Early Outcomes of SARS-CoV-2 Infection in a Multisite Prospective Cohort of Inpatient Veterans.

COVID-19 comorbidity rehospitalization severity veteran

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
Jul 2023
Historique:
received: 06 03 2023
accepted: 23 06 2023
pmc-release: 27 06 2024
medline: 24 7 2023
pubmed: 24 7 2023
entrez: 24 7 2023
Statut: epublish

Résumé

Over 870 000 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections have occurred among Veterans Health Administration users, and 24 000 have resulted in death. We examined early outcomes of SARS-CoV-2 infection in hospitalized veterans. In an ongoing, prospective cohort study, we enrolled veterans age ≥18 tested for SARS-CoV-2 and hospitalized at 15 Department of Veterans Affairs medical centers between February 2021 and June 2022. We estimated adjusted odds ratios (aORs), adjusted incidence rate ratios (aIRRs), and adjusted hazard ratios (aHRs) for maximum illness severity within 30 days of study entry (defined using the 4-category VA Severity Index for coronavirus disease 2019 [COVID-19]), as well as length of hospitalization and rehospitalization within 60 days, in relationship with demographic characteristics, Charlson comorbidity index (CCI), COVID-19 vaccination, and calendar period of enrollment. The 542 participants included 329 (61%) who completed a primary vaccine series (with or without booster; "vaccinated"), 292 (54%) enrolled as SARS-CoV-2-positive, and 503 (93%) men, with a mean age of 64.4 years. High CCI scores (≥5) occurred in 61 (44%) vaccinated and 29 (19%) unvaccinated SARS-CoV-2-positive participants. Severe illness or death occurred in 29 (21%; 6% died) vaccinated and 31 (20%; 2% died) unvaccinated SARS-CoV-2-positive participants. SARS-CoV-2-positive inpatients per unit increase in CCI had greater multivariable-adjusted odds of severe illness (aOR, 1.21; 95% CI, 1.01-1.45), more hospitalization days (aIRR, 1.06; 95% CI, 1.03-1.10), and rehospitalization (aHR, 1.07; 95% CI, 1.01-1.12). In a cohort of hospitalized US veterans with SARS-CoV-2 infection, those with a higher CCI had more severe COVID-19 illness, more hospital days, and rehospitalization, after adjusting for vaccination status, age, sex, and calendar period.

Sections du résumé

Background UNASSIGNED
Over 870 000 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections have occurred among Veterans Health Administration users, and 24 000 have resulted in death. We examined early outcomes of SARS-CoV-2 infection in hospitalized veterans.
Methods UNASSIGNED
In an ongoing, prospective cohort study, we enrolled veterans age ≥18 tested for SARS-CoV-2 and hospitalized at 15 Department of Veterans Affairs medical centers between February 2021 and June 2022. We estimated adjusted odds ratios (aORs), adjusted incidence rate ratios (aIRRs), and adjusted hazard ratios (aHRs) for maximum illness severity within 30 days of study entry (defined using the 4-category VA Severity Index for coronavirus disease 2019 [COVID-19]), as well as length of hospitalization and rehospitalization within 60 days, in relationship with demographic characteristics, Charlson comorbidity index (CCI), COVID-19 vaccination, and calendar period of enrollment.
Results UNASSIGNED
The 542 participants included 329 (61%) who completed a primary vaccine series (with or without booster; "vaccinated"), 292 (54%) enrolled as SARS-CoV-2-positive, and 503 (93%) men, with a mean age of 64.4 years. High CCI scores (≥5) occurred in 61 (44%) vaccinated and 29 (19%) unvaccinated SARS-CoV-2-positive participants. Severe illness or death occurred in 29 (21%; 6% died) vaccinated and 31 (20%; 2% died) unvaccinated SARS-CoV-2-positive participants. SARS-CoV-2-positive inpatients per unit increase in CCI had greater multivariable-adjusted odds of severe illness (aOR, 1.21; 95% CI, 1.01-1.45), more hospitalization days (aIRR, 1.06; 95% CI, 1.03-1.10), and rehospitalization (aHR, 1.07; 95% CI, 1.01-1.12).
Conclusions UNASSIGNED
In a cohort of hospitalized US veterans with SARS-CoV-2 infection, those with a higher CCI had more severe COVID-19 illness, more hospital days, and rehospitalization, after adjusting for vaccination status, age, sex, and calendar period.

Identifiants

pubmed: 37484899
doi: 10.1093/ofid/ofad330
pii: ofad330
pmc: PMC10358428
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofad330

Investigateurs

Mary-Claire Roghmann (MC)
Karen Coffey (K)
Les Katzel (L)
Emily Wan (E)
Federico Perez (F)
Robin Jump (R)
Rohit Manaktala (R)
Lindsay Nicholson (L)
Micah McClain (M)
Christopher Woods (C)
Gary Wang (G)
Amy Vittor (A)
John Theus (J)
North Arkansas (N)
Sheran Mahatme (S)
Milwaukee Nathan Gundacker (MN)
Milwaukee Javeria Haque (MJ)
Milwaukee Harman Paintal (MH)
Matthew Stevenson (M)
Joshua Baker (J)
Chris Pfeiffer (C)
Patrick Powers (P)
Julia Lewis (J)
Patrick Danaher (P)
Antonio Anzueto (A)
McKenna Eastment (M)

Informations de copyright

Published by Oxford University Press on behalf of Infectious Diseases Society of America 2023.

Déclaration de conflit d'intérêts

Potential conflicts of interest. J.D.S. receives funding from the International Vaccine Institute, Seoul, Republic of Korea. R.B. has provided research support to Merck & Co. and consulting services to Merck & Co., Gilead Sciences, Theratechnologies, Shionogi, Janssen, and ViiV Healthcare. C.M.H. has provided consulting services to Adaptive Phage Therapeutics, Akebia, F2G Limited, Intercept, Otsuka, Surrozen, and Palladio. S.N.I. receives payments for contributions to UpToDate on poxviruses and is a shareholder of Johnson & Johnson. All other authors report no potential conflicts.

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Auteurs

Jennifer M Ross (JM)

VA Puget Sound Health Care System, Seattle, Washington, USA.
Division of Allergy and Infectious Diseases, University of Washington, Seattle, Washington, USA.

Jonathan D Sugimoto (JD)

VA Puget Sound Health Care System, Seattle, Washington, USA.

Andrew Timmons (A)

VA Puget Sound Health Care System, Seattle, Washington, USA.

Jonathan Adams (J)

VA Puget Sound Health Care System, Seattle, Washington, USA.

Katrina Deardoff (K)

VA Puget Sound Health Care System, Seattle, Washington, USA.

Anna Korpak (A)

VA Puget Sound Health Care System, Seattle, Washington, USA.

Cindy Liu (C)

VA Puget Sound Health Care System, Seattle, Washington, USA.

Kathryn Moore (K)

VA Puget Sound Health Care System, Seattle, Washington, USA.

Deanna Wilson (D)

VA Palo Alto Health Care System, Palo Alto, California, USA.

Roger Bedimo (R)

VA North Texas Health Care System, Dallas, Texas, USA.
Department of Medicine, University of Texas-Southwestern Medical Center, Dallas, Texas, USA.

Kyong-Mi Chang (KM)

Corporal Michael J. Crescenz VA Medical Center, Philadelphia, Pennsylvania, USA.
Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Kelly Cho (K)

VA Boston Health Care System, Boston, Massachusetts, USA.
Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.

Kristina Crothers (K)

VA Puget Sound Health Care System, Seattle, Washington, USA.
Division of Pulmonary and Critical Care, University of Washington, Seattle, Washington, USA.

Eric Garshick (E)

VA Boston Health Care System, Boston, Massachusetts, USA.
Chobanian & Avedisian School of Medicine, Boston University, Boston, Massachusetts, USA.

J Michael Gaziano (JM)

VA Boston Health Care System, Boston, Massachusetts, USA.
Department of Medicine, Harvard Medical School, Boston, Massachusetts, USA.

Mark Holodniy (M)

VA Palo Alto Health Care System, Palo Alto, California, USA.
Department of Medicine-Infectious Diseases, Stanford University, Palo Alto, California, USA.

Christine M Hunt (CM)

VA Durham Health Care System, Durham, North Carolina, USA.
Department of Medicine, Duke University Medical Center, Durham, North Carolina, USA.

Stuart N Isaacs (SN)

Corporal Michael J. Crescenz VA Medical Center, Philadelphia, Pennsylvania, USA.
Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Elizabeth Le (E)

VA Palo Alto Health Care System, Palo Alto, California, USA.

Barbara E Jones (BE)

VA Salt Lake City Health Care System, Salt Lake City, Utah, USA.
University of Utah School of Medicine, Salt Lake City, Utah, USA.

Javeed A Shah (JA)

VA Puget Sound Health Care System, Seattle, Washington, USA.
Division of Allergy and Infectious Diseases, University of Washington, Seattle, Washington, USA.

Nicholas L Smith (NL)

VA Puget Sound Health Care System, Seattle, Washington, USA.
Department of Epidemiology, University of Washington, Seattle, Washington, USA.

Jennifer S Lee (JS)

VA Palo Alto Health Care System, Palo Alto, California, USA.
Division of Endocrinology, Gerontology, and Metabolism, Department of Medicine, and, by courtesy, Department of Epidemiology and Population Health, Stanford University, Palo Alto, California, USA.

Classifications MeSH