Deriving and validating a risk prediction model for long COVID-19: protocol for an observational cohort study using linked Scottish data.


Journal

BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874

Informations de publication

Date de publication:
06 07 2022
Historique:
entrez: 6 7 2022
pubmed: 7 7 2022
medline: 9 7 2022
Statut: epublish

Résumé

COVID-19 is commonly experienced as an acute illness, yet some people continue to have symptoms that persist for weeks, or months (commonly referred to as 'long-COVID'). It remains unclear which patients are at highest risk of developing long-COVID. In this protocol, we describe plans to develop a prediction model to identify individuals at risk of developing long-COVID. We will use the national Early Pandemic Evaluation and Enhanced Surveillance of COVID-19 (EAVE II) platform, a population-level linked dataset of routine electronic healthcare data from 5.4 million individuals in Scotland. We will identify potential indicators for long-COVID by identifying patterns in primary care data linked to information from out-of-hours general practitioner encounters, accident and emergency visits, hospital admissions, outpatient visits, medication prescribing/dispensing and mortality. We will investigate the potential indicators of long-COVID by performing a matched analysis between those with a positive reverse transcriptase PCR (RT-PCR) test for SARS-CoV-2 infection and two control groups: (1) individuals with at least one negative RT-PCR test and never tested positive; (2) the general population (everyone who did not test positive) of Scotland. Cluster analysis will then be used to determine the final definition of the outcome measure for long-COVID. We will then derive, internally and externally validate a prediction model to identify the epidemiological risk factors associated with long-COVID. The EAVE II study has obtained approvals from the Research Ethics Committee (reference: 12/SS/0201), and the Public Benefit and Privacy Panel for Health and Social Care (reference: 1920-0279). Study findings will be published in peer-reviewed journals and presented at conferences. Understanding the predictors for long-COVID and identifying the patient groups at greatest risk of persisting symptoms will inform future treatments and preventative strategies for long-COVID.

Identifiants

pubmed: 35793922
pii: bmjopen-2021-059385
doi: 10.1136/bmjopen-2021-059385
pmc: PMC9260199
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e059385

Subventions

Organisme : Chief Scientist Office
ID : COV/LTE/20/15
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_19004
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_00022/2
Pays : United Kingdom
Organisme : Chief Scientist Office
ID : SCAF/15/02
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: AS is a member of the Scottish Government Chief Medical Officer’s COVID-19 Advisory Group and its Standing Committee on Pandemics. He is a member of the UK Government’s Risk Stratification Subgroup and Astra-Zeneca's Thrombotic Thrombocytopenic Taskforce. All roles are unremunerated. SVK was co-chair of the Scottish Government’s Expert Reference Group on Ethnicity and COVID-19 and a member of the UK Government’s Scientific Advisory Group on Emergencies (SAGE) subgroup on ethnicity. All other authors declare no competing interests.

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Auteurs

Luke Daines (L)

Usher Institute, The University of Edinburgh, Edinburgh, UK luke.daines@ed.ac.uk.

Rachel H Mulholland (RH)

Usher Institute, The University of Edinburgh, Edinburgh, UK.

Eleftheria Vasileiou (E)

Usher Institute, The University of Edinburgh, Edinburgh, UK.

Vicky Hammersley (V)

Usher Institute, The University of Edinburgh, Edinburgh, UK.

David Weatherill (D)

Usher Institute, The University of Edinburgh, Edinburgh, UK.

Srinivasa Vittal Katikireddi (SV)

MRC/CSO Social & Public Health Sciences Unit, University of Glasgow, Glasgow, UK.

Steven Kerr (S)

Usher Institute, The University of Edinburgh, Edinburgh, UK.

Emily Moore (E)

Public Health Scotland, Glasgow and Edinburgh, UK.

Elisa Pesenti (E)

Institute of Cell Biology, University of Edinburgh, Edinburgh, UK.

Jennifer K Quint (JK)

Faculty of Medicine, National Heart and Lung Institute, Imperial College London, London, UK.

Syed Ahmar Shah (SA)

Usher Institute, The University of Edinburgh, Edinburgh, UK.

Ting Shi (T)

Usher Institute, The University of Edinburgh, Edinburgh, UK.

Colin R Simpson (CR)

Usher Institute, The University of Edinburgh, Edinburgh, UK.
School of Health, Wellington Faculty of Health, Victoria University of Wellington, Wellington, New Zealand.

Chris Robertson (C)

Public Health Scotland, Glasgow and Edinburgh, UK.
Department of Mathematics and Statistics, University of Strathclyde, Glasgow, UK.

Aziz Sheikh (A)

Usher Institute, The University of Edinburgh, Edinburgh, UK.

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