PMID- 31437480 OWN - NLM STAT- MEDLINE DCOM- 20210104 LR - 20210104 IS - 1878-4216 (Electronic) IS - 0278-5846 (Linking) VI - 96 DP - 2020 Jan 10 TI - Efficacy of 3,4-methylenedioxymethamphetamine (MDMA)-assisted psychotherapy for posttraumatic stress disorder: A systematic review and meta-analysis. PG - 109735 LID - S0278-5846(19)30148-4 [pii] LID - 10.1016/j.pnpbp.2019.109735 [doi] AB - BACKGROUND: Posttraumatic stress disorder (PTSD) is a common psychiatric condition that can develop following a traumatic experience. PTSD is associated with significant disability, a large economic burden, and despite the range of therapies to treat PTSD, response to antidepressants is limited. A growing body of clinical research suggests the efficacy of 3,4-methylenedioxymethamphetamine (MDMA)-assisted psychotherapy in individuals with treatment-refractory PTSD. AIM: To assess the effectiveness and safety of MDMA-assisted psychotherapy for reducing symptoms of PTSD, a systematic review and meta-analysis was undertaken. METHODS: Six online databases were searched from inception to December 2018. Reference lists of relevant articles were manually searched as well as electronic sources of ongoing trials and conference proceedings. Researchers active in the subject were also contacted. Eligible studies included randomized and quasi-randomized clinical trials using MDMA-assisted psychotherapy for PTSD in comparison with other medications, placebo or no medication (supportive care). We used standard methodological procedures expected by the Cochrane Collaboration. Two authors assessed studies for inclusion and extracted data. Using random-effects meta-analysis with Cochrane's Review Manager 5.3, we obtained standardized mean differences [SMD] and rate ratios [RR] for reduction in PTSD symptomatology. RESULTS: A total of 5 trials met inclusion criteria, totaling 106 participants (average age: 35-40 years, 70% female). Studies were rated as moderate in quality. MDMA-assisted psychotherapy demonstrated a high rate of clinical response (RR = 3.47, 95% CI: 1.70, 7.06), remission (RR = 2.63, 95% CI: 1.37, 5.02), with a large effect size at reducing the symptoms of PTSD (SMD = 1.30, 95% CI: 0.66, 1.94). Available evidence indicates that MDMA was well-tolerated, with few serious adverse events reported across studies. CONCLUSIONS: MDMA-assisted psychotherapy appears to be a potentially safe, effective, and durable treatment for individuals with chronic, treatment-refractory PTSD. However, future studies involving larger samples and longer durations of treatment and follow-up are warranted-and underway. CI - Copyright (c) 2019 Elsevier Inc. All rights reserved. FAU - Bahji, Anees AU - Bahji A AD - Department of Psychiatry, Queen's University, Kingston, Ontario, Canada; Department of Public Health Sciences, Queen's University, Kingston, Ontario, Canada. Electronic address: 0ab104@queensu.ca. FAU - Forsyth, Ashleigh AU - Forsyth A AD - Department of Psychiatry, Queen's University, Kingston, Ontario, Canada; Providence Care Hospital, Kingston, Ontario, Canada. FAU - Groll, Dianne AU - Groll D AD - Department of Psychiatry, Queen's University, Kingston, Ontario, Canada. FAU - Hawken, Emily R AU - Hawken ER AD - Department of Psychiatry, Queen's University, Kingston, Ontario, Canada; Providence Care Hospital, Kingston, Ontario, Canada. LA - eng PT - Journal Article PT - Meta-Analysis PT - Systematic Review DEP - 20190819 PL - England TA - Prog Neuropsychopharmacol Biol Psychiatry JT - Progress in neuro-psychopharmacology & biological psychiatry JID - 8211617 RN - 0 (Adrenergic Uptake Inhibitors) RN - 0 (Antidepressive Agents) RN - KE1SEN21RM (N-Methyl-3,4-methylenedioxyamphetamine) SB - IM MH - Adrenergic Uptake Inhibitors/*administration & dosage MH - Antidepressive Agents/administration & dosage MH - Cognitive Behavioral Therapy/methods MH - Combined Modality Therapy/methods MH - Humans MH - N-Methyl-3,4-methylenedioxyamphetamine/*administration & dosage MH - Psychotherapy/*methods MH - Randomized Controlled Trials as Topic/methods MH - Stress Disorders, Post-Traumatic/diagnosis/*psychology/*therapy MH - Treatment Outcome EDAT- 2019/08/23 06:00 MHDA- 2021/01/05 06:00 CRDT- 2019/08/23 06:00 PHST- 2019/02/19 00:00 [received] PHST- 2019/06/27 00:00 [revised] PHST- 2019/08/10 00:00 [accepted] PHST- 2019/08/23 06:00 [pubmed] PHST- 2021/01/05 06:00 [medline] PHST- 2019/08/23 06:00 [entrez] AID - S0278-5846(19)30148-4 [pii] AID - 10.1016/j.pnpbp.2019.109735 [doi] PST - ppublish SO - Prog Neuropsychopharmacol Biol Psychiatry. 2020 Jan 10;96:109735. doi: 10.1016/j.pnpbp.2019.109735. Epub 2019 Aug 19.