Prognostic Impact of the Symptom of New-Onset Atrial Fibrillation in Acute Myocardial Infarction: Insights From the NOAFCAMI-SH Registry

Jiachen Luo, Baoxin Liu, Hongqiang Li, Siling Xu, Mengmeng Gong, Zhiqiang Li, Xiaoming Qin, Beibei Shi, Chuanzhen Hao, Ji Zhang, Yidong Wei, Jiachen Luo, Baoxin Liu, Hongqiang Li, Siling Xu, Mengmeng Gong, Zhiqiang Li, Xiaoming Qin, Beibei Shi, Chuanzhen Hao, Ji Zhang, Yidong Wei

Abstract

Background: New-onset atrial fibrillation (NOAF) is a common complication during acute myocardial infarction (AMI) and sometimes can be completely asymptomatic, but the clinical implications of these asymptomatic episodes require further characterization. The objective of this study was to investigate the short- and long-term prognostic impact of post-MI NOAF based on the presence of AF-related symptoms. Methods: The New-Onset Atrial Fibrillation Complicating Acute Myocardial Infarction in ShangHai (NOAFCAMI-SH) registry was a retrospective cohort including participants with AMI without a documented history of AF. Patients with NOAF were divided into two groups according to the AF-related symptoms. The primary endpoint was all-cause mortality. Results: Of 2,399 patients included, 278 (11.6%) developed NOAF of whom 145 (6.0%) with asymptomatic episodes and 133 (5.5%) with symptomatic ones. During hospitalization, 148 patients died [106, 10, and 32 in the sinus rhythm (SR), asymptomatic, and symptomatic NOAF groups, respectively]. After multivariable adjustment, only symptomatic NOAF was associated with in-hospital mortality [odds ratio (OR): 2.32, 95% confidence interval (CI): 1.36-3.94] compared with SR. Over a median follow-up of 2.7 years, all-cause mortality was 3.2, 12.4, and 11.8% per year in the SR, asymptomatic, and symptomatic NOAF groups, respectively. After adjustment for confounders, it was the asymptomatic NOAF [hazard ratio (HR): 1.61, 95% CI: 1.09-2.37) rather than the symptomatic one (HR: 1.37, 95% CI: 0.88-2.12) that was significantly related to mortality. Similar results were also observed for cardiovascular mortality [HRs and 95% CI were 1.71 (1.10-2.67) and 1.25 (0.74-2.11) for asymptomatic and symptomatic NOAF, respectively]. Both asymptomatic and symptomatic NOAF episodes were associated with heart failure, whereas only those with symptomatic NOAF were at heightened risk of ischemic stroke. Our exploratory analysis further identified patients with asymptomatic high-burden NOAF as the highest-risk population (mortality: 19.6% per year). Conclusion: Among patients with AMI, symptomatic NOAF is related to in-hospital mortality and asymptomatic NOAF is associated with poor long-term survival. Registration: URL: https://ichgcp.net/clinical-trials-registry/NCT03533543" title="See in ClinicalTrials.gov">NCT03533543.

Keywords: acute myocardial infarction; atrial fibrillation; heart failure; ischemic stroke; mortality; symptom.

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Copyright © 2021 Luo, Liu, Li, Xu, Gong, Li, Qin, Shi, Hao, Zhang and Wei.

Figures

Figure 1
Figure 1
(A) Long-term all-cause death; (B) cardiovascular death; (C) HF hospitalization-free survival; (D) ischemic stroke-free survival based on the symptom of NOAF during AMI. HF, heart failure; NOAF, new-onset atrial fibrillation; PS, propensity score; SR, sinus rhythm.
Figure 2
Figure 2
Long-term survival in PSM cohorts for (A) SR vs. asymptomatic NOAF and (B) SR vs. symptomatic NOAF and in IPTW cohorts for (C) SR vs. asymptomatic NOAF and (D) SR vs. symptomatic NOAF. IPTW, inverse probability of treatment weighting; PSM, propensity score matching.
Figure 3
Figure 3
Subgroup analysis. MI, myocardial infarction; PCI, percutaneous coronary intervention.
Figure 4
Figure 4
Long-term survival in the whole cohort stratified by the symptom and burden level of NOAF during AMI. HF, heart failure; NOAF, new-onset atrial fibrillation; PS, propensity score; SR, sinus rhythm.

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Source: PubMed

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