首页> 外文期刊>The American journal of geriatric psychiatry: official journal of the American Association for Geriatric Psychiatry >Randomized, double-blind study of the efficacy and tolerability of extended release quetiapine fumarate (quetiapine XR) monotherapy in elderly patients with major depressive disorder
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Randomized, double-blind study of the efficacy and tolerability of extended release quetiapine fumarate (quetiapine XR) monotherapy in elderly patients with major depressive disorder

机译:延缓释放富马酸喹硫平(喹硫平XR)单药治疗重度抑郁症老年患者的疗效和耐受性的随机,双盲研究

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Objectives: This study assessed the efficacy and tolerability of once-daily extended release quetiapine fumarate (quetiapine XR) monotherapy in elderly patients with major depressive disorder (MDD). Design: An 11-week (9-week randomized; 2-week posttreatment phase), double-blind, placebo-controlled, Phase III study (D1448C00014). Setting: A total of 53 centers in Argentina, Estonia, Finland, Russia, Ukraine, and the United States. Participants: A total of 338 patients (Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition diagnosis of MDD, age ≥66 years, Hamilton Rating Scale for Depression [HAM-D] total score ≥22, HAM-D Item 1 [depressed mood] score ≥2) were randomized (mean age: 71.3 years). Intervention: Patients were randomized to quetiapine XR (n = 166; flexible-dosing 50e300 mg/ day) or placebo (n = 172). Measurements: Primary outcome was Montgomery ?sberg Depression Rating Scale (MADRS) total score change from randomization at Week 9. Results: At Week 9, quetiapine XR (least squares [LS] means: -16.33, standard error [SE]: 0.95; mean change: -16.0, standard deviation [SD]: 9.3) significantly reduced MADRS total score from randomization versus placebo (LS means [SE]: -8.79 [0.94]; mean [SD]: -9.0 [9.9]); significant improvements were also seen at Week 1 (LS means [SE]: -4.65 [0.53] versus -2.56 [0.53], respectively; mean [SD]: -4.3 [5.1] versus -2.4 [3.7], respectively). At Week 9, secondary outcome variables significantly improved with quetiapine XR versus placebo, including MADRS response (≥50% reduction in total score); MADRS remission (total score ≤8); HAM-D total, HAM-A total, HAM-A psychic and somatic cluster, and Clinical Global ImpressionseSeverityof Illness (CGI-S) total scores; proportion of patients with CGI-Improvement score of 2 or less; Q-LES-Q-SF% maximum total, Pittsburgh Sleep Quality Index global, and pain Visual Analog Scale scores. Common adverse events (>10% patients with quetiapine XR) were somnolence, headache, dry mouth, and dizziness. Conclusion: In elderly patients with MDD, quetiapine XR monotherapy (50-300 mg/day, flexibly dosed) is effective at improving depressive symptoms, with symptom improvement observed as early as Week 1. Overall tolerability and safety were consistent with the known profile of quetiapine.
机译:目的:本研究评估了每日一次缓释富马酸喹硫平(quetiapine XR)单药治疗老年重症抑郁症(MDD)的疗效和耐受性。设计:一项为期11周(9周随机;治疗2周)的双盲,安慰剂对照的III期研究(D1448C00014)。地点:在阿根廷,爱沙尼亚,芬兰,俄罗斯,乌克兰和美国共有53个中心。参与者:338名患者(《精神障碍诊断和统计手册》,第四版MDD诊断,年龄≥66岁,汉密尔顿抑郁量表[HAM-D]总分≥22,HAM-D项目1 [情绪低落]得分≥2)被随机分配(平均年龄:71.3岁)。干预措施:患者被随机分配到喹硫平XR(n = 166;灵活剂量50e300 mg /天)或安慰剂(n = 172)中。测量:主要结果为蒙哥马利抑郁评分量表(MADRS)在第9周随机化后的总评分变化。结果:在第9周,喹硫平XR(最小二乘法[LS]表示:-16.33,标准误[SE]:0.95;平均变化:-16.0,标准差[SD]:9.3),与安慰剂相比,随机分组的MADRS总分明显降低(LS平均值[SE]:-8.79 [0.94];平均值[SD]:-9.0 [9.9]);在第1周也看到了显着的改善(LS分别为[SE]:-4.65 [0.53]和-2.56 [0.53];平均值[SD]:分别为-4.3 [5.1]和-2.4 [3.7])。在第9周,喹硫平XR与安慰剂相比,次要结局变量显着改善,包括MADRS反应(总得分降低≥50%); MADRS缓解(总分≤8); HAM-D总分,HAM-A总分,HAM-A心理和躯体分类以及临床总体印象疾病严重程度(CGI-S)总分; CGI改善评分不超过2的患者比例; Q-LES-Q-SF%最大总数,匹兹堡睡眠质量指数总体和疼痛视觉模拟量表得分。常见的不良事件(> 10%的喹硫平XR患者)为嗜睡,头痛,口干和头晕。结论:在患有MDD的老年患者中,喹硫平XR单一疗法(50-300 mg /天,灵活剂量)可有效改善抑郁症状,最早在第1周即可观察到症状改善。喹硫平。

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