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Residual lung abnormalities following COVID-19 hospitalisation: interim analysis of the UKILD Post-COVID study

Residual lung abnormalities following COVID-19 hospitalisation: interim analysis of the UKILD Post-COVID study
Residual lung abnormalities following COVID-19 hospitalisation: interim analysis of the UKILD Post-COVID study
Rationale: shared symptoms and genetic architecture between COVID-19 and lung fibrosis suggests SARS-CoV-2 infection may lead to progressive lung damage.

Objectives: the UKILD Post-COVID study interim analysis was planned to estimate the prevalence of residual lung abnormalities in people hospitalised with COVID-19 based on risk strata.

Methods: the Post-HOSPitalisation COVID Study (PHOSP-COVID) was used for capture of routine and research follow-up within 240 days from discharge. Thoracic CTs were linked by PHOSP-COVID identifiers and scored for percentage involvement of residual abnormalities (ground glass opacities and reticulations). Risk factors in linked CT were estimated with Bayesian binomial regression and used to generate risk strata. Numbers of cases within strata were used to estimate post-hospitalisation prevalence using Bayesian binomial distributions. Sensitivity was performed in research follow-up participants.

Measurements and Main Results: the interim cohort comprised 3700 people. Of 209 linked CTs (median 119 days, interquartile range 83-155), 164 people (79.6%) had >10% involvement of residual lung abnormalities. Major risk factors included abnormal chest X-ray (RR 1·21 95%CrI 1·05; 1·40), percent predicted DLco<80% (RR 1·25 95%CrI 1·00; 1·56) and severe admission requiring ventilation support (RR 1·27 95%CrI 1·07; 1·55). Moderate to very-high risk was classified in 7·8% of the remaining 3491 people, post-hospitalisation prevalence was estimated at 8.5% (95%CI CrI 7.6%; 9.5%) rising to 11.7% (95%CrI 10.3%; 13.1%) in sensitivity analysis.

Conclusions: prevalence of residual lung abnormalities were estimated in up to 11% of people discharged following COVID-19 related hospitalisation. Health services should monitor at-risk individuals to elucidate long term functional implications.
COVID-19, HRCT, hospitalization, lung abnormalities, lung damage
1073-449X
693-703
Stewart, I.
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Jacob, J.
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George, P.M.
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Porter, J.C .
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Allen, R.J.
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Aslani, S.
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Baillie, J.K.
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Baratt, S.L.
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Bianchi, S.M.
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Blaikley, J.F.
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Chalmers, J.
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Chambers, R.C.
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Chadhuri, N.
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Coleman, C.
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Jones, Mark
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Weeks, M.
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Wild, J.M.
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Wootton, D.G.
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Brightling, C.E.
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Ho, L.P.
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Wain, L.V.
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Jenkins, R.G.
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Stewart, I.
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Jacob, J.
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George, P.M.
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Porter, J.C .
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Allen, R.J.
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Aslani, S.
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Baillie, J.K.
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Baratt, S.L.
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Bianchi, S.M.
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Blaikley, J.F.
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Chalmers, J.
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Chambers, R.C.
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Chadhuri, N.
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Coleman, C.
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Jones, Mark
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Weeks, M.
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Wild, J.M.
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Wootton, D.G.
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Brightling, C.E.
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Ho, L.P.
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Wain, L.V.
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Jenkins, R.G.
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Stewart, I., Jacob, J., George, P.M., Porter, J.C ., Allen, R.J., Aslani, S., Baillie, J.K., Baratt, S.L., Bianchi, S.M., Blaikley, J.F., Chalmers, J., Chambers, R.C., Chadhuri, N., Coleman, C., Jones, Mark, Weeks, M., Wild, J.M., Wootton, D.G., Brightling, C.E., Ho, L.P., Wain, L.V. and Jenkins, R.G. (2023) Residual lung abnormalities following COVID-19 hospitalisation: interim analysis of the UKILD Post-COVID study. American Journal of Respiratory and Critical Care Medicine, 207 (6), 693-703. (doi:10.1164/rccm.202203-0564OC).

Record type: Article

Abstract

Rationale: shared symptoms and genetic architecture between COVID-19 and lung fibrosis suggests SARS-CoV-2 infection may lead to progressive lung damage.

Objectives: the UKILD Post-COVID study interim analysis was planned to estimate the prevalence of residual lung abnormalities in people hospitalised with COVID-19 based on risk strata.

Methods: the Post-HOSPitalisation COVID Study (PHOSP-COVID) was used for capture of routine and research follow-up within 240 days from discharge. Thoracic CTs were linked by PHOSP-COVID identifiers and scored for percentage involvement of residual abnormalities (ground glass opacities and reticulations). Risk factors in linked CT were estimated with Bayesian binomial regression and used to generate risk strata. Numbers of cases within strata were used to estimate post-hospitalisation prevalence using Bayesian binomial distributions. Sensitivity was performed in research follow-up participants.

Measurements and Main Results: the interim cohort comprised 3700 people. Of 209 linked CTs (median 119 days, interquartile range 83-155), 164 people (79.6%) had >10% involvement of residual lung abnormalities. Major risk factors included abnormal chest X-ray (RR 1·21 95%CrI 1·05; 1·40), percent predicted DLco<80% (RR 1·25 95%CrI 1·00; 1·56) and severe admission requiring ventilation support (RR 1·27 95%CrI 1·07; 1·55). Moderate to very-high risk was classified in 7·8% of the remaining 3491 people, post-hospitalisation prevalence was estimated at 8.5% (95%CI CrI 7.6%; 9.5%) rising to 11.7% (95%CrI 10.3%; 13.1%) in sensitivity analysis.

Conclusions: prevalence of residual lung abnormalities were estimated in up to 11% of people discharged following COVID-19 related hospitalisation. Health services should monitor at-risk individuals to elucidate long term functional implications.

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Accepted/In Press date: 27 October 2022
Published date: 15 March 2023
Additional Information: Funding Information: (Received in original form March 21, 2022; accepted in final form December 1, 2022) This article is open access and distributed under the terms of the Creative Commons Attribution 4.0 International License. Supported by the National Institute of Health Research (COV0319) and UK Research and Innovation (MR/V027859/1). Publisher Copyright: Copyright © 2023 by the American Thoracic Society.
Keywords: COVID-19, HRCT, hospitalization, lung abnormalities, lung damage

Identifiers

Local EPrints ID: 472324
URI: http://eprints.soton.ac.uk/id/eprint/472324
ISSN: 1073-449X
PURE UUID: 646caf5f-1413-4cb5-9b60-c88db33ba374
ORCID for Mark Jones: ORCID iD orcid.org/0000-0001-6308-6014

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Date deposited: 01 Dec 2022 17:39
Last modified: 17 Mar 2024 03:12

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Contributors

Author: I. Stewart
Author: J. Jacob
Author: P.M. George
Author: J.C . Porter
Author: R.J. Allen
Author: S. Aslani
Author: J.K. Baillie
Author: S.L. Baratt
Author: S.M. Bianchi
Author: J.F. Blaikley
Author: J. Chalmers
Author: R.C. Chambers
Author: N. Chadhuri
Author: C. Coleman
Author: Mark Jones ORCID iD
Author: M. Weeks
Author: J.M. Wild
Author: D.G. Wootton
Author: C.E. Brightling
Author: L.P. Ho
Author: L.V. Wain
Author: R.G. Jenkins

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