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首页> 外文期刊>Journal of affective disorders >Effect of asenapine on manic and depressive symptoms in bipolar i patients with mixed episodes: Results from post hoc analyses
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Effect of asenapine on manic and depressive symptoms in bipolar i patients with mixed episodes: Results from post hoc analyses

机译:阿塞那平对混合性发作的躁郁症双相情感障碍患者的躁狂和抑郁症状的影响:事后分析的结果

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Background: The efficacy of agents useful for mania is largely unproven in patients with mixed episodes. Methods: The efficacy of asenapine in the treatment of mixed episodes was assessed using post hoc analyses on pooled data from two identically designed 3-week, randomized, double-blind, flexible dose, placebo- and olanzapine-controlled trials and their 9-week, double-blind olanzapine-controlled extension study. Efficacy was measured by changes on Young Mania Rating Scale (YMRS) and Montgomery-?sberg Depression Rating Scale (MADRS) total scores, and was analysed through analysis of covariance on observed cases of the intent-to-treat dataset. Results: In the intent-to-treat population, 295 patients had a DSM-IV-TR mixed episode (placebo: 66; olanzapine: 122; asenapine: 107) in the 3-week trials. Of these, 102 patients (olanzapine: 56; asenapine: 46) entered the 9-week extension study. At week 3, decreases in YMRS and MADRS total scores, were significantly (p<0.01) greater with asenapine (YMRS: -15.0; MADRS: -8.2) versus placebo (YMRS: -11.5; MADRS: -4.5); olanzapine did not separate from placebo (YMRS: -13.3; MADRS: -6.5). At week 12, further decreases in YMRS and MADRS total scores were observed with asenapine (YMRS: -22.4; MADRS: -11.9); non-statistically different from olanzapine (YMRS: -20.2; MADRS: -7.9). Limitations: Results are from post hoc analyses of trials that were not designed to specifically evaluate mixed episodes. Conclusions: These exploratory analyses provide supportive evidence for the efficacy of asenapine in treating the associated symptoms of mania and depression in bipolar I patients with mixed episodes.
机译:背景:对于混合发作的患者,用于躁狂症的药物的疗效尚未得到证实。方法:使用事后分析,对来自两个相同设计的3周,随机,双盲,灵活剂量,安慰剂和奥氮平对照试验及其9周的汇总数据进行事后分析,评估阿塞那平治疗混合性发作的疗效,双盲奥氮平控制的延伸研究。通过年轻躁狂评分量表(YMRS)和蒙哥马利抑郁量表(MADRS)总评分的变化来衡量疗效,并通过对意向治疗数据集的观察病例进行协方差分析来进行分析。结果:在为期3周的试验中,意向性治疗人群中有295例患者发生了DSM-IV-TR混合发作(安慰剂:66;奥氮平:122;阿塞那平:107)。在这些患者中,有102名患者(奥氮平:56;阿塞那平:46)参加了为期9周的延长研究。在第3周,与安慰剂组(YMRS:-11.5; MADRS:-4.5)相比,阿塞那平(YMRS:-15.0; MADRS:-8.2)的YMRS和MADRS总评分的下降幅度明显更大(p <0.01)。奥氮平未与安慰剂分开(YMRS:-13.3; MADRS:-6.5)。在第12周,阿塞那平的YMRS和MADRS总得分进一步下降(YMRS:-22.4; MADRS:-11.9);与奥氮平没有统计学差异(YMRS:-20.2; MADRS:-7.9)。局限性:结果来自对试验的事后分析,这些试验并非专为评估混合发作而设计。结论:这些探索性分析为阿塞那平治疗混合性发作的双相I型患者躁狂和抑郁相关症状提供了支持性证据。

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