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      Change in Effectiveness of Sotrovimab for Preventing Hospitalization and Mortality for At-risk COVID-19 Outpatients During an Omicron BA.1 and BA.1.1-Predominant Phase

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          Abstract

          Objectives

          Sotrovimab effectively prevented progression to severe disease and mortality following infection with pre-Omicron SARS-CoV-2 variants. We sought to determine whether sotrovimab is similarly effective against SARS-CoV-2 Omicron variant infection.

          Methods

          Observational cohort study of non-hospitalized adult patients with SARS-CoV-2 infection from December 26, 2021 to March 10, 2022, using electronic health records from a statewide health system. We propensity matching patients not receiving authorized treatment for each patient treated with sotrovimab . The primary outcome was 28-day hospitalization; secondary outcomes included mortality. We also propensity matched sotrovimab-treated patients from the Omicron and Delta phases. Logistic regression was used to determine sotrovimab effectiveness during Omicron and between variant phases.

          Results

          Of 30,247 SARS-CoV-2 Omicron variant infected outpatients, we matched 1,542 receiving sotrovimab to 3,663 not receiving treatment. Sotrovimab treatment was not associated with reduced odds of 28-day hospitalization (2.5% versus 3.2%; adjusted OR 0.82, 95% CI 0.55, 1.19) or mortality (0.1% versus 0.2%; adjusted OR 0.62, 95% CI 0.07, 2.78). Between phases, the observed treatment odds ratio was higher during Omicron than during Delta (OR 0.85 vs. 0.39, respectively; interaction p=0.053).

          Conclusions

          Real-world evidence demonstrated sotrovimab was not associated with reduced 28-day hospitalization or mortality among COVID-19 outpatients during the Omicron BA.1 phase.

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          Author and article information

          Journal
          Int J Infect Dis
          Int J Infect Dis
          International Journal of Infectious Diseases
          The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.
          1201-9712
          1878-3511
          10 October 2022
          10 October 2022
          Affiliations
          [a ]Department of Medicine, University of Colorado School of Medicine, Aurora, 80045, USA
          [b ]Department of Biostatistics and Informatics, Colorado School of Public Health, Aurora, 80045, USA
          [c ]Section of Informatics and Data Science, Department of Pediatrics, University of Colorado School of Medicine, Aurora, 80045, USA
          [d ]Department of Emergency Medicine, University of Colorado School of Medicine, Aurora, 80045, USA
          [e ]Colorado Clinical and Translational Sciences Institute, University of Colorado Anschutz Medical Campus, Aurora, 80045, USA
          [f ]UCHealth Pharmacy, Aurora, 80045, USA
          [g ]Center for Bioethics and Humanities, University of Colorado, Anschutz Medical Campus, Aurora, 80045, USA
          [h ]Department of Health Systems Management and Policy, Colorado School of Public Health, Aurora, 80045, USA
          Author notes
          [* ]Corresponding author: Neil R. Aggarwal, Department of Medicine, University of Colorado School of Medicine, 12700 E. 19th Ave, Mail Stop C-272, Aurora, CO 80045, USA. Phone: +1-303-724-6038
          [1]

          Contributed equally to this manuscript

          Article
          S1201-9712(22)00540-9
          10.1016/j.ijid.2022.10.002
          9549713
          36229005
          bf206342-2178-4f98-ba96-cfda743080d0
          © 2022 The Author(s). Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.

          Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

          History
          : 19 August 2022
          : 28 September 2022
          : 3 October 2022
          Categories
          Article

          Infectious disease & Microbiology
          real-world evidence,monoclonal antibody,covid-19
          Infectious disease & Microbiology
          real-world evidence, monoclonal antibody, covid-19

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