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Acute and Post-Acute COVID-19 Outcomes Among Immunologically Naïve Adults During Delta Versus Omicron Waves.
Doll, Margaret K; Waghmare, Alpana; Heit, Antje; Levenson Shakoor, Brianna; Kimball, Louise E; Ozbek, Nina; Blazevic, Rachel L; Mose, Larry; Boonyaratanakornkit, Jim; Stevens-Ayers, Terry L; Cornell, Kevin; Sheppard, Benjamin D; Hampson, Emma; Sharmin, Faria; Goodwin, Benjamin; Dan, Jennifer M; Archie, Tom; O'Connor, Terry; Heckerman, David; Schmitz, Frank; Boeckh, Michael; Crotty, Shane.
Afiliación
  • Doll MK; Department of Population Health Sciences, Albany College of Pharmacy & Health Sciences, Albany, NY, USA.
  • Waghmare A; Division of Infectious Diseases, Department of Pediatrics, University of Washington, Seattle, WA, USA.
  • Heit A; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Levenson Shakoor B; Amazon, Inc., Seattle, WA, USA.
  • Kimball LE; Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California, USA.
  • Ozbek N; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Blazevic RL; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Mose L; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Boonyaratanakornkit J; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Stevens-Ayers TL; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Cornell K; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Sheppard BD; St. Luke's Medical Center, Ketchum, ID, USA.
  • Hampson E; St. Luke's Medical Center, Ketchum, ID, USA.
  • Sharmin F; St. Luke's Medical Center, Ketchum, ID, USA.
  • Goodwin B; Department of Population Health Sciences, Albany College of Pharmacy & Health Sciences, Albany, NY, USA.
  • Dan JM; Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California, USA.
  • Archie T; Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California, USA.
  • O'Connor T; Division of Infectious Diseases and Global Public Health, Department of Medicine, University of California, San Diego, La Jolla, California, USA.
  • Heckerman D; St. Luke's Medical Center, Ketchum, ID, USA.
  • Schmitz F; St. Luke's Medical Center, Ketchum, ID, USA.
  • Boeckh M; Department of Emergency Medicine, University of Washington, Seattle, WA, USA.
  • Crotty S; Amazon, Inc., Seattle, WA, USA.
medRxiv ; 2022 Nov 14.
Article en En | MEDLINE | ID: mdl-36425923
ABSTRACT
Importance The U.S. arrival of the Omicron variant led to a rapid increase in SARS-CoV-2 infections. While numerous studies report characteristics of Omicron infections among vaccinated individuals and/or persons with a prior history of infection, comprehensive data describing infections among immunologically naïve adults is lacking.

Objective:

To examine COVID-19 acute and post-acute clinical outcomes among a well-characterized cohort of unvaccinated and previously uninfected adults who contracted SARS-CoV-2 during the Omicron (BA.1/BA.2) surge, and to compare outcomes with infections that occurred during the Delta wave.

Design:

A prospective cohort undergoing high-resolution symptom and virologic monitoring between June 2021 and September 2022.

Setting:

Multisite recruitment of community-dwelling adults in 8 U.S. states.

Participants:

Healthy, unvaccinated adults between 30 to 64 years of age without an immunological history of SARS-CoV-2 who were at high-risk of infection were recruited. Participants were followed for up to 48 weeks, submitting regular COVID-19 symptom surveys and nasal swabs for SARS-CoV-2 PCR testing. Exposures Omicron (BA.1/BA.2 lineages) versus Delta SARS-CoV-2 infection, defined as a positive PCR that occurred during a period when the variant represented ≥50% of circulating SARS-CoV-2 variants in the participant's geographic region. Main Outcomes and

Measures:

The main outcomes examined were the prevalence and severity of acute (≤28 days post-onset) and post-acute (≥5 weeks post-onset) symptoms.

Results:

Among 274 immunologically naïve participants, 166 (61%) contracted SARS-CoV-2. Of these, 137 (83%) and 29 (17%) infections occurred during the Omicron- and Delta-predominant periods, respectively. Asymptomatic infections occurred among 6.7% (95% CI 3.1%, 12.3%) of Omicron cases and 0.0% (95% CI 0.0%, 11.9%) of Delta cases. Healthcare utilization among Omicron cases was 79% (95% CI 43%, 92%, P =0.001) lower relative to Delta cases. Relative to Delta, Omicron infections also experienced a 56% (95% CI 26%, 74%, P =0.004) and 79% (95% CI 54%, 91%, P <0.001) reduction in the risk and rate of post-acute symptoms, respectively. Conclusions and Relevance These findings suggest that among previously immunologically naïve adults, few Omicron (BA.1/BA.2) and Delta infections are asymptomatic, and relative to Delta, Omicron infections were less likely to seek healthcare and experience post-acute symptoms.

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: MedRxiv Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: MedRxiv Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos