Nugawela, MD;
Stephenson, T;
Shafran, R;
De Stavola, BL;
Ladhani, SN;
Simmons, R;
McOwat, K;
Rojas, N;
Dalrymple, E;
Cheung, EY;
et al.
Nugawela, MD; Stephenson, T; Shafran, R; De Stavola, BL; Ladhani, SN; Simmons, R; McOwat, K; Rojas, N; Dalrymple, E; Cheung, EY; Ford, T; Heyman, I; Crawley, E; Pinto Pereira, SM
(2022)
Predictive model for long COVID in children 3 months after a SARS-CoV-2 PCR test.
BMC Med, 20 (1).
p. 465.
ISSN 1741-7015
https://doi.org/10.1186/s12916-022-02664-y
SGUL Authors: Ladhani, Shamez Nizarali
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Abstract
BACKGROUND: To update and internally validate a model to predict children and young people (CYP) most likely to experience long COVID (i.e. at least one impairing symptom) 3 months after SARS-CoV-2 PCR testing and to determine whether the impact of predictors differed by SARS-CoV-2 status. METHODS: Data from a nationally matched cohort of SARS-CoV-2 test-positive and test-negative CYP aged 11-17 years was used. The main outcome measure, long COVID, was defined as one or more impairing symptoms 3 months after PCR testing. Potential pre-specified predictors included SARS-CoV-2 status, sex, age, ethnicity, deprivation, quality of life/functioning (five EQ-5D-Y items), physical and mental health and loneliness (prior to testing) and number of symptoms at testing. The model was developed using logistic regression; performance was assessed using calibration and discrimination measures; internal validation was performed via bootstrapping and the final model was adjusted for overfitting. RESULTS: A total of 7139 (3246 test-positives, 3893 test-negatives) completing a questionnaire 3 months post-test were included. 25.2% (817/3246) of SARS-CoV-2 PCR-positives and 18.5% (719/3893) of SARS-CoV-2 PCR-negatives had one or more impairing symptoms 3 months post-test. The final model contained SARS-CoV-2 status, number of symptoms at testing, sex, age, ethnicity, physical and mental health, loneliness and four EQ-5D-Y items before testing. Internal validation showed minimal overfitting with excellent calibration and discrimination measures (optimism-adjusted calibration slope: 0.96575; C-statistic: 0.83130). CONCLUSIONS: We updated a risk prediction equation to identify those most at risk of long COVID 3 months after a SARS-CoV-2 PCR test which could serve as a useful triage and management tool for CYP during the ongoing pandemic. External validation is required before large-scale implementation.
Item Type: | Article | ||||||||||||
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Additional Information: | © The Author(s) 2022. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. | ||||||||||||
Keywords: | COVID-19, Children and young people, Long COVID, Predictive model, Public health, Symptoms, Child, Humans, Adolescent, SARS-CoV-2, COVID-19, Quality of Life, Polymerase Chain Reaction, Post-Acute COVID-19 Syndrome, Humans, Polymerase Chain Reaction, Quality of Life, Adolescent, Child, COVID-19, SARS-CoV-2, Post-Acute COVID-19 Syndrome, COVID-19, Long COVID, Symptoms, Predictive model, Public health, Children and young people, 11 Medical and Health Sciences, General & Internal Medicine | ||||||||||||
SGUL Research Institute / Research Centre: | Academic Structure > Infection and Immunity Research Institute (INII) | ||||||||||||
Journal or Publication Title: | BMC Med | ||||||||||||
ISSN: | 1741-7015 | ||||||||||||
Language: | eng | ||||||||||||
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Publisher License: | Creative Commons: Attribution 4.0 | ||||||||||||
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PubMed ID: | 36447237 | ||||||||||||
Web of Science ID: | WOS:000890278000004 | ||||||||||||
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URI: | https://openaccess.sgul.ac.uk/id/eprint/115117 | ||||||||||||
Publisher's version: | https://doi.org/10.1186/s12916-022-02664-y |
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