University Hospitals Cleveland Medical Center, Cleveland, OH, USA.
Otsuka Pharmaceutical Development & Commercialization, Inc., Princeton, NJ, USA.
J Affect Disord. 2018 Feb;227:649-656. doi: 10.1016/j.jad.2017.10.035. Epub 2017 Oct 24.
Effects of maintenance treatment with aripiprazole once-monthly 400mg (AOM 400) on symptoms and functioning were assessed in adults with bipolar I disorder (BP-I) after a manic episode.
Patients were stabilized on oral aripiprazole, cross-titrated to AOM 400, then randomized in a 52-week, double-blind, placebo-controlled, withdrawal phase. Prespecified secondary outcomes are reported: time to hospitalization for mood episode, Young Mania Rating Scale (YMRS), Montgomery-Åsberg Depression Rating Scale (MADRS), Clinical Global Impression-Bipolar scale, Functioning Assessment Short Test (FAST), and Brief Quality of Life in Bipolar Disorder questionnaire. Time to hospitalization for mood episode was analyzed using log-rank test and changes from baseline using mixed model for repeated measures or analysis of covariance.
AOM 400 significantly increased time to hospitalization for any mood episode versus placebo (P=0.0002). YMRS total scores decreased with oral aripiprazole; improvements were maintained with AOM 400. After randomization, YMRS scores changed little with AOM 400 but worsened with placebo (P=0.0016), and MADRS scores, already low at trial initiation, did not differ between groups. FAST score improvements were maintained with AOM 400 but not placebo (P=0.0287).
Results are generalizable to patients with BP-I stabilized on aripiprazole following a manic episode.
Patients with BP-I experiencing an acute manic episode exhibited symptomatic and functional improvements during stabilization with oral aripiprazole and AOM 400 that were maintained with continued AOM 400 treatment but not placebo. AOM 400 is the first once-monthly long-acting injectable antipsychotic to demonstrate efficacy in maintenance treatment of the manic phase of BP-I.
在单相躁狂发作后,评估了长效阿立哌唑每月 400mg(AOM 400)维持治疗对双相 I 型障碍(BP-I)成人患者的症状和功能的影响。
患者在口服阿立哌唑稳定后,交叉滴定至 AOM 400,然后进入 52 周、双盲、安慰剂对照、停药期。报告了预先指定的次要结局:心境发作住院时间、Young Mania Rating Scale(YMRS)、Montgomery-Åsberg Depression Rating Scale(MADRS)、Clinical Global Impression-Bipolar 量表、Functioning Assessment Short Test(FAST)和 Bipolar 障碍简要生活质量问卷。使用对数秩检验分析心境发作住院时间,使用混合模型重复测量或协方差分析分析从基线的变化。
与安慰剂相比,AOM 400 显著延长了任何心境发作的住院时间(P=0.0002)。口服阿立哌唑降低 YMRS 总分;AOM 400 维持改善。随机分组后,AOM 400 对 YMRS 评分的影响较小,但安慰剂组评分恶化(P=0.0016),而在试验开始时已经较低的 MADRS 评分在两组间无差异。FAST 评分的改善在 AOM 400 治疗中维持,但在安慰剂组中没有(P=0.0287)。
结果可推广至在躁狂发作后使用阿立哌唑稳定的 BP-I 患者。
经历急性躁狂发作的 BP-I 患者在口服阿立哌唑和 AOM 400 稳定治疗期间表现出症状和功能改善,继续使用 AOM 400 治疗可维持改善,但安慰剂组无改善。AOM 400 是第一个证明在 BP-I 躁狂期维持治疗中有效的每月一次的长效注射抗精神病药物。