The efficacy and safety of botulinum toxin type A in treatment of trigeminal neuralgia and peripheral neuropathic pain: A meta-analysis of randomized controlled trials

被引:43
|
作者
Wei, Jiangshan [1 ]
Zhu, Xiangyu [2 ]
Yang, Guang [3 ]
Shen, Jun [3 ]
Xie, Peng [4 ]
Zuo, Xiaohua [5 ]
Xia, Lei [6 ]
Han, Qiu [6 ]
Zhao, Ying [3 ]
机构
[1] Hongze Huaian Dist Peoples Hosp, Dept Neurol, Huaian, Peoples R China
[2] Xuzhou Med Univ, Huaian Affiliated Hosp, Peoples Hosp Huaian 2, ICU, Huaian, Peoples R China
[3] Xuzhou Med Univ, Affiliated Huaian Hosp, Peoples Hosp Huaian 2, Dept Neurol, 62 Huaihai South Rd, Huaian 223002, Jiangsu, Peoples R China
[4] Xuzhou Med Univ, Affiliated Huaian Hosp, Peoples Hosp Huaian 2, Dept Neurosurg, Huaian, Peoples R China
[5] Xuzhou Med Univ, Affiliated Huaian Hosp, Peoples Hosp Huaian 2, Dept Pain Management, Huaian, Peoples R China
[6] Nanjing Med Univ, Affiliated Huaian Peoples Hosp 1, Huaian Peoples Hosp 1, Dept Neurol, 1 Huanghe West Rd, Huaian 223000, Jiangsu, Peoples R China
来源
BRAIN AND BEHAVIOR | 2019年 / 9卷 / 10期
关键词
botulinum toxin-A; meta-analysis; peripheral neuropathic pain; randomized controlled trials; trigeminal neuralgia; DOUBLE-BLIND; INJECTIONS; BURDEN; CROSSOVER; MIGRAINE;
D O I
10.1002/brb3.1409
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Background Although recent studies have shown that botulinum toxin-A (BTX-A) has a good analgesic effect on trigeminal neuralgia (TN) and peripheral neuropathic pain (PNP), the quality of evidence is low due to limited data. This meta-analysis is used to synthesize existing evidence for the treatment of these conditions with BTX-A. Methods Relevant trials were accessed by using an electronic search in databases (Web of Science, PubMed, EMBASE, Cochrane Library, and ). Data from included randomized controlled trials (RCTs) on the efficacy and safety of BTX-A in treating TN and PNP were extracted for meta-analysis. Results Finally, 10 RCTs (n = 391) were included in this meta-analysis. The pooled effect of BTX-A was superior to placebo based on pain intensity (SMD = -0.48, 95% CI [-0.74, 0.23] at 1 month, SMD = -0.58, 95% CI [-0.91, -0.24] at 2 months, and SMD = -0.55, 95% CI [-0.87, -0.22] at 3 months). Number needed to treat (NNT) for 50% pain intensity reduction showed better effect of BTX-A on TN and postherpetic neuralgia (PN). Adverse events associated with BTX-A were similar to placebo (OR = 1.58, 95% CI [0.51, 4.87], p = .424). Conclusion Pooled data from our meta-analysis suggest that BTX-A is efficacious and safe in treating TN and PNP. However, due to the limited sample size and heterogeneity, further larger and well-designed RCTs are imperative to validate these findings.
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页数:10
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