Fischer P, Tauscher J, Küfferle B, Kasper S
Department of General Psychiatry, University Hospital for Psychiatry, Vienna, Austria.
Int Clin Psychopharmacol. 1998 Mar;13(2):83-6. doi: 10.1097/00004850-199803000-00005.
Since 1990 open clinical studies and case descriptions reported full or partial antidepressant response after the addition of buspirone to various ongoing antidepressive treatments. Buspirone acts as a partial serotonin agonist at the 5-HT1A receptor. We tried to augment the effect of serotonin-selective re-uptake inhibitors (SSRI) with 30 mg buspirone in a series of 10 in-patients suffering from refractory depression. We observed two cases of partial remission and five other cases with minimal improvement but no case with complete recovery following buspirone augmentation. On the basis of our naturalistic drug surveillance in 10 refractory depressives, we cannot recommend 30 mg-buspirone augmentation of SSRI treatment in severely ill depressives.
自1990年以来,开放性临床研究和病例描述报告称,在各种正在进行的抗抑郁治疗中添加丁螺环酮后出现了完全或部分抗抑郁反应。丁螺环酮在5-HT1A受体上作为部分5-羟色胺激动剂发挥作用。我们尝试在一系列10例难治性抑郁症住院患者中,用30毫克丁螺环酮增强5-羟色胺选择性再摄取抑制剂(SSRI)的疗效。我们观察到2例部分缓解病例和其他5例有轻微改善的病例,但在丁螺环酮增强治疗后没有完全康复的病例。基于我们对10例难治性抑郁症患者的自然药物监测,我们不建议在重症抑郁症患者中用30毫克丁螺环酮增强SSRI治疗。