<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(6)</volume><submitter>Jalbert JJ</submitter><funding>Regeneron Pharmaceuticals</funding><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Data on real-world effectiveness of subcutaneous (SC) casirivimab and imdevimab (CAS+IMD) for the treatment of coronavirus disease 2019 (COVID-19) are limited. The objective of this study was to assess the effectiveness of SC CAS+IMD versus no antibody treatment among patients with COVID-19.&lt;h4>Methods&lt;/h4>This retrospective cohort study linked Komodo Health and CDR Maguire Health and Medical data. Patients diagnosed with COVID-19 in ambulatory settings (August 1-October 30, 2021) treated with SC CAS+IMD were exact- and propensity score-matched to fewer than five untreated treatment-eligible patients and followed for the composite endpoint of 30-day all-cause mortality or COVID-19-related hospitalization. Kaplan-Meier estimators were used to calculate outcome risk over</pubmed_abstract><journal>Infectious diseases and therapy</journal><pagination>2125-2139</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9526200</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Effectiveness of Subcutaneous Casirivimab and Imdevimab in Ambulatory Patients with COVID-19.</pubmed_title><pmcid>PMC9526200</pmcid><pubmed_authors>Murdock D</pubmed_authors><pubmed_authors>Wang D</pubmed_authors><pubmed_authors>Jalbert JJ</pubmed_authors><pubmed_authors>Hussein M</pubmed_authors><pubmed_authors>Mastey V</pubmed_authors><pubmed_authors>Sanchez RJ</pubmed_authors><pubmed_authors>Bussey J</pubmed_authors><pubmed_authors>Hirshberg B</pubmed_authors><pubmed_authors>Weinreich DM</pubmed_authors><pubmed_authors>Wei W</pubmed_authors><pubmed_authors>Farinas L</pubmed_authors><pubmed_authors>Duart C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Effectiveness of Subcutaneous Casirivimab and Imdevimab in Ambulatory Patients with COVID-19.</name><description>&lt;h4>Introduction&lt;/h4>Data on real-world effectiveness of subcutaneous (SC) casirivimab and imdevimab (CAS+IMD) for the treatment of coronavirus disease 2019 (COVID-19) are limited. The objective of this study was to assess the effectiveness of SC CAS+IMD versus no antibody treatment among patients with COVID-19.&lt;h4>Methods&lt;/h4>This retrospective cohort study linked Komodo Health and CDR Maguire Health and Medical data. Patients diagnosed with COVID-19 in ambulatory settings (August 1-October 30, 2021) treated with SC CAS+IMD were exact- and propensity score-matched to fewer than five untreated treatment-eligible patients and followed for the composite endpoint of 30-day all-cause mortality or COVID-19-related hospitalization. Kaplan-Meier estimators were used to calculate outcome risk over</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Dec</publication><modification>2025-04-05T11:40:11.384Z</modification><creation>2025-04-05T11:40:11.384Z</creation></dates><accession>S-EPMC9526200</accession><cross_references><pubmed>36181639</pubmed><doi>10.1007/s40121-022-00691-z</doi></cross_references></HashMap>