养心氏与曲美他嗪对冠心病患者经皮冠状动脉介入治疗后运动耐量的有效性和安全性:多中心双盲临床试验。

IF 6.7 1区 医学 Q1 CHEMISTRY, MEDICINAL Phytomedicine Pub Date : 2024-11-07 DOI:10.1016/j.phymed.2024.156198
Yang Li, Yi Li, Zhijie Zhang, Jian Zhang, Hong Chen, Haichu Yu, Xiaoping Meng, Haitao Yuan, Lili Shao, Yan Lu, Bin Liu, Jiayao Xu, Yi Zhang, Jing Li, Yaling Han
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引用次数: 0

摘要

背景:对于经皮冠状动脉介入治疗(PCI)后的冠心病(CHD)患者,改善其运动耐量的优化药物有限。养心氏片是一种中药口服药,能缓解心绞痛症状,可能是因为它能改善缺血心肌的能量代谢。我们进行了一项随机试验,以评估养心氏片与曲美他嗪相比,在PCI术后改善冠心病患者运动耐量方面的有效性和安全性:这项前瞻性、随机、双盲、双哑剂、多中心、非劣效性研究招募了年龄在 18-75 岁、在确诊后 2 个月内首次接受 PCI 治疗的冠心病患者。患者随机接受养心氏加曲美他嗪-安慰剂或曲美他嗪加养心氏-安慰剂治疗,疗程为24周。主要终点是心肺运动测试(CPET)评估的代谢当量(METs)在0至24周之间的变化。次要终点是 CPET 的综合变量、健康状况和不良事件。本研究已在 ClinicalTrials.gov (NCT03809273) 注册:2019年8月1日至2022年3月31日期间,共有681名患者随机接受了养心氏(n = 341)或曲美他嗪(n = 340)治疗。24周后,养心氏组患者的运动耐量增加了0.77±1.25 METs,曲美他嗪组增加了0.76±1.00 METs(差异,0.01;95%置信区间[CI],-0.17至0.19),达到了预先设定的非劣效性阈值。在患者报告的抑郁(PHQ-9;-1.88±3.32 vs. -0.93±3.68;P<0.001)和焦虑(GAD-7;-1.70±3.26 vs. -0.39±3.29;P<0.001)方面,观察到养心氏组优于曲美他嗪组。两组的不良反应相似:结论:对于PCI术后的冠心病患者,在24周的治疗期间,养心氏在改善运动耐量方面的效果不劣于曲美他嗪。值得注意的是,与曲美他嗪受试者相比,养心氏组患者的心理健康状况更好。
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Efficacy and safety of yangxinshi versus trimetazidine on exercise tolerance in patients with coronary heart disease after percutaneous coronary intervention: Multicenter, double-blind clinical trial.

Background: Optimizing medication to improve exercise tolerance in patients with coronary heart disease (CHD) after percutaneous coronary intervention (PCI) is limited. Yangxinshi tablets, an herbal-based oral medicine, relieve symptoms of angina might be that they can improve energy metabolism of the ischemic myocardium. We conducted a randomized trial to assess the efficacy and safety of Yangxinshi vs. trimetazidine in improving exercise tolerance in patients with CHD after PCI.

Methods: This prospective, randomized, double-blind, double-dummy, multicenter, non-inferiority study enrolled patients aged 18-75 years with CHD who underwent their first PCI within 2 months of diagnosis. Patients were randomized to Yangxinshi plus trimetazidine-placebo or trimetazidine plus Yangxinshi-placebo for 24 weeks. The primary endpoint was the change in metabolic equivalents (METs) assessed by cardiopulmonary exercise test (CPET) between 0 and 24 weeks. Secondary endpoints were comprehensive variables of the CPET, health status and adverse events. This study has been registered at ClinicalTrials. gov (NCT03809273).

Results: Between August 1, 2019, and March 31, 2022, a total of 681 patients were randomized to Yangxinshi (n = 341) or trimetazidine (n = 340). After 24 weeks, the exercise tolerance of patients increased by 0.77±1.25 METs in the Yangxinshi group and 0.76±1.00 METs in the trimetazidine group (difference, 0.01; 95 % confidence interval [CI], -0.17 to 0.19), meeting the predefined non-inferiority threshold. Better outcomes were observed in the Yangxinshi group compared with the trimetazidine group for patient-reported depression (PHQ-9; -1.88±3.32 vs. -0.93±3.68; p < 0.001) and anxiety (GAD-7; -1.70±3.26 vs. -0.39±3.29; p < 0.001). Adverse events were similar in both groups.

Conclusions: In patients with CHD after PCI, Yangxinshi was non-inferior to trimetazidine in improving exercise tolerance during the 24-week treatment period. Notably, patients in the Yangxinshi group showed a better mental health profile compared with trimetazidine recipients.

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来源期刊
Phytomedicine
Phytomedicine 医学-药学
CiteScore
10.30
自引率
5.10%
发文量
670
审稿时长
91 days
期刊介绍: Phytomedicine is a therapy-oriented journal that publishes innovative studies on the efficacy, safety, quality, and mechanisms of action of specified plant extracts, phytopharmaceuticals, and their isolated constituents. This includes clinical, pharmacological, pharmacokinetic, and toxicological studies of herbal medicinal products, preparations, and purified compounds with defined and consistent quality, ensuring reproducible pharmacological activity. Founded in 1994, Phytomedicine aims to focus and stimulate research in this field and establish internationally accepted scientific standards for pharmacological studies, proof of clinical efficacy, and safety of phytomedicines.
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