Mortality and readmission following heart failure | TCRM - Dove Medical Press
Heart failure (HF) represents a global public health threat. The effect of HF on the elderly population is disproportionate. Even assuming that the incidence for a specific age, sex, or ethnicity is stable, heart failure prevalence shows a steady elevation over the next 20 years, 1 mainly in association with population ageing. 2 Epidemiological changes in usual risk factors for heart failure may influence the above prediction. Even if the incidence for a specific age, sex, or race remains stable, the prevalence rates of hypertension and coronary heart disease would rise due to demographic changes. 3 Meanwhile, the incidence rates of obesity 4 and diabetes 5 for specific ages, sexes, and races are also expected to increase, and the increased prevalence rates of these risk factors may further elevate the prevalence of HF. As a result, heart failure remains a substantial and growing public health burden. According to available data in Europe and the United States, 2–6 the prevalence of heart failure ranges from 1% to 14%. When all adults are included, heart failure is considered a chronic debilitating disease regardless of age. 2,5
In other developed countries, the one-year mortality rate after hospitalization for HF is 25%-30%, 7 which is higher than those of many common cancers. 8 The prevalence of heart failure increases with age. 9,10 In addition, heart failure is the main cause of hospitalization in individuals over 64 years of age. 11 The treatment of heart failure is important for improving the prognosis of patients and reducing health system expenditures. 12 In addition, the in-hospital mortality rate of HF patients is relatively low; however, high rates of death and readmission are found after discharge. 13
Readmission constitutes a common negative result for health care facilities and patients and a huge financial burden imposed on medical insurance beneficiaries and private payers. 11 Decreased 30-day readmission and 30-day hospital mortality rates are weak but significantly correlated. 14 From 2001–2003 to 2009–2011, the 30-day readmission rate following myocardial infarction declined from 20.5% to 15.8%, although the trend decreased slightly upon adjustment for patient features and treatments. 15 Predicting the risk factors for and causes of 30-day rehospitalization would help optimize the allocation of meagre medical resources and design profitable and viable interventions. 16,17
However, multiple previous trials have been conducted in single centres with few patients, with inconsistent readmission and mortality rates in heart failure patients. For instance, 30-day readmission rates for heart failure in previous reports ranged between 4.3% and 30.4%. 18–28 Based on the above, further assessing the prevalence and potential causes of and risk factors for readmission is of prime importance. Therefore, this meta-analysis aimed to examine the prevalence of readmission after HF, as well as the potential risk factors for and causes of HF. In addition, we discussed potential intervention approaches for mitigating the risk of readmission after HF.
Two independent medical librarians systematically searched three electronic databases, including PubMed, Web of Science, and the Cochrane Library. All articles published in English were obtained before May 26, 2019. The Keywords/terms were “Heart Failure”, “Patient Readmission” and “Mortality”.
Two investigators performed screening of all titles and abstracts in an independent fashion, retrieving and evaluating the retrieved studies based on full texts. In the final analysis, studies selected for inclusion must have provided data for 30-day and/or 1-year readmission or mortality in hospitalized individuals with HF. Studies were excluded for the following reasons: 1) Did not report risk factors or causes; 2) had already sub-grouped patients; 3) were cell culture or animal studies; 4) provided no available data; 5) had a small sample size (100); and 6) was a systematic review, meta-analysis, case report or comments. In the case of patient cohort overlap, studies with the longest follow-up were included.
Data Extraction and Methodological Quality Assessment
To facilitate the data extraction process, two researchers generated a standardized form and independently extracted the data. From all eligible articles, the extracted information included the first author, year, country, study period, method of HF diagnosis and data source, study design, study population, sample size, demographic features, 30-day and 1-year readmission rates, mortality, and risk factors for readmission and mortality.
Study quality was evaluated based on the Critical Appraisal of the Health Research Literature 29 taking into account the sample size, sample design, sampling frame, study and setting, measures, unbiased assessors, response rate and refusers, and prevalence rates. Each item was given a score. A study with a total score below 6 was considered to be of low quality; otherwise, it was considered to be of high quality (≥6).
The estimated effect sizes for readmission and mortality are expressed as the mean and 95% confidence interval (CI). The random-effects model was used to pool 30-day and 1-year mortality or readmission rates across studies, as well as the mean age, sex, and comorbidities. 30 Heterogeneity was assessed by I2 statistics. Subgroup analysis was carried out based on the region, study population, and study quality to determine the sources of heterogeneity. The median and interquartile range for age were converted to the mean and standard deviation (SD) as previously proposed. 31 Inverse funnel plots were generated to visually assess publication bias. STATA/SE 15.1 was utilized for data analysis.
Patient and Public Involvement Statement
No patients were involved.
In total, 2691 articles were reviewed for titles/abstracts, and 2609 articles were excluded. The remaining 27 reports were further assessed. The flow diagram of the study selection process is shown in Figure 1. We identified 27 studies included in this meta-analysis that reported 30-day and 1-year readmission data and mortality after HF, 18–28,32–47 including 1 trial conducted in Japan, 18 12 in the US, 19,21,23–25,27,33,34,36,38,44,47 1 in Italy, 20 2 in Spain, 22,39 1 in India, 40 1 in Singapore, 41 1 in Romania, 42 1 in France, 26 1 in Australia, 28 1 in Switzerland, 32 1 in Korea, 35 1 in Argentina, 37 1 in South Africa, 43 1 in Europe 45 and 1 in England. 46 The total number of participants was 515,238. Two articles reported both mortality and readmission rates, eleven reported mortality only, and fourteen assessed readmissions only. Ten and four studies were single centre and multicentre trials, respectively, and 13 assessed data from a large national database (Table 1). Twenty-one and 8 studies were of low and high quality, respectively ( Tables S1 and S2 ).
Table 1 Characteristics of Included Studies
Figure 1 Flow diagram of the study.
30-Day and 1-Year Readmission Rates
A pooled 30-day readmission rate of 0.19 (95% CI 0.14–0.23; Figure 2) was recorded in 11 studies that included 194,161 patients. Heterogeneity was extremely high (I2 =99.9%, P0.001), and the funnel plot displayed asymmetry. Then, the studies were grouped by region, sample size, and quality for the subgroup analysis ( Table S2 ). The rate was reduced for the non-American region (0.15, 95% CI 0.08–0.21) compared with the American region (0.22, 95% CI, 0.15–0.28) at 30 days ( Table S3 ). The 30-day readmission rates in studies with sample sizes10,000 (0.21, 95% CI 0.18–0.24) and high quality (score ≥6; 0.22, 95% CI 0.16–0.27) were higher than those for trials with sample sizes10,000 (0.16, 95% CI 0.09–0.23) and low quality (score6; 0.17, 95% CI 0.11–0.23). For 1-year readmissions, the results were similar. The rate was lower for the non-American region (0.50, 95% CI 0.31–0.68) than for the American region (0.59, 95% CI 0.56–0.62, Table S4 ). However, the 1-year admission rate was lower in studies with sample sizes 10,000 (0.49, 95% CI 0.30–0.69) compared with those with sample sizes 10,000 (0.59, 95% CI 0.56–0.61). Only one study had a quality assessment score above 6.
Figure 2 Meta-analysis of 30-day readmission rates.
Six studies with 35,147 patients reported 1-year readmission rates. A pooled 1-year readmission rate of 0.53 (95% CI 0.46–0.59; Figure 3) was obtained, with significant heterogeneity among the trials (I2 =99%, P0.001).
Figure 3 Meta-analysis of 1-year readmission rates.
Risk Factors for Readmission
Fourteen risk factors were revealed by ≥2 trials by multivariate analysis. Common comorbidities, including kidney disease, diabetes, chronic obstructive pulmonary disease (COPD), and cardiac arrhythmia, were tightly associated with elevated 30-day readmission rates. Table 2 depicts all the risk factors for readmission.
Table 2 Risk Factors for Readmission
30-Day and 1-Year Mortality Rates
A pooled 30-day mortality rate of 0.14 (95% CI 0.10–0.18; Figure 4) in 7 studies that included 317,128 participants was found. Heterogeneity was extremely high (I2 =99.9%, P0.001), and the funnel plot showed asymmetry. The results of the subgroup analyses were not significantly different for 30-day mortality rates ( Table S5 ). It is worth noting that heterogeneity for studies with a sample size10,000 was low (I2 =23%). The 1-year mortality rate for the non-American region (0.28, 95% CI 0.25–0.32) was reduced in comparison with the American rate (0.31, 95% CI 0.31–0.31; I2 =0%) ( Table S6 ).
Figure 4 Meta-analysis of 30-day mortality rates.
A pooled 1-year mortality rate of 0.29 (95% CI 0.25–0.33; Figure 5) was obtained in 10 studies that included 231,019 participants. Heterogeneity was extremely high (I2 =98.8%, P0.001), and the funnel plot showed asymmetry.
Figure 5 Meta-analysis of 1-year mortality rates.
Risk Factors for Mortality
Fifteen risk factors were revealed by the multivariable analysis in 2 or more trials (Table 3). The risk factors for 30-day mortality included ischaemic heart disease (IHD) in 4 studies. The use of beta-blockers was positively correlated with elevated readmission rates in 3 trials. Meanwhile, a history of lung disease was negatively correlated with readmission in 3 trials.
Table 3 Risk Factors for Mortality
The results of this study may be more than expected based on chance alone, with a P ≤0.10 in the heterogeneity test. Given the potential statistical heterogeneity, we formed a hypothesis before conducting the above analysis, which may help explain the differences in the results: differences in intervention methods, such as telephone follow-up, home visits, and heart failure clinic visits, may explain the variability leading to the differences in the results.
This was the first comprehensive systematic review and meta-analysis of 30-day and 1-year readmission and mortality rates following HF. Readmission and mortality mostly resulted from cardiac and noncardiac factors. Nonspecific chest pain was the top noncardiac cause of readmission, while cardiac factors encompassed angina and acute ischaemic heart disease, chest pain, etc. In addition, kidney disease, female sex, diabetes mellitus, chronic obstructive pulmonary disease (COPD), and HF were the major predictive factors of early readmission, 48 which may provide a possible correct direction for reducing the readmission rate of HF patients. Among the 13,171 newly hospitalized HF patients, respiratory disease accounted for 18.7%, arrhythmia accounted for 18.5%, coronary/aortic disease accounted for 15.8%, and renal dysfunction accounted for 6.7%. 20 The 3 most common reasons for readmission were HF (36.0%), renal disorders (8.4%), and other cardiac diseases (6.9%). 19 In addition, comparing the baseline patients and clinical characteristics of the readmission and nonrehospitalization HF patient groups, COPD and renal disease accounted for the majority of readmissions. 19
The results indicated that the 30-day readmission rate recorded in 11 studies was 0.19 (95% CI 0.14–0.23; Figure 2). Our findings corroborate the data from other nations. For instance, 30-day HF readmission rates after HF hospitalization in the USA and France are both 18%. 24,26 Meanwhile, the 1-year HF readmission and 30-day mortality rates in South Africa are 14.7%. 43 Most of the articles reported similar data for 1-year all-cause mortality, ie, 29%. 32,34,36,38–40,43,45–47 The careful management of HF outpatients who are elderly, high disease severity, multiple comorbidities, or taking beta-blockers, loop diuretics, thiazide, or nitrates when discharged from the hospital may be critical to reducing the 30-day readmission. 18
In some studies assessed in this meta-analysis, the authors identified multiple predictive factors of readmission, including age 18,20,21 and clinical comorbidities. 20,33,40–42 Some reports revealed multiple parameters that increased 30-day readmission rates, including elevated New York Heart Association functional class (NYHA) and Charlson Comorbidity Index (CCI) and treatment with beta-blockers, loop diuretics, thiazide, or nitrates. 18 In addition, retired and/or disabled patients had one or more emergency room visits in the last 3 months, hospitalization durations above 5 days, and BUN levels 45 mg/dL at discharge. 19 However, only one study reported that age, sex, race, marital status, payer type, and multiple patient features did not predict readmission in their model from Bradford et al. 19
This study had limitations. First, due to limited data, the original causes or comorbidities of CHF patients are not yet clear. Second, multiple risk factors for and/or causes of readmission had no clear definitions, and various reports classified and grouped the causes and risk factors differently with variable definitions of the parameters, which were hardly combined for the meta-analysis. Finally, the studies were highly heterogeneous. Most reports had incomplete datasets, and subgroup analyses could not be performed for all variables.
We found that multiple diseases are very common in hospitalized chronic HF patients. In addition, the increase in recurrent diseases itself was shown to be parallel to an elevated all-cause 30-day readmission rate. This is a major problem for individuals and the health care system as a whole. Based on the present evidence of common comorbid disease clusters in chronic HF, the development and testing of new interventions tailored to patients in each cluster may be a key direction for future clinical trials.
Data Sharing Statement
No additional data available.
Our work was funded by fundamental research funds for the National Center for Clinical Medicine of Digestive Diseases (No. 2015BAI13B07, to Dai-Ming Fan).
The authors declare that they have no conflict of interest.
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