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中药活血化瘀专利口服药联合西药治疗冠心病心绞痛的系统评价概述

Overview of systematic reviews on Chinese patented oral medicines for promoting blood circulation and removing blood stasis combined with western medicine in the treatment of coronary heart disease angina pectoris.

作者信息

Chen Xinyi, Liu Huan, Wu Hongli, Deng Yi, Peng Wenxi, Xie Yanming, Jiang Junjie

机构信息

Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, China.

出版信息

Front Cardiovasc Med. 2025 Jun 20;12:1553735. doi: 10.3389/fcvm.2025.1553735. eCollection 2025.

Abstract

OBJECTIVE

To evaluate the methodology quality, reporting quality, and evidence quality of systematic reviews and meta-analyses on Chinese patented oral medicines that promote blood circulation and remove blood stasis combined with conventional Western medicine in the treatment of coronary heart disease angina pectoris. The aim is to identify and address methodological issues in systematic reviews of Chinese patented oral medicines for promoting blood circulation and removing blood stasis in angina pectoris. This study also offers methodological guidance for future research design and implementation, and provides a basis for clinical decision-making.

METHODS

A systematic search was performed using CNKI, Wanfang, VIP, CBM, PubMed, Cochrane Library, Embase, and Web of Science databases, covering the period from the inception of each database to July 18, 2024, and meta-analyses on randomized controlled trials were included. Methodological quality was evaluated using AMSTAR-2, reporting quality using PRISMA 2020, and evidence quality of the outcome indicators using GRADE.

RESULTS

Twenty meta-analyses were examined, involving a total of 41,231 patients with angina pectoris. The methodological quality of all studies was rated as "critically low," with notable deficiencies in the registration of the study protocol, study inclusion criteria, assessment of individual study risk of bias, evaluation of the likelihood of publication bias, and discussion of the effects of publication bias on the results. The assessment of the three qualities mentioned above revealed common issues, including incomplete abstracts, lack of characteristics for pooled outcomes, failure to report risk of bias across studies, missing registration information, lack of accessibility details for protocols, and unreported modifications to registered protocols or plans. Evidence quality assessment revealed that 16 outcome indicators were rated as "moderate," 29 as "low," and 46 as "very low."

CONCLUSION

Despite the demonstrated efficacy and safety of Chinese patented oral medicines that promote blood circulation and remove blood stasis in the adjuvant treatment of angina pectoris, the low methodological and reporting quality of current systematic reviews and meta-analyses compromises the reliability of these findings. Future research should focus on standardizing study design and reporting to improve the reliability of evidence.

摘要

目的

评价关于治疗冠心病心绞痛的中药活血化瘀口服制剂联合常规西药的系统评价和Meta分析的方法学质量、报告质量及证据质量。旨在识别并解决中药活血化瘀口服制剂治疗心绞痛系统评价中的方法学问题。本研究还为未来的研究设计和实施提供方法学指导,并为临床决策提供依据。

方法

通过检索中国知网、万方、维普、中国生物医学文献数据库、PubMed、Cochrane图书馆、Embase和Web of Science数据库进行系统检索,检索时间范围为各数据库建库至2024年7月18日,纳入随机对照试验的Meta分析。采用AMSTAR-2评价方法学质量,PRISMA 2020评价报告质量,GRADE评价结局指标的证据质量。

结果

共纳入20项Meta分析,涉及41231例心绞痛患者。所有研究的方法学质量均被评为“极低”,在研究方案注册、研究纳入标准、单个研究偏倚风险评估、发表偏倚可能性评估以及发表偏倚对结果影响的讨论方面存在明显不足。上述三种质量评估均发现了一些常见问题,包括摘要不完整、合并结局缺乏特征描述、未报告各研究的偏倚风险、缺少注册信息、方案可获取细节缺失以及未报告对注册方案或计划的修改。证据质量评估显示,16个结局指标被评为“中等”,29个为“低”,46个为“极低”。

结论

尽管中药活血化瘀口服制剂在辅助治疗心绞痛方面已显示出疗效和安全性,但当前系统评价和Meta分析的方法学和报告质量较低,影响了这些研究结果的可靠性。未来的研究应侧重于规范研究设计和报告,以提高证据的可靠性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b58f/12226556/7608ee4cd794/fcvm-12-1553735-g001.jpg

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