Volz H P, Gleiter C H, Möller H J
Department of Psychiatry, Jena University, Germany.
J Affect Disord. 1997 Jul;44(2-3):91-9. doi: 10.1016/s0165-0327(97)00031-1.
Brofaromine is a selective and reversible inhibitor of monoamine oxidase A. The efficacy and safety of this compound as compared with tricyclic antidepressants, classical monoamine oxidase inhibitors and placebo has been demonstrated in several clinical trials. The present 6-week, double-blind, randomized trial compared brofaromine with imipramine in in-patients with major depression. Brofaromine was as effective as imipramine in the treatment of major depression, but exhibited a different side-effect profile, in particular lacking the anticholinergic and certain cardiovascular side-effects of the tricyclic imipramine, but more likely to induce sleep disturbances. In this study, in-patients were examined, since the majority of controlled clinical trials on depressed patients conducted so far have focused on the evaluation of out-patients. If one assumes that a different degree of severity of depression exists between these two patient groups, then the results of those trials conducted on out-patients cannot readily be transferred to in-patients.
溴法罗明是一种选择性且可逆的单胺氧化酶A抑制剂。在多项临床试验中已证实该化合物与三环类抗抑郁药、经典单胺氧化酶抑制剂及安慰剂相比的疗效和安全性。本为期6周的双盲随机试验,将溴法罗明与丙咪嗪用于重度抑郁症住院患者进行比较。溴法罗明在治疗重度抑郁症方面与丙咪嗪效果相当,但副作用情况不同,尤其没有三环类丙咪嗪的抗胆碱能及某些心血管副作用,但更易引发睡眠障碍。在本研究中对住院患者进行了检查,因为迄今为止针对抑郁症患者开展的大多数对照临床试验都集中在对门诊患者的评估上。如果假定这两组患者之间存在不同程度的抑郁严重程度,那么针对门诊患者开展的那些试验结果就不能轻易推广到住院患者身上。