Affiliations
Clalit Research Institute, Chief Physician's Office, Clalit Health Services
Given name(s)
Efrat
Family name
Shadmi
Degrees
PhD

Functional Status and Readmission

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Functional status before and during acute hospitalization and readmission risk identification

A continuing focus on readmission prevention as a means to improve quality and reduce waste and costs has led to abundant research on the identification of factors that put older patients at risk for readmission.[1, 2] Recently, research has focused on the development of prediction tools that are based on information from electronic health records (EHR) and that enable early, at‐admission, identification of patients at high risk for readmission.[3, 4, 5] Through such identification, patients are already targeted for inclusion in readmission‐prevention interventions early in their hospital stay.[6, 7] Yet, the ability to rely on these early‐identification tools is contingent on the stability of risk during the hospital stay. Of the in‐hospital factors that can affect readmission, change in functioning has been identified as a potentially major contributor, especially in older patients.[8]

Older adults' deterioration in functioning is a common, troubling phenomenon. Approximately 20% of patients older than 70 years and hospitalized for a medical illness deteriorate in functioning during the hospitalization.[9] Recent evidence points to the contribution of functioning to 30‐day readmission risk, with studies showing that pre‐ or posthospitalization functional impairment is associated with a 1.5 to 3 times greater likelihood of readmission.[10, 11, 12, 13] Whether in‐hospital changes in functioning add to patients' baseline risk, however, is unknown. The only readmission study that examined functional decline during hospitalization was a retrospective study performed in a population of older adults receiving rehabilitation services and therefore may not be generalizable to acutely hospitalized adults.[14] To fill the current knowledge gap, we examined whether in‐hospital functional decline significantly contributes to at‐admission readmission risk factors in its ability to accurately identify high readmission risk in older adults hospitalized in internal medicine units.

METHODS

Design and Participants

Previously collected data from a prospective cohort study, Hospitalization Process Effects on Functional Outcomes and Recovery (HoPE‐FOR), designed to assess the effect of hospitalization‐care processes on functional outcomes in older adults, were combined with EHR data. The population considered for recruitment to HoPE‐FOR comprised older patients (aged 70 years) admitted during the period 2009 to 2011 to 1 of the 8 internal medicine wards at 2 tertiary medical centers in Israel. Patients recruited for the study had an unplanned admission, and were not completely dependent in their basic functions. Cognitively impaired patients (scoring 5 or less on the Short Portable Mental Status Questionnaire [SPMSQ][15]) who had no available caregiver and patients admitted for stroke, coma, or respiratory failure requiring mechanical ventilation were not eligible for participation in the study. The recruitment process for the study is fully described elsewhere.[16, 17]

At‐admission functional, cognitive, mental, and nutritional status were assessed during the first 48 hours of hospitalization. Additional functional assessment was performed at discharge. Data on severity of acute disease, length of stay (LOS), and mortality were collected from the hospitals' EHR. Preadmission healthcare utilization and readmission information were retrieved from the EHR database of Clalit Health Services (Clalit), a large not‐for‐profit integrated healthcare provider and insurer in Israel; more than 80% of the HoPE‐FOR population were Clalit members.

Of the 969 community‐dwelling participants recruited to the HoPE‐FOR study, a subset of 758 (78%) members of Clalit was used for the current study, as data on readmissions to any general hospital were accurately and readily available from Clalit's EHR system.[18] Of those, we excluded 199 due to the following reasons: 13 (2%) died during the hospitalization, 46 (6%) transferred to another ward, 16 (2%) were discharged to a postacute care facility, and 124 (16%) dropped‐out from the HoPE‐FOR study during the hospitalization (due to unavailability because of intensive tests or procedures[16]) or had missing data on the main variables, leaving a final sample of 559 participants. The admission functional, cognitive, and clinical status; LOS; and readmission rates of the participants who dropped‐out were comparable to those of participants retained in the final sample except for albumin levels and age (see Supporting Information, Appendix A, in the online version of this article). The study was approved by the institutional reviews boards of each of the hospitals, Clalit, and the Israeli Ministry of Health.

Variables and Instruments

Outcome Measure

Readmission was defined as any unplanned hospitalization at any of 27 general hospitals in Israel, occurring within 30 days of discharge from the index hospitalization.

Predictors

We collected information on baseline and in‐hospital characteristics. Baseline characteristics included chronic clinical conditions known as risk factors for readmission; number of different drugs as classified by the fifth level of the Anatomical Therapeutic Chemical classification system; number of hospitalizations in the year preceding the index hospitalization; clinical, functional, cognitive, mental, and nutritional status at admission; and sociodemographic characteristics.

Chronic conditions included: congestive heart failure (HF), chronic renal failure (CRF), chronic obstructive pulmonary disease (COPD), diabetes mellitus, ischemic heart disease, arrhythmia, malignancy, and asthma, and were retrieved from the Clalit's EHR data warehouse.[19] Severity of acute disease was assessed with the Acute Physiology and Chronic Health Evaluation.[20] Functional status was measured as self‐reported independence in performing basic activities of daily living (ADL),[21] using the modified Barthel Index (mBI).[22] The mBI consists of 10 items including personal hygiene, bathing, eating, toileting, dressing, chair/bed transfers, ambulation, stair climbing, and bowel and bladder control. Each item is ranked on 5‐point scale, indicating the amount of assistance required in functional independence in each task. The scores are summarized into a total score ranging from 0 (totally dependent) to 100 (fully independent).

Cognitive status was assessed using the SPMSQ.[15] Mental status was assessed based on self‐report of depressive and anxiety symptoms using the 10‐item Tucker's short Zung Instrument (TSZI)[23] and the 10‐item Anxiety Symptoms Questionnaire Short Anxiety Screening Test (SAST),[24] respectively. Both the TSZI and the SAST were validated in Hebrew as screening tools in older adults.[24, 25]

Assessment of nutritional status included malnutrition risk (Malnutrition Universal Screening Tool [MUST]) and admission serum albumin level (g/dL). MUST provides classification into 3 malnutrition risk groups: low (being overweight or obese, with no loss of weight or loss of less than 5% of the weight and without expectation of fasting), medium (normal body mass index [BMI] or weight loss of 510%), and high (normal BMI and inadequate weight loss or malnutrition by BMI and/or 10% weight loss and/or expectations of fasting).[26] Classification of BMI in the current study was according to thresholds for older adults.[27]

In‐hospital risk factors include LOS, a well‐known risk factor of readmission[28] and ADL decline during the index hospitalization. ADL decline was defined as the change in mBI score, calculated by subtracting the discharge score from the at‐admission score and transforming negative scores (functional improvement) to 0.

Statistical Analysis

The relationship between each of the study variables and readmission was examined using 2 tests for categorical variables and t tests for continuous variables. We took a conservative approach, and used a 0.10 threshold level in univariate analysis to decide on variable inclusion in the multivariate models. To examine the at‐admission readmission risk, baseline multivariate logistic regression was modeled with all pre‐ or at‐admission variables that were associated with readmission risk in the univariate analysis. To capture the contribution of in‐hospital data on readmission risk, the at‐discharge multivariate logistic regression was constructed by adding in‐hospital risk factors to the baseline model. To capture the odds of clinically significant functional decline that is equivalent to functional loss in 1 ADL task,[29] we divided the original mBI decline score by 10. Adjusted odds ratios (OR) and 95% confidence intervals (CI) were estimated for each predictor. We used the bootstrapping technique[30] (100 bootstrap subsamples) to test the ADL parameter estimates of both models. The calibration of both models was determined by the Hosmer‐Lemeshow test. The discrimination of the baseline model was compared with that of the at‐discharge model using the C statistic.[31] We derived the prediction score for each patient by adding the coefficients of all applicable factors from the baseline and at‐discharge multivariate logistic regression models and categorized patients' risk of readmission into 5 groups: very low (019th centile), low (2039th centile), medium (4059th percentile), high (6079th percentile), very high (8099th percentile) and extremely high (9099th percentile). We also examined whether when comparing the at‐admission versus discharge model, new patients are identified as high risk (top 10% and 20% of risk score), as these are the patients who are targeted for intervention. Analysis was performed using IBM SPSS Statistical package version 21.0 (IBM, Armonk, NY) and Stata version 10 (StataCorp, College Station, TX).

RESULTS

Table 1 presents the baseline and in‐hospital characteristics of participants with and without readmissions. The sample includes 559 community‐dwelling older adults (49% men) aged 70 to 98 years (mean age 79 years). One‐third (36%) of the participants were fully independent in ADL at admission. Eighty‐five (15.2%) patients were readmitted within 30 days of discharge. Participants who were readmitted had lower at‐admission ADL levels; had 1 more hospitalization in the previous year; and were more likely to have HF, CRF, arrhythmia, and malignancy, and to be at risk of malnutrition, than those who were not readmitted. Participants who were readmitted were more likely to suffer from functional decline during the index hospitalization. No significant differences were found in living arrangements or in at‐admission mental and cognitive status.

Patient Characteristics and Association With 30‐Day Readmission
Characteristic Entire Cohort, N = 559 No Readmission, n = 474 30‐Day Readmission, n = 85 P Value
  • NOTE: Abbreviations: ADL, activities of daily living; APACHE II, Acute Physiology and Chronic Health Evaluation II; mBI, modified Barthel Index; MUST, Malnutrition Universal Screening Tool; SAST, Short Anxiety Screening Test; SD, standard deviation; SPMSQ, Short Portable Mental Status Questionnaire; TZI, Tucker short Depression Rating Scale.

Baseline characteristics
Sociodemographic characteristics
Age, y, mean SD 78.8 5.6 78.7 5.6 79.7 6.6 0.19
Male, n (%) 274 (49.0) 222 (46.8) 52 (61.2) 0.015
Living alone, n (%) 167 (29.9) 148 (31.2) 19 (22.4) 0.10
Education, y, mean SD 9.6 5.0 9.8 4.9 8.7 5.3 0.074
Chronic condition, n (%)
Congestive heart failure 169 (30.2) 130 (27.4) 39 (45.9) 0.001
Chronic renal failure 188 (33.6) 138 (29.1) 50 (58.8) <0.001
Chronic obstructive pulmonary disease 93 (16.6) 77 (16.2) 16 (18.8) 0.56
Diabetes mellitus 249 (44.5) 212 (44.7) 37 (43.5) 0.84
Ischemic heart disease 353 (63.1) 295 (62.2) 58 (68.2) 0.29
Arrhythmia 242 (43.3) 192 (40.5) 50 (58.8) 0.002
Malignancy 176 (31.5) 132 (27.8) 44 (51.8) <0.001
Asthma 72 (12.9) 61 (12.9) 11 (12.9) 0.99
No. of medications prescribed year before index hospitalization, mean SD 12.1 5.7 11.9 5.5 13.7 6.3 0.007
Prior hospitalizations
No. of hospitalizations the year before index hospitalization, mean SD 1.2 1.6 1.00 1.3 2.20 2.2 <0.001
At‐admission health status
APACHE II (071), mean SD 11.5 4.4 11.2 4.2 12.9 4.6 0.003
ADL (mBI) (0100), mean SD 76.9 28.9 78.4 28.4 68.7 30.4 0.004
Cognitive impairment (SPMSQ 5), n (%) 8.1 2.2 8.1 2.2 7.9 2.2 0.32
Depression symptoms (TZI 70), n (%) 106 (19.0) 89 (18.8) 17 (20.0) 0.85
Anxiety symptoms (SAST 24), n (%) 138 (24.7) 115 (24.3) 23 (27.1) 0.63
Risk of malnutrition (MUST), n (%) 0.002
Low risk 177 (31.7) 163 (34.4) 14 (16.5)
Moderate risk 169 (30.2) 142 (30.0) 27 (31.8)
High risk 213 (38.1) 169 (35.7) 44 (51.8)
Serum albumin (g/dL) (1.54.9), mean SD 3.4 0.5 3.3 0.5 3.0 0.5 <0.001
In‐hospital risk factors
ADL decline (mBI) (0100), mean SD 3.2 8.7 2.6 7.4 7.0 13.2 0.003
Length of stay (130), mean SD 5.7 3.7 5.6 3.4 6.7 5.1 0.055

Multivariate analysis (Table 2) shows that higher at‐admission mBI score was associated with lower odds of readmission (OR for 1‐unit increase: 0.99, 95% CI: 0.98‐0.99). Other predictors of higher readmission risk were: high or medium at‐admission risk of malnutrition, malignancy, CRF, each additional hospitalization during the previous year, and lower albumin levels. Severity of illness and demographic characteristics were not significantly associated with readmission.

Multivariate Baseline and Discharge Logistic Regression Models Predicting of 30‐Day Readmission
Characteristic Baseline Model Discharge Model
OR (95% CI) P Value OR (95% CI) P Value
  • NOTE: Abbreviations: ADL, activities of daily living; APACHE II, Acute Physiology and Chronic Health Evaluation II; CI, confidence interval; MUST, Malnutrition Universal Screening Tool; OR, odds ratio. *Odds ratio for 10‐unit increase in modified Barthel index.

Male 1.57 (0.892.77) 0.12 1.75 (0.983.15) 0.06
Living alone 1.04 (0.551.95) 0.91 1.06 (0.562.01) 0.86
Education (years) 0.98 (0.921.03) 0.33 0.98 (0.931.03) 0.38
Chronic conditions
Chronic renal failure 2.54 (1.394.66) 0.003 2.51 (1.364.64) 0.003
Malignancy 2.45 (1.384.32) 0.002 2.35 (1.324.18) 0.004
Congestive heart failure 1.84 (1.983.46) 0.06 1.83 (0.973.46) 0.06
Arrhythmia 1.64 (0.922.93) 0.10 1.66 (0.953.00) 0.09
No. of medications prescribed year before index admission 0.98 (0.931.04) 0.50 0.98 (0.931.04) 0.51
APACHE II 0.98 (0.921.04) 0.49 0.97 (0.911.04) 0.36
No. of hospitalizations year before index admission 1.27 (1.091.48) 0.002 1.26 (1.081.46) 0.004
Risk of malnutrition (MUST)
Low Ref Ref
Moderate 2.21 (1.054.66) 0.042 2.10 (0.984.46) 0.055
High 3.01 (1.486.12) 0.002 2.88 (1.415.91) 0.004
Serum albumin (g/dL) 0.41 (0.240.69) 0.001 0.50 (0.300.83) 0.03
At‐admission ADL 0.99 (0.980.99) 0.037 0.99 (0.980.99) 0.025
In‐hospital ADL decline* 1.32 (1.021.72) 0.034
Length of stay 1.02 (0.951.09) 0.66
Model fit C statistic = 0.81 C statistic = 0.81

The at‐discharge model that combined the baseline model and in‐hospital risk factors showed that in‐hospital (from admission to discharge) ADL decline was significantly associated with readmission, as a 10‐point decrease in the mBI from admission to discharge was associated with 1.32 (95% CI: 1.02‐1.72) greater odds of readmission. LOS was not significantly associated with readmission, after controlling for baseline health status and in‐hospital ADL decline. All other predictors did not markedly change from the baseline to the at‐discharge model either in significance levels or in magnitude.

The discriminatory power of the baseline model was good (C statistic=0.81). Adding ADL decline and LOS did not change the discriminatory power of the model (C statistic=0.81). The P value of the Hosmer‐Lemeshow test equaled 0.67 for the baseline model and 0.48 for the at‐discharge model, indicating good calibration of both models. The P values for the regression coefficients of bootstrap inference assessing the relationship between the at‐admission and in‐hospital ADL decline odds of readmission remained stable (P < 0.05).

Classification of patients into risk categories by the baseline model and the discharge model (Table 3) shows that identifying patients in the top‐tier category (20th highest percentile) according to information available before or at admission does not detect 6/111 (5.4%) of patients who would have been categorized as highest‐risk if information on ADL decline had been incorporated in the predictive algorithm. Additional partitioning of the top fifth group into 2 tiers (8089th and 9099th percentiles) shows that selection of patients in the top 10% of the baseline risk score would not have detected 7/55 (12.7%) patients who would have been identified as high risk at discharge (data not shown).

Classification of Patients into Risk Groups* by Baseline Characteristics (Baseline Model) and by Baseline Characteristics and In‐hospital Functional Change (Discharge Model)
Discharge Model Risk Group
0 1 2 3 4 Total No.
  • NOTE: *0 = 019th percentile, 1 = 2039th percentile, 2 = 4059th percentile, 3 = 6079th percentile, 4 = 8099th percentile

Baseline model risk group 0 99 (89.2) 11 (9.8) 0 1 (0.9) 0 111
1 12 (10.8) 88 (78.6) 12 (10.7) 0 0 112
2 0 13 (11.6) 90 (80.4) 8 (7.1) 1 (0.9) 112
3 0 0 10 (8.9) 98 (86.7) 5 (4.5) 113
4 0 0 0 6 (5.3) 105 (94.6) 111
Total no. 111 112 112 113 111

DISCUSSION

To our knowledge, ours is the first empirical test of the simultaneous role of functioning along the hospitalization course in explaining readmission risk.[8] Our results show that at‐admission lower functional status and in‐hospital functional decline are significant predictors of early unplanned readmission in older adults, beyond other well‐known risk factors.

The major purpose of this study was to examine whether at‐admission data can be used to detect high‐risk patients for potential inclusion in readmission prevention interventions, or whether changes in ADL occurring during the index hospitalization could affect patients' risk, therefore necessitating an additional assessment at discharge. Our results show that some patients would not have been detected at admission, as their in‐hospital ADL decline affects their at‐discharge risk. Nonetheless, this is a small group (only 5% of patients if a targeting threshold of the highest 20% risk is used). Our findings also show that information on ADL decline during the index hospitalization does not contribute to the accuracy of readmission‐risk prediction in a model that utilizes data on prior hospitalizations, baseline nutritional and functional status, and chronic morbidity (CRF and malignancy). Our results are consistent with previous studies showing the association between baseline,[11, 13, 32] or at‐admission[13] functional status and readmission. However, these studies did not analyze the related contribution of in‐hospital functioning to readmission risk, which was recently suggested as a feature that may significantly affect readmission risk, especially in older patients.[8]

Our findings are also congruent with those of a study in which LOS was not significantly associated with readmission in an elderly population.[33] Our null finding can be explained by the broad set of pre‐ and at‐admission variables, such as nutritional and functional status as well as in‐hospital functional decline, included in our model, making LOS a less significant contributor than in more parsimonious models.[28]

Our results also show that malnutrition contributes to readmission risk beyond other well‐known risk factors. Previous studies showed that malnutrition in the elderly is associated with early readmission.[11, 34] These studies, however, did not examine other well‐known risk factors, such as previous hospitalizations, which were tested in our study, precluding identification of the contribution of malnutrition beyond other well‐known risks.

Our findings should be interpreted in light of several limitations. First, the functional, nutritional, and cognitive data were collected from participants' self‐reports, which are prone to recall bias. Nonetheless, self‐report is often used in large‐scale studies, which preclude actual performance measurement.[21] Second, our sample is of adults aged 70 years or older, and may not be representative of the 65 and older population, which is the target population for many readmission reduction interventions.[35] Yet, participants were from a relatively high‐functioning group of patients who were discharged to their homes, thus may resemble the over age 65 years group. Moreover, these inclusion criteria may have affected their readmission rates, which at 15% are lower than the average reported in other older adult populations.[36] Nonetheless, a more heterogenic sample (in terms of baseline functional status) is needed to address the association between in‐hospital functional change and readmissions as well as the discrimination of the model. Third, the attrition rate (16%) might impact the predictive ability of the models, as patients dropped‐out from the study might have had higher in‐hospital deterioration. However, no significant differences between study sample and dropped‐out patients in the wide range of baseline characteristics except for age and baseline albumin levels were found. Fourth, the unique characteristics of the Israeli healthcare system may affect study's generalizability. The high hospital‐bed occupancy rate, stretched to the limit at 99%, which is much higher than in other developed countries,[37] may affect readmission rates and risk. Nonetheless, our findings may be of relevance to other populations and healthcare systems, as variables included in our model have been previously shown to affect readmission risk in other settings,[4, 6] and the percent of in‐hospital ADL decline is similar to that reported by others.[9] Future studies should examine the significance of in‐hospital functioning in other older adult populations, such as greater mix of baseline functioning and myocardial infarction, HF, and COPD patients, that have been emphasized for readmission prevention by the Centers for Medicare and Medicaid Services.

CONCLUSIONS

This study shows that although both functional status and functional decline are significant predictors of readmission, in‐hospital functional decline did not contribute to the discriminative ability of the model, beyond the risk factors known at admission: malnutrition, prior hospitalizations, and being previously diagnosed with CRF or malignancy. These findings call attention to the ability to predict readmission early in the index hospitalization, to enable early intervention in targeted high‐risk patients. Nonetheless, further at‐discharge functional assessment can detect additional patients whose readmission risk changes during the index hospitalization and who should be considered for inclusion in readmission reduction interventions. As suggested in previous prediction models,[3, 38] most of the at‐admission variables examined in this study, including patient‐reported measures such as functioning, are readily available in the EHR or during the at‐admission intake.[39, 40] In settings where these assessments are not routinely performed, their implementation should be considered. These tools could be used to potentially identify patients at high risk of readmission, and accordingly, address physical function as part of routine medical care and during the acute hospitalization, and tailor adequate follow‐up care after discharge.[11]

Disclosures: This work was supported by the Israeli Science Foundation (grant number 565/08); Clalit Health Services(grant number 04‐121/2010); and the Israel National Institute for Health Policy Research (thesis scholarship number 35/2012). The funding agencies had no role in the design and conduct of this study, the analysis or interpretation of the data, or the preparation of the manuscript. The authors report no conflicts of interest.

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Journal of Hospital Medicine - 11(9)
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A continuing focus on readmission prevention as a means to improve quality and reduce waste and costs has led to abundant research on the identification of factors that put older patients at risk for readmission.[1, 2] Recently, research has focused on the development of prediction tools that are based on information from electronic health records (EHR) and that enable early, at‐admission, identification of patients at high risk for readmission.[3, 4, 5] Through such identification, patients are already targeted for inclusion in readmission‐prevention interventions early in their hospital stay.[6, 7] Yet, the ability to rely on these early‐identification tools is contingent on the stability of risk during the hospital stay. Of the in‐hospital factors that can affect readmission, change in functioning has been identified as a potentially major contributor, especially in older patients.[8]

Older adults' deterioration in functioning is a common, troubling phenomenon. Approximately 20% of patients older than 70 years and hospitalized for a medical illness deteriorate in functioning during the hospitalization.[9] Recent evidence points to the contribution of functioning to 30‐day readmission risk, with studies showing that pre‐ or posthospitalization functional impairment is associated with a 1.5 to 3 times greater likelihood of readmission.[10, 11, 12, 13] Whether in‐hospital changes in functioning add to patients' baseline risk, however, is unknown. The only readmission study that examined functional decline during hospitalization was a retrospective study performed in a population of older adults receiving rehabilitation services and therefore may not be generalizable to acutely hospitalized adults.[14] To fill the current knowledge gap, we examined whether in‐hospital functional decline significantly contributes to at‐admission readmission risk factors in its ability to accurately identify high readmission risk in older adults hospitalized in internal medicine units.

METHODS

Design and Participants

Previously collected data from a prospective cohort study, Hospitalization Process Effects on Functional Outcomes and Recovery (HoPE‐FOR), designed to assess the effect of hospitalization‐care processes on functional outcomes in older adults, were combined with EHR data. The population considered for recruitment to HoPE‐FOR comprised older patients (aged 70 years) admitted during the period 2009 to 2011 to 1 of the 8 internal medicine wards at 2 tertiary medical centers in Israel. Patients recruited for the study had an unplanned admission, and were not completely dependent in their basic functions. Cognitively impaired patients (scoring 5 or less on the Short Portable Mental Status Questionnaire [SPMSQ][15]) who had no available caregiver and patients admitted for stroke, coma, or respiratory failure requiring mechanical ventilation were not eligible for participation in the study. The recruitment process for the study is fully described elsewhere.[16, 17]

At‐admission functional, cognitive, mental, and nutritional status were assessed during the first 48 hours of hospitalization. Additional functional assessment was performed at discharge. Data on severity of acute disease, length of stay (LOS), and mortality were collected from the hospitals' EHR. Preadmission healthcare utilization and readmission information were retrieved from the EHR database of Clalit Health Services (Clalit), a large not‐for‐profit integrated healthcare provider and insurer in Israel; more than 80% of the HoPE‐FOR population were Clalit members.

Of the 969 community‐dwelling participants recruited to the HoPE‐FOR study, a subset of 758 (78%) members of Clalit was used for the current study, as data on readmissions to any general hospital were accurately and readily available from Clalit's EHR system.[18] Of those, we excluded 199 due to the following reasons: 13 (2%) died during the hospitalization, 46 (6%) transferred to another ward, 16 (2%) were discharged to a postacute care facility, and 124 (16%) dropped‐out from the HoPE‐FOR study during the hospitalization (due to unavailability because of intensive tests or procedures[16]) or had missing data on the main variables, leaving a final sample of 559 participants. The admission functional, cognitive, and clinical status; LOS; and readmission rates of the participants who dropped‐out were comparable to those of participants retained in the final sample except for albumin levels and age (see Supporting Information, Appendix A, in the online version of this article). The study was approved by the institutional reviews boards of each of the hospitals, Clalit, and the Israeli Ministry of Health.

Variables and Instruments

Outcome Measure

Readmission was defined as any unplanned hospitalization at any of 27 general hospitals in Israel, occurring within 30 days of discharge from the index hospitalization.

Predictors

We collected information on baseline and in‐hospital characteristics. Baseline characteristics included chronic clinical conditions known as risk factors for readmission; number of different drugs as classified by the fifth level of the Anatomical Therapeutic Chemical classification system; number of hospitalizations in the year preceding the index hospitalization; clinical, functional, cognitive, mental, and nutritional status at admission; and sociodemographic characteristics.

Chronic conditions included: congestive heart failure (HF), chronic renal failure (CRF), chronic obstructive pulmonary disease (COPD), diabetes mellitus, ischemic heart disease, arrhythmia, malignancy, and asthma, and were retrieved from the Clalit's EHR data warehouse.[19] Severity of acute disease was assessed with the Acute Physiology and Chronic Health Evaluation.[20] Functional status was measured as self‐reported independence in performing basic activities of daily living (ADL),[21] using the modified Barthel Index (mBI).[22] The mBI consists of 10 items including personal hygiene, bathing, eating, toileting, dressing, chair/bed transfers, ambulation, stair climbing, and bowel and bladder control. Each item is ranked on 5‐point scale, indicating the amount of assistance required in functional independence in each task. The scores are summarized into a total score ranging from 0 (totally dependent) to 100 (fully independent).

Cognitive status was assessed using the SPMSQ.[15] Mental status was assessed based on self‐report of depressive and anxiety symptoms using the 10‐item Tucker's short Zung Instrument (TSZI)[23] and the 10‐item Anxiety Symptoms Questionnaire Short Anxiety Screening Test (SAST),[24] respectively. Both the TSZI and the SAST were validated in Hebrew as screening tools in older adults.[24, 25]

Assessment of nutritional status included malnutrition risk (Malnutrition Universal Screening Tool [MUST]) and admission serum albumin level (g/dL). MUST provides classification into 3 malnutrition risk groups: low (being overweight or obese, with no loss of weight or loss of less than 5% of the weight and without expectation of fasting), medium (normal body mass index [BMI] or weight loss of 510%), and high (normal BMI and inadequate weight loss or malnutrition by BMI and/or 10% weight loss and/or expectations of fasting).[26] Classification of BMI in the current study was according to thresholds for older adults.[27]

In‐hospital risk factors include LOS, a well‐known risk factor of readmission[28] and ADL decline during the index hospitalization. ADL decline was defined as the change in mBI score, calculated by subtracting the discharge score from the at‐admission score and transforming negative scores (functional improvement) to 0.

Statistical Analysis

The relationship between each of the study variables and readmission was examined using 2 tests for categorical variables and t tests for continuous variables. We took a conservative approach, and used a 0.10 threshold level in univariate analysis to decide on variable inclusion in the multivariate models. To examine the at‐admission readmission risk, baseline multivariate logistic regression was modeled with all pre‐ or at‐admission variables that were associated with readmission risk in the univariate analysis. To capture the contribution of in‐hospital data on readmission risk, the at‐discharge multivariate logistic regression was constructed by adding in‐hospital risk factors to the baseline model. To capture the odds of clinically significant functional decline that is equivalent to functional loss in 1 ADL task,[29] we divided the original mBI decline score by 10. Adjusted odds ratios (OR) and 95% confidence intervals (CI) were estimated for each predictor. We used the bootstrapping technique[30] (100 bootstrap subsamples) to test the ADL parameter estimates of both models. The calibration of both models was determined by the Hosmer‐Lemeshow test. The discrimination of the baseline model was compared with that of the at‐discharge model using the C statistic.[31] We derived the prediction score for each patient by adding the coefficients of all applicable factors from the baseline and at‐discharge multivariate logistic regression models and categorized patients' risk of readmission into 5 groups: very low (019th centile), low (2039th centile), medium (4059th percentile), high (6079th percentile), very high (8099th percentile) and extremely high (9099th percentile). We also examined whether when comparing the at‐admission versus discharge model, new patients are identified as high risk (top 10% and 20% of risk score), as these are the patients who are targeted for intervention. Analysis was performed using IBM SPSS Statistical package version 21.0 (IBM, Armonk, NY) and Stata version 10 (StataCorp, College Station, TX).

RESULTS

Table 1 presents the baseline and in‐hospital characteristics of participants with and without readmissions. The sample includes 559 community‐dwelling older adults (49% men) aged 70 to 98 years (mean age 79 years). One‐third (36%) of the participants were fully independent in ADL at admission. Eighty‐five (15.2%) patients were readmitted within 30 days of discharge. Participants who were readmitted had lower at‐admission ADL levels; had 1 more hospitalization in the previous year; and were more likely to have HF, CRF, arrhythmia, and malignancy, and to be at risk of malnutrition, than those who were not readmitted. Participants who were readmitted were more likely to suffer from functional decline during the index hospitalization. No significant differences were found in living arrangements or in at‐admission mental and cognitive status.

Patient Characteristics and Association With 30‐Day Readmission
Characteristic Entire Cohort, N = 559 No Readmission, n = 474 30‐Day Readmission, n = 85 P Value
  • NOTE: Abbreviations: ADL, activities of daily living; APACHE II, Acute Physiology and Chronic Health Evaluation II; mBI, modified Barthel Index; MUST, Malnutrition Universal Screening Tool; SAST, Short Anxiety Screening Test; SD, standard deviation; SPMSQ, Short Portable Mental Status Questionnaire; TZI, Tucker short Depression Rating Scale.

Baseline characteristics
Sociodemographic characteristics
Age, y, mean SD 78.8 5.6 78.7 5.6 79.7 6.6 0.19
Male, n (%) 274 (49.0) 222 (46.8) 52 (61.2) 0.015
Living alone, n (%) 167 (29.9) 148 (31.2) 19 (22.4) 0.10
Education, y, mean SD 9.6 5.0 9.8 4.9 8.7 5.3 0.074
Chronic condition, n (%)
Congestive heart failure 169 (30.2) 130 (27.4) 39 (45.9) 0.001
Chronic renal failure 188 (33.6) 138 (29.1) 50 (58.8) <0.001
Chronic obstructive pulmonary disease 93 (16.6) 77 (16.2) 16 (18.8) 0.56
Diabetes mellitus 249 (44.5) 212 (44.7) 37 (43.5) 0.84
Ischemic heart disease 353 (63.1) 295 (62.2) 58 (68.2) 0.29
Arrhythmia 242 (43.3) 192 (40.5) 50 (58.8) 0.002
Malignancy 176 (31.5) 132 (27.8) 44 (51.8) <0.001
Asthma 72 (12.9) 61 (12.9) 11 (12.9) 0.99
No. of medications prescribed year before index hospitalization, mean SD 12.1 5.7 11.9 5.5 13.7 6.3 0.007
Prior hospitalizations
No. of hospitalizations the year before index hospitalization, mean SD 1.2 1.6 1.00 1.3 2.20 2.2 <0.001
At‐admission health status
APACHE II (071), mean SD 11.5 4.4 11.2 4.2 12.9 4.6 0.003
ADL (mBI) (0100), mean SD 76.9 28.9 78.4 28.4 68.7 30.4 0.004
Cognitive impairment (SPMSQ 5), n (%) 8.1 2.2 8.1 2.2 7.9 2.2 0.32
Depression symptoms (TZI 70), n (%) 106 (19.0) 89 (18.8) 17 (20.0) 0.85
Anxiety symptoms (SAST 24), n (%) 138 (24.7) 115 (24.3) 23 (27.1) 0.63
Risk of malnutrition (MUST), n (%) 0.002
Low risk 177 (31.7) 163 (34.4) 14 (16.5)
Moderate risk 169 (30.2) 142 (30.0) 27 (31.8)
High risk 213 (38.1) 169 (35.7) 44 (51.8)
Serum albumin (g/dL) (1.54.9), mean SD 3.4 0.5 3.3 0.5 3.0 0.5 <0.001
In‐hospital risk factors
ADL decline (mBI) (0100), mean SD 3.2 8.7 2.6 7.4 7.0 13.2 0.003
Length of stay (130), mean SD 5.7 3.7 5.6 3.4 6.7 5.1 0.055

Multivariate analysis (Table 2) shows that higher at‐admission mBI score was associated with lower odds of readmission (OR for 1‐unit increase: 0.99, 95% CI: 0.98‐0.99). Other predictors of higher readmission risk were: high or medium at‐admission risk of malnutrition, malignancy, CRF, each additional hospitalization during the previous year, and lower albumin levels. Severity of illness and demographic characteristics were not significantly associated with readmission.

Multivariate Baseline and Discharge Logistic Regression Models Predicting of 30‐Day Readmission
Characteristic Baseline Model Discharge Model
OR (95% CI) P Value OR (95% CI) P Value
  • NOTE: Abbreviations: ADL, activities of daily living; APACHE II, Acute Physiology and Chronic Health Evaluation II; CI, confidence interval; MUST, Malnutrition Universal Screening Tool; OR, odds ratio. *Odds ratio for 10‐unit increase in modified Barthel index.

Male 1.57 (0.892.77) 0.12 1.75 (0.983.15) 0.06
Living alone 1.04 (0.551.95) 0.91 1.06 (0.562.01) 0.86
Education (years) 0.98 (0.921.03) 0.33 0.98 (0.931.03) 0.38
Chronic conditions
Chronic renal failure 2.54 (1.394.66) 0.003 2.51 (1.364.64) 0.003
Malignancy 2.45 (1.384.32) 0.002 2.35 (1.324.18) 0.004
Congestive heart failure 1.84 (1.983.46) 0.06 1.83 (0.973.46) 0.06
Arrhythmia 1.64 (0.922.93) 0.10 1.66 (0.953.00) 0.09
No. of medications prescribed year before index admission 0.98 (0.931.04) 0.50 0.98 (0.931.04) 0.51
APACHE II 0.98 (0.921.04) 0.49 0.97 (0.911.04) 0.36
No. of hospitalizations year before index admission 1.27 (1.091.48) 0.002 1.26 (1.081.46) 0.004
Risk of malnutrition (MUST)
Low Ref Ref
Moderate 2.21 (1.054.66) 0.042 2.10 (0.984.46) 0.055
High 3.01 (1.486.12) 0.002 2.88 (1.415.91) 0.004
Serum albumin (g/dL) 0.41 (0.240.69) 0.001 0.50 (0.300.83) 0.03
At‐admission ADL 0.99 (0.980.99) 0.037 0.99 (0.980.99) 0.025
In‐hospital ADL decline* 1.32 (1.021.72) 0.034
Length of stay 1.02 (0.951.09) 0.66
Model fit C statistic = 0.81 C statistic = 0.81

The at‐discharge model that combined the baseline model and in‐hospital risk factors showed that in‐hospital (from admission to discharge) ADL decline was significantly associated with readmission, as a 10‐point decrease in the mBI from admission to discharge was associated with 1.32 (95% CI: 1.02‐1.72) greater odds of readmission. LOS was not significantly associated with readmission, after controlling for baseline health status and in‐hospital ADL decline. All other predictors did not markedly change from the baseline to the at‐discharge model either in significance levels or in magnitude.

The discriminatory power of the baseline model was good (C statistic=0.81). Adding ADL decline and LOS did not change the discriminatory power of the model (C statistic=0.81). The P value of the Hosmer‐Lemeshow test equaled 0.67 for the baseline model and 0.48 for the at‐discharge model, indicating good calibration of both models. The P values for the regression coefficients of bootstrap inference assessing the relationship between the at‐admission and in‐hospital ADL decline odds of readmission remained stable (P < 0.05).

Classification of patients into risk categories by the baseline model and the discharge model (Table 3) shows that identifying patients in the top‐tier category (20th highest percentile) according to information available before or at admission does not detect 6/111 (5.4%) of patients who would have been categorized as highest‐risk if information on ADL decline had been incorporated in the predictive algorithm. Additional partitioning of the top fifth group into 2 tiers (8089th and 9099th percentiles) shows that selection of patients in the top 10% of the baseline risk score would not have detected 7/55 (12.7%) patients who would have been identified as high risk at discharge (data not shown).

Classification of Patients into Risk Groups* by Baseline Characteristics (Baseline Model) and by Baseline Characteristics and In‐hospital Functional Change (Discharge Model)
Discharge Model Risk Group
0 1 2 3 4 Total No.
  • NOTE: *0 = 019th percentile, 1 = 2039th percentile, 2 = 4059th percentile, 3 = 6079th percentile, 4 = 8099th percentile

Baseline model risk group 0 99 (89.2) 11 (9.8) 0 1 (0.9) 0 111
1 12 (10.8) 88 (78.6) 12 (10.7) 0 0 112
2 0 13 (11.6) 90 (80.4) 8 (7.1) 1 (0.9) 112
3 0 0 10 (8.9) 98 (86.7) 5 (4.5) 113
4 0 0 0 6 (5.3) 105 (94.6) 111
Total no. 111 112 112 113 111

DISCUSSION

To our knowledge, ours is the first empirical test of the simultaneous role of functioning along the hospitalization course in explaining readmission risk.[8] Our results show that at‐admission lower functional status and in‐hospital functional decline are significant predictors of early unplanned readmission in older adults, beyond other well‐known risk factors.

The major purpose of this study was to examine whether at‐admission data can be used to detect high‐risk patients for potential inclusion in readmission prevention interventions, or whether changes in ADL occurring during the index hospitalization could affect patients' risk, therefore necessitating an additional assessment at discharge. Our results show that some patients would not have been detected at admission, as their in‐hospital ADL decline affects their at‐discharge risk. Nonetheless, this is a small group (only 5% of patients if a targeting threshold of the highest 20% risk is used). Our findings also show that information on ADL decline during the index hospitalization does not contribute to the accuracy of readmission‐risk prediction in a model that utilizes data on prior hospitalizations, baseline nutritional and functional status, and chronic morbidity (CRF and malignancy). Our results are consistent with previous studies showing the association between baseline,[11, 13, 32] or at‐admission[13] functional status and readmission. However, these studies did not analyze the related contribution of in‐hospital functioning to readmission risk, which was recently suggested as a feature that may significantly affect readmission risk, especially in older patients.[8]

Our findings are also congruent with those of a study in which LOS was not significantly associated with readmission in an elderly population.[33] Our null finding can be explained by the broad set of pre‐ and at‐admission variables, such as nutritional and functional status as well as in‐hospital functional decline, included in our model, making LOS a less significant contributor than in more parsimonious models.[28]

Our results also show that malnutrition contributes to readmission risk beyond other well‐known risk factors. Previous studies showed that malnutrition in the elderly is associated with early readmission.[11, 34] These studies, however, did not examine other well‐known risk factors, such as previous hospitalizations, which were tested in our study, precluding identification of the contribution of malnutrition beyond other well‐known risks.

Our findings should be interpreted in light of several limitations. First, the functional, nutritional, and cognitive data were collected from participants' self‐reports, which are prone to recall bias. Nonetheless, self‐report is often used in large‐scale studies, which preclude actual performance measurement.[21] Second, our sample is of adults aged 70 years or older, and may not be representative of the 65 and older population, which is the target population for many readmission reduction interventions.[35] Yet, participants were from a relatively high‐functioning group of patients who were discharged to their homes, thus may resemble the over age 65 years group. Moreover, these inclusion criteria may have affected their readmission rates, which at 15% are lower than the average reported in other older adult populations.[36] Nonetheless, a more heterogenic sample (in terms of baseline functional status) is needed to address the association between in‐hospital functional change and readmissions as well as the discrimination of the model. Third, the attrition rate (16%) might impact the predictive ability of the models, as patients dropped‐out from the study might have had higher in‐hospital deterioration. However, no significant differences between study sample and dropped‐out patients in the wide range of baseline characteristics except for age and baseline albumin levels were found. Fourth, the unique characteristics of the Israeli healthcare system may affect study's generalizability. The high hospital‐bed occupancy rate, stretched to the limit at 99%, which is much higher than in other developed countries,[37] may affect readmission rates and risk. Nonetheless, our findings may be of relevance to other populations and healthcare systems, as variables included in our model have been previously shown to affect readmission risk in other settings,[4, 6] and the percent of in‐hospital ADL decline is similar to that reported by others.[9] Future studies should examine the significance of in‐hospital functioning in other older adult populations, such as greater mix of baseline functioning and myocardial infarction, HF, and COPD patients, that have been emphasized for readmission prevention by the Centers for Medicare and Medicaid Services.

CONCLUSIONS

This study shows that although both functional status and functional decline are significant predictors of readmission, in‐hospital functional decline did not contribute to the discriminative ability of the model, beyond the risk factors known at admission: malnutrition, prior hospitalizations, and being previously diagnosed with CRF or malignancy. These findings call attention to the ability to predict readmission early in the index hospitalization, to enable early intervention in targeted high‐risk patients. Nonetheless, further at‐discharge functional assessment can detect additional patients whose readmission risk changes during the index hospitalization and who should be considered for inclusion in readmission reduction interventions. As suggested in previous prediction models,[3, 38] most of the at‐admission variables examined in this study, including patient‐reported measures such as functioning, are readily available in the EHR or during the at‐admission intake.[39, 40] In settings where these assessments are not routinely performed, their implementation should be considered. These tools could be used to potentially identify patients at high risk of readmission, and accordingly, address physical function as part of routine medical care and during the acute hospitalization, and tailor adequate follow‐up care after discharge.[11]

Disclosures: This work was supported by the Israeli Science Foundation (grant number 565/08); Clalit Health Services(grant number 04‐121/2010); and the Israel National Institute for Health Policy Research (thesis scholarship number 35/2012). The funding agencies had no role in the design and conduct of this study, the analysis or interpretation of the data, or the preparation of the manuscript. The authors report no conflicts of interest.

A continuing focus on readmission prevention as a means to improve quality and reduce waste and costs has led to abundant research on the identification of factors that put older patients at risk for readmission.[1, 2] Recently, research has focused on the development of prediction tools that are based on information from electronic health records (EHR) and that enable early, at‐admission, identification of patients at high risk for readmission.[3, 4, 5] Through such identification, patients are already targeted for inclusion in readmission‐prevention interventions early in their hospital stay.[6, 7] Yet, the ability to rely on these early‐identification tools is contingent on the stability of risk during the hospital stay. Of the in‐hospital factors that can affect readmission, change in functioning has been identified as a potentially major contributor, especially in older patients.[8]

Older adults' deterioration in functioning is a common, troubling phenomenon. Approximately 20% of patients older than 70 years and hospitalized for a medical illness deteriorate in functioning during the hospitalization.[9] Recent evidence points to the contribution of functioning to 30‐day readmission risk, with studies showing that pre‐ or posthospitalization functional impairment is associated with a 1.5 to 3 times greater likelihood of readmission.[10, 11, 12, 13] Whether in‐hospital changes in functioning add to patients' baseline risk, however, is unknown. The only readmission study that examined functional decline during hospitalization was a retrospective study performed in a population of older adults receiving rehabilitation services and therefore may not be generalizable to acutely hospitalized adults.[14] To fill the current knowledge gap, we examined whether in‐hospital functional decline significantly contributes to at‐admission readmission risk factors in its ability to accurately identify high readmission risk in older adults hospitalized in internal medicine units.

METHODS

Design and Participants

Previously collected data from a prospective cohort study, Hospitalization Process Effects on Functional Outcomes and Recovery (HoPE‐FOR), designed to assess the effect of hospitalization‐care processes on functional outcomes in older adults, were combined with EHR data. The population considered for recruitment to HoPE‐FOR comprised older patients (aged 70 years) admitted during the period 2009 to 2011 to 1 of the 8 internal medicine wards at 2 tertiary medical centers in Israel. Patients recruited for the study had an unplanned admission, and were not completely dependent in their basic functions. Cognitively impaired patients (scoring 5 or less on the Short Portable Mental Status Questionnaire [SPMSQ][15]) who had no available caregiver and patients admitted for stroke, coma, or respiratory failure requiring mechanical ventilation were not eligible for participation in the study. The recruitment process for the study is fully described elsewhere.[16, 17]

At‐admission functional, cognitive, mental, and nutritional status were assessed during the first 48 hours of hospitalization. Additional functional assessment was performed at discharge. Data on severity of acute disease, length of stay (LOS), and mortality were collected from the hospitals' EHR. Preadmission healthcare utilization and readmission information were retrieved from the EHR database of Clalit Health Services (Clalit), a large not‐for‐profit integrated healthcare provider and insurer in Israel; more than 80% of the HoPE‐FOR population were Clalit members.

Of the 969 community‐dwelling participants recruited to the HoPE‐FOR study, a subset of 758 (78%) members of Clalit was used for the current study, as data on readmissions to any general hospital were accurately and readily available from Clalit's EHR system.[18] Of those, we excluded 199 due to the following reasons: 13 (2%) died during the hospitalization, 46 (6%) transferred to another ward, 16 (2%) were discharged to a postacute care facility, and 124 (16%) dropped‐out from the HoPE‐FOR study during the hospitalization (due to unavailability because of intensive tests or procedures[16]) or had missing data on the main variables, leaving a final sample of 559 participants. The admission functional, cognitive, and clinical status; LOS; and readmission rates of the participants who dropped‐out were comparable to those of participants retained in the final sample except for albumin levels and age (see Supporting Information, Appendix A, in the online version of this article). The study was approved by the institutional reviews boards of each of the hospitals, Clalit, and the Israeli Ministry of Health.

Variables and Instruments

Outcome Measure

Readmission was defined as any unplanned hospitalization at any of 27 general hospitals in Israel, occurring within 30 days of discharge from the index hospitalization.

Predictors

We collected information on baseline and in‐hospital characteristics. Baseline characteristics included chronic clinical conditions known as risk factors for readmission; number of different drugs as classified by the fifth level of the Anatomical Therapeutic Chemical classification system; number of hospitalizations in the year preceding the index hospitalization; clinical, functional, cognitive, mental, and nutritional status at admission; and sociodemographic characteristics.

Chronic conditions included: congestive heart failure (HF), chronic renal failure (CRF), chronic obstructive pulmonary disease (COPD), diabetes mellitus, ischemic heart disease, arrhythmia, malignancy, and asthma, and were retrieved from the Clalit's EHR data warehouse.[19] Severity of acute disease was assessed with the Acute Physiology and Chronic Health Evaluation.[20] Functional status was measured as self‐reported independence in performing basic activities of daily living (ADL),[21] using the modified Barthel Index (mBI).[22] The mBI consists of 10 items including personal hygiene, bathing, eating, toileting, dressing, chair/bed transfers, ambulation, stair climbing, and bowel and bladder control. Each item is ranked on 5‐point scale, indicating the amount of assistance required in functional independence in each task. The scores are summarized into a total score ranging from 0 (totally dependent) to 100 (fully independent).

Cognitive status was assessed using the SPMSQ.[15] Mental status was assessed based on self‐report of depressive and anxiety symptoms using the 10‐item Tucker's short Zung Instrument (TSZI)[23] and the 10‐item Anxiety Symptoms Questionnaire Short Anxiety Screening Test (SAST),[24] respectively. Both the TSZI and the SAST were validated in Hebrew as screening tools in older adults.[24, 25]

Assessment of nutritional status included malnutrition risk (Malnutrition Universal Screening Tool [MUST]) and admission serum albumin level (g/dL). MUST provides classification into 3 malnutrition risk groups: low (being overweight or obese, with no loss of weight or loss of less than 5% of the weight and without expectation of fasting), medium (normal body mass index [BMI] or weight loss of 510%), and high (normal BMI and inadequate weight loss or malnutrition by BMI and/or 10% weight loss and/or expectations of fasting).[26] Classification of BMI in the current study was according to thresholds for older adults.[27]

In‐hospital risk factors include LOS, a well‐known risk factor of readmission[28] and ADL decline during the index hospitalization. ADL decline was defined as the change in mBI score, calculated by subtracting the discharge score from the at‐admission score and transforming negative scores (functional improvement) to 0.

Statistical Analysis

The relationship between each of the study variables and readmission was examined using 2 tests for categorical variables and t tests for continuous variables. We took a conservative approach, and used a 0.10 threshold level in univariate analysis to decide on variable inclusion in the multivariate models. To examine the at‐admission readmission risk, baseline multivariate logistic regression was modeled with all pre‐ or at‐admission variables that were associated with readmission risk in the univariate analysis. To capture the contribution of in‐hospital data on readmission risk, the at‐discharge multivariate logistic regression was constructed by adding in‐hospital risk factors to the baseline model. To capture the odds of clinically significant functional decline that is equivalent to functional loss in 1 ADL task,[29] we divided the original mBI decline score by 10. Adjusted odds ratios (OR) and 95% confidence intervals (CI) were estimated for each predictor. We used the bootstrapping technique[30] (100 bootstrap subsamples) to test the ADL parameter estimates of both models. The calibration of both models was determined by the Hosmer‐Lemeshow test. The discrimination of the baseline model was compared with that of the at‐discharge model using the C statistic.[31] We derived the prediction score for each patient by adding the coefficients of all applicable factors from the baseline and at‐discharge multivariate logistic regression models and categorized patients' risk of readmission into 5 groups: very low (019th centile), low (2039th centile), medium (4059th percentile), high (6079th percentile), very high (8099th percentile) and extremely high (9099th percentile). We also examined whether when comparing the at‐admission versus discharge model, new patients are identified as high risk (top 10% and 20% of risk score), as these are the patients who are targeted for intervention. Analysis was performed using IBM SPSS Statistical package version 21.0 (IBM, Armonk, NY) and Stata version 10 (StataCorp, College Station, TX).

RESULTS

Table 1 presents the baseline and in‐hospital characteristics of participants with and without readmissions. The sample includes 559 community‐dwelling older adults (49% men) aged 70 to 98 years (mean age 79 years). One‐third (36%) of the participants were fully independent in ADL at admission. Eighty‐five (15.2%) patients were readmitted within 30 days of discharge. Participants who were readmitted had lower at‐admission ADL levels; had 1 more hospitalization in the previous year; and were more likely to have HF, CRF, arrhythmia, and malignancy, and to be at risk of malnutrition, than those who were not readmitted. Participants who were readmitted were more likely to suffer from functional decline during the index hospitalization. No significant differences were found in living arrangements or in at‐admission mental and cognitive status.

Patient Characteristics and Association With 30‐Day Readmission
Characteristic Entire Cohort, N = 559 No Readmission, n = 474 30‐Day Readmission, n = 85 P Value
  • NOTE: Abbreviations: ADL, activities of daily living; APACHE II, Acute Physiology and Chronic Health Evaluation II; mBI, modified Barthel Index; MUST, Malnutrition Universal Screening Tool; SAST, Short Anxiety Screening Test; SD, standard deviation; SPMSQ, Short Portable Mental Status Questionnaire; TZI, Tucker short Depression Rating Scale.

Baseline characteristics
Sociodemographic characteristics
Age, y, mean SD 78.8 5.6 78.7 5.6 79.7 6.6 0.19
Male, n (%) 274 (49.0) 222 (46.8) 52 (61.2) 0.015
Living alone, n (%) 167 (29.9) 148 (31.2) 19 (22.4) 0.10
Education, y, mean SD 9.6 5.0 9.8 4.9 8.7 5.3 0.074
Chronic condition, n (%)
Congestive heart failure 169 (30.2) 130 (27.4) 39 (45.9) 0.001
Chronic renal failure 188 (33.6) 138 (29.1) 50 (58.8) <0.001
Chronic obstructive pulmonary disease 93 (16.6) 77 (16.2) 16 (18.8) 0.56
Diabetes mellitus 249 (44.5) 212 (44.7) 37 (43.5) 0.84
Ischemic heart disease 353 (63.1) 295 (62.2) 58 (68.2) 0.29
Arrhythmia 242 (43.3) 192 (40.5) 50 (58.8) 0.002
Malignancy 176 (31.5) 132 (27.8) 44 (51.8) <0.001
Asthma 72 (12.9) 61 (12.9) 11 (12.9) 0.99
No. of medications prescribed year before index hospitalization, mean SD 12.1 5.7 11.9 5.5 13.7 6.3 0.007
Prior hospitalizations
No. of hospitalizations the year before index hospitalization, mean SD 1.2 1.6 1.00 1.3 2.20 2.2 <0.001
At‐admission health status
APACHE II (071), mean SD 11.5 4.4 11.2 4.2 12.9 4.6 0.003
ADL (mBI) (0100), mean SD 76.9 28.9 78.4 28.4 68.7 30.4 0.004
Cognitive impairment (SPMSQ 5), n (%) 8.1 2.2 8.1 2.2 7.9 2.2 0.32
Depression symptoms (TZI 70), n (%) 106 (19.0) 89 (18.8) 17 (20.0) 0.85
Anxiety symptoms (SAST 24), n (%) 138 (24.7) 115 (24.3) 23 (27.1) 0.63
Risk of malnutrition (MUST), n (%) 0.002
Low risk 177 (31.7) 163 (34.4) 14 (16.5)
Moderate risk 169 (30.2) 142 (30.0) 27 (31.8)
High risk 213 (38.1) 169 (35.7) 44 (51.8)
Serum albumin (g/dL) (1.54.9), mean SD 3.4 0.5 3.3 0.5 3.0 0.5 <0.001
In‐hospital risk factors
ADL decline (mBI) (0100), mean SD 3.2 8.7 2.6 7.4 7.0 13.2 0.003
Length of stay (130), mean SD 5.7 3.7 5.6 3.4 6.7 5.1 0.055

Multivariate analysis (Table 2) shows that higher at‐admission mBI score was associated with lower odds of readmission (OR for 1‐unit increase: 0.99, 95% CI: 0.98‐0.99). Other predictors of higher readmission risk were: high or medium at‐admission risk of malnutrition, malignancy, CRF, each additional hospitalization during the previous year, and lower albumin levels. Severity of illness and demographic characteristics were not significantly associated with readmission.

Multivariate Baseline and Discharge Logistic Regression Models Predicting of 30‐Day Readmission
Characteristic Baseline Model Discharge Model
OR (95% CI) P Value OR (95% CI) P Value
  • NOTE: Abbreviations: ADL, activities of daily living; APACHE II, Acute Physiology and Chronic Health Evaluation II; CI, confidence interval; MUST, Malnutrition Universal Screening Tool; OR, odds ratio. *Odds ratio for 10‐unit increase in modified Barthel index.

Male 1.57 (0.892.77) 0.12 1.75 (0.983.15) 0.06
Living alone 1.04 (0.551.95) 0.91 1.06 (0.562.01) 0.86
Education (years) 0.98 (0.921.03) 0.33 0.98 (0.931.03) 0.38
Chronic conditions
Chronic renal failure 2.54 (1.394.66) 0.003 2.51 (1.364.64) 0.003
Malignancy 2.45 (1.384.32) 0.002 2.35 (1.324.18) 0.004
Congestive heart failure 1.84 (1.983.46) 0.06 1.83 (0.973.46) 0.06
Arrhythmia 1.64 (0.922.93) 0.10 1.66 (0.953.00) 0.09
No. of medications prescribed year before index admission 0.98 (0.931.04) 0.50 0.98 (0.931.04) 0.51
APACHE II 0.98 (0.921.04) 0.49 0.97 (0.911.04) 0.36
No. of hospitalizations year before index admission 1.27 (1.091.48) 0.002 1.26 (1.081.46) 0.004
Risk of malnutrition (MUST)
Low Ref Ref
Moderate 2.21 (1.054.66) 0.042 2.10 (0.984.46) 0.055
High 3.01 (1.486.12) 0.002 2.88 (1.415.91) 0.004
Serum albumin (g/dL) 0.41 (0.240.69) 0.001 0.50 (0.300.83) 0.03
At‐admission ADL 0.99 (0.980.99) 0.037 0.99 (0.980.99) 0.025
In‐hospital ADL decline* 1.32 (1.021.72) 0.034
Length of stay 1.02 (0.951.09) 0.66
Model fit C statistic = 0.81 C statistic = 0.81

The at‐discharge model that combined the baseline model and in‐hospital risk factors showed that in‐hospital (from admission to discharge) ADL decline was significantly associated with readmission, as a 10‐point decrease in the mBI from admission to discharge was associated with 1.32 (95% CI: 1.02‐1.72) greater odds of readmission. LOS was not significantly associated with readmission, after controlling for baseline health status and in‐hospital ADL decline. All other predictors did not markedly change from the baseline to the at‐discharge model either in significance levels or in magnitude.

The discriminatory power of the baseline model was good (C statistic=0.81). Adding ADL decline and LOS did not change the discriminatory power of the model (C statistic=0.81). The P value of the Hosmer‐Lemeshow test equaled 0.67 for the baseline model and 0.48 for the at‐discharge model, indicating good calibration of both models. The P values for the regression coefficients of bootstrap inference assessing the relationship between the at‐admission and in‐hospital ADL decline odds of readmission remained stable (P < 0.05).

Classification of patients into risk categories by the baseline model and the discharge model (Table 3) shows that identifying patients in the top‐tier category (20th highest percentile) according to information available before or at admission does not detect 6/111 (5.4%) of patients who would have been categorized as highest‐risk if information on ADL decline had been incorporated in the predictive algorithm. Additional partitioning of the top fifth group into 2 tiers (8089th and 9099th percentiles) shows that selection of patients in the top 10% of the baseline risk score would not have detected 7/55 (12.7%) patients who would have been identified as high risk at discharge (data not shown).

Classification of Patients into Risk Groups* by Baseline Characteristics (Baseline Model) and by Baseline Characteristics and In‐hospital Functional Change (Discharge Model)
Discharge Model Risk Group
0 1 2 3 4 Total No.
  • NOTE: *0 = 019th percentile, 1 = 2039th percentile, 2 = 4059th percentile, 3 = 6079th percentile, 4 = 8099th percentile

Baseline model risk group 0 99 (89.2) 11 (9.8) 0 1 (0.9) 0 111
1 12 (10.8) 88 (78.6) 12 (10.7) 0 0 112
2 0 13 (11.6) 90 (80.4) 8 (7.1) 1 (0.9) 112
3 0 0 10 (8.9) 98 (86.7) 5 (4.5) 113
4 0 0 0 6 (5.3) 105 (94.6) 111
Total no. 111 112 112 113 111

DISCUSSION

To our knowledge, ours is the first empirical test of the simultaneous role of functioning along the hospitalization course in explaining readmission risk.[8] Our results show that at‐admission lower functional status and in‐hospital functional decline are significant predictors of early unplanned readmission in older adults, beyond other well‐known risk factors.

The major purpose of this study was to examine whether at‐admission data can be used to detect high‐risk patients for potential inclusion in readmission prevention interventions, or whether changes in ADL occurring during the index hospitalization could affect patients' risk, therefore necessitating an additional assessment at discharge. Our results show that some patients would not have been detected at admission, as their in‐hospital ADL decline affects their at‐discharge risk. Nonetheless, this is a small group (only 5% of patients if a targeting threshold of the highest 20% risk is used). Our findings also show that information on ADL decline during the index hospitalization does not contribute to the accuracy of readmission‐risk prediction in a model that utilizes data on prior hospitalizations, baseline nutritional and functional status, and chronic morbidity (CRF and malignancy). Our results are consistent with previous studies showing the association between baseline,[11, 13, 32] or at‐admission[13] functional status and readmission. However, these studies did not analyze the related contribution of in‐hospital functioning to readmission risk, which was recently suggested as a feature that may significantly affect readmission risk, especially in older patients.[8]

Our findings are also congruent with those of a study in which LOS was not significantly associated with readmission in an elderly population.[33] Our null finding can be explained by the broad set of pre‐ and at‐admission variables, such as nutritional and functional status as well as in‐hospital functional decline, included in our model, making LOS a less significant contributor than in more parsimonious models.[28]

Our results also show that malnutrition contributes to readmission risk beyond other well‐known risk factors. Previous studies showed that malnutrition in the elderly is associated with early readmission.[11, 34] These studies, however, did not examine other well‐known risk factors, such as previous hospitalizations, which were tested in our study, precluding identification of the contribution of malnutrition beyond other well‐known risks.

Our findings should be interpreted in light of several limitations. First, the functional, nutritional, and cognitive data were collected from participants' self‐reports, which are prone to recall bias. Nonetheless, self‐report is often used in large‐scale studies, which preclude actual performance measurement.[21] Second, our sample is of adults aged 70 years or older, and may not be representative of the 65 and older population, which is the target population for many readmission reduction interventions.[35] Yet, participants were from a relatively high‐functioning group of patients who were discharged to their homes, thus may resemble the over age 65 years group. Moreover, these inclusion criteria may have affected their readmission rates, which at 15% are lower than the average reported in other older adult populations.[36] Nonetheless, a more heterogenic sample (in terms of baseline functional status) is needed to address the association between in‐hospital functional change and readmissions as well as the discrimination of the model. Third, the attrition rate (16%) might impact the predictive ability of the models, as patients dropped‐out from the study might have had higher in‐hospital deterioration. However, no significant differences between study sample and dropped‐out patients in the wide range of baseline characteristics except for age and baseline albumin levels were found. Fourth, the unique characteristics of the Israeli healthcare system may affect study's generalizability. The high hospital‐bed occupancy rate, stretched to the limit at 99%, which is much higher than in other developed countries,[37] may affect readmission rates and risk. Nonetheless, our findings may be of relevance to other populations and healthcare systems, as variables included in our model have been previously shown to affect readmission risk in other settings,[4, 6] and the percent of in‐hospital ADL decline is similar to that reported by others.[9] Future studies should examine the significance of in‐hospital functioning in other older adult populations, such as greater mix of baseline functioning and myocardial infarction, HF, and COPD patients, that have been emphasized for readmission prevention by the Centers for Medicare and Medicaid Services.

CONCLUSIONS

This study shows that although both functional status and functional decline are significant predictors of readmission, in‐hospital functional decline did not contribute to the discriminative ability of the model, beyond the risk factors known at admission: malnutrition, prior hospitalizations, and being previously diagnosed with CRF or malignancy. These findings call attention to the ability to predict readmission early in the index hospitalization, to enable early intervention in targeted high‐risk patients. Nonetheless, further at‐discharge functional assessment can detect additional patients whose readmission risk changes during the index hospitalization and who should be considered for inclusion in readmission reduction interventions. As suggested in previous prediction models,[3, 38] most of the at‐admission variables examined in this study, including patient‐reported measures such as functioning, are readily available in the EHR or during the at‐admission intake.[39, 40] In settings where these assessments are not routinely performed, their implementation should be considered. These tools could be used to potentially identify patients at high risk of readmission, and accordingly, address physical function as part of routine medical care and during the acute hospitalization, and tailor adequate follow‐up care after discharge.[11]

Disclosures: This work was supported by the Israeli Science Foundation (grant number 565/08); Clalit Health Services(grant number 04‐121/2010); and the Israel National Institute for Health Policy Research (thesis scholarship number 35/2012). The funding agencies had no role in the design and conduct of this study, the analysis or interpretation of the data, or the preparation of the manuscript. The authors report no conflicts of interest.

References
  1. Vest JR, Gamm LD, Oxford BA, Gonzalez MI, Slawson KM. Determinants of preventable readmissions in the United States: a systematic review. Implement Sci. 2010;5:127.
  2. Garcia‐Perez L, Linertova R, Lorenzo‐Riera A, Vazquez‐Diaz JR, Duque‐Gonzalez B, Sarria‐Santamera A. Risk factors for hospital readmissions in elderly patients: a systematic review. QJM. 2011;104:639651.
  3. Shadmi E, Flaks‐Manov N, Hoshen M, Goldman O, Bitterman H, Balicer RD. Predicting 30‐day readmissions with preadmission electronic health record data. Med Care. 2015;53:283289.
  4. Amarasingham R, Velasco F, Xie B, et al. Electronic medical record‐based multicondition models to predict the risk of 30 day readmission or death among adult medicine patients: validation and comparison to existing models. BMC Med Inform Decis Mak. 2015;15:39.
  5. Amarasingham R, Moore BJ, Tabak YP, et al. An automated model to identify heart failure patients at risk for 30‐day readmission or death using electronic medical record data. Med Care. 2010;48:981988.
  6. Billings J, Blunt I, Steventon A, Georghiou T, Lewis G, Bardsley M. Development of a predictive model to identify inpatients at risk of re‐admission within 30 days of discharge (PARR‐30). BMJ Open. 2012;2:10.
  7. Kansagara D, Chiovaro JC, Kagen D, et al. So many options, where do we start? An overview of the care transitions literature. J Hosp Med. 2016;11(3):221230.
  8. Greysen SR, Covinsky KE. Functional status—an important but overlooked variable in the readmissions equation. J Hosp Med. 2014;9:330331.
  9. Covinsky KE, Palmer RM, Fortinsky RH, et al. Loss of independence in activities of daily living in older adults hospitalized with medical illnesses: increased vulnerability with age. J Am Geriatr Soc. 2003;51:451458.
  10. Kwok T, Lau E, Woo J, et al. Hospital readmission among older medical patients in Hong Kong. J R Coll Physicians Lond. 1999;33:153156.
  11. Greysen SR, Stijacic Cenzer I, Auerbach AD, Covinsky KE. Functional impairment and hospital readmission in Medicare seniors. JAMA Intern Med. 2015;175:559565.
  12. Hoyer EH, Needham DM, Atanelov L, Knox B, Friedman M, Brotman DJ. Association of impaired functional status at hospital discharge and subsequent rehospitalization. J Hosp Med. 2014;9:277282.
  13. Laniece I, Couturier P, Drame M, et al. Incidence and main factors associated with early unplanned hospital readmission among French medical inpatients aged 75 and over admitted through emergency units. Age Ageing. 2008;37:416422.
  14. Morandi A, Bellelli G, Vasilevskis EE, et al. Predictors of rehospitalization among elderly patients admitted to a rehabilitation hospital: the role of polypharmacy, functional status, and length of stay. J Am Med Dir Assoc. 2013;14:761767.
  15. Pfeiffer E. A short portable mental status questionnaire for the assessment of organic brain deficit in elderly patients. J Am Geriatr Soc. 1975;23:433441.
  16. Zisberg A, Shadmi E, Sinoff G, Gur‐Yaish N, Srulovici E, Admi H. Low mobility during hospitalization and functional decline in older adults. J Am Geriatr Soc. 2011;59:266273.
  17. Zisberg A, Shadmi E, Gur‐Yaish N, Tonkikh O, Sinoff G. Hospital associated functional decline: the role of hospitalization processes beyond individual risk factors. J Am Geriatr Soc. 2015;63:5562.
  18. Flaks‐Manov N, Shadmi E, Hoshen M, Balicer RD. Health information exchange systems and length of stay in readmissions to a different hospital [published online December 29, 2015]. J Hosp Med. doi: 10.1002/jhm.2535.
  19. Rennert G, Peterburg Y. Prevalence of selected chronic diseases in Israel. Isr Med Assoc J. 2001;3:404408.
  20. Knaus WA, Draper EA, Wagner DP, Zimmerman JE. APACHE II: a severity of disease classification system. Crit Care Med. 1985;13:818829.
  21. Covinsky KE, Palmer RM, Counsell SR, Pine ZM, Walter LC, Chren MM. Functional status before hospitalization in acutely ill older adults: validity and clinical importance of retrospective reports. J Am Geriatr Soc. 2000;48:164169.
  22. Shah S, Vanclay F, Cooper B. Improving the sensitivity of the Barthel index for stroke rehabilitation. J Clin Epidemiol. 1989;42:703709.
  23. Tucker M, Ogle S, Davison J, Eilenberg M. Validation of a brief screening test for depression in the elderly. Age Ageing. 1987;16:139144.
  24. Sinoff G, Ore L, Zlotogorsky D, Tamir A. Short Anxiety Screening Test—a brief instrument for detecting anxiety in the elderly. Int J Geriatr Psychiatry. 1999;14:10621071.
  25. Sinoff G, Ore L, Zlotogorsky D, Tamir A. Does the presence of anxiety affect the validity of a screening test for depression in the elderly? Int J Geriatr Psychiatry. 2002;17:309314.
  26. Elia M. The ‘MUST’ report. Nutritional screening of adults: a multidisciplinary responsibility (executive summary). Available at: http://www.bapen.org.uk/pdfs/must/must_exec_sum.pdf. Accessed July 10, 2015.
  27. Somes GW, Kritchevsky SB, Shorr RI, Pahor M, Applegate WB. Body mass index, weight change, and death in older adults: the systolic hypertension in the elderly program. Am J Epidemiol. 2002;156:132138.
  28. Walraven C, Dhalla I, Bell C, Etchells E, et al. Derivation and validation of an index to predict early death or unplanned readmission after discharge from hospital to the community. CMAJ. 2010;182:551557.
  29. Buurman BM, Munster BC, Korevaar JC, Haan RJ, Rooij SE. Variability in measuring (instrumental) activities of daily living functioning and functional decline in hospitalized older medical patients: a systematic review. J Clin Epidemiol. 2011;64:619627.
  30. Steyerberg EW, Harrell FE, Borsboom GJ, Eijkemans MJ, Vergouwe Y, Habbema JD. Internal validation of predictive models: efficiency of some procedures for logistic regression analysis. J Clin Epidemiol. 2001;54:774781.
  31. Kansagara D, Englander H, Salanitro A, et al. Risk prediction models for hospital readmission: a systematic review. JAMA. 2011;306:16881698.
  32. Soley‐Bori M, Soria‐Saucedo R, Ryan CM, et al. Functional status and hospital readmissions using the medical expenditure panel survey. J Gen Intern Med. 2015;30:965972.
  33. Cotter PE, Bhalla VK, Wallis SJ, Biram RW. Predicting readmissions: poor performance of the LACE index in an older UK population. Age Ageing. 2012;41:784789.
  34. Silverstein MD, Qin H, Mercer SQ, Fong J, Haydar Z. Risk factors for 30‐day hospital readmission in patients ≥65 years of age. Proc (Bayl Univ Med Cent). 2008;21:363372.
  35. Center for Outcomes Research 360:14181428.
  36. Meydan C, Haklai Z, Gordon B, Mendlovic J, Afek A. Managing the increasing shortage of acute care hospital beds in Israel. J Eval Clin Pract. 2015;21:7984.
  37. Billings J, Dixon J, Mijanovich T, Wennberg D. Case finding for patients at risk of readmission to hospital: development of algorithm to identify high risk patients. BMJ. 2006;333:327.
  38. Rasmussen HH, Holst M, Kondrup J. Measuring nutritional risk in hospitals. Clin Epidemiol. 2010;2:209216.
  39. Hinami K, Smith J, Deamant CD, DuBeshter K, Trick WE. When do patient‐reported outcome measures inform readmission risk? J Hosp Med. 2015;10:294300.
References
  1. Vest JR, Gamm LD, Oxford BA, Gonzalez MI, Slawson KM. Determinants of preventable readmissions in the United States: a systematic review. Implement Sci. 2010;5:127.
  2. Garcia‐Perez L, Linertova R, Lorenzo‐Riera A, Vazquez‐Diaz JR, Duque‐Gonzalez B, Sarria‐Santamera A. Risk factors for hospital readmissions in elderly patients: a systematic review. QJM. 2011;104:639651.
  3. Shadmi E, Flaks‐Manov N, Hoshen M, Goldman O, Bitterman H, Balicer RD. Predicting 30‐day readmissions with preadmission electronic health record data. Med Care. 2015;53:283289.
  4. Amarasingham R, Velasco F, Xie B, et al. Electronic medical record‐based multicondition models to predict the risk of 30 day readmission or death among adult medicine patients: validation and comparison to existing models. BMC Med Inform Decis Mak. 2015;15:39.
  5. Amarasingham R, Moore BJ, Tabak YP, et al. An automated model to identify heart failure patients at risk for 30‐day readmission or death using electronic medical record data. Med Care. 2010;48:981988.
  6. Billings J, Blunt I, Steventon A, Georghiou T, Lewis G, Bardsley M. Development of a predictive model to identify inpatients at risk of re‐admission within 30 days of discharge (PARR‐30). BMJ Open. 2012;2:10.
  7. Kansagara D, Chiovaro JC, Kagen D, et al. So many options, where do we start? An overview of the care transitions literature. J Hosp Med. 2016;11(3):221230.
  8. Greysen SR, Covinsky KE. Functional status—an important but overlooked variable in the readmissions equation. J Hosp Med. 2014;9:330331.
  9. Covinsky KE, Palmer RM, Fortinsky RH, et al. Loss of independence in activities of daily living in older adults hospitalized with medical illnesses: increased vulnerability with age. J Am Geriatr Soc. 2003;51:451458.
  10. Kwok T, Lau E, Woo J, et al. Hospital readmission among older medical patients in Hong Kong. J R Coll Physicians Lond. 1999;33:153156.
  11. Greysen SR, Stijacic Cenzer I, Auerbach AD, Covinsky KE. Functional impairment and hospital readmission in Medicare seniors. JAMA Intern Med. 2015;175:559565.
  12. Hoyer EH, Needham DM, Atanelov L, Knox B, Friedman M, Brotman DJ. Association of impaired functional status at hospital discharge and subsequent rehospitalization. J Hosp Med. 2014;9:277282.
  13. Laniece I, Couturier P, Drame M, et al. Incidence and main factors associated with early unplanned hospital readmission among French medical inpatients aged 75 and over admitted through emergency units. Age Ageing. 2008;37:416422.
  14. Morandi A, Bellelli G, Vasilevskis EE, et al. Predictors of rehospitalization among elderly patients admitted to a rehabilitation hospital: the role of polypharmacy, functional status, and length of stay. J Am Med Dir Assoc. 2013;14:761767.
  15. Pfeiffer E. A short portable mental status questionnaire for the assessment of organic brain deficit in elderly patients. J Am Geriatr Soc. 1975;23:433441.
  16. Zisberg A, Shadmi E, Sinoff G, Gur‐Yaish N, Srulovici E, Admi H. Low mobility during hospitalization and functional decline in older adults. J Am Geriatr Soc. 2011;59:266273.
  17. Zisberg A, Shadmi E, Gur‐Yaish N, Tonkikh O, Sinoff G. Hospital associated functional decline: the role of hospitalization processes beyond individual risk factors. J Am Geriatr Soc. 2015;63:5562.
  18. Flaks‐Manov N, Shadmi E, Hoshen M, Balicer RD. Health information exchange systems and length of stay in readmissions to a different hospital [published online December 29, 2015]. J Hosp Med. doi: 10.1002/jhm.2535.
  19. Rennert G, Peterburg Y. Prevalence of selected chronic diseases in Israel. Isr Med Assoc J. 2001;3:404408.
  20. Knaus WA, Draper EA, Wagner DP, Zimmerman JE. APACHE II: a severity of disease classification system. Crit Care Med. 1985;13:818829.
  21. Covinsky KE, Palmer RM, Counsell SR, Pine ZM, Walter LC, Chren MM. Functional status before hospitalization in acutely ill older adults: validity and clinical importance of retrospective reports. J Am Geriatr Soc. 2000;48:164169.
  22. Shah S, Vanclay F, Cooper B. Improving the sensitivity of the Barthel index for stroke rehabilitation. J Clin Epidemiol. 1989;42:703709.
  23. Tucker M, Ogle S, Davison J, Eilenberg M. Validation of a brief screening test for depression in the elderly. Age Ageing. 1987;16:139144.
  24. Sinoff G, Ore L, Zlotogorsky D, Tamir A. Short Anxiety Screening Test—a brief instrument for detecting anxiety in the elderly. Int J Geriatr Psychiatry. 1999;14:10621071.
  25. Sinoff G, Ore L, Zlotogorsky D, Tamir A. Does the presence of anxiety affect the validity of a screening test for depression in the elderly? Int J Geriatr Psychiatry. 2002;17:309314.
  26. Elia M. The ‘MUST’ report. Nutritional screening of adults: a multidisciplinary responsibility (executive summary). Available at: http://www.bapen.org.uk/pdfs/must/must_exec_sum.pdf. Accessed July 10, 2015.
  27. Somes GW, Kritchevsky SB, Shorr RI, Pahor M, Applegate WB. Body mass index, weight change, and death in older adults: the systolic hypertension in the elderly program. Am J Epidemiol. 2002;156:132138.
  28. Walraven C, Dhalla I, Bell C, Etchells E, et al. Derivation and validation of an index to predict early death or unplanned readmission after discharge from hospital to the community. CMAJ. 2010;182:551557.
  29. Buurman BM, Munster BC, Korevaar JC, Haan RJ, Rooij SE. Variability in measuring (instrumental) activities of daily living functioning and functional decline in hospitalized older medical patients: a systematic review. J Clin Epidemiol. 2011;64:619627.
  30. Steyerberg EW, Harrell FE, Borsboom GJ, Eijkemans MJ, Vergouwe Y, Habbema JD. Internal validation of predictive models: efficiency of some procedures for logistic regression analysis. J Clin Epidemiol. 2001;54:774781.
  31. Kansagara D, Englander H, Salanitro A, et al. Risk prediction models for hospital readmission: a systematic review. JAMA. 2011;306:16881698.
  32. Soley‐Bori M, Soria‐Saucedo R, Ryan CM, et al. Functional status and hospital readmissions using the medical expenditure panel survey. J Gen Intern Med. 2015;30:965972.
  33. Cotter PE, Bhalla VK, Wallis SJ, Biram RW. Predicting readmissions: poor performance of the LACE index in an older UK population. Age Ageing. 2012;41:784789.
  34. Silverstein MD, Qin H, Mercer SQ, Fong J, Haydar Z. Risk factors for 30‐day hospital readmission in patients ≥65 years of age. Proc (Bayl Univ Med Cent). 2008;21:363372.
  35. Center for Outcomes Research 360:14181428.
  36. Meydan C, Haklai Z, Gordon B, Mendlovic J, Afek A. Managing the increasing shortage of acute care hospital beds in Israel. J Eval Clin Pract. 2015;21:7984.
  37. Billings J, Dixon J, Mijanovich T, Wennberg D. Case finding for patients at risk of readmission to hospital: development of algorithm to identify high risk patients. BMJ. 2006;333:327.
  38. Rasmussen HH, Holst M, Kondrup J. Measuring nutritional risk in hospitals. Clin Epidemiol. 2010;2:209216.
  39. Hinami K, Smith J, Deamant CD, DuBeshter K, Trick WE. When do patient‐reported outcome measures inform readmission risk? J Hosp Med. 2015;10:294300.
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Functional status before and during acute hospitalization and readmission risk identification
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Address for correspondence and reprint requests: Orly Tonkikh, The Cheryl Spencer Department of Nursing, Faculty of Social Welfare and Health Sciences, University of Haifa, Haifa 31905, Israel; Telephone: 972‐508885845; Fax: 972‐48288017; E‐mail: [email protected]
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Length of Different‐Hospital Readmissions

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Health information exchange systems and length of stay in readmissions to a different hospital

Readmissions within a relatively short time after discharge are receiving considerable attention as an area of quality improvement,[1, 2] with increasing emphasis on the relatively large share of readmissions to different hospitals, accounting for 20% to 30% of all readmissions.[3, 4, 5, 6] Returning to a different hospital may affect patient and healthcare outcomes due to breaches in continuity. When information from the previous recent hospitalization is not transferred efficiently and accurately to the next admitting hospital, omissions and duplications can occur, resulting in delayed care and potentially worse outcomes (compared to same hospital readmissions [SHRs]), such as longer length of readmission stay (LORS) and increased costs.[7]

Electronic health records (EHRs) and health information exchange (HIE) systems are increasingly used for storage and retrieval of patient information from various sources, such as laboratories and previous physician visits and hospitalizations, enabling informational continuity by providing vital historical medical information for decision‐making. Whereas EHRs collect, store, and present information that is locally created within a specific clinic or hospital, HIEs connect EHR systems between multiple institutions, allowing providers to share clinical data and achieve interorganizational continuity. Such integrative systems are increasingly being implemented across healthcare systems worldwide.[8, 9, 10] Yet, technical difficulties, costs, competitive concerns, data privacy, and workflow implementation challenges have been described as hindering HIE participation.[11, 12, 13, 14] Moreover, major concerns exist regarding the poor usability of EHRs, their limited ability to support multidisciplinary care, and major difficulties in achieving interoperability with HIEs, which undermine efforts to deliver integrated patient‐centered care.[15] Nonetheless, previous research has demonstrated that HIEs can positively affect healthcare resource use and outcomes, including reduced rates of repeated diagnostic imaging in the emergency evaluation of back pain,[16] reduction in admissions via the emergency department (ED),[17] and reduced rates of readmissions within 7 days.[18] However, it is not known whether HIEs can contribute to positive outcomes when patients are readmitted to a different hospital than the hospital from which they were recently (within the previous 30 days) discharged, potentially bridging the transitional‐care information divide.

In Israel, an innovative HIE system, OFEK (literally horizon), was implemented in 2005 at the largest not‐for‐profit insurer and provider of services, Clalit Health Services (Clalit). Clalit operates as an integrated healthcare delivery system, serving more than 50% of the Israeli population, as part of the country's national health insurance system. OFEK links information on all Clalit enrollees from all hospitals, primary care, and specialty care clinics, laboratories, and diagnostic services into a single, virtual, patient file, enabling providers to obtain complete, real‐time information needed for healthcare decision making at the point of care. Like similar HIE systems, OFEK includes information on previous medical encounters and hospitalizations, previous diagnoses, chronically prescribed medications, previous lab and imaging tests, known allergies, and some demographic information.[19] At the time of this study, OFEK was available in all Clalit hospitals as well as in 2 non‐Clalit (government‐owned and operated) large tertiary‐care centers, resulting in 40% coverage of all hospitalizations through the OFEK HIE system. As part of a large organization‐wide readmission reduction program recently implemented by Clalit for all its members admitted to any hospital in Israel, aimed at early detection and intervention,[20] OFEK was viewed as an important mechanism to help maintain continuity and improve transitions.

To inform current knowledge on different‐hospital readmissions (DHRs) and HIEs, we examined whether having HIE systems can contribute to information continuity and prevent delays in care and the need for more expensive, lengthy readmission stays when patients are readmitted to a different hospital. More specifically, we tested whether there is a difference in the LORS between SHRs and DHRs, and whether DHRs the LORS differ by the availability of an HIE (whether index and readmitting hospital are or are not connected through HIE systems).

METHODS

Study Design and Setting

We conducted a retrospective cohort study based on data of hospitalized Clalit members. Clalit has a centralized data warehouse with a comprehensive EHR containing data on all patients' medical encounters, administrative data, and clinical data compiled from laboratories, imaging centers, and hospitals. At the time of the study, OFEK was operating in all 8 Clalit hospitals and in 2 large government‐owned and operated hospitals in the central and northern parts of the country. Information is linked in the Clalit system and OFEK‐affiliated hospitals through an individual identity number assigned by the Israeli Interior Ministry to every Israeli resident for general identification purposes.

Population

The study examined all internal medicine and intensive‐care unit (ICU) readmissions of adult Clalit members (aged 18 years and older) previously (within the prior 30 days) discharged from internal medicine departments during January 1, 2010 until December 31, 2010 (ie, index hospitalizations). Only readmissions of index hospitalizations with more than a 24‐hour stay were included. A total of 146,266 index hospitalizations met the inclusion criteria. Index admissions that resulted in a transfer to another hospital, a long‐term care facility, or rehabilitation center were not included (N = 11,831). The final study sample included 27,057 readmissions (20.1% of the 134,435 index admissions), which could have resulted in any type of discharge (to patient's home, a long‐term care or rehabilitation facility, or due to death). The study was approved by Clalit's institutional review board.

Outcome Variable

We defined the LORS as the number of days from admission to discharge during readmission.

Main Independent Variable

We assessed information continuity as a categorical variable in which 0 = no information continuity (DHRs with either no HIE at either hospital or an HIE in only 1 of the hospitals), 1 = information continuity through an HIE (DHRs with both hospitals having an HIE), and 2 = full information continuity (readmission to the same hospital).

Covariates

We examined the following known correlates of length of stay (LOS): age, gender, residency in a nursing home, socioeconomic status (SES) based on an indicator of social security entitlement received by low‐income members,[21] and the occurrence of common chronic conditions registered in Clalit's EHR registries[22]: congestive heart failure (CHF), chronic obstructive pulmonary disease (COPD), chronic renal failure (CRF), malignancy, diabetes, hypertension, ischemic heart disease, atrial fibrillation, asthma, and disability (indication of a functional limitation). To provide comorbidity adjustment we used the Charlson Comorbidity Index.[23] Additionally, we assessed LOS of the index hospitalization. We included an indicator for the size of the index hospital: small, fewer than 100 beds; medium, 100 to 200 beds; and large, more than 200 beds. Finally, to account for a well‐known correlate of length of hospital stay,[24] we included an indicator for an ICU stay during the readmission.

Statistical Analysis

We first examined the study populations' characteristics and calculated the average LORS for each SHR and DHR category. Due to the skewed distribution of LORS, we also calculated the median and interquartile range (IQR) of LORS and evaluated the difference between categories using the Kruskall‐Wallis test.[25] Sample‐size calculations showed that we would need a sample of >3000 admissions to have 80% power to detect a difference of 0.8 hospitalization days given the 1:3 ratio between the DHR groups. To examine the association between LORS and information continuity, we employed a univariate marginal Cox model.[26] Variables that were significantly (P < 0.05) associated with LORS in the univariate model were entered into a multivariate marginal Cox model, clustering by patient and using a robust sandwich covariance matrix estimate. Additionally, we performed a sensitivity analysis using hierarchichal modeling to account for potential variations due to hospital level factors. A low hazard ratio (<1) represented an association of the covariate with decreased likelihood of discharge, that is, longer LORS. All analyses were conducted with SPSS version 20 (IBM, Armonk, NY) and SAS version 9.3 (SAS Institute Inc., Cary, NC).

RESULTS

The study included a total of 27,057 readmissions, of which 23,927 (88.4%) were SHRs and 3130 (11.6%) were DHRs. Of all DHRs, in 792 (2.9%) of the cases, both hospitals had HIEs (partial information continuity), and in 2338 (8.6%), either 1 or both did not have an HIE system (thus meaning there was no information continuity). Characteristics of the study population are shown in Table 1. Most (75%) of the readmissions were of patients over the age of 65 years, though only 7% were nursing home residents. More than half the study's population consisted of patients with low SES. The most common chronic conditions were hypertension (77%), ischemic heart disease (52%), and diabetes (48%). Other chronic conditions were arrhythmia (38%), CHF (35%), disability (31%), COPD (28%), malignancy (28%), and asthma (16%). In more than 55% of the index hospitalizations, the LOS was 4 days or less, and most index admissions (64%) were in large hospitals. Table 1 also displays the study population by the type of readmission: SHR, DHR with HIE, and DHR without HIE. As compared to patients readmitted to the same hospital, patients with DHRs were younger (P < 0.001), less likely to be nursing home residents (P < 0.001), and had longer LOS during the index admission (P < 0.001). Additionally, patients with SHRs were more likely to have their index admission at a large hospital (P < 0.001), had a higher comorbidity score (P < 0.043), and were less likely be treated in the ICU during their readmission (P < 0.001) compared to their DHR counterparts. Patients with DHRs without an HIE were similar in most characteristics to those with an HIE, except for having an ICU stay during their readmission (6.4% compared with 9.2%, respectively).

Characteristics of Readmissions Within 30 Days
CharacteristicsAll Readmissions, n = 27,057SHR, n = 23,927DHR With HIE, n = 792DHR Without HIE, n = 2,338P Value
  • NOTE: Abbreviations: DHR, different hospital readmission; HIE, health information exchanges; LOS, length of stay; SD, standard deviation; SHR, same hospital readmission.

All personal characteristics 
Age, n (%)<0.001
1844 years1,328 (4.9)1,095 (4.6)58 (7.3)175 (7.5) 
4564 years5,370 (19.8)4,597 (19.2)197 (24.9)576 (24.6) 
6584 years14,059 (52.0)12,500 (52.2)402 (50.8)1,157 (49.5) 
85+ years6,300 (23.3)5,735 (24.0)135 (17.0)430 (18.4) 
Female sex, n (%)13,742 (50.8)12,040 (50.3)418 (52.8)1,284 (54.9)<0.001
Low socioeconomic status, n (%)15,473 (57.2)13,670 (57.1)453 (57.2)1,350 (57.7) 
Residency in a nursing home, n (%)1,857 (6.9)1,743 (7.3)27 (3.4)87 (3.7)<0.001
Common chronic conditions, n (%) 
Hypertension20,797 (76.9)18,484 (77.3)588 (74.2)1,725 (73.8)<0.001
Ischemic heart disease14,150 (52.3)12,577 (52.6)397 (50.1)1,176 (50.3)0.052
Diabetes13,052 (48.2)11,589 (48.4)345 (43.6)1,118 (47.8)0.024
Arrhythmia10,306 (38.1)9,197 (38.4)292 (36.9)817 (34.9)0.003
Chronic renal failure9,486 (35.1)8,454 (35.3)262 (33.1)770 (32.9)0.034
Congestive heart failure9,216 (34.1)8,232 (34.4)270 (34.1)714 (30.5)0.001
Disability8,362 (30.9)7,600 (31.8)165 (20.8)597 (25.5)<0.001
Chronic obstructive pulmonary disease7,671 (28.4)6,888 (28.8)201 (25.4)582 (24.9)<0.001
Malignancy7,642 (28.2)6,763 (28.3)220 (27.8)659 (28.2)0.954
Asthma4,491 (16.6)4,040 (16.9)109 (13.8)342 (14.6)0.002
Charlson score, mean [SD]4.54 [3.15]4.58 [3.14]4.14 [3.08]4.25 [3.24]0.043
Index hospitalization characteristics (LOS during index hospitalization), n (%)<0.001
24 days14,961 (55.3)13,310 (55.6)428 (54.0)1,223 (52.3) 
57 days6,366 (23.5)5,654 (23.6)174 (22.0)538 (23.0) 
8 days and more5,730 (21.2)4,963 (20.7)190 (24.0)577 (24.7) 
Hospital size in index hospitalization (no. of hospitals in each category), n (%)<0.001
Small, <100 beds (8)1,498 (5.5)1,166 (4.9)23 (2.9)309 (13.2) 
Medium, 100200 beds (9)8,129 (30.0)7,113 (29.7)316 (39.9)700 (29.9) 
Large, >200 beds (10)17,430 (64.4)15,648 (65.4)453 (57.2)1,329 (56.8) 
Intensive care unit during readmission, n (%)869 (3.2)647 (2.7)73 (9.2)149 (6.4)<0.001

The mean LORS in SHRs was shorter by 1 day than the mean LORS for DHRs: 6.3 (95% confidence interval [CI]: 6.2‐6.4) versus 7.3 (95% CI: 7.0‐7.6), respectively. Mean LORS in DHRs with or without HIE was 7.6 (95% CI: 7.0‐8.3) and 7.2 (95% CI: 6.8‐7.6), respectively. Although median LORS was similar (4 days), the IQR differed, resulting in significant differences between the SHR and DHR groups (Table 2).

LORS by Information Continuity
Information ContinuityNo. of ReadmissionsMean LORS (95% CI)Median (Q1Q3)Kruskal‐Wallis P Value
  • NOTE: Abbreviations: CI, confidence interval; DHRs, different hospital readmissions; HIE, health information exchanges; LORS, length of readmission stay; SHRs, same hospital readmissions.

SHRs23,927 (88.4)6.3 (6.26.4)4 (27) 
DHRs3,130 (11.6)7.3 (7.07.6)4 (28) 
DHRs with HIE792 (2.9)7.6 (7.08.3)4 (29) 
DHRs without HIE2,338 (8.7)7.2 (6.87.6)4 (28) 
Total27,0576.4 (6.36.5)4 (27)<0.001

In the multivariate model, partial continuity (DHRs with an HIE) was associated with decreased likelihood of discharge on any given day compared with full continuity (SHR) (hazard ratio [HR] = 0.85, 95% CI: 0.79‐0.91). Similar results were obtained for no continuity (DHRs without an HIE) (HR = 0.90, 95% CI: 0.86‐0.94). The difference between DHRs with and without an HIE was not significant (overlapping confidence intervals). Other factors associated with a lower HR for discharge during each day of the readmission were older age, residency in a nursing home, CHF, CRF, disability, malignancy, and long LOS (8+ days) during the index hospitalization. Patients with asthma or ischemic heart disease had a higher HR for discharge during each readmission day (Table 3). We performed a sensitivity analysis using hierarchical modeling (patients nested within hospitals), which resulted in similar findings in terms of directionality and magnitude of the relationships and significance levels.

Univariate and Multivariate Marginal Cox Model Predicting Time to Discharge in Readmissions
CharacteristicsUnivariate ModelMultivariate Model
Hazard Ratio (95% CI)P ValueHazard Ratio (95% CI)P Value
  • NOTE: Abbreviations: CI, confidence interval; DHRs, different hospital readmissions; HIE, health information exchanges; LOS, length of stay;

  • SHRs, same hospital readmissions.

Information continuity  
SHRReference Reference 
DHR with HIE0.87 (0.810.93)<0.0010.86 (0.800.93)<0.001
DHR without HIE0.91 (0.870.94)<0.0010.90 (0.870.94)<0.001
Age    
844 years1.22 (1.181.26)<0.0011.14 (1.071.22)<0.001
4564 years1.16 (1.141.18)<0.0011.11 (1.061.1)<0.001
6584 years1.01 (0.991.02)0.530.99 (0.961.02)0.60
85+ yearsReference Reference 
Sex    
Male0.97 (0.950.99)0.0080.98 (0.961.01)0.19
FemaleReference Reference 
Socioeconomic status   
Low0.98 (0.970.99)0.11  
OtherReference   
Residency in a nursing home  
Nursing home0.90 (0.880.92)<0.0010.90 (0.860.95)<0.001
All othersReference Reference 
Common chronic conditions (reference: without condition)  
Hypertension0.94 (0.930.96)<0.0011.01 (0.971.04)0.69
Ischemic heart disease1.00 (0.991.01)0.931.06 (1.031.09)<0.001
Diabetes0.97 (0.950.98)0.0040.99 (0.971.02)0.64
Arrhythmia0.96 (0.950.97)0.0021.01 (0.981.04)0.39
Chronic renal failure0.92 (0.910.93)<0.0010.96 (0.930.99)0.01
Congestive heart failure0.93 (0.920.94)<0.0010.96 (0.930.99)0.01
Disability0.86 (0.850.87)<0.0010.90 (0.870.92)<0.001
Chronic obstructive pulmonary disease0.99 (0.981.01)0.66  
Malignancy0.97 (0.960.98)0.030.98 (0.961.01)0.28
Asthma1.04 (1.021.06)0.031.04 (1.001.07)0.03
Charlson score0.99 (0.980.99)<0.0010.99 (0.991.00)0.04
LOS during index hospitalization  
Days 241.52 (1.491.54)<0.0011.49 (1.451.54)<0.001
Days 571.21 (1.191.23)<0.0011.20 (1.161.24)<0.001
8 days and moreReference Reference 
Hospital size in index hospitalization   
Small, <100 beds (8)0.94 (0.920.97)0.021.00 (0.951.05)0.93
Medium, 100200 beds (9)1.00 (0.991.02)0.781.01 (0.991.04)0.38
Large, >200 beds (10)Reference Reference 
Intensive care unit in readmission   
Yes0.75 (0.700.80)<0.0010.74 (0.690.79)<0.001
NoReference Reference 

DISCUSSION

This study shows that readmission to a different hospital results in longer duration of the readmission stay compared with readmission to the same index hospital. Our results also show that having HIE systems in both the index and readmitting hospitals does not protect against these negative outcomes, as there was no difference in the length of the readmission stay based on the availability of HIE systems. Factors that were found to be associated with longer readmission stays are well known indicators of the complexity of the patient's medical condition, such as the presence of disability, comorbidity, and ICU treatment during the readmission.[24, 27]

The shorter LORS in SHRs may be due to the familiarity of physicians and other healthcare providers with the patient and his or her condition, especially as the policy in SHRs in Israel is to readmit to the same unit from which the patient was recently discharged. This same hospital familiarity is especially important as hospital care in Israel follows the hospitalist model, in which responsibility for patient care is transferred from the patient's primary care physician to the hospital's physician, resulting in increased need for integration through HIE systems, especially when patients are readmitted to a different hospital.[28, 29]

Our findings, congruent with previous research on DHRs and poor outcomes,[7] could also be explained by the inefficiency associated with transitions. For example, patients frequently leave the hospital with pending lab tests, often with abnormal results that would change the course of care.[30] Because these pending tests are often omitted from the hospital discharge summaries,[31] if patients are hospitalized in a different hospital, the same tests may be ordered again, or a course of treatment that does not acknowledge the test results could be taken. Such time‐consuming duplication can be prevented in SHRs, where the index‐hospital records may be already more complete.

Our null findings regarding the contribution of HIE systems may be explained by the low levels of HIE actual use. Although we did not directly assess use, previous research reports that actual use of HIE is limited.[12] An Israeli study on the effects of the use of the OFEK system on ED physicians' admission decisions found that the patient's medical history was viewed in only 31.2% of all 281,750 ED referrals.[19] In another Israeli‐based ED study, even lower usage levels were found, with the OFEK system having been accessed in only 16% of all 3,219,910 ED referrals.[32] Low levels of HIE use have also been reported in the United States. An additional study, which tested the implementation of HIE in hospitals and clinics, showed that in only 2.3% of encounters did providers access the HIE record.[33] Another study conducted in 12 ED sites and 2 ambulatory clinics reported rates of 6.8% HIE use.[34] Moreover, the null effect of integrated health information reported here is congruent with findings from a US study on implementation of an electronic discharge instructions form with embedded computerized medication reconciliation, which was not found to be associated with postdischarge outcomes.[35]

A wide range of factors may influence decisions on HIE use: patient‐level factors,[36] perceived medical complexity of the patient,[33, 34] and the number of prior hospitalizations.[33, 34, 36] Healthcare systemlevel factors may include: time constraints, which may be positively[32] or negatively[33] associated with HIE use, and organizational policies or incentives.[33] Use may also be associated with features of the HIE technology itself, such as difficulty to access, difficulty to use once accessed, and the quality of information it contains.[37] Additionally, there is some evidence of the link between tight functional integration and higher proportions of usage.[38] Although comprehensive studies on factors affecting the use of the OFEK system in Israeli internal medicine units are still needed, the lack of its integration within each hospital's EHR system may serve as a major explanatory factor for the low usage levels.

The findings from this study should be interpreted in light of its limitations. First, compared with previously reported DHR rates (20%30%),[3, 5] the rate observed in our population was relatively low (about 12%). Previous research was restricted to heart failure patients[3] or assessed DHR in surgical, as well as internal medicine, patients.[5] Our lower rates may have been affected by the type of population (hospitalized internal medicine patients) and/or by characteristics of the Clalit healthcare system, which serves as an integrated provider network as well as insurer. Generalization from 1 health care system to others should be made with caution. Nonetheless, our results may underestimate the potential effect in other healthcare systems with less structural integration. Additionally, as noted above, information on the actual use of an HIE in the course of medical decision making during readmission was absent. Future studies should examine the potential benefit of an HIE with measures that capture providers' use of HIEs. Also, the LORS may be influenced by other factors not investigated here, and further future studies should examine additional outcomes such as costs, patient well‐being, and satisfaction. Finally, causality could not be determined, and future research in this realm should aim to search for the pathways connecting readmission to a different hospital, with and without HIEs, to readmission LOS and additional outcomes.

To conclude, our findings show that patients readmitted to a different hospital are at risk for prolonged LORS, regardless of the availability of HIE systems. Implementing HIE systems is the focus of substantial efforts by policymakers and is considered a key part of the meaningful use of electronic health information. HIE features in the provisions of the Health Information Technology for Economic and Clinical Health Act[39] because it can furnish providers with complete, timely information at the point of care. Moreover, although there has been substantial growth in the number of healthcare organizations that have operational an HIE, its ability to lead to improved outcomes has yet to be realized.[8, 10] The Israeli experience reported here suggests that provisions are needed that will ensure actual use of HIEs, which might in turn minimize the difference between DHRs and SHRs.

Acknowledgements

The authors acknowledge Chandra Cohen‐Stavi, MPA, and Orly Tonkikh, MA, for their contribution to this study.

Disclosures

The study was supported in part by a grant from the Israel National Institute for Health Policy Research (NIHP) (10/127). The authors report no conflicts of interest.

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Readmissions within a relatively short time after discharge are receiving considerable attention as an area of quality improvement,[1, 2] with increasing emphasis on the relatively large share of readmissions to different hospitals, accounting for 20% to 30% of all readmissions.[3, 4, 5, 6] Returning to a different hospital may affect patient and healthcare outcomes due to breaches in continuity. When information from the previous recent hospitalization is not transferred efficiently and accurately to the next admitting hospital, omissions and duplications can occur, resulting in delayed care and potentially worse outcomes (compared to same hospital readmissions [SHRs]), such as longer length of readmission stay (LORS) and increased costs.[7]

Electronic health records (EHRs) and health information exchange (HIE) systems are increasingly used for storage and retrieval of patient information from various sources, such as laboratories and previous physician visits and hospitalizations, enabling informational continuity by providing vital historical medical information for decision‐making. Whereas EHRs collect, store, and present information that is locally created within a specific clinic or hospital, HIEs connect EHR systems between multiple institutions, allowing providers to share clinical data and achieve interorganizational continuity. Such integrative systems are increasingly being implemented across healthcare systems worldwide.[8, 9, 10] Yet, technical difficulties, costs, competitive concerns, data privacy, and workflow implementation challenges have been described as hindering HIE participation.[11, 12, 13, 14] Moreover, major concerns exist regarding the poor usability of EHRs, their limited ability to support multidisciplinary care, and major difficulties in achieving interoperability with HIEs, which undermine efforts to deliver integrated patient‐centered care.[15] Nonetheless, previous research has demonstrated that HIEs can positively affect healthcare resource use and outcomes, including reduced rates of repeated diagnostic imaging in the emergency evaluation of back pain,[16] reduction in admissions via the emergency department (ED),[17] and reduced rates of readmissions within 7 days.[18] However, it is not known whether HIEs can contribute to positive outcomes when patients are readmitted to a different hospital than the hospital from which they were recently (within the previous 30 days) discharged, potentially bridging the transitional‐care information divide.

In Israel, an innovative HIE system, OFEK (literally horizon), was implemented in 2005 at the largest not‐for‐profit insurer and provider of services, Clalit Health Services (Clalit). Clalit operates as an integrated healthcare delivery system, serving more than 50% of the Israeli population, as part of the country's national health insurance system. OFEK links information on all Clalit enrollees from all hospitals, primary care, and specialty care clinics, laboratories, and diagnostic services into a single, virtual, patient file, enabling providers to obtain complete, real‐time information needed for healthcare decision making at the point of care. Like similar HIE systems, OFEK includes information on previous medical encounters and hospitalizations, previous diagnoses, chronically prescribed medications, previous lab and imaging tests, known allergies, and some demographic information.[19] At the time of this study, OFEK was available in all Clalit hospitals as well as in 2 non‐Clalit (government‐owned and operated) large tertiary‐care centers, resulting in 40% coverage of all hospitalizations through the OFEK HIE system. As part of a large organization‐wide readmission reduction program recently implemented by Clalit for all its members admitted to any hospital in Israel, aimed at early detection and intervention,[20] OFEK was viewed as an important mechanism to help maintain continuity and improve transitions.

To inform current knowledge on different‐hospital readmissions (DHRs) and HIEs, we examined whether having HIE systems can contribute to information continuity and prevent delays in care and the need for more expensive, lengthy readmission stays when patients are readmitted to a different hospital. More specifically, we tested whether there is a difference in the LORS between SHRs and DHRs, and whether DHRs the LORS differ by the availability of an HIE (whether index and readmitting hospital are or are not connected through HIE systems).

METHODS

Study Design and Setting

We conducted a retrospective cohort study based on data of hospitalized Clalit members. Clalit has a centralized data warehouse with a comprehensive EHR containing data on all patients' medical encounters, administrative data, and clinical data compiled from laboratories, imaging centers, and hospitals. At the time of the study, OFEK was operating in all 8 Clalit hospitals and in 2 large government‐owned and operated hospitals in the central and northern parts of the country. Information is linked in the Clalit system and OFEK‐affiliated hospitals through an individual identity number assigned by the Israeli Interior Ministry to every Israeli resident for general identification purposes.

Population

The study examined all internal medicine and intensive‐care unit (ICU) readmissions of adult Clalit members (aged 18 years and older) previously (within the prior 30 days) discharged from internal medicine departments during January 1, 2010 until December 31, 2010 (ie, index hospitalizations). Only readmissions of index hospitalizations with more than a 24‐hour stay were included. A total of 146,266 index hospitalizations met the inclusion criteria. Index admissions that resulted in a transfer to another hospital, a long‐term care facility, or rehabilitation center were not included (N = 11,831). The final study sample included 27,057 readmissions (20.1% of the 134,435 index admissions), which could have resulted in any type of discharge (to patient's home, a long‐term care or rehabilitation facility, or due to death). The study was approved by Clalit's institutional review board.

Outcome Variable

We defined the LORS as the number of days from admission to discharge during readmission.

Main Independent Variable

We assessed information continuity as a categorical variable in which 0 = no information continuity (DHRs with either no HIE at either hospital or an HIE in only 1 of the hospitals), 1 = information continuity through an HIE (DHRs with both hospitals having an HIE), and 2 = full information continuity (readmission to the same hospital).

Covariates

We examined the following known correlates of length of stay (LOS): age, gender, residency in a nursing home, socioeconomic status (SES) based on an indicator of social security entitlement received by low‐income members,[21] and the occurrence of common chronic conditions registered in Clalit's EHR registries[22]: congestive heart failure (CHF), chronic obstructive pulmonary disease (COPD), chronic renal failure (CRF), malignancy, diabetes, hypertension, ischemic heart disease, atrial fibrillation, asthma, and disability (indication of a functional limitation). To provide comorbidity adjustment we used the Charlson Comorbidity Index.[23] Additionally, we assessed LOS of the index hospitalization. We included an indicator for the size of the index hospital: small, fewer than 100 beds; medium, 100 to 200 beds; and large, more than 200 beds. Finally, to account for a well‐known correlate of length of hospital stay,[24] we included an indicator for an ICU stay during the readmission.

Statistical Analysis

We first examined the study populations' characteristics and calculated the average LORS for each SHR and DHR category. Due to the skewed distribution of LORS, we also calculated the median and interquartile range (IQR) of LORS and evaluated the difference between categories using the Kruskall‐Wallis test.[25] Sample‐size calculations showed that we would need a sample of >3000 admissions to have 80% power to detect a difference of 0.8 hospitalization days given the 1:3 ratio between the DHR groups. To examine the association between LORS and information continuity, we employed a univariate marginal Cox model.[26] Variables that were significantly (P < 0.05) associated with LORS in the univariate model were entered into a multivariate marginal Cox model, clustering by patient and using a robust sandwich covariance matrix estimate. Additionally, we performed a sensitivity analysis using hierarchichal modeling to account for potential variations due to hospital level factors. A low hazard ratio (<1) represented an association of the covariate with decreased likelihood of discharge, that is, longer LORS. All analyses were conducted with SPSS version 20 (IBM, Armonk, NY) and SAS version 9.3 (SAS Institute Inc., Cary, NC).

RESULTS

The study included a total of 27,057 readmissions, of which 23,927 (88.4%) were SHRs and 3130 (11.6%) were DHRs. Of all DHRs, in 792 (2.9%) of the cases, both hospitals had HIEs (partial information continuity), and in 2338 (8.6%), either 1 or both did not have an HIE system (thus meaning there was no information continuity). Characteristics of the study population are shown in Table 1. Most (75%) of the readmissions were of patients over the age of 65 years, though only 7% were nursing home residents. More than half the study's population consisted of patients with low SES. The most common chronic conditions were hypertension (77%), ischemic heart disease (52%), and diabetes (48%). Other chronic conditions were arrhythmia (38%), CHF (35%), disability (31%), COPD (28%), malignancy (28%), and asthma (16%). In more than 55% of the index hospitalizations, the LOS was 4 days or less, and most index admissions (64%) were in large hospitals. Table 1 also displays the study population by the type of readmission: SHR, DHR with HIE, and DHR without HIE. As compared to patients readmitted to the same hospital, patients with DHRs were younger (P < 0.001), less likely to be nursing home residents (P < 0.001), and had longer LOS during the index admission (P < 0.001). Additionally, patients with SHRs were more likely to have their index admission at a large hospital (P < 0.001), had a higher comorbidity score (P < 0.043), and were less likely be treated in the ICU during their readmission (P < 0.001) compared to their DHR counterparts. Patients with DHRs without an HIE were similar in most characteristics to those with an HIE, except for having an ICU stay during their readmission (6.4% compared with 9.2%, respectively).

Characteristics of Readmissions Within 30 Days
CharacteristicsAll Readmissions, n = 27,057SHR, n = 23,927DHR With HIE, n = 792DHR Without HIE, n = 2,338P Value
  • NOTE: Abbreviations: DHR, different hospital readmission; HIE, health information exchanges; LOS, length of stay; SD, standard deviation; SHR, same hospital readmission.

All personal characteristics 
Age, n (%)<0.001
1844 years1,328 (4.9)1,095 (4.6)58 (7.3)175 (7.5) 
4564 years5,370 (19.8)4,597 (19.2)197 (24.9)576 (24.6) 
6584 years14,059 (52.0)12,500 (52.2)402 (50.8)1,157 (49.5) 
85+ years6,300 (23.3)5,735 (24.0)135 (17.0)430 (18.4) 
Female sex, n (%)13,742 (50.8)12,040 (50.3)418 (52.8)1,284 (54.9)<0.001
Low socioeconomic status, n (%)15,473 (57.2)13,670 (57.1)453 (57.2)1,350 (57.7) 
Residency in a nursing home, n (%)1,857 (6.9)1,743 (7.3)27 (3.4)87 (3.7)<0.001
Common chronic conditions, n (%) 
Hypertension20,797 (76.9)18,484 (77.3)588 (74.2)1,725 (73.8)<0.001
Ischemic heart disease14,150 (52.3)12,577 (52.6)397 (50.1)1,176 (50.3)0.052
Diabetes13,052 (48.2)11,589 (48.4)345 (43.6)1,118 (47.8)0.024
Arrhythmia10,306 (38.1)9,197 (38.4)292 (36.9)817 (34.9)0.003
Chronic renal failure9,486 (35.1)8,454 (35.3)262 (33.1)770 (32.9)0.034
Congestive heart failure9,216 (34.1)8,232 (34.4)270 (34.1)714 (30.5)0.001
Disability8,362 (30.9)7,600 (31.8)165 (20.8)597 (25.5)<0.001
Chronic obstructive pulmonary disease7,671 (28.4)6,888 (28.8)201 (25.4)582 (24.9)<0.001
Malignancy7,642 (28.2)6,763 (28.3)220 (27.8)659 (28.2)0.954
Asthma4,491 (16.6)4,040 (16.9)109 (13.8)342 (14.6)0.002
Charlson score, mean [SD]4.54 [3.15]4.58 [3.14]4.14 [3.08]4.25 [3.24]0.043
Index hospitalization characteristics (LOS during index hospitalization), n (%)<0.001
24 days14,961 (55.3)13,310 (55.6)428 (54.0)1,223 (52.3) 
57 days6,366 (23.5)5,654 (23.6)174 (22.0)538 (23.0) 
8 days and more5,730 (21.2)4,963 (20.7)190 (24.0)577 (24.7) 
Hospital size in index hospitalization (no. of hospitals in each category), n (%)<0.001
Small, <100 beds (8)1,498 (5.5)1,166 (4.9)23 (2.9)309 (13.2) 
Medium, 100200 beds (9)8,129 (30.0)7,113 (29.7)316 (39.9)700 (29.9) 
Large, >200 beds (10)17,430 (64.4)15,648 (65.4)453 (57.2)1,329 (56.8) 
Intensive care unit during readmission, n (%)869 (3.2)647 (2.7)73 (9.2)149 (6.4)<0.001

The mean LORS in SHRs was shorter by 1 day than the mean LORS for DHRs: 6.3 (95% confidence interval [CI]: 6.2‐6.4) versus 7.3 (95% CI: 7.0‐7.6), respectively. Mean LORS in DHRs with or without HIE was 7.6 (95% CI: 7.0‐8.3) and 7.2 (95% CI: 6.8‐7.6), respectively. Although median LORS was similar (4 days), the IQR differed, resulting in significant differences between the SHR and DHR groups (Table 2).

LORS by Information Continuity
Information ContinuityNo. of ReadmissionsMean LORS (95% CI)Median (Q1Q3)Kruskal‐Wallis P Value
  • NOTE: Abbreviations: CI, confidence interval; DHRs, different hospital readmissions; HIE, health information exchanges; LORS, length of readmission stay; SHRs, same hospital readmissions.

SHRs23,927 (88.4)6.3 (6.26.4)4 (27) 
DHRs3,130 (11.6)7.3 (7.07.6)4 (28) 
DHRs with HIE792 (2.9)7.6 (7.08.3)4 (29) 
DHRs without HIE2,338 (8.7)7.2 (6.87.6)4 (28) 
Total27,0576.4 (6.36.5)4 (27)<0.001

In the multivariate model, partial continuity (DHRs with an HIE) was associated with decreased likelihood of discharge on any given day compared with full continuity (SHR) (hazard ratio [HR] = 0.85, 95% CI: 0.79‐0.91). Similar results were obtained for no continuity (DHRs without an HIE) (HR = 0.90, 95% CI: 0.86‐0.94). The difference between DHRs with and without an HIE was not significant (overlapping confidence intervals). Other factors associated with a lower HR for discharge during each day of the readmission were older age, residency in a nursing home, CHF, CRF, disability, malignancy, and long LOS (8+ days) during the index hospitalization. Patients with asthma or ischemic heart disease had a higher HR for discharge during each readmission day (Table 3). We performed a sensitivity analysis using hierarchical modeling (patients nested within hospitals), which resulted in similar findings in terms of directionality and magnitude of the relationships and significance levels.

Univariate and Multivariate Marginal Cox Model Predicting Time to Discharge in Readmissions
CharacteristicsUnivariate ModelMultivariate Model
Hazard Ratio (95% CI)P ValueHazard Ratio (95% CI)P Value
  • NOTE: Abbreviations: CI, confidence interval; DHRs, different hospital readmissions; HIE, health information exchanges; LOS, length of stay;

  • SHRs, same hospital readmissions.

Information continuity  
SHRReference Reference 
DHR with HIE0.87 (0.810.93)<0.0010.86 (0.800.93)<0.001
DHR without HIE0.91 (0.870.94)<0.0010.90 (0.870.94)<0.001
Age    
844 years1.22 (1.181.26)<0.0011.14 (1.071.22)<0.001
4564 years1.16 (1.141.18)<0.0011.11 (1.061.1)<0.001
6584 years1.01 (0.991.02)0.530.99 (0.961.02)0.60
85+ yearsReference Reference 
Sex    
Male0.97 (0.950.99)0.0080.98 (0.961.01)0.19
FemaleReference Reference 
Socioeconomic status   
Low0.98 (0.970.99)0.11  
OtherReference   
Residency in a nursing home  
Nursing home0.90 (0.880.92)<0.0010.90 (0.860.95)<0.001
All othersReference Reference 
Common chronic conditions (reference: without condition)  
Hypertension0.94 (0.930.96)<0.0011.01 (0.971.04)0.69
Ischemic heart disease1.00 (0.991.01)0.931.06 (1.031.09)<0.001
Diabetes0.97 (0.950.98)0.0040.99 (0.971.02)0.64
Arrhythmia0.96 (0.950.97)0.0021.01 (0.981.04)0.39
Chronic renal failure0.92 (0.910.93)<0.0010.96 (0.930.99)0.01
Congestive heart failure0.93 (0.920.94)<0.0010.96 (0.930.99)0.01
Disability0.86 (0.850.87)<0.0010.90 (0.870.92)<0.001
Chronic obstructive pulmonary disease0.99 (0.981.01)0.66  
Malignancy0.97 (0.960.98)0.030.98 (0.961.01)0.28
Asthma1.04 (1.021.06)0.031.04 (1.001.07)0.03
Charlson score0.99 (0.980.99)<0.0010.99 (0.991.00)0.04
LOS during index hospitalization  
Days 241.52 (1.491.54)<0.0011.49 (1.451.54)<0.001
Days 571.21 (1.191.23)<0.0011.20 (1.161.24)<0.001
8 days and moreReference Reference 
Hospital size in index hospitalization   
Small, <100 beds (8)0.94 (0.920.97)0.021.00 (0.951.05)0.93
Medium, 100200 beds (9)1.00 (0.991.02)0.781.01 (0.991.04)0.38
Large, >200 beds (10)Reference Reference 
Intensive care unit in readmission   
Yes0.75 (0.700.80)<0.0010.74 (0.690.79)<0.001
NoReference Reference 

DISCUSSION

This study shows that readmission to a different hospital results in longer duration of the readmission stay compared with readmission to the same index hospital. Our results also show that having HIE systems in both the index and readmitting hospitals does not protect against these negative outcomes, as there was no difference in the length of the readmission stay based on the availability of HIE systems. Factors that were found to be associated with longer readmission stays are well known indicators of the complexity of the patient's medical condition, such as the presence of disability, comorbidity, and ICU treatment during the readmission.[24, 27]

The shorter LORS in SHRs may be due to the familiarity of physicians and other healthcare providers with the patient and his or her condition, especially as the policy in SHRs in Israel is to readmit to the same unit from which the patient was recently discharged. This same hospital familiarity is especially important as hospital care in Israel follows the hospitalist model, in which responsibility for patient care is transferred from the patient's primary care physician to the hospital's physician, resulting in increased need for integration through HIE systems, especially when patients are readmitted to a different hospital.[28, 29]

Our findings, congruent with previous research on DHRs and poor outcomes,[7] could also be explained by the inefficiency associated with transitions. For example, patients frequently leave the hospital with pending lab tests, often with abnormal results that would change the course of care.[30] Because these pending tests are often omitted from the hospital discharge summaries,[31] if patients are hospitalized in a different hospital, the same tests may be ordered again, or a course of treatment that does not acknowledge the test results could be taken. Such time‐consuming duplication can be prevented in SHRs, where the index‐hospital records may be already more complete.

Our null findings regarding the contribution of HIE systems may be explained by the low levels of HIE actual use. Although we did not directly assess use, previous research reports that actual use of HIE is limited.[12] An Israeli study on the effects of the use of the OFEK system on ED physicians' admission decisions found that the patient's medical history was viewed in only 31.2% of all 281,750 ED referrals.[19] In another Israeli‐based ED study, even lower usage levels were found, with the OFEK system having been accessed in only 16% of all 3,219,910 ED referrals.[32] Low levels of HIE use have also been reported in the United States. An additional study, which tested the implementation of HIE in hospitals and clinics, showed that in only 2.3% of encounters did providers access the HIE record.[33] Another study conducted in 12 ED sites and 2 ambulatory clinics reported rates of 6.8% HIE use.[34] Moreover, the null effect of integrated health information reported here is congruent with findings from a US study on implementation of an electronic discharge instructions form with embedded computerized medication reconciliation, which was not found to be associated with postdischarge outcomes.[35]

A wide range of factors may influence decisions on HIE use: patient‐level factors,[36] perceived medical complexity of the patient,[33, 34] and the number of prior hospitalizations.[33, 34, 36] Healthcare systemlevel factors may include: time constraints, which may be positively[32] or negatively[33] associated with HIE use, and organizational policies or incentives.[33] Use may also be associated with features of the HIE technology itself, such as difficulty to access, difficulty to use once accessed, and the quality of information it contains.[37] Additionally, there is some evidence of the link between tight functional integration and higher proportions of usage.[38] Although comprehensive studies on factors affecting the use of the OFEK system in Israeli internal medicine units are still needed, the lack of its integration within each hospital's EHR system may serve as a major explanatory factor for the low usage levels.

The findings from this study should be interpreted in light of its limitations. First, compared with previously reported DHR rates (20%30%),[3, 5] the rate observed in our population was relatively low (about 12%). Previous research was restricted to heart failure patients[3] or assessed DHR in surgical, as well as internal medicine, patients.[5] Our lower rates may have been affected by the type of population (hospitalized internal medicine patients) and/or by characteristics of the Clalit healthcare system, which serves as an integrated provider network as well as insurer. Generalization from 1 health care system to others should be made with caution. Nonetheless, our results may underestimate the potential effect in other healthcare systems with less structural integration. Additionally, as noted above, information on the actual use of an HIE in the course of medical decision making during readmission was absent. Future studies should examine the potential benefit of an HIE with measures that capture providers' use of HIEs. Also, the LORS may be influenced by other factors not investigated here, and further future studies should examine additional outcomes such as costs, patient well‐being, and satisfaction. Finally, causality could not be determined, and future research in this realm should aim to search for the pathways connecting readmission to a different hospital, with and without HIEs, to readmission LOS and additional outcomes.

To conclude, our findings show that patients readmitted to a different hospital are at risk for prolonged LORS, regardless of the availability of HIE systems. Implementing HIE systems is the focus of substantial efforts by policymakers and is considered a key part of the meaningful use of electronic health information. HIE features in the provisions of the Health Information Technology for Economic and Clinical Health Act[39] because it can furnish providers with complete, timely information at the point of care. Moreover, although there has been substantial growth in the number of healthcare organizations that have operational an HIE, its ability to lead to improved outcomes has yet to be realized.[8, 10] The Israeli experience reported here suggests that provisions are needed that will ensure actual use of HIEs, which might in turn minimize the difference between DHRs and SHRs.

Acknowledgements

The authors acknowledge Chandra Cohen‐Stavi, MPA, and Orly Tonkikh, MA, for their contribution to this study.

Disclosures

The study was supported in part by a grant from the Israel National Institute for Health Policy Research (NIHP) (10/127). The authors report no conflicts of interest.

Readmissions within a relatively short time after discharge are receiving considerable attention as an area of quality improvement,[1, 2] with increasing emphasis on the relatively large share of readmissions to different hospitals, accounting for 20% to 30% of all readmissions.[3, 4, 5, 6] Returning to a different hospital may affect patient and healthcare outcomes due to breaches in continuity. When information from the previous recent hospitalization is not transferred efficiently and accurately to the next admitting hospital, omissions and duplications can occur, resulting in delayed care and potentially worse outcomes (compared to same hospital readmissions [SHRs]), such as longer length of readmission stay (LORS) and increased costs.[7]

Electronic health records (EHRs) and health information exchange (HIE) systems are increasingly used for storage and retrieval of patient information from various sources, such as laboratories and previous physician visits and hospitalizations, enabling informational continuity by providing vital historical medical information for decision‐making. Whereas EHRs collect, store, and present information that is locally created within a specific clinic or hospital, HIEs connect EHR systems between multiple institutions, allowing providers to share clinical data and achieve interorganizational continuity. Such integrative systems are increasingly being implemented across healthcare systems worldwide.[8, 9, 10] Yet, technical difficulties, costs, competitive concerns, data privacy, and workflow implementation challenges have been described as hindering HIE participation.[11, 12, 13, 14] Moreover, major concerns exist regarding the poor usability of EHRs, their limited ability to support multidisciplinary care, and major difficulties in achieving interoperability with HIEs, which undermine efforts to deliver integrated patient‐centered care.[15] Nonetheless, previous research has demonstrated that HIEs can positively affect healthcare resource use and outcomes, including reduced rates of repeated diagnostic imaging in the emergency evaluation of back pain,[16] reduction in admissions via the emergency department (ED),[17] and reduced rates of readmissions within 7 days.[18] However, it is not known whether HIEs can contribute to positive outcomes when patients are readmitted to a different hospital than the hospital from which they were recently (within the previous 30 days) discharged, potentially bridging the transitional‐care information divide.

In Israel, an innovative HIE system, OFEK (literally horizon), was implemented in 2005 at the largest not‐for‐profit insurer and provider of services, Clalit Health Services (Clalit). Clalit operates as an integrated healthcare delivery system, serving more than 50% of the Israeli population, as part of the country's national health insurance system. OFEK links information on all Clalit enrollees from all hospitals, primary care, and specialty care clinics, laboratories, and diagnostic services into a single, virtual, patient file, enabling providers to obtain complete, real‐time information needed for healthcare decision making at the point of care. Like similar HIE systems, OFEK includes information on previous medical encounters and hospitalizations, previous diagnoses, chronically prescribed medications, previous lab and imaging tests, known allergies, and some demographic information.[19] At the time of this study, OFEK was available in all Clalit hospitals as well as in 2 non‐Clalit (government‐owned and operated) large tertiary‐care centers, resulting in 40% coverage of all hospitalizations through the OFEK HIE system. As part of a large organization‐wide readmission reduction program recently implemented by Clalit for all its members admitted to any hospital in Israel, aimed at early detection and intervention,[20] OFEK was viewed as an important mechanism to help maintain continuity and improve transitions.

To inform current knowledge on different‐hospital readmissions (DHRs) and HIEs, we examined whether having HIE systems can contribute to information continuity and prevent delays in care and the need for more expensive, lengthy readmission stays when patients are readmitted to a different hospital. More specifically, we tested whether there is a difference in the LORS between SHRs and DHRs, and whether DHRs the LORS differ by the availability of an HIE (whether index and readmitting hospital are or are not connected through HIE systems).

METHODS

Study Design and Setting

We conducted a retrospective cohort study based on data of hospitalized Clalit members. Clalit has a centralized data warehouse with a comprehensive EHR containing data on all patients' medical encounters, administrative data, and clinical data compiled from laboratories, imaging centers, and hospitals. At the time of the study, OFEK was operating in all 8 Clalit hospitals and in 2 large government‐owned and operated hospitals in the central and northern parts of the country. Information is linked in the Clalit system and OFEK‐affiliated hospitals through an individual identity number assigned by the Israeli Interior Ministry to every Israeli resident for general identification purposes.

Population

The study examined all internal medicine and intensive‐care unit (ICU) readmissions of adult Clalit members (aged 18 years and older) previously (within the prior 30 days) discharged from internal medicine departments during January 1, 2010 until December 31, 2010 (ie, index hospitalizations). Only readmissions of index hospitalizations with more than a 24‐hour stay were included. A total of 146,266 index hospitalizations met the inclusion criteria. Index admissions that resulted in a transfer to another hospital, a long‐term care facility, or rehabilitation center were not included (N = 11,831). The final study sample included 27,057 readmissions (20.1% of the 134,435 index admissions), which could have resulted in any type of discharge (to patient's home, a long‐term care or rehabilitation facility, or due to death). The study was approved by Clalit's institutional review board.

Outcome Variable

We defined the LORS as the number of days from admission to discharge during readmission.

Main Independent Variable

We assessed information continuity as a categorical variable in which 0 = no information continuity (DHRs with either no HIE at either hospital or an HIE in only 1 of the hospitals), 1 = information continuity through an HIE (DHRs with both hospitals having an HIE), and 2 = full information continuity (readmission to the same hospital).

Covariates

We examined the following known correlates of length of stay (LOS): age, gender, residency in a nursing home, socioeconomic status (SES) based on an indicator of social security entitlement received by low‐income members,[21] and the occurrence of common chronic conditions registered in Clalit's EHR registries[22]: congestive heart failure (CHF), chronic obstructive pulmonary disease (COPD), chronic renal failure (CRF), malignancy, diabetes, hypertension, ischemic heart disease, atrial fibrillation, asthma, and disability (indication of a functional limitation). To provide comorbidity adjustment we used the Charlson Comorbidity Index.[23] Additionally, we assessed LOS of the index hospitalization. We included an indicator for the size of the index hospital: small, fewer than 100 beds; medium, 100 to 200 beds; and large, more than 200 beds. Finally, to account for a well‐known correlate of length of hospital stay,[24] we included an indicator for an ICU stay during the readmission.

Statistical Analysis

We first examined the study populations' characteristics and calculated the average LORS for each SHR and DHR category. Due to the skewed distribution of LORS, we also calculated the median and interquartile range (IQR) of LORS and evaluated the difference between categories using the Kruskall‐Wallis test.[25] Sample‐size calculations showed that we would need a sample of >3000 admissions to have 80% power to detect a difference of 0.8 hospitalization days given the 1:3 ratio between the DHR groups. To examine the association between LORS and information continuity, we employed a univariate marginal Cox model.[26] Variables that were significantly (P < 0.05) associated with LORS in the univariate model were entered into a multivariate marginal Cox model, clustering by patient and using a robust sandwich covariance matrix estimate. Additionally, we performed a sensitivity analysis using hierarchichal modeling to account for potential variations due to hospital level factors. A low hazard ratio (<1) represented an association of the covariate with decreased likelihood of discharge, that is, longer LORS. All analyses were conducted with SPSS version 20 (IBM, Armonk, NY) and SAS version 9.3 (SAS Institute Inc., Cary, NC).

RESULTS

The study included a total of 27,057 readmissions, of which 23,927 (88.4%) were SHRs and 3130 (11.6%) were DHRs. Of all DHRs, in 792 (2.9%) of the cases, both hospitals had HIEs (partial information continuity), and in 2338 (8.6%), either 1 or both did not have an HIE system (thus meaning there was no information continuity). Characteristics of the study population are shown in Table 1. Most (75%) of the readmissions were of patients over the age of 65 years, though only 7% were nursing home residents. More than half the study's population consisted of patients with low SES. The most common chronic conditions were hypertension (77%), ischemic heart disease (52%), and diabetes (48%). Other chronic conditions were arrhythmia (38%), CHF (35%), disability (31%), COPD (28%), malignancy (28%), and asthma (16%). In more than 55% of the index hospitalizations, the LOS was 4 days or less, and most index admissions (64%) were in large hospitals. Table 1 also displays the study population by the type of readmission: SHR, DHR with HIE, and DHR without HIE. As compared to patients readmitted to the same hospital, patients with DHRs were younger (P < 0.001), less likely to be nursing home residents (P < 0.001), and had longer LOS during the index admission (P < 0.001). Additionally, patients with SHRs were more likely to have their index admission at a large hospital (P < 0.001), had a higher comorbidity score (P < 0.043), and were less likely be treated in the ICU during their readmission (P < 0.001) compared to their DHR counterparts. Patients with DHRs without an HIE were similar in most characteristics to those with an HIE, except for having an ICU stay during their readmission (6.4% compared with 9.2%, respectively).

Characteristics of Readmissions Within 30 Days
CharacteristicsAll Readmissions, n = 27,057SHR, n = 23,927DHR With HIE, n = 792DHR Without HIE, n = 2,338P Value
  • NOTE: Abbreviations: DHR, different hospital readmission; HIE, health information exchanges; LOS, length of stay; SD, standard deviation; SHR, same hospital readmission.

All personal characteristics 
Age, n (%)<0.001
1844 years1,328 (4.9)1,095 (4.6)58 (7.3)175 (7.5) 
4564 years5,370 (19.8)4,597 (19.2)197 (24.9)576 (24.6) 
6584 years14,059 (52.0)12,500 (52.2)402 (50.8)1,157 (49.5) 
85+ years6,300 (23.3)5,735 (24.0)135 (17.0)430 (18.4) 
Female sex, n (%)13,742 (50.8)12,040 (50.3)418 (52.8)1,284 (54.9)<0.001
Low socioeconomic status, n (%)15,473 (57.2)13,670 (57.1)453 (57.2)1,350 (57.7) 
Residency in a nursing home, n (%)1,857 (6.9)1,743 (7.3)27 (3.4)87 (3.7)<0.001
Common chronic conditions, n (%) 
Hypertension20,797 (76.9)18,484 (77.3)588 (74.2)1,725 (73.8)<0.001
Ischemic heart disease14,150 (52.3)12,577 (52.6)397 (50.1)1,176 (50.3)0.052
Diabetes13,052 (48.2)11,589 (48.4)345 (43.6)1,118 (47.8)0.024
Arrhythmia10,306 (38.1)9,197 (38.4)292 (36.9)817 (34.9)0.003
Chronic renal failure9,486 (35.1)8,454 (35.3)262 (33.1)770 (32.9)0.034
Congestive heart failure9,216 (34.1)8,232 (34.4)270 (34.1)714 (30.5)0.001
Disability8,362 (30.9)7,600 (31.8)165 (20.8)597 (25.5)<0.001
Chronic obstructive pulmonary disease7,671 (28.4)6,888 (28.8)201 (25.4)582 (24.9)<0.001
Malignancy7,642 (28.2)6,763 (28.3)220 (27.8)659 (28.2)0.954
Asthma4,491 (16.6)4,040 (16.9)109 (13.8)342 (14.6)0.002
Charlson score, mean [SD]4.54 [3.15]4.58 [3.14]4.14 [3.08]4.25 [3.24]0.043
Index hospitalization characteristics (LOS during index hospitalization), n (%)<0.001
24 days14,961 (55.3)13,310 (55.6)428 (54.0)1,223 (52.3) 
57 days6,366 (23.5)5,654 (23.6)174 (22.0)538 (23.0) 
8 days and more5,730 (21.2)4,963 (20.7)190 (24.0)577 (24.7) 
Hospital size in index hospitalization (no. of hospitals in each category), n (%)<0.001
Small, <100 beds (8)1,498 (5.5)1,166 (4.9)23 (2.9)309 (13.2) 
Medium, 100200 beds (9)8,129 (30.0)7,113 (29.7)316 (39.9)700 (29.9) 
Large, >200 beds (10)17,430 (64.4)15,648 (65.4)453 (57.2)1,329 (56.8) 
Intensive care unit during readmission, n (%)869 (3.2)647 (2.7)73 (9.2)149 (6.4)<0.001

The mean LORS in SHRs was shorter by 1 day than the mean LORS for DHRs: 6.3 (95% confidence interval [CI]: 6.2‐6.4) versus 7.3 (95% CI: 7.0‐7.6), respectively. Mean LORS in DHRs with or without HIE was 7.6 (95% CI: 7.0‐8.3) and 7.2 (95% CI: 6.8‐7.6), respectively. Although median LORS was similar (4 days), the IQR differed, resulting in significant differences between the SHR and DHR groups (Table 2).

LORS by Information Continuity
Information ContinuityNo. of ReadmissionsMean LORS (95% CI)Median (Q1Q3)Kruskal‐Wallis P Value
  • NOTE: Abbreviations: CI, confidence interval; DHRs, different hospital readmissions; HIE, health information exchanges; LORS, length of readmission stay; SHRs, same hospital readmissions.

SHRs23,927 (88.4)6.3 (6.26.4)4 (27) 
DHRs3,130 (11.6)7.3 (7.07.6)4 (28) 
DHRs with HIE792 (2.9)7.6 (7.08.3)4 (29) 
DHRs without HIE2,338 (8.7)7.2 (6.87.6)4 (28) 
Total27,0576.4 (6.36.5)4 (27)<0.001

In the multivariate model, partial continuity (DHRs with an HIE) was associated with decreased likelihood of discharge on any given day compared with full continuity (SHR) (hazard ratio [HR] = 0.85, 95% CI: 0.79‐0.91). Similar results were obtained for no continuity (DHRs without an HIE) (HR = 0.90, 95% CI: 0.86‐0.94). The difference between DHRs with and without an HIE was not significant (overlapping confidence intervals). Other factors associated with a lower HR for discharge during each day of the readmission were older age, residency in a nursing home, CHF, CRF, disability, malignancy, and long LOS (8+ days) during the index hospitalization. Patients with asthma or ischemic heart disease had a higher HR for discharge during each readmission day (Table 3). We performed a sensitivity analysis using hierarchical modeling (patients nested within hospitals), which resulted in similar findings in terms of directionality and magnitude of the relationships and significance levels.

Univariate and Multivariate Marginal Cox Model Predicting Time to Discharge in Readmissions
CharacteristicsUnivariate ModelMultivariate Model
Hazard Ratio (95% CI)P ValueHazard Ratio (95% CI)P Value
  • NOTE: Abbreviations: CI, confidence interval; DHRs, different hospital readmissions; HIE, health information exchanges; LOS, length of stay;

  • SHRs, same hospital readmissions.

Information continuity  
SHRReference Reference 
DHR with HIE0.87 (0.810.93)<0.0010.86 (0.800.93)<0.001
DHR without HIE0.91 (0.870.94)<0.0010.90 (0.870.94)<0.001
Age    
844 years1.22 (1.181.26)<0.0011.14 (1.071.22)<0.001
4564 years1.16 (1.141.18)<0.0011.11 (1.061.1)<0.001
6584 years1.01 (0.991.02)0.530.99 (0.961.02)0.60
85+ yearsReference Reference 
Sex    
Male0.97 (0.950.99)0.0080.98 (0.961.01)0.19
FemaleReference Reference 
Socioeconomic status   
Low0.98 (0.970.99)0.11  
OtherReference   
Residency in a nursing home  
Nursing home0.90 (0.880.92)<0.0010.90 (0.860.95)<0.001
All othersReference Reference 
Common chronic conditions (reference: without condition)  
Hypertension0.94 (0.930.96)<0.0011.01 (0.971.04)0.69
Ischemic heart disease1.00 (0.991.01)0.931.06 (1.031.09)<0.001
Diabetes0.97 (0.950.98)0.0040.99 (0.971.02)0.64
Arrhythmia0.96 (0.950.97)0.0021.01 (0.981.04)0.39
Chronic renal failure0.92 (0.910.93)<0.0010.96 (0.930.99)0.01
Congestive heart failure0.93 (0.920.94)<0.0010.96 (0.930.99)0.01
Disability0.86 (0.850.87)<0.0010.90 (0.870.92)<0.001
Chronic obstructive pulmonary disease0.99 (0.981.01)0.66  
Malignancy0.97 (0.960.98)0.030.98 (0.961.01)0.28
Asthma1.04 (1.021.06)0.031.04 (1.001.07)0.03
Charlson score0.99 (0.980.99)<0.0010.99 (0.991.00)0.04
LOS during index hospitalization  
Days 241.52 (1.491.54)<0.0011.49 (1.451.54)<0.001
Days 571.21 (1.191.23)<0.0011.20 (1.161.24)<0.001
8 days and moreReference Reference 
Hospital size in index hospitalization   
Small, <100 beds (8)0.94 (0.920.97)0.021.00 (0.951.05)0.93
Medium, 100200 beds (9)1.00 (0.991.02)0.781.01 (0.991.04)0.38
Large, >200 beds (10)Reference Reference 
Intensive care unit in readmission   
Yes0.75 (0.700.80)<0.0010.74 (0.690.79)<0.001
NoReference Reference 

DISCUSSION

This study shows that readmission to a different hospital results in longer duration of the readmission stay compared with readmission to the same index hospital. Our results also show that having HIE systems in both the index and readmitting hospitals does not protect against these negative outcomes, as there was no difference in the length of the readmission stay based on the availability of HIE systems. Factors that were found to be associated with longer readmission stays are well known indicators of the complexity of the patient's medical condition, such as the presence of disability, comorbidity, and ICU treatment during the readmission.[24, 27]

The shorter LORS in SHRs may be due to the familiarity of physicians and other healthcare providers with the patient and his or her condition, especially as the policy in SHRs in Israel is to readmit to the same unit from which the patient was recently discharged. This same hospital familiarity is especially important as hospital care in Israel follows the hospitalist model, in which responsibility for patient care is transferred from the patient's primary care physician to the hospital's physician, resulting in increased need for integration through HIE systems, especially when patients are readmitted to a different hospital.[28, 29]

Our findings, congruent with previous research on DHRs and poor outcomes,[7] could also be explained by the inefficiency associated with transitions. For example, patients frequently leave the hospital with pending lab tests, often with abnormal results that would change the course of care.[30] Because these pending tests are often omitted from the hospital discharge summaries,[31] if patients are hospitalized in a different hospital, the same tests may be ordered again, or a course of treatment that does not acknowledge the test results could be taken. Such time‐consuming duplication can be prevented in SHRs, where the index‐hospital records may be already more complete.

Our null findings regarding the contribution of HIE systems may be explained by the low levels of HIE actual use. Although we did not directly assess use, previous research reports that actual use of HIE is limited.[12] An Israeli study on the effects of the use of the OFEK system on ED physicians' admission decisions found that the patient's medical history was viewed in only 31.2% of all 281,750 ED referrals.[19] In another Israeli‐based ED study, even lower usage levels were found, with the OFEK system having been accessed in only 16% of all 3,219,910 ED referrals.[32] Low levels of HIE use have also been reported in the United States. An additional study, which tested the implementation of HIE in hospitals and clinics, showed that in only 2.3% of encounters did providers access the HIE record.[33] Another study conducted in 12 ED sites and 2 ambulatory clinics reported rates of 6.8% HIE use.[34] Moreover, the null effect of integrated health information reported here is congruent with findings from a US study on implementation of an electronic discharge instructions form with embedded computerized medication reconciliation, which was not found to be associated with postdischarge outcomes.[35]

A wide range of factors may influence decisions on HIE use: patient‐level factors,[36] perceived medical complexity of the patient,[33, 34] and the number of prior hospitalizations.[33, 34, 36] Healthcare systemlevel factors may include: time constraints, which may be positively[32] or negatively[33] associated with HIE use, and organizational policies or incentives.[33] Use may also be associated with features of the HIE technology itself, such as difficulty to access, difficulty to use once accessed, and the quality of information it contains.[37] Additionally, there is some evidence of the link between tight functional integration and higher proportions of usage.[38] Although comprehensive studies on factors affecting the use of the OFEK system in Israeli internal medicine units are still needed, the lack of its integration within each hospital's EHR system may serve as a major explanatory factor for the low usage levels.

The findings from this study should be interpreted in light of its limitations. First, compared with previously reported DHR rates (20%30%),[3, 5] the rate observed in our population was relatively low (about 12%). Previous research was restricted to heart failure patients[3] or assessed DHR in surgical, as well as internal medicine, patients.[5] Our lower rates may have been affected by the type of population (hospitalized internal medicine patients) and/or by characteristics of the Clalit healthcare system, which serves as an integrated provider network as well as insurer. Generalization from 1 health care system to others should be made with caution. Nonetheless, our results may underestimate the potential effect in other healthcare systems with less structural integration. Additionally, as noted above, information on the actual use of an HIE in the course of medical decision making during readmission was absent. Future studies should examine the potential benefit of an HIE with measures that capture providers' use of HIEs. Also, the LORS may be influenced by other factors not investigated here, and further future studies should examine additional outcomes such as costs, patient well‐being, and satisfaction. Finally, causality could not be determined, and future research in this realm should aim to search for the pathways connecting readmission to a different hospital, with and without HIEs, to readmission LOS and additional outcomes.

To conclude, our findings show that patients readmitted to a different hospital are at risk for prolonged LORS, regardless of the availability of HIE systems. Implementing HIE systems is the focus of substantial efforts by policymakers and is considered a key part of the meaningful use of electronic health information. HIE features in the provisions of the Health Information Technology for Economic and Clinical Health Act[39] because it can furnish providers with complete, timely information at the point of care. Moreover, although there has been substantial growth in the number of healthcare organizations that have operational an HIE, its ability to lead to improved outcomes has yet to be realized.[8, 10] The Israeli experience reported here suggests that provisions are needed that will ensure actual use of HIEs, which might in turn minimize the difference between DHRs and SHRs.

Acknowledgements

The authors acknowledge Chandra Cohen‐Stavi, MPA, and Orly Tonkikh, MA, for their contribution to this study.

Disclosures

The study was supported in part by a grant from the Israel National Institute for Health Policy Research (NIHP) (10/127). The authors report no conflicts of interest.

References
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  2. Leppin AL, Gionfriddo MR, Kessler M, et al. Preventing 30‐day hospital readmissions: a systematic review and meta‐analysis of randomized trials. JAMA Intern Med. 2014;174:10951107.
  3. Nasir K, Lin Z, Bueno H, et al. Is same‐hospital readmission rate a good surrogate for all‐hospital readmission rate? Med Care. 2010;48:477481.
  4. Fuller RL, Atkinson G, McCullough EC, Hughes JS. Hospital readmission rates: the impacts of age, payer, and mental health diagnoses. J Ambul Care Manage. 2013;36(2):147155.
  5. Davies SM, Saynina O, McDonald KM, Baker LC. Limitations of using same‐hospital readmission metrics. Int J Qual Health Care. 2013;25(6):633639.
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  19. Nirel N, Rosen B, Sharon A, et al. The impact of an integrated hospital‐community medical information system on quality and service utilization in hospital departments. Int J Med Inform. 2010;79(9):649657.
  20. Shadmi E, Flaks‐Manov N, Hoshen M, Goldman O, Bitterman H, Balicer R.D. Predicting 30‐day readmissions with preadmission electronic health record data. Med Care. 2015;53:283289.
  21. Shadmi E, Balicer RD, Kinder K, Abrams C, Weiner JP. Assessing socioeconomic health care utilization inequity in Israel: impact of alternative approaches to morbidity adjustment. BMC Public Health. 2011;11(1):609.
  22. Rennert G, Peterburg Y. Prevalence of selected chronic diseases in Israel. Isr Med Assoc J. 2001;3:404408.
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  28. McMahon LF. The hospitalist movement—time to move on. N Engl J Med. 2007;357:26272629.
  29. Jungerwirth R, Wheeler SB, Paul JE. Association of hospitalist presence and hospital‐level outcome measures among Medicare patients. J Hosp Med. 2014;9:16.
  30. 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.
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  32. Ben‐Assuli O, Leshno M, Shabtai I. Using electronic medical record systems for admission decisions in emergency departments: examining the crowdedness effect. J Med Syst. 2012;36:37953803.
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References
  1. Lavenberg JG, Leas B, Umscheid CA, Williams K, Goldmann DR, Kripalani S. Assessing preventability in the quest to reduce hospital readmissions. J Hosp Med. 2014;9:598603.
  2. Leppin AL, Gionfriddo MR, Kessler M, et al. Preventing 30‐day hospital readmissions: a systematic review and meta‐analysis of randomized trials. JAMA Intern Med. 2014;174:10951107.
  3. Nasir K, Lin Z, Bueno H, et al. Is same‐hospital readmission rate a good surrogate for all‐hospital readmission rate? Med Care. 2010;48:477481.
  4. Fuller RL, Atkinson G, McCullough EC, Hughes JS. Hospital readmission rates: the impacts of age, payer, and mental health diagnoses. J Ambul Care Manage. 2013;36(2):147155.
  5. Davies SM, Saynina O, McDonald KM, Baker LC. Limitations of using same‐hospital readmission metrics. Int J Qual Health Care. 2013;25(6):633639.
  6. Hospital inpatient and outpatient services. In: Report to the Congress: promoting greater efficiency in Medicare. Washington, DC: Medicare Payment Advisory Commission., March 2012;4566.
  7. Kind AJH, Bartels C, Mell MW, Mullahy J, Smith M. For‐profit hospital status and rehospitalizations at different hospitals: an analysis of Medicare data. Ann Intern Med. 2010;153:718727.
  8. Jones SS, Rudin RS, Perry T, Shekelle PG. Health information technology: an updated systematic review with a focus on meaningful use. Ann Intern Med. 2014;160:4854.
  9. Buntin MB, Burke MF, Hoaglin MC, Blumenthal D. The benefits of health information technology: a review of the recent literature shows predominantly positive results. Health Aff (Millwood). 2011;30(3):464471.
  10. Adler‐Milstein J, DesRoches CM, Jha AK. Health information exchange among US hospitals. Am J Manag Care. 2011;17:761768.
  11. Adler‐Milstein J, Bates DW, Jha AK. A survey of health information exchange organizations in the United States: implications for meaningful use. Ann Intern Med. 2011;54:666671.
  12. Patel V, Abramson EL, Edwards A, Malhotra S, Kaushal R. Physicians' potential use and preferences related to health information exchange. Int J Med Inform. 2011;80:171180.
  13. Pevnick JM, Claver M, Dobalian , et al. Provider stakeholders' perceived benefit from a nascent health information exchange: a qualitative analysis. J Med Syst. 2012;36:601613.
  14. Vest JR. More than just a question of technology: factors related to hospitals' adoption and implementation of health information exchange. Int J Med Inform. 2010;79:797806.
  15. Sheikh A, Sood HS, Bates DW. Leveraging health information technology to achieve the “triple aim” of healthcare reform. J Am Med Inform Assoc. 2015;22(4):849856.
  16. Bailey JE, Pope RA, Elliott EC, Wan JY, Waters TM, Frisse ME. Health information exchange reduces repeated diagnostic imaging for back pain. Ann Emerg Med. 2013;62:1624.
  17. Vest JR, Kern LM, Campion TR, Silver MD, Kaushal R. Association between use of a health information exchange system and hospital admissions. Appl Clin Inform. 2014;5:219.
  18. Ben‐Assuli O, Shabtai I, Leshno M. The impact of EHR and HIE on reducing avoidable admissions: controlling main differential diagnoses. BMC Med Inform Decis Mak. 2013;13:49.
  19. Nirel N, Rosen B, Sharon A, et al. The impact of an integrated hospital‐community medical information system on quality and service utilization in hospital departments. Int J Med Inform. 2010;79(9):649657.
  20. Shadmi E, Flaks‐Manov N, Hoshen M, Goldman O, Bitterman H, Balicer R.D. Predicting 30‐day readmissions with preadmission electronic health record data. Med Care. 2015;53:283289.
  21. Shadmi E, Balicer RD, Kinder K, Abrams C, Weiner JP. Assessing socioeconomic health care utilization inequity in Israel: impact of alternative approaches to morbidity adjustment. BMC Public Health. 2011;11(1):609.
  22. Rennert G, Peterburg Y. Prevalence of selected chronic diseases in Israel. Isr Med Assoc J. 2001;3:404408.
  23. Charlson ME, Pompei P, Ales KL, MacKenzie CR. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chron Dis. 1987;40:373383.
  24. Lu M, Sajobi T, Lucyk K, Lorenzetti D, Quan H. Systematic review of risk adjustment models of hospital length of stay (LOS). Med Care. 2015;53:355365.
  25. Kruskal WH, Wallis WA. Use of ranks in one‐criterion variance analysis. J Am Stat Assoc. 1952;47:583621.
  26. Wei LJ, Lin DY, Weissfeld L. Regression analysis of multivariate incomplete failure time data by modeling marginal distributions. J Am Stat Assoc. 1989;84:10651073.
  27. Tan C, Ng YS, Koh GC, Silva DA, Earnest A, Barbier S. Disability impacts length of stay in general internal medicine patients. J Gen Intern Med. 2014;29:885890.
  28. McMahon LF. The hospitalist movement—time to move on. N Engl J Med. 2007;357:26272629.
  29. Jungerwirth R, Wheeler SB, Paul JE. Association of hospitalist presence and hospital‐level outcome measures among Medicare patients. J Hosp Med. 2014;9:16.
  30. 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.
  31. Were MC, Li X, Kesterson J, et al. Adequacy of hospital discharge summaries in documenting tests with pending results and outpatient follow‐up providers. J Gen Intern Med. 2009;24:10021006.
  32. Ben‐Assuli O, Leshno M, Shabtai I. Using electronic medical record systems for admission decisions in emergency departments: examining the crowdedness effect. J Med Syst. 2012;36:37953803.
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Issue
Journal of Hospital Medicine - 11(6)
Issue
Journal of Hospital Medicine - 11(6)
Page Number
401-406
Page Number
401-406
Article Type
Display Headline
Health information exchange systems and length of stay in readmissions to a different hospital
Display Headline
Health information exchange systems and length of stay in readmissions to a different hospital
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© 2015 Society of Hospital Medicine

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Address for correspondence and reprint requests: Efrat Shadmi, PhD, Faculty of Social Welfare and Health Sciences, University of Haifa, Eshkol Tower Room 715, Haifa 31905, Israel; Telephone: 972‐48288557; Fax: 972‐48288017; E‐mail: [email protected]
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