Predicting post-COVID-19 condition in children and young people up to 24 months after a positive SARS-CoV-2 PCR-test: the CLoCk study.

IF 7 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL BMC Medicine Pub Date : 2024-11-07 DOI:10.1186/s12916-024-03708-1
Manjula D Nugawela, Terence Stephenson, Roz Shafran, Trudie Chalder, Emma Dalrymple, Tamsin Ford, Lana Fox-Smith, Anthony Harnden, Isobel Heyman, Shamez N Ladhani, Kelsey McOwat, Ruth Simmons, Olivia Swann, Elizabeth Whittaker, Snehal M Pinto Pereira
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Abstract

Background: Predicting which children and young people (CYP) are at the highest risk of developing post-COVID-19 condition (PCC) could improve care pathways. We aim to develop and validate prediction models for persistent PCC up to 24 months post-infection in CYP.

Methods: CYP who were PCR-positive between September 2020 and March 2021, with follow-up data up to 24-months post-infection, were analysed. Persistent PCC was defined in two ways, as PCC at (a) 3, 6, 12 and 24 months post-infection (N = 943) or (b) 6, 12 and 24 months post-infection (N = 2373). Prediction models were developed using logistic regression; performance was assessed using calibration and discrimination measures; internal validation was performed via bootstrapping; the final model was adjusted for overfitting.

Results: While 24.7% (233/943) of CYP met the PCC definition 3 months post-infection, only 7.2% (68/943) continued to meet the PCC definition at all three subsequent timepoints, i.e. at 6, 12 and 24 months. The final models predicting risk of persistent PCC (at 3, 6, 12 and 24 months and at 6, 12 and 24 months) contained sex (female), history of asthma, allergy problems, learning difficulties at school and family history of ongoing COVID-19 problems, with additional variables (e.g. older age at infection and region of residence) in the model predicting PCC at 6, 12 and 24 months. Internal validation showed minimal overfitting of models with good calibration and discrimination measures (optimism-adjusted calibration slope: 1.064-1.142; C-statistic: 0.724-0.755).

Conclusions: To our knowledge, these are the only prediction models estimating the risk of CYP persistently meeting the PCC definition up to 24 months post-infection. The models could be used to triage CYP after infection. CYP with factors predicting longer-term symptomology, may benefit from earlier support.

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预测儿童和青少年在 SARS-CoV-2 PCR 检测呈阳性后 24 个月内的 COVID-19 后病情:CLoCk 研究。
背景:预测哪些儿童和青少年 (CYP) 最有可能罹患后 COVID-19 病症 (PCC),可以改善护理路径。我们的目标是开发并验证针对儿童和青少年感染后 24 个月内持续性 PCC 的预测模型:我们对 2020 年 9 月至 2021 年 3 月期间 PCR 阳性的 CYP 感染后 24 个月的随访数据进行了分析。持续性 PCC 有两种定义方式,即 (a) 感染后 3、6、12 和 24 个月(N = 943)或 (b) 感染后 6、12 和 24 个月(N = 2373)的 PCC。采用逻辑回归法建立预测模型;采用校准和判别指标评估模型的性能;通过引导法进行内部验证;对最终模型进行过拟合调整:24.7%的CYP(233/943)在感染后3个月符合PCC定义,但只有7.2%的CYP(68/943)在随后的三个时间点,即6个月、12个月和24个月继续符合PCC定义。预测持续 PCC 风险(3、6、12 和 24 个月时以及 6、12 和 24 个月时)的最终模型包含性别(女性)、哮喘病史、过敏问题、在校学习困难和持续 COVID-19 问题家族史,预测 6、12 和 24 个月时 PCC 的模型中还包含其他变量(如感染时年龄较大和居住地区)。内部验证显示,模型的过拟合程度极低,校准和区分度良好(乐观调整校准斜率:1.064-1.142;C统计量:0.724-0.755):据我们所知,这些预测模型是唯一可估算感染后 24 个月内持续符合 PCC 定义的 CYP 风险的模型。这些模型可用于对感染后的 CYP 进行分流。具有预测长期症状因素的 CYP 可能会从早期支持中获益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Medicine
BMC Medicine 医学-医学:内科
CiteScore
13.10
自引率
1.10%
发文量
435
审稿时长
4-8 weeks
期刊介绍: BMC Medicine is an open access, transparent peer-reviewed general medical journal. It is the flagship journal of the BMC series and publishes outstanding and influential research in various areas including clinical practice, translational medicine, medical and health advances, public health, global health, policy, and general topics of interest to the biomedical and sociomedical professional communities. In addition to research articles, the journal also publishes stimulating debates, reviews, unique forum articles, and concise tutorials. All articles published in BMC Medicine are included in various databases such as Biological Abstracts, BIOSIS, CAS, Citebase, Current contents, DOAJ, Embase, MEDLINE, PubMed, Science Citation Index Expanded, OAIster, SCImago, Scopus, SOCOLAR, and Zetoc.
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