The incidence of COVID-19 infection following emergency use authorization of BBIBP-CORV inactivated vaccine in frontline workers in the United Arab Emirates

Nawal Al Kaabi(Shaikh Khalifa Medical City), Abderrahim Oulhaj(Khalifa University of Science and Technology), Farida Ismail Al Hosani(Abu Dhabi University), Shamma Al Mazrouei(Shaikh Khalifa Medical City), Omer Najim, Salah Eldin Hussein(Shaikh Khalifa Medical City), Jehad Saleh Abdalla(Shaikh Khalifa Medical City), Mohammed Saifuddin Fasihuddin(Shaikh Khalifa Medical City), Afnan Hassan(Shaikh Khalifa Medical City), Gehad ElGhazali(United Arab Emirates University), Ahmed Al Rumaithi(Shaikh Khalifa Medical City), Jumana Al Azazi(Shaikh Khalifa Medical City), Stefan Weber(Shaikh Khalifa Medical City), Rami Beiram(United Arab Emirates University), Khatija Parekh(United Arab Emirates University), Mohamud Sheek‐Hussein(United Arab Emirates University), Yunkai Yang, Yang Xiaoming, Jenny Quliang, Islam Eltantawy(INSEAD), Sally Mahmoud, Ashish Koshy, Peng Xiao, Subhashini Ganesan, Wael Elamin, Walid Zaher(Khalifa University of Science and Technology)
Scientific Reports
January 11, 2022
Cited by 16Open Access
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Abstract

Based on the findings from the Phase III clinical trials of inactivated SARS COV-2 Vaccine, (BBIBP-CORV) emergency use authorization (EUA) was granted for the vaccine to frontline workers in the UAE. A prospective cohort study was conducted among frontline workers to estimate the incidence rate and risk of symptomatic COVID-19 infection 14 days after the second dose of inoculation with BBIBP-CORV inactivated vaccine. Those who received two doses of the BBIBP-CORV vaccine in the period from 14th of September 2020 (first dose) to 21st of December 2020 (second dose) were followed up for COVID-19 infections. 11,322 individuals who received the two-dose BBIBP-CORV vaccine were included and were followed up post the second dose plus fourteen days. The incidence rate of symptomatic infection was 0.08 per 1000-person days (95% CI 0.07, 0.10). The estimated absolute risk of developing symptomatic infection was 0.97% (95% CI 0.77%, 1.17%). The confirmed seroconversion rate was 92.8%. There were no serious adverse events reported and no individuals suffered from severe disease. Our findings show that vaccinated individuals are likely to remain protected against symptomatic infection or becoming PCR positive for SARS COV 2 following the second dose of the vaccination.


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