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文拉法辛与阿米替林治疗伴或不伴 melancholia 的重度抑郁症门诊患者的双盲对照研究

Double-blind comparison of venlafaxine and amitriptyline in outpatients with major depression with or without melancholia.

作者信息

Gentil V, Kerr-Correa F, Moreno R, D'Arrigo Busnello E, De Campos J A, Juruena M F, Lafer B, Moreno D H, De Cassia Rodrigues R L, Tiosso A, Benedictis E

机构信息

Departamento de Psiquiatria, Instituto de Psiquiatria, Hospital das Clinicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.

出版信息

J Psychopharmacol. 2000 Mar;14(1):61-6. doi: 10.1177/026988110001400108.

Abstract

The purpose of this study was to compare the efficacy and tolerability of venlafaxine and amitriptyline in outpatients with major depression with or without melancholia. This was an 8-week, multicentre, randomized, double-blind, parallel-group comparison of venlafaxine and amitriptyline. Outpatients with DSM-IV major depression, a minimum score of 20 on the 21-item Hamilton Depression Rating Scale (HAM-D), and depressive symptoms for at least 1 month were eligible. Patients were randomly assigned to venlafaxine or amitriptyline, both drugs titrated to a maximum of 150 mg/day until study day 15. The primary efficacy variables were the final on-therapy scores on the HAM-D, Montgomery-Asberg Depression Rating Scale and Clinical Global Impression severity scales. Data were evaluated on an intent-to-treat basis using the LOCF method. One hundred and 16 patients were randomized, and 115 were evaluated for efficacy. Both drugs showed efficacy in the treatment of depression with or without melancholia. No significant differences were noted between treatments for any efficacy parameter. However, significantly (p < 0.05) more patients in the amitriptyline group had at least one adverse event. These results should support the efficacy and tolerability of venlafaxine in comparison with amitriptyline for treating major depression with or without melancholia.

摘要

本研究旨在比较文拉法辛和阿米替林对伴有或不伴有 melancholia 的重度抑郁症门诊患者的疗效和耐受性。这是一项为期 8 周的多中心、随机、双盲、平行组比较文拉法辛和阿米替林的研究。符合条件的门诊患者需患有 DSM-IV 重度抑郁症,21 项汉密尔顿抑郁量表(HAM-D)得分至少为 20 分,且抑郁症状持续至少 1 个月。患者被随机分配至文拉法辛组或阿米替林组,两种药物均滴定至最大剂量 150mg/天,直至研究第 15 天。主要疗效变量为 HAM-D、蒙哥马利-阿斯伯格抑郁量表和临床总体印象严重程度量表的最终治疗得分。数据采用末次观察结转(LOCF)法进行意向性分析。116 例患者被随机分组,115 例患者接受了疗效评估。两种药物对伴有或不伴有 melancholia 的抑郁症均显示出疗效。各疗效参数在治疗组间未观察到显著差异。然而,阿米替林组中至少发生 1 次不良事件的患者显著更多(p < 0.05)。这些结果支持了与阿米替林相比,文拉法辛治疗伴有或不伴有 melancholia 的重度抑郁症的疗效和耐受性。

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