Department of Clinical Korean Medicine, Graduate School, Kyung Hee University, Kyungheedae-ro, Dongdaemun-gu, Seoul, Korea.
Medicine (Baltimore). 2021 Apr 23;100(16):e25652. doi: 10.1097/MD.0000000000025652.
Lumbar herniated intervertebral disc (LHIVD) is a common disease that causes low back pain. Traditional Chinese medicine (TCM) with conservative conventional treatment is known to be effective at treating LHIVD, but evidence for complex TCM therapies with conventional intervention has not been sufficiently collected to facilitate quality assessment and synthesis of data.
Studies were retrieved from the following databases: the Cochrane Central Register of Controlled Trials, EMBASE, MEDLINE/PubMed, 7 Korean databases (Korean Studies Information Service System, Korean Traditional Knowledge Portal, Oriental Medicine Advanced Searching Integrated System, Korean National Assembly Digital Library, Korean Association of Medical Journal Editors, National Digital Science Library, and Database Periodical Information Academic), Japan Medical Abstracts Society, and Chinese National Knowledge Infrastructure. The risk of bias of the included studies will be assessed using the Cochrane Assessment Tool for Risk of Bias. Eligible studies were quantitatively synthesized through a meta-analysis. The primary outcome will be pain scales, and the secondary outcomes will include range of motion, questionnaires for lumbar function, questionnaire for quality of life, etc.
Ethical approval was waived for this study protocol because it does not provide any patient data. The results of this review will be disseminated through peer-reviewed publications.
DOI 10.17605/OSF.IO/K7NJ8 (https://osf.io/k7nj8).
腰椎间盘突出症(LHIVD)是一种常见的引起腰痛的疾病。传统的中医保守常规治疗被认为对治疗 LHIVD 有效,但对于常规干预的复杂中医治疗方法的证据尚未充分收集,难以进行质量评估和数据综合。
研究从以下数据库中检索:Cochrane 对照试验中心注册库、EMBASE、MEDLINE/PubMed、7 个韩国数据库(韩国研究信息服务系统、韩国传统知识门户、东方医学高级搜索综合系统、韩国国家议会数字图书馆、韩国医学期刊编辑协会、国家数字科学图书馆和期刊信息学术数据库)、日本医学摘要学会和中国国家知识基础设施。使用 Cochrane 评估工具评估纳入研究的偏倚风险。通过荟萃分析对合格研究进行定量综合。主要结局指标为疼痛量表,次要结局指标包括运动范围、腰椎功能问卷、生活质量问卷等。
本研究方案无需提供任何患者数据,因此豁免了伦理审查。本综述的结果将通过同行评审出版物进行传播。
DOI 10.17605/OSF.IO/K7NJ8(https://osf.io/k7nj8)。