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COVID-19 vaccines and adverse events of special interest: A multinational Global Vaccine Data Network (GVDN) cohort study of 99 million vaccinated individuals

Authors :
Faksova, K
Walsh, D
Jiang, Y
Griffin, J
Phillips, A
Gentile, A
Kwong, JC
Macartney, K
Naus, M
Grange, Z
Escolano, S
Sepulveda, G
Shetty, A
Pillsbury, A
Sullivan, C
Naveed, Z
Janjua, NZ
Giglio, N
Perala, J
Nasreen, S
Gidding, H
Hovi, P
Vo, T
Cui, F
Deng, L
Cullen, L
Artama, M
Lu, H
Clothier, HJ
Batty, K
Paynter, J
Petousis-Harris, H
Buttery, J
Black, S
Hviid, A
Faksova, K
Walsh, D
Jiang, Y
Griffin, J
Phillips, A
Gentile, A
Kwong, JC
Macartney, K
Naus, M
Grange, Z
Escolano, S
Sepulveda, G
Shetty, A
Pillsbury, A
Sullivan, C
Naveed, Z
Janjua, NZ
Giglio, N
Perala, J
Nasreen, S
Gidding, H
Hovi, P
Vo, T
Cui, F
Deng, L
Cullen, L
Artama, M
Lu, H
Clothier, HJ
Batty, K
Paynter, J
Petousis-Harris, H
Buttery, J
Black, S
Hviid, A
Publication Year :
2024

Abstract

BACKGROUND: The Global COVID Vaccine Safety (GCoVS) Project, established in 2021 under the multinational Global Vaccine Data Network™ (GVDN®), facilitates comprehensive assessment of vaccine safety. This study aimed to evaluate the risk of adverse events of special interest (AESI) following COVID-19 vaccination from 10 sites across eight countries. METHODS: Using a common protocol, this observational cohort study compared observed with expected rates of 13 selected AESI across neurological, haematological, and cardiac outcomes. Expected rates were obtained by participating sites using pre-COVID-19 vaccination healthcare data stratified by age and sex. Observed rates were reported from the same healthcare datasets since COVID-19 vaccination program rollout. AESI occurring up to 42 days following vaccination with mRNA (BNT162b2 and mRNA-1273) and adenovirus-vector (ChAdOx1) vaccines were included in the primary analysis. Risks were assessed using observed versus expected (OE) ratios with 95 % confidence intervals. Prioritised potential safety signals were those with lower bound of the 95 % confidence interval (LBCI) greater than 1.5. RESULTS: Participants included 99,068,901 vaccinated individuals. In total, 183,559,462 doses of BNT162b2, 36,178,442 doses of mRNA-1273, and 23,093,399 doses of ChAdOx1 were administered across participating sites in the study period. Risk periods following homologous vaccination schedules contributed 23,168,335 person-years of follow-up. OE ratios with LBCI > 1.5 were observed for Guillain-Barré syndrome (2.49, 95 % CI: 2.15, 2.87) and cerebral venous sinus thrombosis (3.23, 95 % CI: 2.51, 4.09) following the first dose of ChAdOx1 vaccine. Acute disseminated encephalomyelitis showed an OE ratio of 3.78 (95 % CI: 1.52, 7.78) following the first dose of mRNA-1273 vaccine. The OE ratios for myocarditis and pericarditis following BNT162b2, mRNA-1273, and ChAdOx1 were significantly increased with LBCIs > 1.5. CONCLUSION: This multi-country a

Details

Database :
OAIster
Publication Type :
Electronic Resource
Accession number :
edsoai.on1456030045
Document Type :
Electronic Resource