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舍曲林与阿米替林治疗门诊重度抑郁症患者的双盲、多中心对照研究

Double-blind, multicenter comparative study of sertraline versus amitriptyline in outpatients with major depression.

作者信息

Möller H J, Glaser K, Leverkus F, Göbel C

机构信息

Psychiatric Department, University of Munich, Germany.

出版信息

Pharmacopsychiatry. 2000 Nov;33(6):206-12. doi: 10.1055/s-2000-8357.

Abstract

OBJECTIVE

To compare the efficacy and safety of sertraline and amitriptyline in a German outpatient population.

METHODS

Patients with Major Depression (DSM-III-R) and HAM-D (21 items) > or = 21 in 19 German centers received double-blind treatment with sertraline (initial dose 50 mg, titration up to 100 mg) or amitriptyline (75 mg, up to 150 mg) over 6 weeks. HAM-D (21 items), HAM-D Bech, CGI, DSI and SDS were evaluated for the efficacy analysis. FSUCL (Fischer Somatic and Undesired Effects Check List) and spontaneously reported adverse events were used for safety analysis.

RESULTS

Of the 240 patients enrolled in the study, 205 (100 sertraline; 105 amitriptyline) were evaluable for efficacy. No statistically significant differences were detected between the two groups in the ITT and ATP efficacy analyses. Response, defined as score 1 (very much improved) or 2 (much improved) of the CGI improvement score, was 76% in the sertraline and 81% in the amitriptyline group (efficacy evaluable patients = ATP population). In the structured FSUCL, the side-effect burden (FSUCL score >2 for drug related symptoms) was significantly higher in the amitriptyline group at all follow up visits (p<0.05).

CONCLUSION

Both sertraline and amitriptyline are suitable for the treatment of Major Depression; sertraline is comparable to amitriptyline with regard to efficacy, and offers the additional benefit of a more favorable safety profile.

摘要

目的

比较舍曲林和阿米替林在德国门诊患者中的疗效和安全性。

方法

19个德国中心中,汉密尔顿抑郁量表(HAM-D,21项)评分≥21分的重度抑郁症(DSM-III-R)患者接受为期6周的双盲治疗,分别服用舍曲林(初始剂量50mg,滴定至100mg)或阿米替林(75mg,滴定至150mg)。采用HAM-D(21项)、HAM-D贝克版、临床总体印象量表(CGI)、药物不良反应量表(DSI)和抑郁自评量表(SDS)进行疗效分析。采用FSUCL(费舍尔躯体和不良反应检查表)及自发报告的不良事件进行安全性分析。

结果

研究共纳入240例患者,其中205例(100例服用舍曲林;105例服用阿米替林)可进行疗效评估。意向性分析(ITT)和符合方案集分析(ATP)中,两组疗效无统计学显著差异。以CGI改善评分1分(显著改善)或2分(中度改善)定义为有效,舍曲林组有效率为76%,阿米替林组为81%(疗效可评估患者=符合方案集人群)。在结构化FSUCL中,阿米替林组在所有随访中副作用负担(FSUCL评分>2分表示与药物相关症状)均显著更高(p<0.05)。

结论

舍曲林和阿米替林均适用于重度抑郁症的治疗;舍曲林在疗效上与阿米替林相当,且安全性更佳。

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