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Human Immunodeficiency Virus Status, Tenofovir Exposure, and the Risk of Poor Coronavirus Disease 19 Outcomes: Real-World Analysis From 6 United States Cohorts Before Vaccine Rollout.
Lea, Alexandra N; Leyden, Wendy A; Sofrygin, Oleg; Marafino, Ben J; Skarbinski, Jacek; Napravnik, Sonia; Agil, Deana; Augenbraun, Michael; Benning, Lorie; Horberg, Michael A; Jefferson, Celeena; Marconi, Vincent C; Park, Lesley S; Gordon, Kirsha S; Bastarache, Lisa; Gangireddy, Srushti; Althoff, Keri N; Coburn, Sally B; Gebo, Kelly A; Lang, Raynell; Williams, Carolyn; Silverberg, Michael J.
Afiliação
  • Lea AN; Division of Research, Kaiser Permanente Northern California, Oakland, California, USA.
  • Leyden WA; Division of Research, Kaiser Permanente Northern California, Oakland, California, USA.
  • Sofrygin O; Division of Research, Kaiser Permanente Northern California, Oakland, California, USA.
  • Marafino BJ; Division of Research, Kaiser Permanente Northern California, Oakland, California, USA.
  • Skarbinski J; Division of Research, Kaiser Permanente Northern California, Oakland, California, USA.
  • Napravnik S; Oakland Medical Center, Kaiser Permanente Northern California, Oakland, California, USA.
  • Agil D; Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Augenbraun M; Department of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
  • Benning L; Division of Infectious Diseases, State University of New York Health Sciences University, Brooklyn, USA.
  • Horberg MA; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
  • Jefferson C; Mid-Atlantic Permanente Research Institute, Kaiser Permanente Mid-Atlantic States, Rockville, Maryland, USA.
  • Marconi VC; Mid-Atlantic Permanente Research Institute, Kaiser Permanente Mid-Atlantic States, Rockville, Maryland, USA.
  • Park LS; Emory University School of Medicine and Rollins School of Public Health, Atlanta Veterans Affairs Medical Center, Atlanta, Georgia, USA.
  • Gordon KS; Stanford Department of Epidemiology & Population Health, Stanford University School of Medicine, Palo Alto, California, USA.
  • Bastarache L; VA Connecticut Healthcare System, West Haven, Connecticut, USA.
  • Gangireddy S; Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut, USA.
  • Althoff KN; Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Coburn SB; Department of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Gebo KA; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
  • Lang R; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
  • Williams C; Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
  • Silverberg MJ; Department of Medicine, University of Calgary, Calgary, Alberta, Canada.
Clin Infect Dis ; 76(10): 1727-1734, 2023 05 24.
Article em En | MEDLINE | ID: mdl-36861341
BACKGROUND: People with human immunodeficiency virus (HIV) (PWH) may be at increased risk for severe coronavirus disease 2019 (COVID-19) outcomes. We examined HIV status and COVID-19 severity, and whether tenofovir, used by PWH for HIV treatment and people without HIV (PWoH) for HIV prevention, was associated with protection. METHODS: Within 6 cohorts of PWH and PWoH in the United States, we compared the 90-day risk of any hospitalization, COVID-19 hospitalization, and mechanical ventilation or death by HIV status and by prior exposure to tenofovir, among those with severe acute respiratory syndrome coronavirus 2 infection between 1 March and 30 November 2020. Adjusted risk ratios (aRRs) were estimated by targeted maximum likelihood estimation, with adjustment for demographics, cohort, smoking, body mass index, Charlson comorbidity index, calendar period of first infection, and CD4 cell counts and HIV RNA levels (in PWH only). RESULTS: Among PWH (n = 1785), 15% were hospitalized for COVID-19 and 5% received mechanical ventilation or died, compared with 6% and 2%, respectively, for PWoH (n = 189 351). Outcome prevalence was lower for PWH and PWoH with prior tenofovir use. In adjusted analyses, PWH were at increased risk compared with PWoH for any hospitalization (aRR, 1.31 [95% confidence interval, 1.20-1.44]), COVID-19 hospitalizations (1.29 [1.15-1.45]), and mechanical ventilation or death (1.51 [1.19-1.92]). Prior tenofovir use was associated with reduced hospitalizations among PWH (aRR, 0.85 [95% confidence interval, .73-.99]) and PWoH (0.71 [.62-.81]). CONCLUSIONS: Before COVID-19 vaccine availability, PWH were at greater risk for severe outcomes than PWoH. Tenofovir was associated with a significant reduction in clinical events for both PWH and PWoH.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / COVID-19 Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Infecções por HIV / COVID-19 Idioma: En Ano de publicação: 2023 Tipo de documento: Article