Herbal medicine for cervicogenic dizziness A protocol for a systematic review and meta-analysis

被引:2
|
作者
Oh, Hyunjoo [1 ]
Shin, Seungwon [2 ,3 ]
Lee, Euiju [4 ]
机构
[1] Kyung Hee Univ, Dept Clin Korean Med, Grad Sch, Seoul, South Korea
[2] Natl Dev Inst Korean Med, Natl Agcy Dev Innovat Technol Korean Med, Seoul, South Korea
[3] Kyung Hee Univ, Grad Sch, Dept Clin Korean Med, Seoul, South Korea
[4] Kyung Hee Univ, Coll Korean Med, Dept Sasang Constitut Med, 23 Kyungheedae Ro, Seoul, South Korea
来源
MEDICINE | 2020年 / 99卷 / 51期
基金
新加坡国家研究基金会;
关键词
cervicogenic dizziness; herbal medicine; protocol; systematic review; MANUAL THERAPY; DIAGNOSIS;
D O I
10.1097/MD.0000000000023852
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Herbal medicines are empirically used to treat cervicogenic dizziness. However, till date there have been no systematic review to evaluate the efficacy and safety of these medicines. Therefore, this study protocol describes the methods for evaluating the efficacy and safety of herbal medicine for cervicogenic dizziness. Methods and analysis: The following electronic academic databases will be searched up to December 2019 without language or publication status restrictions: Medical Literature Analysis and Retrieval System Online (MEDLINE), Excerpta Medica database (EMBASE), and the Cochrane Central Register of Controlled Trials (CENTRAL), together with Korean, Chinese, and Japanese databases. Any randomized controlled trials related to herbal medicine for cervicogenic dizziness will be included. The functional outcomes and the vertebrobasilar artery hemodynamic states will be evaluated as primary outcomes. The total effective rate, hematological conditions, and adverse events will be assessed as secondary outcomes. Study selection, data extraction, quality assessment of studies, and qualitative evaluation of clinical evidence will be performed by 2 independent reviewers. The methodological quality of the included studies will be evaluated using a revised Cochrane risk-of-bias tool for randomized trials. The strength of evidence from the included data will be evaluated using the Grading of Recommendations Assessment, Development, and Evaluation approach. Data synthesis will be performed as either a fixed-effects or a random-effects model using Review Manager software version 5.3. The results will be reported as a risk ratio for dichotomous outcomes and as a mean difference or standardized mean difference for continuous outcomes. Ethics and dissemination: No ethical approval is required since the individual clinical information of the patient is not used. The findings of this systematic review will be disseminated through the peer-reviewed publications or conference presentations. Review Registry Unique Identifying Number: reviewregistry1036.
引用
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页数:5
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