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Sustained beneficial effect of β-blockers on clinical outcomes after discontinuation in patients with ST elevation myocardial infarction

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dc.contributor.authorPark, JS-
dc.contributor.authorSeo, KW-
dc.contributor.authorChoi, SY-
dc.contributor.authorYoon, MH-
dc.contributor.authorHwang, GS-
dc.contributor.authorTahk, SJ-
dc.contributor.authorShin, JH-
dc.date.accessioned2023-10-24T07:46:25Z-
dc.date.available2023-10-24T07:46:25Z-
dc.date.issued2023-
dc.identifier.issn0025-7974-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/26449-
dc.description.abstractOur previous study demonstrated that beneficial effect of β-blockers on clinical outcomes in patients with ST elevation myocardial infarction (STEMI). In clinical practice, β-blocker treatment is occasionally discontinued due to their side effect. The purpose of this study is to assess the impact of discontinuation of β-blockers on long-term clinical outcomes in patients with STEMI. We analyzed the data and clinical outcomes of 901 patients (716 males, 58 ± 13-year-old) STEMI patients who underwent successful primary percutaneous coronary intervention. At discharge of index STEMI, 598 patients were treated with β-blockers (491 males, 56 ± 12-year-old). After more than 1-month β-blocker treatment, β-blockers were stopped in 188 patients for any reason. We classified patients into continuation of β-blockers (410 patients, 56 ± 12-year-old) and discontinuation of β-blockers groups (188 patients, 57 ± 11-year-old) according to discontinuation of β-blockers. Occurrence of major adverse cardiovascular events (MACEs; death, recurrent MI and target vessel revascularization) during up to 10 years of follow-up was evaluated. Mean follow-up month was 56 ± 28 month. In 132 patients (22%), MACEs were occurred. The MACE-free survival rates in the 2 groups were not statistically different (log-rank P = .461). Adjusted hazard ratio (HR) of discontinuation of β-blockers for MACEs was 1.006 (95% confidence interval (CI) 0.701-1.445, P = .973; all cause of death, HR = 0.942, 95% CI = 0.547-1.622, P = .828; recurrent MI, HR = 0.476, 95% CI = 0.179-1.262, P = .136; target vessel revascularization, HR = 1.417, 95% CI = 0.865-2.321, P = .166). The MACE-free survival and survival rates of the non β-blockers treatment group was significantly worse than the discontinuation of β-blockers group (log-rank P = .003 and < 0.001, respectively). This study demonstrated that discontinuation of β-blockers was not associated with adverse cardiovascular outcomes after STEMI. The beneficial effect of β-blockers on clinical outcomes may persist in patients with initial β-blockers treatment at index STEMI.-
dc.language.isoen-
dc.subject.MESHAdrenergic beta-Antagonists-
dc.subject.MESHAdult-
dc.subject.MESHAged-
dc.subject.MESHBody Fluids-
dc.subject.MESHDrug-Related Side Effects and Adverse Reactions-
dc.subject.MESHHumans-
dc.subject.MESHMale-
dc.subject.MESHMiddle Aged-
dc.subject.MESHPatient Discharge-
dc.subject.MESHST Elevation Myocardial Infarction-
dc.titleSustained beneficial effect of β-blockers on clinical outcomes after discontinuation in patients with ST elevation myocardial infarction-
dc.typeArticle-
dc.identifier.pmid37713877-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10508429-
dc.subject.keywordβ-blockers-
dc.subject.keywordmyocardial infarction-
dc.subject.keywordprognosis-
dc.contributor.affiliatedAuthorPark, JS-
dc.contributor.affiliatedAuthorSeo, KW-
dc.contributor.affiliatedAuthorChoi, SY-
dc.contributor.affiliatedAuthorYoon, MH-
dc.contributor.affiliatedAuthorHwang, GS-
dc.contributor.affiliatedAuthorShin, JH-
dc.type.localJournal Papers-
dc.identifier.doi10.1097/MD.0000000000035187-
dc.citation.titleMedicine-
dc.citation.volume102-
dc.citation.number37-
dc.citation.date2023-
dc.citation.startPagee35187-
dc.citation.endPagee35187-
dc.identifier.bibliographicCitationMedicine, 102(37). : e35187-e35187, 2023-
dc.identifier.eissn1536-5964-
dc.relation.journalidJ000257974-
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Journal Papers > School of Medicine / Graduate School of Medicine > Cardiology
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