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Acta Cardiologica Sinica logoLink to Acta Cardiologica Sinica
. 2016 Nov;32(6):698–707. doi: 10.6515/ACS20151113A

Worse Prognosis in Heart Failure Patients with 30-Day Readmission

Ying-Chang Tung 1,2, Shing-Hsien Chou 1,2, Kuan-Liang Liu 1,2, I-Chang Hsieh 1,2, Lung-Sheng Wu 1, Chia-Pin Lin 1,2, Ming-Shien Wen 1,2, Pao-Hsien Chu 1,2,3
PMCID: PMC5126448  PMID: 27899857

Abstract

Background

Heart failure (HF) readmission results in substantial expenditure on HF management. This study aimed to evaluate the readmission rate, outcome, and predictors of HF readmission.

Methods

Patients with reduced left ventricular ejection fraction (LVEF < 40%) who were admitted for acute decompensation of de novo HF were enrolled to analyze readmission rate, mortality and predictors of readmission.

Results

A total of 433 de novo HF patients with LVEF < 40% were enrolled during the period August 2013 to December 2014. The in-hospital and 6-month mortality rates were 3.9% and 15.2%, respectively. In those patients surviving the index HF hospitalization, the 30-day and 6-month readmission rates were 10.9% and 27%, respectively. At the end of the 6-month follow-up, the readmission group had higher mortality than the non-readmission group (27.66% vs. 10.36%; p = 0.001). The survivors of the 30-day readmission had similar mortality rates at 6 months, regardless of the cause of readmission (cardiovascular vs. non-cardiovascular: 25% vs. 30.43%, p = 0.677). Among all the parameters, prescription of beta blockers independently reduced the risk of 30-day readmission (odds ratio 0.15; 95% confidence interval 0.02-0.99; p = 0.049).

Conclusions

Those HF patients who suffered from 30-day readmission had worse prognosis at the 6-month follow-up. Regardless of the readmission causes, the patients surviving the 30-day readmission had similar mortality rates at 6-month follow-up. These results underscored the importance of reducing readmission as a means to improve HF outcome.

Keywords: Heart failure, Prognosis, Readmission

INTRODUCTION

Heart failure (HF), a growing epidemic worldwide, affects 1-2% of the adult population in developed countries, and the prevalence rises to more than 10% in people aged 70 years or older.1 The prevalence of HF is estimated to increase to 3.5% in the United States by 2030, and the medical costs of HF are projected to increase from $24.7 billion in 2010 to $77.7 billion in 2030.2 Hospital admission accounts for more than 50% of healthcare costs associated with HF treatment both in the United States and Europe.3,4 In a medicare database study, HF is the most frequent reason for readmission within 30 days of discharge in both medical and surgery populations.5 Despite the advances in management and improved prognosis of chronic HF in the past two decades, patients with acute decompensated HF continue to have a high mortality rate, varying from 5-15% at 60 to 90 days post-discharge.6 The readmission rate remains high, however, wherein approximately 24% at 30 days7-9 and 30% at 60 to 90 days post-discharge10 and ≥ 50% within 6 months.11,12 This all leads to the large burden of disease and heavy expenditure on HF management, implicating the desperate need to improve prediction and intervention strategies of HF readmissions.

Epidemiologic data of HF in Asia are limited. A community-based cohort study has revealed a HF prevalence of approximately 5.5% in an ethnic Chinese population in northern Taiwan, with the 5- and 10-year mortality rates being 14.1% and 24.4%, respectively, in patients with HF with preserved left ventricular ejection fraction (LVEF), and 29.2% and 48.2%, respectively, in those with HF with reduced ejection fraction (EF).13 The major etiology of HF in this study is hypertension, consistent with the result of another study in an Asian-Chinese population, in which the prevalence of coronary heart disease has been proposed to be less than in western countries.14 Nevertheless, given the high prevalence of cigarette smoking and westernization of dietary patterns, myocardial infarction (MI) has been supposed to be an increasingly common cause of HF in Taiwan.15 As the population ages and survival of various cardiovascular (CV) diseases improves, challenges have emerged with respect to the escalating burden of HF, a situation paralleling that seen in western societies. Owing to the comprehensive coverage of the National Health Insurance, the health care system in Taiwan has been recognized for its good accessibility, relatively low costs and short waiting times.16 Despite the efficiency of the Taiwanese healthcare facilities, prior studies have reported high in-hospital and annual mortality rate, 23.5% and 40-50%, respectively, in patients with New York Heart Association (NYHA) functional class III to IV waiting for cardiac transplantation,17,18 appearing to be inferior to those in the western countries.

Apart from the similarities and differences regarding HF epidemiology between the eastern and the western countries, data on the pattern of HF readmission and related outcomes in Asia population is scarce. Readmission would increase health care costs and may be associated with higher morbidity and mortality compared with the index HF admission. The present study aimed to evaluate the readmission rate, subsequent outcome and predictors of readmission in de novo HF patients with reduced EF (HFrEF) after the index admission for acute decompensated heart failure (ADHF).

METHODS

Study population and protocol

This retrospective study enrolled de novo HFrEF, defined as LVEF < 40%,19 who were admitted for ADHF to the Department of Cardiology of the Linkou Chang Gung Memorial Hospital in Taiwan from August 2013 to December 2014. ADHF is defined as gradual or rapid change in HF signs and symptoms resulting in a need for urgent therapy, usually resulting in unplanned office visits, emergency room visits, or hospitalization.20-22 Patients with a history of HF or LFEF < 40% on previous echocardiography were excluded from this study. Patients with in-hospital mortality or lost to follow-up and not further contacted by telephone during the follow-up period of 6 months were excluded from the readmission analysis. The remaining patients were then grouped into the readmission and the non-readmission groups. Readmission was defined as any rehospitalization or emergency department visit longer than 24 hours (Figure 1).

Figure 1.

Figure 1

Patient enrollment. ADHF, acute decompensated heart failure; HF, heart failure; LVEF, left ventricular ejection fraction.

Data collection

Patients’ baseline characteristics were recorded in a standard case report form. The demographic data included age, sex, occupation, marital status, and educational background. The clinical variables included CV risk factors and comorbidities such as hypertension, diabetes, coronary artery disease (CAD), MI, dyslipidemia, peripheral artery disease, valvular heart disease, atrial fibrillation, smoking, family history, stroke, chronic kidney disease (CKD), chronic obstructive pulmonary disease (COPD), and baseline medications. Past intervention history included percutaneous coronary intervention (PCI), cardiac implantable electronic devices, and coronary artery bypass graft (CABG) and valve surgeries. Other information included body mass index (BMI), blood pressure and heart rate on admission date, precipitating factors of HF admission, and NYHA functional class. Other data collected were daily input/output records, body weight (BW), dosage and duration of diuretics and inotropic agents, use of intra-aortic balloon pump (IABP), extracorporeal membrane oxygenation (ECMO) and mechanical ventilation. Laboratory data included complete blood count and leukocyte differential count, biochemistry and urinalysis. Additionally, 12-lead electrocardiography and chest X-ray findings were recorded, M-mode, 2-dimensional, and Doppler echocardiography were performed according to standard criteria.23 In-hospital outcomes included in-hospital mortality, length of hospital stay, and development of acute kidney injury (AKI). AKI was defined according to the Acute Kidney Injury Network as an absolute increase in serum creatinine of at least 0.3 mg/dL, or a minimum increment of 50% within 48 hours, or oliguria of < 0.5 mL/kg per hour for more than six hours.24

Follow-up evaluation

Patients enrolled in this study were followed for a period of 6 months. After discharge from the index admission, the first follow-up clinic visit was scheduled within the first two weeks post-discharge. Readmission information was obtained mainly from the primary care physicians in the outpatient department, electronic medical records, and telephone contact with the patients or their relatives by the HF case managers. Information collected during the follow-up period included symptoms and signs of HF, medication compliance and adverse effects, dietary pattern, nutritional status, BW changes, and rehabilitation program. Information on readmission included the frequency and reasons for readmission, and the date of readmission and discharge. The CV causes of readmission included HF exacerbation, angina, acute coronary syndrome, ventricular tachyarrhythmia, atrial tachyarrhythmia, and bradycardia. The non-CV causes of readmission included but were not limited to pneumonia, urinary tract infection, other infection, gastrointestinal tract bleeding, renal function deterioration, and COPD with acute exacerbation.

Statistical analysis

The patients were divided into the readmission and the non-readmission groups. Categorical variables were expressed as percentages, and continuous variables were expressed as mean ± standard deviation. The chi-square test with Fisher’s exact test was used to compare categorical variables between the two groups. Continuous variables were compared utilizing the student’s t-test. Variables with a p value < 0.05 were considered to be statistically different between the two groups, and then were incorporated into the multivariate logistic regression to determine the independent predictors of readmission. Kaplan-Meier survival curves and the log-rank test were used to compare survival of the readmission vs. the non-readmission groups and the CV vs. the non-CV causes of readmissions. Data were analyzed with the SPSS version 19.0 (SPSS, Chicago, Illinois, USA).

RESULTS

In-hospital and 6-month mortality and readmission rates

A total of 984 patients with reduced LVEF were admitted to Linkou Chang Memorial Hospital during the study period. Among them, 466 were diagnosed as de novo HF with acute decompensation. The in-hospital mortality of the index HF admission was 3.9%, and the 6-month mortality was 15.2%. Fourteen patients (3%) were excluded from the readmission analysis because of loss to follow-up and lack of telephone contact. The 30-day readmission rate was 10.9%. One hundred seventeen patients (27%) were readmitted at least once at the end of the 6-month follow-up. Twenty-six of the 117 patients were admitted twice, 8 patients three times, 6 patients four times, and one patient was admitted 5 times. Overall, the CV and the non-CV causes comprised 56.7% and 43.3% of the readmissions, respectively (Figure 2).

Figure 2.

Figure 2

Cardiovascular and non-cardiovascular readmissions during 6-month follow-up. CV, cardiovascular.

Clinical characteristics associated with readmission

Table 1 demonstrated the baseline characteristics of the study population. The cohort of all patients had an average age of 65.4 years, with 68.6% men. Patients in the readmission group were older (69.4 vs. 64.93; p = 0.025) and more frequently diagnosed with hypertension (85.11% vs. 61.92%; p = 0.002) than those in the non-readmission group. The non-readmission group tended to be male gender (69.9% vs. 57.4%, p = 0.081) and had higher BMI (25.3 kg/m2 vs. 25.3 kg/m2, p = 0.097) than the readmission group. There was no significant difference between the two study groups in terms of percentage of NYHA function class III or IV, admission blood pressure and heart rate, and comorbidities such as CAD, MI, diabetes, CKD, atrial fibrillation, COPD and malignancy. Regarding the laboratory data, the readmitted patients had relatively higher levels of blood urea nitrogen (45 mg/dL vs. 29.86 mg/dL; p = 0.06) and creatinine on admission (2.8 mg/dL vs. 1.95 mg/dL; p = 0.06; Table 2). The readmitted patients also had lower levels of eGFR (31.33 mL/min vs. 54.03 mL/min; p = 0.034), sodium (137.37 mg/dL vs. 138.98 mg/dL, p = 0.016), and hemoglobin (11.78 mg/dL vs. 12.87 mg/dL; p = 0.006). In spite of the lack of statistical difference, more patients in the readmission group had moderate to severe mitral (42.55% vs. 29.79%; p = 0.075) and tricuspid regurgitation (29.79% vs. 15.54%; p = 0.094).

Table 1. Baseline characteristics of heart failure patients.

All patients (n = 433) Readmission (n = 47) Non-readmission (n = 386) p value
Age (years) 65.42 ± 15.67 69.4 ± 12.17 64.93 ± 15.99 0.025
Male gender (%) 68.6 57.4 69.9 0.081
Body mass index (kg/m2) 25.23 ± 4.62 24.4 ± 4.23 25.33 ± 4.66 0.097
NYHA functional class III or IV (%) 82.91 82.98 82.9 0.989
Systolic blood pressure (mm Hg) 138.73 ± 32.99 137.51 ± 31.72 138.88 ± 33.18 0.8
Diastolic blood pressure (mm Hg) 84.25 ± 21.55 81.34 ± 19.35 84.6 ± 21.8 0.328
Heart rate (beasts/min) 101.03 ± 26.06 101.66 ± 20.58 100.95 ± 26.67 0.861
Cardiovascular risk factors/comorbidities (%)
 Coronary artery disease 52.19 55.32 51.81 0.168
 Myocardial infarction 18.24 14.89 13.73 0.366
 Diabetes mellitus 41.57 48.94 40.67 0.278
 Hypertension 64.43 85.11 61.92 0.002
 Dyslipidemia 57.04 63.83 56.22 0.32
 Smoking 44.8 34.04 46.11 0.266
 CKD stage ≥ 3 41.28 51.35 40 0.187
 Dialysis 10.17 12.77 9.84 0.531
 Stroke 16.4 23.4 15.54 0.169
 Atrial fibrillation 27.02 25.53 27.2 0.945
 COPD 11.78 14.89 11.4 0.483
 Malignancy 3.75 6.52 3.41 0.417

CKD, chronic kidney disease; COPD, chronic obstructive pulmonary disease; NYHA, New York Heart Association.

Table 2. Laboratory tests and cardiac examinations on admission.

All patients (n = 433) Readmission (n = 47) Non-readmission (n = 386) p value
Laboratory tests
 Blood urea nitrogen (mg/dL) 31.55 ± 21.5 45 ± 32.85 29.86 ± 19.04 0.06
 Creatinine (mg/dL) 2.05 ± 2.22 2.8 ± 2.88 1.95 ± 2.11 0.06
 eGFR (ml/min) 52.54 ± 29.37 31.33 ± 20.93 54.03 ± 29.37 0.034
 Sodium (mg/dL) 138.81 ± 4.28 137.37 ± 5 138.98 ± 4.15 0.016
 Potassium (mg/dL) 4.07 ± 0.56 4.02 ± 0.66 4.07 ± 0.55 0.546
 AST (mg/dL) 67.33 ± 239.88 38.49 ± 27.35 70.79 ± 253.5 0.452
 ALT (mg/dL) 52.86 ± 137.65 42.12 ± 47.97 54.15 ± 144.67 0.598
 Total bilirubin (mg/dL) 0.91 ± 1.13 0.88 ± 0.82 0.91 ± 1.16 0.87
 Fasting glucose (mg/dL) 124.08 ± 61.68 117.86 ± 38.83 124.97 ± 64.32 0.623
 HbA1C (%) 6.71 ± 1.51 6.66 ± 1.08 6.71 ± 1.55 0.858
 BNP (pg/mL) 1574.39 ± 1331.19 1509.21 ± 1405.97 1583.13 ± 1323.43 0.758
 Troponin I (ng/mL) 3.44 ± 13.09 4.89 ± 16.91 3.26 ± 12.57 0.475
 Uric acid (mg/dL) 8.19 ± 3.19 7.64 ± 3.46 8.27 ± 3.16 0.323
 Hemoglobin (mg/dL) 12.76 ± 2.53 11.78 ± 2.69 12.87 ± 2.48 0.006
 Proteinuria ≥ 2+ 29.6 41.94 28.05 0.11
Electrocardiography (%)
 Rhythm (%) 0.789
  Sinus 72.66 73.91 72.51
  Atrial fibrillation/flutter 24.77 23.91 24.87
  Pacemaker 1.4 0 1.57
  Others 1.17 2.17 1.05
 LBBB (%) 6.06 4.35 6.27 0.606
 LV hypertrophy (%) 17.95 15.22 18.28 0.609
 Pathologic Q wave (%) 0.47 0 0.52 0.623
 QRS duration (ms) 103.51 ± 25.58 103.65 ± 27.5 103.49 ± 25.38 0.967
 Corrected QT interval (ms) 476.4 ± 43.11 481.09 ± 42.71 475.84 ± 43.18 0.436
Echocardiography
 LVEF (%) 30.45 ± 7.34 31.78 ± 6.73 30.29 ± 7.41 0.19
 Left atrial diameter (mm) 44.39 ± 8.24 43.15 ± 7.54 44.54 ± 8.32 0.248
 LVEDD (mm) 58.19 ± 8.69 56.52 ± 9.73 58.39 ± 8.54 0.165
 Left ventricular mass (g) 284.25 ± 105.13 265.25 ± 98.65 286.12 ± 105.76 0.365
 E/A ratio 1.39 ± .87 1.46 ± 0.83 1.38 ± 0.88 0.666
 E/E’ 23.1 ± 11.8 23.08 ± 7.08 23.11 ± 12.15 0.63
 Moderate or severe MR (%) 31.18 42.55 29.79 0.075
 Moderate or severe TR (%) 17.09 29.79 15.54 0.094
 Moderate or severe AR (%) 6.46 4.26 6.74 0.878

ALT, alanine aminotransferase; AR, aortic regurgitation; AST, aspartate aminotransferase; BNP, B-type natriuretic peptide; EF, ejection fraction; eGFR, estimated glomerular filtration rate; LBBB, left bundle branch block; LV, left ventricular; LVEDD, left ventricular end-diastolic diameter; MR, mitral regurgitation; TR, tricuspid regurgitation.

Comparison of management during the index admission

The average length of hospital stay of all study patients was 16.2 days, with 20.4% requiring inotropic agents and 29.2% developing AKI (Table 3). The readmission group had a numerically longer length of stay (21.11 days vs. 15.62 days; p = 0.091) and a higher risk of AKI (45% vs. 27.84%; p = 0.09). There was no significant difference in revascularization procedures, valve surgery, implantation of electronic devices, or the use of inotropic agents, IABP and ECMO between the two groups. After treatment, there was an average weight reduction of 3.3 kg in all patients upon discharge. However, the readmission group had a higher average heart rate (83.74 beats/min vs. 77.73 beats/min; p = 0.015) upon discharge and a higher percentage of patients discharged with NYHA function class 3 or 4 (47.83% vs. 22.87%; p < 0.001).

Table 3. Comparison of management during the index admission and post-discharge mortality at 6 months.

All patients (n = 433) Readmission (n = 47) Non-readmission (n = 386) p value
Length of hospital stay (days) 16.22 ± 17.86 21.11 ± 20.98 15.62 ± 17.38 0.091
Inotropic agents (%) 20.37 21.74 20.21 0.807
IV diuretics use (%) 64.35 69.57 63.73 0.435
Development of AKI (%) 29.16 45 27.84 0.09
Interventional therapy (%)
 CIED 0.468
  Pacemaker 1.85 2.13 1.81
  ICD 0.69 2.13 0.52
  CRT 0.46 0 0.52
 PCI 16.01 19.15 15.63 0.524
 CABG 4.39 6.38 4.15 0.479
 Valve surgery 1.85 2.13 1.81 0.88
 IABP 3.94 0 4.4 0.146
 ECMO 1.39 0 1.55 0.394
 Cardiac rehabilitation 20.09 23.91 19.63 0.494
Discharge status
 Systolic blood pressure (mm Hg) 121.54 ± 22.58 122.51 ± 20.91 121.49 ± 22.75 0.771
 Diastolic blood pressure (mm Hg) 73.20 ± 14.03 72.68 ± 14.92 73.20 ± 13.95 0.811
 Heart rate (beasts/min) 78.56 ± 15.90 83.74 ± 16.91 77.73 ± 15.76 0.015
 Weight changes (kg) -3.33 ± 4.68 -3.28 ± 4.27 -3.33 ± 4.73 0.928
 NYHA functional class III or IV on discharge (%) 25.59 47.83 22.87 < 0.001
Discharge medications (%)
 ACEI 24.04 25.53 23.85 0.799
 ARB 59.62 40.43 53.93 0.081
 Beta blocker 75.06 65.96 76.17 0.032
 Aldosterone antagonist 34.86 19.14 36.85 0.016
 CCB 9.86 14.89 9.21 0.219
 Thiazide or loop diuretics 54.04 46.81 54.92 0.292
 Antiplatelet agent 60.74 57.44 61.14 0.23
 Anticoagulation agent 20.67 17.02 21.14 0.512
 Antiarrhythmic agent 4.33 2.13 4.61 0.431
 Nitrate 38.22 29.79 39.3 0.206
 Digoxin 17.79 14.89 18.16 0.582
6-month mortality (%) 0.001
 All-cause mortality 12.24 27.66 10.36
 Cardiovascular 7.85 14.89 6.99
 Non-cardiovascular 4.39 12.77 3.37

ACEI, angiotensin-converting-enzyme inhibitor; AKI, acute kidney injury; ARB, angiotensin receptor blocker; CABG, coronary artery bypass graft; CCB, calcium channel blocker; CIED, cardiac implantable electronic device; CRT, cardiac resynchronization therapy; ECMO, extracorporeal membrane oxygenation; IABP, intraaortic balloon pumping; ICD, implantable cardioverter defibrillator; ICU, intensive care unit; IV, intravenous; NYHA, New York Heart Association; PCI, percutaneous coronary intervention.

Predictors of readmission

Table 4 revealed the result of the multivariate logistic regression analysis. Among all the parameters, prescription of beta blockers independently reduced the risk of readmissionin HF patients (odds ratio 0.15; 95% confidence interval 0.02-0.99; p = 0.049).

Table 4. Multivariate analysis of predictors of 30-day readmission.

Odds ratio 95% confidence interval p value
Low Upper
Age 1.04 0.97 0.90 0.335
Hypertension 52.21 4.66 0.42 0.212
eGFR 1.03 1.00 0.96 0.894
Hemoglobin 1.10 0.74 0.50 0.141
Heart rate on discharge 1.13 1.05 0.99 0.126
NYHA functional class III or IV on discharge 45.10 5.26 0.61 0.130
Beta blocker 0.99 0.15 0.02 0.049
Aldosterone antagonist - - - 0.997

eGFR, estimated glomerular filtration rate; NYHA, New York Heart Association.

Association of 30-day readmission and 6-month mortality

In patients surviving the index HF admission, the post-discharge 6-month mortality rate was 12.2%. The post-discharge 6-month mortality was significantly higher in the readmission group than in the non-readmission group (27.66% vs. 10.36%; p = 0.001; Table 3). We also evaluated the influence of the causes of 30-day readmission on outcome. There was no significant difference in 6-month mortality between the patients readmitted for CV and non-CV causes (25% vs. 30.43%, p = 0.677). Figure 3 illustrates the Kaplan-Meier survival analysis of readmission vs. non-readmission groups (A) and CV vs. non-CV causes of readmission (B).

Figure 3.

Figure 3

Kaplan-Meier survival analysis of readmission vs. non-readmission groups (A) and cardiovascular (CV) vs. non-CV causes of readmission (B).

DISCUSSION

This retrospective study analyzed readmission rate, subsequent outcome, and predictors of readmission in patients with LVEF < 40% who were admitted for de novo HF with decompensation. The 30-day and 6-month readmission rates were 10.9% and 27%, respectively. The post-discharge mortality at 6 months was significantly higher in the readmission group than in the non-readmission group. The patients surviving the 30-day readmission had similar mortality rate at the end of follow-up, regardless of the causes of the initial readmission.

The common comorbidities of HF patients in this study included hypertension (64.4%), CAD (52.2%), and diabetes (41.3%), a pattern similar to the ADHF registries the EHFS II study in Europe (hypertension 62.5%, 53.6%, and diabetes 32.8%)25 and the ADHERE study in the United States (hypertension 73%, CAD 57%, and diabetes 44%).26 In contrast to the prior belief of low prevalence of CAD among Taiwan’s HF patients (2.5% in a community cohort study13 and 31.5% in a more recent claims database study27), it is worth noting that the prevalence of CAD in this study was comparable to that in the western societies.25,26 Although there was potential selection bias of higher comorbidity burden in patients admitted to this tertiary referral center, increasing prevalence of western dietary pattern may also in part account for the changes in epidemiology of cardiovascular disease in Taiwan. Furthermore, there was a trend that BMI was lower in the readmission group than that in the non-readmission group, a finding that may be attributed to the “obesity paradox” — clinical outcomes of CV diseases, including HF, are better in obese patients than in their leaner counterparts.28-30 However, data on the association between BMI and HF readmission are scarce. In a retrospective study by Zapatero et al., obesity in patients admitted for ADHF substantially reduces in-hospital mortality and the possibility of 30-day readmission, whereas malnutrition was associated with increases in in-hospital mortality and the risk 30-day readmission.31 Further large, multicenter studies are warranted to establish the association between BMI and HF readmission.

The 30-day and 6-month readmission rates in this study were much lower than the 24%7-9 and ≥ 50% observed in western societies, respectively.11,12 It has been estimated that worsening chronic HF, de novo HF and advanced or end-stage HF comprised 80%, 15% and 5% of hospitalization for HF, respectively.32 The present study only analyzed patients with de novo HF and therefore the readmission rates may be underestimated. In addition, the average length of stay was 16.22 days, much longer than that of the United States (6.4 ± 85.2 days).32 The longer hospital stay in this study may be due to comprehensive assessment of de novo HF patients as well as cardiac rehabilitation during hospitalization. Whether longer hospital stay leads to reduction of 30-day readmission is yet to be determined. Furthermore, we could not exclude the possibility that some patients were admitted to other hospitals, an inherent limitation of this retrospective analysis that may lead to underestimation of the readmission rates.

Although rehospitalizations of HF patients are frequently due to congestion, a significant number of readmissions are associated with cardiac and noncardiac comorbidities.33,34 It is noteworthy that the non-CV causes comprised 43.3% of all readmissions during the 6-month follow-up in this study. Importantly, we found that the 6-month mortality of the patients who were readmitted for non-CV causes within 30 days of discharge was similar to those rehospitalized for CV causes. This suggested that any causes of 30-day readmission in patients with HFrEF were relevant for HF prognosis and should be given equal attention to prevent adverse outcomes. A recent analysis of the CHARM studies (CHARM-Added, CHARM-Preserved, and CHARM-Alternative) also reported a similar risk of subsequent mortality in HF patients across the spectrum of EF, regardless of whether they were first hospitalized for CV or non-CV causes.33

Analysis of readmission in one institution may help improve its efficiency and quality of care and facilitate risk stratification based on patient characteristics. In this study, the lack of beta blocker prescription on discharge was an independent predictor of HF readmission. However, we should also note that patients in the readmission group were discharged with a higher average heart rate, and a higher percentage of them had NYHA functional class 3 or 4 upon discharge, indicating that many of the readmitted patients had been discharged from the index hospitalization without adequate decongestion. So far, a robust and well-validated statistical model for prediction of HF readmission or risk stratification is not yet available.35,36 It has been demonstrated that physiologic indicators of HF severity and serum makers of neurohormonal activation foretell higher readmission rates.37-40 Associated non-CV comorbidities, including diabetes,41-43 renal dysfunction,44,45 anemia46 and pulmonary disease,11 also increased HF or non-HF related complications, including readmission. The inconsistencies in data on readmission prediction may result from a diverse patient spectrum and other non-measurable life events that dominate the clinical variables from the large administrative database. Nevertheless, given the high prevalence of HF comorbidities and their association with readmission and outcome, addressing the non-CV comorbidities is still an important adjunct to the multidisciplinary approach of HF management.

Limitations

This retrospective study had several inherent limitations. First, it was conducted in a tertiary referral center in Taiwan and only de novo HF patients with LVEF < 40% were analyzed. These results could not be generalized to the whole spectrum of HF patients because of potential selection bias. A larger and multicenter registry is needed to represent the epidemiology of HF readmission in Taiwan. Second, despite the extensive effort to identify all readmissions, some readmissions to other hospitals may not be recorded. Third, psychosocial and/or social economic factors were not analyzed in this study. Furthermore, the patient number was relatively small, and only one independent predictor of readmission was derived from the multivariate analysis. This result may be a chance finding and could not allow for the development of a risk prediction model.

CONCLUSIONS

The readmission rates in de novo HF patients with LV EF < 40% in this study were 10.9% and 27% at 30 and 6 months, respectively. The readmitted patients had a higher mortality rate than the non-readmitted patients upon 6-month follow-up. The patients surviving the CV or the non-CV readmissions within 30 days of discharge had a similar mortality rateat the end of follow-up. These results underscored the importance of reducing readmission as a means to improve HF outcome. The high burden of HF comorbidities and the association with readmission rate and mortality also underscored the idea that addressing the non-CV comorbidities should serve as an adjunct to the multidisciplinary approach of HF management.

DISCLOSURES

The authors have no conflicts of interest to declare in this study. This work is supported by Chang Gung Memorial Hospital, CIRPG3E0011 and CMRPG3F1631.

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