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西酞普兰与阿米替林治疗伴有或不伴有轻度认知功能障碍的老年抑郁症患者:丹麦全科医学多中心试验

Citalopram versus amitriptyline in elderly depressed patients with or without mild cognitive dysfunction: a danish multicentre trial in general practice.

作者信息

Rosenberg Claus, Lauritzen Lise, Brix Jørgen, Jørgensen Jørgen B, Kofod Palle, Bayer Liselotte Been

机构信息

Psychiatric Hospital in Hillerød, Denmark.

出版信息

Psychopharmacol Bull. 2007;40(1):63-73.

Abstract

This double-blind, multicenter trial, carried out in general practice in Denmark, comprised 221 women and 70 men, aged 58 to 97 years, with major depression (with or without mild cognitive dysfunction) or dysthymia (DSM-III-R). Patients had a total score > or =13 on the 17-item Hamilton Depression Rating Scale (HDRS) and a score > or =20 on the Mini Mental State Examination scale. The efficacy and tolerability of citalopram (20-40 mg daily) and amitriptyline (50-100 mg daily) were compared over 12 weeks. The participating general practitioners were trained at corating sessions in the use of the HDRS and Melancholia Scale (MES) prior to and during the study. The inter-observer reliability was assessed to investigate if general practitioners were able to use scales that measure the severity of depression. The two treatments were considered equally effective; the 90% confidence interval for the difference between the treatment groups in change from baseline to end-point in HDRS total score (-0.84 to +1.23) was within the predefined interval (-4 to +4). Significantly more patients on citalopram (50%) than on amitriptyline (31%) reported no adverse events at all (P = .001). Moreover, patients on amitriptyline reported adverse events significantly earlier and more frequently than patients on citalopram. The inter-observer reliability was highly satisfactory, with intra-class correlation coefficients (ICC-U) of .83 for the HDRS and .82 for the MES; however, the ICC-U for the Clinical Global Impressions was .54, indicating a poorer consensus in the investigators clinical judgment. Training in the use of the HDRS and MES scales improved the inter-observer reliability.

摘要

这项双盲、多中心试验在丹麦的普通医疗实践中进行,纳入了221名女性和70名男性,年龄在58至97岁之间,患有重度抑郁症(伴或不伴有轻度认知功能障碍)或心境恶劣障碍(DSM-III-R)。患者在17项汉密尔顿抑郁量表(HDRS)上的总分≥13分,在简易精神状态检查表上的得分≥20分。比较了西酞普兰(每日20 - 40毫克)和阿米替林(每日50 - 100毫克)在12周内的疗效和耐受性。参与研究的全科医生在研究前和研究期间接受了关于使用HDRS和忧郁量表(MES)的评分培训。评估了观察者间的可靠性,以调查全科医生是否能够使用测量抑郁严重程度的量表。两种治疗方法被认为同样有效;治疗组之间从基线到终点HDRS总分变化的90%置信区间(-0.84至+1.23)在预定义区间(-4至+4)内。报告无不良事件的西酞普兰组患者(50%)显著多于阿米替林组患者(31%)(P = .001)。此外,阿米替林组患者报告不良事件的时间显著早于且频率高于西酞普兰组患者。观察者间的可靠性非常令人满意,HDRS的组内相关系数(ICC-U)为.83,MES的为.82;然而,临床总体印象的ICC-U为.54,表明研究者的临床判断共识较差。使用HDRS和MES量表的培训提高了观察者间的可靠性。

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