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预测儿童哮喘风险工具的临床队列外部验证。

External validation of the Predicting Asthma Risk in Children tool in a clinical cohort.

机构信息

Institute of Social and Preventive Medicine, University of Bern, Bern, Switzerland.

Graduate School for Health Sciences, University of Bern, Bern, Switzerland.

出版信息

Pediatr Pulmonol. 2022 Nov;57(11):2715-2723. doi: 10.1002/ppul.26088. Epub 2022 Aug 12.

Abstract

INTRODUCTION

The Predicting Asthma Risk in Children (PARC) tool uses questionnaire-based respiratory symptoms collected from preschool children to predict asthma risk 5 years later. The tool was developed and validated in population cohorts but not validated using a clinical cohort. We aimed to externally validate the PARC tool in a pediatric pulmonology clinic setting.

METHODS

The Swiss Paediatric Airway Cohort (SPAC) is a prospective cohort of children seen in pediatric pulmonology clinics across Switzerland. We included children aged 1-6 years with cough or wheeze at baseline who completed the 2-year follow-up questionnaire. The outcome was defined as current wheeze plus use of asthma medication. We assessed performance using: sensitivity, specificity, negative predictive value (NPV) and positive predictive value (PPV), area under the curve (AUC), scaled Brier's score, and Nagelkerke's R scores. We compared performance in SPAC to that in the original population, the Leicester Respiratory Cohort (LRC).

RESULTS

Among 346 children included, 125 (36%) reported the outcome after 2 years. At a PARC score of 4: sensitivity was higher (95% vs. 79%), specificity lower (14% vs. 57%), and NPV and PPV comparable (0.84 vs. 0.87 and 0.37 vs. 0.42) in SPAC versus LRC. AUC (0.71 vs. 0.78), R (0.18 vs. 0.28) and Brier's scores (0.13 vs. 0.22) were lower in SPAC.

CONCLUSIONS

The PARC tool shows some clinical utility, particularly for ruling out the development of asthma in young children, but performance limitations highlight the need for new prediction tools to be developed specifically for the clinical setting.

摘要

简介

预测儿童哮喘风险(PARC)工具使用基于问卷的学龄前儿童呼吸症状来预测 5 年后的哮喘风险。该工具是在人群队列中开发和验证的,但尚未在临床队列中验证。我们旨在儿科肺病学诊所环境中对 PARC 工具进行外部验证。

方法

瑞士儿科气道队列(SPAC)是一项前瞻性队列研究,纳入了瑞士各地儿科肺病诊所就诊的 1-6 岁儿童,这些儿童在基线时有咳嗽或喘息,并完成了为期 2 年的随访问卷。主要结局为当前喘息和使用哮喘药物。我们使用以下方法评估性能:敏感性、特异性、阴性预测值(NPV)和阳性预测值(PPV)、曲线下面积(AUC)、缩放 Brier 评分和 Nagelkerke 的 R 评分。我们将 SPAC 中的表现与原始人群莱斯特呼吸队列(LRC)进行了比较。

结果

在 346 名入组儿童中,125 名(36%)在 2 年后报告了结局。在 PARC 评分为 4 分的情况下,敏感性更高(95% vs. 79%),特异性更低(14% vs. 57%),NPV 和 PPV 相当(0.84 vs. 0.87 和 0.37 vs. 0.42),但 AUC(0.71 vs. 0.78)、R (0.18 vs. 0.28)和 Brier 评分(0.13 vs. 0.22)在 SPAC 中较低。

结论

PARC 工具具有一定的临床实用性,特别是在排除幼儿哮喘方面,但性能限制突出表明需要开发专门针对临床环境的新预测工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b8b/9804745/caec008e56e3/PPUL-57-2715-g003.jpg

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