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缓释文拉法辛用于预防重度抑郁症患者复发

Extended-release venlafaxine in relapse prevention for patients with major depressive disorder.

作者信息

Simon Jeffrey S, Aguiar Loren M, Kunz Nadia R, Lei Dean

机构信息

Northbrooke Research Center, 9275 North 49th Street, Suite 200, Brown Deer, WI 53223, USA.

出版信息

J Psychiatr Res. 2004 May-Jun;38(3):249-57. doi: 10.1016/j.jpsychires.2003.10.004.

Abstract

Many studies have demonstrated that venlafaxine is an efficacious and safe treatment for major depressive disorder (MDD). This double-blind, placebo-controlled study was performed to evaluate the efficacy of venlafaxine extended-release (XR) (75-225 mg/day) in the prevention of relapse of depression. Patients with MDD who responded to an 8-week course of venlafaxine XR treatment, i.e., had a score < or = 3 on the Clinical Global Impressions scale-Severity of Illness item (CGI-S) and a 21-item Hamilton Rating Scale for Depression (HAM-D(21)) score < or = 10, were randomly assigned to receive continuation treatment (up to 6 months) with venlafaxine XR (n=161) or placebo (n=157). The main efficacy outcome measure was the number of patients who experienced a relapse of depression. Relapse was defined by either a combination of a patient meeting Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition criteria for MDD and a CGI-S score > or = 4, two consecutive CGI-S scores > or = 4, or a final CGI-S score > or = 4 for a patient who withdrew from the study. The cumulative probability of relapse was calculated using the Kaplan-Meier method of survival analysis. During the 6-month evaluation period, significantly more patients in the placebo group had a relapse of MDD than did patients who continued treatment with venlafaxine XR. Cumulative relapse rates at 3 and 6 months were 19 and 28%, respectively, for venlafaxine XR, and 44 and 52%, respectively, for placebo. This study demonstrates that venlafaxine XR is an effective and safe continuation therapy.

摘要

许多研究表明,文拉法辛是治疗重度抑郁症(MDD)的一种有效且安全的药物。本双盲、安慰剂对照研究旨在评估缓释文拉法辛(75 - 225毫克/天)预防抑郁症复发的疗效。对8周疗程的缓释文拉法辛治疗有反应的MDD患者,即临床总体印象量表-疾病严重程度项目(CGI-S)评分≤3且21项汉密尔顿抑郁量表(HAM-D(21))评分≤10的患者,被随机分配接受缓释文拉法辛(n = 161)或安慰剂(n = 157)的持续治疗(长达6个月)。主要疗效指标是经历抑郁症复发的患者数量。复发定义为符合《精神障碍诊断与统计手册》第四版MDD标准且CGI-S评分≥4、连续两次CGI-S评分≥4,或退出研究的患者最终CGI-S评分≥4。使用Kaplan-Meier生存分析方法计算复发的累积概率。在6个月的评估期内,安慰剂组中抑郁症复发的患者明显多于继续接受缓释文拉法辛治疗的患者。缓释文拉法辛在3个月和6个月时的累积复发率分别为19%和28%,安慰剂组分别为44%和52%。本研究表明,缓释文拉法辛是一种有效且安全的持续治疗药物。

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