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Nonpharmacological therapies for central poststroke pain: A systematic review

BACKGROUND: Central poststroke pain (CPSP) is a neuropathic pain syndrome that can occur after a cerebrovascular accident. It has negative effects on mood, sleep, rehabilitation, and quality of life in stroke patients. This systematic review assessed the efficacy and safety of nonpharmacological the...

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Autores principales: Xu, Xiao-Min, Luo, Hua, Rong, Ben-bing, Zheng, Xiao-Mei, Wang, Feng-tao, Zhang, Shu-Jiang, Li, Zuo-Xiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7572005/
https://www.ncbi.nlm.nih.gov/pubmed/33080696
http://dx.doi.org/10.1097/MD.0000000000022611
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author Xu, Xiao-Min
Luo, Hua
Rong, Ben-bing
Zheng, Xiao-Mei
Wang, Feng-tao
Zhang, Shu-Jiang
Li, Zuo-Xiao
author_facet Xu, Xiao-Min
Luo, Hua
Rong, Ben-bing
Zheng, Xiao-Mei
Wang, Feng-tao
Zhang, Shu-Jiang
Li, Zuo-Xiao
author_sort Xu, Xiao-Min
collection PubMed
description BACKGROUND: Central poststroke pain (CPSP) is a neuropathic pain syndrome that can occur after a cerebrovascular accident. It has negative effects on mood, sleep, rehabilitation, and quality of life in stroke patients. This systematic review assessed the efficacy and safety of nonpharmacological therapies for treating CPSP. METHODS: The Cochrane, PubMed, Embase, and Web of Science databases were systematically searched for studies from inception to August 2020. Two authors worked independently and in duplicate to identify suitable studies. RESULTS: Eleven studies were identified. Pain related to CPSP was ameliorated by precentral gyrus stimulation (P = .01), caloric vestibular stimulation (P = 0.004), transcranial direct current stimulation (P < .05), and bee venom acupuncture point injection (P = .009). Acupuncture (P = .72) and electroacupuncture therapies (P > .05) were as effective for thalamic pain as oral carbamazepine treatment. Motor cortex stimulation, but not deep brain stimulation (DBS), was effective for treating refractory CPSP, and appeared to be more effective than thalamic stimulation for controlling bulbar pain secondary to Wallenberg syndrome. However, DBS in the ventral striatum or anterior limb of the internal capsule improved depression (P = .020) and anxiety in patients with refractory CPSP. Some serious adverse events were reported in response to invasive electrical brain stimulation, but most of these effects recovered with treatment. CONCLUSIONS: Nonpharmacological therapies appear to be effective in CPSP, but the evidence is relatively weak. Invasive electrical brain stimulation can be accompanied by serious adverse events, but most patients recover from these effects.
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spelling pubmed-75720052020-10-29 Nonpharmacological therapies for central poststroke pain: A systematic review Xu, Xiao-Min Luo, Hua Rong, Ben-bing Zheng, Xiao-Mei Wang, Feng-tao Zhang, Shu-Jiang Li, Zuo-Xiao Medicine (Baltimore) 3800 BACKGROUND: Central poststroke pain (CPSP) is a neuropathic pain syndrome that can occur after a cerebrovascular accident. It has negative effects on mood, sleep, rehabilitation, and quality of life in stroke patients. This systematic review assessed the efficacy and safety of nonpharmacological therapies for treating CPSP. METHODS: The Cochrane, PubMed, Embase, and Web of Science databases were systematically searched for studies from inception to August 2020. Two authors worked independently and in duplicate to identify suitable studies. RESULTS: Eleven studies were identified. Pain related to CPSP was ameliorated by precentral gyrus stimulation (P = .01), caloric vestibular stimulation (P = 0.004), transcranial direct current stimulation (P < .05), and bee venom acupuncture point injection (P = .009). Acupuncture (P = .72) and electroacupuncture therapies (P > .05) were as effective for thalamic pain as oral carbamazepine treatment. Motor cortex stimulation, but not deep brain stimulation (DBS), was effective for treating refractory CPSP, and appeared to be more effective than thalamic stimulation for controlling bulbar pain secondary to Wallenberg syndrome. However, DBS in the ventral striatum or anterior limb of the internal capsule improved depression (P = .020) and anxiety in patients with refractory CPSP. Some serious adverse events were reported in response to invasive electrical brain stimulation, but most of these effects recovered with treatment. CONCLUSIONS: Nonpharmacological therapies appear to be effective in CPSP, but the evidence is relatively weak. Invasive electrical brain stimulation can be accompanied by serious adverse events, but most patients recover from these effects. Lippincott Williams & Wilkins 2020-10-16 /pmc/articles/PMC7572005/ /pubmed/33080696 http://dx.doi.org/10.1097/MD.0000000000022611 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 3800
Xu, Xiao-Min
Luo, Hua
Rong, Ben-bing
Zheng, Xiao-Mei
Wang, Feng-tao
Zhang, Shu-Jiang
Li, Zuo-Xiao
Nonpharmacological therapies for central poststroke pain: A systematic review
title Nonpharmacological therapies for central poststroke pain: A systematic review
title_full Nonpharmacological therapies for central poststroke pain: A systematic review
title_fullStr Nonpharmacological therapies for central poststroke pain: A systematic review
title_full_unstemmed Nonpharmacological therapies for central poststroke pain: A systematic review
title_short Nonpharmacological therapies for central poststroke pain: A systematic review
title_sort nonpharmacological therapies for central poststroke pain: a systematic review
topic 3800
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7572005/
https://www.ncbi.nlm.nih.gov/pubmed/33080696
http://dx.doi.org/10.1097/MD.0000000000022611
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