Jeong Jun-Chang, Park Jong-Il, Kim Byung-Jun, Kim Hong-Ju, Choi Kang-Un, Nam Jong-Ho, Lee Chan-Hee, Son Jang-Won, Park Jong-Seon, Her Sung-Ho, Chang Ki-Yuk, Ahn Tae-Hoon, Jeong Myung-Ho, Rha Seung-Woon, Kim Hyo-Soo, Gwon Hyeon-Cheol, Seong In-Whan, Hwang Kyung-Kuk, Hur Seung-Ho, Cha Kwang-Soo, Oh Seok-Kyu, Chae Jei-Keon, Kim Ung
Division of Cardiology, Yeungnam University Medical Center, Daegu, Republic of Korea.
Division of Cardiology, Hanmaeum Medical Center, Changwon-si, Gyeongsangnam-do, Republic of Korea.
Front Cardiovasc Med. 2024 Nov 21;11:1447952. doi: 10.3389/fcvm.2024.1447952. eCollection 2024.
Data on the clinical impact of beta-blockers (BBs) in patients with myocardial infarction (MI) who had non-reduced left ventricular ejection fraction (LVEF) after percutaneous coronary intervention are limited.
From 2016 to 2020, we evaluated a cohort of 12,101 myocardial infarction patients with a non-reduced LVEF (≥40%) from the Korean Acute Myocardial Infarction Registry V. Patients were divided into two groups based on their BB (carvedilol, bisoprolol, or nebivolol) treatment at discharge: with beta-blocker treatment (BB, = 9,468) and without beta-blocker treatment (non-BB, = 2,633). The primary endpoint after discharge was the occurrence of patient-oriented composite endpoints (POCEs), including all-cause mortality, any MI, or any revascularization at 1-year follow-up.
The median follow-up period was 353 days (interquartile range, 198-378 days). At 1-year follow-up, no significant differences were observed in the primary endpoint between the BB group and the non-BB group. Before propensity score (PS) matching, the POCE incidence was 3.1% in the BB group vs. 3.4% in the non-BB group [hazard ratio (HR) 0.86, 95% confidence interval (CI) 0.68-1.09, = 0.225]. After PS matching, the POCE incidence remained similar between the two groups (3.7% vs. 3.4%, HR 1.01, 95% CI 0.76-1.35, = 0.931). Individual outcomes, including all-cause mortality, myocardial infarction, and revascularization, also showed no significant differences between the two groups. Independent predictors of 1-year POCEs after discharge were age, chronic kidney disease, reduced LVEF, and multivessel disease.
BB treatment in patients with acute MI and non-reduced LVEF was not associated with a significant reduction in cardiovascular outcomes at 1-year follow-up.
关于β受体阻滞剂(BBs)对经皮冠状动脉介入治疗后左心室射血分数(LVEF)未降低的心肌梗死(MI)患者的临床影响的数据有限。
2016年至2020年,我们对来自韩国急性心肌梗死注册研究V的12101例LVEF未降低(≥40%)的心肌梗死患者进行了评估。根据出院时是否接受BB(卡维地洛、比索洛尔或奈必洛尔)治疗将患者分为两组:接受β受体阻滞剂治疗(BB组,n = 9468)和未接受β受体阻滞剂治疗(非BB组,n = 2633)。出院后的主要终点是患者导向性复合终点(POCEs)的发生情况,包括1年随访时的全因死亡率、任何心肌梗死或任何血管重建术。
中位随访期为353天(四分位间距,198 - 378天)。在1年随访时,BB组和非BB组在主要终点方面未观察到显著差异。在倾向评分(PS)匹配前,BB组的POCE发生率为3.1%,非BB组为3.4%[风险比(HR)0.86,95%置信区间(CI)0.68 - 1.09,P = 0.225]。PS匹配后,两组之间的POCE发生率仍然相似(3.7%对3.4%,HR 1.01,95% CI 0.76 - 1.35,P = 0.931)。包括全因死亡率、心肌梗死和血管重建术在内的个体结局在两组之间也未显示出显著差异。出院后1年POCEs的独立预测因素为年龄、慢性肾脏病、LVEF降低和多支血管病变。
急性心肌梗死且LVEF未降低的患者接受BB治疗在1年随访时与心血管结局的显著降低无关。