Curbing the Delta Surge: Clinical Outcomes Check for updates After Treatment With Bamlanivimab-Etesevimab, Casirivimab-Imdevimab, or Sotrovimab for Mild to Moderate Coronavirus Disease 2019

Objective: To describe and compare the clinical outcomes of bamlanivimab-etesevimab, casirivimab-imdevimab, and sotrovimab treatment of mild to moderate coronavirus disease 2019 (COVID-19) during the severe acute respiratory coronavirus 2 (SARS-CoV-2) B.1.617.2 Delta surge. Methods: This is a retros...

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Veröffentlicht in:Mayo Clinic proceedings 2022-09, Vol.97 (9), p.1641
Hauptverfasser: Clune, Caroline G, O'Horo, John C, Arndt, Richard F, Culbertson, Tracy L, Kennedy, Brian D, Jackson, Tammy A, Tulledge-Scheitel, Sidna M, Challener, Douglas W, Larsen, Jennifer, Arndt, Lori, Hall, Scott T, Sweeten, Perry W, Razonable, Raymund R, Hanson, Sara N, Ganesh, Ravindra, Heyliger, Alexander
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Sprache:eng
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Zusammenfassung:Objective: To describe and compare the clinical outcomes of bamlanivimab-etesevimab, casirivimab-imdevimab, and sotrovimab treatment of mild to moderate coronavirus disease 2019 (COVID-19) during the severe acute respiratory coronavirus 2 (SARS-CoV-2) B.1.617.2 Delta surge. Methods: This is a retrospective study of high-risk patients who received bamlanivimab-etesevimab, casirivimab-imdevimab, and sotrovimab for mild to moderate COVID-19 between August 1, 2021, and December 1, 2021. Rates of severe disease, hospitalization, intensive care unit admission, and death were assessed. Results: Among 10,775 high-risk patients who received bamlanivimab-etesevimab, casirivimab-imdevimab, or sotrovimab for mild to moderate COVID-19 during the Delta surge, 287 patients (2.7%) developed severe disease that led to hospitalization, oxygen supplementation, or death within 30 days after treatment. The rates of severe disease were low among patients treated with bamlanivimab-etesevimab (1.2%), casirivimab-imdevimab (2.9%), and sotrovimab (1.6%; P
ISSN:0025-6196
DOI:10.1016/j.mayocp.2022.06.0151641