Low level light therapy/photobiomodulation for diabetic peripheral neuropathy: protocol of a systematic review and meta-analysis

被引:4
作者
Wang, Jia-You [1 ]
Huang, Zou-Qin [2 ]
Deng, Hai-Ping [1 ,3 ]
Zhao, Ling [1 ]
Deng, Hong-Yong [4 ]
Liu, Jian-Ping [5 ]
Shen, Xue-Yong [1 ,3 ]
Cheng, Ke [1 ,3 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Sch Acupuncture Moxibust & Tuina, Shanghai, Peoples R China
[2] Shanghai Pudong Hosp Tradit Chinese Med, Acupuncture Moxibust Dept, Shanghai, Peoples R China
[3] Shanghai Res Ctr Acupuncture & Meridian, Shanghai, Peoples R China
[4] Shanghai Univ Tradit Chinese Med, Collaborat Innovat Ctr, Shanghai, Peoples R China
[5] Beijing Univ Chinese Med, Ctr Evidence Based Chinese Med, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
Laser therapy; Diabetic neuropathy; Neurological pain; SENSITIVITY; THERAPY;
D O I
10.1136/bmjopen-2021-059476
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Diabetic peripheral neuropathy (DPN) is one of the most common complications of diabetes that strongly impact the patients' quality of life and working ability. Evidence indicated that low level light therapy (LLLT)/photobiomodulation might be effective for neuropathy. However, the effect of LLLT for DPN is not clear. The objective of this systematic review and meta-analysis is to determine the effects and safety of LLLT/photobiomodulation for DPN, in comparison with other methods such as sham light, no treatment, other active treatment and LLLT as an additional treatment compared with another treatment alone. Methods and analysis We will search eight databases from their inception to the date before the review submission. Randomised controlled trials (RCTs) will be included. Two reviewers will independently extract data using a structured data extraction method and assess the risk of bias in the included studies. Data will be synthesised using standardised mean difference or risk ratio with 95% CIs for continuous and dichotomous data, respectively. The primary outcome will be change in pain and secondary outcomes will include global symptom improvement, functional impairment and disability, impairment of sensation, quality of life, nerve conduction, and adverse events. Sensitivity and subgroup analysis will be employed to explore the influence of possible clinical and methodological characteristics. Publication bias will be assessed using funnel plot. We will conduct meta-analysis with RevMan V.5.4 and evaluate quality of the evidence using GRADE approach. Ethics and dissemination This study does not require ethics approval. Our findings will be disseminated in the peer-reviewed publications. PROSPERO registration number CRD42021276056.
引用
收藏
页数:5
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