Handoffs

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Handoffs: A story in evolution

In this issue of the Journal of Hospital Medicine, the results of 2 inpatient handoff studies further shape our evolving understanding of in‐hospital care transitions. Schouten and colleagues,[1] report no difference in adverse outcomes when admissions were handed off to the primary team using face‐to‐face compared to nonface‐to‐face interactions. Meanwhile, Hanson and colleagues[2] report that a written handoff tool is used infrequently by covering interns.

Schouten et al.'s study attempted to isolate the impact of the verbal portion of the handoff between admitting and accepting team by evaluating whether early adverse outcomes differed between patients whose teams performed a face‐to‐face handoffs compared to those who did not. Their study was a retrospective chart review, and no additional process changes, training, or instruction regarding handoffs were implemented or measured. Handoffs occurred primarily between advanced practice providers, hospitalists, and a small number of resident physicians, so generalizability of this study to other institutions may be limited. No difference in adverse events was noted between admissions with face‐to‐face compared to those without face‐to‐face handoffs (2.6% vs 3.2%). Unfortunately, this study was likely underpowered to detect significant changes in adverse events, with a sample size of 805 total patients with a 3% baseline rate of adverse events (by our estimate, over 5000 patients would be needed in each group10,000 overallto detect a 30% relative difference in event rates). Further, this study did not examine other outcomes that could be impacted by the handoff process such as provider efficiency or patient experience.

Face‐to‐face handoffs, the gold standard for handoffs between providers, was 1 of the sign‐out approaches examined in a study by Graham and colleagues.[3] This study, in contrast to the Schouten et al. study, prospectively evaluated adverse events before and after implementation of face‐to‐face handoffs, with structured written sign‐out from the primary team to nighttime covering physicians. Prior to implementation, handoffs consisted of a double handoff involving an intermediary physician and unstructured written sign‐out. Although no statistically significant reduction in adverse events was found in the Graham et al. study, significant improvements were noted in physician satisfaction, documentation of key elements in handoffs, and reduced data omissions; importantly, a trend of fewer near misses was noted comparing the pre‐ and postintervention periods. Although the Schouten et al. and Graham et al. studies suggest questionable benefit of face‐to‐face handoffs, we would caution that limitations in sample size and methodological sensitivity to detect adverse events in both studies could explain the lack of association between face‐to‐face handoffs and reduced adverse events. Furthermore, the promising findings of fewer data omissions and near misses in the intervention group in the Graham et al. study suggest benefit from a multipronged approach to improving handoffs including both face‐to‐face interactions and a structured written component.

In this issue, Hanson and colleagues also evaluated the use of a handoff tool by cross‐covering interns in a convenience sample of overnight clinical interactions. Despite finding that standard written documentation was considered beneficial by nearly all respondents (94.3%), the interns reported that the handoff tool was used in only 27.7% of encounters. This pales in comparison to the use of the nurse or chart in 94.4% of cross‐coverage encounters. The authors speculate that a handoff tool, for many years the only timely source of information, may not be as useful when information can be easily accessed in an electronic health record. Yet, in a prior systematic review that included 6 studies of computerized handoff tools, Li and colleagues found that computerized handoff tools may improve physician efficiency, enhance the completeness of handoff information, and even potentially reduce adverse events.[4]

The Schouten et al. and Hanson et al. studies raise important questions for the fields of hospital medicine and patient safety. Is it time to do away with the written and verbal portions of the handoff process? Should the handoff of patients simply consist of transferring a list of patients to covering providers? We do not believe this is the correct course of action. Rather, we recommend a more evolutionary, not revolutionary, interpretation of these results, especially when considered as part of a broader story of in‐hospital transitions of care.

For example, a recently published evaluation of a resident handoff‐improvement program in 9 hospitals and 10,740 patient admissions by Starmer and collegues[5] focused on a handoff bundle, I‐PASS, which is a pneumonic for Illness severity, Patient summary, Action items, Situation awareness and contingency planning, Synthesis by receiver. The authors report a reduction in medical errors and preventable adverse events without significant increases in the duration of oral handoff per patient. The handoff in this study included both oral and written elements in the I‐PASS format. Implementation was multipronged, and the I‐PASS bundle included (1) use of the I‐PASS pneumonic to standardize handoffs; (2) resident physician training in handoffs and communication through a 2‐hour workshop, followed by a 1‐hour role‐playing and simulation session, and a computer module for practice; (3) faculty development and observation with use of direct‐observation tools to provide structured feedback to residents; (4) active surveillance for errors (rather than relying on self‐report); and (5) a sustainability campaign to promote continuation of culture change. The complexity and robust nature of the I‐PASS handoff bundle suggests that having multiple structured components included in a handoff program with active, rather than retrospective, evaluation might increase the likelihood of improved, sustained outcomes. In addition, one might also conclude from the Starmer et al. study that it takes commitment from all levels, including residents, faculty, and administration, to improve handoffs between teams for inpatient care.

We commend Schouten et al. and Hanson et al. on their contributions to the literature, but believe that the story of the in‐hospital handoff has yet to be fully written. Although results from these 2 articles may cause speculation about the value of oral and written handoffs, we believe that the balance of evidence favors the use of a multipronged approach that involves both structured oral and written handoffs to improve the value and efficiency of handoffs. In addition, findings from the I‐PASS study support dedicated handoff training for providers, evaluation of handoffs using structured tools, and active surveillance for medical errors. Future areas of work should include a systematic review of the inpatient handoff literature and further evaluation of precisely which specific intervention components (eg, structured content of handoffs, sensemaking content) or modes of delivery (eg, face‐to‐face vs other) are most likely to reduce medical errors and improve patient outcomes. As the hospital medicine movement continues to grow, handoffs will continue to be paramount. Establishing the safest method to complete handoffs to promote patient safety should be a common goal for hospitalists.

The handoff story is still in evolution; as hospitalists, we are poised to be its author.

Files
References
  1. Schouten WM, Burton MC, Jones LD, et al. Association of Face‐to‐Face Handoffs and Outcomes of Hospitalized Internal Medicine Patients. J Hosp Med. 2015;10(3):137141.
  2. Hanson JT, Leykum LK, Pugh JA, et al. Nighttime Clinical Encounters: How Residents Perceive and Respond to Calls at Night. J Hosp Med. 2015;10(3):142146.
  3. Graham KL, Marcantonio ER, Huang GC, Yang J, Davis RB, Smith CC. Effect of a systems intervention on the quality and safety of patient handoffs in an internal medicine residency program. J Gen Intern Med. 2013;28(8):986993.
  4. Li P, Ali S, Tang C, Ghali WA, Stelfox HT. Review of computerized physician handoff tools for improving the quality of patient care. J Hosp Med. 2013;8(8):456463.
  5. Starmer AJ, Spector ND, Srivastava R, et al. Changes in medical errors after implementation of a handoff program. N Engl J Med. 2014;371(19):18031812.
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In this issue of the Journal of Hospital Medicine, the results of 2 inpatient handoff studies further shape our evolving understanding of in‐hospital care transitions. Schouten and colleagues,[1] report no difference in adverse outcomes when admissions were handed off to the primary team using face‐to‐face compared to nonface‐to‐face interactions. Meanwhile, Hanson and colleagues[2] report that a written handoff tool is used infrequently by covering interns.

Schouten et al.'s study attempted to isolate the impact of the verbal portion of the handoff between admitting and accepting team by evaluating whether early adverse outcomes differed between patients whose teams performed a face‐to‐face handoffs compared to those who did not. Their study was a retrospective chart review, and no additional process changes, training, or instruction regarding handoffs were implemented or measured. Handoffs occurred primarily between advanced practice providers, hospitalists, and a small number of resident physicians, so generalizability of this study to other institutions may be limited. No difference in adverse events was noted between admissions with face‐to‐face compared to those without face‐to‐face handoffs (2.6% vs 3.2%). Unfortunately, this study was likely underpowered to detect significant changes in adverse events, with a sample size of 805 total patients with a 3% baseline rate of adverse events (by our estimate, over 5000 patients would be needed in each group10,000 overallto detect a 30% relative difference in event rates). Further, this study did not examine other outcomes that could be impacted by the handoff process such as provider efficiency or patient experience.

Face‐to‐face handoffs, the gold standard for handoffs between providers, was 1 of the sign‐out approaches examined in a study by Graham and colleagues.[3] This study, in contrast to the Schouten et al. study, prospectively evaluated adverse events before and after implementation of face‐to‐face handoffs, with structured written sign‐out from the primary team to nighttime covering physicians. Prior to implementation, handoffs consisted of a double handoff involving an intermediary physician and unstructured written sign‐out. Although no statistically significant reduction in adverse events was found in the Graham et al. study, significant improvements were noted in physician satisfaction, documentation of key elements in handoffs, and reduced data omissions; importantly, a trend of fewer near misses was noted comparing the pre‐ and postintervention periods. Although the Schouten et al. and Graham et al. studies suggest questionable benefit of face‐to‐face handoffs, we would caution that limitations in sample size and methodological sensitivity to detect adverse events in both studies could explain the lack of association between face‐to‐face handoffs and reduced adverse events. Furthermore, the promising findings of fewer data omissions and near misses in the intervention group in the Graham et al. study suggest benefit from a multipronged approach to improving handoffs including both face‐to‐face interactions and a structured written component.

In this issue, Hanson and colleagues also evaluated the use of a handoff tool by cross‐covering interns in a convenience sample of overnight clinical interactions. Despite finding that standard written documentation was considered beneficial by nearly all respondents (94.3%), the interns reported that the handoff tool was used in only 27.7% of encounters. This pales in comparison to the use of the nurse or chart in 94.4% of cross‐coverage encounters. The authors speculate that a handoff tool, for many years the only timely source of information, may not be as useful when information can be easily accessed in an electronic health record. Yet, in a prior systematic review that included 6 studies of computerized handoff tools, Li and colleagues found that computerized handoff tools may improve physician efficiency, enhance the completeness of handoff information, and even potentially reduce adverse events.[4]

The Schouten et al. and Hanson et al. studies raise important questions for the fields of hospital medicine and patient safety. Is it time to do away with the written and verbal portions of the handoff process? Should the handoff of patients simply consist of transferring a list of patients to covering providers? We do not believe this is the correct course of action. Rather, we recommend a more evolutionary, not revolutionary, interpretation of these results, especially when considered as part of a broader story of in‐hospital transitions of care.

For example, a recently published evaluation of a resident handoff‐improvement program in 9 hospitals and 10,740 patient admissions by Starmer and collegues[5] focused on a handoff bundle, I‐PASS, which is a pneumonic for Illness severity, Patient summary, Action items, Situation awareness and contingency planning, Synthesis by receiver. The authors report a reduction in medical errors and preventable adverse events without significant increases in the duration of oral handoff per patient. The handoff in this study included both oral and written elements in the I‐PASS format. Implementation was multipronged, and the I‐PASS bundle included (1) use of the I‐PASS pneumonic to standardize handoffs; (2) resident physician training in handoffs and communication through a 2‐hour workshop, followed by a 1‐hour role‐playing and simulation session, and a computer module for practice; (3) faculty development and observation with use of direct‐observation tools to provide structured feedback to residents; (4) active surveillance for errors (rather than relying on self‐report); and (5) a sustainability campaign to promote continuation of culture change. The complexity and robust nature of the I‐PASS handoff bundle suggests that having multiple structured components included in a handoff program with active, rather than retrospective, evaluation might increase the likelihood of improved, sustained outcomes. In addition, one might also conclude from the Starmer et al. study that it takes commitment from all levels, including residents, faculty, and administration, to improve handoffs between teams for inpatient care.

We commend Schouten et al. and Hanson et al. on their contributions to the literature, but believe that the story of the in‐hospital handoff has yet to be fully written. Although results from these 2 articles may cause speculation about the value of oral and written handoffs, we believe that the balance of evidence favors the use of a multipronged approach that involves both structured oral and written handoffs to improve the value and efficiency of handoffs. In addition, findings from the I‐PASS study support dedicated handoff training for providers, evaluation of handoffs using structured tools, and active surveillance for medical errors. Future areas of work should include a systematic review of the inpatient handoff literature and further evaluation of precisely which specific intervention components (eg, structured content of handoffs, sensemaking content) or modes of delivery (eg, face‐to‐face vs other) are most likely to reduce medical errors and improve patient outcomes. As the hospital medicine movement continues to grow, handoffs will continue to be paramount. Establishing the safest method to complete handoffs to promote patient safety should be a common goal for hospitalists.

The handoff story is still in evolution; as hospitalists, we are poised to be its author.

In this issue of the Journal of Hospital Medicine, the results of 2 inpatient handoff studies further shape our evolving understanding of in‐hospital care transitions. Schouten and colleagues,[1] report no difference in adverse outcomes when admissions were handed off to the primary team using face‐to‐face compared to nonface‐to‐face interactions. Meanwhile, Hanson and colleagues[2] report that a written handoff tool is used infrequently by covering interns.

Schouten et al.'s study attempted to isolate the impact of the verbal portion of the handoff between admitting and accepting team by evaluating whether early adverse outcomes differed between patients whose teams performed a face‐to‐face handoffs compared to those who did not. Their study was a retrospective chart review, and no additional process changes, training, or instruction regarding handoffs were implemented or measured. Handoffs occurred primarily between advanced practice providers, hospitalists, and a small number of resident physicians, so generalizability of this study to other institutions may be limited. No difference in adverse events was noted between admissions with face‐to‐face compared to those without face‐to‐face handoffs (2.6% vs 3.2%). Unfortunately, this study was likely underpowered to detect significant changes in adverse events, with a sample size of 805 total patients with a 3% baseline rate of adverse events (by our estimate, over 5000 patients would be needed in each group10,000 overallto detect a 30% relative difference in event rates). Further, this study did not examine other outcomes that could be impacted by the handoff process such as provider efficiency or patient experience.

Face‐to‐face handoffs, the gold standard for handoffs between providers, was 1 of the sign‐out approaches examined in a study by Graham and colleagues.[3] This study, in contrast to the Schouten et al. study, prospectively evaluated adverse events before and after implementation of face‐to‐face handoffs, with structured written sign‐out from the primary team to nighttime covering physicians. Prior to implementation, handoffs consisted of a double handoff involving an intermediary physician and unstructured written sign‐out. Although no statistically significant reduction in adverse events was found in the Graham et al. study, significant improvements were noted in physician satisfaction, documentation of key elements in handoffs, and reduced data omissions; importantly, a trend of fewer near misses was noted comparing the pre‐ and postintervention periods. Although the Schouten et al. and Graham et al. studies suggest questionable benefit of face‐to‐face handoffs, we would caution that limitations in sample size and methodological sensitivity to detect adverse events in both studies could explain the lack of association between face‐to‐face handoffs and reduced adverse events. Furthermore, the promising findings of fewer data omissions and near misses in the intervention group in the Graham et al. study suggest benefit from a multipronged approach to improving handoffs including both face‐to‐face interactions and a structured written component.

In this issue, Hanson and colleagues also evaluated the use of a handoff tool by cross‐covering interns in a convenience sample of overnight clinical interactions. Despite finding that standard written documentation was considered beneficial by nearly all respondents (94.3%), the interns reported that the handoff tool was used in only 27.7% of encounters. This pales in comparison to the use of the nurse or chart in 94.4% of cross‐coverage encounters. The authors speculate that a handoff tool, for many years the only timely source of information, may not be as useful when information can be easily accessed in an electronic health record. Yet, in a prior systematic review that included 6 studies of computerized handoff tools, Li and colleagues found that computerized handoff tools may improve physician efficiency, enhance the completeness of handoff information, and even potentially reduce adverse events.[4]

The Schouten et al. and Hanson et al. studies raise important questions for the fields of hospital medicine and patient safety. Is it time to do away with the written and verbal portions of the handoff process? Should the handoff of patients simply consist of transferring a list of patients to covering providers? We do not believe this is the correct course of action. Rather, we recommend a more evolutionary, not revolutionary, interpretation of these results, especially when considered as part of a broader story of in‐hospital transitions of care.

For example, a recently published evaluation of a resident handoff‐improvement program in 9 hospitals and 10,740 patient admissions by Starmer and collegues[5] focused on a handoff bundle, I‐PASS, which is a pneumonic for Illness severity, Patient summary, Action items, Situation awareness and contingency planning, Synthesis by receiver. The authors report a reduction in medical errors and preventable adverse events without significant increases in the duration of oral handoff per patient. The handoff in this study included both oral and written elements in the I‐PASS format. Implementation was multipronged, and the I‐PASS bundle included (1) use of the I‐PASS pneumonic to standardize handoffs; (2) resident physician training in handoffs and communication through a 2‐hour workshop, followed by a 1‐hour role‐playing and simulation session, and a computer module for practice; (3) faculty development and observation with use of direct‐observation tools to provide structured feedback to residents; (4) active surveillance for errors (rather than relying on self‐report); and (5) a sustainability campaign to promote continuation of culture change. The complexity and robust nature of the I‐PASS handoff bundle suggests that having multiple structured components included in a handoff program with active, rather than retrospective, evaluation might increase the likelihood of improved, sustained outcomes. In addition, one might also conclude from the Starmer et al. study that it takes commitment from all levels, including residents, faculty, and administration, to improve handoffs between teams for inpatient care.

We commend Schouten et al. and Hanson et al. on their contributions to the literature, but believe that the story of the in‐hospital handoff has yet to be fully written. Although results from these 2 articles may cause speculation about the value of oral and written handoffs, we believe that the balance of evidence favors the use of a multipronged approach that involves both structured oral and written handoffs to improve the value and efficiency of handoffs. In addition, findings from the I‐PASS study support dedicated handoff training for providers, evaluation of handoffs using structured tools, and active surveillance for medical errors. Future areas of work should include a systematic review of the inpatient handoff literature and further evaluation of precisely which specific intervention components (eg, structured content of handoffs, sensemaking content) or modes of delivery (eg, face‐to‐face vs other) are most likely to reduce medical errors and improve patient outcomes. As the hospital medicine movement continues to grow, handoffs will continue to be paramount. Establishing the safest method to complete handoffs to promote patient safety should be a common goal for hospitalists.

The handoff story is still in evolution; as hospitalists, we are poised to be its author.

References
  1. Schouten WM, Burton MC, Jones LD, et al. Association of Face‐to‐Face Handoffs and Outcomes of Hospitalized Internal Medicine Patients. J Hosp Med. 2015;10(3):137141.
  2. Hanson JT, Leykum LK, Pugh JA, et al. Nighttime Clinical Encounters: How Residents Perceive and Respond to Calls at Night. J Hosp Med. 2015;10(3):142146.
  3. Graham KL, Marcantonio ER, Huang GC, Yang J, Davis RB, Smith CC. Effect of a systems intervention on the quality and safety of patient handoffs in an internal medicine residency program. J Gen Intern Med. 2013;28(8):986993.
  4. Li P, Ali S, Tang C, Ghali WA, Stelfox HT. Review of computerized physician handoff tools for improving the quality of patient care. J Hosp Med. 2013;8(8):456463.
  5. Starmer AJ, Spector ND, Srivastava R, et al. Changes in medical errors after implementation of a handoff program. N Engl J Med. 2014;371(19):18031812.
References
  1. Schouten WM, Burton MC, Jones LD, et al. Association of Face‐to‐Face Handoffs and Outcomes of Hospitalized Internal Medicine Patients. J Hosp Med. 2015;10(3):137141.
  2. Hanson JT, Leykum LK, Pugh JA, et al. Nighttime Clinical Encounters: How Residents Perceive and Respond to Calls at Night. J Hosp Med. 2015;10(3):142146.
  3. Graham KL, Marcantonio ER, Huang GC, Yang J, Davis RB, Smith CC. Effect of a systems intervention on the quality and safety of patient handoffs in an internal medicine residency program. J Gen Intern Med. 2013;28(8):986993.
  4. Li P, Ali S, Tang C, Ghali WA, Stelfox HT. Review of computerized physician handoff tools for improving the quality of patient care. J Hosp Med. 2013;8(8):456463.
  5. Starmer AJ, Spector ND, Srivastava R, et al. Changes in medical errors after implementation of a handoff program. N Engl J Med. 2014;371(19):18031812.
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Handoffs: A story in evolution
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Address for correspondence and reprint requests: Christine Jones, MD, Department of Medicine, Division of General Internal Medicine, Hospital Medicine Section, University of Colorado, Mail Stop F782, 12401 East 17th Avenue, Aurora, CO 80045; Telephone 720‐848‐4289; Fax 720‐848‐4293; E‐mail: [email protected]
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Face‐to‐Face Handoffs and Outcomes

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Association of face‐to‐face handoffs and outcomes of hospitalized internal medicine patients

Handoffs are key events in the care of hospitalized patients whereby vital information is relayed between healthcare providers. Resident duty hour restrictions and the popularity of shift‐based work schedules have increased the frequency of inpatient handoffs.[1, 2] Failures in communication at the time of patient handoff have been implicated as contributing factors to preventable adverse events.[3, 4, 5, 6] With patient safety in mind, accreditation organizations and professional societies have made the standardization of hospital handoff procedures a priority.[7, 8] A variety of strategies have been utilized to standardize handoffs. Examples include the use of mnemonics,[9] electronic resources,[10, 11, 12] preformatted handoff sheets,[13, 14, 15, 16] and optimization of the handoff environment.[17] The primary outcomes for many of these studies center on the provider by measuring their retention of patient facts[18, 19] and completion of tasks[14, 16] after handoff, for example. Few studies examined patient‐centered outcomes such as transfer to a higher level of care,[20] length of stay,[11] mortality,[21] or readmission rate.[22] A study in the pediatric population found that implementation of a handoff bundle was associated with a decrease in medical errors and preventable adverse events.[23]

The Society of Hospital Medicine recommends that patient handoffs consist of both a written and verbal component.[8] Providers in our division work on 3 shifts: day, evening, and night. In 2009, we developed a face‐to‐face morning handoff, during which night‐shift providers hand off patient care to day‐shift providers incorporating an electronically generated service information list.[17] Given that the evening shift ends well before the day shift begins, the evening‐shift providers do not participate in this face‐to‐face handoff of care for patients they admit to day providers.

We wished to compare the clinical outcomes and adverse events of patients admitted by the night‐shift providers to those admitted by the evening‐shift providers. We hypothesized that transfer of care using a face‐to‐face handoff would be associated with fewer adverse events and improved clinical outcomes.

METHODS

The study was deemed exempt by the Mayo Clinic Institutional Review Board.

Study Population

Hospitalists at the study institution, a 1157‐bed academic tertiary referral hospital, admit general medical patients from the emergency department, as transfers from other institutions, and as direct admissions from outpatient offices. Patients included in the study were all adults admitted by evening‐ and night‐shift hospitalists from August 1, 2011 through August 1, 2012 between 6:45 pm and midnight. Our institution primarily uses 2 levels of care for adult inpatients on internal medicine services, including a general care floor for low‐acuity patients and an intensive care unit for high‐acuity patients. All of the patients in this study were triaged as low acuity at the time of admission and were initially admitted to general care units.

Setting

The division's shift schedule during the study period is depicted in Figure 1. Day‐shift providers included a physician and nurse practitioner (NP) or physician assistant (PA) on each of 7 teams. Each service had an average daily patient census between 10 and 15 patients with 3 to 4 new admissions every 24 hours, with 1 to 2 of these admissions occurring during the evening and night shifts, on average. The day shift started at 7:45 am and ended at 7:45 pm, at which time the day teams transitioned care of their patients to 1 of 2 overnight NP/PAs who provided cross‐cover for all teams through the night. The overnight NP/PAs then transitioned care back to the day teams at 7:45 am the following morning.

Figure 1
Provider schedules. Abbreviations: NP, nurse practitioner; PA, physician assistant.

Two evening‐shift providers, both physicians, including a staff hospitalist and a hospital medicine fellowship trainee, admitted patients without any cross‐cover responsibility. Their shifts had the same start time, but staggered end times (2 pm10 pm and 2 pmmidnight). At the end of their shifts, the evening‐shift providers relayed concerns or items for follow‐up to the night cross‐cover NP/PAs; however, this handoff was nonstandardized and provider dependent. The cross‐cover providers could also choose to pass on any relevant information to day‐shift providers if thought to be necessary, but this, again, was not required or standardized. A printed electronic handoff tool (including the patient's problem list, medications, vital signs, laboratory results, and to do list as determined by the admitting provider) as well as all clinical notes generated since admission were made available to day‐shift providers who assumed care at 7:45 am; however, there was no face‐to‐face handoff between the evening‐ and day‐shift providers.

Two night‐shift physicians, including a moonlighting board‐eligible internal medicine physician and staff hospitalist, also started at staggered times, 6:45 pm and 10 pm, but their shifts both ended at 7:45 am. These physicians also admitted patients without cross‐cover responsibilities. At 7:45 am, in a face‐to‐face meeting, they transitioned care of patients admitted overnight to day‐shift providers. This handoff occurred at a predesignated place with assigned start times for each team. During the meeting, printed electronic documents, including the aforementioned electronic handoff tool as well as all clinical notes generated since admission, were made available to the oncoming day‐shift providers. The face‐to‐face interaction between night‐ and day‐shift providers lasted approximately 5 minutes and allowed for a brief presentation of the patient, review of the diagnostic testing and treatments performed so far, as well as anticipatory guidance regarding potential issues throughout the remainder of the hospitalization. Although inclusion of the above components was encouraged during the face‐to‐face handoff, the interaction was not scripted and topics discussed were at the providers' discretion.

Patients admitted during the evening and night shifts were assigned to day‐shift services primarily based on the current census of each team, so as to distribute the workload evenly.

Chart Review

Patients included in the study were admitted by evening‐ or night‐shift providers between 6:45 pm and midnight. This time period accounts for when the evening shift and night shift overlap, allowing for direct comparison of patients admitted during the same time of day, so as to avoid confounding factors. Patients were grouped by whether they were admitted by an evening‐shift provider or a night‐shift provider. Each study patient's chart was retrospectively reviewed and relevant demographic and clinical data were collected. Demographic information included age, gender, and race. Clinical information included medical comorbidities, Charlson Comorbidity Index score, rapid response team calls, code team calls, transfers to a higher level of care, death in hospital, 30‐day readmission rate, length of stay (LOS), and adverse events. The Charlson Comorbidity Index score[24] was determined from diagnoses in the institution's medical index database. The 30‐day readmission rate included observation stays and full hospital admissions that occurred at our institution in the 30 days following the patient's hospital discharge from the index admission. LOS was determined based on the time of admission and discharge, as reported in the hospital billing system, and is reported as the median and mean LOS in hours for all patients in each group.

The Global Trigger Tool (GTT) was used to identify adverse events, as defined within the GTT whitepaper to be unintended physical injury resulting from or contributed to by medical care that requires additional monitoring, treatment or hospitalization, or that results in death.[25] Developed by the Institute for Healthcare Improvement, the GTT uses triggers, clues in the medical record that suggest an adverse event may have occurred, to cue a more detailed chart review. Registered nurses trained in use of the GTT reviewed all of the included patients' electronic medical records. If a trigger was identified (such as a patient fall suffered in the hospital), further chart review was prompted to determine if patient harm occurred. If there was evidence of harm, an adverse event was determined to have occurred and was then categorized using the National Coordinating Council for Medication Error Reporting and Prevention Index for Categorizing Errors.[26] For example, in the case of a patient fall whereby the patient was determined to have fallen in the hospital and suffered a laceration requiring wound care, but the hospital stay was not prolonged, this adverse event was categorized as category E (an adverse event that caused the patient temporary harm necessitating intervention, without prolongation of the hospital stay).

Outcomes including rapid response team calls, code team calls, transfers to a higher level of care, death in the hospital, and adverse events, as identified using the GTT, were counted if they occurred between 7:45 am on the first morning of admission until 12 hours later at 7:45 pm, at the time of the first evening handoff of the admitted patients' care.

Statistical Methods

Study data were collected and managed using REDCap (Research Electronic Data Capture) electronic data capture tools hosted at Mayo Clinic.[27] When comparing outcomes between the 2 groups, Fisher exact test was used for categorical variables and Student t test was used for continuous variables. Global Trigger Tool data were analyzed using the SAS GENMOD procedure, assuming a negative binomial distribution. All the above analyses were performed using SAS version 9.3 software (SAS Institute Inc., Cary, NC). Rates of adverse events were compared using MedCalc version 13 software (MedCalc Software, Ostend, Belgium).[28] A P value <0.05 was considered significant.

RESULTS

Of 805 patients admitted between 6:45 pm and midnight during the study period, 305 (37.9%) patients were handed off to day‐shift providers without face‐to‐face handoff, and 500 (62.1%) patients were transferred to the care of day‐shift providers with the use of a face‐to‐face handoff.

Baseline characteristics of both groups are depicted in Table 1. Demographic characteristics, including age, gender, and race, were not significantly different between groups. The mean Charlson Comorbidity Index score was not significantly different between the groups without and with a face‐to‐face handoff. In addition, the presence of medical comorbidities including type 2 diabetes mellitus, hypertension, coronary artery disease, hyperlipidemia, heart failure, body mass index (BMI) <18, active cancer, and current cigarette smoking were not significantly different between the 2 groups. There was a trend to a significantly increased proportion of patients with a BMI >30 in the group without face‐to‐face handoff (P=0.05).

Baseline Patient Characteristics
 Without Face‐to‐Face Handoff, N=305With Face‐to‐Face Handoff, N=500P Value
  • NOTE: Abbreviations: BMI, body mass index; SD, standard deviation.

Age, y, mean (SD)65.8 (19.0)64.2 (20.0)0.25
Sex, n (%)  0.69
Female166 (54%)265 (53%) 
Male139 (46%)235 (47%) 
Race, n (%)  0.94
White287 (95%)466 (93%) 
African American5 (2%)9 (2%) 
Arab/Middle Eastern3 (1%)8 (2%) 
Asian1 (0%)3 (1%) 
Indian subcontinental1 (0%)1 (0%) 
American Indian/Alaskan1 (0%)1 (0%) 
Other3 (1%)8 (2%) 
Unknown1 (0%)4 (1%) 
Charlson Comorbidity Index, mean ( SD)2.98 ( 3.73)2.93 ( 3.72)0.85
Comorbidities, n (%)   
Type 2 diabetes82 (27%)143 (29%)0.60
Hypertension195 (64%)303 (61%)0.34
Coronary artery disease76 (25%)137 (27%)0.44
Hyperlipidemia122 (40%)206 (41%)0.74
Heart failure30 (10%)66 (13%)0.15
BMI >30109 (36%)146 (29%)0.05
BMI <187 (2%)12 (2%)0.92
Active cancer29 (10%)46 (9%)0.88
Current smoker49 (16%)90 (18%)0.48

Results for the outcomes of this study are depicted in Table 2. The frequency of rapid response team calls, code team calls, transfers to a higher level of care, and death in the hospital in the 12 hours following the first morning handoff of the admission were not significantly different between the 2 groups. Both 30‐day readmission rate and LOS (median and mean) were not significantly different between groups.

Patient Outcomes
 Without Face‐to‐Face Handoff, N=305With Face‐to‐Face Handoff, N=500P Value
  • NOTE: Abbreviations: IQR, interquartile range; SD, standard deviation.

  • Global Trigger Tool adverse events were categorized by the National Coordinating Council for Medication Error Reporting and Prevention Index for Categorizing Medication Errors, using categories E through I.

Rapid response team call, n (%)4 (1%)5 (1%)0.68
Code team call, n (%)0 (0%)1 (0%)0.43
Transfer to higher level of care, n (%)7 (2%)11 (2%)0.93
Patient death, n (%)0 (0%)0 (0%)1.00
30‐day readmission, n (%)50 (16%)67 (13%)0.23
Hospital length of stay   
Median, h (IQR)66.5 (41.3115.6)70.3 (41.9131.2)0.30
Mean, h ( SD)102.0 ( 110.0)102.9 ( 94.0)0.90
Adverse events (Global Trigger Tool)
Temporary harm and required intervention (E)470.92
Temporary harm and required initial or prolonged hospitalization (F)780.53
Permanent harm (G)010.44
Intervention required to sustain life (H)060.14
Death (I)001.00
Total adverse events per 100 admissions3.614.400.59
% of admissions with an adverse event2.6%3.2%0.64

There was no significant difference between the 2 groups in the frequency of adverse events resulting in harm for any of the categories (categories EI). Total adverse events between groups were also compared. Adverse events per 100 admissions were not significantly different between the group without face‐to‐face handoff compared to the group with face‐to‐face handoff. The percentage of admissions with an adverse event was also similar between groups.

DISCUSSION

We found no significant difference in the rate of rapid response team calls, code team calls, transfers to a higher level of care, death in hospital, or adverse events when comparing patients transitioned to the care of day‐shift providers with or without a face‐to‐face handoff. We hypothesize that a reason adverse events were no different between the 2 groups may be that providers were more vigilant when they did not receive a face‐to‐face handoff from the previous provider. As a result, providers may have dedicated additional time reviewing the medical record, speaking with the patients, and communicating with other healthcare providers to ensure a safe care transition. Similarly, other studies found no significant reduction in adverse events when using a standardized handoff.[10, 13, 29] This may be because patient handoff is 1 of a multitude of factors that impact the rate of adverse events, and a handoff may play a less vital role in a system where documentation of care for a given patient is readily accessible, uniform, and detailed. A face‐to‐face interaction itself in a patient handoff may be less pertinent if key information can be communicated through other channels, such as an electronic handoff tool, email, or phone.

Another potential explanation for the lack of a significant difference in patient outcomes with and without a face‐to‐face handoff is related to the study design and inherent rate of the events measured. With the exception of 30‐day readmission rate and LOS, the outcomes of the study were recorded only if they occurred in the 12 hours following the first morning handoff of the admission. This was done in an attempt to isolate the effect of the nonface‐to‐face versus face‐to‐face handoff on the first morning of the admission, and to avoid confounding effects by subsequent transitions of care later in the hospitalization. The frequency of hospital admissions in which an adverse event occurred during this relatively short 12‐hour window was approximately 3% for all patients in the study. With 805 total patients in the study, there may have been insufficient statistical power to detect a difference in the rate of outcomes, if a difference did exist, considering the event rate for both groups and the sample size.

There are several additional limitations to our study. First, the GTT was designed to be applied across the entirety of a hospitalization. By screening for adverse events over the span of only 12 hours for each hospitalization, the sensitivity of the tool may have been diminished, with a proportion of adverse events not captured, even when the sequence of events leading to patient harm began during the 12 hours in question. Second, this is a retrospective study, and all adverse events may not be documented in the medical record. Third, although not formally structured and infrequent, some evening‐shift providers did send an email or call the oncoming day‐shift provider to discuss patients admitted. This process, however, was provider dependent, unstructured, uncommon, and erratic, and thus we were not able to capture it from medical record review. Finally, the patients in this study were deemed low acuity upon triage prior to admission. A face‐to‐face handoff may be less important in ensuring patient safety when caring for low‐acuity compared to high‐acuity patients, considering the rapidity at which the critically ill can deteriorate.

Handoffs of patient care in the hospital have certainly increased in recent years. Consequently, communication among providers is undoubtedly important, with patient safety being the primary goal. Our work suggests that a face‐to‐face component of a handoff is not vital to ensure a safe care transition. Because of the increasing frequency of handoffs, providers' ability to do so face‐to‐face will likely be challenged by time and logistical constraints. Future work is needed to delineate the most effective components of the handoff so that we can design information transfer that promotes safe and efficient care, even without a face‐to‐face interaction.

Acknowledgements

The authors are grateful for support from the Mayo Clinic Department of Medicine Clinical Research Office, Ms. Donna Lawson, and Mr. Stephen Cha.

Disclosures: This publication was made possible by the Mayo Clinic Center for Clinical and Translational Science through grant number UL1 TR000135 from the National Center for Advancing Translational Science, a component of the National Institutes of Health. The authors report no conflicts of interest.

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References
  1. Desai SV, Feldman L, Brown L, et al. Effect of the 2011 vs 2003 duty hour regulation‐compliant models on sleep duration, trainee education, and continuity of patient care among internal medicine house staff: a randomized trial. JAMA Intern Med. 2013;173(8):649655.
  2. Robeznieks A. 'Shift work': 24‐hour workdays are out as residents, hospitals deal with changes, mixed feelings on restrictions. Mod Healthc. 2011;41(30):67, 16, 1.
  3. Horwitz LI, Moin T, Krumholz HM, Wang L, Bradley EH. Consequences of inadequate sign‐out for patient care. Arch Intern Med. 2008;168(16):17551760.
  4. Arora V, Johnson J, Lovinger D, Humphrey HJ, Meltzer DO. Communication failures in patient sign‐out and suggestions for improvement: a critical incident analysis. Qual Saf Health Care. 2005;14(6):401407.
  5. Singh H, Thomas EJ, Petersen LA, Studdert DM. Medical errors involving trainees: a study of closed malpractice claims from 5 insurers. Archives of internal medicine. 2007;167(19):20302036.
  6. Greenberg CC, Regenbogen SE, Studdert DM, et al. Patterns of communication breakdowns resulting in injury to surgical patients. J Am Coll Surg. 2007;204(4):533540.
  7. Joint Commission International. Standard PC.02.02.01. 2013 Hospital Accreditation Standards. Oak Brook, IL: Joint Commission Resources; 2013.
  8. Arora VM, Manjarrez E, Dressler DD, Basaviah P, Halasyamani L, Kripalani S. Hospitalist handoffs: a systematic review and task force recommendations. J Hosp Med. 2009;4(7):433440.
  9. Riesenberg LA, Leitzsch J, Little BW. Systematic review of handoff mnemonics literature. Am J Med Qual. 2009;24(3):196204.
  10. Petersen LA, Orav EJ, Teich JM, O'Neil AC, Brennan TA. Using a computerized sign‐out program to improve continuity of inpatient care and prevent adverse events. Jt Comm J Qual Improv. 1998;24(2):7787.
  11. Ryan S, O'Riordan JM, Tierney S, Conlon KC, Ridgway PF. Impact of a new electronic handover system in surgery. Int J Surg. 2011;9(3):217220.
  12. Eaton EG, Horvath KD, Lober WB, Pellegrini CA. Organizing the transfer of patient care information: the development of a computerized resident sign‐out system. Surgery. 2004;136(1):513.
  13. Zavalkoff SR, Razack SI, Lavoie J, Dancea AB. Handover after pediatric heart surgery: a simple tool improves information exchange. Pediatr Crit Care Med. 2011;12(3):309313.
  14. Wayne JD, Tyagi R, Reinhardt G, et al. Simple standardized patient handoff system that increases accuracy and completeness. J Surg Educ. 2008;65(6):476485.
  15. Stahl K, Palileo A, Schulman CI, et al. Enhancing patient safety in the trauma/surgical intensive care unit. J Trauma. 2009;67(3):430433; discussion 433–435.
  16. Salerno SM, Arnett MV, Domanski JP. Standardized sign‐out reduces intern perception of medical errors on the general internal medicine ward. Teach Learn Med. 2009;21(2):121126.
  17. Burton MC, Kashiwagi DT, Kirkland LL, Manning D, Varkey P. Gaining efficiency and satisfaction in the handoff process. J Hosp Med. 2010;5(9):547552.
  18. Pickering BW, Hurley K, Marsh B. Identification of patient information corruption in the intensive care unit: using a scoring tool to direct quality improvements in handover. Crit Care Med. 2009;37(11):29052912.
  19. Dowding D. Examining the effects that manipulating information given in the change of shift report has on nurses' care planning ability. J Adv Nurs. 2001;33(6):836846.
  20. Horwitz LI, Parwani V, Shah NR, et al. Evaluation of an asynchronous physician voicemail sign‐out for emergency department admissions. Ann Emerg Med. 2009;54(3):368378.
  21. Mazzocco K, Petitti DB, Fong KT, et al. Surgical team behaviors and patient outcomes. Am J Surg. 2009;197(5):678685.
  22. Hess DR, Tokarczyk A, O'Malley M, Gavaghan S, Sullivan J, Schmidt U. The value of adding a verbal report to written handoffs on early readmission following prolonged respiratory failure. Chest. 2010;138(6):14751479.
  23. Starmer AJ, Sectish TC, Simon DW, et al. Rates of medical errors and preventable adverse events among hospitalized children following implementation of a resident handoff bundle. JAMA. 2013;310(21):22622270.
  24. Charlson ME, Pompei P, Ales KL, MacKenzie CR. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis. 1987;40(5):373383.
  25. Griffin FA, Resar RK. IHI Global Trigger Tool for measuring adverse events (second edition). IHI Innovation Series white paper. Cambridge, MA: Institute for Healthcare Improvement; 2009. Available at: http://www.ihi.org/resources/Pages/IHIWhitePapers/IHIGlobalTriggerToolWhitePaper.aspx. www.IHI.org). Accessed June 1, 2014.
  26. National Coordinating Council for Medication Error Reporting and Prevention (NCC MERP) index for categorizing errors. Available at: http://www.nccmerp.org/medErrorCatIndex.html. Accessed June 1, 2014.
  27. Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG. Research electronic data capture (REDCap)—a metadata‐driven methodology and workflow process for providing translational research informatics support. J Biomed Inform. 2009;42(2):377381.
  28. Sahai H, Khurshid A. Statistics in Epidemiology: Methods, Techniques, and Applications. Boca Raton, FL: CRC Press; 1996.
  29. Eaton EG, McDonough K, Lober WB, Johnson EA, Pellegrini CA, Horvath KD. Safety of using a computerized rounding and sign‐out system to reduce resident duty hours. Acad Med. 2010;85(7):11891195.
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Handoffs are key events in the care of hospitalized patients whereby vital information is relayed between healthcare providers. Resident duty hour restrictions and the popularity of shift‐based work schedules have increased the frequency of inpatient handoffs.[1, 2] Failures in communication at the time of patient handoff have been implicated as contributing factors to preventable adverse events.[3, 4, 5, 6] With patient safety in mind, accreditation organizations and professional societies have made the standardization of hospital handoff procedures a priority.[7, 8] A variety of strategies have been utilized to standardize handoffs. Examples include the use of mnemonics,[9] electronic resources,[10, 11, 12] preformatted handoff sheets,[13, 14, 15, 16] and optimization of the handoff environment.[17] The primary outcomes for many of these studies center on the provider by measuring their retention of patient facts[18, 19] and completion of tasks[14, 16] after handoff, for example. Few studies examined patient‐centered outcomes such as transfer to a higher level of care,[20] length of stay,[11] mortality,[21] or readmission rate.[22] A study in the pediatric population found that implementation of a handoff bundle was associated with a decrease in medical errors and preventable adverse events.[23]

The Society of Hospital Medicine recommends that patient handoffs consist of both a written and verbal component.[8] Providers in our division work on 3 shifts: day, evening, and night. In 2009, we developed a face‐to‐face morning handoff, during which night‐shift providers hand off patient care to day‐shift providers incorporating an electronically generated service information list.[17] Given that the evening shift ends well before the day shift begins, the evening‐shift providers do not participate in this face‐to‐face handoff of care for patients they admit to day providers.

We wished to compare the clinical outcomes and adverse events of patients admitted by the night‐shift providers to those admitted by the evening‐shift providers. We hypothesized that transfer of care using a face‐to‐face handoff would be associated with fewer adverse events and improved clinical outcomes.

METHODS

The study was deemed exempt by the Mayo Clinic Institutional Review Board.

Study Population

Hospitalists at the study institution, a 1157‐bed academic tertiary referral hospital, admit general medical patients from the emergency department, as transfers from other institutions, and as direct admissions from outpatient offices. Patients included in the study were all adults admitted by evening‐ and night‐shift hospitalists from August 1, 2011 through August 1, 2012 between 6:45 pm and midnight. Our institution primarily uses 2 levels of care for adult inpatients on internal medicine services, including a general care floor for low‐acuity patients and an intensive care unit for high‐acuity patients. All of the patients in this study were triaged as low acuity at the time of admission and were initially admitted to general care units.

Setting

The division's shift schedule during the study period is depicted in Figure 1. Day‐shift providers included a physician and nurse practitioner (NP) or physician assistant (PA) on each of 7 teams. Each service had an average daily patient census between 10 and 15 patients with 3 to 4 new admissions every 24 hours, with 1 to 2 of these admissions occurring during the evening and night shifts, on average. The day shift started at 7:45 am and ended at 7:45 pm, at which time the day teams transitioned care of their patients to 1 of 2 overnight NP/PAs who provided cross‐cover for all teams through the night. The overnight NP/PAs then transitioned care back to the day teams at 7:45 am the following morning.

Figure 1
Provider schedules. Abbreviations: NP, nurse practitioner; PA, physician assistant.

Two evening‐shift providers, both physicians, including a staff hospitalist and a hospital medicine fellowship trainee, admitted patients without any cross‐cover responsibility. Their shifts had the same start time, but staggered end times (2 pm10 pm and 2 pmmidnight). At the end of their shifts, the evening‐shift providers relayed concerns or items for follow‐up to the night cross‐cover NP/PAs; however, this handoff was nonstandardized and provider dependent. The cross‐cover providers could also choose to pass on any relevant information to day‐shift providers if thought to be necessary, but this, again, was not required or standardized. A printed electronic handoff tool (including the patient's problem list, medications, vital signs, laboratory results, and to do list as determined by the admitting provider) as well as all clinical notes generated since admission were made available to day‐shift providers who assumed care at 7:45 am; however, there was no face‐to‐face handoff between the evening‐ and day‐shift providers.

Two night‐shift physicians, including a moonlighting board‐eligible internal medicine physician and staff hospitalist, also started at staggered times, 6:45 pm and 10 pm, but their shifts both ended at 7:45 am. These physicians also admitted patients without cross‐cover responsibilities. At 7:45 am, in a face‐to‐face meeting, they transitioned care of patients admitted overnight to day‐shift providers. This handoff occurred at a predesignated place with assigned start times for each team. During the meeting, printed electronic documents, including the aforementioned electronic handoff tool as well as all clinical notes generated since admission, were made available to the oncoming day‐shift providers. The face‐to‐face interaction between night‐ and day‐shift providers lasted approximately 5 minutes and allowed for a brief presentation of the patient, review of the diagnostic testing and treatments performed so far, as well as anticipatory guidance regarding potential issues throughout the remainder of the hospitalization. Although inclusion of the above components was encouraged during the face‐to‐face handoff, the interaction was not scripted and topics discussed were at the providers' discretion.

Patients admitted during the evening and night shifts were assigned to day‐shift services primarily based on the current census of each team, so as to distribute the workload evenly.

Chart Review

Patients included in the study were admitted by evening‐ or night‐shift providers between 6:45 pm and midnight. This time period accounts for when the evening shift and night shift overlap, allowing for direct comparison of patients admitted during the same time of day, so as to avoid confounding factors. Patients were grouped by whether they were admitted by an evening‐shift provider or a night‐shift provider. Each study patient's chart was retrospectively reviewed and relevant demographic and clinical data were collected. Demographic information included age, gender, and race. Clinical information included medical comorbidities, Charlson Comorbidity Index score, rapid response team calls, code team calls, transfers to a higher level of care, death in hospital, 30‐day readmission rate, length of stay (LOS), and adverse events. The Charlson Comorbidity Index score[24] was determined from diagnoses in the institution's medical index database. The 30‐day readmission rate included observation stays and full hospital admissions that occurred at our institution in the 30 days following the patient's hospital discharge from the index admission. LOS was determined based on the time of admission and discharge, as reported in the hospital billing system, and is reported as the median and mean LOS in hours for all patients in each group.

The Global Trigger Tool (GTT) was used to identify adverse events, as defined within the GTT whitepaper to be unintended physical injury resulting from or contributed to by medical care that requires additional monitoring, treatment or hospitalization, or that results in death.[25] Developed by the Institute for Healthcare Improvement, the GTT uses triggers, clues in the medical record that suggest an adverse event may have occurred, to cue a more detailed chart review. Registered nurses trained in use of the GTT reviewed all of the included patients' electronic medical records. If a trigger was identified (such as a patient fall suffered in the hospital), further chart review was prompted to determine if patient harm occurred. If there was evidence of harm, an adverse event was determined to have occurred and was then categorized using the National Coordinating Council for Medication Error Reporting and Prevention Index for Categorizing Errors.[26] For example, in the case of a patient fall whereby the patient was determined to have fallen in the hospital and suffered a laceration requiring wound care, but the hospital stay was not prolonged, this adverse event was categorized as category E (an adverse event that caused the patient temporary harm necessitating intervention, without prolongation of the hospital stay).

Outcomes including rapid response team calls, code team calls, transfers to a higher level of care, death in the hospital, and adverse events, as identified using the GTT, were counted if they occurred between 7:45 am on the first morning of admission until 12 hours later at 7:45 pm, at the time of the first evening handoff of the admitted patients' care.

Statistical Methods

Study data were collected and managed using REDCap (Research Electronic Data Capture) electronic data capture tools hosted at Mayo Clinic.[27] When comparing outcomes between the 2 groups, Fisher exact test was used for categorical variables and Student t test was used for continuous variables. Global Trigger Tool data were analyzed using the SAS GENMOD procedure, assuming a negative binomial distribution. All the above analyses were performed using SAS version 9.3 software (SAS Institute Inc., Cary, NC). Rates of adverse events were compared using MedCalc version 13 software (MedCalc Software, Ostend, Belgium).[28] A P value <0.05 was considered significant.

RESULTS

Of 805 patients admitted between 6:45 pm and midnight during the study period, 305 (37.9%) patients were handed off to day‐shift providers without face‐to‐face handoff, and 500 (62.1%) patients were transferred to the care of day‐shift providers with the use of a face‐to‐face handoff.

Baseline characteristics of both groups are depicted in Table 1. Demographic characteristics, including age, gender, and race, were not significantly different between groups. The mean Charlson Comorbidity Index score was not significantly different between the groups without and with a face‐to‐face handoff. In addition, the presence of medical comorbidities including type 2 diabetes mellitus, hypertension, coronary artery disease, hyperlipidemia, heart failure, body mass index (BMI) <18, active cancer, and current cigarette smoking were not significantly different between the 2 groups. There was a trend to a significantly increased proportion of patients with a BMI >30 in the group without face‐to‐face handoff (P=0.05).

Baseline Patient Characteristics
 Without Face‐to‐Face Handoff, N=305With Face‐to‐Face Handoff, N=500P Value
  • NOTE: Abbreviations: BMI, body mass index; SD, standard deviation.

Age, y, mean (SD)65.8 (19.0)64.2 (20.0)0.25
Sex, n (%)  0.69
Female166 (54%)265 (53%) 
Male139 (46%)235 (47%) 
Race, n (%)  0.94
White287 (95%)466 (93%) 
African American5 (2%)9 (2%) 
Arab/Middle Eastern3 (1%)8 (2%) 
Asian1 (0%)3 (1%) 
Indian subcontinental1 (0%)1 (0%) 
American Indian/Alaskan1 (0%)1 (0%) 
Other3 (1%)8 (2%) 
Unknown1 (0%)4 (1%) 
Charlson Comorbidity Index, mean ( SD)2.98 ( 3.73)2.93 ( 3.72)0.85
Comorbidities, n (%)   
Type 2 diabetes82 (27%)143 (29%)0.60
Hypertension195 (64%)303 (61%)0.34
Coronary artery disease76 (25%)137 (27%)0.44
Hyperlipidemia122 (40%)206 (41%)0.74
Heart failure30 (10%)66 (13%)0.15
BMI >30109 (36%)146 (29%)0.05
BMI <187 (2%)12 (2%)0.92
Active cancer29 (10%)46 (9%)0.88
Current smoker49 (16%)90 (18%)0.48

Results for the outcomes of this study are depicted in Table 2. The frequency of rapid response team calls, code team calls, transfers to a higher level of care, and death in the hospital in the 12 hours following the first morning handoff of the admission were not significantly different between the 2 groups. Both 30‐day readmission rate and LOS (median and mean) were not significantly different between groups.

Patient Outcomes
 Without Face‐to‐Face Handoff, N=305With Face‐to‐Face Handoff, N=500P Value
  • NOTE: Abbreviations: IQR, interquartile range; SD, standard deviation.

  • Global Trigger Tool adverse events were categorized by the National Coordinating Council for Medication Error Reporting and Prevention Index for Categorizing Medication Errors, using categories E through I.

Rapid response team call, n (%)4 (1%)5 (1%)0.68
Code team call, n (%)0 (0%)1 (0%)0.43
Transfer to higher level of care, n (%)7 (2%)11 (2%)0.93
Patient death, n (%)0 (0%)0 (0%)1.00
30‐day readmission, n (%)50 (16%)67 (13%)0.23
Hospital length of stay   
Median, h (IQR)66.5 (41.3115.6)70.3 (41.9131.2)0.30
Mean, h ( SD)102.0 ( 110.0)102.9 ( 94.0)0.90
Adverse events (Global Trigger Tool)
Temporary harm and required intervention (E)470.92
Temporary harm and required initial or prolonged hospitalization (F)780.53
Permanent harm (G)010.44
Intervention required to sustain life (H)060.14
Death (I)001.00
Total adverse events per 100 admissions3.614.400.59
% of admissions with an adverse event2.6%3.2%0.64

There was no significant difference between the 2 groups in the frequency of adverse events resulting in harm for any of the categories (categories EI). Total adverse events between groups were also compared. Adverse events per 100 admissions were not significantly different between the group without face‐to‐face handoff compared to the group with face‐to‐face handoff. The percentage of admissions with an adverse event was also similar between groups.

DISCUSSION

We found no significant difference in the rate of rapid response team calls, code team calls, transfers to a higher level of care, death in hospital, or adverse events when comparing patients transitioned to the care of day‐shift providers with or without a face‐to‐face handoff. We hypothesize that a reason adverse events were no different between the 2 groups may be that providers were more vigilant when they did not receive a face‐to‐face handoff from the previous provider. As a result, providers may have dedicated additional time reviewing the medical record, speaking with the patients, and communicating with other healthcare providers to ensure a safe care transition. Similarly, other studies found no significant reduction in adverse events when using a standardized handoff.[10, 13, 29] This may be because patient handoff is 1 of a multitude of factors that impact the rate of adverse events, and a handoff may play a less vital role in a system where documentation of care for a given patient is readily accessible, uniform, and detailed. A face‐to‐face interaction itself in a patient handoff may be less pertinent if key information can be communicated through other channels, such as an electronic handoff tool, email, or phone.

Another potential explanation for the lack of a significant difference in patient outcomes with and without a face‐to‐face handoff is related to the study design and inherent rate of the events measured. With the exception of 30‐day readmission rate and LOS, the outcomes of the study were recorded only if they occurred in the 12 hours following the first morning handoff of the admission. This was done in an attempt to isolate the effect of the nonface‐to‐face versus face‐to‐face handoff on the first morning of the admission, and to avoid confounding effects by subsequent transitions of care later in the hospitalization. The frequency of hospital admissions in which an adverse event occurred during this relatively short 12‐hour window was approximately 3% for all patients in the study. With 805 total patients in the study, there may have been insufficient statistical power to detect a difference in the rate of outcomes, if a difference did exist, considering the event rate for both groups and the sample size.

There are several additional limitations to our study. First, the GTT was designed to be applied across the entirety of a hospitalization. By screening for adverse events over the span of only 12 hours for each hospitalization, the sensitivity of the tool may have been diminished, with a proportion of adverse events not captured, even when the sequence of events leading to patient harm began during the 12 hours in question. Second, this is a retrospective study, and all adverse events may not be documented in the medical record. Third, although not formally structured and infrequent, some evening‐shift providers did send an email or call the oncoming day‐shift provider to discuss patients admitted. This process, however, was provider dependent, unstructured, uncommon, and erratic, and thus we were not able to capture it from medical record review. Finally, the patients in this study were deemed low acuity upon triage prior to admission. A face‐to‐face handoff may be less important in ensuring patient safety when caring for low‐acuity compared to high‐acuity patients, considering the rapidity at which the critically ill can deteriorate.

Handoffs of patient care in the hospital have certainly increased in recent years. Consequently, communication among providers is undoubtedly important, with patient safety being the primary goal. Our work suggests that a face‐to‐face component of a handoff is not vital to ensure a safe care transition. Because of the increasing frequency of handoffs, providers' ability to do so face‐to‐face will likely be challenged by time and logistical constraints. Future work is needed to delineate the most effective components of the handoff so that we can design information transfer that promotes safe and efficient care, even without a face‐to‐face interaction.

Acknowledgements

The authors are grateful for support from the Mayo Clinic Department of Medicine Clinical Research Office, Ms. Donna Lawson, and Mr. Stephen Cha.

Disclosures: This publication was made possible by the Mayo Clinic Center for Clinical and Translational Science through grant number UL1 TR000135 from the National Center for Advancing Translational Science, a component of the National Institutes of Health. The authors report no conflicts of interest.

Handoffs are key events in the care of hospitalized patients whereby vital information is relayed between healthcare providers. Resident duty hour restrictions and the popularity of shift‐based work schedules have increased the frequency of inpatient handoffs.[1, 2] Failures in communication at the time of patient handoff have been implicated as contributing factors to preventable adverse events.[3, 4, 5, 6] With patient safety in mind, accreditation organizations and professional societies have made the standardization of hospital handoff procedures a priority.[7, 8] A variety of strategies have been utilized to standardize handoffs. Examples include the use of mnemonics,[9] electronic resources,[10, 11, 12] preformatted handoff sheets,[13, 14, 15, 16] and optimization of the handoff environment.[17] The primary outcomes for many of these studies center on the provider by measuring their retention of patient facts[18, 19] and completion of tasks[14, 16] after handoff, for example. Few studies examined patient‐centered outcomes such as transfer to a higher level of care,[20] length of stay,[11] mortality,[21] or readmission rate.[22] A study in the pediatric population found that implementation of a handoff bundle was associated with a decrease in medical errors and preventable adverse events.[23]

The Society of Hospital Medicine recommends that patient handoffs consist of both a written and verbal component.[8] Providers in our division work on 3 shifts: day, evening, and night. In 2009, we developed a face‐to‐face morning handoff, during which night‐shift providers hand off patient care to day‐shift providers incorporating an electronically generated service information list.[17] Given that the evening shift ends well before the day shift begins, the evening‐shift providers do not participate in this face‐to‐face handoff of care for patients they admit to day providers.

We wished to compare the clinical outcomes and adverse events of patients admitted by the night‐shift providers to those admitted by the evening‐shift providers. We hypothesized that transfer of care using a face‐to‐face handoff would be associated with fewer adverse events and improved clinical outcomes.

METHODS

The study was deemed exempt by the Mayo Clinic Institutional Review Board.

Study Population

Hospitalists at the study institution, a 1157‐bed academic tertiary referral hospital, admit general medical patients from the emergency department, as transfers from other institutions, and as direct admissions from outpatient offices. Patients included in the study were all adults admitted by evening‐ and night‐shift hospitalists from August 1, 2011 through August 1, 2012 between 6:45 pm and midnight. Our institution primarily uses 2 levels of care for adult inpatients on internal medicine services, including a general care floor for low‐acuity patients and an intensive care unit for high‐acuity patients. All of the patients in this study were triaged as low acuity at the time of admission and were initially admitted to general care units.

Setting

The division's shift schedule during the study period is depicted in Figure 1. Day‐shift providers included a physician and nurse practitioner (NP) or physician assistant (PA) on each of 7 teams. Each service had an average daily patient census between 10 and 15 patients with 3 to 4 new admissions every 24 hours, with 1 to 2 of these admissions occurring during the evening and night shifts, on average. The day shift started at 7:45 am and ended at 7:45 pm, at which time the day teams transitioned care of their patients to 1 of 2 overnight NP/PAs who provided cross‐cover for all teams through the night. The overnight NP/PAs then transitioned care back to the day teams at 7:45 am the following morning.

Figure 1
Provider schedules. Abbreviations: NP, nurse practitioner; PA, physician assistant.

Two evening‐shift providers, both physicians, including a staff hospitalist and a hospital medicine fellowship trainee, admitted patients without any cross‐cover responsibility. Their shifts had the same start time, but staggered end times (2 pm10 pm and 2 pmmidnight). At the end of their shifts, the evening‐shift providers relayed concerns or items for follow‐up to the night cross‐cover NP/PAs; however, this handoff was nonstandardized and provider dependent. The cross‐cover providers could also choose to pass on any relevant information to day‐shift providers if thought to be necessary, but this, again, was not required or standardized. A printed electronic handoff tool (including the patient's problem list, medications, vital signs, laboratory results, and to do list as determined by the admitting provider) as well as all clinical notes generated since admission were made available to day‐shift providers who assumed care at 7:45 am; however, there was no face‐to‐face handoff between the evening‐ and day‐shift providers.

Two night‐shift physicians, including a moonlighting board‐eligible internal medicine physician and staff hospitalist, also started at staggered times, 6:45 pm and 10 pm, but their shifts both ended at 7:45 am. These physicians also admitted patients without cross‐cover responsibilities. At 7:45 am, in a face‐to‐face meeting, they transitioned care of patients admitted overnight to day‐shift providers. This handoff occurred at a predesignated place with assigned start times for each team. During the meeting, printed electronic documents, including the aforementioned electronic handoff tool as well as all clinical notes generated since admission, were made available to the oncoming day‐shift providers. The face‐to‐face interaction between night‐ and day‐shift providers lasted approximately 5 minutes and allowed for a brief presentation of the patient, review of the diagnostic testing and treatments performed so far, as well as anticipatory guidance regarding potential issues throughout the remainder of the hospitalization. Although inclusion of the above components was encouraged during the face‐to‐face handoff, the interaction was not scripted and topics discussed were at the providers' discretion.

Patients admitted during the evening and night shifts were assigned to day‐shift services primarily based on the current census of each team, so as to distribute the workload evenly.

Chart Review

Patients included in the study were admitted by evening‐ or night‐shift providers between 6:45 pm and midnight. This time period accounts for when the evening shift and night shift overlap, allowing for direct comparison of patients admitted during the same time of day, so as to avoid confounding factors. Patients were grouped by whether they were admitted by an evening‐shift provider or a night‐shift provider. Each study patient's chart was retrospectively reviewed and relevant demographic and clinical data were collected. Demographic information included age, gender, and race. Clinical information included medical comorbidities, Charlson Comorbidity Index score, rapid response team calls, code team calls, transfers to a higher level of care, death in hospital, 30‐day readmission rate, length of stay (LOS), and adverse events. The Charlson Comorbidity Index score[24] was determined from diagnoses in the institution's medical index database. The 30‐day readmission rate included observation stays and full hospital admissions that occurred at our institution in the 30 days following the patient's hospital discharge from the index admission. LOS was determined based on the time of admission and discharge, as reported in the hospital billing system, and is reported as the median and mean LOS in hours for all patients in each group.

The Global Trigger Tool (GTT) was used to identify adverse events, as defined within the GTT whitepaper to be unintended physical injury resulting from or contributed to by medical care that requires additional monitoring, treatment or hospitalization, or that results in death.[25] Developed by the Institute for Healthcare Improvement, the GTT uses triggers, clues in the medical record that suggest an adverse event may have occurred, to cue a more detailed chart review. Registered nurses trained in use of the GTT reviewed all of the included patients' electronic medical records. If a trigger was identified (such as a patient fall suffered in the hospital), further chart review was prompted to determine if patient harm occurred. If there was evidence of harm, an adverse event was determined to have occurred and was then categorized using the National Coordinating Council for Medication Error Reporting and Prevention Index for Categorizing Errors.[26] For example, in the case of a patient fall whereby the patient was determined to have fallen in the hospital and suffered a laceration requiring wound care, but the hospital stay was not prolonged, this adverse event was categorized as category E (an adverse event that caused the patient temporary harm necessitating intervention, without prolongation of the hospital stay).

Outcomes including rapid response team calls, code team calls, transfers to a higher level of care, death in the hospital, and adverse events, as identified using the GTT, were counted if they occurred between 7:45 am on the first morning of admission until 12 hours later at 7:45 pm, at the time of the first evening handoff of the admitted patients' care.

Statistical Methods

Study data were collected and managed using REDCap (Research Electronic Data Capture) electronic data capture tools hosted at Mayo Clinic.[27] When comparing outcomes between the 2 groups, Fisher exact test was used for categorical variables and Student t test was used for continuous variables. Global Trigger Tool data were analyzed using the SAS GENMOD procedure, assuming a negative binomial distribution. All the above analyses were performed using SAS version 9.3 software (SAS Institute Inc., Cary, NC). Rates of adverse events were compared using MedCalc version 13 software (MedCalc Software, Ostend, Belgium).[28] A P value <0.05 was considered significant.

RESULTS

Of 805 patients admitted between 6:45 pm and midnight during the study period, 305 (37.9%) patients were handed off to day‐shift providers without face‐to‐face handoff, and 500 (62.1%) patients were transferred to the care of day‐shift providers with the use of a face‐to‐face handoff.

Baseline characteristics of both groups are depicted in Table 1. Demographic characteristics, including age, gender, and race, were not significantly different between groups. The mean Charlson Comorbidity Index score was not significantly different between the groups without and with a face‐to‐face handoff. In addition, the presence of medical comorbidities including type 2 diabetes mellitus, hypertension, coronary artery disease, hyperlipidemia, heart failure, body mass index (BMI) <18, active cancer, and current cigarette smoking were not significantly different between the 2 groups. There was a trend to a significantly increased proportion of patients with a BMI >30 in the group without face‐to‐face handoff (P=0.05).

Baseline Patient Characteristics
 Without Face‐to‐Face Handoff, N=305With Face‐to‐Face Handoff, N=500P Value
  • NOTE: Abbreviations: BMI, body mass index; SD, standard deviation.

Age, y, mean (SD)65.8 (19.0)64.2 (20.0)0.25
Sex, n (%)  0.69
Female166 (54%)265 (53%) 
Male139 (46%)235 (47%) 
Race, n (%)  0.94
White287 (95%)466 (93%) 
African American5 (2%)9 (2%) 
Arab/Middle Eastern3 (1%)8 (2%) 
Asian1 (0%)3 (1%) 
Indian subcontinental1 (0%)1 (0%) 
American Indian/Alaskan1 (0%)1 (0%) 
Other3 (1%)8 (2%) 
Unknown1 (0%)4 (1%) 
Charlson Comorbidity Index, mean ( SD)2.98 ( 3.73)2.93 ( 3.72)0.85
Comorbidities, n (%)   
Type 2 diabetes82 (27%)143 (29%)0.60
Hypertension195 (64%)303 (61%)0.34
Coronary artery disease76 (25%)137 (27%)0.44
Hyperlipidemia122 (40%)206 (41%)0.74
Heart failure30 (10%)66 (13%)0.15
BMI >30109 (36%)146 (29%)0.05
BMI <187 (2%)12 (2%)0.92
Active cancer29 (10%)46 (9%)0.88
Current smoker49 (16%)90 (18%)0.48

Results for the outcomes of this study are depicted in Table 2. The frequency of rapid response team calls, code team calls, transfers to a higher level of care, and death in the hospital in the 12 hours following the first morning handoff of the admission were not significantly different between the 2 groups. Both 30‐day readmission rate and LOS (median and mean) were not significantly different between groups.

Patient Outcomes
 Without Face‐to‐Face Handoff, N=305With Face‐to‐Face Handoff, N=500P Value
  • NOTE: Abbreviations: IQR, interquartile range; SD, standard deviation.

  • Global Trigger Tool adverse events were categorized by the National Coordinating Council for Medication Error Reporting and Prevention Index for Categorizing Medication Errors, using categories E through I.

Rapid response team call, n (%)4 (1%)5 (1%)0.68
Code team call, n (%)0 (0%)1 (0%)0.43
Transfer to higher level of care, n (%)7 (2%)11 (2%)0.93
Patient death, n (%)0 (0%)0 (0%)1.00
30‐day readmission, n (%)50 (16%)67 (13%)0.23
Hospital length of stay   
Median, h (IQR)66.5 (41.3115.6)70.3 (41.9131.2)0.30
Mean, h ( SD)102.0 ( 110.0)102.9 ( 94.0)0.90
Adverse events (Global Trigger Tool)
Temporary harm and required intervention (E)470.92
Temporary harm and required initial or prolonged hospitalization (F)780.53
Permanent harm (G)010.44
Intervention required to sustain life (H)060.14
Death (I)001.00
Total adverse events per 100 admissions3.614.400.59
% of admissions with an adverse event2.6%3.2%0.64

There was no significant difference between the 2 groups in the frequency of adverse events resulting in harm for any of the categories (categories EI). Total adverse events between groups were also compared. Adverse events per 100 admissions were not significantly different between the group without face‐to‐face handoff compared to the group with face‐to‐face handoff. The percentage of admissions with an adverse event was also similar between groups.

DISCUSSION

We found no significant difference in the rate of rapid response team calls, code team calls, transfers to a higher level of care, death in hospital, or adverse events when comparing patients transitioned to the care of day‐shift providers with or without a face‐to‐face handoff. We hypothesize that a reason adverse events were no different between the 2 groups may be that providers were more vigilant when they did not receive a face‐to‐face handoff from the previous provider. As a result, providers may have dedicated additional time reviewing the medical record, speaking with the patients, and communicating with other healthcare providers to ensure a safe care transition. Similarly, other studies found no significant reduction in adverse events when using a standardized handoff.[10, 13, 29] This may be because patient handoff is 1 of a multitude of factors that impact the rate of adverse events, and a handoff may play a less vital role in a system where documentation of care for a given patient is readily accessible, uniform, and detailed. A face‐to‐face interaction itself in a patient handoff may be less pertinent if key information can be communicated through other channels, such as an electronic handoff tool, email, or phone.

Another potential explanation for the lack of a significant difference in patient outcomes with and without a face‐to‐face handoff is related to the study design and inherent rate of the events measured. With the exception of 30‐day readmission rate and LOS, the outcomes of the study were recorded only if they occurred in the 12 hours following the first morning handoff of the admission. This was done in an attempt to isolate the effect of the nonface‐to‐face versus face‐to‐face handoff on the first morning of the admission, and to avoid confounding effects by subsequent transitions of care later in the hospitalization. The frequency of hospital admissions in which an adverse event occurred during this relatively short 12‐hour window was approximately 3% for all patients in the study. With 805 total patients in the study, there may have been insufficient statistical power to detect a difference in the rate of outcomes, if a difference did exist, considering the event rate for both groups and the sample size.

There are several additional limitations to our study. First, the GTT was designed to be applied across the entirety of a hospitalization. By screening for adverse events over the span of only 12 hours for each hospitalization, the sensitivity of the tool may have been diminished, with a proportion of adverse events not captured, even when the sequence of events leading to patient harm began during the 12 hours in question. Second, this is a retrospective study, and all adverse events may not be documented in the medical record. Third, although not formally structured and infrequent, some evening‐shift providers did send an email or call the oncoming day‐shift provider to discuss patients admitted. This process, however, was provider dependent, unstructured, uncommon, and erratic, and thus we were not able to capture it from medical record review. Finally, the patients in this study were deemed low acuity upon triage prior to admission. A face‐to‐face handoff may be less important in ensuring patient safety when caring for low‐acuity compared to high‐acuity patients, considering the rapidity at which the critically ill can deteriorate.

Handoffs of patient care in the hospital have certainly increased in recent years. Consequently, communication among providers is undoubtedly important, with patient safety being the primary goal. Our work suggests that a face‐to‐face component of a handoff is not vital to ensure a safe care transition. Because of the increasing frequency of handoffs, providers' ability to do so face‐to‐face will likely be challenged by time and logistical constraints. Future work is needed to delineate the most effective components of the handoff so that we can design information transfer that promotes safe and efficient care, even without a face‐to‐face interaction.

Acknowledgements

The authors are grateful for support from the Mayo Clinic Department of Medicine Clinical Research Office, Ms. Donna Lawson, and Mr. Stephen Cha.

Disclosures: This publication was made possible by the Mayo Clinic Center for Clinical and Translational Science through grant number UL1 TR000135 from the National Center for Advancing Translational Science, a component of the National Institutes of Health. The authors report no conflicts of interest.

References
  1. Desai SV, Feldman L, Brown L, et al. Effect of the 2011 vs 2003 duty hour regulation‐compliant models on sleep duration, trainee education, and continuity of patient care among internal medicine house staff: a randomized trial. JAMA Intern Med. 2013;173(8):649655.
  2. Robeznieks A. 'Shift work': 24‐hour workdays are out as residents, hospitals deal with changes, mixed feelings on restrictions. Mod Healthc. 2011;41(30):67, 16, 1.
  3. Horwitz LI, Moin T, Krumholz HM, Wang L, Bradley EH. Consequences of inadequate sign‐out for patient care. Arch Intern Med. 2008;168(16):17551760.
  4. Arora V, Johnson J, Lovinger D, Humphrey HJ, Meltzer DO. Communication failures in patient sign‐out and suggestions for improvement: a critical incident analysis. Qual Saf Health Care. 2005;14(6):401407.
  5. Singh H, Thomas EJ, Petersen LA, Studdert DM. Medical errors involving trainees: a study of closed malpractice claims from 5 insurers. Archives of internal medicine. 2007;167(19):20302036.
  6. Greenberg CC, Regenbogen SE, Studdert DM, et al. Patterns of communication breakdowns resulting in injury to surgical patients. J Am Coll Surg. 2007;204(4):533540.
  7. Joint Commission International. Standard PC.02.02.01. 2013 Hospital Accreditation Standards. Oak Brook, IL: Joint Commission Resources; 2013.
  8. Arora VM, Manjarrez E, Dressler DD, Basaviah P, Halasyamani L, Kripalani S. Hospitalist handoffs: a systematic review and task force recommendations. J Hosp Med. 2009;4(7):433440.
  9. Riesenberg LA, Leitzsch J, Little BW. Systematic review of handoff mnemonics literature. Am J Med Qual. 2009;24(3):196204.
  10. Petersen LA, Orav EJ, Teich JM, O'Neil AC, Brennan TA. Using a computerized sign‐out program to improve continuity of inpatient care and prevent adverse events. Jt Comm J Qual Improv. 1998;24(2):7787.
  11. Ryan S, O'Riordan JM, Tierney S, Conlon KC, Ridgway PF. Impact of a new electronic handover system in surgery. Int J Surg. 2011;9(3):217220.
  12. Eaton EG, Horvath KD, Lober WB, Pellegrini CA. Organizing the transfer of patient care information: the development of a computerized resident sign‐out system. Surgery. 2004;136(1):513.
  13. Zavalkoff SR, Razack SI, Lavoie J, Dancea AB. Handover after pediatric heart surgery: a simple tool improves information exchange. Pediatr Crit Care Med. 2011;12(3):309313.
  14. Wayne JD, Tyagi R, Reinhardt G, et al. Simple standardized patient handoff system that increases accuracy and completeness. J Surg Educ. 2008;65(6):476485.
  15. Stahl K, Palileo A, Schulman CI, et al. Enhancing patient safety in the trauma/surgical intensive care unit. J Trauma. 2009;67(3):430433; discussion 433–435.
  16. Salerno SM, Arnett MV, Domanski JP. Standardized sign‐out reduces intern perception of medical errors on the general internal medicine ward. Teach Learn Med. 2009;21(2):121126.
  17. Burton MC, Kashiwagi DT, Kirkland LL, Manning D, Varkey P. Gaining efficiency and satisfaction in the handoff process. J Hosp Med. 2010;5(9):547552.
  18. Pickering BW, Hurley K, Marsh B. Identification of patient information corruption in the intensive care unit: using a scoring tool to direct quality improvements in handover. Crit Care Med. 2009;37(11):29052912.
  19. Dowding D. Examining the effects that manipulating information given in the change of shift report has on nurses' care planning ability. J Adv Nurs. 2001;33(6):836846.
  20. Horwitz LI, Parwani V, Shah NR, et al. Evaluation of an asynchronous physician voicemail sign‐out for emergency department admissions. Ann Emerg Med. 2009;54(3):368378.
  21. Mazzocco K, Petitti DB, Fong KT, et al. Surgical team behaviors and patient outcomes. Am J Surg. 2009;197(5):678685.
  22. Hess DR, Tokarczyk A, O'Malley M, Gavaghan S, Sullivan J, Schmidt U. The value of adding a verbal report to written handoffs on early readmission following prolonged respiratory failure. Chest. 2010;138(6):14751479.
  23. Starmer AJ, Sectish TC, Simon DW, et al. Rates of medical errors and preventable adverse events among hospitalized children following implementation of a resident handoff bundle. JAMA. 2013;310(21):22622270.
  24. Charlson ME, Pompei P, Ales KL, MacKenzie CR. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis. 1987;40(5):373383.
  25. Griffin FA, Resar RK. IHI Global Trigger Tool for measuring adverse events (second edition). IHI Innovation Series white paper. Cambridge, MA: Institute for Healthcare Improvement; 2009. Available at: http://www.ihi.org/resources/Pages/IHIWhitePapers/IHIGlobalTriggerToolWhitePaper.aspx. www.IHI.org). Accessed June 1, 2014.
  26. National Coordinating Council for Medication Error Reporting and Prevention (NCC MERP) index for categorizing errors. Available at: http://www.nccmerp.org/medErrorCatIndex.html. Accessed June 1, 2014.
  27. Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG. Research electronic data capture (REDCap)—a metadata‐driven methodology and workflow process for providing translational research informatics support. J Biomed Inform. 2009;42(2):377381.
  28. Sahai H, Khurshid A. Statistics in Epidemiology: Methods, Techniques, and Applications. Boca Raton, FL: CRC Press; 1996.
  29. Eaton EG, McDonough K, Lober WB, Johnson EA, Pellegrini CA, Horvath KD. Safety of using a computerized rounding and sign‐out system to reduce resident duty hours. Acad Med. 2010;85(7):11891195.
References
  1. Desai SV, Feldman L, Brown L, et al. Effect of the 2011 vs 2003 duty hour regulation‐compliant models on sleep duration, trainee education, and continuity of patient care among internal medicine house staff: a randomized trial. JAMA Intern Med. 2013;173(8):649655.
  2. Robeznieks A. 'Shift work': 24‐hour workdays are out as residents, hospitals deal with changes, mixed feelings on restrictions. Mod Healthc. 2011;41(30):67, 16, 1.
  3. Horwitz LI, Moin T, Krumholz HM, Wang L, Bradley EH. Consequences of inadequate sign‐out for patient care. Arch Intern Med. 2008;168(16):17551760.
  4. Arora V, Johnson J, Lovinger D, Humphrey HJ, Meltzer DO. Communication failures in patient sign‐out and suggestions for improvement: a critical incident analysis. Qual Saf Health Care. 2005;14(6):401407.
  5. Singh H, Thomas EJ, Petersen LA, Studdert DM. Medical errors involving trainees: a study of closed malpractice claims from 5 insurers. Archives of internal medicine. 2007;167(19):20302036.
  6. Greenberg CC, Regenbogen SE, Studdert DM, et al. Patterns of communication breakdowns resulting in injury to surgical patients. J Am Coll Surg. 2007;204(4):533540.
  7. Joint Commission International. Standard PC.02.02.01. 2013 Hospital Accreditation Standards. Oak Brook, IL: Joint Commission Resources; 2013.
  8. Arora VM, Manjarrez E, Dressler DD, Basaviah P, Halasyamani L, Kripalani S. Hospitalist handoffs: a systematic review and task force recommendations. J Hosp Med. 2009;4(7):433440.
  9. Riesenberg LA, Leitzsch J, Little BW. Systematic review of handoff mnemonics literature. Am J Med Qual. 2009;24(3):196204.
  10. Petersen LA, Orav EJ, Teich JM, O'Neil AC, Brennan TA. Using a computerized sign‐out program to improve continuity of inpatient care and prevent adverse events. Jt Comm J Qual Improv. 1998;24(2):7787.
  11. Ryan S, O'Riordan JM, Tierney S, Conlon KC, Ridgway PF. Impact of a new electronic handover system in surgery. Int J Surg. 2011;9(3):217220.
  12. Eaton EG, Horvath KD, Lober WB, Pellegrini CA. Organizing the transfer of patient care information: the development of a computerized resident sign‐out system. Surgery. 2004;136(1):513.
  13. Zavalkoff SR, Razack SI, Lavoie J, Dancea AB. Handover after pediatric heart surgery: a simple tool improves information exchange. Pediatr Crit Care Med. 2011;12(3):309313.
  14. Wayne JD, Tyagi R, Reinhardt G, et al. Simple standardized patient handoff system that increases accuracy and completeness. J Surg Educ. 2008;65(6):476485.
  15. Stahl K, Palileo A, Schulman CI, et al. Enhancing patient safety in the trauma/surgical intensive care unit. J Trauma. 2009;67(3):430433; discussion 433–435.
  16. Salerno SM, Arnett MV, Domanski JP. Standardized sign‐out reduces intern perception of medical errors on the general internal medicine ward. Teach Learn Med. 2009;21(2):121126.
  17. Burton MC, Kashiwagi DT, Kirkland LL, Manning D, Varkey P. Gaining efficiency and satisfaction in the handoff process. J Hosp Med. 2010;5(9):547552.
  18. Pickering BW, Hurley K, Marsh B. Identification of patient information corruption in the intensive care unit: using a scoring tool to direct quality improvements in handover. Crit Care Med. 2009;37(11):29052912.
  19. Dowding D. Examining the effects that manipulating information given in the change of shift report has on nurses' care planning ability. J Adv Nurs. 2001;33(6):836846.
  20. Horwitz LI, Parwani V, Shah NR, et al. Evaluation of an asynchronous physician voicemail sign‐out for emergency department admissions. Ann Emerg Med. 2009;54(3):368378.
  21. Mazzocco K, Petitti DB, Fong KT, et al. Surgical team behaviors and patient outcomes. Am J Surg. 2009;197(5):678685.
  22. Hess DR, Tokarczyk A, O'Malley M, Gavaghan S, Sullivan J, Schmidt U. The value of adding a verbal report to written handoffs on early readmission following prolonged respiratory failure. Chest. 2010;138(6):14751479.
  23. Starmer AJ, Sectish TC, Simon DW, et al. Rates of medical errors and preventable adverse events among hospitalized children following implementation of a resident handoff bundle. JAMA. 2013;310(21):22622270.
  24. Charlson ME, Pompei P, Ales KL, MacKenzie CR. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis. 1987;40(5):373383.
  25. Griffin FA, Resar RK. IHI Global Trigger Tool for measuring adverse events (second edition). IHI Innovation Series white paper. Cambridge, MA: Institute for Healthcare Improvement; 2009. Available at: http://www.ihi.org/resources/Pages/IHIWhitePapers/IHIGlobalTriggerToolWhitePaper.aspx. www.IHI.org). Accessed June 1, 2014.
  26. National Coordinating Council for Medication Error Reporting and Prevention (NCC MERP) index for categorizing errors. Available at: http://www.nccmerp.org/medErrorCatIndex.html. Accessed June 1, 2014.
  27. Harris PA, Taylor R, Thielke R, Payne J, Gonzalez N, Conde JG. Research electronic data capture (REDCap)—a metadata‐driven methodology and workflow process for providing translational research informatics support. J Biomed Inform. 2009;42(2):377381.
  28. Sahai H, Khurshid A. Statistics in Epidemiology: Methods, Techniques, and Applications. Boca Raton, FL: CRC Press; 1996.
  29. Eaton EG, McDonough K, Lober WB, Johnson EA, Pellegrini CA, Horvath KD. Safety of using a computerized rounding and sign‐out system to reduce resident duty hours. Acad Med. 2010;85(7):11891195.
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ACP guidelines for preventing, treating pressure ulcers

‘Dire’ need for good science
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ACP guidelines for preventing, treating pressure ulcers

Alternating-air and low-air-loss mattresses and overlays have little data to support their use for preventing or treating pressure ulcers, the Clinical Guidelines Committee of the American College of Physicians has concluded.

Many U.S. acute-care hospitals, home caregivers, and long-term nursing facilities use alternating-air and low-air-loss mattresses and overlays, even though the evidence in favor of using these surfaces is sparse and of poor quality, the guideline writers said.

The devices have not been show to actually reduce pressure ulcers. The harms have been poorly reported but could be significant. “Using these support systems is expensive and adds unnecessary burden on the health care system. Based on a review of the current evidence, lower-cost support surfaces should be the preferred approach to care,” Dr. Amir Qaseem, of the ACP, Philadelphia, and his associates wrote.

The committee performed an extensive review of the literature on pressure ulcers and compiled two Clinical Practice Guidelines – one concerning prevention (Ann. Intern. Med. 2015;162 [doi:10.7326/M14-1567]) and the other concerning treatment (Ann. Intern. Med. 2015;162 [doi:10.7326/M14-1568]) – in part because “a growing industry” has developed in recent years and aggressively pitches a wide array of products for this patient population. The guidelines present the available evidence on the comparative effectiveness of tools and strategies but state repeatedly that evidence regarding pressure ulcers is sparse and of poor quality.

The prevention guideline strongly recommends that clinicians choose advanced static mattresses or advanced static overlays rather than standard hospital mattresses for at-risk patients. Static mattresses and advanced static overlays provide a constant level of inflation or support and evenly distribute body weight. These products are among the few actually shown to reduce the incidence of pressure ulcers. They are also preferable to alternating-air mattresses and overlays, which change the distribution of pressure by inflating or deflating cells within the devices, and to low-air-loss mattresses and overlays, which use flowing air to regulate heat and humidity and adjust pressure.

Evidence is similarly poor or lacking concerning the use of other support surfaces such as heel supports or boots and a variety of wheelchair cushions. Also lacking evidence are other preventive interventions that extend beyond “usual care,” such as different types of repositioning schemes, a variety of leg elevations, various nutritional supplements, and a wide variety of skin care strategies and topical treatments.

The prevention guideline advises patient assessments to identify those at risk of developing pressure ulcers. However, there is not enough evidence to demonstrate that any one of the many risk assessment tools for this purpose is superior to the others, nor that any of these tools is superior to simple clinical judgment. Risk factors for pressure ulcers include older age; black race or Hispanic ethnicity; low body weight; cognitive impairment; physical impairments; and comorbid conditions that may affect soft-tissue integrity and healing, such as urinary or fecal incontinence, diabetes, edema, impaired microcirculation, hypoalbuminemia, and malnutrition, Dr. Qaseem and his associates wrote (Ann. Intern. Med. 2015 March 2 [doi:10.7326/M14-1567]).

The treatment guideline for patients who already have pressure ulcers similarly notes that the lack of evidence for advanced support surfaces such as alternating-air and low-air-loss mattresses and overlays. It similarly recommends advanced static mattresses or overlays for these patients.

The treatment guideline recommends protein or amino acid supplements as well as hydrocolloid or foam dressings to reduce wound size, and electrical stimulation to accelerate wound healing. The evidence for these recommendations is “weak” and of low- to moderate-quality, Dr. Qaseem and his associates said (Ann. Intern. Med. 2015 March 2 [doi:10.7326/M14-1568]).

The evidence for the safety and efficacy of hyperbaric oxygen therapy, even though it is often used to treat pressure ulcers in hospitals, is similarly inconclusive. Also lacking good-quality evidence are the use of alternating-air chair cushions, three-dimensional polyester overlays, zinc supplements, L-carnosine supplements, wound dressings other than the ones already discussed, debriding enzymes, topical phenytoin, maggot therapy, biological agents other than platelet-derived growth factor, or hydrotherapy in which wounds are cleaned using a whirlpool or pulsed lavage.

References

Body

These guidelines emphasize the dire need for good science to guide both prevention and treatment of pressure ulcers. Despite the ubiquity of pressure ulcers and their potential to threaten life and limb, clinical management varies greatly. Most of the research in this field to date has been underpowered and focused on early signs of healing rather than on more definitive outcomes.

Joyce Black, Ph.D., R.N., is at the University of Nebraska Medical Center, Omaha. Her financial disclosures are available at www.acponline.org. Dr. Black made these remarks in an editorial accompanying the ACP Clinical Practice Guidelines on prevention and treatment of pressure ulcers (Ann. Intern. Med. 2015 March 2 [doi:10.1326/M15-0190]).

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Body

These guidelines emphasize the dire need for good science to guide both prevention and treatment of pressure ulcers. Despite the ubiquity of pressure ulcers and their potential to threaten life and limb, clinical management varies greatly. Most of the research in this field to date has been underpowered and focused on early signs of healing rather than on more definitive outcomes.

Joyce Black, Ph.D., R.N., is at the University of Nebraska Medical Center, Omaha. Her financial disclosures are available at www.acponline.org. Dr. Black made these remarks in an editorial accompanying the ACP Clinical Practice Guidelines on prevention and treatment of pressure ulcers (Ann. Intern. Med. 2015 March 2 [doi:10.1326/M15-0190]).

Body

These guidelines emphasize the dire need for good science to guide both prevention and treatment of pressure ulcers. Despite the ubiquity of pressure ulcers and their potential to threaten life and limb, clinical management varies greatly. Most of the research in this field to date has been underpowered and focused on early signs of healing rather than on more definitive outcomes.

Joyce Black, Ph.D., R.N., is at the University of Nebraska Medical Center, Omaha. Her financial disclosures are available at www.acponline.org. Dr. Black made these remarks in an editorial accompanying the ACP Clinical Practice Guidelines on prevention and treatment of pressure ulcers (Ann. Intern. Med. 2015 March 2 [doi:10.1326/M15-0190]).

Title
‘Dire’ need for good science
‘Dire’ need for good science

Alternating-air and low-air-loss mattresses and overlays have little data to support their use for preventing or treating pressure ulcers, the Clinical Guidelines Committee of the American College of Physicians has concluded.

Many U.S. acute-care hospitals, home caregivers, and long-term nursing facilities use alternating-air and low-air-loss mattresses and overlays, even though the evidence in favor of using these surfaces is sparse and of poor quality, the guideline writers said.

The devices have not been show to actually reduce pressure ulcers. The harms have been poorly reported but could be significant. “Using these support systems is expensive and adds unnecessary burden on the health care system. Based on a review of the current evidence, lower-cost support surfaces should be the preferred approach to care,” Dr. Amir Qaseem, of the ACP, Philadelphia, and his associates wrote.

The committee performed an extensive review of the literature on pressure ulcers and compiled two Clinical Practice Guidelines – one concerning prevention (Ann. Intern. Med. 2015;162 [doi:10.7326/M14-1567]) and the other concerning treatment (Ann. Intern. Med. 2015;162 [doi:10.7326/M14-1568]) – in part because “a growing industry” has developed in recent years and aggressively pitches a wide array of products for this patient population. The guidelines present the available evidence on the comparative effectiveness of tools and strategies but state repeatedly that evidence regarding pressure ulcers is sparse and of poor quality.

The prevention guideline strongly recommends that clinicians choose advanced static mattresses or advanced static overlays rather than standard hospital mattresses for at-risk patients. Static mattresses and advanced static overlays provide a constant level of inflation or support and evenly distribute body weight. These products are among the few actually shown to reduce the incidence of pressure ulcers. They are also preferable to alternating-air mattresses and overlays, which change the distribution of pressure by inflating or deflating cells within the devices, and to low-air-loss mattresses and overlays, which use flowing air to regulate heat and humidity and adjust pressure.

Evidence is similarly poor or lacking concerning the use of other support surfaces such as heel supports or boots and a variety of wheelchair cushions. Also lacking evidence are other preventive interventions that extend beyond “usual care,” such as different types of repositioning schemes, a variety of leg elevations, various nutritional supplements, and a wide variety of skin care strategies and topical treatments.

The prevention guideline advises patient assessments to identify those at risk of developing pressure ulcers. However, there is not enough evidence to demonstrate that any one of the many risk assessment tools for this purpose is superior to the others, nor that any of these tools is superior to simple clinical judgment. Risk factors for pressure ulcers include older age; black race or Hispanic ethnicity; low body weight; cognitive impairment; physical impairments; and comorbid conditions that may affect soft-tissue integrity and healing, such as urinary or fecal incontinence, diabetes, edema, impaired microcirculation, hypoalbuminemia, and malnutrition, Dr. Qaseem and his associates wrote (Ann. Intern. Med. 2015 March 2 [doi:10.7326/M14-1567]).

The treatment guideline for patients who already have pressure ulcers similarly notes that the lack of evidence for advanced support surfaces such as alternating-air and low-air-loss mattresses and overlays. It similarly recommends advanced static mattresses or overlays for these patients.

The treatment guideline recommends protein or amino acid supplements as well as hydrocolloid or foam dressings to reduce wound size, and electrical stimulation to accelerate wound healing. The evidence for these recommendations is “weak” and of low- to moderate-quality, Dr. Qaseem and his associates said (Ann. Intern. Med. 2015 March 2 [doi:10.7326/M14-1568]).

The evidence for the safety and efficacy of hyperbaric oxygen therapy, even though it is often used to treat pressure ulcers in hospitals, is similarly inconclusive. Also lacking good-quality evidence are the use of alternating-air chair cushions, three-dimensional polyester overlays, zinc supplements, L-carnosine supplements, wound dressings other than the ones already discussed, debriding enzymes, topical phenytoin, maggot therapy, biological agents other than platelet-derived growth factor, or hydrotherapy in which wounds are cleaned using a whirlpool or pulsed lavage.

Alternating-air and low-air-loss mattresses and overlays have little data to support their use for preventing or treating pressure ulcers, the Clinical Guidelines Committee of the American College of Physicians has concluded.

Many U.S. acute-care hospitals, home caregivers, and long-term nursing facilities use alternating-air and low-air-loss mattresses and overlays, even though the evidence in favor of using these surfaces is sparse and of poor quality, the guideline writers said.

The devices have not been show to actually reduce pressure ulcers. The harms have been poorly reported but could be significant. “Using these support systems is expensive and adds unnecessary burden on the health care system. Based on a review of the current evidence, lower-cost support surfaces should be the preferred approach to care,” Dr. Amir Qaseem, of the ACP, Philadelphia, and his associates wrote.

The committee performed an extensive review of the literature on pressure ulcers and compiled two Clinical Practice Guidelines – one concerning prevention (Ann. Intern. Med. 2015;162 [doi:10.7326/M14-1567]) and the other concerning treatment (Ann. Intern. Med. 2015;162 [doi:10.7326/M14-1568]) – in part because “a growing industry” has developed in recent years and aggressively pitches a wide array of products for this patient population. The guidelines present the available evidence on the comparative effectiveness of tools and strategies but state repeatedly that evidence regarding pressure ulcers is sparse and of poor quality.

The prevention guideline strongly recommends that clinicians choose advanced static mattresses or advanced static overlays rather than standard hospital mattresses for at-risk patients. Static mattresses and advanced static overlays provide a constant level of inflation or support and evenly distribute body weight. These products are among the few actually shown to reduce the incidence of pressure ulcers. They are also preferable to alternating-air mattresses and overlays, which change the distribution of pressure by inflating or deflating cells within the devices, and to low-air-loss mattresses and overlays, which use flowing air to regulate heat and humidity and adjust pressure.

Evidence is similarly poor or lacking concerning the use of other support surfaces such as heel supports or boots and a variety of wheelchair cushions. Also lacking evidence are other preventive interventions that extend beyond “usual care,” such as different types of repositioning schemes, a variety of leg elevations, various nutritional supplements, and a wide variety of skin care strategies and topical treatments.

The prevention guideline advises patient assessments to identify those at risk of developing pressure ulcers. However, there is not enough evidence to demonstrate that any one of the many risk assessment tools for this purpose is superior to the others, nor that any of these tools is superior to simple clinical judgment. Risk factors for pressure ulcers include older age; black race or Hispanic ethnicity; low body weight; cognitive impairment; physical impairments; and comorbid conditions that may affect soft-tissue integrity and healing, such as urinary or fecal incontinence, diabetes, edema, impaired microcirculation, hypoalbuminemia, and malnutrition, Dr. Qaseem and his associates wrote (Ann. Intern. Med. 2015 March 2 [doi:10.7326/M14-1567]).

The treatment guideline for patients who already have pressure ulcers similarly notes that the lack of evidence for advanced support surfaces such as alternating-air and low-air-loss mattresses and overlays. It similarly recommends advanced static mattresses or overlays for these patients.

The treatment guideline recommends protein or amino acid supplements as well as hydrocolloid or foam dressings to reduce wound size, and electrical stimulation to accelerate wound healing. The evidence for these recommendations is “weak” and of low- to moderate-quality, Dr. Qaseem and his associates said (Ann. Intern. Med. 2015 March 2 [doi:10.7326/M14-1568]).

The evidence for the safety and efficacy of hyperbaric oxygen therapy, even though it is often used to treat pressure ulcers in hospitals, is similarly inconclusive. Also lacking good-quality evidence are the use of alternating-air chair cushions, three-dimensional polyester overlays, zinc supplements, L-carnosine supplements, wound dressings other than the ones already discussed, debriding enzymes, topical phenytoin, maggot therapy, biological agents other than platelet-derived growth factor, or hydrotherapy in which wounds are cleaned using a whirlpool or pulsed lavage.

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Patient fact sheet on the risks of pneumococcal disease

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The National Foundation for Infectious Diseases offers basic information to share with patients about the risks of pneumococcal disease and the importance of vaccination in at-risk adults and adults over age 65. Get the facts and a handy information sheet for your patients at their web site.

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Patient handout on the importance of vaccines

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The Immunization Action Coalition offers a single-page handout for adult patients on the need for vaccinations and emphasizes that "getting immunized is a lifelong, life-protecting job." To access a copy of the handout for your adult patients, click here.

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Adult vaccination record

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The Centers for Disease Control and Prevention offer a handy adult immunization record that can be easily appended to medical charts. Click here to access a copy of the form. 

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Vaccine storage and handling toolkit

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Vaccine storage and handling toolkit
A free resource from the Centers for Disease Control and Prevention

The Vaccine Storage and Handling Toolkit is based on the recommendations of the Advisory Committee on Immunization Practices (ACIP), the manufacturer's product information and studies from the National Institute for Scientific Technology (NIST). Click here to view or print a free copy of the Toolkit.

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The Vaccine Storage and Handling Toolkit is based on the recommendations of the Advisory Committee on Immunization Practices (ACIP), the manufacturer's product information and studies from the National Institute for Scientific Technology (NIST). Click here to view or print a free copy of the Toolkit.

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Overcoming misconceptions about hospice

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Neurology, like any other field, has its share of tragic and incurable diseases. We do our best to shepherd patients and their families through a disorder by offering advice, symptomatic treatment, Family and Medical Leave Act signatures, and a shoulder.

But, inevitably, we come down to one of the most difficult discussions: the end game.

Hospice is never an easy subject to raise. I try to initiate the discussion in advance, so that the decisions and paperwork are in place.

One of the hardest parts is the misconception that hospice means you’re giving up: giving up on caring, giving up on hoping, giving up on treating. I work to try and overcome this.

Hospice may be a change in the treatment plan, but it’s still part of treatment. Finding a way to relieve suffering and provide comfortable surroundings in the final days, while often overlooked, is very important. Peace at a difficult time is sorely needed, more so than another round of tests or invasive procedures.

Yet, it’s not seen that way. Maybe this is cultural. Here, medicine is seen as a cutting-edge field, where there’s always something else that can be done: more scans, another hi-tech bioengineered drug, or some sort of amazing interventional procedure. Although we usually think of all the things we can do, it’s equally important to focus on what we should do. They aren’t always the same – a point that’s often lost.

Sometimes the best thing to do is … everything you can to just make someone comfortable. That’s not giving up. It’s recognizing when it becomes the right decision for the patient and not their family, friends, or anyone else. The patient is the one who really matters.

In an age when newer and flashier facilities and treatments are promoted, keeping the patient’s best interests in mind is critical. Sometimes we get blindsided by the amazing breakthroughs we didn’t have 20, 10, even 5 years ago. So we need to recognize when the best treatment is … to stop.

Quality of life extends all the way up to the moment of death. Part of our job is to keep the Grim Reaper away, but we inevitably lose. It is equally important, though, and sometimes forgotten, to keep the patient as comfortable as possible on the journey. And that isn’t giving up.

Dr. Block has a solo neurology practice in Scottsdale, Ariz.

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Neurology, like any other field, has its share of tragic and incurable diseases. We do our best to shepherd patients and their families through a disorder by offering advice, symptomatic treatment, Family and Medical Leave Act signatures, and a shoulder.

But, inevitably, we come down to one of the most difficult discussions: the end game.

Hospice is never an easy subject to raise. I try to initiate the discussion in advance, so that the decisions and paperwork are in place.

One of the hardest parts is the misconception that hospice means you’re giving up: giving up on caring, giving up on hoping, giving up on treating. I work to try and overcome this.

Hospice may be a change in the treatment plan, but it’s still part of treatment. Finding a way to relieve suffering and provide comfortable surroundings in the final days, while often overlooked, is very important. Peace at a difficult time is sorely needed, more so than another round of tests or invasive procedures.

Yet, it’s not seen that way. Maybe this is cultural. Here, medicine is seen as a cutting-edge field, where there’s always something else that can be done: more scans, another hi-tech bioengineered drug, or some sort of amazing interventional procedure. Although we usually think of all the things we can do, it’s equally important to focus on what we should do. They aren’t always the same – a point that’s often lost.

Sometimes the best thing to do is … everything you can to just make someone comfortable. That’s not giving up. It’s recognizing when it becomes the right decision for the patient and not their family, friends, or anyone else. The patient is the one who really matters.

In an age when newer and flashier facilities and treatments are promoted, keeping the patient’s best interests in mind is critical. Sometimes we get blindsided by the amazing breakthroughs we didn’t have 20, 10, even 5 years ago. So we need to recognize when the best treatment is … to stop.

Quality of life extends all the way up to the moment of death. Part of our job is to keep the Grim Reaper away, but we inevitably lose. It is equally important, though, and sometimes forgotten, to keep the patient as comfortable as possible on the journey. And that isn’t giving up.

Dr. Block has a solo neurology practice in Scottsdale, Ariz.

Neurology, like any other field, has its share of tragic and incurable diseases. We do our best to shepherd patients and their families through a disorder by offering advice, symptomatic treatment, Family and Medical Leave Act signatures, and a shoulder.

But, inevitably, we come down to one of the most difficult discussions: the end game.

Hospice is never an easy subject to raise. I try to initiate the discussion in advance, so that the decisions and paperwork are in place.

One of the hardest parts is the misconception that hospice means you’re giving up: giving up on caring, giving up on hoping, giving up on treating. I work to try and overcome this.

Hospice may be a change in the treatment plan, but it’s still part of treatment. Finding a way to relieve suffering and provide comfortable surroundings in the final days, while often overlooked, is very important. Peace at a difficult time is sorely needed, more so than another round of tests or invasive procedures.

Yet, it’s not seen that way. Maybe this is cultural. Here, medicine is seen as a cutting-edge field, where there’s always something else that can be done: more scans, another hi-tech bioengineered drug, or some sort of amazing interventional procedure. Although we usually think of all the things we can do, it’s equally important to focus on what we should do. They aren’t always the same – a point that’s often lost.

Sometimes the best thing to do is … everything you can to just make someone comfortable. That’s not giving up. It’s recognizing when it becomes the right decision for the patient and not their family, friends, or anyone else. The patient is the one who really matters.

In an age when newer and flashier facilities and treatments are promoted, keeping the patient’s best interests in mind is critical. Sometimes we get blindsided by the amazing breakthroughs we didn’t have 20, 10, even 5 years ago. So we need to recognize when the best treatment is … to stop.

Quality of life extends all the way up to the moment of death. Part of our job is to keep the Grim Reaper away, but we inevitably lose. It is equally important, though, and sometimes forgotten, to keep the patient as comfortable as possible on the journey. And that isn’t giving up.

Dr. Block has a solo neurology practice in Scottsdale, Ariz.

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Telemedicine: Tuning in to teens

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Telemedicine: Tuning in to teens

Times are changing! To compete in to today’s times, doctors are faced with the challenge of seeing 30-plus patients per day, keeping the wait times down, adhering to the meaningful use guidelines – all while participating in the endless maintenance of certification activities. But like it or not, medicine has changed, and you have to keep up or you likely are going to be left behind.

Pediatricians and family physicians more than other specialties are inundated with phone calls and lengthy conversations on constipation and congestion. Most of us just take the call with a smile, and chalk it up to part of the job. But what if you could provide a service that allowed you to get paid for those lengthy conversations, offered the convenience of a consultation without the patient having to come in the office – without the risk of your giving faulty advice because you haven’t actually evaluated the patient. Well, that’s what telemedicine has to offer. For a nominal monthly fee, your patients can subscribe to your “virtual” office. Whether you schedule during your office hours or set aside time before or after clinic, you now can capture a whole new clientele.

Dr. Francine Pearce

For teens, access to their doctors through their electronic devices would provide the convenience they need. Even if the issue cannot be treated without a visit, it allows for early evaluation. Acne, skin rashes, emotional issues, menstrual issues, hair issues, weight issues – all of these can be addressed via telemedicine.

The American Academy of Pediatrics’ Section on Telehealth Care (SOTC) helps guide you on how to bill for telemedicine services. It provides newsletters, educational series, and liability information. Much of the concern with telemedicine is the inconsistency of reimbursement for the service, but things are changing, and more and more of these services are being recognized for their value in meeting the needs of the patient.

There are different products on the market to assist you in setting up your virtual office. Understanding the differences in services is important. Services such as Doctor on Demand have a team of doctors available for fee-for-consult, at approximately $40. Other services, such as myowndoctor.com, set up a virtual office for you, which allows more of a concierge type service for a nominal monthly fee – approximately the amount of a copay – to allow patients access to the telemedicine service with their own physicians. This a great option that can create a cash revenue for you and broader access to patients.

There are several services provided by insurance companies – MDLIVE (Cigna), LiveHealth Online (WellPoint), and Online Care Anywhere (BC/BS Minnesota) – where providers are reimbursed at $45-$49 per visit. What is important to know when choosing a company is to be sure that the software is HIPAA (Health Insurance Portability and Accountability Act) compliant. Currently there are more than 15 companies on the market, and many more to come.

Staying up with the times is going to be key in surviving the current changes in health care. Teens in particular are a difficult group to access, but telemedicine provides that access and the comfort in continuity of care with their own physicians.

Dr. Pearce is a pediatrician in Frankfort, Ill. She said she had no relevant financial disclosures. E-mail her at [email protected].

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Times are changing! To compete in to today’s times, doctors are faced with the challenge of seeing 30-plus patients per day, keeping the wait times down, adhering to the meaningful use guidelines – all while participating in the endless maintenance of certification activities. But like it or not, medicine has changed, and you have to keep up or you likely are going to be left behind.

Pediatricians and family physicians more than other specialties are inundated with phone calls and lengthy conversations on constipation and congestion. Most of us just take the call with a smile, and chalk it up to part of the job. But what if you could provide a service that allowed you to get paid for those lengthy conversations, offered the convenience of a consultation without the patient having to come in the office – without the risk of your giving faulty advice because you haven’t actually evaluated the patient. Well, that’s what telemedicine has to offer. For a nominal monthly fee, your patients can subscribe to your “virtual” office. Whether you schedule during your office hours or set aside time before or after clinic, you now can capture a whole new clientele.

Dr. Francine Pearce

For teens, access to their doctors through their electronic devices would provide the convenience they need. Even if the issue cannot be treated without a visit, it allows for early evaluation. Acne, skin rashes, emotional issues, menstrual issues, hair issues, weight issues – all of these can be addressed via telemedicine.

The American Academy of Pediatrics’ Section on Telehealth Care (SOTC) helps guide you on how to bill for telemedicine services. It provides newsletters, educational series, and liability information. Much of the concern with telemedicine is the inconsistency of reimbursement for the service, but things are changing, and more and more of these services are being recognized for their value in meeting the needs of the patient.

There are different products on the market to assist you in setting up your virtual office. Understanding the differences in services is important. Services such as Doctor on Demand have a team of doctors available for fee-for-consult, at approximately $40. Other services, such as myowndoctor.com, set up a virtual office for you, which allows more of a concierge type service for a nominal monthly fee – approximately the amount of a copay – to allow patients access to the telemedicine service with their own physicians. This a great option that can create a cash revenue for you and broader access to patients.

There are several services provided by insurance companies – MDLIVE (Cigna), LiveHealth Online (WellPoint), and Online Care Anywhere (BC/BS Minnesota) – where providers are reimbursed at $45-$49 per visit. What is important to know when choosing a company is to be sure that the software is HIPAA (Health Insurance Portability and Accountability Act) compliant. Currently there are more than 15 companies on the market, and many more to come.

Staying up with the times is going to be key in surviving the current changes in health care. Teens in particular are a difficult group to access, but telemedicine provides that access and the comfort in continuity of care with their own physicians.

Dr. Pearce is a pediatrician in Frankfort, Ill. She said she had no relevant financial disclosures. E-mail her at [email protected].

Times are changing! To compete in to today’s times, doctors are faced with the challenge of seeing 30-plus patients per day, keeping the wait times down, adhering to the meaningful use guidelines – all while participating in the endless maintenance of certification activities. But like it or not, medicine has changed, and you have to keep up or you likely are going to be left behind.

Pediatricians and family physicians more than other specialties are inundated with phone calls and lengthy conversations on constipation and congestion. Most of us just take the call with a smile, and chalk it up to part of the job. But what if you could provide a service that allowed you to get paid for those lengthy conversations, offered the convenience of a consultation without the patient having to come in the office – without the risk of your giving faulty advice because you haven’t actually evaluated the patient. Well, that’s what telemedicine has to offer. For a nominal monthly fee, your patients can subscribe to your “virtual” office. Whether you schedule during your office hours or set aside time before or after clinic, you now can capture a whole new clientele.

Dr. Francine Pearce

For teens, access to their doctors through their electronic devices would provide the convenience they need. Even if the issue cannot be treated without a visit, it allows for early evaluation. Acne, skin rashes, emotional issues, menstrual issues, hair issues, weight issues – all of these can be addressed via telemedicine.

The American Academy of Pediatrics’ Section on Telehealth Care (SOTC) helps guide you on how to bill for telemedicine services. It provides newsletters, educational series, and liability information. Much of the concern with telemedicine is the inconsistency of reimbursement for the service, but things are changing, and more and more of these services are being recognized for their value in meeting the needs of the patient.

There are different products on the market to assist you in setting up your virtual office. Understanding the differences in services is important. Services such as Doctor on Demand have a team of doctors available for fee-for-consult, at approximately $40. Other services, such as myowndoctor.com, set up a virtual office for you, which allows more of a concierge type service for a nominal monthly fee – approximately the amount of a copay – to allow patients access to the telemedicine service with their own physicians. This a great option that can create a cash revenue for you and broader access to patients.

There are several services provided by insurance companies – MDLIVE (Cigna), LiveHealth Online (WellPoint), and Online Care Anywhere (BC/BS Minnesota) – where providers are reimbursed at $45-$49 per visit. What is important to know when choosing a company is to be sure that the software is HIPAA (Health Insurance Portability and Accountability Act) compliant. Currently there are more than 15 companies on the market, and many more to come.

Staying up with the times is going to be key in surviving the current changes in health care. Teens in particular are a difficult group to access, but telemedicine provides that access and the comfort in continuity of care with their own physicians.

Dr. Pearce is a pediatrician in Frankfort, Ill. She said she had no relevant financial disclosures. E-mail her at [email protected].

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STS releases public surgical outcomes report

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The Society of Thoracic Surgeons has released a public online report of national surgical outcomes from its Congenital Heart Surgery Database, the association has announced.

The STS report focuses on pediatric and congenital cardiac malformations, and includes 4-year observed, expected, and risk-adjusted mortality rates, the society said in a statement.

Twenty-five sites participated in the first round of STS public online reporting, similar to the observed participation in the first round of public reporting in the STS Adult Cardiac Surgery Database, which started in 2010.

“Reporting hospital surgical outcomes using risk-adjusted analysis is extremely important because it allows for a fair assessment, on a level playing field, of outcomes across hospitals that treat different populations of patients,” Dr. Marshall L. Jacobs, STS CHSD Task Force chair, said in the statement.

For more information, visit http://www.sts.org/quality-research-patient-safety/sts-public-reporting-online.

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The Society of Thoracic Surgeons has released a public online report of national surgical outcomes from its Congenital Heart Surgery Database, the association has announced.

The STS report focuses on pediatric and congenital cardiac malformations, and includes 4-year observed, expected, and risk-adjusted mortality rates, the society said in a statement.

Twenty-five sites participated in the first round of STS public online reporting, similar to the observed participation in the first round of public reporting in the STS Adult Cardiac Surgery Database, which started in 2010.

“Reporting hospital surgical outcomes using risk-adjusted analysis is extremely important because it allows for a fair assessment, on a level playing field, of outcomes across hospitals that treat different populations of patients,” Dr. Marshall L. Jacobs, STS CHSD Task Force chair, said in the statement.

For more information, visit http://www.sts.org/quality-research-patient-safety/sts-public-reporting-online.

The Society of Thoracic Surgeons has released a public online report of national surgical outcomes from its Congenital Heart Surgery Database, the association has announced.

The STS report focuses on pediatric and congenital cardiac malformations, and includes 4-year observed, expected, and risk-adjusted mortality rates, the society said in a statement.

Twenty-five sites participated in the first round of STS public online reporting, similar to the observed participation in the first round of public reporting in the STS Adult Cardiac Surgery Database, which started in 2010.

“Reporting hospital surgical outcomes using risk-adjusted analysis is extremely important because it allows for a fair assessment, on a level playing field, of outcomes across hospitals that treat different populations of patients,” Dr. Marshall L. Jacobs, STS CHSD Task Force chair, said in the statement.

For more information, visit http://www.sts.org/quality-research-patient-safety/sts-public-reporting-online.

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