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首页> 外文期刊>Expert opinion on pharmacotherapy >Beneficial acute antidepressant effects of aripiprazole as an adjunctive treatment or monotherapy in bipolar patients unresponsive to mood stabilizers: results from a 16-week open-label trial.
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Beneficial acute antidepressant effects of aripiprazole as an adjunctive treatment or monotherapy in bipolar patients unresponsive to mood stabilizers: results from a 16-week open-label trial.

机译:阿立哌唑作为对情绪稳定剂无反应的躁郁症患者的辅助治疗或单一疗法的有益急性抗抑郁作用:一项为期16周的开放标签试验得出的结果。

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OBJECTIVE: Several lines of research suggested that aripiprazole might be a useful treatment for acute bipolar depression. The aim of this open-label trial is to give more evidence of the clinical effectiveness and tolerability of aripiprazole in acute bipolar depression. RESEARCH DESIGN AND METHODS: Aripiprazole response was prospectively assessed for 16 weeks using the Montgomery-Asberg Depression Rating Scale (MADRS), the Clinical Global Impression Severity Scale (CGI-S), and the Young Mania Rating Scale in 85 bipolar patients with acute depression inadequately responsive to one mood stabilizer. MAIN OUTCOME MEASURES: Aripiprazole was well tolerated. Only three (3.5%) patients discontinued the study for side effects. The most common side effect was akathisia, occurring in 17/80 (21.2%) patients. Patients showed statistically insignificant weight gain (0.9 +/- 2.64 kg) over the 16-week trial. RESULTS: Patients showed a significant decrease in mean MADRS and CGI-S, and 80 (94.1%) patients completed the 16-week trial. Thirty-nine (45.8%) patients received aripiprazole as monotherapy and 46 received the drug adjunctively (54.1%). Fifty-two (65%) patients met criteria for response (>/= 50% reduction in MADRS total score), 30 (37.5%) patients met criteria for remission (final MADRS total score
机译:目的:几项研究表明,阿立哌唑可能是治疗急性双相抑郁症的有效方法。这项开放性试验的目的是为阿立哌唑在急性双相抑郁症中的临床有效性和耐受性提供更多证据。研究设计和方法:使用蒙哥马利-阿斯伯格抑郁量表(MADRS),临床总体印象严重度量表(CGI-S)和年轻躁狂症量表对85名双相情感障碍急性抑郁患者进行了前16周的阿立哌唑反应评估。对一种情绪稳定剂反应不足。主要观察指标:阿立哌唑耐受良好。只有三名(3.5%)患者因副作用而终止研究。最常见的副作用是静坐不全,发生在17/80(21.2%)患者中。在16周的试验中,患者的体重增加无统计学意义(0.9 +/- 2.64 kg)。结果:患者的平均MADRS和CGI-S显着降低,并且80位患者(94.1%)完成了16周的试验。三十九(45.8%)例患者接受阿立哌唑单药治疗,46例辅助治疗(54.1%)。五十二(65%)位患者符合缓解标准(> / = MADRS总得分降低50%),30位(37.5%)患者符合缓解标准(最终MADRS总得分

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