Pecknold J C, Luthe L, Scott-Fleury M H, Jenkins S
Douglas Hospital Research Centre, Verdun, Quebec, Canada.
J Clin Psychopharmacol. 1993 Apr;13(2):145-9.
Gepirone, an azapirone, is a potent 5-hydroxytryptamine 1A (5-HT1A) agonist. We report an uncontrolled 6-week study in 21 patients (4 men, 17 women: mean age, 36.71 years) with a concurrent DSM-III-R diagnosis of generalized anxiety disorder and panic disorder with agoraphobia. After a 2-week medication-free period, patients were started on 2 mg of gepirone per day increasing over 3 weeks to 12 mg/day. Three patients dropped out in the first week, and one patient violated the protocol. They were therefore excluded from analysis. Two patients who dropped out at weeks 4 and 5 because they found the treatment ineffective were included. Twelve of the 17 patients (70.6%) had at least a 50% reduction in their panic attacks by week 6, and 9 of them had at least a 50% reduction by week 3. Ten patients had "0" panic attacks by week 6 (59%). On the Hamilton Anxiety Scale, 65% had a 50% or greater reduction in total score, mostly beginning in week 1. On Global Assessment, by week 6, 11 were much improved or better (65%). Adverse effects were rare and consisted of stomach upset, dizziness, or headaches. This preliminary study suggests the possible efficacy of gepirone in panic disorder.
吉哌隆是一种氮杂哌隆,是一种强效的5-羟色胺1A(5-HT1A)激动剂。我们报告了一项针对21例患者(4名男性,17名女性:平均年龄36.71岁)的非对照6周研究,这些患者同时符合《精神疾病诊断与统计手册》第三版修订本(DSM-III-R)中广泛性焦虑症和伴有广场恐惧症的惊恐障碍的诊断标准。在经过2周的无药期后,患者开始每天服用2毫克吉哌隆,在3周内逐渐增加至12毫克/天。有3名患者在第一周退出,1名患者违反了方案。因此,他们被排除在分析之外。纳入了2名在第4周和第5周因觉得治疗无效而退出的患者。17名患者中有12名(70.6%)在第6周时惊恐发作至少减少了50%,其中9名在第3周时至少减少了50%。到第6周时,有10名患者(59%)的惊恐发作次数为“0”。在汉密尔顿焦虑量表上,65%的患者总分降低了50%或更多,大多从第1周开始。在总体评估中,到第6周时,11名患者的情况有很大改善或更好(65%)。不良反应很少见,包括胃部不适、头晕或头痛。这项初步研究表明吉哌隆治疗惊恐障碍可能有效。