Department of Psychiatry, Faculty of Medicine, Chiang Mai University, 110 Inthawarorot Road, Si Phum, Mueang, Chiang Mai, 50200, Thailand.
Department of Psychiatry, Faculty of Medicine, Chiang Mai University, 110 Inthawarorot Road, Si Phum, Mueang, Chiang Mai, 50200, Thailand.
Drug Alcohol Depend. 2021 Feb 1;219:108467. doi: 10.1016/j.drugalcdep.2020.108467. Epub 2020 Dec 23.
This study aimed to compare the treatment effects of different antipsychotics for methamphetamine psychosis (MAP).
Clinical Trials, Cochrane Library, Pubmed, Scopus, and Web of Science were searched for short-term, randomized controlled trials (RCTs) from the inception to June 15, 2020. Standardized mean differences (SMDs) and odds ratios (ORs) were aggregated using random-effects pairwise comparisons and frequentist network meta-analyses (NMAs). Primary outcomes of interest were the main psychotic symptoms and dropout rates. We also rated the quality of NMA estimates.
This NMA included six RCTs of 395 patients with MAP. Six studied antipsychotics were aripiprazole, haloperidol, olanzapine, paliperidone extended-release, quetiapine, and risperidone. Risperidone is the most frequently studied antipsychotic, being investigated in four trials. Low quality of evidence was available to determine the efficacy of those antipsychotics for main psychotic symptoms. Aripiprazole was significantly inferior to olanzapine (SMD = 1.36, 95 % CI = 0.46-2.26), quetiapine (SMD = 1.13, 95 % CI = 0.28-1.98), haloperidol (SMD = 0.87, 95 % CI = 0.14-1.60), and paliperidone extended-release (SMD = 0.60, 95 % CI = 0.06-1.14). Olanzapine and quetiapine were superior to risperidone (SMD = -1.09, 95 % CI = -1.89 to -0.28 and SMD = -0.86, 95 % CI = -1.61 to -0.11, respectively). The dropout rates were not significantly different among the studied antipsychotics.
This analysis suggests that olanzapine or quetiapine may be a preferred antipsychotic for MAP, although the evidence for this was rated low-quality due to the high risk of bias or indirectness/intransitivity.
本研究旨在比较不同抗精神病药物治疗甲基苯丙胺精神病(MAP)的疗效。
检索ClinicalTrials、Cochrane Library、Pubmed、Scopus 和 Web of Science 数据库,从建库至 2020 年 6 月 15 日,纳入短期、随机对照试验(RCT)。采用随机效应模型进行二分类变量的合并,使用贝叶斯网络荟萃分析(NMA)进行连续变量的合并。主要结局指标为主要精神病症状和脱落率。我们还对 NMA 估计值的质量进行了评级。
该 NMA 共纳入 6 项 RCT,共 395 例 MAP 患者。6 种研究的抗精神病药物分别为阿立哌唑、氟哌啶醇、奥氮平、帕利哌酮长效、喹硫平和利培酮。利培酮是最常被研究的抗精神病药物,有 4 项试验对其进行了研究。由于证据质量低,我们无法确定这些抗精神病药物对主要精神病症状的疗效。阿立哌唑显著劣于奥氮平(SMD=1.36,95%CI=0.46-2.26)、喹硫平(SMD=1.13,95%CI=0.28-1.98)、氟哌啶醇(SMD=0.87,95%CI=0.14-1.60)和帕利哌酮长效(SMD=0.60,95%CI=0.06-1.14)。奥氮平和喹硫平优于利培酮(SMD=-1.09,95%CI=-1.89 至-0.28 和 SMD=-0.86,95%CI=-1.61 至-0.11)。研究中的抗精神病药物的脱落率无显著差异。
本分析表明,奥氮平或喹硫平可能是 MAP 的首选抗精神病药物,尽管由于偏倚风险高或间接性/不稳定性,证据质量被评为低质量。