrolytes, magnesium, phosphorus, and glucose checked before nutrition support starts. The degree of laboratory abnormalities, if any, and the clinical course of refeeding guides the frequency of subsequent blood tests.56 These consequences of refeeding can adversely affect every major organ system and may result in death.57

Starvation physiology underlies all risk factors for refeeding syndrome. In hospitalized patients, those at risk for refeeding include, but are not limited to, the elderly, oncology patients, postoperative patients, alcohol‐dependent patients, those with malabsorptive states, those who are fasting or chronically malnourished, and those on diuretic therapy.54, 57 The National Institute for Health and Clinical Excellence (NICE) of England and Wales has published criteria to identify patients at high risk for refeeding (Table 3).56 Identification of at‐risk patients and attention to their nutritional needs prevents refeeding syndrome.

NICE Criteria of Risk Factors for Refeeding
  • NOTE: National Institute for Health and Clinical Excellence (2006) CG 32 Nutrition support in adults: oral nutrition support, enteral tube feeding and parenteral nutrition. London: NICE. Available from www.nice.org.uk/guidance/CG32 Reproduced with permission.

  • Abbreviations: BMI, body mass index.

Patient has 1 or more of the following:
BMI <16 kg/m2
Unintentional weight loss >15% within the last 36 mo
Little or no nutritional intake for more than 10 d
Low levels of potassium, phosphate, or magnesium prior to feeding
Or patient has 2 or more of the following:
BMI <18.5 kg/m2
Unintentional weight loss >10% within the last 36 mo
Little or no nutritional intake for more than 5 d
A history of alcohol abuse or drugs including insulin, chemotherapy, antacids, or diuretics

ASPEN and NICE have each issued guidelines for initiating nutrition support in patients at risk for refeeding. ASPEN guidelines recommend feeding start at approximately 25% of the estimated goal, with advancement to goal over 35 days. ASPEN recommends fluid and electrolyte status be monitored as needed.50 The NICE guidelines recommend starting nutrition support at a maximum of 10 kcal/kg/d with slow increase to meet or exceed full needs by 47 days. For extremely malnourished patients (eg, BMI <14 kg/m2, or negligible intake for >15 days), they recommend starting at 5 kcal/kg/d. For patients at high risk of developing refeeding syndrome, the NICE guidelines recommend vitamin repletion immediately before and during the first 10 days of feeding (thiamine, vitamin B, and a balanced multivitamin/trace element supplement). Cardiac monitoring is recommended for this group as well as any patients who are at risk for cardiac arrhythmias. Careful monitoring of fluid balance and restoring circulatory volume is recommended, as is repletion of potassium, phosphate, and magnesium.56

TERMINATION OF THERAPY

Termination of nutrition support often involves transitioning from one mode of support to another. PN can be discontinued when oral or enteral intake reaches 60% of total calories; enteral intake can be discontinued when oral intake reaches the same level. However, the patient should be observed maintaining their intake; if they cannot, nutrition support should be resumed.12

TRANSITION OF CARE PLAN

Patients discharged from the hospital on enteral or parenteral nutrition require the support of a coordinated multidisciplinary team including dietitians, home nutrition delivery companies, primary care physicians trained in specialized nutrition support, community pharmacists, and other healthcare professionals, if indicated. These relationships should be established prior to discharge, with education about the patient's individualized nutrition plan, and training with the equipment and supplies.10, 56

CONCLUSION

This review provides an overview of managing the at‐risk or malnourished patient by describing the processes of screening, assessment, and development and implementation of a nutrition care plan in the acutely ill hospitalized patient. Malnutrition is a relatively common, yet underdiagnosed entity that impacts patient outcomes, length of stay, hospital costs, and readmissions. Acute illness in a patient already nutritionally debilitated by chronic disease may cause rapid depletion in nutritional stores. Hospitals are required to screen patients for malnutrition on admission and at regular intervals, and to develop and implement a nutrition care plan for those at risk. The plan guides how nutrition therapy is provided, monitored for adequacy and adverse effects, and assessed for achievement of nutritional goals. It encompasses the use of dietary modifications, and enteral and parenteral nutrition. Clinicians must be aware of serious but avoidable adverse effects, particularly refeeding syndrome in malnourished patients. Prior to discharge, the patient should have already been transitioned from EN or PN to taking adequate amounts of calories by mouth; otherwise, careful discharge planning to educate the patients and/or caregivers, and coordinate the necessary multidisciplinary community services is necessary.

Acknowledgements

The authors express their appreciation to Ms Susan Lundy, for her helpful and timely information, and Ms Lisa Boucher, for her invaluable assistance with this manuscript and its submission.

Disclosures: Susan Brantley is on the Speaker's Bureau for Nestle Nutrition and for Abbott Nutrition. Authors Kirkland, Kashiwagi, Scheurer, and Varkey have nothing to report.

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References
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  9. White JV,Guenter P,Jensen G,Malone A,Schofield M.Consensus statement: Academy of Nutrition and Dietetics and American Society for Parenteral and Enteral Nutrition: characteristics recommended for the identification and documentation of adult malnutrition (undernutrition).J Parenter Enteral Nutr.2012;36(3):275283.
  10. Ukleja A,Freeman KL,Gilbert K, et al.Standards for nutrition support: adult hospitalized patients.Nutr Clin Pract.2010;25(4):403414.
  11. American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.), Board of Directors and Clinical Practice Committee. Definition of Terms, Style, and Conventions used in A.S.P.E.N. Board of Directors‐Approved Documents. May2012. Available at: http://www.nutritioncare.org/Library.aspx. Accessed June 29, 2012.
  12. Joint Commission on Accreditation of Healthcare Organizations.Comprehensive Accreditation for Hospitals.Chicago, IL:Joint Commission on Accreditation for Healthcare Organizations;2007.
  13. Russell MK,Mueller C.Nutrition screening and assessment. In: Gottschlich MM, ed.The ASPEN Nutrition Support Core Curriculum: A Case‐Based Approach—The Adult Patient.1st ed.Silver Spring, MD:American Society for Parenteral and Enteral Nutrition;2007:163186.
  14. Anthony PS.Nutrition screening tools for hospitalized patients.Nutr Clin Pract.2008;23(4):373382.
  15. Charney P.Nutrition screening and assessment. In: Skipper A, ed.Dietitian's Handbook of Enteral and Parenteral Nutrition.3rd ed.Sudbury, MA:Jones 2012:421.
  16. Waitzberg DL,Correia MITD.Nutritional assessment in the hospitalized patient.Curr Opin Clin Nutr Metab Care.2003;6(5):531538.
  17. Blackburn GL,Bistrian BR,Maini BS,Schlamm HT,Smith MF.Nutritional and metabolic assessment of the hospitalized patient.J Parenter Enteral Nutr.1977;1(1):1122.
  18. Fuhrman MP,Charney P,Mueller CM.Hepatic proteins and nutrition assessment.J Am Diet Assoc.2004;104(8):12581264.
  19. Fuhrman MP.The albumin‐nutrition connection: separating myth from fact.Nutrition.2002;18(2):199200.
  20. Walker RN,Heuberger RA.Predictive equations for energy needs for the critically ill.Respir Care.2009;54(4):509521.
  21. Dhaliwal R,Madden SM,Cahill N, et al.Guidelines, guidelines, guidelines: what are we to do with all of these North American guidelines?J Parenter Enteral Nutr.2010;34(6):625643.
  22. Cerra FB,Benitez MR,Blackburn GL, et al.Applied nutrition in ICU patients. A consensus statement of the American College of Chest Physicians.Chest.1997;111(3):769778.
  23. Anderegg BA,Worrall C,Barbour E,Simpson KN,Delegge M.Comparison of resting energy expenditure prediction methods with measured resting energy expenditure in obese, hospitalized adults.J Parenter Enteral Nutr.2009;33(2):168175.
  24. Mifflin MD,St Jeor ST,Hill LA,Scott BJ,Daugherty SA,Koh YO.A new predictive equation for resting energy expenditure in healthy individuals.Am J Clin Nutr.1990;51(2):241247.
  25. American Society for Parenteral and Enteral Nutrition.Guidelines for the use of parenteral and enteral nutrition in adult and pediatric patients.J Parenter Enteral Nutr.2002;26(suppl):1SA138SA.
  26. Kirby DF,Delegge MH,Fleming CR.American Gastroenterological Association technical review on tube feeding for enteral nutrition.Gastroenterology.1995;108(4):12821301.
  27. Kreymann KG,Berger MM,Deutz NE, et al.ESPEN guidelines on enteral nutrition: intensive care.Clin Nutr.2006;25(2):210223.
  28. Winawer N,Williams MV.Nutritional support. In: Shojania KG, Duncan BW, McDonald KM, et al, eds.Making Health Care Safer: A Critical Analysis of Patient Safety Practices. Evidence Report/Technology Assessment Number 43.Rockville, MD:Agency for Healthcare Research and Quality, US Department of Health and Human Services, July2001. AHRQ Publication 01‐E058. Available at: http://www.ahrq.gov.
  29. Veterans Affairs Total Parenteral Nutrition Cooperative Study Group.Perioperative total parenteral nutrition in surgical patients.N Engl J Med.1991;328(8):525532.
  30. Koretz RL,Avenell A,Lipman TO,Braunschweig CL,Milne AC.Does enteral nutrition affect clinical outcome? A systematic review of the randomized trials.Am J Gastroenterol.2007;102(2):412429.
  31. Corrigan ML,Escuro AA,Celestin J,Kirby DF.Nutrition in the stroke patient.Nutr Clin Pract.2011;26(3):242252.
  32. Charney P,Escott‐Stump S,Mahan LK.Nutrition diagnosis and intervention. In: Mahan LK, Escott‐Stump S, eds.Krause's Food and Nutrition Therapy.12th ed.St Louis, MO:Saunders Elsevier;2008:454469.
  33. Dietary Supplement Health and Education Act (DSHEA) of 1994. Available at: http://www.gpo.gov/fdsys/pkg/BILLS‐103s784es/pdf/BILLS‐103s784es.pdf. Accessed June 29,2012.
  34. Thompson CA.Intervention: dietary supplementation and integrative care. In: Mahan LK, Escott‐Stump S, eds.Krause's Food and Nutrition Therapy.12th ed.St Louis, MO:Saunders Elsevier;2008:470474.
  35. Martindale RG,McClave SA,Vanek VW, et al.Guidelines for the provision and assessment of nutrition support therapy in the adult critically ill patient: Society of Critical Care Medicine and American Society for Parenteral and Enteral Nutrition: executive summary.Crit Care Med.2009;37(5):17571761.
  36. Heyland DK,Dhaliwal R,Drover JW,Gramlich L,Dodek P;for the. Canadian Critical Care Clinical Practice Guidelines Committee.Canadian clinical practice guidelines for nutrition support in mechanically ventilated, critically ill adult patients.J Parenter Enteral Nutr.2003;27(5):355373.
  37. American Dietetic Association Evidence Library. Critical Illness. Available at: http://www.adaevidencelibrary.com/template.cfm?key=767115(5 suppl):64S70S.
  38. Skipper A.Enteral nutrition. In: Skipper A, ed.Dietitian's Handbook of Enteral and Parenteral Nutrition.3rd ed.Sudbury, MA:Jones 2012:259280.
  39. Malone A.Enteral formula selection. In: Charney P, Malone A, eds.ADA Pocket Guide to Enteral Nutrition.Chicago, IL:American Dietetic Association;2006:63122.
  40. Marian M,McGinnis C.Overview of enteral nutrition. In: Gottschlich MM, ed.The ASPEN Nutrition Support Core Curriculum: A Case‐Based Approach—The Adult Patient.1st ed.Silver Spring, MD:American Society for Parenteral and Enteral Nutrition;2007:187208.
  41. McClave SA,Martindale RG,Vanek VW, et al.Guidelines for the provision and assessment of nutrition support therapy in the adult critically ill patient: Society of Critical Care Medicine (SCCM) and American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.).J Parenter Enteral Nutr.2009;33(3):277316.
  42. Braga M,Ljungqvist O,Soeters P,Fearon K,Weimann A,Bozzetti F.ESPEN guidelines on parenteral nutrition: surgery.Clin Nutr.2009;28(4):378386.
  43. Mirtallo J,Canada T,Johnson D, et al.Safe practices for parenteral nutrition.J Parenter Enteral Nutr.2004;28(6):S39S70.
  44. DeChicco R,Matarese L,Hummell AC,Speerhas R,Seidner D,Steiger E.Contribution of calories from propofol to total energy intake.J Am Diet Assoc.1995;95(9 supplement):A25.
  45. Forsberg E,Soop M,Lepapea A,Thorne A.Metabolic and thermogenic response to continuous and cyclic total parenteral nutrition in traumatised and infected patients.Clin Nutr.1994;13(5):291301.
  46. Nirula R,Yamada K,Waxman K.The effect of abrupt cessation of total parenteral nutrition on serum glucose: a randomized trial.Am Surg.2000;66(9):866869.
  47. Wagman LD,Newsome HH,Miller KB,Thomas RB,Weir GC.The effect of acute discontinuation of total parenteral nutrition.Ann Surg.1986;204(5):524529.
  48. Mehanna HM,Moledina J,Travis J.Refeeding syndrome: what it is, and how to prevent and treat it.BMJ.2008;336(7659):14951498.
  49. Bankhead R,Boullata J,Brantley S, et al.Enteral nutrition practice recommendations.J Parenter Enteral Nutr.2009;33(2):122167.
  50. Rushdi TATA,Pichard C,Khater YHYH.Control of diarrhea by fiber‐enriched diet in ICU patients on enteral nutrition: a prospective randomized controlled trial.Clin Nutr.2004;23(6):13441352.
  51. Drakulovic MB,Torres A,Bauer TT,Nicolas JM,Nogue S,Ferrer M.Supine body position as a risk factor for nosocomial pneumonia in mechanically ventilated patients: a randomised trial.Lancet.1999;354(9193):18511858.
  52. Ziegler TR.Parenteral nutrition in the critically ill patient.N Engl J Med.2009;361(11):10881097.
  53. Boateng AA,Sriram K,Meguid MM,Crook M.Refeeding syndrome: treatment considerations based on collective analysis of literature case reports.Nutrition.2010;26(2):156167.
  54. Ahmed S,Travis J,Mehanna H.Re‐feeding syndrome in head and neck cancer‐prevention and management.Oral Oncol.2011;47(9):792796.
  55. Nutrition Support in Adults. NICE Clinical Guideline No. 32. 2006. Available at: http://guidance.nice.org.uk/CG32/NICEGuidance. Accessed November 29,2011.
  56. Crook MA,Hally V,Panteli JV.The importance of the refeeding syndrome.Nutrition.2001;17(7–8):632637.
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Malnutrition is present in 20% to 50% of hospitalized patients.1, 2 Despite simple, validated screening tools, malnutrition tends to be underdiagnosed.3, 4 Over 90% of elderly patients transitioning from an acute care hospital to a subacute care facility are either malnourished or at risk of malnutrition.5 Malnutrition has been associated with increased risk of nosocomial infections,6 worsened discharge functional status,7 and higher mortality,8 as well as longer lengths of stay7, 8 and higher hospital costs.2

Malnutrition describes either overnutrition or undernutrition that causes a change in body composition and decreased function.9 Malnutrition in hospitalized patients is typically related to undernutrition due to either reduced intake or increased metabolic rate. Reasons for reduced intake include poor appetite, reduced ability to chew or swallow, and nil per os (NPO) status. Patients with acute or chronic illnesses may either be malnourished on admission, or develop malnutrition within a few days of hospital admission, due to the effects of the inflammatory state on metabolism. Given that malnutrition is potentially modifiable, it is important to screen for malnutrition and, when present, develop, implement, and monitor a nutrition care plan10 (Figure 1).

Figure 1
Algorithm for nutrition care (adapted from Ukleja et al. Standard for nutrition support: adult hospitalized patients. Nutr Clin Pract. 2010;24(4):403–414; copyright 2010 by American Society of Parenteral and Enteral Nutrition. Reprinted by permission of SAGE Publications).

The purpose of this review is to provide the hospitalist with an overview of screening, assessment, and development and implementation of a nutrition care plan in the acutely ill hospitalized patient.

PATIENT SCREENING

Nutrition screening identifies patients with nutritional deficits who may benefit from further detailed nutrition assessment and intervention.11 The Joint Commission requires that all patients admitted to acute care hospitals be screened for risk of malnutrition within 24 hours.12 Those considered at risk for malnutrition have significant weight changes, chronic disease or an acute inflammatory process, or have been unable to ingest adequate calories for 7 days.13

Those not at risk should be regularly rescreened throughout their hospital stay. The American Society of Parenteral and Enteral Nutrition (ASPEN) recommends that institutions create and approve a screening process according to the patient population served.10 There are several tools validated for use in the acute care setting.14 Many institutions trigger an automatic nutrition consult when certain screening criteria are met.

PATIENT ASSESSMENT

Nutrition assessment should be performed by a dietitian or nutrition consult provider in patients who screen at risk for malnutrition to characterize and determine the cause of nutritional deficits.10 The nutrition assessment identifies history and physical examination elements to diagnose malnutrition. An ASPEN consensus statement recommends the diagnosis of malnutrition if 2 or more of the following are present: insufficient energy intake, weight loss, loss of muscle mass, loss of subcutaneous fat, localized or generalized fluid accumulation, and decreased functional status measured by hand‐grip strength.9 The nutrition assessment should also consider how long the patient has been without adequate nutrition, document baseline nutrition parameters,15 and estimate caloric requirements to determine nutrition support therapy needs.10 Nutrition assessment typically includes the following components.

History

A careful history elicits the majority of information needed to determine the cause and severity of malnutrition.16 Patients should be questioned about a typical day's oral intake prior to hospitalization, and about factors that affect their intake such as sensory deficits, fine motor dysfunction, or chewing and swallowing difficulties, which often decline in chronically ill and elderly patients. Nutrition may be affected by financial difficulties or limited social support, and access to food should be assessed.

Physical Findings

Weight loss is the best physical exam predictor of malnutrition risk, although nutritional depletion can occur in a very short time in acutely ill or injured patients before substantial weight loss has occurred. The likelihood of malnutrition is increased if a patient has: a body mass index (BMI) <18.5 kg/m2; unintentional loss of >2.3 kg (5 lb) or 5% of body weight over 1 month; and unintentional loss of >4.5 kg (10 lb) or 10% of body weight over 6 months.17 Weight loss may be masked by fluid retention from chronic conditions, such as heart failure, or from volume resuscitation in the acutely ill patient.9, 16

Body mass index can be misleading, as age‐related height loss may artificially increase BMI, and height may be difficult to accurately measure in a kyphotic, unsteady, or bedridden patient. The clinician may find evidence of loss of subcutaneous fat or muscle mass in patients with chronic illness, but these findings may not be evident in the acutely ill patient.9 Other physical exam assessments of malnutrition, such as arm span, skinfold thickness, and arm circumference are not reliable.16

Laboratory Tests

Biochemical markers, including transferrin, albumin, and prealbumin, have not been proven as accurate predictors of nutrition status because they may change as a result of other factors not related to nutrition.15, 18 Serum albumin, for example, may be more reflective of the degree of metabolic stress.19 Prealbumin has a serum half‐life much shorter than albumin or transferrin (approximately 2448 hours) and is perhaps the most useful protein marker to assess the adequacy of nutritional replacement after the inflammatory state is resolved.18

Calculating Caloric Requirements

Energy expenditure measurement is considered the gold standard to determine patients' caloric needs. Actual measurement by methods such as indirect calorimetry, which measures oxygen consumption and carbon dioxide production, and calculates energy expenditure, is challenging in everyday clinical settings. Predictive equations often are used as alternative methods to estimate patients' caloric requirements.20 There is no consensus among the 3 North American societies' guidelines (the Canadian Clinical Practice Guidelines; the American Dietetics Association's evidence‐based guideline for critical illness; and the Society of Critical Care Medicine and American Society of Parenteral and Enteral Nutrition's joint guideline) as to the best method.21

In the simplest equation, caloric needs are estimated by calories per kilogram.22 In obese patients, using actual body weight will overestimate needs, but using ideal body weight may cause underfeeding. A small study comparing predictive equations in obese hospitalized patients found the Harris‐Benedict equations (H‐BE) using adjusted body weight and a stress factor to be most accurate, but only in 50% of patients.23 Most clinicians are familiar with the H‐BE, but alternatives such as calories per kilogram or the Mifflin St.‐Jeor equation24 are often used (S. Brantley (May 5, 2012), S. Lundy (May 23, 2012), personal communication).

Indications for Nutritional Intervention

In adults without preexisting malnutrition, inadequate nutritional intake for approximately 714 days should prompt nutritional intervention.25, 26 This timeline should be shorter (37 days) in those with lower energy reserves (eg, underweight or recent weight loss) or significant catabolic stress (eg, acutely ill patients).27, 28 Other patient populations shown to benefit from nutritional intervention include: postoperative patients who are anticipated to be NPO for more than 7 days or to be taking less than 60% of estimated caloric needs by postoperative day 10; preoperative patients with severe malnutrition29; those with gastrointestinal cancer undergoing elective surgery30; and stroke patients with persistent dysphagia for more than 7 days.31

DEVELOPMENT OF A NUTRITION CARE PLAN

The formal nutrition assessment of the at‐risk patient derives the information needed for the development of a nutrition care plan. This plan guides the provision of nutrition therapy, the intervention, the monitoring protocols, evaluation, and reassessment of nutrition goals or termination of specialized nutrition support.10 Assessments for adequacy of nutritional repletion are best done by repeated screening and physical examinations.18

IMPLEMENTATION OF NUTRITION CARE PLAN

Nutritional interventions include dietary modifications, enteral nutrition, and parenteral nutrition.

Dietary Modifications

The purpose of the diet is to provide the necessary nutrients to the body in a well‐tolerated form. Diets can be modified to provide for individual requirements, personal eating patterns and food preferences, and disease process and digestive capacity. Dietary adjustments include change in consistency of foods (eg, pureed, mechanical soft), increase or decrease in energy value, increase or decrease in the type of food or nutrient consumed (eg, sodium restriction, fiber enhancement), elimination of specific foods (eg, gluten‐free diet), adjustment in protein, fat, and carbohydrate content (eg, ketogenic diet, renal diet, cholesterol‐lowering diet), and adjustment of the number and frequency of meals.32

Dietary supplementation (eg, Boost, Ensure) is common practice in persons diagnosed with such conditions as cancer, diabetes, and cardiovascular disease. Supplements enhance the diet by increasing the total daily intake of a vitamin, a mineral, an amino acid, an herb or other botanical33, and should not be used as a meal substitute.34 These supplements are varied in content of calories, protein, vitamins, and minerals. Various flavors and consistencies are also available. Several oral supplements are reviewed in Table 1.

Nutritional Content of Oral Supplements
Oral Supplement* (Serving Size; mL) Kcal/svg Protein (g/svg) Fat (g/svg) CHO (g/svg) Na (mg/svg) K (mg/svg) Ca (mg/svg) Phos (mg/svg) Mg (mg/svg)
  • Abbreviations: Ca, calcium; CHO, carbohydrate; g, gram; K, potassium; Kcal, kilocalories; Mg, magnesium; mg, milligram; Na, sodium; Phos, phosphorus; svg, serving. *All information provided for vanilla‐flavored supplement, unless otherwise noted.

Boost Original (237) 240 10 4 41 150 460 300 300 100
Ensure Nutrition Shake (237) 250 9 6 40 200 370 300 250 100
Carnation Instant Breakfast Ready to Drink (325) 250 14 5 34 180 330 500 500 120
Resource Breeze (fruit‐flavored) clear liquid (237) 250 9 0 54 80 10 10 150 1
Glucerna 1.0 Ready to Drink low‐CHO (237) 240 10 13 23 220 370 170 170 67
Re/Gen low K and Phos (180) 375 12 17 47 180 23 15 68 3

Enteral Nutrition

Enteral nutrition (EN) support should be provided to patients who have functioning gastrointestinal (GI) tracts but are unable to take adequate calories orally. Compared to parenteral nutrition (PN), EN is associated with favorable improvements in inflammatory cytokines, acute phase proteins, hyperglycemia, insulin resistance, nosocomial infections, mortality, and cost.35 Enteral feeds are more physiologic than parenteral feeds, maintain GI structure and integrity, and avoid intravenous (IV) access complications. Patients with normal nutritional status on admission who require EN should be receiving over 50% of their caloric needs within the first week of hospital stay.25 Malnourished patients should reach this minimum goal within 35 days of admission.27, 28 EN is not contraindicated in the absence of bowel sounds or in the presence of increased gastric residuals.35 Withholding enteral feedings for gastric residual volumes <250 mL36, 37 or reduced bowel sounds can result in inadequate caloric intake or inappropriate use of PN.27

Gastric feedings are more physiologic than small bowel feedings, can be given by bolus or continuous infusion, and can be given by tubes that are easy to place at the bedside. Post‐pyloric feedings (nasoduodenal or nasojejunal) may be associated with a lower risk of pneumonia, and should be considered in high‐risk patients such as those receiving continuous sedatives or neuromuscular blockers.36 Post‐pyloric tube placement usually requires endoscopy, fluoroscopy, or electromagnetic guidance. Percutaneous feeding tubes (gastrostomy or jejunostomy) should be considered in those who require tube feedings for longer than 30 days.38

Assessment of patient requirements and disease state, as well as extensive knowledge of available formulas, is important in the selection of the appropriate enteral formula.39 Standardized formulas are used for most patients. The provision of adequate water must be considered with these formulas, particularly in the long‐term care and home settings.40 Many specialized formulas are designed for a particular disease state or condition, some of which are further reviewed in Table 2.

Nutritional Content of Tube Feed Formulas
Formula Kcal/mL Protein (g/L) Fat (g/L) CHO (g/L) Osmolality (mOsm/kg H2O) Na (mEq/L) K (mEq/L) Ca (mg/L) Mg (mg/L) Phos (mg/L)
  • Abbreviations: Ca, calcium; CHO, carbohydrate; g, gram; H2O, water; K, potassium; Kcal, kilocalories; kg, kilogram; L, liter; mEq, milliequivalent; Mg, magnesium; mL, milliliter; mOsm, milliosmoles; Na, sodium; Phos, phosphorus; RTF, ready to feed.

Nutren 1.0‐low residue 1 40 38 127 315 38 32 668 268 668
Osmolite 1.0 Cal low residue 1 44.3 34.7 143.9 300 40.4 40.2 760 305 1760
Replete high protein, low residue 1 62.4 34 112 300 38.1 38.5 1000 400 1000
Replete Fiber high protein with fiber 1 62.4 34 112 310 38.1 38.5 1000 400 1000
Osmolite 1.5 low residue, calorically dense 1.5 62.7 49.1 203.6 525 60.9 46 1000 400 1000
Two Cal calorie and protein dense 2 83.5 91 219 725 64 63 1050 425 1050
Vivonex RTF‐elemental 1 50 11.6 176 630 30.4 31 668 268 668
Nepro with Carb Steady‐for electrolyte, fluid restriction (eg, dialysis) 1.8 81 96 161 745 46 27 1060 210 720
Nutren Glytrol low CHO 1 45.2 47.6 100 280 32.2 35.9 720 286 720
NutriHep‐for hepatic disease 1.5 40 21.2 290 790 160 33.9 956 376 1000

If concerned about formula tolerance, one solution is to initiate the formula at a low rate and increase to the goal rate over 2448 hours. Dilution of enteral formulas is not necessary to assure optimal tolerance. Continuous feedings are recommended for most patients initially and after tolerance has been established, bolus feedings can be attempted if the feeding tube terminates in the stomach. Bolus feedings, where 240480 mL of formula are delivered through a syringe over 1015 minutes, may be more physiological for patients. This regimen can be repeated 46 times daily to meet nutrition goals.41

Parenteral Nutrition

PN provides macronutrients such as carbohydrates, protein, and fat; micronutrients such as vitamins, minerals, electrolytes, and trace elements are added in appropriate concentrations. PN may also provide the patient's daily fluid needs. The timing of PN initiation depends upon the patient's initial nutritional status. ASPEN does not recommend PN during the first 7 days of hospitalization in critically ill patients with normal nutritional status. If the patient is not receiving 100% of caloric needs from EN after 7 days, supplemental PN should be considered. However, if on admission a patient is already malnourished and EN is not feasible, PN should be initiated and continued until the patient is receiving at least 60% of caloric needs by enteral route.42 This includes patients with intestinal obstruction, ileus, peritonitis, malabsorption, high output enterocutaneous fistulae, intestinal ischemia, intractable vomiting and diarrhea, severe shock, and fulminant sepsis.10, 43

Standardized commercial PN products are available and reduce the number of steps required between ordering and administration, as compared to customized PN, which is compounded for a particular patient. However, despite improved efficiency and lower cost, there is no evidence that standardized preparations are safer to patients than customized solutions. Institutions utilizing standardized PN must also have a mechanism to customize formulas for those with complex needs.44

Creating a customized parenteral solution involves several basic steps. Total caloric requirement may be estimated using a predictive formula, as previously discussed; calories/kg of ideal body weight is the simplest method. Most hospitalized patients require 2030 calories/kg/d. Daily fluid requirement may be based on kilocalories (kcal) delivered, or by ideal body weight (eg, 1 mL/kcal or 3040 mL/kg). More fluid may be needed in patients with significant sensible or insensible losses; those with renal failure or heart failure should receive less fluid.

Protein needs are calculated by multiplying ideal body weight (kg) by estimated protein needs in g/kg/d (1.22 g/kg/d for catabolic patients). Protein should provide approximately 20% of total calories. Protein restriction is not required in renal impairment; acutely ill patients on renal replacement therapy should receive 1.51.8 g/kg/d. In hepatic failure patients, protein should be restricted only if hepatic encephalopathy fails to improve with other measures.

Knowing the protein, kcal, and fluid needs of the patient, the practitioner divides the remaining non‐protein calories between carbohydrates and fat. Approximately 70%85% of non‐protein calories should be provided as carbohydrates (dextrose), up to 7 g/kg/d. The other 15%30% are as fat, in lipid solutions, providing a maximum of 2.5 g/kg/d. Lipid solutions are provided as either 10% (1.1 kcal/mL) or 20% (2.2 kcal/mL) concentrations.43, 44 Propofol's contribution to fat intake complicates estimating total fat intake in critically ill patients.45

Standardized parenteral multivitamin preparations are available; the clinician must determine if preparations containing vitamin K are appropriate. Of the trace elements, copper and manganese should be restricted in hepatobiliary disease.44

Acutely ill patients receive PN as a 24‐hour infusion, to minimize its impact on volume status and energy expenditure,46 providing 50% of needs on infusion day one and reaching goal within 4872 hours, rather than cyclic infusions over shorter intervals. Daily assessments of vital signs, intake and output, and weight are necessary to monitor volume status.

Once a patient is taking at least 60% of caloric needs either by mouth or by EN, PN can be discontinued. Tapering the infusion is not required, as abrupt discontinuation has not been demonstrated to cause symptomatic hypoglycemia.47, 48

PATIENT MONITORING

Laboratory monitoring with nutrition support should include baseline electrolytes, glucose, renal function, coagulation studies, triglycerides, magnesium, phosphorus, cholesterol, platelet count, and hepatobiliary enzymes. Electrolytes, calcium, magnesium, and phosphorus should be checked daily for 3 days and, if normal, should then be checked biweekly. Capillary glucose should be monitored several times a day until stable. Weekly triglycerides, albumin, cholesterol, coagulation studies, and liver enzymes should also be checked in patients while on parenteral nutrition.25 Patients at risk for refeeding syndrome should have potassium, phosphate, calcium, and magnesium measured daily for 7 days, with repletion as necessary. These electrolytes should be monitored 3 times the following week if stable.49

Patients should be monitored clinically for gastrointestinal tolerance of enteral nutrition. All 3 North American guidelines recommend monitoring gastric residual volumes (GRV); however, there is no consensus on the volume considered to require intervention. Motility agents are recommended as first line treatment of high GRV.36, 37, 42 If high GRV continues, tube feeding should be held, and tube placement, medications, and metabolic assessment should be reviewed. Placement of a transpyloric feeding tube may be indicated.50

Adverse Effects and Complications of Nutrition Support

Regarding EN, complications include those related to tube placement and maintenance, infections, and medical complications of the feeds themselves. Some of the adverse effects of the enteral formulas may be attenuated. Diarrhea, which occurs in up to 20% of patients, may be avoided with slow feed advancement, use of low‐osmotic formulas, or fiber additives.51 Gastric distention and abdominal pain may improve with slow feed advancement and continuous (rather than bolus) feeds. Small‐bore tubes and acid‐reducing medications may decrease gastroesophageal reflux, and aspiration pneumonia may be avoided by semi‐recumbent positioning and post‐pyloric feeding.52

Complications of PN may be grouped as mechanical, infectious, and metabolic. The mechanical complications of central line placement include pneumothorax, arterial puncture, hematoma, air embolism, and line malpositioning. Catheter‐related deep venous thrombosis may occur. Patients on PN through a central line are at risk for central line‐associated bloodstream infections.25 The metabolic complications such as hyperglycemia, electrolyte disorders, hepatic steatosis, and volume overload may have severe consequences, such as heart failure or neuromuscular dysfunction, thus they require close attention.53

A complication of nutrition support that may occur regardless of route is the refeeding syndrome. Refeeding syndrome describes fluid shifts and electrolyte abnormalities that occur after initiation of oral, enteral, or parenteral nutrition in a malnourished or starved patient.54, 55 There are no formal criteria for diagnosing refeeding syndrome.

In the starved state, the body switches from carbohydrate to protein and fat metabolism. Reintroduction of carbohydrates stimulates insulin release with glycogen, fat, and protein synthesis. Associated uptake of glucose, potassium, magnesium, phosphate, and water into cells causes electrolyte and fluid abnormalities. Although hypophosphatemia is the hallmark of refeeding syndrome, it is not pathognomonic. Additional disturbances include hypokalemia, hyperglycemia, hypomagnesemia, thiamine deficiency, and fluid imbalance.49 Patients at risk of refeeding should have serum electrolytes, magnesium, phosphorus, and glucose checked before nutrition support starts. The degree of laboratory abnormalities, if any, and the clinical course of refeeding guides the frequency of subsequent blood tests.56 These consequences of refeeding can adversely affect every major organ system and may result in death.57

Starvation physiology underlies all risk factors for refeeding syndrome. In hospitalized patients, those at risk for refeeding include, but are not limited to, the elderly, oncology patients, postoperative patients, alcohol‐dependent patients, those with malabsorptive states, those who are fasting or chronically malnourished, and those on diuretic therapy.54, 57 The National Institute for Health and Clinical Excellence (NICE) of England and Wales has published criteria to identify patients at high risk for refeeding (Table 3).56 Identification of at‐risk patients and attention to their nutritional needs prevents refeeding syndrome.

NICE Criteria of Risk Factors for Refeeding
  • NOTE: National Institute for Health and Clinical Excellence (2006) CG 32 Nutrition support in adults: oral nutrition support, enteral tube feeding and parenteral nutrition. London: NICE. Available from www.nice.org.uk/guidance/CG32 Reproduced with permission.

  • Abbreviations: BMI, body mass index.

Patient has 1 or more of the following:
BMI <16 kg/m2
Unintentional weight loss >15% within the last 36 mo
Little or no nutritional intake for more than 10 d
Low levels of potassium, phosphate, or magnesium prior to feeding
Or patient has 2 or more of the following:
BMI <18.5 kg/m2
Unintentional weight loss >10% within the last 36 mo
Little or no nutritional intake for more than 5 d
A history of alcohol abuse or drugs including insulin, chemotherapy, antacids, or diuretics

ASPEN and NICE have each issued guidelines for initiating nutrition support in patients at risk for refeeding. ASPEN guidelines recommend feeding start at approximately 25% of the estimated goal, with advancement to goal over 35 days. ASPEN recommends fluid and electrolyte status be monitored as needed.50 The NICE guidelines recommend starting nutrition support at a maximum of 10 kcal/kg/d with slow increase to meet or exceed full needs by 47 days. For extremely malnourished patients (eg, BMI <14 kg/m2, or negligible intake for >15 days), they recommend starting at 5 kcal/kg/d. For patients at high risk of developing refeeding syndrome, the NICE guidelines recommend vitamin repletion immediately before and during the first 10 days of feeding (thiamine, vitamin B, and a balanced multivitamin/trace element supplement). Cardiac monitoring is recommended for this group as well as any patients who are at risk for cardiac arrhythmias. Careful monitoring of fluid balance and restoring circulatory volume is recommended, as is repletion of potassium, phosphate, and magnesium.56

TERMINATION OF THERAPY

Termination of nutrition support often involves transitioning from one mode of support to another. PN can be discontinued when oral or enteral intake reaches 60% of total calories; enteral intake can be discontinued when oral intake reaches the same level. However, the patient should be observed maintaining their intake; if they cannot, nutrition support should be resumed.12

TRANSITION OF CARE PLAN

Patients discharged from the hospital on enteral or parenteral nutrition require the support of a coordinated multidisciplinary team including dietitians, home nutrition delivery companies, primary care physicians trained in specialized nutrition support, community pharmacists, and other healthcare professionals, if indicated. These relationships should be established prior to discharge, with education about the patient's individualized nutrition plan, and training with the equipment and supplies.10, 56

CONCLUSION

This review provides an overview of managing the at‐risk or malnourished patient by describing the processes of screening, assessment, and development and implementation of a nutrition care plan in the acutely ill hospitalized patient. Malnutrition is a relatively common, yet underdiagnosed entity that impacts patient outcomes, length of stay, hospital costs, and readmissions. Acute illness in a patient already nutritionally debilitated by chronic disease may cause rapid depletion in nutritional stores. Hospitals are required to screen patients for malnutrition on admission and at regular intervals, and to develop and implement a nutrition care plan for those at risk. The plan guides how nutrition therapy is provided, monitored for adequacy and adverse effects, and assessed for achievement of nutritional goals. It encompasses the use of dietary modifications, and enteral and parenteral nutrition. Clinicians must be aware of serious but avoidable adverse effects, particularly refeeding syndrome in malnourished patients. Prior to discharge, the patient should have already been transitioned from EN or PN to taking adequate amounts of calories by mouth; otherwise, careful discharge planning to educate the patients and/or caregivers, and coordinate the necessary multidisciplinary community services is necessary.

Acknowledgements

The authors express their appreciation to Ms Susan Lundy, for her helpful and timely information, and Ms Lisa Boucher, for her invaluable assistance with this manuscript and its submission.

Disclosures: Susan Brantley is on the Speaker's Bureau for Nestle Nutrition and for Abbott Nutrition. Authors Kirkland, Kashiwagi, Scheurer, and Varkey have nothing to report.

Malnutrition is present in 20% to 50% of hospitalized patients.1, 2 Despite simple, validated screening tools, malnutrition tends to be underdiagnosed.3, 4 Over 90% of elderly patients transitioning from an acute care hospital to a subacute care facility are either malnourished or at risk of malnutrition.5 Malnutrition has been associated with increased risk of nosocomial infections,6 worsened discharge functional status,7 and higher mortality,8 as well as longer lengths of stay7, 8 and higher hospital costs.2

Malnutrition describes either overnutrition or undernutrition that causes a change in body composition and decreased function.9 Malnutrition in hospitalized patients is typically related to undernutrition due to either reduced intake or increased metabolic rate. Reasons for reduced intake include poor appetite, reduced ability to chew or swallow, and nil per os (NPO) status. Patients with acute or chronic illnesses may either be malnourished on admission, or develop malnutrition within a few days of hospital admission, due to the effects of the inflammatory state on metabolism. Given that malnutrition is potentially modifiable, it is important to screen for malnutrition and, when present, develop, implement, and monitor a nutrition care plan10 (Figure 1).

Figure 1
Algorithm for nutrition care (adapted from Ukleja et al. Standard for nutrition support: adult hospitalized patients. Nutr Clin Pract. 2010;24(4):403–414; copyright 2010 by American Society of Parenteral and Enteral Nutrition. Reprinted by permission of SAGE Publications).

The purpose of this review is to provide the hospitalist with an overview of screening, assessment, and development and implementation of a nutrition care plan in the acutely ill hospitalized patient.

PATIENT SCREENING

Nutrition screening identifies patients with nutritional deficits who may benefit from further detailed nutrition assessment and intervention.11 The Joint Commission requires that all patients admitted to acute care hospitals be screened for risk of malnutrition within 24 hours.12 Those considered at risk for malnutrition have significant weight changes, chronic disease or an acute inflammatory process, or have been unable to ingest adequate calories for 7 days.13

Those not at risk should be regularly rescreened throughout their hospital stay. The American Society of Parenteral and Enteral Nutrition (ASPEN) recommends that institutions create and approve a screening process according to the patient population served.10 There are several tools validated for use in the acute care setting.14 Many institutions trigger an automatic nutrition consult when certain screening criteria are met.

PATIENT ASSESSMENT

Nutrition assessment should be performed by a dietitian or nutrition consult provider in patients who screen at risk for malnutrition to characterize and determine the cause of nutritional deficits.10 The nutrition assessment identifies history and physical examination elements to diagnose malnutrition. An ASPEN consensus statement recommends the diagnosis of malnutrition if 2 or more of the following are present: insufficient energy intake, weight loss, loss of muscle mass, loss of subcutaneous fat, localized or generalized fluid accumulation, and decreased functional status measured by hand‐grip strength.9 The nutrition assessment should also consider how long the patient has been without adequate nutrition, document baseline nutrition parameters,15 and estimate caloric requirements to determine nutrition support therapy needs.10 Nutrition assessment typically includes the following components.

History

A careful history elicits the majority of information needed to determine the cause and severity of malnutrition.16 Patients should be questioned about a typical day's oral intake prior to hospitalization, and about factors that affect their intake such as sensory deficits, fine motor dysfunction, or chewing and swallowing difficulties, which often decline in chronically ill and elderly patients. Nutrition may be affected by financial difficulties or limited social support, and access to food should be assessed.

Physical Findings

Weight loss is the best physical exam predictor of malnutrition risk, although nutritional depletion can occur in a very short time in acutely ill or injured patients before substantial weight loss has occurred. The likelihood of malnutrition is increased if a patient has: a body mass index (BMI) <18.5 kg/m2; unintentional loss of >2.3 kg (5 lb) or 5% of body weight over 1 month; and unintentional loss of >4.5 kg (10 lb) or 10% of body weight over 6 months.17 Weight loss may be masked by fluid retention from chronic conditions, such as heart failure, or from volume resuscitation in the acutely ill patient.9, 16

Body mass index can be misleading, as age‐related height loss may artificially increase BMI, and height may be difficult to accurately measure in a kyphotic, unsteady, or bedridden patient. The clinician may find evidence of loss of subcutaneous fat or muscle mass in patients with chronic illness, but these findings may not be evident in the acutely ill patient.9 Other physical exam assessments of malnutrition, such as arm span, skinfold thickness, and arm circumference are not reliable.16

Laboratory Tests

Biochemical markers, including transferrin, albumin, and prealbumin, have not been proven as accurate predictors of nutrition status because they may change as a result of other factors not related to nutrition.15, 18 Serum albumin, for example, may be more reflective of the degree of metabolic stress.19 Prealbumin has a serum half‐life much shorter than albumin or transferrin (approximately 2448 hours) and is perhaps the most useful protein marker to assess the adequacy of nutritional replacement after the inflammatory state is resolved.18

Calculating Caloric Requirements

Energy expenditure measurement is considered the gold standard to determine patients' caloric needs. Actual measurement by methods such as indirect calorimetry, which measures oxygen consumption and carbon dioxide production, and calculates energy expenditure, is challenging in everyday clinical settings. Predictive equations often are used as alternative methods to estimate patients' caloric requirements.20 There is no consensus among the 3 North American societies' guidelines (the Canadian Clinical Practice Guidelines; the American Dietetics Association's evidence‐based guideline for critical illness; and the Society of Critical Care Medicine and American Society of Parenteral and Enteral Nutrition's joint guideline) as to the best method.21

In the simplest equation, caloric needs are estimated by calories per kilogram.22 In obese patients, using actual body weight will overestimate needs, but using ideal body weight may cause underfeeding. A small study comparing predictive equations in obese hospitalized patients found the Harris‐Benedict equations (H‐BE) using adjusted body weight and a stress factor to be most accurate, but only in 50% of patients.23 Most clinicians are familiar with the H‐BE, but alternatives such as calories per kilogram or the Mifflin St.‐Jeor equation24 are often used (S. Brantley (May 5, 2012), S. Lundy (May 23, 2012), personal communication).

Indications for Nutritional Intervention

In adults without preexisting malnutrition, inadequate nutritional intake for approximately 714 days should prompt nutritional intervention.25, 26 This timeline should be shorter (37 days) in those with lower energy reserves (eg, underweight or recent weight loss) or significant catabolic stress (eg, acutely ill patients).27, 28 Other patient populations shown to benefit from nutritional intervention include: postoperative patients who are anticipated to be NPO for more than 7 days or to be taking less than 60% of estimated caloric needs by postoperative day 10; preoperative patients with severe malnutrition29; those with gastrointestinal cancer undergoing elective surgery30; and stroke patients with persistent dysphagia for more than 7 days.31

DEVELOPMENT OF A NUTRITION CARE PLAN

The formal nutrition assessment of the at‐risk patient derives the information needed for the development of a nutrition care plan. This plan guides the provision of nutrition therapy, the intervention, the monitoring protocols, evaluation, and reassessment of nutrition goals or termination of specialized nutrition support.10 Assessments for adequacy of nutritional repletion are best done by repeated screening and physical examinations.18

IMPLEMENTATION OF NUTRITION CARE PLAN

Nutritional interventions include dietary modifications, enteral nutrition, and parenteral nutrition.

Dietary Modifications

The purpose of the diet is to provide the necessary nutrients to the body in a well‐tolerated form. Diets can be modified to provide for individual requirements, personal eating patterns and food preferences, and disease process and digestive capacity. Dietary adjustments include change in consistency of foods (eg, pureed, mechanical soft), increase or decrease in energy value, increase or decrease in the type of food or nutrient consumed (eg, sodium restriction, fiber enhancement), elimination of specific foods (eg, gluten‐free diet), adjustment in protein, fat, and carbohydrate content (eg, ketogenic diet, renal diet, cholesterol‐lowering diet), and adjustment of the number and frequency of meals.32

Dietary supplementation (eg, Boost, Ensure) is common practice in persons diagnosed with such conditions as cancer, diabetes, and cardiovascular disease. Supplements enhance the diet by increasing the total daily intake of a vitamin, a mineral, an amino acid, an herb or other botanical33, and should not be used as a meal substitute.34 These supplements are varied in content of calories, protein, vitamins, and minerals. Various flavors and consistencies are also available. Several oral supplements are reviewed in Table 1.

Nutritional Content of Oral Supplements
Oral Supplement* (Serving Size; mL) Kcal/svg Protein (g/svg) Fat (g/svg) CHO (g/svg) Na (mg/svg) K (mg/svg) Ca (mg/svg) Phos (mg/svg) Mg (mg/svg)
  • Abbreviations: Ca, calcium; CHO, carbohydrate; g, gram; K, potassium; Kcal, kilocalories; Mg, magnesium; mg, milligram; Na, sodium; Phos, phosphorus; svg, serving. *All information provided for vanilla‐flavored supplement, unless otherwise noted.

Boost Original (237) 240 10 4 41 150 460 300 300 100
Ensure Nutrition Shake (237) 250 9 6 40 200 370 300 250 100
Carnation Instant Breakfast Ready to Drink (325) 250 14 5 34 180 330 500 500 120
Resource Breeze (fruit‐flavored) clear liquid (237) 250 9 0 54 80 10 10 150 1
Glucerna 1.0 Ready to Drink low‐CHO (237) 240 10 13 23 220 370 170 170 67
Re/Gen low K and Phos (180) 375 12 17 47 180 23 15 68 3

Enteral Nutrition

Enteral nutrition (EN) support should be provided to patients who have functioning gastrointestinal (GI) tracts but are unable to take adequate calories orally. Compared to parenteral nutrition (PN), EN is associated with favorable improvements in inflammatory cytokines, acute phase proteins, hyperglycemia, insulin resistance, nosocomial infections, mortality, and cost.35 Enteral feeds are more physiologic than parenteral feeds, maintain GI structure and integrity, and avoid intravenous (IV) access complications. Patients with normal nutritional status on admission who require EN should be receiving over 50% of their caloric needs within the first week of hospital stay.25 Malnourished patients should reach this minimum goal within 35 days of admission.27, 28 EN is not contraindicated in the absence of bowel sounds or in the presence of increased gastric residuals.35 Withholding enteral feedings for gastric residual volumes <250 mL36, 37 or reduced bowel sounds can result in inadequate caloric intake or inappropriate use of PN.27

Gastric feedings are more physiologic than small bowel feedings, can be given by bolus or continuous infusion, and can be given by tubes that are easy to place at the bedside. Post‐pyloric feedings (nasoduodenal or nasojejunal) may be associated with a lower risk of pneumonia, and should be considered in high‐risk patients such as those receiving continuous sedatives or neuromuscular blockers.36 Post‐pyloric tube placement usually requires endoscopy, fluoroscopy, or electromagnetic guidance. Percutaneous feeding tubes (gastrostomy or jejunostomy) should be considered in those who require tube feedings for longer than 30 days.38

Assessment of patient requirements and disease state, as well as extensive knowledge of available formulas, is important in the selection of the appropriate enteral formula.39 Standardized formulas are used for most patients. The provision of adequate water must be considered with these formulas, particularly in the long‐term care and home settings.40 Many specialized formulas are designed for a particular disease state or condition, some of which are further reviewed in Table 2.

Nutritional Content of Tube Feed Formulas
Formula Kcal/mL Protein (g/L) Fat (g/L) CHO (g/L) Osmolality (mOsm/kg H2O) Na (mEq/L) K (mEq/L) Ca (mg/L) Mg (mg/L) Phos (mg/L)
  • Abbreviations: Ca, calcium; CHO, carbohydrate; g, gram; H2O, water; K, potassium; Kcal, kilocalories; kg, kilogram; L, liter; mEq, milliequivalent; Mg, magnesium; mL, milliliter; mOsm, milliosmoles; Na, sodium; Phos, phosphorus; RTF, ready to feed.

Nutren 1.0‐low residue 1 40 38 127 315 38 32 668 268 668
Osmolite 1.0 Cal low residue 1 44.3 34.7 143.9 300 40.4 40.2 760 305 1760
Replete high protein, low residue 1 62.4 34 112 300 38.1 38.5 1000 400 1000
Replete Fiber high protein with fiber 1 62.4 34 112 310 38.1 38.5 1000 400 1000
Osmolite 1.5 low residue, calorically dense 1.5 62.7 49.1 203.6 525 60.9 46 1000 400 1000
Two Cal calorie and protein dense 2 83.5 91 219 725 64 63 1050 425 1050
Vivonex RTF‐elemental 1 50 11.6 176 630 30.4 31 668 268 668
Nepro with Carb Steady‐for electrolyte, fluid restriction (eg, dialysis) 1.8 81 96 161 745 46 27 1060 210 720
Nutren Glytrol low CHO 1 45.2 47.6 100 280 32.2 35.9 720 286 720
NutriHep‐for hepatic disease 1.5 40 21.2 290 790 160 33.9 956 376 1000

If concerned about formula tolerance, one solution is to initiate the formula at a low rate and increase to the goal rate over 2448 hours. Dilution of enteral formulas is not necessary to assure optimal tolerance. Continuous feedings are recommended for most patients initially and after tolerance has been established, bolus feedings can be attempted if the feeding tube terminates in the stomach. Bolus feedings, where 240480 mL of formula are delivered through a syringe over 1015 minutes, may be more physiological for patients. This regimen can be repeated 46 times daily to meet nutrition goals.41

Parenteral Nutrition

PN provides macronutrients such as carbohydrates, protein, and fat; micronutrients such as vitamins, minerals, electrolytes, and trace elements are added in appropriate concentrations. PN may also provide the patient's daily fluid needs. The timing of PN initiation depends upon the patient's initial nutritional status. ASPEN does not recommend PN during the first 7 days of hospitalization in critically ill patients with normal nutritional status. If the patient is not receiving 100% of caloric needs from EN after 7 days, supplemental PN should be considered. However, if on admission a patient is already malnourished and EN is not feasible, PN should be initiated and continued until the patient is receiving at least 60% of caloric needs by enteral route.42 This includes patients with intestinal obstruction, ileus, peritonitis, malabsorption, high output enterocutaneous fistulae, intestinal ischemia, intractable vomiting and diarrhea, severe shock, and fulminant sepsis.10, 43

Standardized commercial PN products are available and reduce the number of steps required between ordering and administration, as compared to customized PN, which is compounded for a particular patient. However, despite improved efficiency and lower cost, there is no evidence that standardized preparations are safer to patients than customized solutions. Institutions utilizing standardized PN must also have a mechanism to customize formulas for those with complex needs.44

Creating a customized parenteral solution involves several basic steps. Total caloric requirement may be estimated using a predictive formula, as previously discussed; calories/kg of ideal body weight is the simplest method. Most hospitalized patients require 2030 calories/kg/d. Daily fluid requirement may be based on kilocalories (kcal) delivered, or by ideal body weight (eg, 1 mL/kcal or 3040 mL/kg). More fluid may be needed in patients with significant sensible or insensible losses; those with renal failure or heart failure should receive less fluid.

Protein needs are calculated by multiplying ideal body weight (kg) by estimated protein needs in g/kg/d (1.22 g/kg/d for catabolic patients). Protein should provide approximately 20% of total calories. Protein restriction is not required in renal impairment; acutely ill patients on renal replacement therapy should receive 1.51.8 g/kg/d. In hepatic failure patients, protein should be restricted only if hepatic encephalopathy fails to improve with other measures.

Knowing the protein, kcal, and fluid needs of the patient, the practitioner divides the remaining non‐protein calories between carbohydrates and fat. Approximately 70%85% of non‐protein calories should be provided as carbohydrates (dextrose), up to 7 g/kg/d. The other 15%30% are as fat, in lipid solutions, providing a maximum of 2.5 g/kg/d. Lipid solutions are provided as either 10% (1.1 kcal/mL) or 20% (2.2 kcal/mL) concentrations.43, 44 Propofol's contribution to fat intake complicates estimating total fat intake in critically ill patients.45

Standardized parenteral multivitamin preparations are available; the clinician must determine if preparations containing vitamin K are appropriate. Of the trace elements, copper and manganese should be restricted in hepatobiliary disease.44

Acutely ill patients receive PN as a 24‐hour infusion, to minimize its impact on volume status and energy expenditure,46 providing 50% of needs on infusion day one and reaching goal within 4872 hours, rather than cyclic infusions over shorter intervals. Daily assessments of vital signs, intake and output, and weight are necessary to monitor volume status.

Once a patient is taking at least 60% of caloric needs either by mouth or by EN, PN can be discontinued. Tapering the infusion is not required, as abrupt discontinuation has not been demonstrated to cause symptomatic hypoglycemia.47, 48

PATIENT MONITORING

Laboratory monitoring with nutrition support should include baseline electrolytes, glucose, renal function, coagulation studies, triglycerides, magnesium, phosphorus, cholesterol, platelet count, and hepatobiliary enzymes. Electrolytes, calcium, magnesium, and phosphorus should be checked daily for 3 days and, if normal, should then be checked biweekly. Capillary glucose should be monitored several times a day until stable. Weekly triglycerides, albumin, cholesterol, coagulation studies, and liver enzymes should also be checked in patients while on parenteral nutrition.25 Patients at risk for refeeding syndrome should have potassium, phosphate, calcium, and magnesium measured daily for 7 days, with repletion as necessary. These electrolytes should be monitored 3 times the following week if stable.49

Patients should be monitored clinically for gastrointestinal tolerance of enteral nutrition. All 3 North American guidelines recommend monitoring gastric residual volumes (GRV); however, there is no consensus on the volume considered to require intervention. Motility agents are recommended as first line treatment of high GRV.36, 37, 42 If high GRV continues, tube feeding should be held, and tube placement, medications, and metabolic assessment should be reviewed. Placement of a transpyloric feeding tube may be indicated.50

Adverse Effects and Complications of Nutrition Support

Regarding EN, complications include those related to tube placement and maintenance, infections, and medical complications of the feeds themselves. Some of the adverse effects of the enteral formulas may be attenuated. Diarrhea, which occurs in up to 20% of patients, may be avoided with slow feed advancement, use of low‐osmotic formulas, or fiber additives.51 Gastric distention and abdominal pain may improve with slow feed advancement and continuous (rather than bolus) feeds. Small‐bore tubes and acid‐reducing medications may decrease gastroesophageal reflux, and aspiration pneumonia may be avoided by semi‐recumbent positioning and post‐pyloric feeding.52

Complications of PN may be grouped as mechanical, infectious, and metabolic. The mechanical complications of central line placement include pneumothorax, arterial puncture, hematoma, air embolism, and line malpositioning. Catheter‐related deep venous thrombosis may occur. Patients on PN through a central line are at risk for central line‐associated bloodstream infections.25 The metabolic complications such as hyperglycemia, electrolyte disorders, hepatic steatosis, and volume overload may have severe consequences, such as heart failure or neuromuscular dysfunction, thus they require close attention.53

A complication of nutrition support that may occur regardless of route is the refeeding syndrome. Refeeding syndrome describes fluid shifts and electrolyte abnormalities that occur after initiation of oral, enteral, or parenteral nutrition in a malnourished or starved patient.54, 55 There are no formal criteria for diagnosing refeeding syndrome.

In the starved state, the body switches from carbohydrate to protein and fat metabolism. Reintroduction of carbohydrates stimulates insulin release with glycogen, fat, and protein synthesis. Associated uptake of glucose, potassium, magnesium, phosphate, and water into cells causes electrolyte and fluid abnormalities. Although hypophosphatemia is the hallmark of refeeding syndrome, it is not pathognomonic. Additional disturbances include hypokalemia, hyperglycemia, hypomagnesemia, thiamine deficiency, and fluid imbalance.49 Patients at risk of refeeding should have serum electrolytes, magnesium, phosphorus, and glucose checked before nutrition support starts. The degree of laboratory abnormalities, if any, and the clinical course of refeeding guides the frequency of subsequent blood tests.56 These consequences of refeeding can adversely affect every major organ system and may result in death.57

Starvation physiology underlies all risk factors for refeeding syndrome. In hospitalized patients, those at risk for refeeding include, but are not limited to, the elderly, oncology patients, postoperative patients, alcohol‐dependent patients, those with malabsorptive states, those who are fasting or chronically malnourished, and those on diuretic therapy.54, 57 The National Institute for Health and Clinical Excellence (NICE) of England and Wales has published criteria to identify patients at high risk for refeeding (Table 3).56 Identification of at‐risk patients and attention to their nutritional needs prevents refeeding syndrome.

NICE Criteria of Risk Factors for Refeeding
  • NOTE: National Institute for Health and Clinical Excellence (2006) CG 32 Nutrition support in adults: oral nutrition support, enteral tube feeding and parenteral nutrition. London: NICE. Available from www.nice.org.uk/guidance/CG32 Reproduced with permission.

  • Abbreviations: BMI, body mass index.

Patient has 1 or more of the following:
BMI <16 kg/m2
Unintentional weight loss >15% within the last 36 mo
Little or no nutritional intake for more than 10 d
Low levels of potassium, phosphate, or magnesium prior to feeding
Or patient has 2 or more of the following:
BMI <18.5 kg/m2
Unintentional weight loss >10% within the last 36 mo
Little or no nutritional intake for more than 5 d
A history of alcohol abuse or drugs including insulin, chemotherapy, antacids, or diuretics

ASPEN and NICE have each issued guidelines for initiating nutrition support in patients at risk for refeeding. ASPEN guidelines recommend feeding start at approximately 25% of the estimated goal, with advancement to goal over 35 days. ASPEN recommends fluid and electrolyte status be monitored as needed.50 The NICE guidelines recommend starting nutrition support at a maximum of 10 kcal/kg/d with slow increase to meet or exceed full needs by 47 days. For extremely malnourished patients (eg, BMI <14 kg/m2, or negligible intake for >15 days), they recommend starting at 5 kcal/kg/d. For patients at high risk of developing refeeding syndrome, the NICE guidelines recommend vitamin repletion immediately before and during the first 10 days of feeding (thiamine, vitamin B, and a balanced multivitamin/trace element supplement). Cardiac monitoring is recommended for this group as well as any patients who are at risk for cardiac arrhythmias. Careful monitoring of fluid balance and restoring circulatory volume is recommended, as is repletion of potassium, phosphate, and magnesium.56

TERMINATION OF THERAPY

Termination of nutrition support often involves transitioning from one mode of support to another. PN can be discontinued when oral or enteral intake reaches 60% of total calories; enteral intake can be discontinued when oral intake reaches the same level. However, the patient should be observed maintaining their intake; if they cannot, nutrition support should be resumed.12

TRANSITION OF CARE PLAN

Patients discharged from the hospital on enteral or parenteral nutrition require the support of a coordinated multidisciplinary team including dietitians, home nutrition delivery companies, primary care physicians trained in specialized nutrition support, community pharmacists, and other healthcare professionals, if indicated. These relationships should be established prior to discharge, with education about the patient's individualized nutrition plan, and training with the equipment and supplies.10, 56

CONCLUSION

This review provides an overview of managing the at‐risk or malnourished patient by describing the processes of screening, assessment, and development and implementation of a nutrition care plan in the acutely ill hospitalized patient. Malnutrition is a relatively common, yet underdiagnosed entity that impacts patient outcomes, length of stay, hospital costs, and readmissions. Acute illness in a patient already nutritionally debilitated by chronic disease may cause rapid depletion in nutritional stores. Hospitals are required to screen patients for malnutrition on admission and at regular intervals, and to develop and implement a nutrition care plan for those at risk. The plan guides how nutrition therapy is provided, monitored for adequacy and adverse effects, and assessed for achievement of nutritional goals. It encompasses the use of dietary modifications, and enteral and parenteral nutrition. Clinicians must be aware of serious but avoidable adverse effects, particularly refeeding syndrome in malnourished patients. Prior to discharge, the patient should have already been transitioned from EN or PN to taking adequate amounts of calories by mouth; otherwise, careful discharge planning to educate the patients and/or caregivers, and coordinate the necessary multidisciplinary community services is necessary.

Acknowledgements

The authors express their appreciation to Ms Susan Lundy, for her helpful and timely information, and Ms Lisa Boucher, for her invaluable assistance with this manuscript and its submission.

Disclosures: Susan Brantley is on the Speaker's Bureau for Nestle Nutrition and for Abbott Nutrition. Authors Kirkland, Kashiwagi, Scheurer, and Varkey have nothing to report.

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  26. Kirby DF,Delegge MH,Fleming CR.American Gastroenterological Association technical review on tube feeding for enteral nutrition.Gastroenterology.1995;108(4):12821301.
  27. Kreymann KG,Berger MM,Deutz NE, et al.ESPEN guidelines on enteral nutrition: intensive care.Clin Nutr.2006;25(2):210223.
  28. Winawer N,Williams MV.Nutritional support. In: Shojania KG, Duncan BW, McDonald KM, et al, eds.Making Health Care Safer: A Critical Analysis of Patient Safety Practices. Evidence Report/Technology Assessment Number 43.Rockville, MD:Agency for Healthcare Research and Quality, US Department of Health and Human Services, July2001. AHRQ Publication 01‐E058. Available at: http://www.ahrq.gov.
  29. Veterans Affairs Total Parenteral Nutrition Cooperative Study Group.Perioperative total parenteral nutrition in surgical patients.N Engl J Med.1991;328(8):525532.
  30. Koretz RL,Avenell A,Lipman TO,Braunschweig CL,Milne AC.Does enteral nutrition affect clinical outcome? A systematic review of the randomized trials.Am J Gastroenterol.2007;102(2):412429.
  31. Corrigan ML,Escuro AA,Celestin J,Kirby DF.Nutrition in the stroke patient.Nutr Clin Pract.2011;26(3):242252.
  32. Charney P,Escott‐Stump S,Mahan LK.Nutrition diagnosis and intervention. In: Mahan LK, Escott‐Stump S, eds.Krause's Food and Nutrition Therapy.12th ed.St Louis, MO:Saunders Elsevier;2008:454469.
  33. Dietary Supplement Health and Education Act (DSHEA) of 1994. Available at: http://www.gpo.gov/fdsys/pkg/BILLS‐103s784es/pdf/BILLS‐103s784es.pdf. Accessed June 29,2012.
  34. Thompson CA.Intervention: dietary supplementation and integrative care. In: Mahan LK, Escott‐Stump S, eds.Krause's Food and Nutrition Therapy.12th ed.St Louis, MO:Saunders Elsevier;2008:470474.
  35. Martindale RG,McClave SA,Vanek VW, et al.Guidelines for the provision and assessment of nutrition support therapy in the adult critically ill patient: Society of Critical Care Medicine and American Society for Parenteral and Enteral Nutrition: executive summary.Crit Care Med.2009;37(5):17571761.
  36. Heyland DK,Dhaliwal R,Drover JW,Gramlich L,Dodek P;for the. Canadian Critical Care Clinical Practice Guidelines Committee.Canadian clinical practice guidelines for nutrition support in mechanically ventilated, critically ill adult patients.J Parenter Enteral Nutr.2003;27(5):355373.
  37. American Dietetic Association Evidence Library. Critical Illness. Available at: http://www.adaevidencelibrary.com/template.cfm?key=767115(5 suppl):64S70S.
  38. Skipper A.Enteral nutrition. In: Skipper A, ed.Dietitian's Handbook of Enteral and Parenteral Nutrition.3rd ed.Sudbury, MA:Jones 2012:259280.
  39. Malone A.Enteral formula selection. In: Charney P, Malone A, eds.ADA Pocket Guide to Enteral Nutrition.Chicago, IL:American Dietetic Association;2006:63122.
  40. Marian M,McGinnis C.Overview of enteral nutrition. In: Gottschlich MM, ed.The ASPEN Nutrition Support Core Curriculum: A Case‐Based Approach—The Adult Patient.1st ed.Silver Spring, MD:American Society for Parenteral and Enteral Nutrition;2007:187208.
  41. McClave SA,Martindale RG,Vanek VW, et al.Guidelines for the provision and assessment of nutrition support therapy in the adult critically ill patient: Society of Critical Care Medicine (SCCM) and American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.).J Parenter Enteral Nutr.2009;33(3):277316.
  42. Braga M,Ljungqvist O,Soeters P,Fearon K,Weimann A,Bozzetti F.ESPEN guidelines on parenteral nutrition: surgery.Clin Nutr.2009;28(4):378386.
  43. Mirtallo J,Canada T,Johnson D, et al.Safe practices for parenteral nutrition.J Parenter Enteral Nutr.2004;28(6):S39S70.
  44. DeChicco R,Matarese L,Hummell AC,Speerhas R,Seidner D,Steiger E.Contribution of calories from propofol to total energy intake.J Am Diet Assoc.1995;95(9 supplement):A25.
  45. Forsberg E,Soop M,Lepapea A,Thorne A.Metabolic and thermogenic response to continuous and cyclic total parenteral nutrition in traumatised and infected patients.Clin Nutr.1994;13(5):291301.
  46. Nirula R,Yamada K,Waxman K.The effect of abrupt cessation of total parenteral nutrition on serum glucose: a randomized trial.Am Surg.2000;66(9):866869.
  47. Wagman LD,Newsome HH,Miller KB,Thomas RB,Weir GC.The effect of acute discontinuation of total parenteral nutrition.Ann Surg.1986;204(5):524529.
  48. Mehanna HM,Moledina J,Travis J.Refeeding syndrome: what it is, and how to prevent and treat it.BMJ.2008;336(7659):14951498.
  49. Bankhead R,Boullata J,Brantley S, et al.Enteral nutrition practice recommendations.J Parenter Enteral Nutr.2009;33(2):122167.
  50. Rushdi TATA,Pichard C,Khater YHYH.Control of diarrhea by fiber‐enriched diet in ICU patients on enteral nutrition: a prospective randomized controlled trial.Clin Nutr.2004;23(6):13441352.
  51. Drakulovic MB,Torres A,Bauer TT,Nicolas JM,Nogue S,Ferrer M.Supine body position as a risk factor for nosocomial pneumonia in mechanically ventilated patients: a randomised trial.Lancet.1999;354(9193):18511858.
  52. Ziegler TR.Parenteral nutrition in the critically ill patient.N Engl J Med.2009;361(11):10881097.
  53. Boateng AA,Sriram K,Meguid MM,Crook M.Refeeding syndrome: treatment considerations based on collective analysis of literature case reports.Nutrition.2010;26(2):156167.
  54. Ahmed S,Travis J,Mehanna H.Re‐feeding syndrome in head and neck cancer‐prevention and management.Oral Oncol.2011;47(9):792796.
  55. Nutrition Support in Adults. NICE Clinical Guideline No. 32. 2006. Available at: http://guidance.nice.org.uk/CG32/NICEGuidance. Accessed November 29,2011.
  56. Crook MA,Hally V,Panteli JV.The importance of the refeeding syndrome.Nutrition.2001;17(7–8):632637.
References
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  9. White JV,Guenter P,Jensen G,Malone A,Schofield M.Consensus statement: Academy of Nutrition and Dietetics and American Society for Parenteral and Enteral Nutrition: characteristics recommended for the identification and documentation of adult malnutrition (undernutrition).J Parenter Enteral Nutr.2012;36(3):275283.
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  11. American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.), Board of Directors and Clinical Practice Committee. Definition of Terms, Style, and Conventions used in A.S.P.E.N. Board of Directors‐Approved Documents. May2012. Available at: http://www.nutritioncare.org/Library.aspx. Accessed June 29, 2012.
  12. Joint Commission on Accreditation of Healthcare Organizations.Comprehensive Accreditation for Hospitals.Chicago, IL:Joint Commission on Accreditation for Healthcare Organizations;2007.
  13. Russell MK,Mueller C.Nutrition screening and assessment. In: Gottschlich MM, ed.The ASPEN Nutrition Support Core Curriculum: A Case‐Based Approach—The Adult Patient.1st ed.Silver Spring, MD:American Society for Parenteral and Enteral Nutrition;2007:163186.
  14. Anthony PS.Nutrition screening tools for hospitalized patients.Nutr Clin Pract.2008;23(4):373382.
  15. Charney P.Nutrition screening and assessment. In: Skipper A, ed.Dietitian's Handbook of Enteral and Parenteral Nutrition.3rd ed.Sudbury, MA:Jones 2012:421.
  16. Waitzberg DL,Correia MITD.Nutritional assessment in the hospitalized patient.Curr Opin Clin Nutr Metab Care.2003;6(5):531538.
  17. Blackburn GL,Bistrian BR,Maini BS,Schlamm HT,Smith MF.Nutritional and metabolic assessment of the hospitalized patient.J Parenter Enteral Nutr.1977;1(1):1122.
  18. Fuhrman MP,Charney P,Mueller CM.Hepatic proteins and nutrition assessment.J Am Diet Assoc.2004;104(8):12581264.
  19. Fuhrman MP.The albumin‐nutrition connection: separating myth from fact.Nutrition.2002;18(2):199200.
  20. Walker RN,Heuberger RA.Predictive equations for energy needs for the critically ill.Respir Care.2009;54(4):509521.
  21. Dhaliwal R,Madden SM,Cahill N, et al.Guidelines, guidelines, guidelines: what are we to do with all of these North American guidelines?J Parenter Enteral Nutr.2010;34(6):625643.
  22. Cerra FB,Benitez MR,Blackburn GL, et al.Applied nutrition in ICU patients. A consensus statement of the American College of Chest Physicians.Chest.1997;111(3):769778.
  23. Anderegg BA,Worrall C,Barbour E,Simpson KN,Delegge M.Comparison of resting energy expenditure prediction methods with measured resting energy expenditure in obese, hospitalized adults.J Parenter Enteral Nutr.2009;33(2):168175.
  24. Mifflin MD,St Jeor ST,Hill LA,Scott BJ,Daugherty SA,Koh YO.A new predictive equation for resting energy expenditure in healthy individuals.Am J Clin Nutr.1990;51(2):241247.
  25. American Society for Parenteral and Enteral Nutrition.Guidelines for the use of parenteral and enteral nutrition in adult and pediatric patients.J Parenter Enteral Nutr.2002;26(suppl):1SA138SA.
  26. Kirby DF,Delegge MH,Fleming CR.American Gastroenterological Association technical review on tube feeding for enteral nutrition.Gastroenterology.1995;108(4):12821301.
  27. Kreymann KG,Berger MM,Deutz NE, et al.ESPEN guidelines on enteral nutrition: intensive care.Clin Nutr.2006;25(2):210223.
  28. Winawer N,Williams MV.Nutritional support. In: Shojania KG, Duncan BW, McDonald KM, et al, eds.Making Health Care Safer: A Critical Analysis of Patient Safety Practices. Evidence Report/Technology Assessment Number 43.Rockville, MD:Agency for Healthcare Research and Quality, US Department of Health and Human Services, July2001. AHRQ Publication 01‐E058. Available at: http://www.ahrq.gov.
  29. Veterans Affairs Total Parenteral Nutrition Cooperative Study Group.Perioperative total parenteral nutrition in surgical patients.N Engl J Med.1991;328(8):525532.
  30. Koretz RL,Avenell A,Lipman TO,Braunschweig CL,Milne AC.Does enteral nutrition affect clinical outcome? A systematic review of the randomized trials.Am J Gastroenterol.2007;102(2):412429.
  31. Corrigan ML,Escuro AA,Celestin J,Kirby DF.Nutrition in the stroke patient.Nutr Clin Pract.2011;26(3):242252.
  32. Charney P,Escott‐Stump S,Mahan LK.Nutrition diagnosis and intervention. In: Mahan LK, Escott‐Stump S, eds.Krause's Food and Nutrition Therapy.12th ed.St Louis, MO:Saunders Elsevier;2008:454469.
  33. Dietary Supplement Health and Education Act (DSHEA) of 1994. Available at: http://www.gpo.gov/fdsys/pkg/BILLS‐103s784es/pdf/BILLS‐103s784es.pdf. Accessed June 29,2012.
  34. Thompson CA.Intervention: dietary supplementation and integrative care. In: Mahan LK, Escott‐Stump S, eds.Krause's Food and Nutrition Therapy.12th ed.St Louis, MO:Saunders Elsevier;2008:470474.
  35. Martindale RG,McClave SA,Vanek VW, et al.Guidelines for the provision and assessment of nutrition support therapy in the adult critically ill patient: Society of Critical Care Medicine and American Society for Parenteral and Enteral Nutrition: executive summary.Crit Care Med.2009;37(5):17571761.
  36. Heyland DK,Dhaliwal R,Drover JW,Gramlich L,Dodek P;for the. Canadian Critical Care Clinical Practice Guidelines Committee.Canadian clinical practice guidelines for nutrition support in mechanically ventilated, critically ill adult patients.J Parenter Enteral Nutr.2003;27(5):355373.
  37. American Dietetic Association Evidence Library. Critical Illness. Available at: http://www.adaevidencelibrary.com/template.cfm?key=767115(5 suppl):64S70S.
  38. Skipper A.Enteral nutrition. In: Skipper A, ed.Dietitian's Handbook of Enteral and Parenteral Nutrition.3rd ed.Sudbury, MA:Jones 2012:259280.
  39. Malone A.Enteral formula selection. In: Charney P, Malone A, eds.ADA Pocket Guide to Enteral Nutrition.Chicago, IL:American Dietetic Association;2006:63122.
  40. Marian M,McGinnis C.Overview of enteral nutrition. In: Gottschlich MM, ed.The ASPEN Nutrition Support Core Curriculum: A Case‐Based Approach—The Adult Patient.1st ed.Silver Spring, MD:American Society for Parenteral and Enteral Nutrition;2007:187208.
  41. McClave SA,Martindale RG,Vanek VW, et al.Guidelines for the provision and assessment of nutrition support therapy in the adult critically ill patient: Society of Critical Care Medicine (SCCM) and American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.).J Parenter Enteral Nutr.2009;33(3):277316.
  42. Braga M,Ljungqvist O,Soeters P,Fearon K,Weimann A,Bozzetti F.ESPEN guidelines on parenteral nutrition: surgery.Clin Nutr.2009;28(4):378386.
  43. Mirtallo J,Canada T,Johnson D, et al.Safe practices for parenteral nutrition.J Parenter Enteral Nutr.2004;28(6):S39S70.
  44. DeChicco R,Matarese L,Hummell AC,Speerhas R,Seidner D,Steiger E.Contribution of calories from propofol to total energy intake.J Am Diet Assoc.1995;95(9 supplement):A25.
  45. Forsberg E,Soop M,Lepapea A,Thorne A.Metabolic and thermogenic response to continuous and cyclic total parenteral nutrition in traumatised and infected patients.Clin Nutr.1994;13(5):291301.
  46. Nirula R,Yamada K,Waxman K.The effect of abrupt cessation of total parenteral nutrition on serum glucose: a randomized trial.Am Surg.2000;66(9):866869.
  47. Wagman LD,Newsome HH,Miller KB,Thomas RB,Weir GC.The effect of acute discontinuation of total parenteral nutrition.Ann Surg.1986;204(5):524529.
  48. Mehanna HM,Moledina J,Travis J.Refeeding syndrome: what it is, and how to prevent and treat it.BMJ.2008;336(7659):14951498.
  49. Bankhead R,Boullata J,Brantley S, et al.Enteral nutrition practice recommendations.J Parenter Enteral Nutr.2009;33(2):122167.
  50. Rushdi TATA,Pichard C,Khater YHYH.Control of diarrhea by fiber‐enriched diet in ICU patients on enteral nutrition: a prospective randomized controlled trial.Clin Nutr.2004;23(6):13441352.
  51. Drakulovic MB,Torres A,Bauer TT,Nicolas JM,Nogue S,Ferrer M.Supine body position as a risk factor for nosocomial pneumonia in mechanically ventilated patients: a randomised trial.Lancet.1999;354(9193):18511858.
  52. Ziegler TR.Parenteral nutrition in the critically ill patient.N Engl J Med.2009;361(11):10881097.
  53. Boateng AA,Sriram K,Meguid MM,Crook M.Refeeding syndrome: treatment considerations based on collective analysis of literature case reports.Nutrition.2010;26(2):156167.
  54. Ahmed S,Travis J,Mehanna H.Re‐feeding syndrome in head and neck cancer‐prevention and management.Oral Oncol.2011;47(9):792796.
  55. Nutrition Support in Adults. NICE Clinical Guideline No. 32. 2006. Available at: http://guidance.nice.org.uk/CG32/NICEGuidance. Accessed November 29,2011.
  56. Crook MA,Hally V,Panteli JV.The importance of the refeeding syndrome.Nutrition.2001;17(7–8):632637.
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Nutrition in the hospitalized patient
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Nutrition in the hospitalized patient
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Curbside vs Formal Consultation

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Prospective comparison of curbside versus formal consultations

A curbside consultation is an informal process whereby a consultant is asked to provide information or advice about a patient's care without doing a formal assessment of the patient.14 Curbside consultations are common in the practice of medicine2, 3, 5 and are frequently requested by physicians caring for hospitalized patients. Several surveys have documented the quantity of curbside consultations requested of various subspecialties, the types of questions asked, the time it takes to respond, and physicians' perceptions about the quality of the information exchanged.111 While curbside consultations have a number of advantages, physicians' perceptions are that the information conveyed may be inaccurate or incomplete and that the advice offered may be erroneous.13, 5, 10, 12, 13

Cartmill and White14 performed a random audit of 10% of the telephone referrals they received for neurosurgical consultation over a 1‐year period and noted discrepancies between the Glascow Coma Scores reported during the telephone referrals and those noted in the medical records, but the frequency of these discrepancies was not reported. To our knowledge, no studies have compared the quality of the information provided in curbside consultations with that obtained in formal consultations that included direct face‐to‐face patient evaluations and primary data collection, and whether the advice provided in curbside and formal consultations on the same patient differed.

We performed a prospective cohort study to compare the information received by hospitalists during curbside consultations on hospitalized patients, with that obtained from formal consultations done the same day on the same patients, by different hospitalists who were unaware of any details regarding the curbside consultation. We also compared the advice provided by the 2 hospitalists following their curbside and formal consultations. Our hypotheses were that the information received during curbside consultations was frequently inaccurate or incomplete, that the recommendations made after the formal consultation would frequently differ from those made in the curbside consultation, and that these differences would have important implications on patient care.

METHODS

This was a quality improvement study conducted at Denver Health, a 500‐bed university‐affiliated urban safety net hospital from January 10, 2011 to January 9, 2012. The study design was a prospective cohort that included all curbside consultations on hospitalized patients received between 7 AM and 3 PM, on intermittently selected weekdays, by the Internal Medicine Consultation Service that was staffed by 18 hospitalists. Data were collected intermittently based upon hospitalist availability and was done to limit potential alterations in the consulting practices of the providers requesting consultations.

Consultations were defined as being curbside when the consulting provider asked for advice, suggestions, or opinions about a patient's care but did not ask the hospitalist to see the patient.15, 15 Consultations pertaining to administrative issues (eg, whether a patient should be admitted to an intensive care bed as opposed to an acute care floor bed) or on patients who were already being followed by a hospitalist were excluded.

The hospitalist receiving the curbside consultation was allowed to ask questions as they normally would, but could not verify the accuracy of the information received (eg, could not review any portion of the patient's medical record, such as notes or lab data). A standardized data collection sheet was used to record the service and level of training of the requesting provider, the medical issue(s) of concern, all clinical data offered by the provider, the number of questions asked by the hospitalist of the provider, and whether, on the basis of the information provided, the hospitalist felt that the question(s) being asked was (were) of sufficient complexity that a formal consultation should occur. The hospitalist then offered advice based upon the information given during the curbside consultation.

After completing the curbside consultation, the hospitalist requested verbal permission from the requesting provider to perform a formal consultation. If the request was approved, the hospitalist performing the curbside consultation contacted a different hospitalist who performed the formal consultation within the next few hours. The only information given to the second hospitalist was the patient's identifiers and the clinical question(s) being asked. The formal consultation included a complete face‐to‐face history and physical examination, a review of the patient's medical record, documentation of the provider's findings, and recommendations for care.

Upon completion of the formal consultation, the hospitalists who performed the curbside and the formal consultations met to review the advice each gave to the requesting provider and the information on which this advice was based. The 2 hospitalists jointly determined the following: (a) whether the information received during the curbside consultation was correct and complete, (b) whether the advice provided in the formal consultation differed from that provided in the curbside consultation, (c) whether the advice provided in the formal consultation dealt with issues other than one(s) leading to the curbside consultation, (d) whether differences in the recommendations given in the curbside versus the formal consultation changed patient management in a meaningful way, and (e) whether the curbside consultation alone was felt to be sufficient.

Information obtained by the hospitalist performing the formal consultation that was different from, or not included in, the information recorded during the curbside consultation was considered to be incorrect or incomplete, respectively. A change in management was defined as an alteration in the direction or type of care that the patient would have received as a result of the advice being given. A pulmonary and critical care physician, with >35 years of experience in inpatient medicine, reviewed the information provided in the curbside and formal consultations, and independently assessed whether the curbside consultation alone would have been sufficient and whether the formal consultation changed management.

Curbside consultations were neither solicited nor discouraged during the course of the study. The provider requesting the curbside consultation was not informed or debriefed about the study in an attempt to avoid affecting future consultation practices from that provider or service.

Associations were sought between the frequency of inaccurate or incomplete data and the requesting service and provider, the consultative category and medical issue, the number of questions asked by the hospitalist during the curbside consultation, and whether the hospitalist doing the curbside consultation thought that formal consultation was needed. A chi‐square test was used to analyze all associations. A P value of <0.05 was considered significant. All analyses were performed using SAS Enterprise Guide 4.3 (SAS Institute, Inc, Cary, NC) software. The study was approved by the Colorado Multiple Institutional Review Board.

RESULTS

Fifty curbside consultations were requested on a total of 215 study days. The requesting service declined formal consultation in 3 instances, leaving 47 curbside consultations that had a formal consultation. Curbside consultations came from a variety of services and providers, and addressed a variety of issues and concerns (Table 1).

Characteristics of Curbside Consultations (N = 47)
 Curbside Consultations, N (%)
 47 (100)
  • Consultations could be listed in more than one category; accordingly, the totals exceed 100%.

Requesting service 
Psychiatry21 (45)
Emergency Department9 (19)
Obstetrics/Gynecology5 (11)
Neurology4 (8)
Other (Orthopedics, Anesthesia, General Surgery, Neurosurgery, and Interventional Radiology)8 (17)
Requesting provider 
Resident25 (53)
Intern8 (17)
Attending9 (19)
Other5 (11)
Consultative issue* 
Diagnosis10 (21)
Treatment29 (62)
Evaluation20 (43)
Discharge13 (28)
Lab interpretation4 (9)
Medical concern* 
Cardiac27 (57)
Endocrine17 (36)
Infectious disease9 (19)
Pulmonary8 (17)
Gastroenterology6 (13)
Fluid and electrolyte6 (13)
Others23 (49)

The hospitalists asked 0 to 2 questions during 8/47 (17%) of the curbside consultations, 3 to 5 questions during 26/47 (55%) consultations, and more than 5 questions during 13/47 (28%). Based on the information received during the curbside consultations, the hospitalists thought that the curbside consultations were insufficient for 18/47 (38%) of patients. In all instances, the opinions of the 2 hospitalists concurred with respect to this conclusion, and the independent reviewer agreed with this assessment in 17 of these 18 (94%).

The advice rendered in the formal consultations differed from that provided in 26/47 (55%) of the curbside consultations, and the formal consultation was thought to have changed management for 28/47 (60%) of patients (Table 2). The independent reviewer thought that the advice provided in the formal consultations changed management in 29/47 (62%) of the cases, and in 24/28 cases (86%) where the hospitalist felt that the formal consult changed management.

Curbside Consultation Assessment
 Curbside Consultations, N (%)
 TotalAccurate and CompleteInaccurate or Incomplete
47 (100)23 (49)24 (51)
  • P < 0.001

  • P < 0.0001.

Advice in formal consultation differed from advice in curbside consultation26 (55)7 (30)19 (79)*
Formal consultation changed management28 (60)6 (26)22 (92)
Minor change18 (64)6 (100)12 (55)
Major change10 (36)0 (0)10 (45)
Curbside consultation insufficient18 (38)2 (9)16 (67)

Information was felt to be inaccurate or incomplete in 24/47 (51%) of the curbside consultations (13/47 inaccurate, 16/47 incomplete, 5/47 both inaccurate and incomplete), and when inaccurate or incomplete information was obtained, the advice given in the formal consultations more commonly differed from that provided in the curbside consultation (19/24, 79% vs 7/23, 30%; P < 0.001), and was more commonly felt to change management (22/24, 92% vs 6/23, 26%; P < 0.0001) (Table 2). No association was found between whether the curbside consultation contained complete or accurate information and the consulting service from which the curbside originated, the consulting provider, the consultative aspect(s) or medical issue(s) addressed, the number of questions asked by the hospitalist during the curbside consultation, nor whether the hospitalists felt that a formal consultation was needed.

DISCUSSION

The important findings of this study are that (a) the recommendations made by hospitalists in curbside versus formal consultations on the same patient frequently differ, (b) these differences frequently result in changes in clinical management, (c) the information presented in curbside consultations by providers is frequently inaccurate or incomplete, regardless of the providers specialty or seniority, (d) when inaccurate or incomplete information is received, the recommendations made in curbside and formal consultations differ more frequently, and (e) we found no way to predict whether the information provided in a curbside consultation was likely to be inaccurate or incomplete.

Our hospitalists thought that 38% of the curbside consultations they received should have had formal consultations. Manian and McKinsey7 reported that as many as 53% of questions asked of infectious disease consultants were thought to be too complex to be addressed in an informal consultation. Others, however, report that only 11%33% of curbside consultations were thought to require formal consultation.1, 9, 10, 16 Our hospitalists asked 3 or more questions of the consulting providers in more than 80% of the curbside consultations, suggesting that the curbside consultations we received might have had a higher complexity than those seen by others.

Our finding that information provided in curbside consultation was frequently inaccurate or incomplete is consistent with a number of previous studies reporting physicians' perceptions of the accuracy of curbside consultations.2, 3 Hospital medicine is not likely to be the only discipline affected by inaccurate curbside consultation practices, as surveys of specialists in infectious disease, gynecology, and neurosurgery report that practitioners in these disciplines have similar concerns.1, 10, 14 In a survey returned by 34 physicians, Myers1 found that 50% thought the information exchanged during curbside consultations was inaccurate, leading him to conclude that inaccuracies presented during curbside consultations required further study.

We found no way of predicting whether curbside consultations were likely to include inaccurate or incomplete information. This observation is consistent with the results of Bergus et al16 who found that the frequency of curbside consultations being converted to formal consultations was independent of the training status of the consulting physician, and with the data of Myers1 who found no way of predicting the likelihood that a curbside consultation should be converted to a formal consultation.

We found that formal consultations resulted in management changes more often than differences in recommendations (ie, 60% vs 55%, respectively). This small difference occurred because, on occasion, the formal consultations found issues to address other than the one(s) for which the curbside consultation was requested. In the majority of these instances, the management changes were minor and the curbside consultation was still felt to be sufficient.

In some instances, the advice given after the curbside and the formal consultations differed to only a minor extent (eg, varying recommendations for oral diabetes management). In other instances, however, the advice differed substantially (eg, change in antibiotic management in a septic patient with a multidrug resistant organism, when the original curbside question was for when to order a follow‐up chest roentgenogram for hypoxia; see Supporting Information, Appendix, in the online version of this article). In 26 patients (55%), formal consultation resulted in different medications being started or stopped, additional tests being performed, or different decisions being made about admission versus discharge.

Our study has a number of strengths. First, while a number of reports document that physicians' perceptions are that curbside consultations frequently contain errors,2, 3, 5, 12 to our knowledge this is the first study that prospectively compared the information collected and advice given in curbside versus formal consultation. Second, while this study was conducted as a quality improvement project, thereby requiring us to conclude that the results are not generalizable, the data presented were collected by 18 different hospitalists, reducing the potential of bias from an individual provider's knowledge base or practice. Third, there was excellent agreement between the independent reviewer and the 2 hospitalists who performed the curbside and formal consultations regarding whether a curbside consultation would have been sufficient, and whether the formal consultation changed patient management. Fourth, the study was conducted over a 1‐year period, which should have reduced potential bias arising from the increasing experience of residents requesting consultations as their training progressed.

Our study has several limitations. First, the number of curbside consultations we received during the study period (50 over 215 days) was lower than anticipated, and lower than the rates of consultation reported by others.1, 7, 9 This likely relates to the fact that, prior to beginning the study, Denver Health hospitalists already provided mandatory consultations for several surgical services (thereby reducing the number of curbside consultations received from these services), because curbside consultations received during evenings, nights, and weekends were not included in the study for reasons of convenience, and because we excluded all administrative curbside consultations. Our hospitalist service also provides consultative services 24 hours a day, thereby reducing the number of consultations received during daytime hours. Second, the frequency with which curbside consultations included inaccurate or incomplete information might be higher than what occurs in other hospitals, as Denver Health is an urban, university‐affiliated public hospital and the patients encountered may be more complex and trainees may be less adept at recognizing the information that would facilitate accurate curbside consultations (although we found no difference in the frequency with which inaccurate or incomplete information was provided as a function of the seniority of the requesting physician). Third, the disparity between curbside and formal consultations that we observed could have been biased by the Hawthorne effect. We attempted to address this by not providing the hospitalists who did the formal consultation with any information collected by the hospitalist involved with the curbside consultation, and by comparing the conclusions reached by the hospitalists performing the curbside and formal consultations with those of a third party reviewer. Fourth, while we found no association between the frequency of curbside consultations in which information was inaccurate or incomplete and the consulting service, there could be a selection bias of the consulting service requesting the curbside consultations as a result of the mandatory consultations already provided by our hospitalists. Finally, our study was not designed or adequately powered to determine why curbside consultations frequently have inaccurate or incomplete information.

In summary, we found that the information provided to hospitalists during a curbside consultation was often inaccurate and incomplete, and that these problems with information exchange adversely affected the accuracy of the resulting recommendations. While there are a number of advantages to curbside consultations,1, 3, 7, 10, 12, 13 our findings indicate that the risk associated with this practice is substantial.

Acknowledgements

Disclosure: Nothing to report.

Files
References
  1. Myers JP.Curbside consultation in infectious diseases: a prospective study.J Infect Dis.1984;150:797802.
  2. Keating NL,Zaslavsky AM,Ayanian JZ.Physicians' experiences and beliefs regarding informal consultation.JAMA.1998;280:900904.
  3. Kuo D,Gifford DR,Stein MD.Curbside consultation practices and attitudes among primary care physicians and medical subspecialists.JAMA.1998;280:905909.
  4. Grace C,Alston WK,Ramundo M,Polish L,Kirkpatrick B,Huston C.The complexity, relative value, and financial worth of curbside consultations in an academic infectious diseases unit.Clin Infect Dis.2010;51:651655.
  5. Manian FA,Janssen DA.Curbside consultations. A closer look at a common practice.JAMA.1996;275:145147.
  6. Weinberg AD,Ullian L,Richards WD,Cooper P.Informal advice‐ and information‐seeking between physicians.J Med Educ.1981;56;174180.
  7. Manian FA,McKinsey DS.A prospective study of 2,092 “curbside” questions asked of two infectious disease consultants in private practice in the midwest.Clin Infect Dis.1996;22:303307.
  8. Findling JW,Shaker JL,Brickner RC,Riordan PR,Aron DC.Curbside consultation in endocrine practice: a prospective observational study.Endocrinologist.1996;6:328331.
  9. Pearson SD,Moreno R,Trnka Y.Informal consultations provided to general internists by the gastroenterology department of an HMO.J Gen Intern Med.1998;13:435438.
  10. Muntz HG.“Curbside” consultations in gynecologic oncology: a closer look at a common practice.Gynecol Oncol.1999;74:456459.
  11. Leblebicioglu H,Akbulut A,Ulusoy S, et al.Informal consultations in infectious diseases and clinical microbiology practice.Clin Microbiol Infect.2003;9:724726.
  12. Golub RM.Curbside consultations and the viaduct effect.JAMA.1998;280:929930.
  13. Borowsky SJ.What do we really need to know about consultation and referral?J Gen Intern Med.1998;13:497498.
  14. Cartmill M,White BD.Telephone advice for neurosurgical referrals. Who assumes duty of care?Br J Neurosurg.2001;15:453455.
  15. Olick RS,Bergus GR.Malpractice liability for informal consultations.Fam Med.2003;35:476481.
  16. Bergus GR,Randall CS,Sinift SD,Rosenthal DM.Does the structure of clinical questions affect the outcome of curbside consultations with specialty colleagues?Arch Fam Med.2000;9:541547.
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A curbside consultation is an informal process whereby a consultant is asked to provide information or advice about a patient's care without doing a formal assessment of the patient.14 Curbside consultations are common in the practice of medicine2, 3, 5 and are frequently requested by physicians caring for hospitalized patients. Several surveys have documented the quantity of curbside consultations requested of various subspecialties, the types of questions asked, the time it takes to respond, and physicians' perceptions about the quality of the information exchanged.111 While curbside consultations have a number of advantages, physicians' perceptions are that the information conveyed may be inaccurate or incomplete and that the advice offered may be erroneous.13, 5, 10, 12, 13

Cartmill and White14 performed a random audit of 10% of the telephone referrals they received for neurosurgical consultation over a 1‐year period and noted discrepancies between the Glascow Coma Scores reported during the telephone referrals and those noted in the medical records, but the frequency of these discrepancies was not reported. To our knowledge, no studies have compared the quality of the information provided in curbside consultations with that obtained in formal consultations that included direct face‐to‐face patient evaluations and primary data collection, and whether the advice provided in curbside and formal consultations on the same patient differed.

We performed a prospective cohort study to compare the information received by hospitalists during curbside consultations on hospitalized patients, with that obtained from formal consultations done the same day on the same patients, by different hospitalists who were unaware of any details regarding the curbside consultation. We also compared the advice provided by the 2 hospitalists following their curbside and formal consultations. Our hypotheses were that the information received during curbside consultations was frequently inaccurate or incomplete, that the recommendations made after the formal consultation would frequently differ from those made in the curbside consultation, and that these differences would have important implications on patient care.

METHODS

This was a quality improvement study conducted at Denver Health, a 500‐bed university‐affiliated urban safety net hospital from January 10, 2011 to January 9, 2012. The study design was a prospective cohort that included all curbside consultations on hospitalized patients received between 7 AM and 3 PM, on intermittently selected weekdays, by the Internal Medicine Consultation Service that was staffed by 18 hospitalists. Data were collected intermittently based upon hospitalist availability and was done to limit potential alterations in the consulting practices of the providers requesting consultations.

Consultations were defined as being curbside when the consulting provider asked for advice, suggestions, or opinions about a patient's care but did not ask the hospitalist to see the patient.15, 15 Consultations pertaining to administrative issues (eg, whether a patient should be admitted to an intensive care bed as opposed to an acute care floor bed) or on patients who were already being followed by a hospitalist were excluded.

The hospitalist receiving the curbside consultation was allowed to ask questions as they normally would, but could not verify the accuracy of the information received (eg, could not review any portion of the patient's medical record, such as notes or lab data). A standardized data collection sheet was used to record the service and level of training of the requesting provider, the medical issue(s) of concern, all clinical data offered by the provider, the number of questions asked by the hospitalist of the provider, and whether, on the basis of the information provided, the hospitalist felt that the question(s) being asked was (were) of sufficient complexity that a formal consultation should occur. The hospitalist then offered advice based upon the information given during the curbside consultation.

After completing the curbside consultation, the hospitalist requested verbal permission from the requesting provider to perform a formal consultation. If the request was approved, the hospitalist performing the curbside consultation contacted a different hospitalist who performed the formal consultation within the next few hours. The only information given to the second hospitalist was the patient's identifiers and the clinical question(s) being asked. The formal consultation included a complete face‐to‐face history and physical examination, a review of the patient's medical record, documentation of the provider's findings, and recommendations for care.

Upon completion of the formal consultation, the hospitalists who performed the curbside and the formal consultations met to review the advice each gave to the requesting provider and the information on which this advice was based. The 2 hospitalists jointly determined the following: (a) whether the information received during the curbside consultation was correct and complete, (b) whether the advice provided in the formal consultation differed from that provided in the curbside consultation, (c) whether the advice provided in the formal consultation dealt with issues other than one(s) leading to the curbside consultation, (d) whether differences in the recommendations given in the curbside versus the formal consultation changed patient management in a meaningful way, and (e) whether the curbside consultation alone was felt to be sufficient.

Information obtained by the hospitalist performing the formal consultation that was different from, or not included in, the information recorded during the curbside consultation was considered to be incorrect or incomplete, respectively. A change in management was defined as an alteration in the direction or type of care that the patient would have received as a result of the advice being given. A pulmonary and critical care physician, with >35 years of experience in inpatient medicine, reviewed the information provided in the curbside and formal consultations, and independently assessed whether the curbside consultation alone would have been sufficient and whether the formal consultation changed management.

Curbside consultations were neither solicited nor discouraged during the course of the study. The provider requesting the curbside consultation was not informed or debriefed about the study in an attempt to avoid affecting future consultation practices from that provider or service.

Associations were sought between the frequency of inaccurate or incomplete data and the requesting service and provider, the consultative category and medical issue, the number of questions asked by the hospitalist during the curbside consultation, and whether the hospitalist doing the curbside consultation thought that formal consultation was needed. A chi‐square test was used to analyze all associations. A P value of <0.05 was considered significant. All analyses were performed using SAS Enterprise Guide 4.3 (SAS Institute, Inc, Cary, NC) software. The study was approved by the Colorado Multiple Institutional Review Board.

RESULTS

Fifty curbside consultations were requested on a total of 215 study days. The requesting service declined formal consultation in 3 instances, leaving 47 curbside consultations that had a formal consultation. Curbside consultations came from a variety of services and providers, and addressed a variety of issues and concerns (Table 1).

Characteristics of Curbside Consultations (N = 47)
 Curbside Consultations, N (%)
 47 (100)
  • Consultations could be listed in more than one category; accordingly, the totals exceed 100%.

Requesting service 
Psychiatry21 (45)
Emergency Department9 (19)
Obstetrics/Gynecology5 (11)
Neurology4 (8)
Other (Orthopedics, Anesthesia, General Surgery, Neurosurgery, and Interventional Radiology)8 (17)
Requesting provider 
Resident25 (53)
Intern8 (17)
Attending9 (19)
Other5 (11)
Consultative issue* 
Diagnosis10 (21)
Treatment29 (62)
Evaluation20 (43)
Discharge13 (28)
Lab interpretation4 (9)
Medical concern* 
Cardiac27 (57)
Endocrine17 (36)
Infectious disease9 (19)
Pulmonary8 (17)
Gastroenterology6 (13)
Fluid and electrolyte6 (13)
Others23 (49)

The hospitalists asked 0 to 2 questions during 8/47 (17%) of the curbside consultations, 3 to 5 questions during 26/47 (55%) consultations, and more than 5 questions during 13/47 (28%). Based on the information received during the curbside consultations, the hospitalists thought that the curbside consultations were insufficient for 18/47 (38%) of patients. In all instances, the opinions of the 2 hospitalists concurred with respect to this conclusion, and the independent reviewer agreed with this assessment in 17 of these 18 (94%).

The advice rendered in the formal consultations differed from that provided in 26/47 (55%) of the curbside consultations, and the formal consultation was thought to have changed management for 28/47 (60%) of patients (Table 2). The independent reviewer thought that the advice provided in the formal consultations changed management in 29/47 (62%) of the cases, and in 24/28 cases (86%) where the hospitalist felt that the formal consult changed management.

Curbside Consultation Assessment
 Curbside Consultations, N (%)
 TotalAccurate and CompleteInaccurate or Incomplete
47 (100)23 (49)24 (51)
  • P < 0.001

  • P < 0.0001.

Advice in formal consultation differed from advice in curbside consultation26 (55)7 (30)19 (79)*
Formal consultation changed management28 (60)6 (26)22 (92)
Minor change18 (64)6 (100)12 (55)
Major change10 (36)0 (0)10 (45)
Curbside consultation insufficient18 (38)2 (9)16 (67)

Information was felt to be inaccurate or incomplete in 24/47 (51%) of the curbside consultations (13/47 inaccurate, 16/47 incomplete, 5/47 both inaccurate and incomplete), and when inaccurate or incomplete information was obtained, the advice given in the formal consultations more commonly differed from that provided in the curbside consultation (19/24, 79% vs 7/23, 30%; P < 0.001), and was more commonly felt to change management (22/24, 92% vs 6/23, 26%; P < 0.0001) (Table 2). No association was found between whether the curbside consultation contained complete or accurate information and the consulting service from which the curbside originated, the consulting provider, the consultative aspect(s) or medical issue(s) addressed, the number of questions asked by the hospitalist during the curbside consultation, nor whether the hospitalists felt that a formal consultation was needed.

DISCUSSION

The important findings of this study are that (a) the recommendations made by hospitalists in curbside versus formal consultations on the same patient frequently differ, (b) these differences frequently result in changes in clinical management, (c) the information presented in curbside consultations by providers is frequently inaccurate or incomplete, regardless of the providers specialty or seniority, (d) when inaccurate or incomplete information is received, the recommendations made in curbside and formal consultations differ more frequently, and (e) we found no way to predict whether the information provided in a curbside consultation was likely to be inaccurate or incomplete.

Our hospitalists thought that 38% of the curbside consultations they received should have had formal consultations. Manian and McKinsey7 reported that as many as 53% of questions asked of infectious disease consultants were thought to be too complex to be addressed in an informal consultation. Others, however, report that only 11%33% of curbside consultations were thought to require formal consultation.1, 9, 10, 16 Our hospitalists asked 3 or more questions of the consulting providers in more than 80% of the curbside consultations, suggesting that the curbside consultations we received might have had a higher complexity than those seen by others.

Our finding that information provided in curbside consultation was frequently inaccurate or incomplete is consistent with a number of previous studies reporting physicians' perceptions of the accuracy of curbside consultations.2, 3 Hospital medicine is not likely to be the only discipline affected by inaccurate curbside consultation practices, as surveys of specialists in infectious disease, gynecology, and neurosurgery report that practitioners in these disciplines have similar concerns.1, 10, 14 In a survey returned by 34 physicians, Myers1 found that 50% thought the information exchanged during curbside consultations was inaccurate, leading him to conclude that inaccuracies presented during curbside consultations required further study.

We found no way of predicting whether curbside consultations were likely to include inaccurate or incomplete information. This observation is consistent with the results of Bergus et al16 who found that the frequency of curbside consultations being converted to formal consultations was independent of the training status of the consulting physician, and with the data of Myers1 who found no way of predicting the likelihood that a curbside consultation should be converted to a formal consultation.

We found that formal consultations resulted in management changes more often than differences in recommendations (ie, 60% vs 55%, respectively). This small difference occurred because, on occasion, the formal consultations found issues to address other than the one(s) for which the curbside consultation was requested. In the majority of these instances, the management changes were minor and the curbside consultation was still felt to be sufficient.

In some instances, the advice given after the curbside and the formal consultations differed to only a minor extent (eg, varying recommendations for oral diabetes management). In other instances, however, the advice differed substantially (eg, change in antibiotic management in a septic patient with a multidrug resistant organism, when the original curbside question was for when to order a follow‐up chest roentgenogram for hypoxia; see Supporting Information, Appendix, in the online version of this article). In 26 patients (55%), formal consultation resulted in different medications being started or stopped, additional tests being performed, or different decisions being made about admission versus discharge.

Our study has a number of strengths. First, while a number of reports document that physicians' perceptions are that curbside consultations frequently contain errors,2, 3, 5, 12 to our knowledge this is the first study that prospectively compared the information collected and advice given in curbside versus formal consultation. Second, while this study was conducted as a quality improvement project, thereby requiring us to conclude that the results are not generalizable, the data presented were collected by 18 different hospitalists, reducing the potential of bias from an individual provider's knowledge base or practice. Third, there was excellent agreement between the independent reviewer and the 2 hospitalists who performed the curbside and formal consultations regarding whether a curbside consultation would have been sufficient, and whether the formal consultation changed patient management. Fourth, the study was conducted over a 1‐year period, which should have reduced potential bias arising from the increasing experience of residents requesting consultations as their training progressed.

Our study has several limitations. First, the number of curbside consultations we received during the study period (50 over 215 days) was lower than anticipated, and lower than the rates of consultation reported by others.1, 7, 9 This likely relates to the fact that, prior to beginning the study, Denver Health hospitalists already provided mandatory consultations for several surgical services (thereby reducing the number of curbside consultations received from these services), because curbside consultations received during evenings, nights, and weekends were not included in the study for reasons of convenience, and because we excluded all administrative curbside consultations. Our hospitalist service also provides consultative services 24 hours a day, thereby reducing the number of consultations received during daytime hours. Second, the frequency with which curbside consultations included inaccurate or incomplete information might be higher than what occurs in other hospitals, as Denver Health is an urban, university‐affiliated public hospital and the patients encountered may be more complex and trainees may be less adept at recognizing the information that would facilitate accurate curbside consultations (although we found no difference in the frequency with which inaccurate or incomplete information was provided as a function of the seniority of the requesting physician). Third, the disparity between curbside and formal consultations that we observed could have been biased by the Hawthorne effect. We attempted to address this by not providing the hospitalists who did the formal consultation with any information collected by the hospitalist involved with the curbside consultation, and by comparing the conclusions reached by the hospitalists performing the curbside and formal consultations with those of a third party reviewer. Fourth, while we found no association between the frequency of curbside consultations in which information was inaccurate or incomplete and the consulting service, there could be a selection bias of the consulting service requesting the curbside consultations as a result of the mandatory consultations already provided by our hospitalists. Finally, our study was not designed or adequately powered to determine why curbside consultations frequently have inaccurate or incomplete information.

In summary, we found that the information provided to hospitalists during a curbside consultation was often inaccurate and incomplete, and that these problems with information exchange adversely affected the accuracy of the resulting recommendations. While there are a number of advantages to curbside consultations,1, 3, 7, 10, 12, 13 our findings indicate that the risk associated with this practice is substantial.

Acknowledgements

Disclosure: Nothing to report.

A curbside consultation is an informal process whereby a consultant is asked to provide information or advice about a patient's care without doing a formal assessment of the patient.14 Curbside consultations are common in the practice of medicine2, 3, 5 and are frequently requested by physicians caring for hospitalized patients. Several surveys have documented the quantity of curbside consultations requested of various subspecialties, the types of questions asked, the time it takes to respond, and physicians' perceptions about the quality of the information exchanged.111 While curbside consultations have a number of advantages, physicians' perceptions are that the information conveyed may be inaccurate or incomplete and that the advice offered may be erroneous.13, 5, 10, 12, 13

Cartmill and White14 performed a random audit of 10% of the telephone referrals they received for neurosurgical consultation over a 1‐year period and noted discrepancies between the Glascow Coma Scores reported during the telephone referrals and those noted in the medical records, but the frequency of these discrepancies was not reported. To our knowledge, no studies have compared the quality of the information provided in curbside consultations with that obtained in formal consultations that included direct face‐to‐face patient evaluations and primary data collection, and whether the advice provided in curbside and formal consultations on the same patient differed.

We performed a prospective cohort study to compare the information received by hospitalists during curbside consultations on hospitalized patients, with that obtained from formal consultations done the same day on the same patients, by different hospitalists who were unaware of any details regarding the curbside consultation. We also compared the advice provided by the 2 hospitalists following their curbside and formal consultations. Our hypotheses were that the information received during curbside consultations was frequently inaccurate or incomplete, that the recommendations made after the formal consultation would frequently differ from those made in the curbside consultation, and that these differences would have important implications on patient care.

METHODS

This was a quality improvement study conducted at Denver Health, a 500‐bed university‐affiliated urban safety net hospital from January 10, 2011 to January 9, 2012. The study design was a prospective cohort that included all curbside consultations on hospitalized patients received between 7 AM and 3 PM, on intermittently selected weekdays, by the Internal Medicine Consultation Service that was staffed by 18 hospitalists. Data were collected intermittently based upon hospitalist availability and was done to limit potential alterations in the consulting practices of the providers requesting consultations.

Consultations were defined as being curbside when the consulting provider asked for advice, suggestions, or opinions about a patient's care but did not ask the hospitalist to see the patient.15, 15 Consultations pertaining to administrative issues (eg, whether a patient should be admitted to an intensive care bed as opposed to an acute care floor bed) or on patients who were already being followed by a hospitalist were excluded.

The hospitalist receiving the curbside consultation was allowed to ask questions as they normally would, but could not verify the accuracy of the information received (eg, could not review any portion of the patient's medical record, such as notes or lab data). A standardized data collection sheet was used to record the service and level of training of the requesting provider, the medical issue(s) of concern, all clinical data offered by the provider, the number of questions asked by the hospitalist of the provider, and whether, on the basis of the information provided, the hospitalist felt that the question(s) being asked was (were) of sufficient complexity that a formal consultation should occur. The hospitalist then offered advice based upon the information given during the curbside consultation.

After completing the curbside consultation, the hospitalist requested verbal permission from the requesting provider to perform a formal consultation. If the request was approved, the hospitalist performing the curbside consultation contacted a different hospitalist who performed the formal consultation within the next few hours. The only information given to the second hospitalist was the patient's identifiers and the clinical question(s) being asked. The formal consultation included a complete face‐to‐face history and physical examination, a review of the patient's medical record, documentation of the provider's findings, and recommendations for care.

Upon completion of the formal consultation, the hospitalists who performed the curbside and the formal consultations met to review the advice each gave to the requesting provider and the information on which this advice was based. The 2 hospitalists jointly determined the following: (a) whether the information received during the curbside consultation was correct and complete, (b) whether the advice provided in the formal consultation differed from that provided in the curbside consultation, (c) whether the advice provided in the formal consultation dealt with issues other than one(s) leading to the curbside consultation, (d) whether differences in the recommendations given in the curbside versus the formal consultation changed patient management in a meaningful way, and (e) whether the curbside consultation alone was felt to be sufficient.

Information obtained by the hospitalist performing the formal consultation that was different from, or not included in, the information recorded during the curbside consultation was considered to be incorrect or incomplete, respectively. A change in management was defined as an alteration in the direction or type of care that the patient would have received as a result of the advice being given. A pulmonary and critical care physician, with >35 years of experience in inpatient medicine, reviewed the information provided in the curbside and formal consultations, and independently assessed whether the curbside consultation alone would have been sufficient and whether the formal consultation changed management.

Curbside consultations were neither solicited nor discouraged during the course of the study. The provider requesting the curbside consultation was not informed or debriefed about the study in an attempt to avoid affecting future consultation practices from that provider or service.

Associations were sought between the frequency of inaccurate or incomplete data and the requesting service and provider, the consultative category and medical issue, the number of questions asked by the hospitalist during the curbside consultation, and whether the hospitalist doing the curbside consultation thought that formal consultation was needed. A chi‐square test was used to analyze all associations. A P value of <0.05 was considered significant. All analyses were performed using SAS Enterprise Guide 4.3 (SAS Institute, Inc, Cary, NC) software. The study was approved by the Colorado Multiple Institutional Review Board.

RESULTS

Fifty curbside consultations were requested on a total of 215 study days. The requesting service declined formal consultation in 3 instances, leaving 47 curbside consultations that had a formal consultation. Curbside consultations came from a variety of services and providers, and addressed a variety of issues and concerns (Table 1).

Characteristics of Curbside Consultations (N = 47)
 Curbside Consultations, N (%)
 47 (100)
  • Consultations could be listed in more than one category; accordingly, the totals exceed 100%.

Requesting service 
Psychiatry21 (45)
Emergency Department9 (19)
Obstetrics/Gynecology5 (11)
Neurology4 (8)
Other (Orthopedics, Anesthesia, General Surgery, Neurosurgery, and Interventional Radiology)8 (17)
Requesting provider 
Resident25 (53)
Intern8 (17)
Attending9 (19)
Other5 (11)
Consultative issue* 
Diagnosis10 (21)
Treatment29 (62)
Evaluation20 (43)
Discharge13 (28)
Lab interpretation4 (9)
Medical concern* 
Cardiac27 (57)
Endocrine17 (36)
Infectious disease9 (19)
Pulmonary8 (17)
Gastroenterology6 (13)
Fluid and electrolyte6 (13)
Others23 (49)

The hospitalists asked 0 to 2 questions during 8/47 (17%) of the curbside consultations, 3 to 5 questions during 26/47 (55%) consultations, and more than 5 questions during 13/47 (28%). Based on the information received during the curbside consultations, the hospitalists thought that the curbside consultations were insufficient for 18/47 (38%) of patients. In all instances, the opinions of the 2 hospitalists concurred with respect to this conclusion, and the independent reviewer agreed with this assessment in 17 of these 18 (94%).

The advice rendered in the formal consultations differed from that provided in 26/47 (55%) of the curbside consultations, and the formal consultation was thought to have changed management for 28/47 (60%) of patients (Table 2). The independent reviewer thought that the advice provided in the formal consultations changed management in 29/47 (62%) of the cases, and in 24/28 cases (86%) where the hospitalist felt that the formal consult changed management.

Curbside Consultation Assessment
 Curbside Consultations, N (%)
 TotalAccurate and CompleteInaccurate or Incomplete
47 (100)23 (49)24 (51)
  • P < 0.001

  • P < 0.0001.

Advice in formal consultation differed from advice in curbside consultation26 (55)7 (30)19 (79)*
Formal consultation changed management28 (60)6 (26)22 (92)
Minor change18 (64)6 (100)12 (55)
Major change10 (36)0 (0)10 (45)
Curbside consultation insufficient18 (38)2 (9)16 (67)

Information was felt to be inaccurate or incomplete in 24/47 (51%) of the curbside consultations (13/47 inaccurate, 16/47 incomplete, 5/47 both inaccurate and incomplete), and when inaccurate or incomplete information was obtained, the advice given in the formal consultations more commonly differed from that provided in the curbside consultation (19/24, 79% vs 7/23, 30%; P < 0.001), and was more commonly felt to change management (22/24, 92% vs 6/23, 26%; P < 0.0001) (Table 2). No association was found between whether the curbside consultation contained complete or accurate information and the consulting service from which the curbside originated, the consulting provider, the consultative aspect(s) or medical issue(s) addressed, the number of questions asked by the hospitalist during the curbside consultation, nor whether the hospitalists felt that a formal consultation was needed.

DISCUSSION

The important findings of this study are that (a) the recommendations made by hospitalists in curbside versus formal consultations on the same patient frequently differ, (b) these differences frequently result in changes in clinical management, (c) the information presented in curbside consultations by providers is frequently inaccurate or incomplete, regardless of the providers specialty or seniority, (d) when inaccurate or incomplete information is received, the recommendations made in curbside and formal consultations differ more frequently, and (e) we found no way to predict whether the information provided in a curbside consultation was likely to be inaccurate or incomplete.

Our hospitalists thought that 38% of the curbside consultations they received should have had formal consultations. Manian and McKinsey7 reported that as many as 53% of questions asked of infectious disease consultants were thought to be too complex to be addressed in an informal consultation. Others, however, report that only 11%33% of curbside consultations were thought to require formal consultation.1, 9, 10, 16 Our hospitalists asked 3 or more questions of the consulting providers in more than 80% of the curbside consultations, suggesting that the curbside consultations we received might have had a higher complexity than those seen by others.

Our finding that information provided in curbside consultation was frequently inaccurate or incomplete is consistent with a number of previous studies reporting physicians' perceptions of the accuracy of curbside consultations.2, 3 Hospital medicine is not likely to be the only discipline affected by inaccurate curbside consultation practices, as surveys of specialists in infectious disease, gynecology, and neurosurgery report that practitioners in these disciplines have similar concerns.1, 10, 14 In a survey returned by 34 physicians, Myers1 found that 50% thought the information exchanged during curbside consultations was inaccurate, leading him to conclude that inaccuracies presented during curbside consultations required further study.

We found no way of predicting whether curbside consultations were likely to include inaccurate or incomplete information. This observation is consistent with the results of Bergus et al16 who found that the frequency of curbside consultations being converted to formal consultations was independent of the training status of the consulting physician, and with the data of Myers1 who found no way of predicting the likelihood that a curbside consultation should be converted to a formal consultation.

We found that formal consultations resulted in management changes more often than differences in recommendations (ie, 60% vs 55%, respectively). This small difference occurred because, on occasion, the formal consultations found issues to address other than the one(s) for which the curbside consultation was requested. In the majority of these instances, the management changes were minor and the curbside consultation was still felt to be sufficient.

In some instances, the advice given after the curbside and the formal consultations differed to only a minor extent (eg, varying recommendations for oral diabetes management). In other instances, however, the advice differed substantially (eg, change in antibiotic management in a septic patient with a multidrug resistant organism, when the original curbside question was for when to order a follow‐up chest roentgenogram for hypoxia; see Supporting Information, Appendix, in the online version of this article). In 26 patients (55%), formal consultation resulted in different medications being started or stopped, additional tests being performed, or different decisions being made about admission versus discharge.

Our study has a number of strengths. First, while a number of reports document that physicians' perceptions are that curbside consultations frequently contain errors,2, 3, 5, 12 to our knowledge this is the first study that prospectively compared the information collected and advice given in curbside versus formal consultation. Second, while this study was conducted as a quality improvement project, thereby requiring us to conclude that the results are not generalizable, the data presented were collected by 18 different hospitalists, reducing the potential of bias from an individual provider's knowledge base or practice. Third, there was excellent agreement between the independent reviewer and the 2 hospitalists who performed the curbside and formal consultations regarding whether a curbside consultation would have been sufficient, and whether the formal consultation changed patient management. Fourth, the study was conducted over a 1‐year period, which should have reduced potential bias arising from the increasing experience of residents requesting consultations as their training progressed.

Our study has several limitations. First, the number of curbside consultations we received during the study period (50 over 215 days) was lower than anticipated, and lower than the rates of consultation reported by others.1, 7, 9 This likely relates to the fact that, prior to beginning the study, Denver Health hospitalists already provided mandatory consultations for several surgical services (thereby reducing the number of curbside consultations received from these services), because curbside consultations received during evenings, nights, and weekends were not included in the study for reasons of convenience, and because we excluded all administrative curbside consultations. Our hospitalist service also provides consultative services 24 hours a day, thereby reducing the number of consultations received during daytime hours. Second, the frequency with which curbside consultations included inaccurate or incomplete information might be higher than what occurs in other hospitals, as Denver Health is an urban, university‐affiliated public hospital and the patients encountered may be more complex and trainees may be less adept at recognizing the information that would facilitate accurate curbside consultations (although we found no difference in the frequency with which inaccurate or incomplete information was provided as a function of the seniority of the requesting physician). Third, the disparity between curbside and formal consultations that we observed could have been biased by the Hawthorne effect. We attempted to address this by not providing the hospitalists who did the formal consultation with any information collected by the hospitalist involved with the curbside consultation, and by comparing the conclusions reached by the hospitalists performing the curbside and formal consultations with those of a third party reviewer. Fourth, while we found no association between the frequency of curbside consultations in which information was inaccurate or incomplete and the consulting service, there could be a selection bias of the consulting service requesting the curbside consultations as a result of the mandatory consultations already provided by our hospitalists. Finally, our study was not designed or adequately powered to determine why curbside consultations frequently have inaccurate or incomplete information.

In summary, we found that the information provided to hospitalists during a curbside consultation was often inaccurate and incomplete, and that these problems with information exchange adversely affected the accuracy of the resulting recommendations. While there are a number of advantages to curbside consultations,1, 3, 7, 10, 12, 13 our findings indicate that the risk associated with this practice is substantial.

Acknowledgements

Disclosure: Nothing to report.

References
  1. Myers JP.Curbside consultation in infectious diseases: a prospective study.J Infect Dis.1984;150:797802.
  2. Keating NL,Zaslavsky AM,Ayanian JZ.Physicians' experiences and beliefs regarding informal consultation.JAMA.1998;280:900904.
  3. Kuo D,Gifford DR,Stein MD.Curbside consultation practices and attitudes among primary care physicians and medical subspecialists.JAMA.1998;280:905909.
  4. Grace C,Alston WK,Ramundo M,Polish L,Kirkpatrick B,Huston C.The complexity, relative value, and financial worth of curbside consultations in an academic infectious diseases unit.Clin Infect Dis.2010;51:651655.
  5. Manian FA,Janssen DA.Curbside consultations. A closer look at a common practice.JAMA.1996;275:145147.
  6. Weinberg AD,Ullian L,Richards WD,Cooper P.Informal advice‐ and information‐seeking between physicians.J Med Educ.1981;56;174180.
  7. Manian FA,McKinsey DS.A prospective study of 2,092 “curbside” questions asked of two infectious disease consultants in private practice in the midwest.Clin Infect Dis.1996;22:303307.
  8. Findling JW,Shaker JL,Brickner RC,Riordan PR,Aron DC.Curbside consultation in endocrine practice: a prospective observational study.Endocrinologist.1996;6:328331.
  9. Pearson SD,Moreno R,Trnka Y.Informal consultations provided to general internists by the gastroenterology department of an HMO.J Gen Intern Med.1998;13:435438.
  10. Muntz HG.“Curbside” consultations in gynecologic oncology: a closer look at a common practice.Gynecol Oncol.1999;74:456459.
  11. Leblebicioglu H,Akbulut A,Ulusoy S, et al.Informal consultations in infectious diseases and clinical microbiology practice.Clin Microbiol Infect.2003;9:724726.
  12. Golub RM.Curbside consultations and the viaduct effect.JAMA.1998;280:929930.
  13. Borowsky SJ.What do we really need to know about consultation and referral?J Gen Intern Med.1998;13:497498.
  14. Cartmill M,White BD.Telephone advice for neurosurgical referrals. Who assumes duty of care?Br J Neurosurg.2001;15:453455.
  15. Olick RS,Bergus GR.Malpractice liability for informal consultations.Fam Med.2003;35:476481.
  16. Bergus GR,Randall CS,Sinift SD,Rosenthal DM.Does the structure of clinical questions affect the outcome of curbside consultations with specialty colleagues?Arch Fam Med.2000;9:541547.
References
  1. Myers JP.Curbside consultation in infectious diseases: a prospective study.J Infect Dis.1984;150:797802.
  2. Keating NL,Zaslavsky AM,Ayanian JZ.Physicians' experiences and beliefs regarding informal consultation.JAMA.1998;280:900904.
  3. Kuo D,Gifford DR,Stein MD.Curbside consultation practices and attitudes among primary care physicians and medical subspecialists.JAMA.1998;280:905909.
  4. Grace C,Alston WK,Ramundo M,Polish L,Kirkpatrick B,Huston C.The complexity, relative value, and financial worth of curbside consultations in an academic infectious diseases unit.Clin Infect Dis.2010;51:651655.
  5. Manian FA,Janssen DA.Curbside consultations. A closer look at a common practice.JAMA.1996;275:145147.
  6. Weinberg AD,Ullian L,Richards WD,Cooper P.Informal advice‐ and information‐seeking between physicians.J Med Educ.1981;56;174180.
  7. Manian FA,McKinsey DS.A prospective study of 2,092 “curbside” questions asked of two infectious disease consultants in private practice in the midwest.Clin Infect Dis.1996;22:303307.
  8. Findling JW,Shaker JL,Brickner RC,Riordan PR,Aron DC.Curbside consultation in endocrine practice: a prospective observational study.Endocrinologist.1996;6:328331.
  9. Pearson SD,Moreno R,Trnka Y.Informal consultations provided to general internists by the gastroenterology department of an HMO.J Gen Intern Med.1998;13:435438.
  10. Muntz HG.“Curbside” consultations in gynecologic oncology: a closer look at a common practice.Gynecol Oncol.1999;74:456459.
  11. Leblebicioglu H,Akbulut A,Ulusoy S, et al.Informal consultations in infectious diseases and clinical microbiology practice.Clin Microbiol Infect.2003;9:724726.
  12. Golub RM.Curbside consultations and the viaduct effect.JAMA.1998;280:929930.
  13. Borowsky SJ.What do we really need to know about consultation and referral?J Gen Intern Med.1998;13:497498.
  14. Cartmill M,White BD.Telephone advice for neurosurgical referrals. Who assumes duty of care?Br J Neurosurg.2001;15:453455.
  15. Olick RS,Bergus GR.Malpractice liability for informal consultations.Fam Med.2003;35:476481.
  16. Bergus GR,Randall CS,Sinift SD,Rosenthal DM.Does the structure of clinical questions affect the outcome of curbside consultations with specialty colleagues?Arch Fam Med.2000;9:541547.
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There have been four revolutions that have fundamentally changed the way we communicate, according to Clay Shirky, a New York University professor and social media theorist: the printing press, the telephone and telegraph, television and radio, and social media.

On rating sites, such as Yelp and DrScore, and social networking sites, such as LinkedIn and Twitter, patients are connecting and sharing information about their health and about you. You have a choice: You can participate in that conversation, or you can let it happen without you.

In a survey of 4,000 physicians, QuantiaMD found that nearly 90% of physicians reported using Facebook for personal use and 67% used it professionally. So what about the other 33%?

Physicians cite many barriers to using social media. The most common include lack of time, failure to see return on investment, concerns about patient safety, and not knowing where to begin.

While there are scores of social media options available to physicians, I recommend starting with the following: having a website or blog and using Facebook, Twitter, LinkedIn, and YouTube or Vimeo. These sites will help you to engage with and educate your patients and prospective patients, market and build your practice, gain professional clout, and protect your online reputation.

Website/Blog. Having a static practice website that is never updated is passé. Sure, your website should include information about scheduling, hours, and products, but it should also be regularly updated with new information. In this way, your website can also serve as your blog, a place where you can post articles on topics of interest to your current and prospective patients. It’s best to start with a website/blog so you can create relevant content to share on social media sites.

Facebook. The rock star of social networking sites was launched in 2004 and recently reached over 1 billion active users. Your patients, current and prospective, as well as your competition, are on Facebook. And you should be, too. Facebook allows for you to have both personal and professional pages, to add friends, to categorize friends, and to even "unfriend" friends. You can exchange both public and private messages, and unlike Twitter, you have the ability to monitor what others post on your page; and you can delete inappropriate material when necessary.

Twitter. This online social networking site allows users to create messages that are up to 140 characters, known as "tweets." As such, it can be challenging for a newbie to know what to say, how to say it cleverly enough to get "retweeted" or shared, and how to get people engaged long-term. Benefits for physicians, however, include engaging in real-time conversation, sharing breaking news, and discovering hot topics.

LinkedIn. This social networking site is used primarily by professionals and is effective for making business contacts, hiring, and networking.

Video. You should consider having a YouTube or Vimeo account because a video post is 50 times more likely to get picked up in a Google search than is a written post, and because 3 billion videos are watched on YouTube every day. Video also allows prospective patients to get to know you and increases your visibility as an educator and expert in the field.

You can ignore all of this and hope it goes away, but the younger generation of physicians entering the field today isn’t. Or you could contract out your social media work to a professional company. Or you and your staff could do it. I’ll speak about these options in future columns.

DR. BENABIO is in private practice in San Diego. Visit his consumer health blog or connect with him on Twitter @Dermdoc and on Facebook (DermDoc).

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There have been four revolutions that have fundamentally changed the way we communicate, according to Clay Shirky, a New York University professor and social media theorist: the printing press, the telephone and telegraph, television and radio, and social media.

On rating sites, such as Yelp and DrScore, and social networking sites, such as LinkedIn and Twitter, patients are connecting and sharing information about their health and about you. You have a choice: You can participate in that conversation, or you can let it happen without you.

In a survey of 4,000 physicians, QuantiaMD found that nearly 90% of physicians reported using Facebook for personal use and 67% used it professionally. So what about the other 33%?

Physicians cite many barriers to using social media. The most common include lack of time, failure to see return on investment, concerns about patient safety, and not knowing where to begin.

While there are scores of social media options available to physicians, I recommend starting with the following: having a website or blog and using Facebook, Twitter, LinkedIn, and YouTube or Vimeo. These sites will help you to engage with and educate your patients and prospective patients, market and build your practice, gain professional clout, and protect your online reputation.

Website/Blog. Having a static practice website that is never updated is passé. Sure, your website should include information about scheduling, hours, and products, but it should also be regularly updated with new information. In this way, your website can also serve as your blog, a place where you can post articles on topics of interest to your current and prospective patients. It’s best to start with a website/blog so you can create relevant content to share on social media sites.

Facebook. The rock star of social networking sites was launched in 2004 and recently reached over 1 billion active users. Your patients, current and prospective, as well as your competition, are on Facebook. And you should be, too. Facebook allows for you to have both personal and professional pages, to add friends, to categorize friends, and to even "unfriend" friends. You can exchange both public and private messages, and unlike Twitter, you have the ability to monitor what others post on your page; and you can delete inappropriate material when necessary.

Twitter. This online social networking site allows users to create messages that are up to 140 characters, known as "tweets." As such, it can be challenging for a newbie to know what to say, how to say it cleverly enough to get "retweeted" or shared, and how to get people engaged long-term. Benefits for physicians, however, include engaging in real-time conversation, sharing breaking news, and discovering hot topics.

LinkedIn. This social networking site is used primarily by professionals and is effective for making business contacts, hiring, and networking.

Video. You should consider having a YouTube or Vimeo account because a video post is 50 times more likely to get picked up in a Google search than is a written post, and because 3 billion videos are watched on YouTube every day. Video also allows prospective patients to get to know you and increases your visibility as an educator and expert in the field.

You can ignore all of this and hope it goes away, but the younger generation of physicians entering the field today isn’t. Or you could contract out your social media work to a professional company. Or you and your staff could do it. I’ll speak about these options in future columns.

DR. BENABIO is in private practice in San Diego. Visit his consumer health blog or connect with him on Twitter @Dermdoc and on Facebook (DermDoc).

There have been four revolutions that have fundamentally changed the way we communicate, according to Clay Shirky, a New York University professor and social media theorist: the printing press, the telephone and telegraph, television and radio, and social media.

On rating sites, such as Yelp and DrScore, and social networking sites, such as LinkedIn and Twitter, patients are connecting and sharing information about their health and about you. You have a choice: You can participate in that conversation, or you can let it happen without you.

In a survey of 4,000 physicians, QuantiaMD found that nearly 90% of physicians reported using Facebook for personal use and 67% used it professionally. So what about the other 33%?

Physicians cite many barriers to using social media. The most common include lack of time, failure to see return on investment, concerns about patient safety, and not knowing where to begin.

While there are scores of social media options available to physicians, I recommend starting with the following: having a website or blog and using Facebook, Twitter, LinkedIn, and YouTube or Vimeo. These sites will help you to engage with and educate your patients and prospective patients, market and build your practice, gain professional clout, and protect your online reputation.

Website/Blog. Having a static practice website that is never updated is passé. Sure, your website should include information about scheduling, hours, and products, but it should also be regularly updated with new information. In this way, your website can also serve as your blog, a place where you can post articles on topics of interest to your current and prospective patients. It’s best to start with a website/blog so you can create relevant content to share on social media sites.

Facebook. The rock star of social networking sites was launched in 2004 and recently reached over 1 billion active users. Your patients, current and prospective, as well as your competition, are on Facebook. And you should be, too. Facebook allows for you to have both personal and professional pages, to add friends, to categorize friends, and to even "unfriend" friends. You can exchange both public and private messages, and unlike Twitter, you have the ability to monitor what others post on your page; and you can delete inappropriate material when necessary.

Twitter. This online social networking site allows users to create messages that are up to 140 characters, known as "tweets." As such, it can be challenging for a newbie to know what to say, how to say it cleverly enough to get "retweeted" or shared, and how to get people engaged long-term. Benefits for physicians, however, include engaging in real-time conversation, sharing breaking news, and discovering hot topics.

LinkedIn. This social networking site is used primarily by professionals and is effective for making business contacts, hiring, and networking.

Video. You should consider having a YouTube or Vimeo account because a video post is 50 times more likely to get picked up in a Google search than is a written post, and because 3 billion videos are watched on YouTube every day. Video also allows prospective patients to get to know you and increases your visibility as an educator and expert in the field.

You can ignore all of this and hope it goes away, but the younger generation of physicians entering the field today isn’t. Or you could contract out your social media work to a professional company. Or you and your staff could do it. I’ll speak about these options in future columns.

DR. BENABIO is in private practice in San Diego. Visit his consumer health blog or connect with him on Twitter @Dermdoc and on Facebook (DermDoc).

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ONLINE EXCLUSIVE: Listen to Derek C. Angus discuss incorporating hospitalists into a tiered system of ICU care

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ONLINE EXCLUSIVE: Listen to Joaquin Cigarroa, MD, of Oregon Health & Science University, discuss the overlap of cardiology and hospital medicine

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ONLINE EXCLUSIVE: Daniel Dressler, MD, MSc, SFHM, discusses the differences in opinion over the SHM/SCCM critical care fellowship proposal

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ONLINE EXCLUSIVE: Daniel Dressler, MD, MSc, SFHM, discusses the differences in opinion over the SHM/SCCM critical care fellowship proposal
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Special Skills Hospitalists Need for the Intensive Care Unit

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Critical-care experts point to three types of competency that are crucial for any hospitalist working within an ICU environment. First, hospitalists need a solid knowledge base of the pharmacology, physiology, and pathophysiology of critical illnesses and conditions such as renal failure, respiratory failure, cardiac failure, sepsis, and seizures.

Second, providers need to acquire an array of psychomotor and interpersonal skills. Core skills like endotracheal intubation, chest-tube placement, and arterial and central venous catheterization are essential. But so are broader abilities like bringing people together to work as a team, says Timothy Buchman, PhD, MD, director of Emory University’s Center for Critical Care in Atlanta.

Eric Siegal, MD, SFHM, director of critical care medicine at Aurora St Luke’s Medical Center in Milwaukee, concurs. Much of the value of intensivists, he says, comes from their ability to understand the ICU as a multidisciplinary, team-based environment that emphasizes system improvement, quality control, and consistent patient care.

“Does that sound familiar? It’s what hospitalists do,” he says. “So the conceptual structure of a high-functioning intensivist team is nearly identical to the conceptual structure of a high-functioning hospitalist team; it’s just located in a smaller area, with a higher acuity patient population.”

Dr. Siegal emphasizes the importance of inpatient procedural skills, which he says are no longer emphasized in internal-medicine training. “The good news is, those skills are definable, are fairly easily taught, and are simply a matter of repetition,” he says.

Finally, hospitalists need to adopt the right attitude about what care is or isn’t possible for critically-ill patients, and how families can be integrated into complex, culturally-sensitive decision-making about difficult topics such as organ donation.

“That’s very different when the patient is unable to speak for him or herself,” Dr. Buchman says. “There’s a list of what I would call attitudinal competencies, which is longer than I think most people understand it to be to be an effective clinician. … Although all of them, to some degree, overlap with experience during residency training, they are often at a complexity level that can only be mastered through additional training.”

Bryn Nelson is a freelance medical writer in Seattle.

 

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Critical-care experts point to three types of competency that are crucial for any hospitalist working within an ICU environment. First, hospitalists need a solid knowledge base of the pharmacology, physiology, and pathophysiology of critical illnesses and conditions such as renal failure, respiratory failure, cardiac failure, sepsis, and seizures.

Second, providers need to acquire an array of psychomotor and interpersonal skills. Core skills like endotracheal intubation, chest-tube placement, and arterial and central venous catheterization are essential. But so are broader abilities like bringing people together to work as a team, says Timothy Buchman, PhD, MD, director of Emory University’s Center for Critical Care in Atlanta.

Eric Siegal, MD, SFHM, director of critical care medicine at Aurora St Luke’s Medical Center in Milwaukee, concurs. Much of the value of intensivists, he says, comes from their ability to understand the ICU as a multidisciplinary, team-based environment that emphasizes system improvement, quality control, and consistent patient care.

“Does that sound familiar? It’s what hospitalists do,” he says. “So the conceptual structure of a high-functioning intensivist team is nearly identical to the conceptual structure of a high-functioning hospitalist team; it’s just located in a smaller area, with a higher acuity patient population.”

Dr. Siegal emphasizes the importance of inpatient procedural skills, which he says are no longer emphasized in internal-medicine training. “The good news is, those skills are definable, are fairly easily taught, and are simply a matter of repetition,” he says.

Finally, hospitalists need to adopt the right attitude about what care is or isn’t possible for critically-ill patients, and how families can be integrated into complex, culturally-sensitive decision-making about difficult topics such as organ donation.

“That’s very different when the patient is unable to speak for him or herself,” Dr. Buchman says. “There’s a list of what I would call attitudinal competencies, which is longer than I think most people understand it to be to be an effective clinician. … Although all of them, to some degree, overlap with experience during residency training, they are often at a complexity level that can only be mastered through additional training.”

Bryn Nelson is a freelance medical writer in Seattle.

 

Critical-care experts point to three types of competency that are crucial for any hospitalist working within an ICU environment. First, hospitalists need a solid knowledge base of the pharmacology, physiology, and pathophysiology of critical illnesses and conditions such as renal failure, respiratory failure, cardiac failure, sepsis, and seizures.

Second, providers need to acquire an array of psychomotor and interpersonal skills. Core skills like endotracheal intubation, chest-tube placement, and arterial and central venous catheterization are essential. But so are broader abilities like bringing people together to work as a team, says Timothy Buchman, PhD, MD, director of Emory University’s Center for Critical Care in Atlanta.

Eric Siegal, MD, SFHM, director of critical care medicine at Aurora St Luke’s Medical Center in Milwaukee, concurs. Much of the value of intensivists, he says, comes from their ability to understand the ICU as a multidisciplinary, team-based environment that emphasizes system improvement, quality control, and consistent patient care.

“Does that sound familiar? It’s what hospitalists do,” he says. “So the conceptual structure of a high-functioning intensivist team is nearly identical to the conceptual structure of a high-functioning hospitalist team; it’s just located in a smaller area, with a higher acuity patient population.”

Dr. Siegal emphasizes the importance of inpatient procedural skills, which he says are no longer emphasized in internal-medicine training. “The good news is, those skills are definable, are fairly easily taught, and are simply a matter of repetition,” he says.

Finally, hospitalists need to adopt the right attitude about what care is or isn’t possible for critically-ill patients, and how families can be integrated into complex, culturally-sensitive decision-making about difficult topics such as organ donation.

“That’s very different when the patient is unable to speak for him or herself,” Dr. Buchman says. “There’s a list of what I would call attitudinal competencies, which is longer than I think most people understand it to be to be an effective clinician. … Although all of them, to some degree, overlap with experience during residency training, they are often at a complexity level that can only be mastered through additional training.”

Bryn Nelson is a freelance medical writer in Seattle.

 

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Penalties for Hospitals with Excessive Readmissions Take Effect

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The new era of penalizing hospitals for higher-than-predicted 30-day avoidable readmissions rates has begun. Under the federal Hospital Readmissions Reduction Program, some calculate a hospital's excessive readmissions rate for each applicable condition.

Penalties for the current fiscal year—FY 2013, which began Oct. 1, 2012—will be based on discharges that occurred during the three-year period from July 1, 2008, to June 30, 2011, according to the program guidelines. For hospitals that don't improve, the penalty grows to a maximum 2% next year (FY14) and 3% in FY15.

Hospitalists are not penalized directly for readmissions, and many hospitalists are wondering about the extent to which they're responsible for a readmission after the patient leaves the hospital, notes Mark Williams, MD, FACP, MHM, chief of the division of hospital medicine at Northwestern University’s Feinberg School of Medicine in Chicago.

Dr. Williams is the principal investigator of SHM’s Project BOOST (Better Outcomes for Older Adults through Safe Transitions), one of several national quality initiatives that teach hospitals and other healthcare providers how to improve transitions of care through such techniques as patient coaching and community partnerships.


"These new penalties mean that hospitals will start talking to their physicians about readmissions, and looking for methods to incentivize the hospitalists to get involved in preventing them," Dr. Williams says.

 

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The new era of penalizing hospitals for higher-than-predicted 30-day avoidable readmissions rates has begun. Under the federal Hospital Readmissions Reduction Program, some calculate a hospital's excessive readmissions rate for each applicable condition.

Penalties for the current fiscal year—FY 2013, which began Oct. 1, 2012—will be based on discharges that occurred during the three-year period from July 1, 2008, to June 30, 2011, according to the program guidelines. For hospitals that don't improve, the penalty grows to a maximum 2% next year (FY14) and 3% in FY15.

Hospitalists are not penalized directly for readmissions, and many hospitalists are wondering about the extent to which they're responsible for a readmission after the patient leaves the hospital, notes Mark Williams, MD, FACP, MHM, chief of the division of hospital medicine at Northwestern University’s Feinberg School of Medicine in Chicago.

Dr. Williams is the principal investigator of SHM’s Project BOOST (Better Outcomes for Older Adults through Safe Transitions), one of several national quality initiatives that teach hospitals and other healthcare providers how to improve transitions of care through such techniques as patient coaching and community partnerships.


"These new penalties mean that hospitals will start talking to their physicians about readmissions, and looking for methods to incentivize the hospitalists to get involved in preventing them," Dr. Williams says.

 

The new era of penalizing hospitals for higher-than-predicted 30-day avoidable readmissions rates has begun. Under the federal Hospital Readmissions Reduction Program, some calculate a hospital's excessive readmissions rate for each applicable condition.

Penalties for the current fiscal year—FY 2013, which began Oct. 1, 2012—will be based on discharges that occurred during the three-year period from July 1, 2008, to June 30, 2011, according to the program guidelines. For hospitals that don't improve, the penalty grows to a maximum 2% next year (FY14) and 3% in FY15.

Hospitalists are not penalized directly for readmissions, and many hospitalists are wondering about the extent to which they're responsible for a readmission after the patient leaves the hospital, notes Mark Williams, MD, FACP, MHM, chief of the division of hospital medicine at Northwestern University’s Feinberg School of Medicine in Chicago.

Dr. Williams is the principal investigator of SHM’s Project BOOST (Better Outcomes for Older Adults through Safe Transitions), one of several national quality initiatives that teach hospitals and other healthcare providers how to improve transitions of care through such techniques as patient coaching and community partnerships.


"These new penalties mean that hospitals will start talking to their physicians about readmissions, and looking for methods to incentivize the hospitalists to get involved in preventing them," Dr. Williams says.

 

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The Hospitalist - 2012(10)
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The Hospitalist - 2012(10)
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Penalties for Hospitals with Excessive Readmissions Take Effect
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