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Botulinum toxin A treatment for post-herpetic neuralgia: A systematic review and meta-analysis
The present meta-analysis study aimed to investigate the safety and efficacy of local administration of botulinum toxin (BTX-A) vs. lidocaine in the treatment of post-herpetic neuralgia. A systematic search of the Cochrane Library, PubMed, Embase, Chinese National Knowledge Infrastructure, Wanfang,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966161/ https://www.ncbi.nlm.nih.gov/pubmed/32010269 http://dx.doi.org/10.3892/etm.2019.8301 |
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author | Li, Xin-Long Zeng, Xu Zeng, Shan He, Hai-Ping Zeng, Zhen Peng, Li-Lei Chen, Li-Gang |
author_facet | Li, Xin-Long Zeng, Xu Zeng, Shan He, Hai-Ping Zeng, Zhen Peng, Li-Lei Chen, Li-Gang |
author_sort | Li, Xin-Long |
collection | PubMed |
description | The present meta-analysis study aimed to investigate the safety and efficacy of local administration of botulinum toxin (BTX-A) vs. lidocaine in the treatment of post-herpetic neuralgia. A systematic search of the Cochrane Library, PubMed, Embase, Chinese National Knowledge Infrastructure, Wanfang, Chongqing VIP Information Co. and Chinese Biomedical Literature Database was performed to identify randomized controlled trials (RCTs) comparing BTX-A and lidocaine in the treatment of post-herpetic neuralgia. The primary outcomes were Visual Analogue Scale (VAS) pain scores at 1, 2 and 3 months after treatment and the effective rate. Secondary outcomes were scores on the McGill pain questionnaire and adverse event rate. A total of 7 RCTs comprising 752 patients were included. The VAS pain score was significantly lower at 1 month [mean difference (MD)=−2.31; 95% CI: −3.06, −1.56; P<0.00001)], 2 months (MD=−2.18; 95% CI: −2.24, −2.11; P<0.00001) and 3 months (MD=−1.93; 95% CI: −3.05, −0.82; P=0.0007) after treatment, the effective rate was significantly higher (odds ratio=2.9; 95% CI: 1.71, 4.13; P<0.0001) and scores on the McGill pain questionnaire were significantly lower (MD=−10.93; 95% CI: −21.02, −0.83; Z=2.12; P=0.03) in patients who received BTX-A for post-herpetic neuralgia compared to those who received lidocaine. There was no difference in the adverse event rate between treatments. In conclusion, BTX-A has potential as a safe and effective treatment option for post-herpetic neuralgia. Further large and well-designed RCTs are required to confirm this conclusion. |
format | Online Article Text |
id | pubmed-6966161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-69661612020-01-31 Botulinum toxin A treatment for post-herpetic neuralgia: A systematic review and meta-analysis Li, Xin-Long Zeng, Xu Zeng, Shan He, Hai-Ping Zeng, Zhen Peng, Li-Lei Chen, Li-Gang Exp Ther Med Articles The present meta-analysis study aimed to investigate the safety and efficacy of local administration of botulinum toxin (BTX-A) vs. lidocaine in the treatment of post-herpetic neuralgia. A systematic search of the Cochrane Library, PubMed, Embase, Chinese National Knowledge Infrastructure, Wanfang, Chongqing VIP Information Co. and Chinese Biomedical Literature Database was performed to identify randomized controlled trials (RCTs) comparing BTX-A and lidocaine in the treatment of post-herpetic neuralgia. The primary outcomes were Visual Analogue Scale (VAS) pain scores at 1, 2 and 3 months after treatment and the effective rate. Secondary outcomes were scores on the McGill pain questionnaire and adverse event rate. A total of 7 RCTs comprising 752 patients were included. The VAS pain score was significantly lower at 1 month [mean difference (MD)=−2.31; 95% CI: −3.06, −1.56; P<0.00001)], 2 months (MD=−2.18; 95% CI: −2.24, −2.11; P<0.00001) and 3 months (MD=−1.93; 95% CI: −3.05, −0.82; P=0.0007) after treatment, the effective rate was significantly higher (odds ratio=2.9; 95% CI: 1.71, 4.13; P<0.0001) and scores on the McGill pain questionnaire were significantly lower (MD=−10.93; 95% CI: −21.02, −0.83; Z=2.12; P=0.03) in patients who received BTX-A for post-herpetic neuralgia compared to those who received lidocaine. There was no difference in the adverse event rate between treatments. In conclusion, BTX-A has potential as a safe and effective treatment option for post-herpetic neuralgia. Further large and well-designed RCTs are required to confirm this conclusion. D.A. Spandidos 2020-02 2019-12-09 /pmc/articles/PMC6966161/ /pubmed/32010269 http://dx.doi.org/10.3892/etm.2019.8301 Text en Copyright: © Li et al. This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Li, Xin-Long Zeng, Xu Zeng, Shan He, Hai-Ping Zeng, Zhen Peng, Li-Lei Chen, Li-Gang Botulinum toxin A treatment for post-herpetic neuralgia: A systematic review and meta-analysis |
title | Botulinum toxin A treatment for post-herpetic neuralgia: A systematic review and meta-analysis |
title_full | Botulinum toxin A treatment for post-herpetic neuralgia: A systematic review and meta-analysis |
title_fullStr | Botulinum toxin A treatment for post-herpetic neuralgia: A systematic review and meta-analysis |
title_full_unstemmed | Botulinum toxin A treatment for post-herpetic neuralgia: A systematic review and meta-analysis |
title_short | Botulinum toxin A treatment for post-herpetic neuralgia: A systematic review and meta-analysis |
title_sort | botulinum toxin a treatment for post-herpetic neuralgia: a systematic review and meta-analysis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6966161/ https://www.ncbi.nlm.nih.gov/pubmed/32010269 http://dx.doi.org/10.3892/etm.2019.8301 |
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