[中药治疗脑卒中后抑郁的随机对照试验结局指标]。

Q3 Pharmacology, Toxicology and Pharmaceutics Zhongguo Zhongyao Zazhi Pub Date : 2025-01-01 DOI:10.19540/j.cnki.cjcmm.20240826.501
Jin Han, Yue Yuan, Fang-Biao Xu, Yan-Bo Song, Yong-Kang Sun, Xin-Zhi Wang
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引用次数: 0

摘要

本研究系统回顾了中医药治疗脑卒中后抑郁(PSD)的随机对照试验(RCT),分析了临床研究特点和结局指标,旨在优化设计,建立中医治疗PSD的未来临床试验的核心结局集。检索PubMed、Web of Science、Cochrane Library、EMbase、CNKI、VIP、万方、SinoMed近3年发表的相关RCT。提取纳入RCT的基本特征、干预措施及结局指标,并进行描述性分析。最终纳入76项rct,样本量集中在80-100例。以肝郁气滞证型(15次,占31.91%)和痰瘀证型(5次,占10.63%)最为常见。干预方式频次呈下降趋势,以中药汤剂(35次,46.05%)、中药汤剂+针灸(4次,5.26%)、中成药(3次,3.94%)为主,干预时间以1 ~ 3个月为主(43次,60.56%)。患者不良反应主要为消化系统反应(150例,39.37%)和神经系统反应(112例,29.39%)。纳入的大多数研究偏倚风险不明确,共涉及84个结局指标,属于8个指标域。中医药治疗PSD的随机对照试验存在中医辨证不规范、中医证候评分和测量工具名称不一致、质量不高、偏倚风险不明确、忽视终点指标、替代指标选择不合理、主次结局指标不区分、安全性指标报告不规范、对经济指标重视不够等问题。缺乏长期预后评价。建议今后的研究应提高方法学质量,建立规范的核心结果集,促进该领域高质量临床研究的发展。
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[Outcome indicators in randomized controlled trials of traditional Chinese medicine treatment of post-stroke depression].

This study systematically reviewed the randomized controlled trial(RCT) of traditional Chinese medicine(TCM) treatment of post-stroke depression(PSD) and analyzed the clinical study characteristics and outcome indicators, aiming to optimize the design and establish the core outcome set in the future clinical trials of the TCM treatment of PSD. PubMed, Web of Science, Cochrane Library, EMbase, CNKI, VIP, Wanfang, and SinoMed were searched for the relevant RCT published in recent 3 years. The basic characteristics, intervention measures, and outcome indicators of the included RCT were extracted, and the descriptive analysis was carried out. A total of 76 RCTs were eventually included, with the sample size concentrated in 80-100 cases. The most frequent TCM syndromes were liver depression and Qi stagnation(15 times, 31.91%) and phlegm combined with stasis(5 times, 10.63%). The frequency of intervention methods followed a descending trend of TCM decoction(35 times, 46.05%) and TCM decoction + acupuncture(4 times, 5.26%), Chinese patent medicine(3 times, 3.94%), and the intervention mainly lasted for 1 to 3 months(43 times, 60.56%). The adverse reactions of patients were mainly digestive system reaction(150 patients, 39.37%) and nervous system reaction(112 patients, 29.39%). Most of the included studies had unclear risk of bias, involving 84 outcome indicators, which belonged to 8 indicator domains. The RCTs of TCM treatment of PSD showed a variety of problems, such as non-standard TCM syndrome differentiation, inconsistent names of TCM syndrome scores and measurement tools, low quality, unclear risk of bias, neglect of endpoint indicators, unreasonable selection of substitute indicators, lack of differentiation between primary and secondary outcome indicators, non-standard reporting of safety indicators, insufficient attention to economic indicators, and lack of long-term prognosis evaluation. It is suggested that the future research should improve the quality of methodology and build a standardized core outcome set to promote the development of high-quality clinical research in this field.

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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
期刊介绍:
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