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米安色林在治疗抑郁症方面比诺米芬辛 - 氯巴占组合耐受性更好且更有效:一项双盲研究。

Mianserin is better tolerated and more effective in depression than a nomifensine-clobazam combination: a double-blind study.

作者信息

Levin A, Schlebusch L

出版信息

Acta Psychiatr Scand Suppl. 1985;320:75-80. doi: 10.1111/j.1600-0447.1985.tb08079.x.

Abstract

Patients suffering from depression (mostly depressive neurosis) were admitted to a double-blind study which compared the efficacy of a combination of nomifensine and clobazam with mianserin. Therapeutic efficacy was evaluated on the Hamilton Depression Rating Scale, Hamilton Anxiety Rating Scale, Clinical Global Impression Scale, physician's assessments, Global Improvement and Treatment Emergent Symptom Scale for side-effects. Assessments were made before admission to the trial and on days 3, 7, 14 and 21. Forty patients were randomly allocated to two treatment groups. A case is made against polypharmacy and in particular against the use of benzodiazepine combinations in depression. Nineteen patients on nomifensine-clobazam and 14 on mianserin completed the three-week trial. At 7, 14 and 21 days, the Hamilton Depression Rating Scale (HDRS) total scores were significantly improved for mianserin when compared with nomifensine-clobazam. Similarly, at 7 and 14 days the Hamilton Anxiety Rating Scale (HARS) total scores were significantly better for mianserin than for the nomifensine-clobazam combination. There were also significant improvements for mianserin on the HDRS sub-scales of anxiety somatization, cognitive disturbance and sleep disturbance. There were no significant differences for HDRS somatic symptoms between treatment groups. Drowsiness was the most common side-effect in both groups. The incidence of total side-effects was 74% for nomifensine-clobazam and 71% for the mianserin group.

摘要

患有抑郁症(主要是抑郁性神经症)的患者被纳入一项双盲研究,该研究比较了诺米芬辛与氯巴占联合用药和米安色林的疗效。疗效通过汉密尔顿抑郁评定量表、汉密尔顿焦虑评定量表、临床总体印象量表、医生评估、总体改善情况以及副作用的治疗中出现的症状量表进行评估。在试验入组前以及第3、7、14和21天进行评估。40名患者被随机分配到两个治疗组。有观点反对联合用药,尤其是反对在抑郁症中使用苯二氮䓬类药物联合用药。19名服用诺米芬辛 - 氯巴占的患者和14名服用米安色林的患者完成了为期三周的试验。在第7、14和21天,与诺米芬辛 - 氯巴占相比,米安色林的汉密尔顿抑郁评定量表(HDRS)总分有显著改善。同样,在第7和14天,米安色林的汉密尔顿焦虑评定量表(HARS)总分显著优于诺米芬辛 - 氯巴占联合用药组。米安色林在焦虑躯体化、认知障碍和睡眠障碍的HDRS子量表上也有显著改善。治疗组之间在HDRS躯体症状方面无显著差异。嗜睡是两组中最常见的副作用。诺米芬辛 - 氯巴占组的总副作用发生率为74%,米安色林组为71%。

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