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Residual Lung Abnormalities after COVID-19 Hospitalization: Interim Analysis of the UKILD Post–COVID-19 Study

RATIONALE: Shared symptoms and genetic architecture between coronavirus disease (COVID-19) and lung fibrosis suggest severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection may lead to progressive lung damage. OBJECTIVES: The UK Interstitial Lung Disease Consortium (UKILD) post–COVID-...

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Autores principales: Stewart, Iain, Jacob, Joseph, George, Peter M., Molyneaux, Philip L., Porter, Joanna C., Allen, Richard J., Aslani, Shahab, Baillie, J. Kenneth, Barratt, Shaney L., Beirne, Paul, Bianchi, Stephen M., Blaikley, John F., Chalmers, James D., Chambers, Rachel C., Chadhuri, Nazia, Coleman, Christopher, Collier, Guilhem, Denneny, Emma K., Docherty, Annemarie, Elneima, Omer, Evans, Rachael A., Fabbri, Laura, Gibbons, Michael A., Gleeson, Fergus V., Gooptu, Bibek, Greening, Neil J., Guio, Beatriz Guillen, Hall, Ian P., Hanley, Neil A., Harris, Victoria, Harrison, Ewen M., Heightman, Melissa, Hillman, Toby E., Horsley, Alex, Houchen-Wolloff, Linzy, Jarrold, Ian, Johnson, Simon R., Jones, Mark G., Khan, Fasihul, Lawson, Rod, Leavy, Olivia, Lone, Nazir, Marks, Michael, McAuley, Hamish, Mehta, Puja, Parekh, Dhruv, Hanley, Karen Piper, Platé, Manuela, Pearl, John, Poinasamy, Krisnah, Quint, Jennifer K., Raman, Betty, Richardson, Matthew, Rivera-Ortega, Pilar, Saunders, Laura, Saunders, Ruth, Semple, Malcolm G., Sereno, Marco, Shikotra, Aarti, Simpson, A. John, Singapuri, Amisha, Smith, David J. F., Spears, Mark, Spencer, Lisa G., Stanel, Stefan, Thickett, David R., Thompson, A. A. Roger, Thorpe, Mathew, Walsh, Simon L. F., Walker, Samantha, Weatherley, Nicholas David, Weeks, Mark E., Wild, Jim M., Wootton, Dan G., Brightling, Chris E., Ho, Ling-Pei, Wain, Louise V., Jenkins, Gisli R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Thoracic Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037479/
https://www.ncbi.nlm.nih.gov/pubmed/36457159
http://dx.doi.org/10.1164/rccm.202203-0564OC
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author Stewart, Iain
Jacob, Joseph
George, Peter M.
Molyneaux, Philip L.
Porter, Joanna C.
Allen, Richard J.
Aslani, Shahab
Baillie, J. Kenneth
Barratt, Shaney L.
Beirne, Paul
Bianchi, Stephen M.
Blaikley, John F.
Chalmers, James D.
Chambers, Rachel C.
Chadhuri, Nazia
Coleman, Christopher
Collier, Guilhem
Denneny, Emma K.
Docherty, Annemarie
Elneima, Omer
Evans, Rachael A.
Fabbri, Laura
Gibbons, Michael A.
Gleeson, Fergus V.
Gooptu, Bibek
Greening, Neil J.
Guio, Beatriz Guillen
Hall, Ian P.
Hanley, Neil A.
Harris, Victoria
Harrison, Ewen M.
Heightman, Melissa
Hillman, Toby E.
Horsley, Alex
Houchen-Wolloff, Linzy
Jarrold, Ian
Johnson, Simon R.
Jones, Mark G.
Khan, Fasihul
Lawson, Rod
Leavy, Olivia
Lone, Nazir
Marks, Michael
McAuley, Hamish
Mehta, Puja
Parekh, Dhruv
Hanley, Karen Piper
Platé, Manuela
Pearl, John
Poinasamy, Krisnah
Quint, Jennifer K.
Raman, Betty
Richardson, Matthew
Rivera-Ortega, Pilar
Saunders, Laura
Saunders, Ruth
Semple, Malcolm G.
Sereno, Marco
Shikotra, Aarti
Simpson, A. John
Singapuri, Amisha
Smith, David J. F.
Spears, Mark
Spencer, Lisa G.
Stanel, Stefan
Thickett, David R.
Thompson, A. A. Roger
Thorpe, Mathew
Walsh, Simon L. F.
Walker, Samantha
Weatherley, Nicholas David
Weeks, Mark E.
Wild, Jim M.
Wootton, Dan G.
Brightling, Chris E.
Ho, Ling-Pei
Wain, Louise V.
Jenkins, Gisli R.
author_facet Stewart, Iain
Jacob, Joseph
George, Peter M.
Molyneaux, Philip L.
Porter, Joanna C.
Allen, Richard J.
Aslani, Shahab
Baillie, J. Kenneth
Barratt, Shaney L.
Beirne, Paul
Bianchi, Stephen M.
Blaikley, John F.
Chalmers, James D.
Chambers, Rachel C.
Chadhuri, Nazia
Coleman, Christopher
Collier, Guilhem
Denneny, Emma K.
Docherty, Annemarie
Elneima, Omer
Evans, Rachael A.
Fabbri, Laura
Gibbons, Michael A.
Gleeson, Fergus V.
Gooptu, Bibek
Greening, Neil J.
Guio, Beatriz Guillen
Hall, Ian P.
Hanley, Neil A.
Harris, Victoria
Harrison, Ewen M.
Heightman, Melissa
Hillman, Toby E.
Horsley, Alex
Houchen-Wolloff, Linzy
Jarrold, Ian
Johnson, Simon R.
Jones, Mark G.
Khan, Fasihul
Lawson, Rod
Leavy, Olivia
Lone, Nazir
Marks, Michael
McAuley, Hamish
Mehta, Puja
Parekh, Dhruv
Hanley, Karen Piper
Platé, Manuela
Pearl, John
Poinasamy, Krisnah
Quint, Jennifer K.
Raman, Betty
Richardson, Matthew
Rivera-Ortega, Pilar
Saunders, Laura
Saunders, Ruth
Semple, Malcolm G.
Sereno, Marco
Shikotra, Aarti
Simpson, A. John
Singapuri, Amisha
Smith, David J. F.
Spears, Mark
Spencer, Lisa G.
Stanel, Stefan
Thickett, David R.
Thompson, A. A. Roger
Thorpe, Mathew
Walsh, Simon L. F.
Walker, Samantha
Weatherley, Nicholas David
Weeks, Mark E.
Wild, Jim M.
Wootton, Dan G.
Brightling, Chris E.
Ho, Ling-Pei
Wain, Louise V.
Jenkins, Gisli R.
author_sort Stewart, Iain
collection PubMed
description RATIONALE: Shared symptoms and genetic architecture between coronavirus disease (COVID-19) and lung fibrosis suggest severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection may lead to progressive lung damage. OBJECTIVES: The UK Interstitial Lung Disease Consortium (UKILD) post–COVID-19 study interim analysis was planned to estimate the prevalence of residual lung abnormalities in people hospitalized with COVID-19 on the basis of risk strata. METHODS: The PHOSP–COVID-19 (Post-Hospitalization COVID-19) study was used to capture routine and research follow-up within 240 days from discharge. Thoracic computed tomography linked by PHOSP–COVID-19 identifiers was scored for the percentage of residual lung abnormalities (ground-glass opacities and reticulations). Risk factors in linked computed tomography were estimated with Bayesian binomial regression, and risk strata were generated. Numbers within strata were used to estimate posthospitalization prevalence using Bayesian binomial distributions. Sensitivity analysis was restricted to participants with protocol-driven research follow-up. MEASUREMENTS AND MAIN RESULTS: The interim cohort comprised 3,700 people. Of 209 subjects with linked computed tomography (median, 119 d; interquartile range, 83–155), 166 people (79.4%) had more than 10% involvement of residual lung abnormalities. Risk factors included abnormal chest X-ray (risk ratio [RR], 1.21; 95% credible interval [CrI], 1.05–1.40), percent predicted Dl(CO) less than 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). In the remaining 3,491 people, moderate to very high risk of residual lung abnormalities was classified at 7.8%, and posthospitalization prevalence was estimated at 8.5% (95% CrI, 7.6–9.5), rising to 11.7% (95% CrI, 10.3–13.1) in the sensitivity analysis. CONCLUSIONS: Residual lung abnormalities were estimated in up to 11% of people discharged after COVID-19–related hospitalization. Health services should monitor at-risk individuals to elucidate long-term functional implications.
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spelling pubmed-100374792023-03-25 Residual Lung Abnormalities after COVID-19 Hospitalization: Interim Analysis of the UKILD Post–COVID-19 Study Stewart, Iain Jacob, Joseph George, Peter M. Molyneaux, Philip L. Porter, Joanna C. Allen, Richard J. Aslani, Shahab Baillie, J. Kenneth Barratt, Shaney L. Beirne, Paul Bianchi, Stephen M. Blaikley, John F. Chalmers, James D. Chambers, Rachel C. Chadhuri, Nazia Coleman, Christopher Collier, Guilhem Denneny, Emma K. Docherty, Annemarie Elneima, Omer Evans, Rachael A. Fabbri, Laura Gibbons, Michael A. Gleeson, Fergus V. Gooptu, Bibek Greening, Neil J. Guio, Beatriz Guillen Hall, Ian P. Hanley, Neil A. Harris, Victoria Harrison, Ewen M. Heightman, Melissa Hillman, Toby E. Horsley, Alex Houchen-Wolloff, Linzy Jarrold, Ian Johnson, Simon R. Jones, Mark G. Khan, Fasihul Lawson, Rod Leavy, Olivia Lone, Nazir Marks, Michael McAuley, Hamish Mehta, Puja Parekh, Dhruv Hanley, Karen Piper Platé, Manuela Pearl, John Poinasamy, Krisnah Quint, Jennifer K. Raman, Betty Richardson, Matthew Rivera-Ortega, Pilar Saunders, Laura Saunders, Ruth Semple, Malcolm G. Sereno, Marco Shikotra, Aarti Simpson, A. John Singapuri, Amisha Smith, David J. F. Spears, Mark Spencer, Lisa G. Stanel, Stefan Thickett, David R. Thompson, A. A. Roger Thorpe, Mathew Walsh, Simon L. F. Walker, Samantha Weatherley, Nicholas David Weeks, Mark E. Wild, Jim M. Wootton, Dan G. Brightling, Chris E. Ho, Ling-Pei Wain, Louise V. Jenkins, Gisli R. Am J Respir Crit Care Med Original Articles RATIONALE: Shared symptoms and genetic architecture between coronavirus disease (COVID-19) and lung fibrosis suggest severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection may lead to progressive lung damage. OBJECTIVES: The UK Interstitial Lung Disease Consortium (UKILD) post–COVID-19 study interim analysis was planned to estimate the prevalence of residual lung abnormalities in people hospitalized with COVID-19 on the basis of risk strata. METHODS: The PHOSP–COVID-19 (Post-Hospitalization COVID-19) study was used to capture routine and research follow-up within 240 days from discharge. Thoracic computed tomography linked by PHOSP–COVID-19 identifiers was scored for the percentage of residual lung abnormalities (ground-glass opacities and reticulations). Risk factors in linked computed tomography were estimated with Bayesian binomial regression, and risk strata were generated. Numbers within strata were used to estimate posthospitalization prevalence using Bayesian binomial distributions. Sensitivity analysis was restricted to participants with protocol-driven research follow-up. MEASUREMENTS AND MAIN RESULTS: The interim cohort comprised 3,700 people. Of 209 subjects with linked computed tomography (median, 119 d; interquartile range, 83–155), 166 people (79.4%) had more than 10% involvement of residual lung abnormalities. Risk factors included abnormal chest X-ray (risk ratio [RR], 1.21; 95% credible interval [CrI], 1.05–1.40), percent predicted Dl(CO) less than 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). In the remaining 3,491 people, moderate to very high risk of residual lung abnormalities was classified at 7.8%, and posthospitalization prevalence was estimated at 8.5% (95% CrI, 7.6–9.5), rising to 11.7% (95% CrI, 10.3–13.1) in the sensitivity analysis. CONCLUSIONS: Residual lung abnormalities were estimated in up to 11% of people discharged after COVID-19–related hospitalization. Health services should monitor at-risk individuals to elucidate long-term functional implications. American Thoracic Society 2022-12-01 /pmc/articles/PMC10037479/ /pubmed/36457159 http://dx.doi.org/10.1164/rccm.202203-0564OC Text en Copyright © 2023 by the American Thoracic Society https://creativecommons.org/licenses/by/4.0/This article is open access and distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Articles
Stewart, Iain
Jacob, Joseph
George, Peter M.
Molyneaux, Philip L.
Porter, Joanna C.
Allen, Richard J.
Aslani, Shahab
Baillie, J. Kenneth
Barratt, Shaney L.
Beirne, Paul
Bianchi, Stephen M.
Blaikley, John F.
Chalmers, James D.
Chambers, Rachel C.
Chadhuri, Nazia
Coleman, Christopher
Collier, Guilhem
Denneny, Emma K.
Docherty, Annemarie
Elneima, Omer
Evans, Rachael A.
Fabbri, Laura
Gibbons, Michael A.
Gleeson, Fergus V.
Gooptu, Bibek
Greening, Neil J.
Guio, Beatriz Guillen
Hall, Ian P.
Hanley, Neil A.
Harris, Victoria
Harrison, Ewen M.
Heightman, Melissa
Hillman, Toby E.
Horsley, Alex
Houchen-Wolloff, Linzy
Jarrold, Ian
Johnson, Simon R.
Jones, Mark G.
Khan, Fasihul
Lawson, Rod
Leavy, Olivia
Lone, Nazir
Marks, Michael
McAuley, Hamish
Mehta, Puja
Parekh, Dhruv
Hanley, Karen Piper
Platé, Manuela
Pearl, John
Poinasamy, Krisnah
Quint, Jennifer K.
Raman, Betty
Richardson, Matthew
Rivera-Ortega, Pilar
Saunders, Laura
Saunders, Ruth
Semple, Malcolm G.
Sereno, Marco
Shikotra, Aarti
Simpson, A. John
Singapuri, Amisha
Smith, David J. F.
Spears, Mark
Spencer, Lisa G.
Stanel, Stefan
Thickett, David R.
Thompson, A. A. Roger
Thorpe, Mathew
Walsh, Simon L. F.
Walker, Samantha
Weatherley, Nicholas David
Weeks, Mark E.
Wild, Jim M.
Wootton, Dan G.
Brightling, Chris E.
Ho, Ling-Pei
Wain, Louise V.
Jenkins, Gisli R.
Residual Lung Abnormalities after COVID-19 Hospitalization: Interim Analysis of the UKILD Post–COVID-19 Study
title Residual Lung Abnormalities after COVID-19 Hospitalization: Interim Analysis of the UKILD Post–COVID-19 Study
title_full Residual Lung Abnormalities after COVID-19 Hospitalization: Interim Analysis of the UKILD Post–COVID-19 Study
title_fullStr Residual Lung Abnormalities after COVID-19 Hospitalization: Interim Analysis of the UKILD Post–COVID-19 Study
title_full_unstemmed Residual Lung Abnormalities after COVID-19 Hospitalization: Interim Analysis of the UKILD Post–COVID-19 Study
title_short Residual Lung Abnormalities after COVID-19 Hospitalization: Interim Analysis of the UKILD Post–COVID-19 Study
title_sort residual lung abnormalities after covid-19 hospitalization: interim analysis of the ukild post–covid-19 study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10037479/
https://www.ncbi.nlm.nih.gov/pubmed/36457159
http://dx.doi.org/10.1164/rccm.202203-0564OC
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