Additive Benefit of Guideline-Directed Medical Therapies at Discharge in Reducing 30-Day Readmissions in Heart Failure

出院时采用指南指导的药物治疗可进一步降低心力衰竭患者30天内再入院率

阅读:1

Abstract

BACKGROUND: Hospitalization-related costs for heart failure (HF) are a major contributor to the overall health care expenditure in the United States. Despite recommendations, guideline-directed medical therapy (GDMT) is underutilized at discharge in eligible patients, likely contributing to high readmission rates. Describing the effect of GDMT use at discharge may better inform institutions on the value of implementing focused therapy initiatives. OBJECTIVES: This study aimed to examine the association between the number of active GDMT prescriptions at discharge and 30-day readmissions. METHODS: This retrospective cohort study analyzed 2,121 index hospitalizations for HF across 5 institutions from February 1, 2021, to October 31, 2024. Patients included were adults with a baseline left ventricular ejection fraction ≤40%. The primary outcome was 30-day all-cause readmission, and the secondary outcome was 30-day HF readmission. Multivariable mixed-effects Cox proportional hazard models were used to assess the association between GDMT count and readmission rates. RESULTS: Increased GDMT count at discharge was associated with significantly lower hazard of 30-day all-cause readmission: 1 vs 2 GDMT (HR: 0.79; 95% CI: 0.64-0.97), 1 vs 3 GDMT (HR: 0.70; 95% CI: 0.55-0.90), and 1 vs 4 GDMT (HR: 0.56; 95% CI: 0.40-0.77). Trends were similar for HF-specific readmissions. CONCLUSIONS: Increasing number of GDMT classes prescribed at discharge was associated with a gradient reduction in 30-day all-cause and HF readmissions, with a stronger effect seen with higher GDMT counts. Implementing comprehensive GDMT strategies at discharge may reduce health care costs and enhance institutional performance under national quality metrics.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。