Oya Kazuto, Sakuma Kenji, Esumi Satoru, Hashimoto Yasuhiko, Hatano Masakazu, Matsuda Yuki, Matsui Yuki, Miyake Nobumi, Nomura Ikuo, Okuya Makoto, Iwata Nakao, Kato Masaki, Hashimoto Ryota, Mishima Kazuo, Watanabe Norio, Kishi Taro
Department of Psychiatry, Fujita Health University School of Medicine, Toyoake, Japan.
Department of Pharmacy, Okayama University Hospital, Okayama, Japan.
Neuropsychopharmacol Rep. 2019 Sep;39(3):241-246. doi: 10.1002/npr2.12056. Epub 2019 Apr 26.
Whether patients with adult bipolar disorder (BD) who have been clinically stabilized with lithium or lamotrigine should continue this medication is not established fully. This systematic review and meta-analysis evaluated the efficacy and safety of lithium and lamotrigine for maintenance treatment in clinically stable patients with adult BD.
This meta-analysis included only double-blind, randomized, placebo-controlled trials with an enrichment design that selected patients who responded acutely to lithium or lamotrigine. Reports prior to November 15, 2018, were retrieved from the PubMed/Cochrane Library/Embase. The primary outcome was the relapse rate due to any mood episode at the study endpoint. Other outcomes were relapse rates due to a manic/hypomanic/mixed episode or depression at the study endpoint, discontinuation rate, death, and death by suicide. Risk ratios (RRs) (95% confidence intervals) were calculated. When the random-effects model showed significant differences between groups, the number-needed-to-treat (NNT) was estimated.
The search retrieved two studies regarding lithium (N = 218) and four evaluating lamotrigine (N = 706). Both drugs were superior to placebo for reducing the relapse rate due to any mood episode [lithium: RR = 0.52 (0.41-0.66), P < 0.00001, I = 0%, NNT = 2.3 (1.6-4.2); lamotrigine: RR = 0.81 (0.70-0.93), P = 0.004, I = 0%, NNT = 8.3 (5.0-25.0)] and all-cause discontinuation. There were no significant differences in other outcomes between lithium or lamotrigine and the placebo groups.
Both drugs showed benefit for preventing relapse in clinically stable patients with adult BD. However, the number of studies and patients in this analysis was small.
对于已通过锂盐或拉莫三嗪实现临床稳定的成年双相情感障碍(BD)患者是否应继续使用该药物,目前尚未完全明确。本系统评价和荟萃分析评估了锂盐和拉莫三嗪在成年BD临床稳定患者维持治疗中的疗效和安全性。
本荟萃分析仅纳入采用富集设计的双盲、随机、安慰剂对照试验,这些试验选取了对锂盐或拉莫三嗪有急性反应的患者。检索了2018年11月15日前来自PubMed/考克兰图书馆/Embase的报告。主要结局是研究终点时因任何情绪发作导致的复发率。其他结局包括研究终点时因躁狂/轻躁狂/混合发作或抑郁导致的复发率、停药率、死亡率以及自杀死亡率。计算风险比(RRs)(95%置信区间)。当随机效应模型显示组间存在显著差异时,估算需治疗人数(NNT)。
检索到两项关于锂盐的研究(N = 218)和四项评估拉莫三嗪的研究(N = 706)。两种药物在降低因任何情绪发作导致的复发率方面均优于安慰剂[锂盐:RR = 0.52(0.41 - 0.66),P < 0.00001,I² = 0%,NNT = 2.3(1.6 - 4.2);拉莫三嗪:RR = 0.81(0.70 - 0.93),P = 0.004,I² = 0%,NNT = 8.3(5.0 - 25.0)]以及全因停药率。锂盐或拉莫三嗪组与安慰剂组在其他结局方面无显著差异。
两种药物在预防成年BD临床稳定患者复发方面均显示出益处。然而,本分析中的研究数量和患者数量较少。