Assessing competency in less invasive surfactant administration: simulation-based validity evidence for the LISA-AT scores.

IF 3.1 3区 医学 Q1 PEDIATRICS Pediatric Research Pub Date : 2025-01-18 DOI:10.1038/s41390-025-03868-7
Niklas Breindahl, Emma Therese Bay, Christian Heiring, Ingrid Rose MacLean-Nyegaard, Amalie Gudiksen, Andreas Frithioff, Tine Brink Henriksen, Martin Grønnebæk Tolsgaard, Lise Aunsholt
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引用次数: 0

Abstract

Background: The Less Invasive Surfactant Administration Assessment Tool (LISA-AT) was developed to support operator training and competence assessment. This study aimed to gather validity evidence in the simulated setting to support using the LISA-AT scores.

Methods: Validity evidence was gathered using the Messick framework. The lowest quartile (Q1) for the median of the experts' LISA-AT scores defined the minimum passing score.

Results: Ten experts and 23 novices were enrolled in this study. Eight of the original 15 LISA-AT metrics effectively discriminated between novices and experts and demonstrated high test-retest reliability (Spearman's rho = 0.87), high internal consistency, and good inter-rater reliability (Cronbach's alpha = 0.88 and 0.82, respectively). The LISA-AT discriminated between novices' and experts' first two attempts with median [IQR] scores of 29 [26-32] vs 39 [39-40]). The minimum passing score was defined as 39/40 points, and the novices used a median [IQR] of 6 [5-7] attempts, ranging from 4 to 9 attempts, to reach this score. Compared with the expert group, the novices' laryngoscopy skills and time remained significantly different even after attaining the minimum passing score.

Conclusion: We found strong validity evidence to support using the LISA-AT scores to train new LISA operators to the minimum passing score to ensure competence in the simulated setting.

Impact: This study showed robust validity evidence for using the Less Invasive Surfactant Administration Assessment Tool (LISA-AT) to train LISA novices with a high test-retest reliability, high internal consistency, and good inter-rater reliability. Eight of the original 15 LISA-AT metrics effectively discriminated between novices and experts, with a minimum passing score of 39/40 points, corresponding to the lowest quartile (Q1) of the experts' performances. Novices typically needed six attempts in the simulated setting, ranging from four to nine. However, their laryngoscopy skills and duration remained significantly different from experts. Using the LISA-AT score can ensure competence in the simulated setting before advancing to supervised clinical procedures.

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评估低创表面活性剂给药的能力:LISA-AT分数基于模拟的效度证据。
背景:低创表面活性剂给药评估工具(LISA-AT)的开发是为了支持操作人员培训和能力评估。本研究旨在收集模拟情境下的效度证据,以支持使用LISA-AT分数。方法:采用Messick框架收集效度证据。专家的LISA-AT分数中位数的最低四分位数(Q1)定义了最低及格分数。结果:入选专家10名,新手23名。最初的15个LISA-AT指标中有8个有效地区分了新手和专家,并表现出高测试-重测信度(Spearman's rho = 0.87),高内部一致性和良好的评估者间信度(Cronbach's alpha分别= 0.88和0.82)。LISA-AT区分新手和专家的前两次尝试,中位数[IQR]得分为29[26-32]和39[39-40])。最低及格分数定义为39/40分,新手使用6[5-7]次尝试的中位数[IQR]达到该分数,范围从4到9次。与专家组相比,即使达到最低合格分,新手的喉镜检查技能和时间仍有显著差异。结论:我们发现强有力的效度证据支持使用LISA- at分数来培训新的LISA操作员达到最低及格分数,以确保在模拟环境中的能力。影响:本研究显示了使用无创表面活性剂给药评估工具(LISA- at)训练LISA新手具有高重测信度、高内部一致性和良好的量表间信度的强有力的效度证据。在最初的15个LISA-AT指标中,有8个有效地区分了新手和专家,最低通过分数为39/40分,对应于专家表现的最低四分位数(Q1)。新手通常需要在模拟环境中尝试六次,从四次到九次不等。然而,他们的喉镜检查技能和持续时间与专家仍有显著差异。使用LISA-AT评分可以确保在进入有监督的临床程序之前在模拟环境中的能力。
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来源期刊
Pediatric Research
Pediatric Research 医学-小儿科
CiteScore
6.80
自引率
5.60%
发文量
473
审稿时长
3-8 weeks
期刊介绍: Pediatric Research publishes original papers, invited reviews, and commentaries on the etiologies of children''s diseases and disorders of development, extending from molecular biology to epidemiology. Use of model organisms and in vitro techniques relevant to developmental biology and medicine are acceptable, as are translational human studies
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