Clinical InvestigationRoles of Nonclinical and Clinical Data in Prediction of 30-Day Rehospitalization or Death Among Heart Failure Patients
Section snippets
Study Population
This statewide data linkage included all 1,727 HF patients (with either reduced or preserved ejection fraction) who had their 1st admission to a public hospital in Tasmania with HF from July 2009 to June 2012. These patients were identified by their coded diagnoses (International Classification of Diseases, Ninth Revision, Clinical Modification [ICD]: 402.x1, 404.x1, 404.x3, 428.x, and 428.xx). Because this study aimed to evaluate the post-discharge risk of readmission or death, we excluded 190
Baseline Characteristics
There were 1,537 HF patients (89% of all 1st-time HF patients during 2009–2012 in Tasmania) who survived their 1st admission. Nonclinical data were available for all patients, and clinical data were available for 977 patients.
Table 1 presents the nonclinical characteristics of patients at baseline. Their median age was 80 years and 49.5% were men. Nearly one-half were living alone. Although nearly one-half were classified as living outside of major population centers, the median distance to the
Discussion
Short-term outcomes for HF are important targets for quality improvement and are a central focus for patients, health care providers, taxpayers, and policy makers. The risk of readmission or death after a hospitalization with HF is high even in the short term. In the present study, ∼1 in 4 patients who survived their 1st admission with HF was readmitted and/or dead within 30 days of discharge. This finding was similar to those from other studies.2, 5, 26, 27 Targeting more intensive disease
Study Limitations
Our participants were mostly white, so the generalizability of our findings to other ethnic groups is uncertain. The restriction of analysis to patients admitted to public hospitals may have underestimated the roles of socioeconomic and geomapping factors in this study because patients without health insurance are more likely to be socioeconomically disadvantaged. By using log-binomial regression analysis rather than time-to-event analysis, we could not identify HF patients with high risk of
Conclusion
The present findings suggest that clinical data are stronger than nonclinical data in predicting 30-day readmission or death among HF patients. However, combining the 2 sources of data best predicts short-term adverse outcomes among HF patients.
Disclosures
None.
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Cited by (48)
Global Comparison of Readmission Rates for Patients With Heart Failure
2023, Journal of the American College of CardiologyRisk Prediction in Transition: MAGGIC Score Performance at Discharge and Incremental Utility of Natriuretic Peptides
2020, Journal of Cardiac FailureHigh-Sensitivity Troponin T and Incident Heart Failure in Older Men: British Regional Heart Study
2019, Journal of Cardiac FailureCitation Excerpt :For example, in chronic HF patients in the RED-HF (Reduction of Events by Darbepoetin Alfa in Heart Failure) trial, among a range of cardiac biomarkers only hsTnT added to NT-proBNP in the prediction of adverse outcome.26 In the MARATHON (Multicentre Australian Risk Algorithm to Predict Heart Failure Readmission) study, comprising patients hospitalized with preserved or reduced ejection fraction HF, elevated troponin I predicted 30-day readmission to hospital or death, both individually and as part of a panel of variables.27 Therefore, elevated troponin appears to be a predictor of adverse outcomes in the presymptomatic, chronic, and acute phases of HF.
Mortality and Readmission Following Hospitalisation for Heart Failure in Australia: A Systematic Review and Meta-Analysis
2018, Heart Lung and CirculationCitation Excerpt :Again, there was significant heterogeneity between studies (I2 = 98%). Five studies reported all-cause readmission [16,27,33,35,36], while three studies reported unplanned readmission only [28,30,34]. There was an increase of 1-year readmission rate with time (based on year of publication) by 2.3% (95% CI is 1.1–3.6%, p = 0.014).
Funding: Supported in part by a partnership grant (GRT1059738) from the National Health and Medical Research Council, Canberra, the National Heart Foundation of Australia, Tasmania Medicare Local, and the Tasmanian Department of Health and Human Services, Hobart, Australia.
See page 380 for disclosure information.