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A preliminary study of D-cycloserine augmentation of cognitive-behavioral therapy in pediatric obsessive-compulsive disorder.

机译:D-环丝氨酸增强小儿强迫症认知行为治疗的初步研究。

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BACKGROUND: Research on the neural circuitry underlying fear extinction has led to the examination of D-cycloserine (DCS), a partial agonist at the N-methyl-D-aspartate receptor in the amygdala, as a method to enhance exposure therapy outcome. Preliminary results have supported the use of DCS to augment exposure therapy in adult anxiety disorders; however, no data have been reported in any childhood anxiety disorder. Thus, we sought to preliminarily examine whether weight-adjusted DCS doses (25 or 50 mg) enhanced the overall efficacy of cognitive-behavioral therapy (CBT) for pediatric obsessive-compulsive disorder (OCD). METHOD: Participants were 30 youth (aged 8-17) with a primary diagnosis of OCD. The study design was a randomized, double-blinded, placebo-controlled augmentation trial examining CBT + DCS versus CBT + Placebo (15 youth per group). All patients received seven exposure and response prevention sessions paired with DCS or placebo taken 1 hour before sessions. RESULTS: Although not significantly different, compared with the CBT + Placebo group, youth in the CBT + DCS arm showed small-to-moderate treatment effects (d = .31-.47 on primary outcomes). No adverse events were recorded. CONCLUSIONS: These results complement findings in adult OCD and non-OCD anxiety disorders and provide initial support for a more extensive study of DCS augmentation of CBT among youth with OCD.
机译:背景:关于消除恐惧的神经回路的研究已导致对D-环丝氨酸(DCS)的检查,该化合物是杏仁核N-甲基-D-天冬氨酸受体的部分激动剂,可作为提高暴露治疗结果的一种方法。初步结果支持使用DCS增强成人焦虑症的暴露治疗;然而,尚无任何儿童焦虑症的报道。因此,我们试图初步研究体重调整的DCS剂量(25或50 mg)是否能增强认知行为疗法(CBT)对小儿强迫症(OCD)的总体疗效。方法:参加者为30位年龄在8-17岁之间的初次诊断为强迫症的年轻人。该研究设计是一项随机,双盲,安慰剂对照的增强试验,研究了CBT + DCS与CBT +安慰剂的关系(每组15位青年)。所有患者均接受七个暴露和缓解反应预防措施,并在治疗前1小时服用DCS或安慰剂。结果:与CBT +安慰剂组相比,尽管无显着差异,但CBT + DCS组的青年表现出中小治疗效果(主要结局指标d = 0.31-0.47)。没有不良事件的记录。结论:这些结果补充了在成人强迫症和非强迫症焦虑症中的发现,并为在强迫症青年中DCS增强CBT的更广泛研究提供了初步支持。

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