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Massachusetts General Hospital, Department of Medicine, Boston, Massachusetts
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Terrence
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O'Malley
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MD

Embedding a Discharge Facilitator

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Improving the discharge process by embedding a discharge facilitator in a resident team

Recent studies have shown that a patient's discharge from the hospital is a vulnerable period for patient safety.14 With the reduction in length of stay (LOS) and the increase in patient acuity over the past decade, patients are discharged from acute care settings quicker and sicker, resulting in management of ongoing illness in a less‐monitored environment.5, 6 In addition, in teaching hospitals, residents are supervised by hospital‐based physicians who are rarely the primary care physician (PCP) for the residents' patients, which creates discontinuity of care.

One in 5 medical discharges is complicated by an adverse event believed, in part, to be due to poor communication between caregivers during this transition time.2 Discharge summaries, a key form of that communication, are not always done in a timely fashion and may lack key pieces of information.7, 8 For approximately 68% of patient discharges, the PCP will not have a discharge summary available for the patient's first follow‐up visit.911 In a survey of PCPs whose patients were in the hospital, only 23% reported direct communication with the hospital care team.12 This leaves PCPs unaware of pending test results or recommended follow‐up evaluations.10, 11, 13, 14 All of these factors are believed to contribute to adverse events, emergency department (ED) visits, and readmissions.

A recently published consensus statement on transitions of care by 6 major medical societies emphasizes the need for timely communication and transfer of information.15 These important processes are especially challenging to meet at academic medical centers, where discharge summaries and transition communication are done by residents in a hectic and challenging work environment, with multiple simultaneous and competing demands including outpatient clinic and required conferences.12 Residents have little formal training in how to write an effective discharge summary or how to systematically approach discharge planning. One study found higher error rates in discharge summaries written by residents compared with attending physicians.16 While the Accreditation Council for Graduate Medical Education (ACGME) limits the number of admissions per intern for both patient safety and educational reasons, the number of discharges per day is not limited despite the considerable amount of time required for appropriate discharge planning and communication.

Many interventions have been tried to improve the discharge process and reduce patient adverse events.17 Arranging early follow‐up appointments to reduce emergency department visits and readmissions has shown mixed results.13, 1820 Interventions that focus on specific populations, such as the elderly or patients with congestive heart failure, have been more successful.2123 Some interventions employed additional resources, such as a discharge form, transition coach, or discharge advocate, again with varying impact on results.18, 2427 A recent study by Jack et al. used nurse discharge advocates (DAs) to help with discharge planning and communication at an academic medical center.25 These DAs were independent of the care team, and focused on patient education and follow‐up plans, and reduced hospital reutilization in a selected population.

No studies have assessed the potential benefit of helping residents with the physician components of the discharge process. Prior studies have mainly focused on patient communication and follow‐up appointments, yet safe transitions also involve timely discharge summaries, physician‐to‐physician communication, physician‐to‐nurse communication, and medication reconciliation. Without support and time, these tasks can be very challenging for resident physicians with work‐hour limitations. We undertook a randomized, controlled trial to evaluate the impact on the discharge process of embedding a discharge facilitator in a resident medical team to help with the physician discharge process. We studied the effect for all the patients discharged from the resident team, rather than focusing on a select group or patients with a single diagnosis.

METHODS

Study Setting and Participants

This study was conducted on 2 of the 5 resident general medical teams on the inpatient teaching service at Massachusetts General Hospital (MGH), Boston, Massachusettsa large, 907‐bed, urban hospital. The residents' teams are regionalized and each care for approximately 20 patients on a single floor. Each of the study teams consists of a junior resident, 4 interns, and 1 to 2 attendings who rotate on the floor for 2‐week or 4‐week blocks. Attending rounds, which occur 10 AM to 12 PM weekdays, are for new patient presentations and discussion of plans. Interdisciplinary rounds occur 9:30 AM to 10 AM. Sign‐out rounds occur in the afternoon whenever all work is complete. The junior resident is responsible for all the discharge orders and communication with PCPs, and the discharge summaries for patients going to facilities. The interns are responsible for discharge summaries for patients discharged home; these summaries are not mandatory at the time of discharge. The majority of patients were admitted under the team attending(s). Patients were assigned to the teams by the admitting office, based on bed availability. All patients discharged from both resident medical teams over a 5‐month period were included in this study. Those who were not discharged from the hospital by the study teams (ie, transfers to intensive care units or deaths) were excluded. These exclusions accounted for less than 12% of all team patients. Partners Healthcare System Institutional Review Board approved all study activities.

Intervention

We randomly assigned a discharge facilitator (DF), a master's level nurse practitioner with prior inpatient medicine experience, to 1 of the 5 resident medical teams. She had no prior experience on this specific floor. A similar resident team, on a different floor, served as the control. For the intervention team, the DF attended daily resident work rounds and interdisciplinary discharge rounds. The resident and DF collaborated in identifying patients being discharged in the next 1 to 3 days, and the DF scheduled all follow‐up appointments and tests. The DF performed medication reconciliation, wrote prescriptions and faxed them to pharmacies, and arranged all anticoagulation services. In collaboration with the resident, the DF called PCPs' offices with discharge information and faxed discharge summaries to PCPs' offices outside the Partners Healthcare System. The DF wrote part or all of the computer discharge orders and discharge summaries at the request of the resident and interns. All discharge summaries still needed to be reviewed, edited, and signed by the resident or interns. The DF also noted pending tests and studies at time of discharge, and followed up on these tests for the team. The DF met with all patients to answer any questions about their discharge plan, medications, and appointments; while residents are encouraged to do this, it is not done as consistently. She provided her business card for any questions after their discharge. Follow‐up patient calls to the DF were either answered by her or triaged to the appropriate person. The DF also communicated with the patient's nurse about the discharge plans. For all patients discharged over a weekend, the DF would arrange the follow‐up appointments on Mondays and call the patients at home.

For both teams, residents received letters at the start of their rotation notifying them of the study and asking them to complete discharge summaries within 24 hours. All residents in the program were expected to do an online discharge tutorial and attend a didactic lecture on discharge summaries. The residents on the intervention team received a 5‐minute orientation on how best to work with the DF. Residents were given the autonomy to decide how much to use the DF's services. The scheduling of follow‐up appointments on the control team was the responsibility of the team resident as per usual care. The nursing component of the discharge process, including patient discharge education, was the same on both teams. Nurses on both floors are identically trained on these aspects of care. The nurses on both teams were surveyed about perception of the discharge process prior to the intervention and after the intervention. A research assistant (RA) called patients discharged home on both teams, 1 week after discharge, to ask about satisfaction with the discharge process, to determine if the patients had any questions, and to verify patient knowledge regarding whom they should contact for problems. The RA also noted the end time of attending rounds each day and the start time of resident sign‐out.

Outcome Measures and Follow‐Up

At the time of discharge, the RA collected baseline data on all patients discharged from both teams, including the number of follow‐up appointments scheduled. Patients were tracked through electronic medical records to see if and when they attended their follow‐up appointments, whether they changed the appointment, and whether patients returned to a hospital emergency department or were readmitted to MGH or an affiliated Partners hospital within 30 days. For patients outside the MGHPartners system, the research assistant contacted primary care physician offices to document follow‐up. The remaining patient data was obtained through the MGHPartners computerized information system.

The primary outcomes of the study were length of stay, time of discharge, number of emergency department visits, hospital readmissions, numbers of discharge summaries completed in 24 hours, time from discharge to discharge summary completion, and whether the discharge summary was completed before follow‐up. Secondary outcomes were number of follow‐up PCP appointments made at time of discharge, percentage of follow‐up appointments attended and time from discharge to attending a follow‐up appointment, patient phone survey results, and nursing perception of the discharge process, as well as the percentage of attending rounds that ended on time and the time of resident sign‐out.

Statistical Analyses

Patient characteristics were compared between intervention and control teams using 2‐sample t tests or Wilcoxon rank sum tests for continuous variables, and chi‐square tests for categorical variables. Hours to discharge summary completion and hospital length of stay were summarized using median and interquartiles (IQR), and compared between the 2 teams using Wilcoxon rank sum tests. Categorical outcomes were compared using chi‐square tests. Two‐sided P values 0.05 were considered statistically significant. SAS version 9.2 (SAS Institute Inc, Cary, NC) was used for all statistical analyses.

RESULTS

Study Sample

During the 5‐month intervention (November 12, 2008 to April 14, 2009), a combined total of 999 patients were admitted to the intervention and control general medical teams. We excluded 96 patients who were not discharged but transferred to another service or intensive care units, and 24 patients who died. We also excluded 7 patients who were discharged from both teams the first day of the study, because the DF was not involved with the patients' discharge planning. That left 872 patients discharged to either home, a facility, or having left against medical advice (AMA) included in the study: 440 patients on the intervention team and 432 patients on the control team (Figure 1). Baseline patient demographic and clinical characteristics were similar across both teams with only gender being significantly different (Table 1). The mean age was 63 years (range, 1896) and the mean comorbidity score was 2.3 (range, 012). Of note, about a quarter of patients were discharged to facilities, about half were Medicare recipients, and approximately 80% had a PCP. The DF participated in the discharge process for nearly all of the intervention patients; she reported contributing approximately 50% of the content to the discharge summaries.

Figure 1
Enrollment of Patients.
Baseline Participant Characteristics
CharacteristicsIntervention TeamControl Team
 n = 440n = 432
  • Abbreviations: AMA, against medical advice; COPD, chronic obstructive pulmonary disease; PCP, primary care physician; SD, standard deviation.

  • P < 0.05; no other comparisons were statistically significant.

  • Deyo Modification of the Charlson Comorbidity Index.

Mean age (SD), year63 (18)63 (18)
Women, n (%)*181 (41)207 (48)
Race, n (%)  
White non‐Hispanic267 (61)243 (56)
Black non‐Hispanic24 (5)33 (8)
Hispanic21 (5)17 (4)
Unknown/other128 (29)139 (32)
Health insurance, n (%)  
Medicare213 (48)226 (52)
Medicaid85 (19)81 (19)
Private110 (25)91 (21)
Other32 (7)34 (8)
PCP on admission, n (%)370 (84)356 (82)
Discharge disposition, n (%)  
AMA12 (3)14 (3)
Home305 (69)315 (73)
Facility123 (28)103 (24)
Mean comorbidity index score (SD)2.3 (2.4)2.3 (2.4)
Diagnoses  
Congestive heart failure30 (6%)27 (5%)
COPD/asthma34 (7%)47 (9%)
Cardiovascular disease54 (11%)50 (8%)
Alcohol/substance abuse29 (6%)34 (7%)
Gastrointestinal bleeds/ulcers38 (8%)41 (8%)
Hepatobiliary disease30 (6%)36 (7%)
Renal failure/kidney disease33 (7%)37 (7%)
Pneumonia36 (7%)22 (4%)
Musculoskeletal disease26 (5%)23 (5%)
Neurologic disease22 (4%)25 (5%)
Other163 (33%)172 (35%)

Primary Outcomes

Primary outcomes from the 2 medical teams are listed in Table 2. In the intervention group, significantly more discharge summaries were completed within 24 hours compared to the control group (293 [67%] vs 207 [48%]; P < 0.0001). Since nearly all patients discharged to facilities must have a discharge summary at the time of discharge, the overall difference in completion rates came mainly from patients discharged home or having left AMA from the intervention team (177 [56%] vs 112 [34%]; P < 0.0001). For all discharge summaries, the median time to completion on the intervention team was 18.9 hours compared with 73.1 hours on the control team (P < 0.0001). More discharge summaries were completed before the first follow‐up appointment on the intervention team (393 [89%] vs 330 [76%]; P < 0.001). The DF intervention had no effect on 30‐day readmission or emergency department visits. For patients on the DF team, 88 (20%) were readmitted within 30 days of discharge, as compared with 79 (18%) on the control team (P = 0.55). Similarly, 40 (9%) of the intervention team patients, as compared with 39 (9%) of the control team patients, visited the emergency department at least once within 30 days (P = 1.0). There was no difference in length of stay (LOS) between the 2 teams (median 4.0 days for both teams, P = 0.84).

Primary Outcomes
 Intervention TeamControl Team 
Variablesn = 440n = 432P Value
  • Abbreviations: AMA, against medical advice; IQR, interquartile range.

Discharge summaries completed 24 hr, n (%)293 (67)207 (48)<0.0001
Discharges to facilities116 (94)95 (92)0.60
Discharges to home/AMA177 (56)112 (34)<0.0001
Median hours to discharge summary completion for discharges to home/AMA (IQR)18.9 (0138)73.1 (4.3286)<0.0001
Discharge summary complete before time of follow‐up appointment.393 (89)330 (76)<0.0001
Emergency department visits in 30 days, n (%)40 (9)39 (9)1.0
Readmissions in 30 days, n (%)88 (20)79 (18)0.55
Median length of stay, days (IQR)4.0 (37)4.0 (28)0.84
Discharges to facilities6.0 (511)8.0 (513)0.17
Discharges to home/AMA4.0 (26)3.0 (26)0.61
Discharged by noon, n (%)38 (9)42 (10)0.64

Secondary Outcomes

Table 3 shows secondary outcomes from the 2 medical teams. Among the patients discharged from the DF team, 264 (62%) had scheduled follow‐up appointments with PCPs compared to the control team 151 (36%) (P < 0.0001). (Many patients going to rehabilitation hospitals are not given PCP appointments at the time of discharge.) Despite having more scheduled appointments, patients' actual follow‐up with PCPs was similar during the 5‐month study period among both intervention and control group (234 [65%] vs 223 [63%]; P = 0.58). However, there was earlier follow‐up with the primary provider in the first 2 or 4 weeks in the intervention group. At 2 weeks, 129 (36%) patients in the intervention group saw their provider compared to 81 (23%) patients in the control group (P < 0.0002), and at 4 weeks, 159 (44%) of the intervention group was seen compared to 99 (28%) of the control group (P < 0.0001). Of note, among the 415 patients on both teams discharged with scheduled appointments, only 53 (13%) of patients did not show up for the scheduled appointment and this no‐show rate was the same on both teams.

Secondary Outcomes
VariablesIntervention TeamControl TeamP Value
  • Against medical advice (AMA) patients excluded.

  • Patients excluded if AMA, readmitted, died after discharge, or discharged to hospice.

No. of eligible patients*428418 
Patients with follow‐up appointments to primary providers, n (%)264 (62)151 (36)<0.0001
No. of eligible patients359354 
Attended follow‐up appointment with primary provider during study, n (%)234 (65)223 (63)0.58
Within 2 weeks of discharge129 (36)81 (23)0.0002
Within 4 weeks of discharge159 (44)99 (28)<0.0001
No. of days round times were recorded10099 
No. of attending rounds ending by 12 PM45 (45%)31 (31%)0.058
Mean start time of sign‐out rounds16:3817:240.0007

Attending rounds ended on time (12 PM) 45% of the time in the intervention group compared to 31% in the control group (P = 0.058). Mean start time of resident sign‐out rounds was 1638 hours on the intervention team and 1724 hours on the control team (P = 0.0007).

We obtained patient reported outcome data by telephone within 2 to 4 weeks of discharge. Of the 620 patients discharged to home, 6 died or were readmitted to the hospital before being reached by phone. For the remaining 614 patients, we were able to contact 444 (72%). Of those, 321 (52%) agreed to participate in the phone interview. We surveyed similar proportions of intervention and control group patients (158 [52%] vs 163 [52%]) (Table 4). Both groups reported similar rates of having questions about their hospital stay after discharge (43 [27%] vs 49 [30%]; P = 0.62). The intervention group could better identify whom to call with questions (150 [95%] vs 138 [85%]; P = 0.003). The intervention group reported better understanding of their follow‐up plans (157 [99%] vs 141 [87%]; P = 0.001) and better understanding of their discharge medications (152 [96%] vs 142 [87%]; P = 0.001). More patients in the intervention group were satisfied with the discharge process (153 [97%] vs 124 [76%]; P < 0.0001).

Secondary Outcomes Continued: Patient Survey Results
 Intervention TeamControl TeamP Value
  • Patients excluded if died or readmitted prior to phone call.

  • Questions were answered on a 5‐point Likert scale. The number/percentage reflects participants who responded with the top 2 categories on the scale.

Patients discharged home*304310 
Patients contacted by phone after discharge, n (%)213 (70)231 (75)0.24
Agreed to participate in phone interview, n (%)158 (52)163 (53)0.94
Among those agreed to participate, n (%)   
Did you have questions about your hospital stay?43 (27)49 (30)0.62
Would you know who to call if you had questions after discharge?150 (95)138 (85)0.003
Satisfied with the discharge process?153 (97)124 (76)<0.0001
Did you understand your follow‐up plans?157 (99)141 (87)<0.0001
Did you understand your medications?152 (96)142 (87)0.001
Did you feel safe going home?153 (97)151 (92)0.07

Compared with nurses on the control team, nurses on the intervention team more often reported paperwork being completed in a timely fashion (56% vs 29%; P = 0.041) and being less worried about the discharge plan (44% vs 57%; P = 0.027). The intervention team nurses also reported fewer issues with medications/prescriptions (61% vs 82%) and being included more often in the discharge planning (50% vs 38%). However, neither of these results reached statistical significance (P = 0.81 and 0.50, respectively).

DISCUSSION

Our study embedded a nurse practitioner on a busy resident general medical team to help with all aspects of the discharge process for which physicians are responsible. Previous studies have been limited to patients with specific diagnoses, age, or disposition plans.1825 In this study, we included all general medical patients. Our intervention improved several important quality of care elements: the timeliness of completion of discharge summaries; and increased number of early follow‐up appointments, with more patients seen within 2 and 4 weeks after discharge. Patients reported better understanding of their follow‐up plans and more satisfaction with the discharge process. While not statistically significant, there was a trend towards better communication with nurses. For residents with work‐hour limitations, there was time savings with a trend towards finishing attending rounds on time and statistically significant earlier sign‐out rounds (46 minutes earlier). This intervention had no effect on patient length of stay, readmissions, or emergency department visits in the 30 days after discharge.

Despite improving many aspects of the discharge process and communication that have previously been raised as areas of concern for patient safety, there was no improvement in readmissions rates and ED utilization which are often used as the quality indicators for effective discharge planning. Similar types of interventions on general medical patients have generally also failed to show improvement in readmission rates.1820, 25 Weinberger et al. arranged follow‐up appointments within 1 week for patients discharged from a Veterans Administrative hospital; while patients were seen more often, the intervention actually increased readmission rates.20 Fitzgerald et al. had a case manager contact patients at home and encourage follow‐up, which increased follow‐up visits, but again had no effect on readmission.19 Einstadter et al. had a nurse case manager coordinate outpatient follow‐up on a resident team and also did not effect readmission rates or ED visits.18 Jack et al. in project reengineered discharge (RED) did show a significant reduction in combined hospital utilization measures. However, their study focused on a more limited patient population, and employed both a discharge advocate to arrange follow‐up and improve patient education, and a pharmacist to make postdischarge phone calls.25

So why did readmissions rates and ED visits not change in our study? It would be reasonable to think that having earlier follow‐up appointments, better and timely physician‐to‐physician communication, and a facilitator for patient questions should improve the quality of the discharge process. In a recent study, Jha et al. found there was no association between chart‐based measures of discharge quality and readmissions rates, and only a modest association for patient‐reported measures of discharge quality and readmission rates.28 The authors suggest readmission rates are driven by many factors beyond just improved discharge safety. Perhaps readmission rates are too complex a measure to use to assess discharge process improvement. For fiscal reasons, it is understandable that hospitals, insurance companies, and the Centers for Medicare and Medicaid want to reduce readmission rates and ED utilization. Jencks et al. noted the cost of readmissions in 2004 was 17.4 billion dollars.29 However, sweeping efforts to improve the discharge process for all general medical patients may not yield significant reductions in readmissions, as this study suggests. We may need to focus aggressive intervention on smaller target populations, as prior studies on focused groups suggest.2123

There are no evidence‐based studies to suggest when optimal follow‐up should occur after discharge.26 Several medical society guidelines recommend 2 weeks. More patients on the intervention team were seen within 2 weeks, but readmission rates were not affected. The University Health System Consortium recently reported that the majority of readmissions occurred within 6 days, with the average being about 2 to 3 days.30 In this study, the median days to readmit were 12 for the intervention team and 10 for the control. It is possible that even with our improved 2‐week follow‐up, this was not early enough to reduce readmissions. Follow‐up may need to be within 13 days of discharge for highly vulnerable patients, to significantly change readmission rates. Further studies focusing on this question would be helpful.

Finally, with ACGME limitation of work hours, many residency programs are looking for ways to reduce residents' workload and increase time for education. With a significant trend towards finishing attending rounds on time, it is likely that more residents on the intervention team were able to attend the noon‐time educational conferences. We speculate that this was due to fewer interruptions during rounds because the DF was available for nurses' questions. Sign‐out rounds occurred significantly earlier, possibly because of improved resident efficiency due to the DF's help with the discharge process. While residents may lose some educational experience from not performing all discharge tasks, they gain experience working in interdisciplinary teams, have increased time for education, and reduced work hours. Since the ACGME limits the number of residents per program and increasing the residency size is not an option, a DF should be considered as a possible solution to ACGME work‐hour restrictions.

This study had several limitations. First, the intervention team had 1 specific person embedded, and therefore the results of this study may have limited generalizability. Second, the limited number of residents working with the DF could have biased the intervention, as not all residents worked equally well with the DF. However, this may represent the real‐world experience on any teaching service, given variation in working styles and learning curves of residents over their training. Third, this study was done at 1 university‐affiliated urban Academic Medical Center, making it potentially less generalizable to resident teams in community hospitals. Fourth, we were not able to capture readmissions and ED visits at institutions outside the MGHPartners Healthcare System. However, given that patients were assigned at random to either team, this factor should have impacted both teams equally. Fifth, the study occurred during Massachusetts healthcare reform which requires everyone to have health insurance. This may have affected the rates of ED visits and readmission rates, especially with a shortage of primary care physicians and office visits. Finally, this intervention was not cost‐neutral. Paying for a nurse practitioner to help residents with the work of discharge and providing patients with additional services had many advantages, but this quality improvement project did not pay for itself through shorter LOS, or decreases in ED visits or readmissions.

While readmission rates and ED utilization are important patient outcomes, especially in the current healthcare climate, what determines readmissions and ED visits is likely complex and multifactorial. This study suggests that, in the nationwide effort to reduce readmissions, solely improving the discharge process for all general medical patients may not produce the hoped‐for financial savings. Improving the discharge process, however, is something valuable in its own right. Adding a DF to a resident team does improve some quality markers of the discharge process and decreases work hours for residents.

Acknowledgements

Sara Macchiano, RN for her help with the data gathering of this study.

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References
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Recent studies have shown that a patient's discharge from the hospital is a vulnerable period for patient safety.14 With the reduction in length of stay (LOS) and the increase in patient acuity over the past decade, patients are discharged from acute care settings quicker and sicker, resulting in management of ongoing illness in a less‐monitored environment.5, 6 In addition, in teaching hospitals, residents are supervised by hospital‐based physicians who are rarely the primary care physician (PCP) for the residents' patients, which creates discontinuity of care.

One in 5 medical discharges is complicated by an adverse event believed, in part, to be due to poor communication between caregivers during this transition time.2 Discharge summaries, a key form of that communication, are not always done in a timely fashion and may lack key pieces of information.7, 8 For approximately 68% of patient discharges, the PCP will not have a discharge summary available for the patient's first follow‐up visit.911 In a survey of PCPs whose patients were in the hospital, only 23% reported direct communication with the hospital care team.12 This leaves PCPs unaware of pending test results or recommended follow‐up evaluations.10, 11, 13, 14 All of these factors are believed to contribute to adverse events, emergency department (ED) visits, and readmissions.

A recently published consensus statement on transitions of care by 6 major medical societies emphasizes the need for timely communication and transfer of information.15 These important processes are especially challenging to meet at academic medical centers, where discharge summaries and transition communication are done by residents in a hectic and challenging work environment, with multiple simultaneous and competing demands including outpatient clinic and required conferences.12 Residents have little formal training in how to write an effective discharge summary or how to systematically approach discharge planning. One study found higher error rates in discharge summaries written by residents compared with attending physicians.16 While the Accreditation Council for Graduate Medical Education (ACGME) limits the number of admissions per intern for both patient safety and educational reasons, the number of discharges per day is not limited despite the considerable amount of time required for appropriate discharge planning and communication.

Many interventions have been tried to improve the discharge process and reduce patient adverse events.17 Arranging early follow‐up appointments to reduce emergency department visits and readmissions has shown mixed results.13, 1820 Interventions that focus on specific populations, such as the elderly or patients with congestive heart failure, have been more successful.2123 Some interventions employed additional resources, such as a discharge form, transition coach, or discharge advocate, again with varying impact on results.18, 2427 A recent study by Jack et al. used nurse discharge advocates (DAs) to help with discharge planning and communication at an academic medical center.25 These DAs were independent of the care team, and focused on patient education and follow‐up plans, and reduced hospital reutilization in a selected population.

No studies have assessed the potential benefit of helping residents with the physician components of the discharge process. Prior studies have mainly focused on patient communication and follow‐up appointments, yet safe transitions also involve timely discharge summaries, physician‐to‐physician communication, physician‐to‐nurse communication, and medication reconciliation. Without support and time, these tasks can be very challenging for resident physicians with work‐hour limitations. We undertook a randomized, controlled trial to evaluate the impact on the discharge process of embedding a discharge facilitator in a resident medical team to help with the physician discharge process. We studied the effect for all the patients discharged from the resident team, rather than focusing on a select group or patients with a single diagnosis.

METHODS

Study Setting and Participants

This study was conducted on 2 of the 5 resident general medical teams on the inpatient teaching service at Massachusetts General Hospital (MGH), Boston, Massachusettsa large, 907‐bed, urban hospital. The residents' teams are regionalized and each care for approximately 20 patients on a single floor. Each of the study teams consists of a junior resident, 4 interns, and 1 to 2 attendings who rotate on the floor for 2‐week or 4‐week blocks. Attending rounds, which occur 10 AM to 12 PM weekdays, are for new patient presentations and discussion of plans. Interdisciplinary rounds occur 9:30 AM to 10 AM. Sign‐out rounds occur in the afternoon whenever all work is complete. The junior resident is responsible for all the discharge orders and communication with PCPs, and the discharge summaries for patients going to facilities. The interns are responsible for discharge summaries for patients discharged home; these summaries are not mandatory at the time of discharge. The majority of patients were admitted under the team attending(s). Patients were assigned to the teams by the admitting office, based on bed availability. All patients discharged from both resident medical teams over a 5‐month period were included in this study. Those who were not discharged from the hospital by the study teams (ie, transfers to intensive care units or deaths) were excluded. These exclusions accounted for less than 12% of all team patients. Partners Healthcare System Institutional Review Board approved all study activities.

Intervention

We randomly assigned a discharge facilitator (DF), a master's level nurse practitioner with prior inpatient medicine experience, to 1 of the 5 resident medical teams. She had no prior experience on this specific floor. A similar resident team, on a different floor, served as the control. For the intervention team, the DF attended daily resident work rounds and interdisciplinary discharge rounds. The resident and DF collaborated in identifying patients being discharged in the next 1 to 3 days, and the DF scheduled all follow‐up appointments and tests. The DF performed medication reconciliation, wrote prescriptions and faxed them to pharmacies, and arranged all anticoagulation services. In collaboration with the resident, the DF called PCPs' offices with discharge information and faxed discharge summaries to PCPs' offices outside the Partners Healthcare System. The DF wrote part or all of the computer discharge orders and discharge summaries at the request of the resident and interns. All discharge summaries still needed to be reviewed, edited, and signed by the resident or interns. The DF also noted pending tests and studies at time of discharge, and followed up on these tests for the team. The DF met with all patients to answer any questions about their discharge plan, medications, and appointments; while residents are encouraged to do this, it is not done as consistently. She provided her business card for any questions after their discharge. Follow‐up patient calls to the DF were either answered by her or triaged to the appropriate person. The DF also communicated with the patient's nurse about the discharge plans. For all patients discharged over a weekend, the DF would arrange the follow‐up appointments on Mondays and call the patients at home.

For both teams, residents received letters at the start of their rotation notifying them of the study and asking them to complete discharge summaries within 24 hours. All residents in the program were expected to do an online discharge tutorial and attend a didactic lecture on discharge summaries. The residents on the intervention team received a 5‐minute orientation on how best to work with the DF. Residents were given the autonomy to decide how much to use the DF's services. The scheduling of follow‐up appointments on the control team was the responsibility of the team resident as per usual care. The nursing component of the discharge process, including patient discharge education, was the same on both teams. Nurses on both floors are identically trained on these aspects of care. The nurses on both teams were surveyed about perception of the discharge process prior to the intervention and after the intervention. A research assistant (RA) called patients discharged home on both teams, 1 week after discharge, to ask about satisfaction with the discharge process, to determine if the patients had any questions, and to verify patient knowledge regarding whom they should contact for problems. The RA also noted the end time of attending rounds each day and the start time of resident sign‐out.

Outcome Measures and Follow‐Up

At the time of discharge, the RA collected baseline data on all patients discharged from both teams, including the number of follow‐up appointments scheduled. Patients were tracked through electronic medical records to see if and when they attended their follow‐up appointments, whether they changed the appointment, and whether patients returned to a hospital emergency department or were readmitted to MGH or an affiliated Partners hospital within 30 days. For patients outside the MGHPartners system, the research assistant contacted primary care physician offices to document follow‐up. The remaining patient data was obtained through the MGHPartners computerized information system.

The primary outcomes of the study were length of stay, time of discharge, number of emergency department visits, hospital readmissions, numbers of discharge summaries completed in 24 hours, time from discharge to discharge summary completion, and whether the discharge summary was completed before follow‐up. Secondary outcomes were number of follow‐up PCP appointments made at time of discharge, percentage of follow‐up appointments attended and time from discharge to attending a follow‐up appointment, patient phone survey results, and nursing perception of the discharge process, as well as the percentage of attending rounds that ended on time and the time of resident sign‐out.

Statistical Analyses

Patient characteristics were compared between intervention and control teams using 2‐sample t tests or Wilcoxon rank sum tests for continuous variables, and chi‐square tests for categorical variables. Hours to discharge summary completion and hospital length of stay were summarized using median and interquartiles (IQR), and compared between the 2 teams using Wilcoxon rank sum tests. Categorical outcomes were compared using chi‐square tests. Two‐sided P values 0.05 were considered statistically significant. SAS version 9.2 (SAS Institute Inc, Cary, NC) was used for all statistical analyses.

RESULTS

Study Sample

During the 5‐month intervention (November 12, 2008 to April 14, 2009), a combined total of 999 patients were admitted to the intervention and control general medical teams. We excluded 96 patients who were not discharged but transferred to another service or intensive care units, and 24 patients who died. We also excluded 7 patients who were discharged from both teams the first day of the study, because the DF was not involved with the patients' discharge planning. That left 872 patients discharged to either home, a facility, or having left against medical advice (AMA) included in the study: 440 patients on the intervention team and 432 patients on the control team (Figure 1). Baseline patient demographic and clinical characteristics were similar across both teams with only gender being significantly different (Table 1). The mean age was 63 years (range, 1896) and the mean comorbidity score was 2.3 (range, 012). Of note, about a quarter of patients were discharged to facilities, about half were Medicare recipients, and approximately 80% had a PCP. The DF participated in the discharge process for nearly all of the intervention patients; she reported contributing approximately 50% of the content to the discharge summaries.

Figure 1
Enrollment of Patients.
Baseline Participant Characteristics
CharacteristicsIntervention TeamControl Team
 n = 440n = 432
  • Abbreviations: AMA, against medical advice; COPD, chronic obstructive pulmonary disease; PCP, primary care physician; SD, standard deviation.

  • P < 0.05; no other comparisons were statistically significant.

  • Deyo Modification of the Charlson Comorbidity Index.

Mean age (SD), year63 (18)63 (18)
Women, n (%)*181 (41)207 (48)
Race, n (%)  
White non‐Hispanic267 (61)243 (56)
Black non‐Hispanic24 (5)33 (8)
Hispanic21 (5)17 (4)
Unknown/other128 (29)139 (32)
Health insurance, n (%)  
Medicare213 (48)226 (52)
Medicaid85 (19)81 (19)
Private110 (25)91 (21)
Other32 (7)34 (8)
PCP on admission, n (%)370 (84)356 (82)
Discharge disposition, n (%)  
AMA12 (3)14 (3)
Home305 (69)315 (73)
Facility123 (28)103 (24)
Mean comorbidity index score (SD)2.3 (2.4)2.3 (2.4)
Diagnoses  
Congestive heart failure30 (6%)27 (5%)
COPD/asthma34 (7%)47 (9%)
Cardiovascular disease54 (11%)50 (8%)
Alcohol/substance abuse29 (6%)34 (7%)
Gastrointestinal bleeds/ulcers38 (8%)41 (8%)
Hepatobiliary disease30 (6%)36 (7%)
Renal failure/kidney disease33 (7%)37 (7%)
Pneumonia36 (7%)22 (4%)
Musculoskeletal disease26 (5%)23 (5%)
Neurologic disease22 (4%)25 (5%)
Other163 (33%)172 (35%)

Primary Outcomes

Primary outcomes from the 2 medical teams are listed in Table 2. In the intervention group, significantly more discharge summaries were completed within 24 hours compared to the control group (293 [67%] vs 207 [48%]; P < 0.0001). Since nearly all patients discharged to facilities must have a discharge summary at the time of discharge, the overall difference in completion rates came mainly from patients discharged home or having left AMA from the intervention team (177 [56%] vs 112 [34%]; P < 0.0001). For all discharge summaries, the median time to completion on the intervention team was 18.9 hours compared with 73.1 hours on the control team (P < 0.0001). More discharge summaries were completed before the first follow‐up appointment on the intervention team (393 [89%] vs 330 [76%]; P < 0.001). The DF intervention had no effect on 30‐day readmission or emergency department visits. For patients on the DF team, 88 (20%) were readmitted within 30 days of discharge, as compared with 79 (18%) on the control team (P = 0.55). Similarly, 40 (9%) of the intervention team patients, as compared with 39 (9%) of the control team patients, visited the emergency department at least once within 30 days (P = 1.0). There was no difference in length of stay (LOS) between the 2 teams (median 4.0 days for both teams, P = 0.84).

Primary Outcomes
 Intervention TeamControl Team 
Variablesn = 440n = 432P Value
  • Abbreviations: AMA, against medical advice; IQR, interquartile range.

Discharge summaries completed 24 hr, n (%)293 (67)207 (48)<0.0001
Discharges to facilities116 (94)95 (92)0.60
Discharges to home/AMA177 (56)112 (34)<0.0001
Median hours to discharge summary completion for discharges to home/AMA (IQR)18.9 (0138)73.1 (4.3286)<0.0001
Discharge summary complete before time of follow‐up appointment.393 (89)330 (76)<0.0001
Emergency department visits in 30 days, n (%)40 (9)39 (9)1.0
Readmissions in 30 days, n (%)88 (20)79 (18)0.55
Median length of stay, days (IQR)4.0 (37)4.0 (28)0.84
Discharges to facilities6.0 (511)8.0 (513)0.17
Discharges to home/AMA4.0 (26)3.0 (26)0.61
Discharged by noon, n (%)38 (9)42 (10)0.64

Secondary Outcomes

Table 3 shows secondary outcomes from the 2 medical teams. Among the patients discharged from the DF team, 264 (62%) had scheduled follow‐up appointments with PCPs compared to the control team 151 (36%) (P < 0.0001). (Many patients going to rehabilitation hospitals are not given PCP appointments at the time of discharge.) Despite having more scheduled appointments, patients' actual follow‐up with PCPs was similar during the 5‐month study period among both intervention and control group (234 [65%] vs 223 [63%]; P = 0.58). However, there was earlier follow‐up with the primary provider in the first 2 or 4 weeks in the intervention group. At 2 weeks, 129 (36%) patients in the intervention group saw their provider compared to 81 (23%) patients in the control group (P < 0.0002), and at 4 weeks, 159 (44%) of the intervention group was seen compared to 99 (28%) of the control group (P < 0.0001). Of note, among the 415 patients on both teams discharged with scheduled appointments, only 53 (13%) of patients did not show up for the scheduled appointment and this no‐show rate was the same on both teams.

Secondary Outcomes
VariablesIntervention TeamControl TeamP Value
  • Against medical advice (AMA) patients excluded.

  • Patients excluded if AMA, readmitted, died after discharge, or discharged to hospice.

No. of eligible patients*428418 
Patients with follow‐up appointments to primary providers, n (%)264 (62)151 (36)<0.0001
No. of eligible patients359354 
Attended follow‐up appointment with primary provider during study, n (%)234 (65)223 (63)0.58
Within 2 weeks of discharge129 (36)81 (23)0.0002
Within 4 weeks of discharge159 (44)99 (28)<0.0001
No. of days round times were recorded10099 
No. of attending rounds ending by 12 PM45 (45%)31 (31%)0.058
Mean start time of sign‐out rounds16:3817:240.0007

Attending rounds ended on time (12 PM) 45% of the time in the intervention group compared to 31% in the control group (P = 0.058). Mean start time of resident sign‐out rounds was 1638 hours on the intervention team and 1724 hours on the control team (P = 0.0007).

We obtained patient reported outcome data by telephone within 2 to 4 weeks of discharge. Of the 620 patients discharged to home, 6 died or were readmitted to the hospital before being reached by phone. For the remaining 614 patients, we were able to contact 444 (72%). Of those, 321 (52%) agreed to participate in the phone interview. We surveyed similar proportions of intervention and control group patients (158 [52%] vs 163 [52%]) (Table 4). Both groups reported similar rates of having questions about their hospital stay after discharge (43 [27%] vs 49 [30%]; P = 0.62). The intervention group could better identify whom to call with questions (150 [95%] vs 138 [85%]; P = 0.003). The intervention group reported better understanding of their follow‐up plans (157 [99%] vs 141 [87%]; P = 0.001) and better understanding of their discharge medications (152 [96%] vs 142 [87%]; P = 0.001). More patients in the intervention group were satisfied with the discharge process (153 [97%] vs 124 [76%]; P < 0.0001).

Secondary Outcomes Continued: Patient Survey Results
 Intervention TeamControl TeamP Value
  • Patients excluded if died or readmitted prior to phone call.

  • Questions were answered on a 5‐point Likert scale. The number/percentage reflects participants who responded with the top 2 categories on the scale.

Patients discharged home*304310 
Patients contacted by phone after discharge, n (%)213 (70)231 (75)0.24
Agreed to participate in phone interview, n (%)158 (52)163 (53)0.94
Among those agreed to participate, n (%)   
Did you have questions about your hospital stay?43 (27)49 (30)0.62
Would you know who to call if you had questions after discharge?150 (95)138 (85)0.003
Satisfied with the discharge process?153 (97)124 (76)<0.0001
Did you understand your follow‐up plans?157 (99)141 (87)<0.0001
Did you understand your medications?152 (96)142 (87)0.001
Did you feel safe going home?153 (97)151 (92)0.07

Compared with nurses on the control team, nurses on the intervention team more often reported paperwork being completed in a timely fashion (56% vs 29%; P = 0.041) and being less worried about the discharge plan (44% vs 57%; P = 0.027). The intervention team nurses also reported fewer issues with medications/prescriptions (61% vs 82%) and being included more often in the discharge planning (50% vs 38%). However, neither of these results reached statistical significance (P = 0.81 and 0.50, respectively).

DISCUSSION

Our study embedded a nurse practitioner on a busy resident general medical team to help with all aspects of the discharge process for which physicians are responsible. Previous studies have been limited to patients with specific diagnoses, age, or disposition plans.1825 In this study, we included all general medical patients. Our intervention improved several important quality of care elements: the timeliness of completion of discharge summaries; and increased number of early follow‐up appointments, with more patients seen within 2 and 4 weeks after discharge. Patients reported better understanding of their follow‐up plans and more satisfaction with the discharge process. While not statistically significant, there was a trend towards better communication with nurses. For residents with work‐hour limitations, there was time savings with a trend towards finishing attending rounds on time and statistically significant earlier sign‐out rounds (46 minutes earlier). This intervention had no effect on patient length of stay, readmissions, or emergency department visits in the 30 days after discharge.

Despite improving many aspects of the discharge process and communication that have previously been raised as areas of concern for patient safety, there was no improvement in readmissions rates and ED utilization which are often used as the quality indicators for effective discharge planning. Similar types of interventions on general medical patients have generally also failed to show improvement in readmission rates.1820, 25 Weinberger et al. arranged follow‐up appointments within 1 week for patients discharged from a Veterans Administrative hospital; while patients were seen more often, the intervention actually increased readmission rates.20 Fitzgerald et al. had a case manager contact patients at home and encourage follow‐up, which increased follow‐up visits, but again had no effect on readmission.19 Einstadter et al. had a nurse case manager coordinate outpatient follow‐up on a resident team and also did not effect readmission rates or ED visits.18 Jack et al. in project reengineered discharge (RED) did show a significant reduction in combined hospital utilization measures. However, their study focused on a more limited patient population, and employed both a discharge advocate to arrange follow‐up and improve patient education, and a pharmacist to make postdischarge phone calls.25

So why did readmissions rates and ED visits not change in our study? It would be reasonable to think that having earlier follow‐up appointments, better and timely physician‐to‐physician communication, and a facilitator for patient questions should improve the quality of the discharge process. In a recent study, Jha et al. found there was no association between chart‐based measures of discharge quality and readmissions rates, and only a modest association for patient‐reported measures of discharge quality and readmission rates.28 The authors suggest readmission rates are driven by many factors beyond just improved discharge safety. Perhaps readmission rates are too complex a measure to use to assess discharge process improvement. For fiscal reasons, it is understandable that hospitals, insurance companies, and the Centers for Medicare and Medicaid want to reduce readmission rates and ED utilization. Jencks et al. noted the cost of readmissions in 2004 was 17.4 billion dollars.29 However, sweeping efforts to improve the discharge process for all general medical patients may not yield significant reductions in readmissions, as this study suggests. We may need to focus aggressive intervention on smaller target populations, as prior studies on focused groups suggest.2123

There are no evidence‐based studies to suggest when optimal follow‐up should occur after discharge.26 Several medical society guidelines recommend 2 weeks. More patients on the intervention team were seen within 2 weeks, but readmission rates were not affected. The University Health System Consortium recently reported that the majority of readmissions occurred within 6 days, with the average being about 2 to 3 days.30 In this study, the median days to readmit were 12 for the intervention team and 10 for the control. It is possible that even with our improved 2‐week follow‐up, this was not early enough to reduce readmissions. Follow‐up may need to be within 13 days of discharge for highly vulnerable patients, to significantly change readmission rates. Further studies focusing on this question would be helpful.

Finally, with ACGME limitation of work hours, many residency programs are looking for ways to reduce residents' workload and increase time for education. With a significant trend towards finishing attending rounds on time, it is likely that more residents on the intervention team were able to attend the noon‐time educational conferences. We speculate that this was due to fewer interruptions during rounds because the DF was available for nurses' questions. Sign‐out rounds occurred significantly earlier, possibly because of improved resident efficiency due to the DF's help with the discharge process. While residents may lose some educational experience from not performing all discharge tasks, they gain experience working in interdisciplinary teams, have increased time for education, and reduced work hours. Since the ACGME limits the number of residents per program and increasing the residency size is not an option, a DF should be considered as a possible solution to ACGME work‐hour restrictions.

This study had several limitations. First, the intervention team had 1 specific person embedded, and therefore the results of this study may have limited generalizability. Second, the limited number of residents working with the DF could have biased the intervention, as not all residents worked equally well with the DF. However, this may represent the real‐world experience on any teaching service, given variation in working styles and learning curves of residents over their training. Third, this study was done at 1 university‐affiliated urban Academic Medical Center, making it potentially less generalizable to resident teams in community hospitals. Fourth, we were not able to capture readmissions and ED visits at institutions outside the MGHPartners Healthcare System. However, given that patients were assigned at random to either team, this factor should have impacted both teams equally. Fifth, the study occurred during Massachusetts healthcare reform which requires everyone to have health insurance. This may have affected the rates of ED visits and readmission rates, especially with a shortage of primary care physicians and office visits. Finally, this intervention was not cost‐neutral. Paying for a nurse practitioner to help residents with the work of discharge and providing patients with additional services had many advantages, but this quality improvement project did not pay for itself through shorter LOS, or decreases in ED visits or readmissions.

While readmission rates and ED utilization are important patient outcomes, especially in the current healthcare climate, what determines readmissions and ED visits is likely complex and multifactorial. This study suggests that, in the nationwide effort to reduce readmissions, solely improving the discharge process for all general medical patients may not produce the hoped‐for financial savings. Improving the discharge process, however, is something valuable in its own right. Adding a DF to a resident team does improve some quality markers of the discharge process and decreases work hours for residents.

Acknowledgements

Sara Macchiano, RN for her help with the data gathering of this study.

Recent studies have shown that a patient's discharge from the hospital is a vulnerable period for patient safety.14 With the reduction in length of stay (LOS) and the increase in patient acuity over the past decade, patients are discharged from acute care settings quicker and sicker, resulting in management of ongoing illness in a less‐monitored environment.5, 6 In addition, in teaching hospitals, residents are supervised by hospital‐based physicians who are rarely the primary care physician (PCP) for the residents' patients, which creates discontinuity of care.

One in 5 medical discharges is complicated by an adverse event believed, in part, to be due to poor communication between caregivers during this transition time.2 Discharge summaries, a key form of that communication, are not always done in a timely fashion and may lack key pieces of information.7, 8 For approximately 68% of patient discharges, the PCP will not have a discharge summary available for the patient's first follow‐up visit.911 In a survey of PCPs whose patients were in the hospital, only 23% reported direct communication with the hospital care team.12 This leaves PCPs unaware of pending test results or recommended follow‐up evaluations.10, 11, 13, 14 All of these factors are believed to contribute to adverse events, emergency department (ED) visits, and readmissions.

A recently published consensus statement on transitions of care by 6 major medical societies emphasizes the need for timely communication and transfer of information.15 These important processes are especially challenging to meet at academic medical centers, where discharge summaries and transition communication are done by residents in a hectic and challenging work environment, with multiple simultaneous and competing demands including outpatient clinic and required conferences.12 Residents have little formal training in how to write an effective discharge summary or how to systematically approach discharge planning. One study found higher error rates in discharge summaries written by residents compared with attending physicians.16 While the Accreditation Council for Graduate Medical Education (ACGME) limits the number of admissions per intern for both patient safety and educational reasons, the number of discharges per day is not limited despite the considerable amount of time required for appropriate discharge planning and communication.

Many interventions have been tried to improve the discharge process and reduce patient adverse events.17 Arranging early follow‐up appointments to reduce emergency department visits and readmissions has shown mixed results.13, 1820 Interventions that focus on specific populations, such as the elderly or patients with congestive heart failure, have been more successful.2123 Some interventions employed additional resources, such as a discharge form, transition coach, or discharge advocate, again with varying impact on results.18, 2427 A recent study by Jack et al. used nurse discharge advocates (DAs) to help with discharge planning and communication at an academic medical center.25 These DAs were independent of the care team, and focused on patient education and follow‐up plans, and reduced hospital reutilization in a selected population.

No studies have assessed the potential benefit of helping residents with the physician components of the discharge process. Prior studies have mainly focused on patient communication and follow‐up appointments, yet safe transitions also involve timely discharge summaries, physician‐to‐physician communication, physician‐to‐nurse communication, and medication reconciliation. Without support and time, these tasks can be very challenging for resident physicians with work‐hour limitations. We undertook a randomized, controlled trial to evaluate the impact on the discharge process of embedding a discharge facilitator in a resident medical team to help with the physician discharge process. We studied the effect for all the patients discharged from the resident team, rather than focusing on a select group or patients with a single diagnosis.

METHODS

Study Setting and Participants

This study was conducted on 2 of the 5 resident general medical teams on the inpatient teaching service at Massachusetts General Hospital (MGH), Boston, Massachusettsa large, 907‐bed, urban hospital. The residents' teams are regionalized and each care for approximately 20 patients on a single floor. Each of the study teams consists of a junior resident, 4 interns, and 1 to 2 attendings who rotate on the floor for 2‐week or 4‐week blocks. Attending rounds, which occur 10 AM to 12 PM weekdays, are for new patient presentations and discussion of plans. Interdisciplinary rounds occur 9:30 AM to 10 AM. Sign‐out rounds occur in the afternoon whenever all work is complete. The junior resident is responsible for all the discharge orders and communication with PCPs, and the discharge summaries for patients going to facilities. The interns are responsible for discharge summaries for patients discharged home; these summaries are not mandatory at the time of discharge. The majority of patients were admitted under the team attending(s). Patients were assigned to the teams by the admitting office, based on bed availability. All patients discharged from both resident medical teams over a 5‐month period were included in this study. Those who were not discharged from the hospital by the study teams (ie, transfers to intensive care units or deaths) were excluded. These exclusions accounted for less than 12% of all team patients. Partners Healthcare System Institutional Review Board approved all study activities.

Intervention

We randomly assigned a discharge facilitator (DF), a master's level nurse practitioner with prior inpatient medicine experience, to 1 of the 5 resident medical teams. She had no prior experience on this specific floor. A similar resident team, on a different floor, served as the control. For the intervention team, the DF attended daily resident work rounds and interdisciplinary discharge rounds. The resident and DF collaborated in identifying patients being discharged in the next 1 to 3 days, and the DF scheduled all follow‐up appointments and tests. The DF performed medication reconciliation, wrote prescriptions and faxed them to pharmacies, and arranged all anticoagulation services. In collaboration with the resident, the DF called PCPs' offices with discharge information and faxed discharge summaries to PCPs' offices outside the Partners Healthcare System. The DF wrote part or all of the computer discharge orders and discharge summaries at the request of the resident and interns. All discharge summaries still needed to be reviewed, edited, and signed by the resident or interns. The DF also noted pending tests and studies at time of discharge, and followed up on these tests for the team. The DF met with all patients to answer any questions about their discharge plan, medications, and appointments; while residents are encouraged to do this, it is not done as consistently. She provided her business card for any questions after their discharge. Follow‐up patient calls to the DF were either answered by her or triaged to the appropriate person. The DF also communicated with the patient's nurse about the discharge plans. For all patients discharged over a weekend, the DF would arrange the follow‐up appointments on Mondays and call the patients at home.

For both teams, residents received letters at the start of their rotation notifying them of the study and asking them to complete discharge summaries within 24 hours. All residents in the program were expected to do an online discharge tutorial and attend a didactic lecture on discharge summaries. The residents on the intervention team received a 5‐minute orientation on how best to work with the DF. Residents were given the autonomy to decide how much to use the DF's services. The scheduling of follow‐up appointments on the control team was the responsibility of the team resident as per usual care. The nursing component of the discharge process, including patient discharge education, was the same on both teams. Nurses on both floors are identically trained on these aspects of care. The nurses on both teams were surveyed about perception of the discharge process prior to the intervention and after the intervention. A research assistant (RA) called patients discharged home on both teams, 1 week after discharge, to ask about satisfaction with the discharge process, to determine if the patients had any questions, and to verify patient knowledge regarding whom they should contact for problems. The RA also noted the end time of attending rounds each day and the start time of resident sign‐out.

Outcome Measures and Follow‐Up

At the time of discharge, the RA collected baseline data on all patients discharged from both teams, including the number of follow‐up appointments scheduled. Patients were tracked through electronic medical records to see if and when they attended their follow‐up appointments, whether they changed the appointment, and whether patients returned to a hospital emergency department or were readmitted to MGH or an affiliated Partners hospital within 30 days. For patients outside the MGHPartners system, the research assistant contacted primary care physician offices to document follow‐up. The remaining patient data was obtained through the MGHPartners computerized information system.

The primary outcomes of the study were length of stay, time of discharge, number of emergency department visits, hospital readmissions, numbers of discharge summaries completed in 24 hours, time from discharge to discharge summary completion, and whether the discharge summary was completed before follow‐up. Secondary outcomes were number of follow‐up PCP appointments made at time of discharge, percentage of follow‐up appointments attended and time from discharge to attending a follow‐up appointment, patient phone survey results, and nursing perception of the discharge process, as well as the percentage of attending rounds that ended on time and the time of resident sign‐out.

Statistical Analyses

Patient characteristics were compared between intervention and control teams using 2‐sample t tests or Wilcoxon rank sum tests for continuous variables, and chi‐square tests for categorical variables. Hours to discharge summary completion and hospital length of stay were summarized using median and interquartiles (IQR), and compared between the 2 teams using Wilcoxon rank sum tests. Categorical outcomes were compared using chi‐square tests. Two‐sided P values 0.05 were considered statistically significant. SAS version 9.2 (SAS Institute Inc, Cary, NC) was used for all statistical analyses.

RESULTS

Study Sample

During the 5‐month intervention (November 12, 2008 to April 14, 2009), a combined total of 999 patients were admitted to the intervention and control general medical teams. We excluded 96 patients who were not discharged but transferred to another service or intensive care units, and 24 patients who died. We also excluded 7 patients who were discharged from both teams the first day of the study, because the DF was not involved with the patients' discharge planning. That left 872 patients discharged to either home, a facility, or having left against medical advice (AMA) included in the study: 440 patients on the intervention team and 432 patients on the control team (Figure 1). Baseline patient demographic and clinical characteristics were similar across both teams with only gender being significantly different (Table 1). The mean age was 63 years (range, 1896) and the mean comorbidity score was 2.3 (range, 012). Of note, about a quarter of patients were discharged to facilities, about half were Medicare recipients, and approximately 80% had a PCP. The DF participated in the discharge process for nearly all of the intervention patients; she reported contributing approximately 50% of the content to the discharge summaries.

Figure 1
Enrollment of Patients.
Baseline Participant Characteristics
CharacteristicsIntervention TeamControl Team
 n = 440n = 432
  • Abbreviations: AMA, against medical advice; COPD, chronic obstructive pulmonary disease; PCP, primary care physician; SD, standard deviation.

  • P < 0.05; no other comparisons were statistically significant.

  • Deyo Modification of the Charlson Comorbidity Index.

Mean age (SD), year63 (18)63 (18)
Women, n (%)*181 (41)207 (48)
Race, n (%)  
White non‐Hispanic267 (61)243 (56)
Black non‐Hispanic24 (5)33 (8)
Hispanic21 (5)17 (4)
Unknown/other128 (29)139 (32)
Health insurance, n (%)  
Medicare213 (48)226 (52)
Medicaid85 (19)81 (19)
Private110 (25)91 (21)
Other32 (7)34 (8)
PCP on admission, n (%)370 (84)356 (82)
Discharge disposition, n (%)  
AMA12 (3)14 (3)
Home305 (69)315 (73)
Facility123 (28)103 (24)
Mean comorbidity index score (SD)2.3 (2.4)2.3 (2.4)
Diagnoses  
Congestive heart failure30 (6%)27 (5%)
COPD/asthma34 (7%)47 (9%)
Cardiovascular disease54 (11%)50 (8%)
Alcohol/substance abuse29 (6%)34 (7%)
Gastrointestinal bleeds/ulcers38 (8%)41 (8%)
Hepatobiliary disease30 (6%)36 (7%)
Renal failure/kidney disease33 (7%)37 (7%)
Pneumonia36 (7%)22 (4%)
Musculoskeletal disease26 (5%)23 (5%)
Neurologic disease22 (4%)25 (5%)
Other163 (33%)172 (35%)

Primary Outcomes

Primary outcomes from the 2 medical teams are listed in Table 2. In the intervention group, significantly more discharge summaries were completed within 24 hours compared to the control group (293 [67%] vs 207 [48%]; P < 0.0001). Since nearly all patients discharged to facilities must have a discharge summary at the time of discharge, the overall difference in completion rates came mainly from patients discharged home or having left AMA from the intervention team (177 [56%] vs 112 [34%]; P < 0.0001). For all discharge summaries, the median time to completion on the intervention team was 18.9 hours compared with 73.1 hours on the control team (P < 0.0001). More discharge summaries were completed before the first follow‐up appointment on the intervention team (393 [89%] vs 330 [76%]; P < 0.001). The DF intervention had no effect on 30‐day readmission or emergency department visits. For patients on the DF team, 88 (20%) were readmitted within 30 days of discharge, as compared with 79 (18%) on the control team (P = 0.55). Similarly, 40 (9%) of the intervention team patients, as compared with 39 (9%) of the control team patients, visited the emergency department at least once within 30 days (P = 1.0). There was no difference in length of stay (LOS) between the 2 teams (median 4.0 days for both teams, P = 0.84).

Primary Outcomes
 Intervention TeamControl Team 
Variablesn = 440n = 432P Value
  • Abbreviations: AMA, against medical advice; IQR, interquartile range.

Discharge summaries completed 24 hr, n (%)293 (67)207 (48)<0.0001
Discharges to facilities116 (94)95 (92)0.60
Discharges to home/AMA177 (56)112 (34)<0.0001
Median hours to discharge summary completion for discharges to home/AMA (IQR)18.9 (0138)73.1 (4.3286)<0.0001
Discharge summary complete before time of follow‐up appointment.393 (89)330 (76)<0.0001
Emergency department visits in 30 days, n (%)40 (9)39 (9)1.0
Readmissions in 30 days, n (%)88 (20)79 (18)0.55
Median length of stay, days (IQR)4.0 (37)4.0 (28)0.84
Discharges to facilities6.0 (511)8.0 (513)0.17
Discharges to home/AMA4.0 (26)3.0 (26)0.61
Discharged by noon, n (%)38 (9)42 (10)0.64

Secondary Outcomes

Table 3 shows secondary outcomes from the 2 medical teams. Among the patients discharged from the DF team, 264 (62%) had scheduled follow‐up appointments with PCPs compared to the control team 151 (36%) (P < 0.0001). (Many patients going to rehabilitation hospitals are not given PCP appointments at the time of discharge.) Despite having more scheduled appointments, patients' actual follow‐up with PCPs was similar during the 5‐month study period among both intervention and control group (234 [65%] vs 223 [63%]; P = 0.58). However, there was earlier follow‐up with the primary provider in the first 2 or 4 weeks in the intervention group. At 2 weeks, 129 (36%) patients in the intervention group saw their provider compared to 81 (23%) patients in the control group (P < 0.0002), and at 4 weeks, 159 (44%) of the intervention group was seen compared to 99 (28%) of the control group (P < 0.0001). Of note, among the 415 patients on both teams discharged with scheduled appointments, only 53 (13%) of patients did not show up for the scheduled appointment and this no‐show rate was the same on both teams.

Secondary Outcomes
VariablesIntervention TeamControl TeamP Value
  • Against medical advice (AMA) patients excluded.

  • Patients excluded if AMA, readmitted, died after discharge, or discharged to hospice.

No. of eligible patients*428418 
Patients with follow‐up appointments to primary providers, n (%)264 (62)151 (36)<0.0001
No. of eligible patients359354 
Attended follow‐up appointment with primary provider during study, n (%)234 (65)223 (63)0.58
Within 2 weeks of discharge129 (36)81 (23)0.0002
Within 4 weeks of discharge159 (44)99 (28)<0.0001
No. of days round times were recorded10099 
No. of attending rounds ending by 12 PM45 (45%)31 (31%)0.058
Mean start time of sign‐out rounds16:3817:240.0007

Attending rounds ended on time (12 PM) 45% of the time in the intervention group compared to 31% in the control group (P = 0.058). Mean start time of resident sign‐out rounds was 1638 hours on the intervention team and 1724 hours on the control team (P = 0.0007).

We obtained patient reported outcome data by telephone within 2 to 4 weeks of discharge. Of the 620 patients discharged to home, 6 died or were readmitted to the hospital before being reached by phone. For the remaining 614 patients, we were able to contact 444 (72%). Of those, 321 (52%) agreed to participate in the phone interview. We surveyed similar proportions of intervention and control group patients (158 [52%] vs 163 [52%]) (Table 4). Both groups reported similar rates of having questions about their hospital stay after discharge (43 [27%] vs 49 [30%]; P = 0.62). The intervention group could better identify whom to call with questions (150 [95%] vs 138 [85%]; P = 0.003). The intervention group reported better understanding of their follow‐up plans (157 [99%] vs 141 [87%]; P = 0.001) and better understanding of their discharge medications (152 [96%] vs 142 [87%]; P = 0.001). More patients in the intervention group were satisfied with the discharge process (153 [97%] vs 124 [76%]; P < 0.0001).

Secondary Outcomes Continued: Patient Survey Results
 Intervention TeamControl TeamP Value
  • Patients excluded if died or readmitted prior to phone call.

  • Questions were answered on a 5‐point Likert scale. The number/percentage reflects participants who responded with the top 2 categories on the scale.

Patients discharged home*304310 
Patients contacted by phone after discharge, n (%)213 (70)231 (75)0.24
Agreed to participate in phone interview, n (%)158 (52)163 (53)0.94
Among those agreed to participate, n (%)   
Did you have questions about your hospital stay?43 (27)49 (30)0.62
Would you know who to call if you had questions after discharge?150 (95)138 (85)0.003
Satisfied with the discharge process?153 (97)124 (76)<0.0001
Did you understand your follow‐up plans?157 (99)141 (87)<0.0001
Did you understand your medications?152 (96)142 (87)0.001
Did you feel safe going home?153 (97)151 (92)0.07

Compared with nurses on the control team, nurses on the intervention team more often reported paperwork being completed in a timely fashion (56% vs 29%; P = 0.041) and being less worried about the discharge plan (44% vs 57%; P = 0.027). The intervention team nurses also reported fewer issues with medications/prescriptions (61% vs 82%) and being included more often in the discharge planning (50% vs 38%). However, neither of these results reached statistical significance (P = 0.81 and 0.50, respectively).

DISCUSSION

Our study embedded a nurse practitioner on a busy resident general medical team to help with all aspects of the discharge process for which physicians are responsible. Previous studies have been limited to patients with specific diagnoses, age, or disposition plans.1825 In this study, we included all general medical patients. Our intervention improved several important quality of care elements: the timeliness of completion of discharge summaries; and increased number of early follow‐up appointments, with more patients seen within 2 and 4 weeks after discharge. Patients reported better understanding of their follow‐up plans and more satisfaction with the discharge process. While not statistically significant, there was a trend towards better communication with nurses. For residents with work‐hour limitations, there was time savings with a trend towards finishing attending rounds on time and statistically significant earlier sign‐out rounds (46 minutes earlier). This intervention had no effect on patient length of stay, readmissions, or emergency department visits in the 30 days after discharge.

Despite improving many aspects of the discharge process and communication that have previously been raised as areas of concern for patient safety, there was no improvement in readmissions rates and ED utilization which are often used as the quality indicators for effective discharge planning. Similar types of interventions on general medical patients have generally also failed to show improvement in readmission rates.1820, 25 Weinberger et al. arranged follow‐up appointments within 1 week for patients discharged from a Veterans Administrative hospital; while patients were seen more often, the intervention actually increased readmission rates.20 Fitzgerald et al. had a case manager contact patients at home and encourage follow‐up, which increased follow‐up visits, but again had no effect on readmission.19 Einstadter et al. had a nurse case manager coordinate outpatient follow‐up on a resident team and also did not effect readmission rates or ED visits.18 Jack et al. in project reengineered discharge (RED) did show a significant reduction in combined hospital utilization measures. However, their study focused on a more limited patient population, and employed both a discharge advocate to arrange follow‐up and improve patient education, and a pharmacist to make postdischarge phone calls.25

So why did readmissions rates and ED visits not change in our study? It would be reasonable to think that having earlier follow‐up appointments, better and timely physician‐to‐physician communication, and a facilitator for patient questions should improve the quality of the discharge process. In a recent study, Jha et al. found there was no association between chart‐based measures of discharge quality and readmissions rates, and only a modest association for patient‐reported measures of discharge quality and readmission rates.28 The authors suggest readmission rates are driven by many factors beyond just improved discharge safety. Perhaps readmission rates are too complex a measure to use to assess discharge process improvement. For fiscal reasons, it is understandable that hospitals, insurance companies, and the Centers for Medicare and Medicaid want to reduce readmission rates and ED utilization. Jencks et al. noted the cost of readmissions in 2004 was 17.4 billion dollars.29 However, sweeping efforts to improve the discharge process for all general medical patients may not yield significant reductions in readmissions, as this study suggests. We may need to focus aggressive intervention on smaller target populations, as prior studies on focused groups suggest.2123

There are no evidence‐based studies to suggest when optimal follow‐up should occur after discharge.26 Several medical society guidelines recommend 2 weeks. More patients on the intervention team were seen within 2 weeks, but readmission rates were not affected. The University Health System Consortium recently reported that the majority of readmissions occurred within 6 days, with the average being about 2 to 3 days.30 In this study, the median days to readmit were 12 for the intervention team and 10 for the control. It is possible that even with our improved 2‐week follow‐up, this was not early enough to reduce readmissions. Follow‐up may need to be within 13 days of discharge for highly vulnerable patients, to significantly change readmission rates. Further studies focusing on this question would be helpful.

Finally, with ACGME limitation of work hours, many residency programs are looking for ways to reduce residents' workload and increase time for education. With a significant trend towards finishing attending rounds on time, it is likely that more residents on the intervention team were able to attend the noon‐time educational conferences. We speculate that this was due to fewer interruptions during rounds because the DF was available for nurses' questions. Sign‐out rounds occurred significantly earlier, possibly because of improved resident efficiency due to the DF's help with the discharge process. While residents may lose some educational experience from not performing all discharge tasks, they gain experience working in interdisciplinary teams, have increased time for education, and reduced work hours. Since the ACGME limits the number of residents per program and increasing the residency size is not an option, a DF should be considered as a possible solution to ACGME work‐hour restrictions.

This study had several limitations. First, the intervention team had 1 specific person embedded, and therefore the results of this study may have limited generalizability. Second, the limited number of residents working with the DF could have biased the intervention, as not all residents worked equally well with the DF. However, this may represent the real‐world experience on any teaching service, given variation in working styles and learning curves of residents over their training. Third, this study was done at 1 university‐affiliated urban Academic Medical Center, making it potentially less generalizable to resident teams in community hospitals. Fourth, we were not able to capture readmissions and ED visits at institutions outside the MGHPartners Healthcare System. However, given that patients were assigned at random to either team, this factor should have impacted both teams equally. Fifth, the study occurred during Massachusetts healthcare reform which requires everyone to have health insurance. This may have affected the rates of ED visits and readmission rates, especially with a shortage of primary care physicians and office visits. Finally, this intervention was not cost‐neutral. Paying for a nurse practitioner to help residents with the work of discharge and providing patients with additional services had many advantages, but this quality improvement project did not pay for itself through shorter LOS, or decreases in ED visits or readmissions.

While readmission rates and ED utilization are important patient outcomes, especially in the current healthcare climate, what determines readmissions and ED visits is likely complex and multifactorial. This study suggests that, in the nationwide effort to reduce readmissions, solely improving the discharge process for all general medical patients may not produce the hoped‐for financial savings. Improving the discharge process, however, is something valuable in its own right. Adding a DF to a resident team does improve some quality markers of the discharge process and decreases work hours for residents.

Acknowledgements

Sara Macchiano, RN for her help with the data gathering of this study.

References
  1. Forster AJ,Murff HJ,Peterson JF,Gandhi TK,Bates DW.Adverse drug events occurring following hospital discharge.J Gen Intern Med.2005;20(4):317323.
  2. Forster AJ,Murff HJ,Peterson JF,Gandhi TK,Bates DW.The incidence and severity of adverse events affecting patients after discharge from the hospital.Ann Intern Med.2003;138(3):161167.
  3. Moore C,Wisnivesky J,Williams S,McGinn T.Medical errors related to discontinuity of care from an inpatient to an outpatient setting.J Gen Intern Med.2003;18(8):646651.
  4. Coleman EA,Smith JD,Raha D,Min SJ.Posthospital medication discrepancies: Prevalence and contributing factors.Arch Intern Med.2005;165(16):18421847.
  5. Kosecoff J,Kahn KL,Rogers WH, et al.Prospective payment system and impairment at discharge. The ‘quicker‐and‐sicker’ story revisited.JAMA.1990;264(15):19801983.
  6. Cutler D.The incidence of adverse medical outcomes under prospective payment.Econometrica. 1995;63:2950.
  7. Solomon JK,Maxwell RB,Hopkins AP.Content of a discharge summary from a medical ward: Views of general practitioners and hospital doctors.J R Coll Physicians Lond.1995;29(4):307310.
  8. van Walraven C,Weinberg AL.Quality assessment of a discharge summary system.Can Med Assoc J.1995;152(9):14371442.
  9. van Walraven C,Seth R,Laupacis A.Dissemination of discharge summaries. Not reaching follow‐up physicians.Can Fam Physician.2002;48:737742.
  10. van Walraven C,Seth R,Austin PC,Laupacis A.Effect of discharge summary availability during post‐discharge visits on hospital readmission.J Gen Intern Med.2002;17(3):186192.
  11. Kripalani S,LeFevre F,Phillips CO,Williams MV,Basaviah P,Baker DW.Deficits in communication and information transfer between hospital‐based and primary care physicians: Implications for patient safety and continuity of care.JAMA.2007;297(8):831841.
  12. Bell CM,Schnipper JL,Auerbach AD, et al.Association of communication between hospital‐based physicians and primary care providers with patient outcomes.J Gen Intern Med.2009;24(3):381386.
  13. Moore C,McGinn T,Halm E.Tying up loose ends: Discharging patients with unresolved medical issues.Arch Intern Med.2007;167(12):13051311.
  14. Roy CL,Poon EG,Karson AS, et al.Patient safety concerns arising from test results that return after hospital discharge.Ann Intern Med.2005;143(2):121128.
  15. Snow V,Beck D,Budnitz T, et al.Transitions of care consensus policy statement: American College of Physicians, Society of General Internal Medicine, Society of Hospital Medicine, American Geriatrics Society, American College of Emergency Physicians, and Society for Academic Emergency Medicine.J Hosp Med.2009;4(6):364370.
  16. Macaulay EM,Cooper GG,Engeset J,Naylor AR.Prospective audit of discharge summary errors.Br J Surg.1996;83(6):788790.
  17. Coleman EA,Berenson RA.Lost in transition: Challenges and opportunities for improving the quality of transitional care.Ann Intern Med.2004;141(7):533536.
  18. Einstadter D,Cebul RD,Franta PR.Effect of a nurse case manager on postdischarge follow‐up.J Gen Intern Med.1996;11(11):684688.
  19. Fitzgerald JF,Smith DM,Martin DK,Freedman JA,Katz BP.A case manager intervention to reduce readmissions.Arch Intern Med.1994;154(15):17211729.
  20. Weinberger M,Oddone EZ,Henderson WG.Does increased access to primary care reduce hospital readmissions? Veterans Affairs Cooperative Study Group on Primary Care and Hospital Readmission.N Engl J Med.1996;334(22):14411447.
  21. Phillips CO,Wright SM,Kern DE,Singa RM,Shepperd S,Rubin HR.Comprehensive discharge planning with postdischarge support for older patients with congestive heart failure: A meta‐analysis.JAMA.2004;291(11):13581367.
  22. Naylor MD,Brooten DA,Campbell RL,Maislin G,McCauley KM,Schwartz JS.Transitional care of older adults hospitalized with heart failure: A randomized, controlled trial.J Am Geriatr Soc.2004;52(5):675684.
  23. Coleman EA,Smith JD,Frank JC,Min SJ,Parry C,Kramer AM.Preparing patients and caregivers to participate in care delivered across settings: The Care Transitions Intervention.J Am Geriatr Soc.2004;52(11):18171825.
  24. Coleman EA,Parry C,Chalmers S,Min SJ.The care transitions intervention: Results of a randomized controlled trial.Arch Intern Med.2006;166(17):18221828.
  25. Jack BW,Chetty VK,Anthony D, et al.A reengineered hospital discharge program to decrease rehospitalization: A randomized trial.Ann Intern Med.2009;150(3):178187.
  26. Balaban RB,Weissman JS,Samuel PA,Woolhandler S.Redefining and redesigning hospital discharge to enhance patient care: A randomized controlled study.J Gen Intern Med.2008;23(8):12281233.
  27. Forster AJ,Clark HD,Menard A, et al.Effect of a nurse team coordinator on outcomes for hospitalized medicine patients.Am J Med.2005;118(10):11481153.
  28. Jha AK,Orav EJ,Epstein AM.Public reporting of discharge planning and rates of readmissions.N Engl J Med.2009;361(27):26372645.
  29. Jencks SF,Williams MV,Coleman EA.Rehospitalizations among patients in the Medicare fee‐for‐service program.N Engl J Med.2009;360(14):14181428.
  30. Consortium UHS. Reducing Readmissions SC22009. Available at: https://www.uhc.edu/1244.htm
References
  1. Forster AJ,Murff HJ,Peterson JF,Gandhi TK,Bates DW.Adverse drug events occurring following hospital discharge.J Gen Intern Med.2005;20(4):317323.
  2. Forster AJ,Murff HJ,Peterson JF,Gandhi TK,Bates DW.The incidence and severity of adverse events affecting patients after discharge from the hospital.Ann Intern Med.2003;138(3):161167.
  3. Moore C,Wisnivesky J,Williams S,McGinn T.Medical errors related to discontinuity of care from an inpatient to an outpatient setting.J Gen Intern Med.2003;18(8):646651.
  4. Coleman EA,Smith JD,Raha D,Min SJ.Posthospital medication discrepancies: Prevalence and contributing factors.Arch Intern Med.2005;165(16):18421847.
  5. Kosecoff J,Kahn KL,Rogers WH, et al.Prospective payment system and impairment at discharge. The ‘quicker‐and‐sicker’ story revisited.JAMA.1990;264(15):19801983.
  6. Cutler D.The incidence of adverse medical outcomes under prospective payment.Econometrica. 1995;63:2950.
  7. Solomon JK,Maxwell RB,Hopkins AP.Content of a discharge summary from a medical ward: Views of general practitioners and hospital doctors.J R Coll Physicians Lond.1995;29(4):307310.
  8. van Walraven C,Weinberg AL.Quality assessment of a discharge summary system.Can Med Assoc J.1995;152(9):14371442.
  9. van Walraven C,Seth R,Laupacis A.Dissemination of discharge summaries. Not reaching follow‐up physicians.Can Fam Physician.2002;48:737742.
  10. van Walraven C,Seth R,Austin PC,Laupacis A.Effect of discharge summary availability during post‐discharge visits on hospital readmission.J Gen Intern Med.2002;17(3):186192.
  11. Kripalani S,LeFevre F,Phillips CO,Williams MV,Basaviah P,Baker DW.Deficits in communication and information transfer between hospital‐based and primary care physicians: Implications for patient safety and continuity of care.JAMA.2007;297(8):831841.
  12. Bell CM,Schnipper JL,Auerbach AD, et al.Association of communication between hospital‐based physicians and primary care providers with patient outcomes.J Gen Intern Med.2009;24(3):381386.
  13. Moore C,McGinn T,Halm E.Tying up loose ends: Discharging patients with unresolved medical issues.Arch Intern Med.2007;167(12):13051311.
  14. Roy CL,Poon EG,Karson AS, et al.Patient safety concerns arising from test results that return after hospital discharge.Ann Intern Med.2005;143(2):121128.
  15. Snow V,Beck D,Budnitz T, et al.Transitions of care consensus policy statement: American College of Physicians, Society of General Internal Medicine, Society of Hospital Medicine, American Geriatrics Society, American College of Emergency Physicians, and Society for Academic Emergency Medicine.J Hosp Med.2009;4(6):364370.
  16. Macaulay EM,Cooper GG,Engeset J,Naylor AR.Prospective audit of discharge summary errors.Br J Surg.1996;83(6):788790.
  17. Coleman EA,Berenson RA.Lost in transition: Challenges and opportunities for improving the quality of transitional care.Ann Intern Med.2004;141(7):533536.
  18. Einstadter D,Cebul RD,Franta PR.Effect of a nurse case manager on postdischarge follow‐up.J Gen Intern Med.1996;11(11):684688.
  19. Fitzgerald JF,Smith DM,Martin DK,Freedman JA,Katz BP.A case manager intervention to reduce readmissions.Arch Intern Med.1994;154(15):17211729.
  20. Weinberger M,Oddone EZ,Henderson WG.Does increased access to primary care reduce hospital readmissions? Veterans Affairs Cooperative Study Group on Primary Care and Hospital Readmission.N Engl J Med.1996;334(22):14411447.
  21. Phillips CO,Wright SM,Kern DE,Singa RM,Shepperd S,Rubin HR.Comprehensive discharge planning with postdischarge support for older patients with congestive heart failure: A meta‐analysis.JAMA.2004;291(11):13581367.
  22. Naylor MD,Brooten DA,Campbell RL,Maislin G,McCauley KM,Schwartz JS.Transitional care of older adults hospitalized with heart failure: A randomized, controlled trial.J Am Geriatr Soc.2004;52(5):675684.
  23. Coleman EA,Smith JD,Frank JC,Min SJ,Parry C,Kramer AM.Preparing patients and caregivers to participate in care delivered across settings: The Care Transitions Intervention.J Am Geriatr Soc.2004;52(11):18171825.
  24. Coleman EA,Parry C,Chalmers S,Min SJ.The care transitions intervention: Results of a randomized controlled trial.Arch Intern Med.2006;166(17):18221828.
  25. Jack BW,Chetty VK,Anthony D, et al.A reengineered hospital discharge program to decrease rehospitalization: A randomized trial.Ann Intern Med.2009;150(3):178187.
  26. Balaban RB,Weissman JS,Samuel PA,Woolhandler S.Redefining and redesigning hospital discharge to enhance patient care: A randomized controlled study.J Gen Intern Med.2008;23(8):12281233.
  27. Forster AJ,Clark HD,Menard A, et al.Effect of a nurse team coordinator on outcomes for hospitalized medicine patients.Am J Med.2005;118(10):11481153.
  28. Jha AK,Orav EJ,Epstein AM.Public reporting of discharge planning and rates of readmissions.N Engl J Med.2009;361(27):26372645.
  29. Jencks SF,Williams MV,Coleman EA.Rehospitalizations among patients in the Medicare fee‐for‐service program.N Engl J Med.2009;360(14):14181428.
  30. Consortium UHS. Reducing Readmissions SC22009. Available at: https://www.uhc.edu/1244.htm
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Communication and information deficits in patients discharged to rehabilitation facilities: An evaluation of five acute care hospitals

Effective communication among physicians during the hospital discharge process is critical to patient care. Patients are at high risk of having an adverse drug event,1 readmission, or death2 during the transition from hospital to home.3 Ineffective communication between inpatient and outpatient providers has been implicated as a leading cause of adverse events.35 Conversely, efforts to improve communication have been shown to improve compliance with follow‐up tests and decrease readmission rates.6, 7 Recently, the absence of several specific data elements in discharge documentation have been shown to be common and to have potential for patient harm, including test results that are pending at the time of discharge.8, 9 Unexplained discrepancies between preadmission and discharge medication regimens are also common and potentially dangerous.1

According to the Joint Commission for Accreditation of Healthcare Organizations (TJC), the following elements should be included in discharge summaries: the reason for hospitalization; significant findings; procedures performed and care, treatment, and services provided; the patient's condition at discharge; and information provided to the patient and family, as appropriate.10 TJC also advocates medication reconciliation, a process of identifying the most accurate list of all medications a patient is takingincluding name, dosage, frequency, and routeand using this list to provide correct medications for patients anywhere within the health care system.11

Despite the importance of complete communication among providers at hospital discharge, a recent systematic review showed that discharge summaries often lacked important information such as diagnostic test results (missing from 33%‐63%), treatment or hospital course (7%‐22%), discharge medications (2%‐40%), test results pending at discharge (65%), patient or family counseling (90%‐92%), and follow‐up plans (2%‐43%).1

Most of the studies addressing this issue have evaluated communication pitfalls between acute care hospitals and primary care physicians among patients discharged home.17 In contrast, the quality of discharge documentation among patients discharged to rehabilitation centers and other subacute care facilities has been less well studied, perhaps due to relatively smaller numbers of patients discharged to such facilities. This communication is as or more important because these patients are potentially more vulnerable and their medical conditions more active than for patients discharged home.12 Furthermore, discharge information from acute care hospitals will often form the basis for admission orders at subacute facilities. Last, these patients will have a second transition in care (from subacute facility to home) whose quality is dependent at least in part on the quality of communication during the first transition.

The aim of this study was to evaluate the quality of information transfer among patients discharged from acute hospitals to subacute facilities across an integrated healthcare delivery system. The long‐term goals of this effort were to determine the areas most in need of improvement, to guide interventions to address these problems, and to track improvements in these measures over time as interventions are implemented and refined.

Methods

This observational study was conducted as part of a quality improvement project evaluating the quality of information provided during the discharge process across Partners Health Care System. The institutional review boards of the participating institutions approved the study.

Study Sample

We evaluated a sample of discharge documentation packets (eg, discharge summaries, discharge orders, nursing instructions, care coordination, and physical/occupational therapy notes) of patients discharged from all 5 acute care hospitals of the Partners Healthcare System to 30 subacute facilities (rehabilitation hospitals and skilled nursing facilities) from March 2005 through June 2007.

For reviewers at acute sites, discharge documentation packets were randomly selected each quarter using a random number generator within Microsoft Excel (Microsoft, Redmond, WA). At subacute sites, reviewers selected which packets to review, although they were encouraged to review all of them. Random selection of packets could not be achieved at subacute sites because reviews took place on the day of admission to the subacute facility. All reviewers received 1 hour of training on how to evaluate discharge packets, including review of a standardized teaching packet with 1 of the coauthors (J.L.S. or T.O.).

Two of the 5 acute care hospitals in the study are academic medical centers and the other 3 are community hospitals. Reviewers were a mix of trained medical residents or nurse practitioners at acute sites and admitting physicians or nurse practitioners at receiving subacute sites.

Fifty packets were reviewed per acute site per quarter. This provided roughly 10% precision around our estimates (ie, if compliance with a measure were 80%, the 95% confidence interval around this estimate would be 70%‐90%). This sample size is consistent with those used to obtain other national benchmarks, such as those for National Hospital Quality Measures, which generally require at least 35 cases per quarter.13

Measures

A multidisciplinary team at Partners derived, reviewed, and refined a minimum data set required to appropriately care for patients during the first 72 hours after transfer from an acute care hospital to a subacute facility. Several of these measures are required by TJC. Other measures were either modifications of TJC measures made to facilitate uniform data collection (eg, history and physical examination at admission instead of significant findings) or additional data elements (not required by TJC) felt to be important to patient care based on the medical literature and interviews with receiving providers at subacute facilities. All measures were refined by the multidisciplinary team with input from additional subspecialists as needed (see Table 1 for the final list of measures).

Measured Data Elements at Discharge
 Reason(s) for Admission
Joint Commission requirementsA focused history
A focused physical exam
Pertinent past medical history
Treatment rendered
Discharge diagnosis(es)
Condition on discharge
Discharge summary
Any information missing
Non‐Joint Commission requirements
Medication informationDischarge medications
Drug allergies
Preadmission medication information
Explanation for any differences between preadmission and discharge medications
Test results informationLatest pertinent laboratory results
Pertinent radiology results
Test results pending at time of transfer
Overall assessmentWere management and follow‐up plans adequately described?
Did you uncover a significant condition not mentioned in the discharge packet?

Data Collection

After reviewing the entire discharge documentation packet, reviewers completed a survey concerning the inclusion of the required data elements. Surveys were completed online using Perseus Survey Solutions 6.0 (Perseus Development Corp., Braintree, MA) in the month following discharge (for reviewers at acute care sites) or within 24 hours of admission to the subacute facility (for reviewers at subacute sites). To verify the accuracy and completeness of packets, reviewers at acute sites were instructed to compare the discharge documentation to a review of the inpatient medical record. Similarly, reviewers at subacute sites were instructed to complete their evaluations after admitting each patient to their facility.

Outcomes

The primary outcome was the proportion of packets that contained each data element. In addition, we calculated the proportion of packets that contained all applicable elements required by TJC and all applicable data elements measured in the study. Last, we evaluated two global (albeit subjective) measures of satisfaction with the packet: Were management and follow‐up plans adequately described? (both components needed to be adequately described to get credit for this question) and Did you uncover a significant condition not mentioned in the discharge packet? Significant conditions were defined as active medical problems requiring management during or immediately following the hospitalization.

Statistical Analysis

Results were calculated as proportions, odds ratios, and 95% confidence intervals (CI), using SAS version 9.1 (SAS Institute, Inc., Cary, NC). Simple logistic regression was used to compare inclusion of data elements between medical and surgical services and between academic medical centers and community hospitals. To evaluate interrater reliability, 2 reviewers (both at acute sites) independently evaluated 29 randomly chosen charts, each with 12 data elements.

Results

A total of 1501 discharge documentation packets were reviewed, including 980 patients (65%) from a medical unit and 521 patients (35%) from a surgical unit. Based on 2007 data, these packets represent approximately 4% of all eligible discharges to subacute facilities. Patients discharged from 1 of the 2 academic medical centers represented 44% of the sample. A total of 644 discharge packets (43%) were reviewed at acute sites and 814 packets (54%) were reviewed at subacute sites. Information about reviewer site was missing in 43 discharge packets (3%). For the 29 charts independently reviewed by 2 reviewers, there was complete agreement for 331 out of 348 data elements (95.1%).

Only 1055 (70%) discharge summaries had all the information required by TJC (Table 2). Physical examination at admission (a component of significant findings, as noted above) and condition at discharge were the 2 elements most often missing. The defect‐free rate varied by site, with a range of 61% to 76% across the 5 acute care hospitals (data not shown).

Inclusion of Discharge Data Elements
 Sample SizeMissing [n (%)]95% CI Missing %
  • Abbreviation: CI, confidence interval.

Joint Commission requirements
Reason(s) for admission149714 (0.9)0.41.4
A focused history149365 (4.4)3.35.3
A focused physical exam1493170 (11.4)9.713
Pertinent past medical history149469 (4.6)3.55.6
Treatment rendered149433 (2.2)1.42.9
Discharge diagnosis(es)148053 (3.6)2.64.5
Condition on discharge1462208 (14.2)12.416.0
Discharge summary147590 (6.1)4.87.3
Any information missing1501447 (29.7)27.432.0
Non‐Joint Commission requirements
Medication information
Discharge medications149119 (1.3)0.71.8
Drug allergies147088 (6.0)4.77.2
Preadmission medication information1460297 (20.3)18.322.4
Explanation for any differences between preadmission and discharge medications1060374 (35.3)32.038.1
Test results information
Latest pertinent lab results1460261 (17.9)15.919.8
Pertinent radiology results1303139 (10.7)912.4
Test results pending at time of transfer341160 (47.2)41.952.5
Overall assessment
Were management and follow‐up plans adequately described?1461No (%): 161 (11.1)95% CI No %: 9.512.7
Did you uncover a significant condition not mentioned in the discharge packet?1469Yes (%): 162 (11.0)95% CI Yes %: 9.413.0
All applicable elements present1501503 (33.5)31.135.9

The rates of inclusion of other (non‐TJC required) data elements are shown in Table 2. Most often missing were preadmission medication regimens, any documented reason for any difference between preadmission and discharge medications, pertinent laboratory results, and an adequate follow‐up plan (including who to follow up with, when to follow‐up, and a list of tasks to be accomplished at the follow‐up visit). Notation regarding significant test results that were pending at the time of transfer was missing in 160 of 341 applicable patients (47%), and in 162 patients (11%), physicians uncovered a significant condition that was not mentioned in the discharge documentation. Only 503 (33.5%) discharge documentation packets had all applicable measures present. In addition, the discharge summary was not received at all on the day of discharge according to the receiving site in 90 patients (6%).

Reviewers were asked in a separate question which missing data were necessary for patient care. Data elements most often cited were explanations for any medication discrepancies and test results pending at the time of the hospital discharge.

Community hospitals had a higher rate of inclusion of TJC‐required data elements when compared to academic medical centers (Table 3). Also, among non‐TJC required data elements, inclusion rates were higher among the community hospitals, especially regarding information about medication discrepancies, pending test results, and follow‐up information (Table 3).

Completeness of Discharge Documentation by Site and Service
 Total (n)All Elements Present [n (%)]OR (95% CI)
  • Abbreviations: CI, confidence interval; OR, odds ratio.

Joint Commission requirements
Hospital type
Community hospitals949826 (87)2.7 (2.13.6)
Academic medical centers541384 (71)Ref.
Service
Medical services1013745 (73)1.3 (1.01.7)
Surgical services488332 (68)Ref.
Explanation for any medication discrepancies Yes [n (%)] 
Hospital type
Community hospitals718550 (76)5.0 (3.86.5)
Academic medical centers342136 (39)Ref.
Service
Medical services754529 (70)2.2 (1.72.9)
Surgical services306157 (51)Ref.
Test results pending at time of transfer Yes [n (%)] 
Hospital type
Community hospitals172109 (63)2.4 (1.53.7)
Academic medical centers16971 (42)Ref.
Service
Medical services227146 (64)4.2 (2.66.9)
Surgical services11434 (30)Ref.
Follow‐up plans adequately described Yes [n (%)] 
Hospital type
Community hospitals968883 (91)1.7 (1.22.4)
Academic medical centers543466 (85)Ref.
Service
Medical services983862 (87)0.67 (0.51.0)
Surgical services478437 (91)Ref.

Although no differences were found between medical and surgical services regarding compliance with TJC requirements, a difference was noted in documentation of explanations of medication discrepancies and pending test results, with medical services performing better in both measures (Table 3).

In general, reviewers at subacute sites more often evaluated packets as deficient than reviewers at acute sites, up to an absolute difference of 33% in the proportion of missing data, depending on the data element (see Appendix, Table 1).

Discussion

Our study evaluated the completeness of documentation in the discharge summaries of patients discharged from acute care to subacute care facilities. Our results for the inclusion of TJC‐required data elements were similar to those quoted in the literature for patients discharged home.6 Our results also demonstrated a high rate of other missing data elements that are arguably of equal or greater importance, including reasons for discrepancies between preadmission and discharge medication regimens and tests that are pending at the time of discharge.1, 8, 9 Our results also demonstrated the relatively poorer performance of academic centers compared to community hospitals regarding inclusion of information about medication reconciliation, follow‐up, pending test results, and complete information required by TJC. Finally, we found that patients discharged from surgical services more often lacked documentation of medication discrepancies and pending test results compared with patients from medical services.

To our knowledge, this is one of the first studies looking at the quality of information transfer in patients discharged to subacute care facilities. The results of this study are not surprising given the known problems with general information transfer at hospital discharge.1 The fact that community hospitals provided more complete information than academic medical centers for certain data elements may be due to the difference between residents and more senior physicians preparing discharge documentation. Such differences could reflect differences in experience, training, and degree of appreciation for the importance of discharge documentation, and/or restrictions in work hours among residents (eg, resulting in time‐pressure to complete discharge summaries and/or summaries being written by residents who know the patients less well). These hypotheses deserve further exploration. The differences between medical and surgical services should also be validated and explored in other healthcare systems, including both academic and community settings.

The results of this study should be viewed in light of the study's limitations. Packets evaluated by reviewers at subacute facilities were chosen by the reviewers and may not have been representative of all patients received by that facility (in contrast to those reviewed at the acute sites, which were chosen at random and more likely to be representative, although we did not formally test for this). It is possible that reviewers at subacute sites selected the worst discharge documentation packets for evaluation. Second, evaluations by reviewers at subacute sites did not distinguish between information missing from discharge documentation and failure to receive the documentation at all from the acute care hospital (again in contrast to reviewers at acute sites, who always had access to the documentation). Lastly, reviewers at acute and subacute sites may have graded packets differently due to their different clinical perspectives. These 3 factors may explain the relatively poorer results of discharge packets reviewed by reviewers at subacute sites. Further study would be needed to distinguish among these possibilities (eg, having acute and subacute reviewers answer the same questions for the same discharge packets to allow us to measure interrater reliability between the different kinds of reviewers; explicitly asking subacute reviewers about receipt of each piece of documentation; comparing the distribution of diagnosis‐related group [DRG] codes and hospital length of stay in evaluated vs. total discharge packets as a measure of representativeness). We also cannot rule out the possibility of reviewer bias, but all reviewers were trained in a standardized fashion and we know that reliability of assessments were high, at least among reviewers at acute sites. Last, we did not measure actual or potential adverse events caused by these information deficits.

As part of a Partners‐wide initiative to improve transitions in care, the results were presented to the administrations of each of the 5 acute care hospitals. The Partners High Performance Medicine Transition team then began work with a steering committee (composed of representatives from each hospital) to address these deficiencies. Since then, the hospitals have taken several steps to improve the quality of information transfer for discharged patients, including the following:

  • Technological improvements to the hospitals' discharge ordering systems to actively solicit and/or autoimport the required information into discharge documentation.

  • Creation of discharge templates to record the required information on paper.

  • Provision of feedback to clinicians and their service chiefs regarding the ongoing quality of their discharge documentation.

  • Creation of an online Partners‐wide curriculum on discharge summary authorship, with a mandatory quiz to be taken by all incoming clinicians.

 

In conclusion, we found room for improvement in the inclusion of data elements required for the safe transfer of patients from acute hospitals to subacute facilities, especially in areas such as medication reconciliation, pending test results, and adequate follow‐up plans. We also found variation by site and type of service. For patients discharged to rehabilitation and other subacute facilities, improvement is needed in the communication of clinically relevant information to those providing continuing care.

Appendix

0

Differences in evaluation scores between reviewers at acute and Sub‐Acute Sites
JCAHO IndicatorsReviews from Sub‐Acute Sites (N = 814)*Reviews from Acute Sites (N = 644)*
Sample SizeMissing N%95% CISample SizeMissing%95% CI
  • Information about the reviewer was missing in 43 cases

Reason(s) for admission81291.10.41.864340.60.011.2
A focused history810496.14.47.7642162.51.33.7
A focused physical exam81013116.213.718.7641345.33.67.0
Pertinent past medical history810506.24.57.86421422.01.13.3
Treatment rendered811293.62.34.964140.60.011.2
Discharge diagnosis(es)806597.35.59.163071.10.31.9
Condition on discharge8009211.59.313.762210917.514.520.5
Discharge summary809779.57.511.5624111.80.72.8
Any information missing
Medication InformationSample SizeMissing%95% CISample SizeMissing%95% CI
Discharge medications811121.50.72.363860.90.21.7
Drug allergies811475.84.27.4639355.53.77.2
Explanation for any differences between preadmission and discharge medications54227550.746.5554988817.714.321.0
Test results informationSample SizeMissing%95% CISample SizeMissing%95% CI
Latest pertinent lab results79017822.519.625.46297311.69.114.1
Pertinent radiology results66811016.513.719.3601274.52.86.2
Test results pending at time of transfer1838747.540.354.81527348.040.156.0
Management InformationSample SizeNo%95% CISample SizeNo%95% CI
Were management and follow‐up plans adequately described?79412115.212.717.76317912.59.915.1
Sample SizeYes%95% CISample SizeYes%95% CI
Did you uncover a significant condition not mentioned in the discharge packet?79311714.812.317.2635386.04.47.8
References
  1. Schnipper JL, Kirwin JL, Cotugno MC, et al.Role of pharmacist counseling in preventing adverse drug events after hospitalization.Arch Intern Med.2006;166:565571.
  2. Van Walraven C, Mamdani M, Fang J, Austin PC.Continuity of care and patient outcomes after hospital discharge.J Gen Intern Med.1989;19:624631.
  3. Kripalani S, LeFevre F, Phillips CO, Williams MV, Basaviah P, Baker DW.Deficits in communication and information transfer between hospital‐based and primary care physicians: implications for patient safety and continuity of care.JAMA.2007;297:831841.
  4. Van Walraven C, Seth R, Austin PC, Laupacis A.Effect of discharge summary availability during post‐discharge visits on hospital readmission.JGen Intern Med.2002;17:186192.
  5. Moore C, Wisnivesky J, Williams S, McGinn T.Medical errors related to discontinuity of care from an inpatient to an outpatient setting.J Gen Intern Med.2003;18:646651.
  6. Kripalani S, Jackson AT, Schnipper JL, Coleman EA.Promoting effective transitions of care at hospital discharge: a review of key issues for hospitalists.J Hosp Med.2007;2:314323.
  7. Afilalo M, Lang E, Léger R, et al.Impact of a standardized communication system on continuity of care between family physicians and the emergency department.CJEM.2007;9:7986.
  8. Roy CL, Poon EG, Karson AS, et al.Patient safety concerns arising from test results that return after hospital discharge.Ann Intern Med.2005;143:121128.
  9. Moore C, McGinn T, Halm E.Tying up loose ends: discharging patients with unresolved medical issues.Arch Intern Med.2007;167:13051311.
  10. Standard IM.6.10: Hospital Accreditation Standards.Oakbrook Terrace, IL:Joint Commission on Accreditation of Healthcare Organizations;2006:338340.
  11. Joint Commission on Accreditation of Healthcare Organizations. Joint Commission national patient safety goals. Available at: http://www.jointcommission.org/PatientSafety/NationalPatientSafetyGoals. Accessed July 2009.
  12. Prvu Bettger JA, Stineman MG.Effectiveness of multidisciplinary rehabilitation services in post acute care: state‐of‐the‐science. A review.Arch Phys Med Rehabil.2007;88:15261534.
  13. Joint Commission on Accreditation of Healthcare Organizations. Specification Manual for National Hospital Quality Measures: Population and Sampling Specifications Version 2.4. Available at: http://www.jointcommission.org/PerformanceMeasurement/PerformanceMeasurement/Current+NHQM+Manual.htm. Accessed July 2009.
Article PDF
Issue
Journal of Hospital Medicine - 4(8)
Publications
Page Number
E28-E33
Legacy Keywords
patient discharge, quality indicators, rehabilitation centers
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Effective communication among physicians during the hospital discharge process is critical to patient care. Patients are at high risk of having an adverse drug event,1 readmission, or death2 during the transition from hospital to home.3 Ineffective communication between inpatient and outpatient providers has been implicated as a leading cause of adverse events.35 Conversely, efforts to improve communication have been shown to improve compliance with follow‐up tests and decrease readmission rates.6, 7 Recently, the absence of several specific data elements in discharge documentation have been shown to be common and to have potential for patient harm, including test results that are pending at the time of discharge.8, 9 Unexplained discrepancies between preadmission and discharge medication regimens are also common and potentially dangerous.1

According to the Joint Commission for Accreditation of Healthcare Organizations (TJC), the following elements should be included in discharge summaries: the reason for hospitalization; significant findings; procedures performed and care, treatment, and services provided; the patient's condition at discharge; and information provided to the patient and family, as appropriate.10 TJC also advocates medication reconciliation, a process of identifying the most accurate list of all medications a patient is takingincluding name, dosage, frequency, and routeand using this list to provide correct medications for patients anywhere within the health care system.11

Despite the importance of complete communication among providers at hospital discharge, a recent systematic review showed that discharge summaries often lacked important information such as diagnostic test results (missing from 33%‐63%), treatment or hospital course (7%‐22%), discharge medications (2%‐40%), test results pending at discharge (65%), patient or family counseling (90%‐92%), and follow‐up plans (2%‐43%).1

Most of the studies addressing this issue have evaluated communication pitfalls between acute care hospitals and primary care physicians among patients discharged home.17 In contrast, the quality of discharge documentation among patients discharged to rehabilitation centers and other subacute care facilities has been less well studied, perhaps due to relatively smaller numbers of patients discharged to such facilities. This communication is as or more important because these patients are potentially more vulnerable and their medical conditions more active than for patients discharged home.12 Furthermore, discharge information from acute care hospitals will often form the basis for admission orders at subacute facilities. Last, these patients will have a second transition in care (from subacute facility to home) whose quality is dependent at least in part on the quality of communication during the first transition.

The aim of this study was to evaluate the quality of information transfer among patients discharged from acute hospitals to subacute facilities across an integrated healthcare delivery system. The long‐term goals of this effort were to determine the areas most in need of improvement, to guide interventions to address these problems, and to track improvements in these measures over time as interventions are implemented and refined.

Methods

This observational study was conducted as part of a quality improvement project evaluating the quality of information provided during the discharge process across Partners Health Care System. The institutional review boards of the participating institutions approved the study.

Study Sample

We evaluated a sample of discharge documentation packets (eg, discharge summaries, discharge orders, nursing instructions, care coordination, and physical/occupational therapy notes) of patients discharged from all 5 acute care hospitals of the Partners Healthcare System to 30 subacute facilities (rehabilitation hospitals and skilled nursing facilities) from March 2005 through June 2007.

For reviewers at acute sites, discharge documentation packets were randomly selected each quarter using a random number generator within Microsoft Excel (Microsoft, Redmond, WA). At subacute sites, reviewers selected which packets to review, although they were encouraged to review all of them. Random selection of packets could not be achieved at subacute sites because reviews took place on the day of admission to the subacute facility. All reviewers received 1 hour of training on how to evaluate discharge packets, including review of a standardized teaching packet with 1 of the coauthors (J.L.S. or T.O.).

Two of the 5 acute care hospitals in the study are academic medical centers and the other 3 are community hospitals. Reviewers were a mix of trained medical residents or nurse practitioners at acute sites and admitting physicians or nurse practitioners at receiving subacute sites.

Fifty packets were reviewed per acute site per quarter. This provided roughly 10% precision around our estimates (ie, if compliance with a measure were 80%, the 95% confidence interval around this estimate would be 70%‐90%). This sample size is consistent with those used to obtain other national benchmarks, such as those for National Hospital Quality Measures, which generally require at least 35 cases per quarter.13

Measures

A multidisciplinary team at Partners derived, reviewed, and refined a minimum data set required to appropriately care for patients during the first 72 hours after transfer from an acute care hospital to a subacute facility. Several of these measures are required by TJC. Other measures were either modifications of TJC measures made to facilitate uniform data collection (eg, history and physical examination at admission instead of significant findings) or additional data elements (not required by TJC) felt to be important to patient care based on the medical literature and interviews with receiving providers at subacute facilities. All measures were refined by the multidisciplinary team with input from additional subspecialists as needed (see Table 1 for the final list of measures).

Measured Data Elements at Discharge
 Reason(s) for Admission
Joint Commission requirementsA focused history
A focused physical exam
Pertinent past medical history
Treatment rendered
Discharge diagnosis(es)
Condition on discharge
Discharge summary
Any information missing
Non‐Joint Commission requirements
Medication informationDischarge medications
Drug allergies
Preadmission medication information
Explanation for any differences between preadmission and discharge medications
Test results informationLatest pertinent laboratory results
Pertinent radiology results
Test results pending at time of transfer
Overall assessmentWere management and follow‐up plans adequately described?
Did you uncover a significant condition not mentioned in the discharge packet?

Data Collection

After reviewing the entire discharge documentation packet, reviewers completed a survey concerning the inclusion of the required data elements. Surveys were completed online using Perseus Survey Solutions 6.0 (Perseus Development Corp., Braintree, MA) in the month following discharge (for reviewers at acute care sites) or within 24 hours of admission to the subacute facility (for reviewers at subacute sites). To verify the accuracy and completeness of packets, reviewers at acute sites were instructed to compare the discharge documentation to a review of the inpatient medical record. Similarly, reviewers at subacute sites were instructed to complete their evaluations after admitting each patient to their facility.

Outcomes

The primary outcome was the proportion of packets that contained each data element. In addition, we calculated the proportion of packets that contained all applicable elements required by TJC and all applicable data elements measured in the study. Last, we evaluated two global (albeit subjective) measures of satisfaction with the packet: Were management and follow‐up plans adequately described? (both components needed to be adequately described to get credit for this question) and Did you uncover a significant condition not mentioned in the discharge packet? Significant conditions were defined as active medical problems requiring management during or immediately following the hospitalization.

Statistical Analysis

Results were calculated as proportions, odds ratios, and 95% confidence intervals (CI), using SAS version 9.1 (SAS Institute, Inc., Cary, NC). Simple logistic regression was used to compare inclusion of data elements between medical and surgical services and between academic medical centers and community hospitals. To evaluate interrater reliability, 2 reviewers (both at acute sites) independently evaluated 29 randomly chosen charts, each with 12 data elements.

Results

A total of 1501 discharge documentation packets were reviewed, including 980 patients (65%) from a medical unit and 521 patients (35%) from a surgical unit. Based on 2007 data, these packets represent approximately 4% of all eligible discharges to subacute facilities. Patients discharged from 1 of the 2 academic medical centers represented 44% of the sample. A total of 644 discharge packets (43%) were reviewed at acute sites and 814 packets (54%) were reviewed at subacute sites. Information about reviewer site was missing in 43 discharge packets (3%). For the 29 charts independently reviewed by 2 reviewers, there was complete agreement for 331 out of 348 data elements (95.1%).

Only 1055 (70%) discharge summaries had all the information required by TJC (Table 2). Physical examination at admission (a component of significant findings, as noted above) and condition at discharge were the 2 elements most often missing. The defect‐free rate varied by site, with a range of 61% to 76% across the 5 acute care hospitals (data not shown).

Inclusion of Discharge Data Elements
 Sample SizeMissing [n (%)]95% CI Missing %
  • Abbreviation: CI, confidence interval.

Joint Commission requirements
Reason(s) for admission149714 (0.9)0.41.4
A focused history149365 (4.4)3.35.3
A focused physical exam1493170 (11.4)9.713
Pertinent past medical history149469 (4.6)3.55.6
Treatment rendered149433 (2.2)1.42.9
Discharge diagnosis(es)148053 (3.6)2.64.5
Condition on discharge1462208 (14.2)12.416.0
Discharge summary147590 (6.1)4.87.3
Any information missing1501447 (29.7)27.432.0
Non‐Joint Commission requirements
Medication information
Discharge medications149119 (1.3)0.71.8
Drug allergies147088 (6.0)4.77.2
Preadmission medication information1460297 (20.3)18.322.4
Explanation for any differences between preadmission and discharge medications1060374 (35.3)32.038.1
Test results information
Latest pertinent lab results1460261 (17.9)15.919.8
Pertinent radiology results1303139 (10.7)912.4
Test results pending at time of transfer341160 (47.2)41.952.5
Overall assessment
Were management and follow‐up plans adequately described?1461No (%): 161 (11.1)95% CI No %: 9.512.7
Did you uncover a significant condition not mentioned in the discharge packet?1469Yes (%): 162 (11.0)95% CI Yes %: 9.413.0
All applicable elements present1501503 (33.5)31.135.9

The rates of inclusion of other (non‐TJC required) data elements are shown in Table 2. Most often missing were preadmission medication regimens, any documented reason for any difference between preadmission and discharge medications, pertinent laboratory results, and an adequate follow‐up plan (including who to follow up with, when to follow‐up, and a list of tasks to be accomplished at the follow‐up visit). Notation regarding significant test results that were pending at the time of transfer was missing in 160 of 341 applicable patients (47%), and in 162 patients (11%), physicians uncovered a significant condition that was not mentioned in the discharge documentation. Only 503 (33.5%) discharge documentation packets had all applicable measures present. In addition, the discharge summary was not received at all on the day of discharge according to the receiving site in 90 patients (6%).

Reviewers were asked in a separate question which missing data were necessary for patient care. Data elements most often cited were explanations for any medication discrepancies and test results pending at the time of the hospital discharge.

Community hospitals had a higher rate of inclusion of TJC‐required data elements when compared to academic medical centers (Table 3). Also, among non‐TJC required data elements, inclusion rates were higher among the community hospitals, especially regarding information about medication discrepancies, pending test results, and follow‐up information (Table 3).

Completeness of Discharge Documentation by Site and Service
 Total (n)All Elements Present [n (%)]OR (95% CI)
  • Abbreviations: CI, confidence interval; OR, odds ratio.

Joint Commission requirements
Hospital type
Community hospitals949826 (87)2.7 (2.13.6)
Academic medical centers541384 (71)Ref.
Service
Medical services1013745 (73)1.3 (1.01.7)
Surgical services488332 (68)Ref.
Explanation for any medication discrepancies Yes [n (%)] 
Hospital type
Community hospitals718550 (76)5.0 (3.86.5)
Academic medical centers342136 (39)Ref.
Service
Medical services754529 (70)2.2 (1.72.9)
Surgical services306157 (51)Ref.
Test results pending at time of transfer Yes [n (%)] 
Hospital type
Community hospitals172109 (63)2.4 (1.53.7)
Academic medical centers16971 (42)Ref.
Service
Medical services227146 (64)4.2 (2.66.9)
Surgical services11434 (30)Ref.
Follow‐up plans adequately described Yes [n (%)] 
Hospital type
Community hospitals968883 (91)1.7 (1.22.4)
Academic medical centers543466 (85)Ref.
Service
Medical services983862 (87)0.67 (0.51.0)
Surgical services478437 (91)Ref.

Although no differences were found between medical and surgical services regarding compliance with TJC requirements, a difference was noted in documentation of explanations of medication discrepancies and pending test results, with medical services performing better in both measures (Table 3).

In general, reviewers at subacute sites more often evaluated packets as deficient than reviewers at acute sites, up to an absolute difference of 33% in the proportion of missing data, depending on the data element (see Appendix, Table 1).

Discussion

Our study evaluated the completeness of documentation in the discharge summaries of patients discharged from acute care to subacute care facilities. Our results for the inclusion of TJC‐required data elements were similar to those quoted in the literature for patients discharged home.6 Our results also demonstrated a high rate of other missing data elements that are arguably of equal or greater importance, including reasons for discrepancies between preadmission and discharge medication regimens and tests that are pending at the time of discharge.1, 8, 9 Our results also demonstrated the relatively poorer performance of academic centers compared to community hospitals regarding inclusion of information about medication reconciliation, follow‐up, pending test results, and complete information required by TJC. Finally, we found that patients discharged from surgical services more often lacked documentation of medication discrepancies and pending test results compared with patients from medical services.

To our knowledge, this is one of the first studies looking at the quality of information transfer in patients discharged to subacute care facilities. The results of this study are not surprising given the known problems with general information transfer at hospital discharge.1 The fact that community hospitals provided more complete information than academic medical centers for certain data elements may be due to the difference between residents and more senior physicians preparing discharge documentation. Such differences could reflect differences in experience, training, and degree of appreciation for the importance of discharge documentation, and/or restrictions in work hours among residents (eg, resulting in time‐pressure to complete discharge summaries and/or summaries being written by residents who know the patients less well). These hypotheses deserve further exploration. The differences between medical and surgical services should also be validated and explored in other healthcare systems, including both academic and community settings.

The results of this study should be viewed in light of the study's limitations. Packets evaluated by reviewers at subacute facilities were chosen by the reviewers and may not have been representative of all patients received by that facility (in contrast to those reviewed at the acute sites, which were chosen at random and more likely to be representative, although we did not formally test for this). It is possible that reviewers at subacute sites selected the worst discharge documentation packets for evaluation. Second, evaluations by reviewers at subacute sites did not distinguish between information missing from discharge documentation and failure to receive the documentation at all from the acute care hospital (again in contrast to reviewers at acute sites, who always had access to the documentation). Lastly, reviewers at acute and subacute sites may have graded packets differently due to their different clinical perspectives. These 3 factors may explain the relatively poorer results of discharge packets reviewed by reviewers at subacute sites. Further study would be needed to distinguish among these possibilities (eg, having acute and subacute reviewers answer the same questions for the same discharge packets to allow us to measure interrater reliability between the different kinds of reviewers; explicitly asking subacute reviewers about receipt of each piece of documentation; comparing the distribution of diagnosis‐related group [DRG] codes and hospital length of stay in evaluated vs. total discharge packets as a measure of representativeness). We also cannot rule out the possibility of reviewer bias, but all reviewers were trained in a standardized fashion and we know that reliability of assessments were high, at least among reviewers at acute sites. Last, we did not measure actual or potential adverse events caused by these information deficits.

As part of a Partners‐wide initiative to improve transitions in care, the results were presented to the administrations of each of the 5 acute care hospitals. The Partners High Performance Medicine Transition team then began work with a steering committee (composed of representatives from each hospital) to address these deficiencies. Since then, the hospitals have taken several steps to improve the quality of information transfer for discharged patients, including the following:

  • Technological improvements to the hospitals' discharge ordering systems to actively solicit and/or autoimport the required information into discharge documentation.

  • Creation of discharge templates to record the required information on paper.

  • Provision of feedback to clinicians and their service chiefs regarding the ongoing quality of their discharge documentation.

  • Creation of an online Partners‐wide curriculum on discharge summary authorship, with a mandatory quiz to be taken by all incoming clinicians.

 

In conclusion, we found room for improvement in the inclusion of data elements required for the safe transfer of patients from acute hospitals to subacute facilities, especially in areas such as medication reconciliation, pending test results, and adequate follow‐up plans. We also found variation by site and type of service. For patients discharged to rehabilitation and other subacute facilities, improvement is needed in the communication of clinically relevant information to those providing continuing care.

Appendix

0

Differences in evaluation scores between reviewers at acute and Sub‐Acute Sites
JCAHO IndicatorsReviews from Sub‐Acute Sites (N = 814)*Reviews from Acute Sites (N = 644)*
Sample SizeMissing N%95% CISample SizeMissing%95% CI
  • Information about the reviewer was missing in 43 cases

Reason(s) for admission81291.10.41.864340.60.011.2
A focused history810496.14.47.7642162.51.33.7
A focused physical exam81013116.213.718.7641345.33.67.0
Pertinent past medical history810506.24.57.86421422.01.13.3
Treatment rendered811293.62.34.964140.60.011.2
Discharge diagnosis(es)806597.35.59.163071.10.31.9
Condition on discharge8009211.59.313.762210917.514.520.5
Discharge summary809779.57.511.5624111.80.72.8
Any information missing
Medication InformationSample SizeMissing%95% CISample SizeMissing%95% CI
Discharge medications811121.50.72.363860.90.21.7
Drug allergies811475.84.27.4639355.53.77.2
Explanation for any differences between preadmission and discharge medications54227550.746.5554988817.714.321.0
Test results informationSample SizeMissing%95% CISample SizeMissing%95% CI
Latest pertinent lab results79017822.519.625.46297311.69.114.1
Pertinent radiology results66811016.513.719.3601274.52.86.2
Test results pending at time of transfer1838747.540.354.81527348.040.156.0
Management InformationSample SizeNo%95% CISample SizeNo%95% CI
Were management and follow‐up plans adequately described?79412115.212.717.76317912.59.915.1
Sample SizeYes%95% CISample SizeYes%95% CI
Did you uncover a significant condition not mentioned in the discharge packet?79311714.812.317.2635386.04.47.8

Effective communication among physicians during the hospital discharge process is critical to patient care. Patients are at high risk of having an adverse drug event,1 readmission, or death2 during the transition from hospital to home.3 Ineffective communication between inpatient and outpatient providers has been implicated as a leading cause of adverse events.35 Conversely, efforts to improve communication have been shown to improve compliance with follow‐up tests and decrease readmission rates.6, 7 Recently, the absence of several specific data elements in discharge documentation have been shown to be common and to have potential for patient harm, including test results that are pending at the time of discharge.8, 9 Unexplained discrepancies between preadmission and discharge medication regimens are also common and potentially dangerous.1

According to the Joint Commission for Accreditation of Healthcare Organizations (TJC), the following elements should be included in discharge summaries: the reason for hospitalization; significant findings; procedures performed and care, treatment, and services provided; the patient's condition at discharge; and information provided to the patient and family, as appropriate.10 TJC also advocates medication reconciliation, a process of identifying the most accurate list of all medications a patient is takingincluding name, dosage, frequency, and routeand using this list to provide correct medications for patients anywhere within the health care system.11

Despite the importance of complete communication among providers at hospital discharge, a recent systematic review showed that discharge summaries often lacked important information such as diagnostic test results (missing from 33%‐63%), treatment or hospital course (7%‐22%), discharge medications (2%‐40%), test results pending at discharge (65%), patient or family counseling (90%‐92%), and follow‐up plans (2%‐43%).1

Most of the studies addressing this issue have evaluated communication pitfalls between acute care hospitals and primary care physicians among patients discharged home.17 In contrast, the quality of discharge documentation among patients discharged to rehabilitation centers and other subacute care facilities has been less well studied, perhaps due to relatively smaller numbers of patients discharged to such facilities. This communication is as or more important because these patients are potentially more vulnerable and their medical conditions more active than for patients discharged home.12 Furthermore, discharge information from acute care hospitals will often form the basis for admission orders at subacute facilities. Last, these patients will have a second transition in care (from subacute facility to home) whose quality is dependent at least in part on the quality of communication during the first transition.

The aim of this study was to evaluate the quality of information transfer among patients discharged from acute hospitals to subacute facilities across an integrated healthcare delivery system. The long‐term goals of this effort were to determine the areas most in need of improvement, to guide interventions to address these problems, and to track improvements in these measures over time as interventions are implemented and refined.

Methods

This observational study was conducted as part of a quality improvement project evaluating the quality of information provided during the discharge process across Partners Health Care System. The institutional review boards of the participating institutions approved the study.

Study Sample

We evaluated a sample of discharge documentation packets (eg, discharge summaries, discharge orders, nursing instructions, care coordination, and physical/occupational therapy notes) of patients discharged from all 5 acute care hospitals of the Partners Healthcare System to 30 subacute facilities (rehabilitation hospitals and skilled nursing facilities) from March 2005 through June 2007.

For reviewers at acute sites, discharge documentation packets were randomly selected each quarter using a random number generator within Microsoft Excel (Microsoft, Redmond, WA). At subacute sites, reviewers selected which packets to review, although they were encouraged to review all of them. Random selection of packets could not be achieved at subacute sites because reviews took place on the day of admission to the subacute facility. All reviewers received 1 hour of training on how to evaluate discharge packets, including review of a standardized teaching packet with 1 of the coauthors (J.L.S. or T.O.).

Two of the 5 acute care hospitals in the study are academic medical centers and the other 3 are community hospitals. Reviewers were a mix of trained medical residents or nurse practitioners at acute sites and admitting physicians or nurse practitioners at receiving subacute sites.

Fifty packets were reviewed per acute site per quarter. This provided roughly 10% precision around our estimates (ie, if compliance with a measure were 80%, the 95% confidence interval around this estimate would be 70%‐90%). This sample size is consistent with those used to obtain other national benchmarks, such as those for National Hospital Quality Measures, which generally require at least 35 cases per quarter.13

Measures

A multidisciplinary team at Partners derived, reviewed, and refined a minimum data set required to appropriately care for patients during the first 72 hours after transfer from an acute care hospital to a subacute facility. Several of these measures are required by TJC. Other measures were either modifications of TJC measures made to facilitate uniform data collection (eg, history and physical examination at admission instead of significant findings) or additional data elements (not required by TJC) felt to be important to patient care based on the medical literature and interviews with receiving providers at subacute facilities. All measures were refined by the multidisciplinary team with input from additional subspecialists as needed (see Table 1 for the final list of measures).

Measured Data Elements at Discharge
 Reason(s) for Admission
Joint Commission requirementsA focused history
A focused physical exam
Pertinent past medical history
Treatment rendered
Discharge diagnosis(es)
Condition on discharge
Discharge summary
Any information missing
Non‐Joint Commission requirements
Medication informationDischarge medications
Drug allergies
Preadmission medication information
Explanation for any differences between preadmission and discharge medications
Test results informationLatest pertinent laboratory results
Pertinent radiology results
Test results pending at time of transfer
Overall assessmentWere management and follow‐up plans adequately described?
Did you uncover a significant condition not mentioned in the discharge packet?

Data Collection

After reviewing the entire discharge documentation packet, reviewers completed a survey concerning the inclusion of the required data elements. Surveys were completed online using Perseus Survey Solutions 6.0 (Perseus Development Corp., Braintree, MA) in the month following discharge (for reviewers at acute care sites) or within 24 hours of admission to the subacute facility (for reviewers at subacute sites). To verify the accuracy and completeness of packets, reviewers at acute sites were instructed to compare the discharge documentation to a review of the inpatient medical record. Similarly, reviewers at subacute sites were instructed to complete their evaluations after admitting each patient to their facility.

Outcomes

The primary outcome was the proportion of packets that contained each data element. In addition, we calculated the proportion of packets that contained all applicable elements required by TJC and all applicable data elements measured in the study. Last, we evaluated two global (albeit subjective) measures of satisfaction with the packet: Were management and follow‐up plans adequately described? (both components needed to be adequately described to get credit for this question) and Did you uncover a significant condition not mentioned in the discharge packet? Significant conditions were defined as active medical problems requiring management during or immediately following the hospitalization.

Statistical Analysis

Results were calculated as proportions, odds ratios, and 95% confidence intervals (CI), using SAS version 9.1 (SAS Institute, Inc., Cary, NC). Simple logistic regression was used to compare inclusion of data elements between medical and surgical services and between academic medical centers and community hospitals. To evaluate interrater reliability, 2 reviewers (both at acute sites) independently evaluated 29 randomly chosen charts, each with 12 data elements.

Results

A total of 1501 discharge documentation packets were reviewed, including 980 patients (65%) from a medical unit and 521 patients (35%) from a surgical unit. Based on 2007 data, these packets represent approximately 4% of all eligible discharges to subacute facilities. Patients discharged from 1 of the 2 academic medical centers represented 44% of the sample. A total of 644 discharge packets (43%) were reviewed at acute sites and 814 packets (54%) were reviewed at subacute sites. Information about reviewer site was missing in 43 discharge packets (3%). For the 29 charts independently reviewed by 2 reviewers, there was complete agreement for 331 out of 348 data elements (95.1%).

Only 1055 (70%) discharge summaries had all the information required by TJC (Table 2). Physical examination at admission (a component of significant findings, as noted above) and condition at discharge were the 2 elements most often missing. The defect‐free rate varied by site, with a range of 61% to 76% across the 5 acute care hospitals (data not shown).

Inclusion of Discharge Data Elements
 Sample SizeMissing [n (%)]95% CI Missing %
  • Abbreviation: CI, confidence interval.

Joint Commission requirements
Reason(s) for admission149714 (0.9)0.41.4
A focused history149365 (4.4)3.35.3
A focused physical exam1493170 (11.4)9.713
Pertinent past medical history149469 (4.6)3.55.6
Treatment rendered149433 (2.2)1.42.9
Discharge diagnosis(es)148053 (3.6)2.64.5
Condition on discharge1462208 (14.2)12.416.0
Discharge summary147590 (6.1)4.87.3
Any information missing1501447 (29.7)27.432.0
Non‐Joint Commission requirements
Medication information
Discharge medications149119 (1.3)0.71.8
Drug allergies147088 (6.0)4.77.2
Preadmission medication information1460297 (20.3)18.322.4
Explanation for any differences between preadmission and discharge medications1060374 (35.3)32.038.1
Test results information
Latest pertinent lab results1460261 (17.9)15.919.8
Pertinent radiology results1303139 (10.7)912.4
Test results pending at time of transfer341160 (47.2)41.952.5
Overall assessment
Were management and follow‐up plans adequately described?1461No (%): 161 (11.1)95% CI No %: 9.512.7
Did you uncover a significant condition not mentioned in the discharge packet?1469Yes (%): 162 (11.0)95% CI Yes %: 9.413.0
All applicable elements present1501503 (33.5)31.135.9

The rates of inclusion of other (non‐TJC required) data elements are shown in Table 2. Most often missing were preadmission medication regimens, any documented reason for any difference between preadmission and discharge medications, pertinent laboratory results, and an adequate follow‐up plan (including who to follow up with, when to follow‐up, and a list of tasks to be accomplished at the follow‐up visit). Notation regarding significant test results that were pending at the time of transfer was missing in 160 of 341 applicable patients (47%), and in 162 patients (11%), physicians uncovered a significant condition that was not mentioned in the discharge documentation. Only 503 (33.5%) discharge documentation packets had all applicable measures present. In addition, the discharge summary was not received at all on the day of discharge according to the receiving site in 90 patients (6%).

Reviewers were asked in a separate question which missing data were necessary for patient care. Data elements most often cited were explanations for any medication discrepancies and test results pending at the time of the hospital discharge.

Community hospitals had a higher rate of inclusion of TJC‐required data elements when compared to academic medical centers (Table 3). Also, among non‐TJC required data elements, inclusion rates were higher among the community hospitals, especially regarding information about medication discrepancies, pending test results, and follow‐up information (Table 3).

Completeness of Discharge Documentation by Site and Service
 Total (n)All Elements Present [n (%)]OR (95% CI)
  • Abbreviations: CI, confidence interval; OR, odds ratio.

Joint Commission requirements
Hospital type
Community hospitals949826 (87)2.7 (2.13.6)
Academic medical centers541384 (71)Ref.
Service
Medical services1013745 (73)1.3 (1.01.7)
Surgical services488332 (68)Ref.
Explanation for any medication discrepancies Yes [n (%)] 
Hospital type
Community hospitals718550 (76)5.0 (3.86.5)
Academic medical centers342136 (39)Ref.
Service
Medical services754529 (70)2.2 (1.72.9)
Surgical services306157 (51)Ref.
Test results pending at time of transfer Yes [n (%)] 
Hospital type
Community hospitals172109 (63)2.4 (1.53.7)
Academic medical centers16971 (42)Ref.
Service
Medical services227146 (64)4.2 (2.66.9)
Surgical services11434 (30)Ref.
Follow‐up plans adequately described Yes [n (%)] 
Hospital type
Community hospitals968883 (91)1.7 (1.22.4)
Academic medical centers543466 (85)Ref.
Service
Medical services983862 (87)0.67 (0.51.0)
Surgical services478437 (91)Ref.

Although no differences were found between medical and surgical services regarding compliance with TJC requirements, a difference was noted in documentation of explanations of medication discrepancies and pending test results, with medical services performing better in both measures (Table 3).

In general, reviewers at subacute sites more often evaluated packets as deficient than reviewers at acute sites, up to an absolute difference of 33% in the proportion of missing data, depending on the data element (see Appendix, Table 1).

Discussion

Our study evaluated the completeness of documentation in the discharge summaries of patients discharged from acute care to subacute care facilities. Our results for the inclusion of TJC‐required data elements were similar to those quoted in the literature for patients discharged home.6 Our results also demonstrated a high rate of other missing data elements that are arguably of equal or greater importance, including reasons for discrepancies between preadmission and discharge medication regimens and tests that are pending at the time of discharge.1, 8, 9 Our results also demonstrated the relatively poorer performance of academic centers compared to community hospitals regarding inclusion of information about medication reconciliation, follow‐up, pending test results, and complete information required by TJC. Finally, we found that patients discharged from surgical services more often lacked documentation of medication discrepancies and pending test results compared with patients from medical services.

To our knowledge, this is one of the first studies looking at the quality of information transfer in patients discharged to subacute care facilities. The results of this study are not surprising given the known problems with general information transfer at hospital discharge.1 The fact that community hospitals provided more complete information than academic medical centers for certain data elements may be due to the difference between residents and more senior physicians preparing discharge documentation. Such differences could reflect differences in experience, training, and degree of appreciation for the importance of discharge documentation, and/or restrictions in work hours among residents (eg, resulting in time‐pressure to complete discharge summaries and/or summaries being written by residents who know the patients less well). These hypotheses deserve further exploration. The differences between medical and surgical services should also be validated and explored in other healthcare systems, including both academic and community settings.

The results of this study should be viewed in light of the study's limitations. Packets evaluated by reviewers at subacute facilities were chosen by the reviewers and may not have been representative of all patients received by that facility (in contrast to those reviewed at the acute sites, which were chosen at random and more likely to be representative, although we did not formally test for this). It is possible that reviewers at subacute sites selected the worst discharge documentation packets for evaluation. Second, evaluations by reviewers at subacute sites did not distinguish between information missing from discharge documentation and failure to receive the documentation at all from the acute care hospital (again in contrast to reviewers at acute sites, who always had access to the documentation). Lastly, reviewers at acute and subacute sites may have graded packets differently due to their different clinical perspectives. These 3 factors may explain the relatively poorer results of discharge packets reviewed by reviewers at subacute sites. Further study would be needed to distinguish among these possibilities (eg, having acute and subacute reviewers answer the same questions for the same discharge packets to allow us to measure interrater reliability between the different kinds of reviewers; explicitly asking subacute reviewers about receipt of each piece of documentation; comparing the distribution of diagnosis‐related group [DRG] codes and hospital length of stay in evaluated vs. total discharge packets as a measure of representativeness). We also cannot rule out the possibility of reviewer bias, but all reviewers were trained in a standardized fashion and we know that reliability of assessments were high, at least among reviewers at acute sites. Last, we did not measure actual or potential adverse events caused by these information deficits.

As part of a Partners‐wide initiative to improve transitions in care, the results were presented to the administrations of each of the 5 acute care hospitals. The Partners High Performance Medicine Transition team then began work with a steering committee (composed of representatives from each hospital) to address these deficiencies. Since then, the hospitals have taken several steps to improve the quality of information transfer for discharged patients, including the following:

  • Technological improvements to the hospitals' discharge ordering systems to actively solicit and/or autoimport the required information into discharge documentation.

  • Creation of discharge templates to record the required information on paper.

  • Provision of feedback to clinicians and their service chiefs regarding the ongoing quality of their discharge documentation.

  • Creation of an online Partners‐wide curriculum on discharge summary authorship, with a mandatory quiz to be taken by all incoming clinicians.

 

In conclusion, we found room for improvement in the inclusion of data elements required for the safe transfer of patients from acute hospitals to subacute facilities, especially in areas such as medication reconciliation, pending test results, and adequate follow‐up plans. We also found variation by site and type of service. For patients discharged to rehabilitation and other subacute facilities, improvement is needed in the communication of clinically relevant information to those providing continuing care.

Appendix

0

Differences in evaluation scores between reviewers at acute and Sub‐Acute Sites
JCAHO IndicatorsReviews from Sub‐Acute Sites (N = 814)*Reviews from Acute Sites (N = 644)*
Sample SizeMissing N%95% CISample SizeMissing%95% CI
  • Information about the reviewer was missing in 43 cases

Reason(s) for admission81291.10.41.864340.60.011.2
A focused history810496.14.47.7642162.51.33.7
A focused physical exam81013116.213.718.7641345.33.67.0
Pertinent past medical history810506.24.57.86421422.01.13.3
Treatment rendered811293.62.34.964140.60.011.2
Discharge diagnosis(es)806597.35.59.163071.10.31.9
Condition on discharge8009211.59.313.762210917.514.520.5
Discharge summary809779.57.511.5624111.80.72.8
Any information missing
Medication InformationSample SizeMissing%95% CISample SizeMissing%95% CI
Discharge medications811121.50.72.363860.90.21.7
Drug allergies811475.84.27.4639355.53.77.2
Explanation for any differences between preadmission and discharge medications54227550.746.5554988817.714.321.0
Test results informationSample SizeMissing%95% CISample SizeMissing%95% CI
Latest pertinent lab results79017822.519.625.46297311.69.114.1
Pertinent radiology results66811016.513.719.3601274.52.86.2
Test results pending at time of transfer1838747.540.354.81527348.040.156.0
Management InformationSample SizeNo%95% CISample SizeNo%95% CI
Were management and follow‐up plans adequately described?79412115.212.717.76317912.59.915.1
Sample SizeYes%95% CISample SizeYes%95% CI
Did you uncover a significant condition not mentioned in the discharge packet?79311714.812.317.2635386.04.47.8
References
  1. Schnipper JL, Kirwin JL, Cotugno MC, et al.Role of pharmacist counseling in preventing adverse drug events after hospitalization.Arch Intern Med.2006;166:565571.
  2. Van Walraven C, Mamdani M, Fang J, Austin PC.Continuity of care and patient outcomes after hospital discharge.J Gen Intern Med.1989;19:624631.
  3. Kripalani S, LeFevre F, Phillips CO, Williams MV, Basaviah P, Baker DW.Deficits in communication and information transfer between hospital‐based and primary care physicians: implications for patient safety and continuity of care.JAMA.2007;297:831841.
  4. Van Walraven C, Seth R, Austin PC, Laupacis A.Effect of discharge summary availability during post‐discharge visits on hospital readmission.JGen Intern Med.2002;17:186192.
  5. Moore C, Wisnivesky J, Williams S, McGinn T.Medical errors related to discontinuity of care from an inpatient to an outpatient setting.J Gen Intern Med.2003;18:646651.
  6. Kripalani S, Jackson AT, Schnipper JL, Coleman EA.Promoting effective transitions of care at hospital discharge: a review of key issues for hospitalists.J Hosp Med.2007;2:314323.
  7. Afilalo M, Lang E, Léger R, et al.Impact of a standardized communication system on continuity of care between family physicians and the emergency department.CJEM.2007;9:7986.
  8. Roy CL, Poon EG, Karson AS, et al.Patient safety concerns arising from test results that return after hospital discharge.Ann Intern Med.2005;143:121128.
  9. Moore C, McGinn T, Halm E.Tying up loose ends: discharging patients with unresolved medical issues.Arch Intern Med.2007;167:13051311.
  10. Standard IM.6.10: Hospital Accreditation Standards.Oakbrook Terrace, IL:Joint Commission on Accreditation of Healthcare Organizations;2006:338340.
  11. Joint Commission on Accreditation of Healthcare Organizations. Joint Commission national patient safety goals. Available at: http://www.jointcommission.org/PatientSafety/NationalPatientSafetyGoals. Accessed July 2009.
  12. Prvu Bettger JA, Stineman MG.Effectiveness of multidisciplinary rehabilitation services in post acute care: state‐of‐the‐science. A review.Arch Phys Med Rehabil.2007;88:15261534.
  13. Joint Commission on Accreditation of Healthcare Organizations. Specification Manual for National Hospital Quality Measures: Population and Sampling Specifications Version 2.4. Available at: http://www.jointcommission.org/PerformanceMeasurement/PerformanceMeasurement/Current+NHQM+Manual.htm. Accessed July 2009.
References
  1. Schnipper JL, Kirwin JL, Cotugno MC, et al.Role of pharmacist counseling in preventing adverse drug events after hospitalization.Arch Intern Med.2006;166:565571.
  2. Van Walraven C, Mamdani M, Fang J, Austin PC.Continuity of care and patient outcomes after hospital discharge.J Gen Intern Med.1989;19:624631.
  3. Kripalani S, LeFevre F, Phillips CO, Williams MV, Basaviah P, Baker DW.Deficits in communication and information transfer between hospital‐based and primary care physicians: implications for patient safety and continuity of care.JAMA.2007;297:831841.
  4. Van Walraven C, Seth R, Austin PC, Laupacis A.Effect of discharge summary availability during post‐discharge visits on hospital readmission.JGen Intern Med.2002;17:186192.
  5. Moore C, Wisnivesky J, Williams S, McGinn T.Medical errors related to discontinuity of care from an inpatient to an outpatient setting.J Gen Intern Med.2003;18:646651.
  6. Kripalani S, Jackson AT, Schnipper JL, Coleman EA.Promoting effective transitions of care at hospital discharge: a review of key issues for hospitalists.J Hosp Med.2007;2:314323.
  7. Afilalo M, Lang E, Léger R, et al.Impact of a standardized communication system on continuity of care between family physicians and the emergency department.CJEM.2007;9:7986.
  8. Roy CL, Poon EG, Karson AS, et al.Patient safety concerns arising from test results that return after hospital discharge.Ann Intern Med.2005;143:121128.
  9. Moore C, McGinn T, Halm E.Tying up loose ends: discharging patients with unresolved medical issues.Arch Intern Med.2007;167:13051311.
  10. Standard IM.6.10: Hospital Accreditation Standards.Oakbrook Terrace, IL:Joint Commission on Accreditation of Healthcare Organizations;2006:338340.
  11. Joint Commission on Accreditation of Healthcare Organizations. Joint Commission national patient safety goals. Available at: http://www.jointcommission.org/PatientSafety/NationalPatientSafetyGoals. Accessed July 2009.
  12. Prvu Bettger JA, Stineman MG.Effectiveness of multidisciplinary rehabilitation services in post acute care: state‐of‐the‐science. A review.Arch Phys Med Rehabil.2007;88:15261534.
  13. Joint Commission on Accreditation of Healthcare Organizations. Specification Manual for National Hospital Quality Measures: Population and Sampling Specifications Version 2.4. Available at: http://www.jointcommission.org/PerformanceMeasurement/PerformanceMeasurement/Current+NHQM+Manual.htm. Accessed July 2009.
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Journal of Hospital Medicine - 4(8)
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Journal of Hospital Medicine - 4(8)
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Communication and information deficits in patients discharged to rehabilitation facilities: An evaluation of five acute care hospitals
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Communication and information deficits in patients discharged to rehabilitation facilities: An evaluation of five acute care hospitals
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patient discharge, quality indicators, rehabilitation centers
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