Clinical study of Yiqi Liangxue Shengji prescription for improving cardiac function after myocardial ischemia reperfusion injury in patients with acute myocardial infarction: a randomized, double-blind, placebo-controlled trial.

L I Yuxuan, L I Yan, Wang Wujiao, Cui Xiaoyun, Wan Jie, Zhou Kun, L U Jinjin, Liu Jing, Lin Qian, L I Dong
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Abstract

Objective: To evaluate the effect of Yiqi Liangxue Shengji prescription (, YQLXSJ) on cardiac function and outcomes in acute myocardial infarction (AMI) patients with myocardial ischemia-reperfusion injury (MIRI) and to determine its clinical efficacy.

Methods: This prospective, randomized, double-blind, placebo-controlled trial enrolled hospitalized patients with AMI who underwent percutaneous coronary intervention and experienced MIRI either intraoperatively or postoperatively. Participants were randomly allocated to the treatment group, which received YQLXSJ, or the control group, which received a placebo, concurrent with standard Western Medicine therapy. The intervention period lasted 8 weeks. The primary outcome measure was left ventricular ejection fraction (LVEF), determined by echocardiography. Secondary outcomes included N-terminal pro brain natriuretic peptide (NT-proBNP) and cardiac troponin I (cTnI) levels, left ventricular internal diameter, major adverse cardiovascular events (MACE), angina pectoris scores, and Chinese medicine evidence scores.

Results: Following 8 weeks of intervention, the treatment group demonstrated a significant increase in LVEF and a marked reduction in NT-proBNP when compared to the control group. There was also a significant decrease in peak cTnI levels, Chinese medicine evidence scores, and angina pectoris scores. The control group's left ventricular end-systolic diameter (LVESD) significantly increased compared to baseline after 8 weeks (P < 0.05), whereas the treatment group's LVESD showed no significant change from baseline (P > 0.05). Although the treatment group showed a downward trend in MACE incidence compared to the control group, this difference was not statistically significant (P > 0.05).

Conclusions: This study demonstrated that the addition of YQLXSJ to standard therapy can improve cardiac function and alleviate clinical symptoms in AMI patients with MIRI, and also showed a potential to mitigate the incidence of MACE. Furthermore, YQLXSJ displayed a favorable safety profile in clinical application.

益气凉血生积方改善急性心肌梗死患者心肌缺血再灌注损伤后心功能的临床研究:随机、双盲、安慰剂对照试验
目的:评价益气凉血生积方(YQLXSJ)对急性心肌梗死(AMI)合并心肌缺血再灌注损伤(MIRI)患者心功能及转归的影响,探讨其临床疗效。方法:这项前瞻性、随机、双盲、安慰剂对照试验纳入了住院的AMI患者,这些患者接受了经皮冠状动脉介入治疗,并在术中或术后经历了MIRI。参与者被随机分配到治疗组,治疗组接受YQLXSJ,对照组接受安慰剂,同时接受标准的西医治疗。干预期8周。主要结局指标是左心室射血分数(LVEF),由超声心动图测定。次要结局包括n端前脑利钠肽(NT-proBNP)和心肌肌钙蛋白I (cTnI)水平、左心室内径、主要不良心血管事件(MACE)、心绞痛评分和中医证据评分。结果:干预8周后,治疗组与对照组相比,LVEF显著升高,NT-proBNP显著降低。cTnI峰值水平、中医证据评分和心绞痛评分也有显著下降。8周后,对照组左心室收缩末期直径(LVESD)较基线显著升高(P < 0.05),而治疗组左心室收缩末期直径(LVESD)较基线无显著变化(P < 0.05)。治疗组MACE发生率虽较对照组有下降趋势,但差异无统计学意义(P < 0.05)。结论:本研究表明,AMI合并MIRI患者在标准治疗基础上加用YQLXSJ可改善心功能,缓解临床症状,并具有降低MACE发生率的潜力。此外,YQLXSJ在临床应用中显示出良好的安全性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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