Morbidity and Mortality Associated With Heart Failure in Acute Coronary Syndrome: A Pooled Analysis of 4 Clinical Trials

医学 危险系数 狼牙棒 内科学 急性冠脉综合征 心力衰竭 心肌梗塞 心脏病学 置信区间 比例危险模型 入射(几何) 经皮冠状动脉介入治疗 物理 光学
作者
Nathan Goodwin,Robert M. Clare,Josephine Harrington,Anish Badjatiya,Daniel Wojdyla,Jacob A. Udell,Javed Butler,James L. Januzzi,Puja B. Parikh,Stefan James,John H. Alexander,Renato D. Lópes,Lars Wallentin,E. Magnus Ohman,Adrian F. Hernandez,W. Schuyler Jones
出处
期刊:Journal of Cardiac Failure [Elsevier]
卷期号:29 (12): 1603-1614 被引量:4
标识
DOI:10.1016/j.cardfail.2023.07.004
摘要

ABSTRACT

Background

Heart failure (HF) may complicate acute coronary syndrome (ACS) and is associated with a high burden of short- and long-term morbidity and mortality. Only limited data regarding future ischemic events and rehospitalization are available for patients who suffer HF before or during ACS.

Methods

A secondary analysis of 4 large ACS trials (PLATO, APPRAISE-2, TRACER, and TRILOGY ACS) using Cox proportional hazards models was performed to investigate the association of HF status (no HF, chronic HF, de novo HF) at presentation for ACS with all-cause and cardiovascular death, major adverse cardiovascular event (MACE ), myocardial infarction, stroke, and hospitalization for heart failure (HHF) by 1 year. Cumulative incidence plots are presented at 30 days and 1 year.

Results

A total of 11.1% of the 47,474 patients presenting with ACS presented with evidence of acute HF, 55.0% of whom presented with de novo HF. Patients with chronic HF presented with evidence of acute HF at a higher rate than those with no previous HF (40.3% vs 6.9%). Compared to those without HF, those with chronic and de novo HF had higher rates of all-cause mortality (adjusted hazard ratio [aHR] 2.01, 95% confidence interval [CI] 1.72–2.34 and aHR 1.47, 95% CI1.15–1.88, respectively), MACE (aHR 1.47, 95% CI1.31–1-.66 and aHR 1.38, 95% CI1.12–1.69), and HHF (aHR 2.29, 95% CI2.02–2.61 and aHR 1.48, 95% CI 1.20–1.82) at 1 year.

Conclusion

In this large cohort of patients with ACS, both prior and de novo HF complicating ACS were associated with significantly higher risk-adjusted rates of death, ischemic events and HHF at 30 days and 1 year. Further studies examining the association between HF and outcomes in this high-risk population are warranted, especially given the advent of more contemporary HF therapies.
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