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Analysis of severe illness after post-vaccination COVID-19 breakthrough among adults with and without HIV in the United States
Raynell Lang; Elizabeth Humes; Sally B. Coburn; Michael A. Horberg; Lily F. Fathi; Eric Watson; Celeena R. Jefferson; Lesley S. Park; Amy C. Justice; Kirsha S. Gordon; Kathleen M Akgun; Sonia Napravnik; Jessie K. Edwards; Lindsay E. Browne; Deana M. Agil; Michael J. Silverberg; Jacek Skarbinski; Wendy A. Leyden; Cameron Stewart; Brenna C. Hogan; Kelly A. Gebo; Vincent C. Marconi; Carolyn F. Williams; Keri N. Althoff; - for the Corona-Infectious-Virus Epidemiology Team (CIVETs) of the NA-ACCORD of IeDEA.
Affiliation
  • Raynell Lang; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA; Department of Medicine, University of Calgary, Calgary, Canada
  • Elizabeth Humes; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
  • Sally B. Coburn; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
  • Michael A. Horberg; Kaiser Permanente Mid-Atlantic States, Mid- Atlantic Permanente Research Institute, Rockville, MD, USA
  • Lily F. Fathi; Kaiser Permanente Mid-Atlantic States, Mid- Atlantic Permanente Research Institute, Rockville, MD, USA
  • Eric Watson; Kaiser Permanente Mid-Atlantic States, Mid- Atlantic Permanente Research Institute, Rockville, MD, USA
  • Celeena R. Jefferson; Kaiser Permanente Mid-Atlantic States, Mid- Atlantic Permanente Research Institute, Rockville, MD, USA
  • Lesley S. Park; Stanford Center for Population Health Sciences, Palo Alto, CA, USA
  • Amy C. Justice; Department of Health Policy and Management, Yale School of Public Health, New Haven, CT, USA; Department of Medicine, Yale School of Medicine, New Haven, CT, US
  • Kirsha S. Gordon; Department of Medicine, Yale School of Medicine, New Haven, CT, USA; VA Connecticut Healthcare System, West Haven, CT, USA
  • Kathleen M Akgun; Department of Medicine, Yale School of Medicine, New Haven, CT, USA; VA Connecticut Healthcare System, West Haven, CT, USA
  • Sonia Napravnik; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA; Department of Medicine, School of Medicine, University of North C
  • Jessie K. Edwards; Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA
  • Lindsay E. Browne; Department of Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA
  • Deana M. Agil; Department of Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA
  • Michael J. Silverberg; Kaiser Permanente Northern California, Division of Research, Oakland CA, USA
  • Jacek Skarbinski; Kaiser Permanente Northern California, Division of Research, Oakland CA, USA; Department of Infectious Diseases, Oakland Medical Center, Oakland CA, USA
  • Wendy A. Leyden; Kaiser Permanente Northern California, Division of Research, Oakland CA, USA
  • Cameron Stewart; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
  • Brenna C. Hogan; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
  • Kelly A. Gebo; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA; Department of Medicine, Johns Hopkins School of Medicine, Balti
  • Vincent C. Marconi; Emory University School of Medicine and Rollins School of Public Health, Atlanta, GA, USA; Atlanta Veterans Affairs Medical Center, Decatur, GA, USA
  • Carolyn F. Williams; Epidemiology Branch, Division of AIDS at National Institute of Allergy and Infectious Diseases (NIAID), National Institute of Health (NIH), Rockville, MD, USA
  • Keri N. Althoff; Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA
  • - for the Corona-Infectious-Virus Epidemiology Team (CIVETs) of the NA-ACCORD of IeDEA;
Preprint in English | medRxiv | ID: ppmedrxiv-22273913
ABSTRACT
ImportanceUnderstanding the severity of post-vaccination COVID-19 breakthrough illness among people with HIV (PWH) can inform vaccine guidelines and risk-reduction recommendations. ObjectiveEstimate the rate and risk of severe breakthrough illness among vaccinated PWH and people without HIV (PWoH) who experience a breakthrough infection. Design, setting, and participantsThe Corona-Infectious-Virus Epidemiology Team (CIVET-II) collaboration consists of four US longitudinal cohorts from integrated health systems and academic centers. Adults ([≥]18 years old), in-care, fully vaccinated by June 30, 2021 with HIV, and matched PWoH (on date fully vaccinated, age group, race/ethnicity, and sex) were the source population. Those who experienced a post-vaccination SARS-CoV-2 breakthrough infection were eligible. Severe COVID-19 breakthrough illness was defined as hospitalization due to COVID-19. Discrete time proportional hazards models estimated adjusted hazard ratios (aHR) and 95% confidence intervals ([,]) of severe breakthrough illness by HIV status adjusting for demographics, COVID-19 vaccine type, and clinical factors. The proportion of patients requiring mechanical ventilation or died was compared by HIV status. ExposureHIV infection OutcomeSevere 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. ResultsAmong 1,241 PWH and 2,408 PWoH with breakthrough infections, the cumulative incidence of severe illness in the first 28 days was low and comparable between PWoH and PWH (7.3% vs. 6.7%, respectively, risk difference=-0.67% [-2.58%, 1.23%]). The risk of severe breakthrough illness was 59% higher in PWH with CD4 counts <350 cells/mm3 compared with PWoH (aHR=1.59 [0.99, 2.46]). In multivariable analyses among PWH, being female, older, having a cancer diagnosis, and lower CD4 count increased the risk of severe breakthrough illness, while previous COVID-19 reduced the risk. Among all patients, 10% were mechanically ventilated and 8% died, with no difference by HIV status. Conclusions and RelevanceThe risk of severe COVID-19 breakthrough illness within 28 days of a breakthrough infection was low among vaccinated PWH and PWoH. However, PWH with moderate and severe immune suppression had a higher risk of severe breakthrough infection. Recommendations for additional vaccine doses and risk-reduction strategies for PWH with moderate immune suppression may be warranted. Key PointsO_ST_ABSQuestionC_ST_ABSIn 2021, among fully vaccinated people with COVID-19 breakthrough illness, was the risk of severe illness higher in people with HIV (PWH) compared to people without HIV (PWoH)? FindingsPWH with <350 cells/mm3 have a 59% increased risk of severe breakthrough illness compared to PWoH. MeaningVaccinations effectively reduce the risk of severe COVID-19 infection in both PWH and PWoH; however, PWH having a CD4 count <350 cells/mm3 are at higher risk of severe breakthrough infection compared to PWoH. PWH with moderate immune suppression should be considered for additional vaccine dosages and other risk-reduction measures.
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Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Observational study / Prognostic study Language: English Year: 2022 Document type: Preprint
Full text: Available Collection: Preprints Database: medRxiv Type of study: Cohort_studies / Observational study / Prognostic study Language: English Year: 2022 Document type: Preprint
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