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  4. Association of long-COVID with major adverse cardiovascular events and mortality
 
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Association of long-COVID with major adverse cardiovascular events and mortality

Other Title
a real-world data cohort study
Journal
BMC Cardiovascular Disorders
Date Issued
2026-12-01
Author(s)
PAI-YUAN WANG  
SAI-WAI HO  
SHUN-FA YANG  
CHAO-BIN YEH  
DOI
10.1186/s12872-026-06026-x
URI
https://www.scopus.com/pages/publications/105045159596
https://scholars.csmu.edu.tw/handle/123456789/34361
Abstract
Background: There is a limited body of research examining the association between long COVID and major adverse cardiovascular events (MACE) as well as all-cause mortality. This study aimed to investigate the association between long COVID and both MACE and mortality. Methods: This retrospective cohort study utilized multicenter real-world data from the TriNetX research network platform, which contains electronic health records from multiple healthcare organizations. Patients aged 18 years and older who were diagnosed with COVID-19 between 2020 and 2023 were included. The exposure group comprised individuals diagnosed with long-COVID within 3 to 6 months after their initial COVID-19 diagnosis, while the comparison group included COVID-19 patients without a diagnosis of long-COVID. The primary outcomes were the risk of major adverse cardiovascular events (MACE) and all-cause mortality. Follow-up commenced 90 days after the index date and continued until the occurrence of the study outcome or the date of the last available medical record. Results: The risk of MACE was markedly higher in the long-COVID cohort compared to the non-long-COVID cohort. The overall hazard ratio (HR) for MACE was 4.48 (95% CI: 3.95–5.07). Specific conditions such as coronary artery disease and stroke exhibited particularly high HRs, at 6.48 (5.29–7.95) and 3.46 (2.96–4.04) respectively. Mortality was significantly higher in the long-COVID group, with an HR of 1.53 (1.38–1.69). Conclusions: Compared to patients without long COVID, patients with long COVID had a higher risk of developing MACE.
Type
journal article
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