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SARS-CoV-2 vaccine Alpha and Delta variant breakthrough infections are rare and mild, but happen relative early after vaccination
Jelissa Katharina Peter; Fanny Wegner; Severin Gsponer; Fabrice Helfenstein; Tim Roloff; Rahel Tarnutzer; Kerstin Grosheintz; Moritz Back; Carla Schaubhut; Sabina Wagner; Helena M.B. Seth-Smith; Patrick Scotton; Maurice Redondo; Christiane Beckmann; Tanja Stadler; Andrea Salzmann; Henriette Kurth; Karoline Leuzinger; Stefano Bassetti; Roland Bingisser; Martin Siegemund; Maja Weisser; Manuel Battegay; Sarah Tschudin Sutter; Aitana Lebrand; Hans H Hirsch; Simon Fuchs; Adrian Egli.
Afiliação
  • Jelissa Katharina Peter; Health Services for the Canton of Basel-City
  • Fanny Wegner; University of Basel
  • Severin Gsponer; Health Services for the Canton of Basel-City
  • Fabrice Helfenstein; University Hospital Basel
  • Tim Roloff; University Hospital Basel
  • Rahel Tarnutzer; Health Services for the Canton of Basel-City
  • Kerstin Grosheintz; Health Services for the Canton of Basel-City
  • Moritz Back; Health Services for the Canton of Basel-City
  • Carla Schaubhut; Health Services of the Canton of Basel-City
  • Sabina Wagner; Health Services of the Canton of Basel-City
  • Helena M.B. Seth-Smith; University Hospital Basel
  • Patrick Scotton; Corona Vaccination Center for the Canton of Basel-City
  • Maurice Redondo; Viollier AG
  • Christiane Beckmann; Viollier AG
  • Tanja Stadler; ETH Zurich
  • Andrea Salzmann; Viollier AG
  • Henriette Kurth; Viollier AG
  • Karoline Leuzinger; University Hospital Basel
  • Stefano Bassetti; University Hospital Basel
  • Roland Bingisser; University Hospital Basel
  • Martin Siegemund; University Hospital Basel
  • Maja Weisser; University Hospital Basel
  • Manuel Battegay; University Hospital Basel
  • Sarah Tschudin Sutter; University Hospital Basel
  • Aitana Lebrand; Swiss Institute of Bioinformatics
  • Hans H Hirsch; University Hospital Basel
  • Simon Fuchs; Helath Services for the Canton of Basel-City
  • Adrian Egli; University Hospital Basel
Preprint em Inglês | medRxiv | ID: ppmedrxiv-21268324
ABSTRACT
IntroductionCOVID-19 vaccines significantly reduce SARS-CoV-2 (SCoV2)-related hospitalization and mortality in randomized controlled clinical trials, as well as in real-world effectiveness against different circulating SCoV2-lineages. However, some vaccine recipients show breakthrough infection and it remains unknown, which host and viral factors contribute to this risk and how many resulted in severe outcomes. Our aim was to identify demographic and clinical risk factors for SCoV2 breakthrough infections and severe disease in fully vaccinated individuals and to compare patient characteristics in breakthrough infections caused by SCoV2 Alpha or Delta variant. MethodsWe conducted an exploratory retrospective case-control study from 28th of December to 25th of October 2021 dominated by the Delta SCoV2 variant. All cases of infection had to be reported by law to the local health authorities. Vaccine recipients data was anonymously available from the national Vaccination Monitoring Data Lake and the main local vaccine center. We compared anonymized patients characteristics of breakthrough infection (n=492) to two overlapping control groups including all vaccine recipients from the Canton of Basel-City (group 1 n=126586 and group 2 n=109382). We also compared patients with breakthrough infection caused by the Alpha to Delta variant. We used different multivariate generalized linear models (GLM). ResultsWe found only 492/126586 (0.39%) vaccine recipients with a breakthrough infection after vaccination during the 10 months observational period. Most cases were asymptomatic or mild (478/492 97.2%) and only very few required hospitalization (14/492, 2.8%). The time to a positive SCoV2 test shows that most breakthrough infections occurred between a few days to about 170 days after full vaccination, with a median of 78 days (interquartile range, IQR 47-124 days). Factors associated with a lower odds for breakthrough infection were age (OR 0.987, 95%CI 0.983-0.992), previous COVID-19 infection prior to vaccination (OR 0.296, 95%CI 0.117-0.606), and (self-declared) serious side-effects from previous vaccines (OR 0.289, 95%CI 0.033-1.035). Factors associated with a higher odds for breakthrough infection were vaccination with the Pfizer/BioNTech vaccine (OR 1.459, 95%CI 1.238-1.612), chronic disease as vaccine indication (OR 2.109, 95%CI 1.692-2.620), and healthcare workers (OR 1.404, 95%CI 1.042-1.860). We did not observe a significantly increased risk for immunosuppressed patients (OR 1.248, 95% CI 0.806-1.849). ConclusionsOur study shows that breakthrough infections are rare and show mild illness, but that it occurs early after vaccination with more than 50% of cases within 70 to 80 days post-full vaccination. This clearly implies that boost vaccination should be much earlier initiated compared to the currently communicated 180-day threshold. This has important implications especially for risk groups associated with more frequent breakthrough infections such as healthcare workers, and people in high-risk care facilities. Due to changes in the epidemiological dynamic with new variants emerging, continuous monitoring of breakthrough infections is helpful to provide evidence on booster vaccines and patient groups at risk for potential complications.
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Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Estudo observacional / Estudo prognóstico / Rct Idioma: Inglês Ano de publicação: 2021 Tipo de documento: Preprint
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