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Parenchymal lung abnormalities following hospitalisation for COVID-19 and viral pneumonitis: a systematic review and meta-analysis.
Fabbri, Laura; Moss, Samuel; Khan, Fasihul A; Chi, Wenjie; Xia, Jun; Robinson, Karen; Smyth, Alan Robert; Jenkins, Gisli; Stewart, Iain.
  • Fabbri L; National Heart & Lung Institute, Imperial College London, London, UK.
  • Moss S; Nottingham NIHR Biomedical Research Centre, University of Nottingham, Nottingham, UK.
  • Khan FA; National Heart & Lung Institute, Imperial College London, London, UK.
  • Chi W; Nottingham NIHR Biomedical Research Centre, University of Nottingham, Nottingham, UK.
  • Xia J; Nottingham NIHR Biomedical Research Centre, University of Nottingham, Nottingham, UK.
  • Robinson K; Institute of Mental Health, University of Nottingham, Nottingham, UK.
  • Smyth AR; Institute of Mental Health, University of Nottingham, Nottingham, UK.
  • Jenkins G; Department of Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Stewart I; Nottingham NIHR Biomedical Research Centre, University of Nottingham, Nottingham, UK.
Thorax ; 2022 Mar 25.
Article in English | MEDLINE | ID: covidwho-2229843
ABSTRACT

INTRODUCTION:

Persisting respiratory symptoms in COVID-19 survivors may be related to development of pulmonary fibrosis. We assessed the proportion of chest CT scans and pulmonary function tests consistent with parenchymal lung disease in the follow-up of people hospitalised with COVID-19 and viral pneumonitis.

METHODS:

Systematic review and random effects meta-analysis of proportions using studies of adults hospitalised with SARS-CoV-2, SARS-CoV, MERS-CoV or influenza pneumonia and followed up within 12 months. Searches performed in MEDLINE and Embase. Primary outcomes were proportion of radiological sequelae on CT scans; restrictive impairment; impaired gas transfer. Heterogeneity was explored in meta-regression.

RESULTS:

Ninety-five studies (98.9% observational) were included in qualitative synthesis, 70 were suitable for meta-analysis including 60 SARS-CoV-2 studies with a median follow-up of 3 months. In SARS-CoV-2, the overall estimated proportion of inflammatory sequelae was 50% during follow-up (0.50; 95% CI 0.41 to 0.58; I2=95%), fibrotic sequelae were estimated in 29% (0.29; 95% CI 0.22 to 0.37; I2=94.1%). Follow-up time was significantly associated with estimates of inflammatory sequelae (-0.036; 95% CI -0.068 to -0.004; p=0.029), associations with fibrotic sequelae did not reach significance (-0.021; 95% CI -0.051 to 0.009; p=0.176). Impaired gas transfer was estimated at 38% of lung function tests (0.38 95% CI 0.32 to 0.44; I2=92.1%), which was greater than restrictive impairment (0.17; 95% CI 0.13 to 0.23; I2=92.5%), neither were associated with follow-up time (p=0.207; p=0.864).

DISCUSSION:

Sequelae consistent with parenchymal lung disease were observed following COVID-19 and other viral pneumonitis. Estimates should be interpreted with caution due to high heterogeneity, differences in study casemix and initial severity. PROSPERO REGISTRATION NUMBER CRD42020183139.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study / Qualitative research / Randomized controlled trials / Reviews / Systematic review/Meta Analysis Topics: Long Covid Language: English Year: 2022 Document Type: Article Affiliation country: Thoraxjnl-2021-218275

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study / Qualitative research / Randomized controlled trials / Reviews / Systematic review/Meta Analysis Topics: Long Covid Language: English Year: 2022 Document Type: Article Affiliation country: Thoraxjnl-2021-218275