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Experience of the United Arab Emirates in the use of monoclonal antibody drug sotrovimab in high-risk vaccinated and unvaccinated patients with COVID-19: an observational cohort study

OBJECTIVES: Monoclonal antibodies can slow COVID-19 progression. This study describes the experience of using sotrovimab in patients with COVID-19 at high risk for disease progression and hospitalisation within the United Arab Emirates (UAE). DESIGN: Observational cohort study. SETTING: A tertiary h...

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Autores principales: Abdalateef, Sumaya, Al Meheiri, Noor Majed, Nassef, Mohamed, Shorrab, Ahmed A., Hashimi, Obaid Al Rahman, Allam, Samah, Alnaqbi, Mariam Saif, Al-Rifai, Rami H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835446/
https://www.ncbi.nlm.nih.gov/pubmed/36627160
http://dx.doi.org/10.1136/bmjopen-2022-066095
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author Abdalateef, Sumaya
Al Meheiri, Noor Majed
Nassef, Mohamed
Shorrab, Ahmed A.
Hashimi, Obaid Al Rahman
Allam, Samah
Alnaqbi, Mariam Saif
Al-Rifai, Rami H.
author_facet Abdalateef, Sumaya
Al Meheiri, Noor Majed
Nassef, Mohamed
Shorrab, Ahmed A.
Hashimi, Obaid Al Rahman
Allam, Samah
Alnaqbi, Mariam Saif
Al-Rifai, Rami H.
author_sort Abdalateef, Sumaya
collection PubMed
description OBJECTIVES: Monoclonal antibodies can slow COVID-19 progression. This study describes the experience of using sotrovimab in patients with COVID-19 at high risk for disease progression and hospitalisation within the United Arab Emirates (UAE). DESIGN: Observational cohort study. SETTING: A tertiary hospital in the Emirate of Sharjah, UAE. PARTICIPANTS: Patients with mild or moderate COVID-19 at high risk for disease progression. INTERVENTIONS: Infusion with a single 500 mg dose of the monoclonal antibody drug sotrovimab. PRIMARY AND SECONDARY OUTCOME MEASURES: Any adverse effect within 24 hours, disease progression within 5 days, emergency department visit within 10 days, hospital admission within 10 days or mortality within 28 days of infusion. RESULTS: 3227 high-risk COVID-19 patients were infused with sotrovimab during the mild (n=3107, 96.3%) or moderate (n=120, 3.7%) disease stages. The incidence of at least one outcome was recorded in 196 (6.1%) of the patients (60.7 per 1000 patients). The most common outcome was disease progression within 5 days of infusion in 129 patients (4.0%), followed by emergency department visits by 90 patients (2.8%) within 10 days. Twenty-nine (0.9%) patients were hospitalised within 10 days of infusion with only two deaths (0.1%). Patients infused with sotrovimab during the moderate disease stage had 11 times greater odds of developing at least one outcome compared with patients infused during the mild stage (adjusted OR, aOR 10.86, 95% CI 7.14 to 16.54). SARS-CoV-2 vaccinated (aOR 12.8, 95% CI 7.3 to 20.5) and unvaccinated (aOR 7.2, 95% CI 3.4 to 15.3) patients infused with sotrovimab during the moderate disease stage had similar odds of at least one outcome compared with patients infused during the mild stage. CONCLUSIONS: Among high-risk sotrovimab-infused COVID-19 patients, there were relatively low incidences of disease progression and hospitalisation. Regardless of vaccination history, monoclonal antibody intervention during the early stages of COVID-19 results in better outcomes.
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spelling pubmed-98354462023-01-12 Experience of the United Arab Emirates in the use of monoclonal antibody drug sotrovimab in high-risk vaccinated and unvaccinated patients with COVID-19: an observational cohort study Abdalateef, Sumaya Al Meheiri, Noor Majed Nassef, Mohamed Shorrab, Ahmed A. Hashimi, Obaid Al Rahman Allam, Samah Alnaqbi, Mariam Saif Al-Rifai, Rami H. BMJ Open Infectious Diseases OBJECTIVES: Monoclonal antibodies can slow COVID-19 progression. This study describes the experience of using sotrovimab in patients with COVID-19 at high risk for disease progression and hospitalisation within the United Arab Emirates (UAE). DESIGN: Observational cohort study. SETTING: A tertiary hospital in the Emirate of Sharjah, UAE. PARTICIPANTS: Patients with mild or moderate COVID-19 at high risk for disease progression. INTERVENTIONS: Infusion with a single 500 mg dose of the monoclonal antibody drug sotrovimab. PRIMARY AND SECONDARY OUTCOME MEASURES: Any adverse effect within 24 hours, disease progression within 5 days, emergency department visit within 10 days, hospital admission within 10 days or mortality within 28 days of infusion. RESULTS: 3227 high-risk COVID-19 patients were infused with sotrovimab during the mild (n=3107, 96.3%) or moderate (n=120, 3.7%) disease stages. The incidence of at least one outcome was recorded in 196 (6.1%) of the patients (60.7 per 1000 patients). The most common outcome was disease progression within 5 days of infusion in 129 patients (4.0%), followed by emergency department visits by 90 patients (2.8%) within 10 days. Twenty-nine (0.9%) patients were hospitalised within 10 days of infusion with only two deaths (0.1%). Patients infused with sotrovimab during the moderate disease stage had 11 times greater odds of developing at least one outcome compared with patients infused during the mild stage (adjusted OR, aOR 10.86, 95% CI 7.14 to 16.54). SARS-CoV-2 vaccinated (aOR 12.8, 95% CI 7.3 to 20.5) and unvaccinated (aOR 7.2, 95% CI 3.4 to 15.3) patients infused with sotrovimab during the moderate disease stage had similar odds of at least one outcome compared with patients infused during the mild stage. CONCLUSIONS: Among high-risk sotrovimab-infused COVID-19 patients, there were relatively low incidences of disease progression and hospitalisation. Regardless of vaccination history, monoclonal antibody intervention during the early stages of COVID-19 results in better outcomes. BMJ Publishing Group 2023-01-10 /pmc/articles/PMC9835446/ /pubmed/36627160 http://dx.doi.org/10.1136/bmjopen-2022-066095 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Infectious Diseases
Abdalateef, Sumaya
Al Meheiri, Noor Majed
Nassef, Mohamed
Shorrab, Ahmed A.
Hashimi, Obaid Al Rahman
Allam, Samah
Alnaqbi, Mariam Saif
Al-Rifai, Rami H.
Experience of the United Arab Emirates in the use of monoclonal antibody drug sotrovimab in high-risk vaccinated and unvaccinated patients with COVID-19: an observational cohort study
title Experience of the United Arab Emirates in the use of monoclonal antibody drug sotrovimab in high-risk vaccinated and unvaccinated patients with COVID-19: an observational cohort study
title_full Experience of the United Arab Emirates in the use of monoclonal antibody drug sotrovimab in high-risk vaccinated and unvaccinated patients with COVID-19: an observational cohort study
title_fullStr Experience of the United Arab Emirates in the use of monoclonal antibody drug sotrovimab in high-risk vaccinated and unvaccinated patients with COVID-19: an observational cohort study
title_full_unstemmed Experience of the United Arab Emirates in the use of monoclonal antibody drug sotrovimab in high-risk vaccinated and unvaccinated patients with COVID-19: an observational cohort study
title_short Experience of the United Arab Emirates in the use of monoclonal antibody drug sotrovimab in high-risk vaccinated and unvaccinated patients with COVID-19: an observational cohort study
title_sort experience of the united arab emirates in the use of monoclonal antibody drug sotrovimab in high-risk vaccinated and unvaccinated patients with covid-19: an observational cohort study
topic Infectious Diseases
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9835446/
https://www.ncbi.nlm.nih.gov/pubmed/36627160
http://dx.doi.org/10.1136/bmjopen-2022-066095
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