Effect of Compound Danshen Dripping Pills on cardiac function after acute anterior ST-segment elevation myocardial infarction: A randomized trial.

IF 2.4 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL Journal of Biomedical Research Pub Date : 2025-01-10 DOI:10.7555/JBR.38.20240325
Bo Deng, Sibo Wang, Yujie Wu, Qiming Wang, Rui Qiao, Xiwen Zhang, Yuan Lu, Li Wang, Shunzhong Gu, Yuqing Zhang, Kaiqiao Li, Zongliang Yu, Lixing Wu, Shengbiao Zhao, Shuanglin Zhou, Yang Yang, Liansheng Wang
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Abstract

The current study aimed to evaluate the efficacy and safety of Compound Danshen Dripping Pills (CDDP) in improving cardiac function in 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 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 values after 24 weeks of 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 in N-terminal pro-B-type natriuretic peptide levels were observed in both groups at the 24- and 48-week visits with no significant difference between the two groups ( P > 0.1 for all). The incidence of major adverse cardiovascular and cerebrovascular events was 6.35% in the CDDP group and 5.79% in the placebo group ( P = 0.822). Notably, no serious adverse events were attributed to CDDP. These findings suggest that CDDP may be well tolerated and could improve left ventricular ejection fraction in patients with AAMI at 24 and 48 weeks.

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复方丹参滴丸对急性st段抬高型心肌梗死心功能的影响:一项随机试验。
本研究旨在评价复方丹参滴丸(CDDP)改善急性st段前抬高型心肌梗死(AAMI)患者心功能的疗效和安全性。在2021年2月至2023年2月期间,纳入247例经皮冠状动脉介入治疗(pPCI)后符合条件的AAMI患者,随机分配(1∶1)接受CDDP (n = 126)或安慰剂(n = 121),随访48周。与安慰剂组相比,CDDP组在治疗24周后左心室射血分数(LVEF)值显著增加(最小二乘平均值:3.31;95%置信区间[CI]: 1.72-4.90;P < 0.001)和48周随访时(最小二乘平均值:4.35;95% ci: 2.76-5.94;P < 0.001)。在24周和48周的随访中,两组患者的n端前b型利钠肽水平均显著降低,两组之间无差异(P < 0.01), CDDP组和安慰剂组分别有6.35%和5.79%的患者发生了主要的心脑血管不良事件(P = 0.822)。因此,没有严重的不良事件归因于CDDP。这些结果表明,CDDP耐受性良好,并在24周和48周改善AAMI患者的LVEF。
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来源期刊
Journal of Biomedical Research
Journal of Biomedical Research MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
4.60
自引率
0.00%
发文量
69
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