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Analysis of Severe Illness After Postvaccination COVID-19 Breakthrough Among Adults With and Without HIV in the US.
Lang, Raynell; Humes, Elizabeth; Coburn, Sally B; Horberg, Michael A; Fathi, Lily F; Watson, Eric; Jefferson, Celeena R; Park, Lesley S; Gordon, Kirsha S; Akgün, Kathleen M; Justice, Amy C; Napravnik, Sonia; Edwards, Jessie K; Browne, Lindsay E; Agil, Deana M; Silverberg, Michael J; Skarbinski, Jacek; Leyden, Wendy A; Stewart, Cameron; Hogan, Brenna C; Gebo, Kelly A; Marconi, Vincent C; Williams, Carolyn F; Althoff, Keri N.
  • Lang R; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Humes E; Department of Medicine, University of Calgary, Calgary, Canada.
  • Coburn SB; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Horberg MA; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
  • Fathi LF; Kaiser Permanente Mid-Atlantic States, Mid-Atlantic Permanente Research Institute, Rockville, Maryland.
  • Watson E; Kaiser Permanente Mid-Atlantic States, Mid-Atlantic Permanente Research Institute, Rockville, Maryland.
  • Jefferson CR; Kaiser Permanente Mid-Atlantic States, Mid-Atlantic Permanente Research Institute, Rockville, Maryland.
  • Park LS; Kaiser Permanente Mid-Atlantic States, Mid-Atlantic Permanente Research Institute, Rockville, Maryland.
  • Gordon KS; Stanford Center for Population Health Sciences, Palo Alto, California.
  • Akgün KM; VA Connecticut Healthcare System, West Haven.
  • Justice AC; Department of Health Policy and Management, Yale School of Public Health, New Haven, Connecticut.
  • Napravnik S; VA Connecticut Healthcare System, West Haven.
  • Edwards JK; Department of Health Policy and Management, Yale School of Public Health, New Haven, Connecticut.
  • Browne LE; VA Connecticut Healthcare System, West Haven.
  • Agil DM; Department of Health Policy and Management, Yale School of Public Health, New Haven, Connecticut.
  • Silverberg MJ; Department of Medicine, Yale School of Medicine, New Haven, Connecticut.
  • Skarbinski J; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill.
  • Leyden WA; Department of Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill.
  • Stewart C; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill.
  • Hogan BC; Department of Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill.
  • Gebo KA; Department of Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill.
  • Marconi VC; Division of Research, Kaiser Permanente Northern California, Oakland.
  • Williams CF; Division of Research, Kaiser Permanente Northern California, Oakland.
  • Althoff KN; Department of Infectious Diseases, Oakland Medical Center, Oakland, California.
JAMA Netw Open ; 5(10): e2236397, 2022 10 03.
Article in English | MEDLINE | ID: covidwho-2059210
ABSTRACT
Importance Understanding the severity of postvaccination SARS-CoV-2 (ie, COVID-19) breakthrough illness among people with HIV (PWH) can inform vaccine guidelines and risk-reduction recommendations.

Objective:

To estimate the rate and risk of severe breakthrough illness among vaccinated PWH and people without HIV (PWoH) who experience a breakthrough infection. Design, Setting, and

Participants:

In this cohort study, the Corona-Infectious-Virus Epidemiology Team (CIVET-II) collaboration included adults (aged ≥18 years) with HIV who were receiving care and were fully vaccinated by June 30, 2021, along with PWoH matched according to date fully vaccinated, age group, race, ethnicity, and sex from 4 US integrated health systems and academic centers. Those with postvaccination COVID-19 breakthrough before December 31, 2021, were eligible. Exposures HIV infection. Main Outcomes and

Measures:

The main outcome was severe COVID-19 breakthrough illness, defined as hospitalization within 28 days after a breakthrough SARS-CoV-2 infection with a primary or secondary COVID-19 discharge diagnosis. Discrete time proportional hazards models estimated adjusted hazard ratios (aHRs) and 95% CIs of severe breakthrough illness within 28 days of breakthrough COVID-19 by HIV status adjusting for demographic variables, COVID-19 vaccine type, and clinical factors. The proportion of patients who received mechanical ventilation or died was compared by HIV status.

Results:

Among 3649 patients with breakthrough COVID-19 (1241 PWH and 2408 PWoH), most were aged 55 years or older (2182 patients [59.8%]) and male (3244 patients [88.9%]). The cumulative incidence of severe illness in the first 28 days was low and comparable between PWoH and PWH (7.3% vs 6.7%; risk difference, -0.67%; 95% CI, -2.58% to 1.23%). The risk of severe breakthrough illness was 59% higher in PWH with CD4 cell counts less than 350 cells/µL compared with PWoH (aHR, 1.59; 95% CI, 0.99 to 2.46; P = .049). In multivariable analyses among PWH, being female, older, having a cancer diagnosis, and lower CD4 cell count were associated with increased risk of severe breakthrough illness, whereas previous COVID-19 was associated with reduced risk. Among 249 hospitalized patients, 24 (9.6%) were mechanically ventilated and 20 (8.0%) died, with no difference by HIV status. Conclusions and Relevance In this cohort study, the risk of severe COVID-19 breakthrough illness within 28 days of a breakthrough infection was low among vaccinated PWH and PWoH. PWH with moderate or severe immune suppression had a higher risk of severe breakthrough infection and should be included in groups prioritized for additional vaccine doses and risk-reduction strategies.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: HIV Infections / COVID-19 Vaccines / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Long Covid / Vaccines Limits: Adolescent / Adult / Female / Humans / Male Language: English Journal: JAMA Netw Open Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: HIV Infections / COVID-19 Vaccines / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Long Covid / Vaccines Limits: Adolescent / Adult / Female / Humans / Male Language: English Journal: JAMA Netw Open Year: 2022 Document Type: Article