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首页> 外文期刊>Journal of clinical psychopharmacology >Quetiapine addition to serotonin reuptake inhibitors in patients with severe obsessive-compulsive disorder: a double-blind, randomized, placebo-controlled study.
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Quetiapine addition to serotonin reuptake inhibitors in patients with severe obsessive-compulsive disorder: a double-blind, randomized, placebo-controlled study.

机译:重度强迫症患者中除喹硫平和5-羟色胺再摄取抑制剂外:一项双盲,随机,安慰剂对照研究。

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OBJECTIVE: Although many patients with obsessive-compulsive disorder (OCD) benefit from treatment with serotonin reuptake inhibitors (SRIs), it is estimated that 40% to 60% of them do not respond. The objective of the present study was to evaluate the efficacy of quetiapine added to baseline treatment with SRIs for the treatment of OCD in severely ill adult subjects. METHOD: Forty patients (21 men, 19 women) with primary OCD according to Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition criteria participated in a 12-week, double-blind, placebo-controlled trial. They were randomly assigned to dosages of quetiapine titrated up to 400 mg/d (n = 20) or to placebo (n = 20) in addition to their SRI treatment. During the continuation phase (weeks 6-12), subjects received different dosages between 400 and 600 mg/d depending on clinical response. At entry, all patients were unresponsive to at least 1 course of at least 12 weeks of treatment with SRIs at defined doses. The total Yale-Brown Obsessive-Compulsive Scale score was the primary efficacy parameter. RESULTS: Intention-to-treat, last-observation-carried-forward analysis demonstrated a mean +/- SD decrease in Yale-Brown Obsessive-Compulsive Scale score of 5.2 +/- 5.4 in the quetiapine group and 3.9 +/- 4.9 in the placebo group. The analysis of treatment effects between the 2 groups showed no significant difference. There were no significant group differences in any of the other self-rating scales or clinician-administered rating scales. CONCLUSIONS: In this study, augmentation of SRI treatment with quetiapine in severe OCD had no additional effect.
机译:目的:尽管许多强迫症患者都受益于5-羟色胺再摄取抑制剂(SRIs)的治疗,但据估计其中有40%至60%的患者没有反应。本研究的目的是评估喹硫平加用SRI基线治疗对重症成年受试者强迫症的疗效。方法:根据《精神障碍诊断和统计手册》第四版标准,四十名原发性强迫症患者(21名男性,19名女性)参加了为期12周的双盲,安慰剂对照试验。除了他们的SRI治疗外,他们被随机分配至滴定至400 mg / d(n = 20)的喹硫平剂量或安慰剂(n = 20)。在延续阶段(第6-12周),根据临床反应,受试者接受400至600 mg / d的不同剂量。入院时,所有患者对使用定义剂量的SRI至少12周的至少1个疗程无反应。耶鲁-布朗强迫症量表总分是主要的疗效参数。结果:意向性治疗,最后观察进行的分析表明,喹硫平组的耶鲁-布朗强迫症量表得分平均+/- SD降低了5.2 +/- 5.4,而喹硫平组为3.9 +/- 4.9。安慰剂组。两组之间的治疗效果分析无显着差异。在其他任何自评量表或临床医生管理的评量表中,组间均无显着差异。结论:在这项研究中,喹硫平在严重强迫症患者中增强SRI治疗没有其他作用。

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