Quality evaluation of the literature on clinical randomized controlled trials of traditional Chinese medicine for treatment of gastric precancerous lesions in the past 20 years.

Qingqing Zhang, Di Wu, Yichen Wang, Fengyun Guo, Shengnan Yang, Ping Wang
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Abstract

Objectives: To evaluate the methodological quality of randomized controlled trials (RCTs) of traditional Chinese medicines for the treatment of gastric precancerous lesions in the past 20 years.

Methods: The RCTs on traditional Chinese medicines for gastric precancerous lesions were searched from the CNKI, Wanfang database, VIP, PubMed, and Embase from January 2001 to December 2021. The retrieved articles were screened, extracted and evaluated based on the 2010 edition of CONSORT statement, Cochrane Risk of Bias Assessment Scale and additional evaluation indicators.

Results: A total of 840 papers were included. According to the Cochrane Risk of Bias Assessment Scale, the high risk of bias in the application of randomized methods was 5.95%; the risk of uncertainty for the allocation scheme concealment was 98.93%; the risk of uncertainty for blinding of patients or testers was 98.69%; the risk of uncertainty for blinding of the outcome assessor was 100.00%; the risk of bias for completeness of the outcome data was 2.86%; and the risk of uncertainty for selective reporting was 98.45%. The CONSORT statement evaluating the quality of reporting showed that 100.00% of the RCT articles reported the 8 entries; 36.79% of the literature mentioned the method of randomized sequence generation, but only 27.62% of the literature mentioned who implemented the randomized program, 1.07% of the literature hid the randomized program and 1.31% of the studies were blinded; 36.67% of the literature reported adverse reactions; no literature reported sample size prediction methods. Additional evaluation indicators showed that 17.02% of the studies had ethical approval; 43.81% of the literature specified Chinese medicine evidence; 16.55% of the studies excluded severe heterotrophic hyperplasia; 7.26% of the studies conducted follow-up; and 65.12% of the literature used composite efficacy indicators; 46.67% of the literature applied pathological histological evaluation; 2.62% of the literature applied quality of life evaluation.

Conclusions: The overall risk of bias in RCTs of traditional Chinese medicines for gastric precancerous lesions is high, and the quality of most of the study reports needs to be improved. In the future, it is necessary to strengthen the study design of RCTs and refer to appropriate traditional Chinese medicines evidence grading standards, select study protocols according to different purposes, provide objective and strong evidence for clinical studies on traditional Chinese medicines, and carry out clinical study design and result reporting suitable for traditional Chinese medicines according to the CONSORT principle.

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近20年来中医药治疗胃癌前病变临床随机对照试验的文献质量评价。
目的:评价近20年来中药治疗胃癌前病变的随机对照试验的方法学质量。方法:检索2001年1月至2021年12月在中国知网、万方数据库、VIP、PubMed和Embase上进行的胃癌前病变中药随机对照试验。检索到的文章根据2010年版CONSORT声明、Cochrane偏倚风险评估量表和其他评估指标进行筛选、提取和评估。结果:共收录论文840篇。根据Cochrane偏倚风险评估量表,应用随机方法的偏倚高风险为5.95%;分配方案隐蔽的不确定性风险为98.93%;患者或测试人员致盲的不确定性风险为98.69%;结果评估者致盲的不确定性风险为100.00%;结果数据完整性的偏倚风险为2.86%;选择性报告的不确定性风险为98.45%。CONSORT评估报告质量的声明显示,100.00%的RCT文章报告了这8个条目;36.79%的文献提到了随机序列生成的方法,但只有27.62%的文献提到谁实施了随机程序,1.07%的文献隐藏了随机程序和1.31%的研究是盲法的;36.67%的文献报道了不良反应;没有文献报道样本量预测方法。其他评估指标显示,17.02%的研究获得了伦理批准;43.81%的文献有明确的中医证候;16.55%的研究排除了严重的异养性增生;7.26%的研究进行了随访;65.12%的文献使用了复合疗效指标;46.67%的文献采用病理组织学评价;2.62%的文献应用了生活质量评价。结论:胃癌前病变的中药随机对照试验总体偏倚风险较高,大多数研究报告的质量有待提高。未来,有必要加强随机对照试验的研究设计,并参考适当的中药证据分级标准,根据不同目的选择研究方案,为中药临床研究提供客观有力的证据,按照CONSORT原则进行适合中药的临床研究设计和结果报告。
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CiteScore
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67
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