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惊恐障碍中的可逆性单胺氧化酶-A抑制剂

Reversible monoamine oxidase-A inhibitors in panic disorder.

作者信息

Bakish D, Saxena B M, Bowen R, D'Souza J

机构信息

University of Ottawa at Royal Ottawa Hospital, Ontario, Canada.

出版信息

Clin Neuropharmacol. 1993;16 Suppl 2:S77-82.

PMID:8313401
Abstract

Monoamine oxidase (MAO) inhibitors are known to be effective in panic disorder, but a high incidence of adverse reactions have limited their use. The new, selective, and reversible MAO-A inhibitors exemplified by brofaromine and moclobemide do not require dietary restrictions, have fewer drug interactions, and are better tolerated. This paper reports a randomized, double-blind, 8-week trial in which the efficacy and safety of brofaromine was compared to clomipramine in patients with panic disorder with or without agoraphobia. Both treatments achieved a significant and comparable reduction in the number of panic attacks, and were equally effective in all the parameters measured. Side effects were typical of the drug class. Further trials are required to evaluate this promising new treatment.

摘要

已知单胺氧化酶(MAO)抑制剂对惊恐障碍有效,但不良反应发生率高限制了其应用。以溴法罗明和吗氯贝胺为代表的新型、选择性且可逆的MAO - A抑制剂不需要饮食限制,药物相互作用较少,耐受性更好。本文报告了一项随机、双盲、为期8周的试验,该试验比较了溴法罗明与氯米帕明对伴有或不伴有广场恐惧症的惊恐障碍患者的疗效和安全性。两种治疗方法在惊恐发作次数上均实现了显著且相当的减少,并且在所有测量参数上效果相同。副作用是该药物类别的典型特征。需要进一步试验来评估这种有前景的新疗法。

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