Bristol-Myers Squibb, 5 Research Parkway, Wallingford, CT 06492, USA.
Bipolar Disord. 2011 Mar;13(2):133-44. doi: 10.1111/j.1399-5618.2011.00898.x.
To evaluate the efficacy and safety of aripiprazole (ARI) adjunctive to lithium (Li) or valproate (Val) (ARI+Li / Val) compared with placebo (PLB) adjunctive to Li or Val (PLB+Li / Val) as maintenance therapy for patients with bipolar I disorder who had an inadequate response to Li or Val monotherapy.
Patients with a current manic/mixed episode received Li or Val for at least 2 weeks. Those with an inadequate response [Young Mania Rating Scale (YMRS) total score ≥ 16 and ≤ 35% decrease from baseline at 2 weeks] received adjunctive single-blind ARI plus mood stabilizer. Patients who achieved stability [YMRS and Montgomery-Åsberg Depression Rating Scale (MADRS) score ≤ 12] for 12 consecutive weeks were randomized to double-blind ARI (10-30 mg/day) or PLB+Li / Val. Relapse was monitored for 52 weeks. Adverse events (AEs) were also evaluated.
A total of 337 patients were randomized to ARI+ Li / Val (n=168) or PLB+Li / Val (n=169). The Kaplan-Meier relapse rate at 52 weeks was 17% with ARI+Li / Val and 29% with PLB+Li / Val. ARI+Li / Val significantly delayed time to any relapse compared with PLB+Li / Val; hazard ratio=0.54 (95% confidence interval: 0.33-0.89; log-rank p=0.014). The most common AEs ≥ 5%(ARI+Li / Val versus PLB+Li / Val) were headache (13.2% versus 10.8%), weight increase (9.0% versus 6.6%), tremor (6.0% versus 2.4%), and insomnia (5.4% versus 9.6%).
Continuation of ARI+Li / Val treatment increased the time to relapse to any mood episode compared with Li or Val monotherapy, and was relatively well tolerated during the one-year study. These findings suggest that there is a long-term benefit in continuing ARI adjunctive to a mood stabilizer after sustained remission is achieved.
评估阿立哌唑(ARI)联合锂(Li)或丙戊酸(Val)(ARI+Li/Val)与安慰剂(PLB)联合 Li 或 Val(PLB+Li/Val)作为双相 I 型障碍患者的维持治疗的疗效和安全性,这些患者对 Li 或 Val 单药治疗反应不足。
当前有躁狂/混合发作的患者接受 Li 或 Val 治疗至少 2 周。那些反应不足的患者[Young Mania Rating Scale(YMRS)总分≥16 且自基线 2 周后降低≤35%]接受单盲 ARI 联合心境稳定剂辅助治疗。连续 12 周达到稳定[YMRS 和 Montgomery-Åsberg 抑郁评定量表(MADRS)评分≤12]的患者随机接受双盲 ARI(10-30mg/天)或 PLB+Li/Val。监测 52 周的复发情况。还评估了不良事件(AE)。
共有 337 名患者被随机分配至 ARI+Li/Val(n=168)或 PLB+Li/Val(n=169)组。52 周时,ARI+Li/Val 组的复发率为 17%,PLB+Li/Val 组为 29%。ARI+Li/Val 组与 PLB+Li/Val 组相比,显著延迟了任何复发的时间;风险比=0.54(95%置信区间:0.33-0.89;对数秩检验 p=0.014)。最常见的≥5%的不良事件(ARI+Li/Val 与 PLB+Li/Val)为头痛(13.2%与 10.8%)、体重增加(9.0%与 6.6%)、震颤(6.0%与 2.4%)和失眠(5.4%与 9.6%)。
与 Li 或 Val 单药治疗相比,继续 ARI+Li/Val 治疗可延长任何心境发作的复发时间,且在为期一年的研究中具有相对良好的耐受性。这些发现表明,在持续缓解后继续使用 ARI 联合心境稳定剂治疗具有长期获益。