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Impact of SARS-CoV-2 infective exacerbation of chronic obstructive pulmonary disease on clinical outcomes in a prospective cohort study of hospitalised adults.
Hyams, Catherine; Qian, George; Nava, George; Challen, Robert; Begier, Elizabeth; Southern, Jo; Lahuerta, Maria; Nguyen, Jennifer L; King, Jade; Morley, Anna; Clout, Madeleine; Maskell, Nick; Jodar, Luis; Oliver, Jennifer; Ellsbury, Gillian; McLaughlin, John M; Gessner, Bradford D; Finn, Adam; Danon, Leon; Dodd, James W.
Afiliación
  • Hyams C; Academic Respiratory Unit and Bristol Vaccine Centre, University of Bristol, Bristol, BS15, UK.
  • Qian G; Engineering Mathematics, University of Bristol, Bristol, Bristol, BS8, UK.
  • Nava G; Academic Respiratory Unit, University of Bristol, Southmead Hospital, Bristol, Bristol, BS15, UK.
  • Challen R; Engineering Mathematics, University of Bristol, Bristol, Bristol, BS8, UK.
  • Begier E; Vaccines Medical Development, Scientific and Clinical Affairs, Pfizer Inc., Collegeville, PA 19426, USA.
  • Southern J; Vaccines Medical Development, Scientific and Clinical Affairs, Pfizer Inc., Collegeville, PA 19426, USA.
  • Lahuerta M; Vaccines Medical Development, Scientific and Clinical Affairs, Pfizer Inc., Collegeville, PA 19426, USA.
  • Nguyen JL; Vaccines Medical Development, Scientific and Clinical Affairs, Pfizer Inc., Collegeville, PA 19426, USA.
  • King J; Clinical Research and Imaging Centre, UHBW NHS Trust, Bristol, Bristol, BS2, UK.
  • Morley A; Academic Respiratory Unit, Southmead Hospital, Bristol, Bristol, BS15, UK.
  • Clout M; Bristol Vaccine Centre and Population Health Sciences, University of Bristol, Bristol, BS2, UK.
  • Maskell N; Academic Respiratory Unit, University of Bristol, Southmead Hospital, Bristol, Bristol, BS15, UK.
  • Jodar L; Vaccines Medical Development, Scientific and Clinical Affairs, Pfizer Inc., Collegeville, PA 19426, USA.
  • Oliver J; Bristol Vaccine Centre and Population Health Sciences, University of Bristol, Bristol, BS2, UK.
  • Ellsbury G; Vaccines Medical Affairs, Pfizer Ltd, Tadworth, KT20, UK.
  • McLaughlin JM; Vaccines Medical Development, Scientific and Clinical Affairs, Pfizer Inc., Collegeville, PA 19426, USA.
  • Gessner BD; Vaccines Medical Development, Scientific and Clinical Affairs, Pfizer Inc., Collegeville, PA 19426, USA.
  • Finn A; Bristol Vaccine Centre, Cellular and Molecular Medicine and Population Health Sciences, University of Bristol, Bristol, BS2, UK.
  • Danon L; Engineering Mathematics, University of Bristol, Bristol, Bristol, BS8, UK.
  • Dodd JW; Academic Respiratory Unit and Population Health Sciences, University of Bristol, Southmead Hospital, Bristol, BS15, UK.
J R Soc Med ; 116(11): 371-385, 2023 11.
Article en En | MEDLINE | ID: mdl-37404021
OBJECTIVES: To determine whether acute exacerbations of chronic obstructive pulmonary disease (AECOPD) triggered by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), have worse outcomes than AECOPD caused by other infectious agents or non-infective AECOPD (NI-COPD). DESIGN: A two-hospital prospective cohort study of adults hospitalised with acute respiratory disease. We compared outcomes with AECOPD and a positive test for SARS-CoV-2 (n = 816), AECOPD triggered by other infections (n = 3038) and NI-COPD (n = 994). We used multivariable modelling to adjust for potential confounders and assessed variation by seasons associated with different SARS-CoV-2 variants. SETTING: Bristol UK, August 2020-May 2022. PARTICIPANTS: Adults (≥18 y) hospitalised with AECOPD. MAIN OUTCOME MEASURES: We determined the risk of positive pressure support, longer hospital admission and mortality following hospitalisation with AECOPD due to non-SARS-CoV-2 infection compared with SARS-CoV-2 AECOPD and NI-COPD. RESULTS: Patients with SARS-CoV-2 AECOPD, in comparison to non-SARS-CoV-2 infective AECOPD or NI-COPD, more frequently required positive pressure support (18.5% and 7.5% vs. 11.7%, respectively), longer hospital stays (median [interquartile range, IQR]: 7 [3-15] and 5 [2-10] vs. 4 [2-9] days, respectively) and had higher 30-day mortality (16.9% and 11.1% vs. 5.9%, respectively) (all p < 0.001). In adjusted analyses, SARS-CoV-2 AECOPD was associated with a 55% (95% confidence interval [95% CI]: 24-93), 26% (95% CI: 15-37) and 35% (95% CI: 10-65) increase in the risk of positive pressure support, hospitalisation length and 30-day mortality, respectively, relative to non-SARS-CoV-2 infective AECOPD. The difference in risk remained similar during periods of wild-type, Alpha and Delta SARS-CoV-2 strain dominance, but diminished during Omicron dominance. CONCLUSIONS: SARS-CoV-2-related AECOPD had worse patient outcomes compared with non-SARS-CoV-2 AECOPD or NI-AECOPD, although the difference in risks was less pronounced during Omicron dominance.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad Pulmonar Obstructiva Crónica / COVID-19 Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: J R Soc Med Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedad Pulmonar Obstructiva Crónica / COVID-19 Tipo de estudio: Etiology_studies / Observational_studies / Risk_factors_studies Límite: Adult / Humans Idioma: En Revista: J R Soc Med Año: 2023 Tipo del documento: Article