PMID- 33844010 OWN - NLM STAT- MEDLINE DCOM- 20220401 LR - 20220401 IS - 1526-4637 (Electronic) IS - 1526-2375 (Linking) VI - 23 IP - 2 DP - 2022 Feb 1 TI - The Efficacy, Adverse Events, and Withdrawal Rates of the Pharmacological Management of Chronic Spinal Cord Injury Pain: A Systematic Review and Meta-Analysis. PG - 375-395 LID - 10.1093/pm/pnab140 [doi] AB - OBJECTIVE: To establish the efficacy of medications, incidence of adverse events (AEs), and withdrawal rates associated with the pharmacological management of chronic spinal cord injury pain. METHODOLOGY: PubMed, MEDLINE, Embase, CINAHL, Web of Science, CENTRAL, and PsycINFO were searched (November 2017) and updated (January 2020). Two independent review authors screened and identified papers for inclusion. RESULTS: Twenty-one studies met inclusion requirements for efficacy analysis and 17 for AE and withdrawal rate analysis; no additional papers were included from the updated 2020 search. Treatments were divided into six categories: anticonvulsants (n = 6), antidepressants (n = 3), analgesics (n = 8), anti-spasticity medications (n = 2), cannabinoids (n = 1), and other (n = 2). Trials of anticonvulsants, antidepressants, and cannabinoids included long-term follow-up trials (2 weeks to 4 months), and trials of analgesics and anti-spasticity medications, among others, were short-term trials (0-2 days). Effectiveness for neuropathic pain was found for pregabalin (3/3 studies) and lidocaine (2/3 studies). Studies using ketamine also reported effectiveness (2/2), but the quality of these papers was rated as poor. The most frequently reported AEs included dizziness, dry mouth, nausea, and constipation. Pregabalin was associated with a higher risk of somnolence (risk ratio [RR] 3.15, 95% confidence interval [CI]: 2.00-4.98) and dizziness (RR 2.9, 95% CI: 1.58-5.30). Ketamine was associated with a higher risk of reduced vision (RR 9.00, 95% CI: 0.05-146.11), dizziness (RR 8.33, 95% CI: 1.73-40.10), and somnolence (RR 7.00, 95% CI: 1.73-40.1). Withdrawal rates ranged from 18.4% for antidepressants to 0-30% for anticonvulsants, 0-10% for anti-spasticity medications, 0-48% for analgesics, 28.6% for cannabinoids, and 0-22.2% for other medications. CONCLUSION: Pregabalin was found to be effective for neuropathic pain vs placebo. Cannabinoids were ineffective for neuropathic pain. AEs are a common cause for withdrawal. The nature of AEs was poorly reported, and AE reporting should be improved in future randomized controlled trials. CI - (c) The Author(s) 2021. Published by Oxford University Press on behalf of the American Academy of Pain Medicine. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. FAU - Canavan, Clare AU - Canavan C AD - UCD Centre for Translational Pain Research. AD - UCD School of Public Health, Physiotherapy and Sports Science, University College Dublin, Belfield Campus, Dublin, Ireland. FAU - Inoue, Takayoshi AU - Inoue T AUID- ORCID: 0000-0002-1531-2395 AD - UCD Centre for Translational Pain Research. FAU - McMahon, Sinead AU - McMahon S AD - UCD School of Public Health, Physiotherapy and Sports Science, University College Dublin, Belfield Campus, Dublin, Ireland. FAU - Doody, Catherine AU - Doody C AD - UCD Centre for Translational Pain Research. AD - UCD School of Public Health, Physiotherapy and Sports Science, University College Dublin, Belfield Campus, Dublin, Ireland. FAU - Blake, Catherine AU - Blake C AD - UCD Centre for Translational Pain Research. AD - UCD School of Public Health, Physiotherapy and Sports Science, University College Dublin, Belfield Campus, Dublin, Ireland. FAU - Fullen, Brona M AU - Fullen BM AD - UCD Centre for Translational Pain Research. AD - UCD School of Public Health, Physiotherapy and Sports Science, University College Dublin, Belfield Campus, Dublin, Ireland. LA - eng PT - Journal Article PT - Meta-Analysis PT - Systematic Review PL - England TA - Pain Med JT - Pain medicine (Malden, Mass.) JID - 100894201 RN - 0 (Analgesics) RN - 55JG375S6M (Pregabalin) SB - IM MH - Analgesics/adverse effects MH - *Chronic Pain/drug therapy MH - Humans MH - Nausea MH - Pregabalin MH - *Spinal Cord Injuries/complications/drug therapy EDAT- 2021/04/13 06:00 MHDA- 2022/04/02 06:00 CRDT- 2021/04/12 12:44 PHST- 2021/04/13 06:00 [pubmed] PHST- 2022/04/02 06:00 [medline] PHST- 2021/04/12 12:44 [entrez] AID - 6222194 [pii] AID - 10.1093/pm/pnab140 [doi] PST - ppublish SO - Pain Med. 2022 Feb 1;23(2):375-395. doi: 10.1093/pm/pnab140.