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dc.contributor.authorMelhorn, J.
dc.contributor.authorAchaiah, A.
dc.contributor.authorConway, F. M.
dc.contributor.authorThompson, E. M. F.
dc.contributor.authorSkyllberg, E. W.
dc.contributor.authorDurrant, J.
dc.contributor.authorHasan, N. A.
dc.contributor.authorMadani, Y.
dc.contributor.authorNaran, P.
dc.contributor.authorVijayakumar, B.
dc.contributor.authorTate, M. J.
dc.contributor.authorTrevelyan, G. E.
dc.contributor.authorZaki, I.
dc.contributor.authorDoig, C. A.
dc.contributor.authorLynch, G.
dc.contributor.authorWarwick, G.
dc.contributor.authorAujayeb, A.
dc.contributor.authorJackson, K. A.
dc.contributor.authorIftikhar, H.
dc.contributor.authorNoble, J. H.
dc.contributor.authorNg, Aykc
dc.contributor.authorNugent, M.
dc.contributor.authorEvans, P. J.
dc.contributor.authorHastings, R. A.
dc.contributor.authorBellenberg, H. R.
dc.contributor.authorLawrence, H.
dc.contributor.authorSaville, R. L.
dc.contributor.authorJohl, N. T.
dc.contributor.authorGrey, A. N.
dc.contributor.authorEllis, H. C.
dc.contributor.authorChen, C.
dc.contributor.authorJones, T. L.
dc.contributor.authorMaddekar, N.
dc.contributor.authorKhan, S. L.
dc.contributor.authorMuhammad, A. I.
dc.contributor.authorGhani, H.
dc.contributor.authorMyint, Y. M. M.
dc.contributor.authorRafique, C.
dc.contributor.authorPippard, B. J.
dc.contributor.authorIrving, B. R. H.
dc.contributor.authorAli, F.
dc.contributor.authorAsimba, V. H.
dc.contributor.authorAzam, A.
dc.contributor.authorBarton, E. C.
dc.contributor.authorBhatnagar, M.
dc.contributor.authorBlackburn, M. P.
dc.contributor.authorMillington, K. J.
dc.contributor.authorBudhram, N. J.
dc.contributor.authorBunclark, K. L.
dc.contributor.authorSapkal, T. P.
dc.contributor.authorDixon, G.
dc.contributor.authorHarries, A. J. E.
dc.contributor.authorIjaz, M.
dc.contributor.authorKarunanithi, V.
dc.contributor.authorNaik, S.
dc.contributor.authorKhan, M. A.
dc.contributor.authorSavlani, K.
dc.contributor.authorKumar, V.
dc.contributor.authorGallego, B. L.
dc.contributor.authorMahdi, N. A.
dc.contributor.authorMorgan, C.
dc.contributor.authorPatel, N.
dc.contributor.authorRowlands, E. W.
dc.contributor.authorSteward, M. S.
dc.contributor.authorThorley, R. S.
dc.contributor.authorWollerton, R. L.
dc.contributor.authorUllah, S.
dc.contributor.authorSmith, D. M.
dc.contributor.authorLason, W.
dc.contributor.authorRostron, A. J.
dc.contributor.authorRahman, N. M.
dc.contributor.authorHallifax, R. J.
dc.date.accessioned2022-04-21T09:39:10Z
dc.date.available2022-04-21T09:39:10Z
dc.date.issued2022-02-10
dc.identifier.citationEur Respir J. 2022 Feb 10:2102522. doi: 10.1183/13993003.02522-2021.
dc.identifier.pmid35144988
dc.identifier.doi10.1183/13993003.02522-2021
dc.identifier.urihttps://rde.dspace-express.com/handle/11287/622422
dc.description.abstractBACKGROUND: There is an emerging understanding that coronavirus disease 2019 (COVID-19) is associated with increased incidence of pneumomediastinum. We aimed to determine its incidence among patients hospitalised with COVID-19 in the United Kingdom and describe factors associated with outcome. METHODS: A structured survey of pneumomediastinum and its incidence was conducted from September 2020 to February 2021. United Kingdom-wide participation was solicited via respiratory research networks. Identified patients had SARS-CoV-2 infection and radiologically proven pneumomediastinum. The primary outcomes were to determine incidence of pneumomediastinum in COVID-19 and to investigate risk factors associated with patient mortality. RESULTS: 377 cases of pneumomediastinum in COVID-19 were identified from 58 484 inpatients with COVID-19 at 53 hospitals during the study period, giving an incidence of 0.64%. Overall 120-day mortality in COVID-19 pneumomediastinum was 195/377 (51.7%). Pneumomediastinum in COVID-19 was associated with high rates of mechanical ventilation. 172/377 patients (45.6%) were mechanically ventilated at the point of diagnosis. Mechanical ventilation was the most important predictor of mortality in COVID-19 pneumomediastinum at the time of diagnosis and thereafter (p<0.001) along with increasing age (p<0.01) and diabetes mellitus (p=0.08). Switching patients from continuous positive airways pressure support to oxygen or high flow nasal oxygen after the diagnosis of pneumomediastinum was not associated with difference in mortality. CONCLUSIONS: Pneumomediastinum appears to be a marker of severe COVID-19 pneumonitis. The majority of patients in whom pneumomediastinum was identified had not been mechanically ventilated at the point of diagnosis.
dc.language.isoeng
dc.publisherEuropean Respiratory Society
dc.relation.urlhttp://erj.ersjournals.com/lookup/pmidlookup?view=long&pmid=35144988
dc.rights©The authors 2022.
dc.rights.urihttp://creativecommons.org/publicdomain/zero/1.0/
dc.titlePneumomediastinum in COVID-19: a phenotype of severe COVID-19 pneumonitis? The results of the United Kingdom (POETIC) survey
dc.typeJournal Article
dc.identifier.journalThe European respiratory journal
dc.identifier.pmcidPMC8832377
dc.description.noteThe article is available via Open Access. Click on the 'Additional link' above to access the full-text.
dc.type.versionaheadofprint
dc.description.admin-notePublished version, accepted version (12 month embargo), submitted version
dc.date.epub2022-02-12


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