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Potential effectiveness and safety of olanzapine in refractory panic disorder

机译:奥沙明滨在难治性恐慌症中的潜在效果和安全性

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Panic disorder is a common and disabling psychiatric disorder. Despite treatment advances, refractory panic disorder requires novel interventions. One such pharmacologic intervention with theoretical and case study support includes olanzapine, a thienobenzodiazepine medication currently approved for schizophrenia in the United States. Ten people with refractory DSM-IV diagnosed panic disorder completed an 8-week, open-label, flexible-dose clinical trial. Baseline, in-treatment, and end-of-treatment data for panic attacks, anticipatory anxiety, phobic avoidance, and impairment were collected. Data were analyzed using SPSS software. Refractory panic disorder patients required a wide dose range averaging 12.3 mg/day of olanzapine to significantly improve or ablate panic attacks. On the average, number of attacks decreasedfrom 6.1/week at baseline to 1.1/week at the end of treatment, and anticipatory anxiety fi-om 32% of the day to 8% of the day. At treatment end, 5 of 10 participants (50%) were panic free, 4 (40%) bad one attack in the previous week, 1 (10%) bad seven attacks in the previous week, and 6 of 10 participants (60%) were anticipatory anxiety free. There were also statistically and clinically significant improvements in impairment over the course of the trial. There were no significant changes in vital signs, emergent side effects, or average weight, although 6 of 10 people did gain weight. Olanzapine is potentially effective and safe in panic disorder. Due to study limitations, further clinical trials are needed to demonstrate effectiveness. (c) 2005 Wiley-Liss, Inc.
机译:恐慌症是一种常见和致残的精神疾病。尽管治疗进展,但难治性恐慌症需要新的干预措施。一种具有理论和案例研究支持的这种药理学干预包括奥氮平,目前在美国精神分裂症批准的噻吩苯二齐二嗪类药物。十名难治性DSM-IV诊断出的恐慌症,完成了8周,开放式标签,灵活的临床试验。基线,治疗和治疗结束数据,用于恐慌发作,预期焦虑,避免和损害。使用SPSS软件分析数据。难治性恐慌症患者需要宽剂量范围,平均12.3毫克/天奥氮平,以显着改善或消融恐慌发作。平均而言,攻击次数会在基线的基准下跌6.1 /周,在治疗结束时为1.1 /周,预期焦虑症32%的日期为每天的8%。在治疗末端,10名参与者(50%)的5个(50%)是恐慌免费的,前一周的4(40%)不良一次攻击,前一周的七次袭击率为1(10%),10名参与者中有6名(60%) )预期焦虑不安。在审判过程中,在统计上和临床上显着改善。生命体征没有显着变化,突出的副作用或平均重量,尽管有6人的体重是体重。奥拉扎丁潜在有效和安全的恐慌症。由于研究限制,需要进一步的临床试验来证明有效性。 (c)2005 Wiley-Liss,Inc。

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