Schneier F R, Carrasco J L, Hollander E, Campeas R, Fallon B, Saoud J B, Feerick J, Liebowitz M R
Anxiety Disorders Clinic, New York State Psychiatric Institute, NY 10032.
J Clin Psychopharmacol. 1993 Apr;13(2):150-3.
Alpidem, an imidazopyridine that acts at the gamma-aminobutyric acid/benzodiazepine receptor complex, has been reported to be an effective anxiolytic with a more favorable side effect profile than benzodiazepines. The effect of alpidem was investigated in an 8-week, open, clinical trial in 13 patients with panic disorder, with or without agoraphobia. Three patients were responders (much improved or very much improved), five patients were nonresponders, and five patients dropped out after less than 6 weeks of treatment. Significant improvement was seen in the sample as a whole for spontaneous panic attacks, phobic avoidance, and anticipatory anxiety. Most improvement occurred during the first 4 weeks of treatment, and responders had milder panic disorder at baseline. Adverse effects were generally mild. After 8 weeks of treatment, taper of medication over 2 weeks occurred without significant worsening of panic disorder symptoms. The efficacy of alpidem in the treatment of panic disorder remains uncertain and requires assessment in a controlled trial.
阿吡坦是一种作用于γ-氨基丁酸/苯二氮䓬受体复合物的咪唑并吡啶,据报道它是一种有效的抗焦虑药,其副作用比苯二氮䓬类药物更有利。在一项为期8周的开放性临床试验中,对13例有或无广场恐怖症的惊恐障碍患者研究了阿吡坦的疗效。3例患者有反应(明显改善或非常明显改善),5例患者无反应,5例患者在治疗不到6周后退出。整个样本在自发性惊恐发作、恐惧回避和预期性焦虑方面有显著改善。大多数改善发生在治疗的前4周,有反应者在基线时惊恐障碍较轻。不良反应一般较轻。治疗8周后,在2周内逐渐减少药物剂量,惊恐障碍症状没有明显恶化。阿吡坦治疗惊恐障碍的疗效仍不确定,需要在对照试验中进行评估。