PMID- 34251756 OWN - NLM STAT- MEDLINE DCOM- 20221230 LR - 20230215 IS - 2151-4658 (Electronic) IS - 2151-464X (Linking) VI - 75 IP - 1 DP - 2023 Jan TI - Efficacy and Safety of Tramadol for Knee or Hip Osteoarthritis: A Systematic Review and Network Meta-Analysis of Randomized Controlled Trials. PG - 158-165 LID - 10.1002/acr.24750 [doi] AB - OBJECTIVE: To examine efficacy and safety of tramadol for knee or hip osteoarthritis (OA). METHODS: PubMed, Embase, Cochrane Library, and Web of Science were searched up to May 2020 for randomized controlled trials (RCTs) comparing any of the following interventions: tramadol 100 mg/day, 200 mg/day, and 300 mg/day, and placebo for knee or hip OA. Pain and function were measured at or near 12 weeks for efficacy. Gastrointestinal, cardiovascular, and central nervous system (CNS) adverse events (AEs), and withdrawals were measured for safety. Bayesian network meta-analysis was conducted. RESULTS: Six RCTs (3,611 participants) were included. Tramadol 100 mg/day (standardized mean difference [SMD] -0.16 [95% confidence interval (95% CI) -0.34, 0.00]), 200 mg/day (SMD -0.21 [95% CI -0.37, -0.06]), and 300 mg/day (SMD -0.30 [95% CI -0.48, -0.14]) were statistically more effective than placebo in pain relief, but only tramadol 300 mg/day was better than placebo in functional improvement (SMD -0.24 [95% CI -0.47, -0.03]). Tramadol 100 mg/day (relative risk [RR] 2.29 [95% credible interval (CrI) 1.22, 4.25]), 200 mg/day (RR 4.35 [95% CrI 2.31, 8.01]), and 300 mg/day (RR 6.02 [95% CrI 3.22, 11.1]) involved a higher risk of gastrointestinal AEs. Similarly, tramadol 100-300 mg/day showed a higher risk of CNS AEs and withdrawals. However, the risk of cardiovascular AEs remained unclear. CONCLUSION: Only tramadol 300 mg/day showed minimal improvement in pain and function but with increasing AEs compared with placebo. Tramadol may not be sufficiently recommended for knee or hip OA based on the presented evidence, especially in patients with the risk of gastrointestinal and CNS AEs. CI - (c) 2021 American College of Rheumatology. FAU - Zhang, Xiurui AU - Zhang X AUID- ORCID: 0000-0002-5033-2084 AD - Xiangya Hospital, Central South University, Changsha, Hunan, China. FAU - Li, Xiaoxiao AU - Li X AD - Hunan Key Laboratory of Joint Degeneration and Injury, Changsha, Hunan, China. FAU - Xiong, Yilin AU - Xiong Y AD - Xiangya Hospital, Central South University, Changsha, Hunan, China. FAU - Wang, Yilun AU - Wang Y AD - Xiangya Hospital, Central South University, Changsha, Hunan, China. FAU - Wei, Jie AU - Wei J AD - Xiangya Hospital, Central South University, Changsha, Hunan, China. FAU - Zeng, Chao AU - Zeng C AD - Hunan Key Laboratory of Joint Degeneration and Injury and Xiangya Hospital, Central South University, Changsha, Hunan, China. FAU - Sha, Tingting AU - Sha T AD - Hunan Key Laboratory of Joint Degeneration and Injury, Changsha, Hunan, China. FAU - Lei, Guanghua AU - Lei G AUID- ORCID: 0000-0003-2987-138X AD - Hunan Key Laboratory of Joint Degeneration and Injury and Xiangya Hospital, Central South University, Changsha, Hunan, China. LA - eng PT - Journal Article PT - Meta-Analysis PT - Research Support, Non-U.S. Gov't PT - Systematic Review DEP - 20220823 PL - United States TA - Arthritis Care Res (Hoboken) JT - Arthritis care & research JID - 101518086 RN - 39J1LGJ30J (Tramadol) SB - IM MH - Humans MH - *Osteoarthritis, Hip/diagnosis/drug therapy MH - *Tramadol/adverse effects MH - *Osteoarthritis, Knee/diagnosis/drug therapy MH - Network Meta-Analysis MH - Randomized Controlled Trials as Topic MH - Pain EDAT- 2021/07/13 06:00 MHDA- 2022/12/31 06:00 CRDT- 2021/07/12 13:18 PHST- 2021/06/09 00:00 [revised] PHST- 2020/11/23 00:00 [received] PHST- 2021/07/08 00:00 [accepted] PHST- 2021/07/13 06:00 [pubmed] PHST- 2022/12/31 06:00 [medline] PHST- 2021/07/12 13:18 [entrez] AID - 10.1002/acr.24750 [doi] PST - ppublish SO - Arthritis Care Res (Hoboken). 2023 Jan;75(1):158-165. doi: 10.1002/acr.24750. Epub 2022 Aug 23.