Effect of Beta-Blocker on Long-Term Major Cardiovascular Events in High Atherosclerotic Risk Population

dc.contributor.authorOsataphan N.
dc.contributor.authorUdol K.
dc.contributor.authorSiriwattana K.
dc.contributor.authorSukanandachai B.
dc.contributor.authorGunaparn S.
dc.contributor.authorSirikul W.
dc.contributor.authorPhrommintikul A.
dc.contributor.authorWongcharoen W.
dc.contributor.otherMahidol University
dc.date.accessioned2023-08-28T18:02:19Z
dc.date.available2023-08-28T18:02:19Z
dc.date.issued2023-01-01
dc.description.abstractPurpose: Beta-blocker is a frequently used medication in cardiovascular diseases. However, long-term benefit of beta-blocker in patients with preserved left ventricular ejection function (LVEF) on major adverse cardiovascular events (MACEs) is uncertain. Methods: The Cohort Of patients with high Risk for cardiovascular Events (CORE-Thailand) was a prospective study that enrolled Thai patients with high atherosclerotic risk including multiple atherosclerotic risk factors and established atherosclerotic cardiovascular diseases. Baseline demographic data, co-morbidities and medication were recorded. Patients were followed for 5 years. Patients with LVEF<50% were excluded. Primary outcome was the effect of beta-blocker on the occurrence of MACEs including all-cause death, non-fatal myocardial infarction and non-fatal stroke (3P-MACEs). Propensity score matching was used to control confounding factors. Results: There was a total of 8513 patients in the pre-matched cohort, 4418 were taking beta-blocker and 4095 were not. After adjustment of confounders, beta-blocker was an independent predictor of 3P-MACEs (adjusted HR 1.29;95% CI 1.12-1.49;p<0.001). After propensity score matching, 4686 patients remained in the post-matched cohort. Propensity score analysis showed consistent results in which patient taking beta-blocker had higher risk of 3P-MACEs (adjusted HR 1.29;95% CI 1.10-1.53;p=0.002). Subgroup analysis in patients with coronary artery disease (CAD) indicated that taking beta-blocker did not increase the incidence of 3P-MACEs (adjusted HR 0.99;95% CI 0.76-1.29) while those without CAD did (adjusted HR 1.51; 95% CI, 1.22-1.86;p-interaction=0.015). Conclusion: In patients with high atherosclerotic cardiovascular risk, taking beta-blockers had a higher risk of 3P-MACEs. Care should be taken when prescribing beta-blockers to patients without a clear indication. Trial registration: TCTR20130520001 registered in Thai Clinical Trials Registry (TCTR) https://www.thaiclinicaltrials.org/ , date of registration 20 May 2013.
dc.identifier.citationCardiovascular Drugs and Therapy (2023)
dc.identifier.doi10.1007/s10557-023-07502-8
dc.identifier.eissn15737241
dc.identifier.issn09203206
dc.identifier.pmid37594650
dc.identifier.scopus2-s2.0-85168359058
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/88868
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleEffect of Beta-Blocker on Long-Term Major Cardiovascular Events in High Atherosclerotic Risk Population
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85168359058&origin=inward
oaire.citation.titleCardiovascular Drugs and Therapy
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationFaculty of Medicine, Chiang Mai University
oairecerif.author.affiliationNakornping Hospital
oairecerif.author.affiliationMaharaj Nakhon Ratchasima Hospital

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