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The efficacy and safety of moxibustion for chronic fatigue syndrome: A protocol for systematic review and meta-analysis

BACKGROUND: The pathogenesis of chronic fatigue syndrome (CFS) is not clear. The main purpose of treatment is to improve autoimmune function and relieve fatigue symptoms. Moxibustion is often used to treat diseases caused by low autoimmunity, especially in relieving fatigue symptoms. It is a superio...

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Autores principales: Xue, Kaiyang, Wang, Yanping, Wang, Xianzhu, Chen, Pingnan, Xiao, Caihong, Fu, Jing, Cui, Jin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104202/
https://www.ncbi.nlm.nih.gov/pubmed/33950958
http://dx.doi.org/10.1097/MD.0000000000025742
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author Xue, Kaiyang
Wang, Yanping
Wang, Xianzhu
Chen, Pingnan
Xiao, Caihong
Fu, Jing
Cui, Jin
author_facet Xue, Kaiyang
Wang, Yanping
Wang, Xianzhu
Chen, Pingnan
Xiao, Caihong
Fu, Jing
Cui, Jin
author_sort Xue, Kaiyang
collection PubMed
description BACKGROUND: The pathogenesis of chronic fatigue syndrome (CFS) is not clear. The main purpose of treatment is to improve autoimmune function and relieve fatigue symptoms. Moxibustion is often used to treat diseases caused by low autoimmunity, especially in relieving fatigue symptoms. It is a superior therapy for CFS in traditional Chinese medicine. At present, there is a lack of the high level clinical evidence to support the moxibustion in the treatment of CFS, so this study will systematically review and analyze the currently available randomized controlled trials to evaluate the efficacy and safety of moxibustion in the treatment of CFS. METHODS: We will systematically search PubMed, EMBASE, Cochrane library, Sinomed, CNKI, VIP, and Wanfang Database, ClinicalTrials.gov and Chinese Clinical Trial Registry will also be searched. The time range for the search will be from database activation to March 31, 2021. The randomized controlled trials (RCTs) associated with moxibustion for CFS will be included, regardless of language. We will use the standard proposed in Cochrane Handbook 5.1.0 to assess the bias risk of a single RCT. The main outcome index of the study is Fatigue Assessment Instrument (FAI), secondary outcome indexes will include Fatigue Scale -14 (FS-14), Fatigue Severity Scale (FSS), Pittsburgh sleep quality index (PSQI), natural killer (NK) cells, interleukin- 2 (IL-2), T lymphocyte subsets (CD(4)(+), CD(8)(+)), cure rate, total efficiency and adverse reactions. The random effect model meta was used to analyze the effect data of a single RCT. Heterogeneity will be measured by Cochran Q test and I-squared statistics. We will use 2 subgroup analyses to explore the source of heterogeneity. RCTs with high bias risk was excluded and adjustment effect model was used for sensitivity analysis to test the robustness of the meta-analysis results. The publication bias included in RCTs will be assessed by funnel plot and Egger test. RESULTS: This study will objectively and comprehensively evaluate the efficacy and safety of randomized controlled trials of moxibustion in the treatment of chronic fatigue syndrome, and the results will be submitted to peer-reviewed journals for publication. CONCLUSION: This systematic review will provide clinicians with the latest high-quality evidence for the use of moxibustion in the treatment of chronic fatigue syndrome. INPLASY REGISTRATION NUMBER: INPLASY202140063.
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spelling pubmed-81042022021-05-10 The efficacy and safety of moxibustion for chronic fatigue syndrome: A protocol for systematic review and meta-analysis Xue, Kaiyang Wang, Yanping Wang, Xianzhu Chen, Pingnan Xiao, Caihong Fu, Jing Cui, Jin Medicine (Baltimore) 3800 BACKGROUND: The pathogenesis of chronic fatigue syndrome (CFS) is not clear. The main purpose of treatment is to improve autoimmune function and relieve fatigue symptoms. Moxibustion is often used to treat diseases caused by low autoimmunity, especially in relieving fatigue symptoms. It is a superior therapy for CFS in traditional Chinese medicine. At present, there is a lack of the high level clinical evidence to support the moxibustion in the treatment of CFS, so this study will systematically review and analyze the currently available randomized controlled trials to evaluate the efficacy and safety of moxibustion in the treatment of CFS. METHODS: We will systematically search PubMed, EMBASE, Cochrane library, Sinomed, CNKI, VIP, and Wanfang Database, ClinicalTrials.gov and Chinese Clinical Trial Registry will also be searched. The time range for the search will be from database activation to March 31, 2021. The randomized controlled trials (RCTs) associated with moxibustion for CFS will be included, regardless of language. We will use the standard proposed in Cochrane Handbook 5.1.0 to assess the bias risk of a single RCT. The main outcome index of the study is Fatigue Assessment Instrument (FAI), secondary outcome indexes will include Fatigue Scale -14 (FS-14), Fatigue Severity Scale (FSS), Pittsburgh sleep quality index (PSQI), natural killer (NK) cells, interleukin- 2 (IL-2), T lymphocyte subsets (CD(4)(+), CD(8)(+)), cure rate, total efficiency and adverse reactions. The random effect model meta was used to analyze the effect data of a single RCT. Heterogeneity will be measured by Cochran Q test and I-squared statistics. We will use 2 subgroup analyses to explore the source of heterogeneity. RCTs with high bias risk was excluded and adjustment effect model was used for sensitivity analysis to test the robustness of the meta-analysis results. The publication bias included in RCTs will be assessed by funnel plot and Egger test. RESULTS: This study will objectively and comprehensively evaluate the efficacy and safety of randomized controlled trials of moxibustion in the treatment of chronic fatigue syndrome, and the results will be submitted to peer-reviewed journals for publication. CONCLUSION: This systematic review will provide clinicians with the latest high-quality evidence for the use of moxibustion in the treatment of chronic fatigue syndrome. INPLASY REGISTRATION NUMBER: INPLASY202140063. Lippincott Williams & Wilkins 2021-05-07 /pmc/articles/PMC8104202/ /pubmed/33950958 http://dx.doi.org/10.1097/MD.0000000000025742 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/)
spellingShingle 3800
Xue, Kaiyang
Wang, Yanping
Wang, Xianzhu
Chen, Pingnan
Xiao, Caihong
Fu, Jing
Cui, Jin
The efficacy and safety of moxibustion for chronic fatigue syndrome: A protocol for systematic review and meta-analysis
title The efficacy and safety of moxibustion for chronic fatigue syndrome: A protocol for systematic review and meta-analysis
title_full The efficacy and safety of moxibustion for chronic fatigue syndrome: A protocol for systematic review and meta-analysis
title_fullStr The efficacy and safety of moxibustion for chronic fatigue syndrome: A protocol for systematic review and meta-analysis
title_full_unstemmed The efficacy and safety of moxibustion for chronic fatigue syndrome: A protocol for systematic review and meta-analysis
title_short The efficacy and safety of moxibustion for chronic fatigue syndrome: A protocol for systematic review and meta-analysis
title_sort efficacy and safety of moxibustion for chronic fatigue syndrome: a protocol for systematic review and meta-analysis
topic 3800
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104202/
https://www.ncbi.nlm.nih.gov/pubmed/33950958
http://dx.doi.org/10.1097/MD.0000000000025742
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