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速效救心丸治疗长效硝酸酯类药物不耐受的慢性冠脉综合征的疗效和安全性:一项多中心、随机、双盲、安慰剂对照研究。

Efficacy and Safety of Suxiao Jiuxin Pills in the Treatment of Chronic Coronary Syndrome with Intolerance to Adverse Effects of Long-acting Nitrates: A Multicenter, Randomized, Double-blind, Placebo-controlled Study.

机构信息

Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.

Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.

出版信息

BMC Complement Med Ther. 2024 Oct 4;24(1):356. doi: 10.1186/s12906-024-04661-5.

Abstract

BACKGROUND

This study aims to investigate the short-term effects and safety of adjunct Suxiao Jiuxin Pills (SJPs) on conventional therapy in chronic coronary syndrome (CCS) patients who are intolerant to the adverse effects of long-acting nitrates.

METHODS

This was a multicenter, randomized, double-blind, placebo-controlled trial. A total of 174 CCS participants from eight clinical study centers in China were included in the modified intention-to-treat analyses. Participants with CCS and intolerance to the adverse effects of long-acting nitrates were recruited and randomized to either the SJPs or the placebo group for a duration of 4 weeks.

RESULTS

Compared to the placebo group, the SJPs group showed a significant improvement in the efficacy rate after 4 weeks (OR = 2.43, 95% CI = 1.32 to 4.47, P = 0.004). Besides, individuals without a history of alcohol consumption showed a greater improvement in the SAQ summary score compared to those with a history of alcohol consumption.

CONCLUSION

Adjunctive SJPs enhance the effectiveness of short-term conventional anti-angina treatment for patients with CCS who experience intolerance to long-acting nitrates, without significant adverse effects during application.

TRIAL REGISTRATION

Chinese Clinical Trials Registry Platform, ChiCTR2100050066. Registered 16 August 2021, https://www.chictr.org.cn/showproj.html?proj=131470 .

摘要

背景

本研究旨在探讨在不能耐受长效硝酸酯类药物不良反应的慢性冠脉综合征(CCS)患者中,速效救心丸(SJPs)辅助常规治疗的短期疗效和安全性。

方法

这是一项多中心、随机、双盲、安慰剂对照试验。共有来自中国 8 个临床研究中心的 174 名 CCS 参与者被纳入意向治疗分析的修改版。招募并随机分配有 CCS 且不能耐受长效硝酸酯类药物不良反应的参与者至 SJPs 或安慰剂组,治疗持续 4 周。

结果

与安慰剂组相比,SJPs 组在 4 周后疗效率显著提高(OR=2.43,95%CI=1.32 至 4.47,P=0.004)。此外,无饮酒史的个体在 SAQ 综合评分方面的改善大于有饮酒史的个体。

结论

辅助 SJPs 增强了对不能耐受长效硝酸酯类药物的 CCS 患者短期常规抗心绞痛治疗的效果,在应用过程中无明显不良反应。

试验注册

中国临床试验注册平台,ChiCTR2100050066。注册于 2021 年 8 月 16 日,https://www.chictr.org.cn/showproj.html?proj=131470。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/beb7/11451125/42c1f67ad0e2/12906_2024_4661_Fig1_HTML.jpg

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