{"title":"Effectiveness of tixagevimab/cilgavimab in reducing SARS-CoV-2 infections, hospitalizations and mortality in inmunocompromised patients","authors":"Marc Marti-Pastor , Ricardo Bou-Monterde , Lucia Ciancotti-Oliver , Marta Alcover-Pons , Aurora Amorós Cantero , Raquel Sánchez-Lopezosa , Neus Montañana-Rosell","doi":"10.1016/j.medcle.2024.03.018","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Inmunocompromised people have higher SARS-CoV-2 morbi-mortality and they are subsidiary to receive pre-exposure prophylaxis. The objective of this study is to evaluate the effectiveness of tixagevimab/cilgavimab (Evusheld) in preventing SARS-CoV-2 infections, hospitalizations and mortality in immunocompromised patients.</div></div><div><h3>Materials and methods</h3><div>119 immunocompromised people ≥18 years old eligible of receiving Evusheld were followed for 6 months. People with previous SARS-CoV-2 infection or incomplete vaccination regimen were exluded. A total of 19 people who received Evusheld were matched by propensity score, using a 1:1 ratio, with another 19 people who did not receive Evusheld.</div><div>Sociodemographic, related to SARS-CoV-2 risk factors and related to immunosuppression variables were included. The dependent variables were infection, hospitalization, and mortality related to SARS-CoV-2.</div><div>Statistical analyzes were performed using SPSS Statistics 19.0, STATA 11.0, and the R statistical package.</div></div><div><h3>Results</h3><div>In total, 4 people in the Evusheld group and 11 in the control group had SARS-CoV-2 infection, showing an incidence rate of 3.87 and 13.62 per 100 person-months, respectively. The HR (Hazard Ratio) was 0.29 (95% CI = 0.09−0.90) for SARS-CoV-2 infection, 0.37 (0.07−1.92) for SARS-CoV-2 hospitalization and, 0.23 (0.03−2.09) for SARS-CoV-2 mortality in the Evusheld group compared to control group.</div></div><div><h3>Conclusions</h3><div>This study demonstrates that Evusheld reduces the SARS-CoV-2 infections.</div></div>","PeriodicalId":74154,"journal":{"name":"Medicina clinica (English ed.)","volume":"163 6","pages":"Pages 275-280"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medicina clinica (English ed.)","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2387020624003875","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction
Inmunocompromised people have higher SARS-CoV-2 morbi-mortality and they are subsidiary to receive pre-exposure prophylaxis. The objective of this study is to evaluate the effectiveness of tixagevimab/cilgavimab (Evusheld) in preventing SARS-CoV-2 infections, hospitalizations and mortality in immunocompromised patients.
Materials and methods
119 immunocompromised people ≥18 years old eligible of receiving Evusheld were followed for 6 months. People with previous SARS-CoV-2 infection or incomplete vaccination regimen were exluded. A total of 19 people who received Evusheld were matched by propensity score, using a 1:1 ratio, with another 19 people who did not receive Evusheld.
Sociodemographic, related to SARS-CoV-2 risk factors and related to immunosuppression variables were included. The dependent variables were infection, hospitalization, and mortality related to SARS-CoV-2.
Statistical analyzes were performed using SPSS Statistics 19.0, STATA 11.0, and the R statistical package.
Results
In total, 4 people in the Evusheld group and 11 in the control group had SARS-CoV-2 infection, showing an incidence rate of 3.87 and 13.62 per 100 person-months, respectively. The HR (Hazard Ratio) was 0.29 (95% CI = 0.09−0.90) for SARS-CoV-2 infection, 0.37 (0.07−1.92) for SARS-CoV-2 hospitalization and, 0.23 (0.03−2.09) for SARS-CoV-2 mortality in the Evusheld group compared to control group.
Conclusions
This study demonstrates that Evusheld reduces the SARS-CoV-2 infections.