它能有多简单?通过对MAPS-EASI 2.0早期儿童易怒筛查的基于人群的验证,缩小研究与实践之间的差距,并将其转化为临床应用。

IF 1.7 Q3 PSYCHOLOGY
Translational Issues in Psychological Science Pub Date : 2024-12-01 Epub Date: 2024-12-12 DOI:10.1037/tps0000428
Lauren S Wakschlag, Yudong Zhang, Marie E Heffernan, Leigha A MacNeill, Erin O Peterson, Susan Friedland, Aliza Jaffe Sass, Justin D Smith, Matthew M Davis, Jillian Lee Wiggins
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引用次数: 0

摘要

失调的易怒是最强大的早期儿童精神病理的诊断预测因子。然而,由于缺乏有效的、基于发育的筛查工具,这一证据未能转化为实践。根据经过验证的多维评估档案(MAPS)脾气损失量表,初步临床筛选器(MAPS-早期易怒评估筛选器;MAPS- easi 1.0)的早期可行性测试得到了好评。然而,大规模的临床实施需要提高精度,在一个大的代表性样本中,用心理测量学得出年龄带规范。在这里,我们的目标是通过对MAPS-EASI 2.0易怒筛选和影响评级的心理测量验证来优化MAPS-EASI在常规儿科护理中的应用。利用2-5岁儿童的数据(N=1,508)得出MAPS-EASI 2.0的可推广阈值。分析以幼儿(n=463)和学龄前儿童(n=1045)就诊时间为指导,生成两种易怒筛选表:(1)幼儿(18-33个月)3个项目;(2)学龄前儿童(34-66个月)4项。对幼儿和学龄前儿童分别采用良至优分类(曲线下面积=0.84,0.88)、敏感性(0.83,0.82)和特异性(0.72,0.79)建立易怒筛选器严重程度切点。通过MAPS-EASI 2.0 Impact Rating将损伤纳入筛选算法,减少了过度识别。该综合算法的临床阈值分别确定了15%和18%的幼儿和学龄前儿童;这些比率与已确定的人口流行率相符。实用的、跨诊断的常规护理发育筛查工具可能会加速易怒科学对早期心理健康的现实影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
How EASI can it be? Closing the research-to-practice gap via population-based validation of the MAPS-EASI 2.0 early childhood irritability screener for translation to clinical use.

Dysregulated irritability is the most robust early childhood transdiagnostic predictor of psychopathology. However, this evidence has failed to translate to practice due to a dearth of efficient, developmentally-based screening tools. Drawing on the well-validated Multidimensional Assessment Profiles (MAPS) Temper Loss Scale, early feasibility testing of a preliminary clinical screener (MAPS-Early Assessment Screener for Irritability; MAPS-EASI 1.0) was well-received. However, large-scale clinical implementation requires enhanced precision, with age-banded norms psychometrically derived in a large representative sample. Here, we aim to optimize MAPS-EASI for routine pediatric care via psychometric validation of the MAPS-EASI 2.0 Irritability Screener and Impact Rating. Data on 2-5-year-old children (N=1,508) were utilized to derive generalizable thresholds for MAPS-EASI 2.0. Analyses were guided by timing of toddler (n=463) and preschool (n=1045) age well-child visits, generating two Irritability Screener forms: (1) 3 items for toddlers (18-33 months); and (2) 4 items for preschoolers (34-66 months). Irritability Screener severity cut-points were established with good-to-excellent classification (areas under the curve=0.84, 0.88), sensitivity (0.83, 0.82), and specificity (0.72, 0.79), for toddlers and preschoolers respectively. Over-identification was reduced by including impairment in the screening algorithm via the MAPS-EASI 2.0 Impact Rating. The clinical threshold for this integrative algorithm identified 15% and 18% of toddlers and preschoolers, respectively; these rates align with established population prevalence. Pragmatic, transdiagnostic developmental screening tools for routine care may accelerate real-world impact of irritability science for early mental health.

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CiteScore
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