Müller-Siecheneder F, Müller M J, Hillert A, Szegedi A, Wetzel H, Benkert O
Department of Psychiatry, University of Mainz, Germany.
J Clin Psychopharmacol. 1998 Apr;18(2):111-20. doi: 10.1097/00004714-199804000-00003.
In a multicenter, double-blind, parallel group trial, the efficacy of risperidone (RIS) was compared with a combination of haloperidol and amitriptyline (HAL/AMI) over 6 weeks in patients with coexisting psychotic and depressive symptoms with either a schizoaffective disorder, depressive type, a major depression with psychotic features, or a nonresidual schizophrenia with major depressive symptoms according to DSM-III-R criteria. A total of 123 patients (62 RIS; 61 HAL/AMI) were included; the mean daily dosage at endpoint was 6.9 mg RIS versus 9 mg HAL combined with 180 mg AMI. Efficacy results for those 98 patients (47 RIS; 51 HAL/AMI) who completed at least 3 weeks of double-blind treatment revealed in both treatment groups large reductions in the Positive and Negative Syndrome Scale-derived Brief Psychiatric Rating Scale (RIS 37%; HAL/AMI 51%) and the Bech-Rafaelsen Melancholia Scale total scores (RIS 51%; HAL/AMI 70%). The reductions in the Brief Psychiatric Rating Scale and the Bech-Rafaelsen Melancholia Scale scores in the total group were significantly larger in the HAL/AMI group than in the RIS group (p < 0.01), mostly because of significant differences in the subgroup of patients suffering from depression with psychotic features, whereas treatment differences in the other diagnostic subgroups were not significant. The incidence of extrapyramidal side effects as assessed by the Extrapyramidal Symptom Rating Scale was slightly higher under RIS (37%) than under HAL/AMI (31%). Adverse events were reported by 66% of RIS and 75% of HAL/AMI patients. The results of this trial suggest that the therapeutic effect of HAL/AMI is superior to RIS in the total group of patients with combined psychotic and depressive symptoms. However, subgroup differences have to be considered.
在一项多中心、双盲、平行组试验中,根据《精神疾病诊断与统计手册》第三版修订本(DSM-III-R)标准,将利培酮(RIS)与氟哌啶醇和阿米替林联合用药(HAL/AMI)在6周内对同时患有精神病性和抑郁症状的精神分裂症情感障碍(抑郁型)、伴有精神病性特征的重度抑郁症或伴有重度抑郁症状的非残留型精神分裂症患者的疗效进行了比较。共纳入123例患者(62例使用RIS;61例使用HAL/AMI);终点时的平均日剂量为RIS 6.9 mg,而HAL为9 mg加AMI 180 mg。对完成至少3周双盲治疗的98例患者(47例使用RIS;51例使用HAL/AMI)的疗效结果显示,两个治疗组中,阳性和阴性症状量表衍生的简明精神病评定量表得分均大幅降低(RIS组降低37%;HAL/AMI组降低51%),贝克-拉范森抑郁量表总分也降低(RIS组降低51%;HAL/AMI组降低70%)。简明精神病评定量表和贝克-拉范森抑郁量表总分的降低在HAL/AMI组显著大于RIS组(p<0.01),这主要是由于伴有精神病性特征的抑郁症患者亚组存在显著差异,而其他诊断亚组的治疗差异不显著。根据锥体外系症状评定量表评估,锥体外系副作用的发生率在RIS组(37%)略高于HAL/AMI组(31%)。66%的RIS患者和75%的HAL/AMI患者报告了不良事件。该试验结果表明,在同时患有精神病性和抑郁症状的患者总体中,HAL/AMI的治疗效果优于RIS。然而,必须考虑亚组差异。