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Dr Capehart replies

机译:Capehart博士回复

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There are, however, important differences between clinical care and the animal research studies cited by Steenen et al.The article by Bustos et al evaluates midazolam in a rodent model of anxiety. Assuming a number of unresolved questions could be answered, Bustos et al suggest a potential future role for benzodiazepines in psychotherapy of PTSD. When animal research protocols have determined the proper dose and time frame for medications to augment psychotherapy, I would welcome a randomized, placebo-controlled clinical trial based on those animal studies.Clinicians need novel treatment approaches for PTSD. In particular, PTSD care would benefit from treatments that integrate psychotherapy and medication to yield a greater magnitude and longer duration of clinical response. To my knowledge, there are no clinical protocols for benzodiazepines and psychotherapy in routine clinical practice. The preclinical study published by Bustos et al2 does not guide the clinician on if, how, when, or how long to prescribe a benzodiazepine for PTSD, and their findings should not be used to justify routine benzodiazepine prescribing in PTSD.The article by Lund et al and my accompanying commentary both describe clinical practice for PTSD. Until we see results from properly controlled clinical trials that support a change in clinical practice guidelines, benzodiazepines are best avoided when treating patients with PTSD.
机译:然而,临床护理与斯蒂芬等人引用的动物研究研究之间的重要差异。Bustos等人的文章在焦虑的啮齿动物模型中评估咪达唑仑。假设可以回答许多未解决的问题,Bustos等人提出了苯二氮卓在PTSD心理治疗中的潜在未来作用。当动物研究方案确定药物的适当剂量和时间框架以增加心理治疗时,我将根据那些动物研究,欢迎一项随机的安慰剂对照临床试验.Clinicians需要用于PTSD的新型治疗方法。特别是,PTSD护理将受益于整合心理治疗和药物治疗的治疗,以产生更大的临床反应持续时间越来越大。据我所知,常规临床实践中苯二氮卓和心理治疗没有临床方案。 Bustos et al2出版的临床前研究并无指导临床医生,如果如何,何时或多长时间开启苯并二氮卓为应激枢纽,以及他们的调查结果不应用于证明在第四次努力的常规苯二氮卓卓证明处。 AL和我的伴随评论都描述了PTSD的临床实践。直到我们看到支持临床实践准则变化的适当控制的临床试验的结果,在治疗PTSD患者时,最好避免苯并二氮卓。

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