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Placebo Response in Pediatric Anxiety Disorders: Results from the Child/Adolescent Anxiety Multimodal Study

机译:小儿焦虑症中的安慰剂反应:儿童/青少年焦虑多模式研究的结果

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>Objectives: The aim of this study is to identify predictors of pill placebo response and to characterize the temporal course of pill placebo response in anxious youth.>Methods: Data from placebo-treated patients (N = 76) in the Child/Adolescent Anxiety Multimodal Study (CAMS), a multisite, randomized controlled trial that examined the efficacy of cognitive-behavioral therapy, sertraline, their combination, and placebo for the treatment of separation, generalized, and social anxiety disorders, were evaluated. Multiple linear regression models identified features associated with placebo response and models were confirmed with leave-one-out cross-validation. The likelihood of improvement in patients receiving pill placebo—over time—relative to improvement associated with active treatment was determined using probabilistic Bayesian analyses.>Results: Based on a categorical definition of response (Clinical Global Impressions-Improvement Scale score ≤2), nonresponders (n = 48), and pill placebo responders (n = 18) did not differ in age (p = 0.217), sex (p = 0.980), race (p = 0.743), or primary diagnosis (all ps > 0.659). In terms of change in anxiety symptoms, separation anxiety disorder and treatment expectation were associated with the degree of pill placebo response. Greater probability of placebo-related anxiety symptom improvement was observed early in the course of treatment (baseline to week 4, p < 0.0001). No significant change in the probability of placebo-related improvement was observed after week 4 (weeks 4–8, p = 0.07; weeks 8–12, p = 0.85), whereas the probability of improvement, in general, significantly increased week over week with active treatment.>Conclusions: Pill placebo-related improvement occurs early in the course of treatment and both clinical factors and expectation predict this improvement. Additionally, probabilistic approaches may refine our understanding and prediction of pill placebo response.
机译:>目的:该研究的目的是确定焦虑青年中的药物安慰剂反应的预测因素,并表征药物安慰剂反应的时间过程。>方法:来自安慰剂治疗的数据儿童/青少年焦虑多模式研究(CAMS)中的患者(N = 76),该研究是一项多地点,随机对照试验,研究了认知行为疗法,舍曲林,它们的组合和安慰剂在分离,全身和非常规治疗中的功效。社交焦虑症,进行了评估。多个线性回归模型确定了与安慰剂反应相关的特征,并通过留一法交叉验证确认了模型。使用概率贝叶斯分析确定了接受安慰剂的患者随时间推移相对于主动治疗的改善的可能性。>结果:基于对反应的明确定义(临床总体印象-改善量表得分≤2),无反应者(n = 48)和药丸安慰剂反应者(n = 18)在年龄(p = 0.217),性别(p = 0.980),种族(p = 0.743)或主要诊断方面没有差异(p = 0.217)所有ps> 0.659)。就焦虑症状的改变而言,分离性焦虑症和治疗期望与药丸安慰剂反应程度有关。在治疗的早期阶段观察到安慰剂相关的焦虑症状改善的可能性更大(基线至第4周,p <0.0001)。在第4周后,与安慰剂相关的改善可能性没有显着变化(第4-8周,p = 0.07;第8-12周,p = 0.85),而总体而言,改善的可能性周比增加>结论:丸安慰剂相关的改善发生在治疗过程的早期,临床因素和预期都预示了这种改善。此外,概率方法可能会改善我们对药丸安慰剂反应的理解和预测。

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