医学
射血分数
心肌梗塞
安慰剂
不利影响
内科学
心功能曲线
置信区间
经皮冠状动脉介入治疗
心脏病学
ST段
心力衰竭
替代医学
病理
作者
Bo Deng,Sibo Wang,Yujie Wu,Qiming Wang,Rui Qiao,Xiwen Zhang,Yuan Lu,Wang Li,Shunzhong Gu,Yuqing Zhang,Kaiqiao Li,Zongliang Yu,Lixing Wu,Zhao Shitian,Shuanglin Zhou,Yang Yang,Liansheng Wang
标识
DOI:10.7555/jbr.38.20240325
摘要
The current study aimed to evaluate the efficacy and safety of Compound Danshen Dripping Pills (CDDP) in improving cardiac function among patients with acute anterior ST-segment elevation myocardial infarction (AAMI). Between February 2021 and February 2023, 247 eligible patients with AAMI after primary percutaneous coronary intervention (pPCI) were enrolled and randomly assigned (1∶1) to receive CDDP (n = 126) or placebo (n = 121), with a follow-up of 48 weeks. Compared with the placebo group, the CDDP group demonstrated a significant increase in left ventricular ejection fraction (LVEF) values after 24 weeks of the treatment (least squares mean: 3.31; 95% confidence interval CI: 1.72–4.90; P < 0.001) and at the 48-week follow-up (least squares mean: 4.35; 95% CI: 2.76–5.94; P < 0.001). Significant reductions of N-terminal pro-B-type natriuretic peptide levels were observed in both groups at the 24- and 48-week visits without difference between the two groups (P > 0.1 for all), and 6.35% and 5.79% of patients in the CDDP and placebo groups experienced major adverse cardiovascular and cerebrovascular events, respectively (P = 0.822). Therefore, no serious adverse events were attributed to CDDP. These findings sugget that CDDP was well tolerated and improved LVEF of patients with AAMI in 24 and 48 weeks.
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