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[噻奈普汀治疗精神衰弱的疗效。与安慰剂对照研究]

[Efficacy of tianeptine in the treatment of psychasthenia. A study versus placebo].

作者信息

Grivois H, Deniker P, Ganry H

机构信息

Service de Psychiatrie, Hôtel-Dieu de Paris.

出版信息

Encephale. 1992 Sep-Oct;18(5):591-9.

PMID:1340807
Abstract

Tianeptine is an effective antidepressant with original neurochemical properties. Tianeptine increases the serotonin (5-HT) reuptake after acute and chronic treatment. The efficacy of tianeptine (T) versus placebo (P) was evaluated in the treatment of psychasthenia, because of the role of 5-HT in obsessive-compulsive disorders, the last state of psychasthenia in term of severity. Patients were recruited using the psychasthenia scale; then, their MADRS scores limited those who turned out to the depression. Mean inclusion MADRS scores where 12 (T) and 11.8 (P). Tianeptine is an effective treatment for patients suffering from psychasthenia. Tianeptine is more effective than placebo in global score and in sub-scores (asthenia and somatic symptoms) of the psychasthenia scale. In spite of weak inclusion scores in MADRS, patients taking tianeptine also showed significant improvement, greater than with placebo. The percentage of patients with a reduction equal to or greater than 50% of their MADRS score was significantly more important in tianeptine group. These results could be the illustration of the decrease in associated depressive symptoms or the result of an improvement of symptoms common to MADRS and psychasthenia scales. The same favorable results were obtained in symptoms of anxiety scored by HARS. In term of safety, tianeptine is equivalent to a placebo if we consider somatic complaints expressed by the patients, global improvement evaluated by the patient and the investigator, weight and blood pressure. Interruption of treatment for side-effects concerns the placebo group only (3 versus 0). This excellent safety is particularly well-adapted to the treatment of these out-patients.

摘要

噻奈普汀是一种具有独特神经化学特性的有效抗抑郁药。急性和慢性治疗后,噻奈普汀可增加血清素(5-HT)的再摄取。由于5-HT在强迫性障碍(神经衰弱严重程度方面的最终状态)中的作用,对噻奈普汀(T)与安慰剂(P)治疗神经衰弱的疗效进行了评估。使用神经衰弱量表招募患者;然后,他们的蒙哥马利-阿斯伯格抑郁量表(MADRS)评分限制了那些出现抑郁症状的患者。平均纳入时的MADRS评分,噻奈普汀组为12分,安慰剂组为11.8分。噻奈普汀对患有神经衰弱的患者是一种有效的治疗方法。在神经衰弱量表的总体评分以及子评分(无力和躯体症状)方面,噻奈普汀比安慰剂更有效。尽管MADRS的纳入评分较低,但服用噻奈普汀的患者也显示出显著改善,且优于安慰剂组。MADRS评分降低等于或大于其基线评分50%的患者百分比在噻奈普汀组中显著更高。这些结果可能是相关抑郁症状减轻的体现,或者是MADRS和神经衰弱量表共同症状改善的结果。在汉密尔顿焦虑量表(HARS)评分的焦虑症状方面也获得了同样良好的结果。在安全性方面,如果考虑患者表达的躯体不适、患者和研究者评估的总体改善、体重和血压,噻奈普汀与安慰剂相当。因副作用而中断治疗的情况仅出现在安慰剂组(3例对比0例)。这种出色的安全性特别适合这些门诊患者的治疗。

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