Altered lung physiology in two cohorts after COVID-19 infection as assessed by computed cardiopulmonography
<p>The longer-term effects of COVID-19 on lung physiology remain poorly understood. Here, a new technique, computed cardiopulmonography (CCP), was used to study two COVID-19 cohorts (MCOVID and C-MORE-LP) at both ∼6 and ∼12 mo after infection. CCP is comprised of two components. The first is c...
Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Format: | Journal article |
Language: | English |
Published: |
American Physiological Society
2022
|
_version_ | 1797108435639074816 |
---|---|
author | Magor-Elliott, SRM Alamoudi, A Chamley, RR Xu, H Wellalagodage, T McDonald, RP O'Brien, D Collins, J Coombs, B Winchester, J Sellon, E Xie, C Sandhu, D Fullerton, CJ Couper, JH Smith, NMJ Richmond, G Cassar, MP Raman, B Talbot, NP Bennett, AN Nicol, ED Ritchie, GAD Petousi, N Holdsworth, DA Robbins, PA |
author_facet | Magor-Elliott, SRM Alamoudi, A Chamley, RR Xu, H Wellalagodage, T McDonald, RP O'Brien, D Collins, J Coombs, B Winchester, J Sellon, E Xie, C Sandhu, D Fullerton, CJ Couper, JH Smith, NMJ Richmond, G Cassar, MP Raman, B Talbot, NP Bennett, AN Nicol, ED Ritchie, GAD Petousi, N Holdsworth, DA Robbins, PA |
author_sort | Magor-Elliott, SRM |
collection | OXFORD |
description | <p>The longer-term effects of COVID-19 on lung physiology remain poorly understood. Here, a new technique, computed cardiopulmonography (CCP), was used to study two COVID-19 cohorts (MCOVID and C-MORE-LP) at both ∼6 and ∼12 mo after infection. CCP is comprised of two components. The first is collection of highly precise, highly time-resolved measurements of gas exchange with a purpose-built molecular flow sensor based around laser absorption spectroscopy. The second component is estimation of physiological parameters by fitting a cardiopulmonary model to the data set. The measurement protocol involved 7 min of breathing air followed by 5 min of breathing pure O2. One hundred seventy-eight participants were studied, with 97 returning for a repeat assessment. One hundred twenty-six arterial blood gas samples were drawn from MCOVID participants. For participants who had required intensive care and/or invasive mechanical ventilation, there was a significant increase in anatomical dead space of ∼30 mL and a significant increase in alveolar-to-arterial Po2 gradient of ∼0.9 kPa relative to control participants. Those who had been hospitalized had reductions in functional residual capacity of ∼15%. Irrespectively of COVID-19 severity, participants who had had COVID-19 demonstrated a modest increase in ventilation inhomogeneity, broadly equivalent to that associated with 15 yr of aging. This study illustrates the capability of CCP to study aspects of lung function not so easily addressed through standard clinical lung function tests. However, without measurements before infection, it is not possible to conclude whether the findings relate to the effects of COVID-19 or whether they constitute risk factors for more serious disease.</p>
<p><strong>NEW & NOTEWORTHY </strong>This study used a novel technique, computed cardiopulmonography, to study the lungs of patients who have had COVID-19. Depending on severity of infection, there were increases in anatomical dead space, reductions in absolute lung volumes, and increases in ventilation inhomogeneity broadly equivalent to those associated with 15 yr of aging. However, without measurements taken before infection, it is unclear whether the changes result from COVID-19 infection or are risk factors for more severe disease.</p>
|
first_indexed | 2024-03-07T07:29:12Z |
format | Journal article |
id | oxford-uuid:9cb61ef2-4029-415f-8114-4e86398655ff |
institution | University of Oxford |
language | English |
last_indexed | 2024-03-07T07:29:12Z |
publishDate | 2022 |
publisher | American Physiological Society |
record_format | dspace |
spelling | oxford-uuid:9cb61ef2-4029-415f-8114-4e86398655ff2022-12-09T12:07:31ZAltered lung physiology in two cohorts after COVID-19 infection as assessed by computed cardiopulmonographyJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:9cb61ef2-4029-415f-8114-4e86398655ffEnglishSymplectic ElementsAmerican Physiological Society2022Magor-Elliott, SRMAlamoudi, AChamley, RRXu, HWellalagodage, TMcDonald, RPO'Brien, DCollins, JCoombs, BWinchester, JSellon, EXie, CSandhu, DFullerton, CJCouper, JHSmith, NMJRichmond, GCassar, MPRaman, BTalbot, NPBennett, ANNicol, EDRitchie, GADPetousi, NHoldsworth, DARobbins, PA<p>The longer-term effects of COVID-19 on lung physiology remain poorly understood. Here, a new technique, computed cardiopulmonography (CCP), was used to study two COVID-19 cohorts (MCOVID and C-MORE-LP) at both ∼6 and ∼12 mo after infection. CCP is comprised of two components. The first is collection of highly precise, highly time-resolved measurements of gas exchange with a purpose-built molecular flow sensor based around laser absorption spectroscopy. The second component is estimation of physiological parameters by fitting a cardiopulmonary model to the data set. The measurement protocol involved 7 min of breathing air followed by 5 min of breathing pure O2. One hundred seventy-eight participants were studied, with 97 returning for a repeat assessment. One hundred twenty-six arterial blood gas samples were drawn from MCOVID participants. For participants who had required intensive care and/or invasive mechanical ventilation, there was a significant increase in anatomical dead space of ∼30 mL and a significant increase in alveolar-to-arterial Po2 gradient of ∼0.9 kPa relative to control participants. Those who had been hospitalized had reductions in functional residual capacity of ∼15%. Irrespectively of COVID-19 severity, participants who had had COVID-19 demonstrated a modest increase in ventilation inhomogeneity, broadly equivalent to that associated with 15 yr of aging. This study illustrates the capability of CCP to study aspects of lung function not so easily addressed through standard clinical lung function tests. However, without measurements before infection, it is not possible to conclude whether the findings relate to the effects of COVID-19 or whether they constitute risk factors for more serious disease.</p> <p><strong>NEW & NOTEWORTHY </strong>This study used a novel technique, computed cardiopulmonography, to study the lungs of patients who have had COVID-19. Depending on severity of infection, there were increases in anatomical dead space, reductions in absolute lung volumes, and increases in ventilation inhomogeneity broadly equivalent to those associated with 15 yr of aging. However, without measurements taken before infection, it is unclear whether the changes result from COVID-19 infection or are risk factors for more severe disease.</p> |
spellingShingle | Magor-Elliott, SRM Alamoudi, A Chamley, RR Xu, H Wellalagodage, T McDonald, RP O'Brien, D Collins, J Coombs, B Winchester, J Sellon, E Xie, C Sandhu, D Fullerton, CJ Couper, JH Smith, NMJ Richmond, G Cassar, MP Raman, B Talbot, NP Bennett, AN Nicol, ED Ritchie, GAD Petousi, N Holdsworth, DA Robbins, PA Altered lung physiology in two cohorts after COVID-19 infection as assessed by computed cardiopulmonography |
title | Altered lung physiology in two cohorts after COVID-19 infection as assessed by computed cardiopulmonography |
title_full | Altered lung physiology in two cohorts after COVID-19 infection as assessed by computed cardiopulmonography |
title_fullStr | Altered lung physiology in two cohorts after COVID-19 infection as assessed by computed cardiopulmonography |
title_full_unstemmed | Altered lung physiology in two cohorts after COVID-19 infection as assessed by computed cardiopulmonography |
title_short | Altered lung physiology in two cohorts after COVID-19 infection as assessed by computed cardiopulmonography |
title_sort | altered lung physiology in two cohorts after covid 19 infection as assessed by computed cardiopulmonography |
work_keys_str_mv | AT magorelliottsrm alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT alamoudia alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT chamleyrr alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT xuh alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT wellalagodaget alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT mcdonaldrp alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT obriend alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT collinsj alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT coombsb alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT winchesterj alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT sellone alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT xiec alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT sandhud alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT fullertoncj alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT couperjh alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT smithnmj alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT richmondg alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT cassarmp alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT ramanb alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT talbotnp alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT bennettan alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT nicoled alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT ritchiegad alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT petousin alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT holdsworthda alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography AT robbinspa alteredlungphysiologyintwocohortsaftercovid19infectionasassessedbycomputedcardiopulmonography |