Your browser doesn't support javascript.
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.
  • Abdalateef S; Department of Pediatric Cardiology, Al Qassimi Hospital, Sharjah, UAE.
  • Al Meheiri NM; Hospital department, Emirates Health Service, Dubai, UAE.
  • Nassef M; Department of Anesthesia and Critical Care Medicine, Al Qassimi Hospital, Sharjah, UAE.
  • Shorrab AA; Anesthesia department, University Hospital Sharjah, Sharjah, UAE.
  • Hashimi OAR; Department of Medicine, Al Qassimi Hospital, Sharjah, UAE.
  • Allam S; Department of Medicine, Al Qassimi Hospital, Sharjah, UAE.
  • Alnaqbi MS; Hospital department, Emirates Health Service, Dubai, UAE.
  • Al-Rifai RH; Institute of Public Health, College of Medicine and Health Sciences, United Arab Emirates University, Al Ain, UAE rrifai@uaeu.ac.ae.
BMJ Open ; 13(1): e066095, 2023 01 10.
Article in English | MEDLINE | ID: covidwho-2193794
ABSTRACT

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.
Subject(s)
Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Antibodies, Monoclonal Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Country/Region as subject: Asia Language: English Journal: BMJ Open Year: 2023 Document Type: Article

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Antibodies, Monoclonal Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Humans Country/Region as subject: Asia Language: English Journal: BMJ Open Year: 2023 Document Type: Article