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首页> 外文期刊>Human psychopharmacology: clinical and experimental >The comparison of aripiprazole and risperidone augmentation in selective serotonin reuptake inhibitor-refractory obsessive-compulsive disorder: a single-blind, randomised study
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The comparison of aripiprazole and risperidone augmentation in selective serotonin reuptake inhibitor-refractory obsessive-compulsive disorder: a single-blind, randomised study

机译:选择性5-羟色胺再摄取抑制剂-难治性强迫症中阿立哌唑和利培酮增强的比较:单盲,随机研究

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Objective To investigate the comparative efficacy of aripiprazole and risperidone as augmenting agents in the treatment of obsessive-compulsive disorder (OCD) patients who did not show a >35% decrease in the Yale-Brown Obsessive-Compulsive Scale (Y-BOCS) after 12-week monotherapy with selective serotonin reuptake inhibitors (SSRIs). Methods The study consists of two different periods of treatment: a 12-week prospective period to determine resistance to SSRI treatment and an 8-week single-blind addition period for refractory patients only. Ninety patients were randomly assigned to receive one of the SSRI treatments. Sixty-nine patients (76.6%) completed the 12-week SSRI monotherapy period. Forty-one patients (59.4%) were considered refractory and were randomised to receive either risperidone (20 patients, 3 mgr daily) or aripiprazole (21 patients, 15 mgr daily) as augmentation to SSRI treatment. Sixteen patients (76.2%) in the aripiprazole group and 18 patients (84%) in the risperidone group completed the 8-week treatment period. Results Eight patients (50%) in aripiprazole and 13 patients (72.2%) in risperidone group met response criteria of Y-BOCS decrease >=35% at the end of the study. The risperidone group showed a significant improvement in Y-BOCS obsession scores compared with aripiprazole. Conclusions The present findings suggest that risperidone may be more effective than aripiprazole.
机译:目的探讨阿立哌唑和利培酮作为增强剂治疗强迫症(OCD)患者的疗效,这些患者在12岁后Yale-Brown强迫症量表(Y-BOCS)没有下降> 35%选择性5-羟色胺再摄取抑制剂(SSRIs)的单周治疗。方法该研究包括两个不同的治疗期:确定SSRI治疗耐药性的12周预期期和仅针对难治性患者的8周单盲加药期。 90名患者被随机分配接受SSRI治疗之一。 69名患者(76.6%)完成了12周的SSRI单药治疗期。有41名患者(59.4%)被认为是难治性的,并随机接受利培酮(20例患者,每天3 mgr)或阿立哌唑(21例患者,每天15 mgr)作为SSRI治疗的补充。阿立哌唑组有16名患者(76.2%),利培酮组有18名患者(84%)完成了8周的治疗期。结果研究结束时,阿立哌唑组的8例患者(50%)和利培酮组的13例患者(72.2%)符合Y-BOCS缓解标准,即≥35%。与阿立哌唑相比,利培酮组的Y-BOCS痴呆评分显着改善。结论本研究结果表明利培酮可能比阿立哌唑更有效。

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