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An Updated Systematic Review and Meta-analysis of Duloxetine for Knee Osteoarthritis Pain
We conducted the updated systematic review and meta-analysis of the best available quantitative and qualitative evidence to evaluate the effects and safety of duloxetine for the treatment of knee osteoarthritis (OA) pain. METHODS: A comprehensive literature search used 3 English and 4 Chinese biomed...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500362/ https://www.ncbi.nlm.nih.gov/pubmed/34483232 http://dx.doi.org/10.1097/AJP.0000000000000975 |
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author | Chen, Bo Duan, Jingrui Wen, Shengyue Pang, Jian Zhang, Min Zhan, Hongsheng Zheng, Yuxin |
author_facet | Chen, Bo Duan, Jingrui Wen, Shengyue Pang, Jian Zhang, Min Zhan, Hongsheng Zheng, Yuxin |
author_sort | Chen, Bo |
collection | PubMed |
description | We conducted the updated systematic review and meta-analysis of the best available quantitative and qualitative evidence to evaluate the effects and safety of duloxetine for the treatment of knee osteoarthritis (OA) pain. METHODS: A comprehensive literature search used 3 English and 4 Chinese biomedical databases from inception through July 10, 2020. We included randomized controlled trials of duloxetine with intervention duration of 2 weeks or longer for knee OA. The primary outcome was pain intensity measured by Brief Pain Inventory and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain subscale. Secondary outcome measurements included 36-Item Short Form Health Survey, Patient’s Global Impression of Improvement, Clinical Global Impressions of Severity, and adverse events (AEs). The quality of all included studies was evaluated using the Cochrane risk-of-bias criteria. The review was registered in the PROSPERO (CRD 42020194072). RESULTS: Six studies totaling 2059 patients met the eligibility criteria. Duloxetine had significant reductions in Brief Pain Inventory 24 hours average pain (mean difference [MD]=−0.74; 95% confidence interval [CI], −0.92 to −0.57; P<0.00001; I (2)=13%; 5 trials; 1695 patients); patient general activity (MD=−0.76; 95% CI, −0.96 to −0.56; P<0.00001; I (2)=0%; 5 trials; 1694 patients) WOMAC physical function subscale (MD=−4.22; 95% CI, −5.14 to −3.30; P<0.00001; I (2)=26%; 5 trials; 1986 patients); Patient’s Global Impression of Improvement (MD=−0.48; 95% CI, −0.58 to −0.37; P<0.00001; I (2)=29%; 5 trials; 1741 patients); and Clinical Global Impressions of Severity (MD=−0.34; 95% CI, −0.44 to −0.24; P<0.00001; I (2)=0%; 4 trials; 1178 patients) compared with placebo control. However, no difference on WOMAC pain subscale (standard mean difference=−1.68; 95% CI, −3.45 to 0.08; P=0.06; I (2)=100%; 3 trials; 1104 patients) and in serious AEs (risk ratio=0.92; 95% CI, 0.40-2.11; P=0.84; I (2)=0%; 5 trials; 1762 patients) between duloxetine and placebo. Furthermore, duloxetine failed to show superior effects for improving the life quality and demonstrated more treatment-emergent AEs. CONCLUSION: Duloxetine may be an effective treatment option for knee OA patients but further rigorously designed and well-controlled randomized trials are warranted. |
format | Online Article Text |
id | pubmed-8500362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-85003622021-10-13 An Updated Systematic Review and Meta-analysis of Duloxetine for Knee Osteoarthritis Pain Chen, Bo Duan, Jingrui Wen, Shengyue Pang, Jian Zhang, Min Zhan, Hongsheng Zheng, Yuxin Clin J Pain Review Articles We conducted the updated systematic review and meta-analysis of the best available quantitative and qualitative evidence to evaluate the effects and safety of duloxetine for the treatment of knee osteoarthritis (OA) pain. METHODS: A comprehensive literature search used 3 English and 4 Chinese biomedical databases from inception through July 10, 2020. We included randomized controlled trials of duloxetine with intervention duration of 2 weeks or longer for knee OA. The primary outcome was pain intensity measured by Brief Pain Inventory and the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain subscale. Secondary outcome measurements included 36-Item Short Form Health Survey, Patient’s Global Impression of Improvement, Clinical Global Impressions of Severity, and adverse events (AEs). The quality of all included studies was evaluated using the Cochrane risk-of-bias criteria. The review was registered in the PROSPERO (CRD 42020194072). RESULTS: Six studies totaling 2059 patients met the eligibility criteria. Duloxetine had significant reductions in Brief Pain Inventory 24 hours average pain (mean difference [MD]=−0.74; 95% confidence interval [CI], −0.92 to −0.57; P<0.00001; I (2)=13%; 5 trials; 1695 patients); patient general activity (MD=−0.76; 95% CI, −0.96 to −0.56; P<0.00001; I (2)=0%; 5 trials; 1694 patients) WOMAC physical function subscale (MD=−4.22; 95% CI, −5.14 to −3.30; P<0.00001; I (2)=26%; 5 trials; 1986 patients); Patient’s Global Impression of Improvement (MD=−0.48; 95% CI, −0.58 to −0.37; P<0.00001; I (2)=29%; 5 trials; 1741 patients); and Clinical Global Impressions of Severity (MD=−0.34; 95% CI, −0.44 to −0.24; P<0.00001; I (2)=0%; 4 trials; 1178 patients) compared with placebo control. However, no difference on WOMAC pain subscale (standard mean difference=−1.68; 95% CI, −3.45 to 0.08; P=0.06; I (2)=100%; 3 trials; 1104 patients) and in serious AEs (risk ratio=0.92; 95% CI, 0.40-2.11; P=0.84; I (2)=0%; 5 trials; 1762 patients) between duloxetine and placebo. Furthermore, duloxetine failed to show superior effects for improving the life quality and demonstrated more treatment-emergent AEs. CONCLUSION: Duloxetine may be an effective treatment option for knee OA patients but further rigorously designed and well-controlled randomized trials are warranted. Lippincott Williams & Wilkins 2021-11 2021-09-06 /pmc/articles/PMC8500362/ /pubmed/34483232 http://dx.doi.org/10.1097/AJP.0000000000000975 Text en Copyright © 2021 The Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Review Articles Chen, Bo Duan, Jingrui Wen, Shengyue Pang, Jian Zhang, Min Zhan, Hongsheng Zheng, Yuxin An Updated Systematic Review and Meta-analysis of Duloxetine for Knee Osteoarthritis Pain |
title | An Updated Systematic Review and Meta-analysis of Duloxetine for Knee Osteoarthritis Pain |
title_full | An Updated Systematic Review and Meta-analysis of Duloxetine for Knee Osteoarthritis Pain |
title_fullStr | An Updated Systematic Review and Meta-analysis of Duloxetine for Knee Osteoarthritis Pain |
title_full_unstemmed | An Updated Systematic Review and Meta-analysis of Duloxetine for Knee Osteoarthritis Pain |
title_short | An Updated Systematic Review and Meta-analysis of Duloxetine for Knee Osteoarthritis Pain |
title_sort | updated systematic review and meta-analysis of duloxetine for knee osteoarthritis pain |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500362/ https://www.ncbi.nlm.nih.gov/pubmed/34483232 http://dx.doi.org/10.1097/AJP.0000000000000975 |
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