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奈法唑酮治疗创伤后应激障碍:六项开放标签试验的结果

Nefazodone in post-traumatic stress disorder: results from six open-label trials.

作者信息

Hidalgo R, Hertzberg M A, Mellman T, Petty F, Tucker P, Weisler R, Zisook S, Chen S, Churchill E, Davidson J

机构信息

Duke University Medical Center, Durham, North Carolina, USA.

出版信息

Int Clin Psychopharmacol. 1999 Mar;14(2):61-8. doi: 10.1097/00004850-199903000-00001.

Abstract

Nefazodone, an antidepressant which blocks serotonin (5-HT)2 receptors and 5-HT reuptake, was evaluated in the treatment of post-traumatic stress disorder (PTSD) in six open-label studies involving both civilians and combat veterans. Our objective was to report this available pooled data to characterize the response of this drug in PTSD. Specifically, we looked at response rates using three different criteria, the effect of nefazodone on each PTSD cluster and individual symptoms and, lastly, variables that might predict response. One hundred and five outpatients with chronic PTSD were treated with nefazodone titrated up to 600 mg/day, 92 of whom were entered in an intent to treat analysis. We used the percentage drop in score between baseline and endpoint on main scale as a common measure to evaluate outcome. The response criterion of a drop in score of at least 30%, 40% and 50% revealed response rates of 46, 36 and 26%, respectively. Nefazodone showed a broad spectrum of action on PTSD symptoms. This profile might make nefazodone a useful drug to treat PTSD. Predictors of response include age, sex and trauma type. Double-blind, placebo-controlled clinical trials in PTSD are in progress to assess the utility of nefazodone as a treatment in this disorder.

摘要

奈法唑酮是一种能阻断5-羟色胺(5-HT)2受体和5-HT再摄取的抗抑郁药,在六项涉及平民和退伍军人的开放性研究中对其治疗创伤后应激障碍(PTSD)的效果进行了评估。我们的目的是报告这些汇总数据,以描述该药物对PTSD的反应。具体而言,我们使用三种不同标准查看了有效率,奈法唑酮对PTSD每个症状群和个体症状的影响,以及最后可能预测疗效的变量。105例慢性PTSD门诊患者接受了剂量滴定至600mg/天的奈法唑酮治疗,其中92例进入意向性治疗分析。我们将主要量表上基线至终点的分数下降百分比作为评估结果的常用指标。分数下降至少30%、40%和50%的有效标准分别显示有效率为46%、36%和26%。奈法唑酮对PTSD症状显示出广泛的作用。这种情况可能使奈法唑酮成为治疗PTSD的一种有用药物。疗效预测因素包括年龄、性别和创伤类型。关于奈法唑酮作为该疾病治疗药物效用的双盲、安慰剂对照临床试验正在进行中。

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