首页> 外文OA文献 >Refining clinical judgment of treatment response and symptom remission identification in childhood anxiety using a signal detection analysis on the pediatric anxiety rating scale
【2h】

Refining clinical judgment of treatment response and symptom remission identification in childhood anxiety using a signal detection analysis on the pediatric anxiety rating scale

机译:使用小儿焦虑等级量表的信号检测分析完善儿童焦虑症的治疗反应和症状缓解识别的临床判断

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Objective: The purpose of this study was to determine guidelines for delineating treatment response and symptom remission for children with anxiety disorder based on the five item and Pediatric Anxiety Rating Scale (PARS5), and replicate guidelines using the six item PARS (PARS6). Methods: Participants were 73 children 7-13 years of age with a primary anxiety disorder who received computer-assisted cognitive behavioral therapy for anxiety. Signal detection analyses utilizing receiver operating curve procedures were used to determine optimal guidelines for defining treatment response and symptom remission for youth with anxiety disorders on the PARS5 and PARS6. The percent reduction in anxiety severity was used to predict treatment responder status. The percent reduction in symptoms and posttreatment raw score were used to predict remission status. Results: Optimal prediction of treatment response based on gold standard criteria was achieved at 15-20% reduction in symptoms on the PARS5 (with 20% reduction achieving marginally higher accuracy), and 20% reduction on the PARS6. A 25% reduction in symptoms on the PARS5 or a posttreatment raw score cutoff of 9 optimally predicted remission status. For the PARS6, a cutoff of 35% reduction or a posttreatment score of 11, was considered optimal for determining remission in clinical settings, whereas a 30% reduction or score of 12 was considered optimal for research settings. Conclusions: With different scoring options available for the PARS, these results provide guidelines for determining response and remission based on the PARS5 and PARS6 scores. Guidelines have implications for use in clinical trials, as well as for assessment of change in clinical practice.
机译:目的:本研究的目的是根据五项和儿童焦虑评估量表(PARS5)确定描述焦虑症患儿的治疗反应和症状缓解的指南,并使用六项PARS(PARS6)来复制指南。方法:参与者为73名7-13岁的原发性焦虑症儿童,他们接受了计算机辅助认知行为疗法治疗焦虑症。利用接收器工作曲线程序进行信号检测分析,以确定用于确定PARS5和PARS6上患有焦虑症的青年的治疗反应和症状缓解的最佳指南。焦虑严重程度的降低百分比用于预测治疗反应者的状态。症状减少的百分比和治疗后的原始评分用于预测缓解状态。结果:在PARS5上症状减少15-20%(减少20%达到较高的准确度),而在PARS6减少20%时,可以达到基于黄金标准的最佳治疗反应预测。 PARS5的症状减轻25%或治疗后原始评分截止值达到9的最佳预测缓解状态。对于PARS6,降低35%的截止值或11的治疗后分数被认为是确定临床环境中缓解的最佳选择,而对于研究设置,30%的降低或12的分数被认为是最佳的。结论:利用针对PARS的不同评分选项,这些结果提供了基于PARS5和PARS6分数确定反应和缓解的指南。指南对于在临床试验中使用以及对临床实践变化的评估具有影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号