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Comparative efficacy study of haloperidol, olanzapine and risperidone in delirium.

机译:氟哌啶醇,奥氮平和利培酮在del妄中的比较疗效研究。

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OBJECTIVE: The objective of the study was to assess the efficacy and safety of second-generation antipsychotics olanzapine and risperidone vs. haloperidol in patients of delirium admitted to medical and surgical wards. METHODS: Prospective follow-up single-blind randomized controlled trials were performed. Consecutive patients with delirium referred to the consultation-liaison psychiatry team were eligible for the study. The study sample comprised 64 patients, with 20 subjects in the haloperidol group, 21 subjects in the risperidone group and 23 subjects in the olanzapine group. A flexible dose regimen (haloperidol -0.25 to 10 mg; risperidone -0.25 to 4 mg; olanzapine -1.25 to 20 mg) was used. Delirium Rating Scale-Revised-98 (DRS-R98) was used as the primary efficacy measure, and mini mental status examination (MMSE) was used as a secondary efficacy measure. RESULTS: There was no significant difference in mean baseline DRS-R98 severity scores and MMSE scores between the three groups. However, there were a significant reduction in DRS-R98 severity scores and a significant improvement in MMSE scores over the period of 6 days, but there was no difference between the three groups. Four patients in the haloperidol group, six subjects in the risperidone group and two subjects in the olanzapine group experienced some side effects. CONCLUSIONS: Risperidone and olanzapine are as efficacious as haloperidol in the treatment of delirium.
机译:目的:本研究的目的是评估第二代抗精神病药olanzapine和利培酮与氟哌啶醇对入院和外科病房的ir妄患者的疗效和安全性。方法:进行了前瞻性随访单盲随机对照试验。转诊至咨询精神病学小组的连续性ir妄患者符合研究条件。该研究样本包括64位患者,氟哌啶醇组为20名受试者,利培酮组为21名受试者,奥氮平组为23名受试者。使用灵活的剂量方案(氟哌啶醇-0.25至10毫克;利培酮-0.25至4毫克;奥氮平-1.25至20毫克)。妄评定量表修订版98(DRS-R98)被用作主要功效指标,迷你精神状态检查(MMSE)被用作次要功效指标。结果:三组之间的平均基线DRS-R98严重程度得分和MMSE得分无显着差异。但是,在6天内,DRS-R98严重性评分显着降低,而MMSE评分显着提高,但是三组之间没有差异。氟哌啶醇组中的四名患者,利培酮组中的六名受试者和奥氮平组中的两名受试者有一些副作用。结论:利培酮和奥氮平在治疗del妄方面与氟哌啶醇一样有效。

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