Immediate versus delayed coronary angiography in patients with non-ST segment elevation acute coronary syndrome complicated with acute decompensated heart failure: The EARLY-HF randomized clinical trial.

Yongwhan Lim,S. Park,Donghyeon Joo,Yong-Kyu Lee,S. Oh,Seung Hun Lee,J. Ahn,D. Y. Hyun,K. Cho,D. Sim,Young Joon Hong,Ju Han Kim,Youngkeun Ahn,Min Chul Kim

Published 2025 in Cardiovascular Revascularization Medicine

ABSTRACT

BACKGROUND AND OBJECTIVES Immediate coronary angiography (CAG) is recommended for patients with non-ST segment elevation acute coronary syndrome (NSTE-ACS) complicated by acute decompensated heart failure (ADHF). The EARLY-HF trial (ClinicalTrials.gov, NCT04810806) was conducted to evaluate the optimal timing of coronary angiography (CAG) in this population. METHODS Patients were randomized in a 1:1 ratio to receive either immediate CAG within 2 h of randomization (immediate CAG group) or delayed CAG following stabilization of heart failure (HF) (delayed CAG group). The primary outcome was the composite of 12-month composite of all-cause mortality, nonfatal myocardial infarction (MI), and recurrent ischemia. RESULTS A total of 85 patients were randomly divided into the immediate CAG group (43 patients) or delayed CAG group (42 patients, performed at a median of 82.7 h post-randomization). The EARLY-HF trial was prematurely terminated due to COVID-19-related constraints. Revascularization was performed in 67.4 % and 69.1 % of patients in the immediate and delayed CAG groups, respectively. The incidence of the primary outcome was 35.6 % vs. 24.2 % in the two groups, respectively (P = 0.240, HR [95 % CI] =1.60 [0.72-3.57]). No statistically significant differences were observed in the individual components of the primary outcome at 1 month, 12 months, or during hospitalization except for a higher 12-month cardiovascular mortality rate in the immediate CAG group (23.7 % vs. 7.3 %, P = 0.039). CONCLUSION Immediate CAG within 2 h of randomization did not demonstrate a clinical benefit over delayed CAG in this trial. However, the premature termination limits the ability to draw definitive conclusions. TRIAL REGISTRATION URL: https://www. CLINICALTRIALS gov; Unique identifier: NCT04810806, registered on March 14, 2021.

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