COVID-19 vaccines and adverse events of special interest: A multinational Global Vaccine Data Network (GVDN) cohort study of 99 million vaccinated individuals
Faksova, K.; Walsh, D.; Jiang, Y.; Griffin, J.; Phillips, A.; Gentile, A.; Kwong, J. C.; Macartney, K.; Naus, M.; Grange, Z.; Escolano, S.; Sepulveda, G.; Shetty, A.; Pillsbury, A.; Sullivan, C.; Naveed, Z.; Janjua, N. Z.; Giglio, N.; Perälä, J.; Nasreen, S.; Gidding, H.; Hovi, P.; Vo, T.; Cui, F.; Deng, L.; Cullen, L.; Artama, M.; Weintraub, E.; Lu, H.; Clothier, H. J.; Batty, K.; Paynter, J.; Petousis-Harris, H.; Buttery, J.; Black, S.; Hviid, A. (2024)
Faksova, K.
Walsh, D.
Jiang, Y.
Griffin, J.
Phillips, A.
Gentile, A.
Kwong, J. C.
Macartney, K.
Naus, M.
Grange, Z.
Escolano, S.
Sepulveda, G.
Shetty, A.
Pillsbury, A.
Sullivan, C.
Naveed, Z.
Janjua, N. Z.
Giglio, N.
Perälä, J.
Nasreen, S.
Gidding, H.
Hovi, P.
Vo, T.
Cui, F.
Deng, L.
Cullen, L.
Artama, M.
Weintraub, E.
Lu, H.
Clothier, H. J.
Batty, K.
Paynter, J.
Petousis-Harris, H.
Buttery, J.
Black, S.
Hviid, A.
2024
VACCINE
Julkaisun pysyvä osoite on
https://urn.fi/URN:NBN:fi:tuni-202404173699
https://urn.fi/URN:NBN:fi:tuni-202404173699
Kuvaus
Peer reviewed
Tiivistelmä
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 analysis confirmed pre-established safety signals for myocarditis, pericarditis, Guillain-Barré syndrome, and cerebral venous sinus thrombosis. Other potential safety signals that require further investigation were identified.
Kokoelmat
- TUNICRIS-julkaisut [20161]