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舍曲林治疗重度抑郁症的安全性和有效性:与安慰剂的双盲固定剂量对照研究

Sertraline safety and efficacy in major depression: a double-blind fixed-dose comparison with placebo.

作者信息

Fabre L F, Abuzzahab F S, Amin M, Claghorn J L, Mendels J, Petrie W M, Dubé S, Small J G

机构信息

Fabre Research Clinics Inc., Houston, TX 77004, USA.

出版信息

Biol Psychiatry. 1995 Nov 1;38(9):592-602. doi: 10.1016/0006-3223(95)00178-8.

Abstract

In a 6-week, randomized, double-blind, multicenter trial, sertraline 50 mg, 100 mg, or 200 mg, or placebo, was administered once daily to 369 patients with DSM-III-defined major depression. Efficacy variables included changes from baseline scores for total Hamilton Rating Scale for Depression (HAMD), HAMD Bech Depression Cluster, Clinical Global Impressions (CGI) Severity, CGI Improvement, and Profile of Mood States Depression/Dejection Factor. For the evaluable-patients analysis, all sertraline groups showed significantly (p < 0.05 or better) greater improvements in all efficacy variables except one when compared with the placebo group. For the all-patients analysis, all efficacy variables in the 50 mg group were statistically significantly (p < 0.05) better than placebo. Side effects increased with increasing dosage but were usually mild and well tolerated. The results of this study show that sertraline 50 mg once daily is as effective as higher dosages for the treatment of major depression with fewer side effects and therapy discontinuations.

摘要

在一项为期6周的随机、双盲、多中心试验中,369名符合《精神疾病诊断与统计手册》第三版(DSM-III)定义的重度抑郁症患者被随机分配,每天服用一次50毫克、100毫克或200毫克的舍曲林,或服用安慰剂。疗效变量包括汉密尔顿抑郁量表(HAMD)总分、HAMD贝克抑郁因子、临床总体印象量表(CGI)严重程度、CGI改善情况以及情绪状态剖面图抑郁/沮丧因子与基线分数的变化。在可评估患者分析中,与安慰剂组相比,所有舍曲林组在除一项之外的所有疗效变量上均显示出显著(p<0.05或更佳)更大的改善。在所有患者分析中,50毫克组的所有疗效变量在统计学上均显著(p<0.05)优于安慰剂。副作用随剂量增加而增加,但通常较轻且耐受性良好。本研究结果表明,每日一次50毫克的舍曲林在治疗重度抑郁症方面与更高剂量同样有效,且副作用更少,治疗中断情况也更少。

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