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全科医疗中混合性情感障碍的治疗:曲唑酮与多塞平的比较

The treatment of mixed affective disorders in general practice: a comparison of trazodone and dothiepin.

作者信息

Moon C A, Chapman J P, Healey J C, Hannington J A

机构信息

Medical Department, Roussel Laboratories Limited, Denham, England.

出版信息

Curr Med Res Opin. 1990;12(1):34-42. doi: 10.1185/03007999009111489.

Abstract

The efficacy and tolerance of trazodone in the treatment of mixed affective disorder was compared with that of dothiepin in a double-blind, parallel group study in 228 general practice patients at 10 centres. After satisfying entry criteria, patients were randomized to receive either 150 mg trazodone at night, or 75 mg dothiepin at night for a 6-week period. Efficacy was assessed using the Hamilton Rating Scales for Depression and Anxiety. Significant improvements were observed in the condition of patients in each of the two treatment groups during the 6-week treatment period (p = 0.0001), with no statistically significant difference between the groups. There were no marked differences between the two treatment groups in the type of side-effects reported in response to open questioning, although a higher percentage of symptoms in the trazodone group were mild compared to the dothiepin group, and a lower percentage were severe. The incidence side-effects recorded by means of a checklist of common psychotropic side-effects was similar for the two treatment groups: dry mouth and drowsiness were the most frequent. A slightly higher proportion of patients withdrew from the dothiepin group, and of those who withdrew a higher percentage was due to side-effects than in the trazodone group.

摘要

在一项针对10个中心的228名全科患者的双盲平行组研究中,比较了曲唑酮和多塞平治疗混合性情感障碍的疗效和耐受性。符合入选标准后,患者被随机分为两组,一组每晚服用150毫克曲唑酮,另一组每晚服用75毫克多塞平,为期6周。使用汉密尔顿抑郁和焦虑评定量表评估疗效。在为期6周的治疗期间,两个治疗组的患者病情均有显著改善(p = 0.0001),两组之间无统计学显著差异。在开放式询问中报告的副作用类型方面,两个治疗组之间没有明显差异,尽管与多塞平组相比,曲唑酮组症状较轻的比例更高,严重症状的比例更低。通过常见精神药物副作用清单记录的副作用发生率在两个治疗组中相似:口干和嗜睡最为常见。多塞平组退出的患者比例略高,且退出者中因副作用退出的比例高于曲唑酮组。

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