Features of Inflammatory Heart Reactions Following mRNA COVID-19 Vaccination at a Global Level.


Journal

Clinical pharmacology and therapeutics
ISSN: 1532-6535
Titre abrégé: Clin Pharmacol Ther
Pays: United States
ID NLM: 0372741

Informations de publication

Date de publication:
03 2022
Historique:
received: 13 09 2021
accepted: 25 11 2021
pubmed: 4 12 2021
medline: 19 2 2022
entrez: 3 12 2021
Statut: ppublish

Résumé

Myocarditis and pericarditis may constitute adverse reactions of mRNA coronavirus disease 2019 (COVID-19) vaccines. This study aimed to document these reactions and to assess the association with patient sex and age. This is as an observational retrospective study using a case-non-case design (also called disproportionality study) on inflammatory heart reactions reported with mRNA COVID-19 vaccines within the World Health Organization (WHO) global safety database (VigiBase), up to June 30, 2021. Results are expressed using reporting odds ratios (RORs) and their 95% confidence interval (95% CI). Of 716,576 reports related to mRNA COVID-19 vaccines, 2,277 were cases of inflammatory heart reactions, including 1241 (55%) myocarditis and 851 (37%) pericarditis. The main age group was 18-29 years (704, 31%), and mostly male patients (1,555, 68%). Pericarditis onset was delayed compared with myocarditis with a median time to onset of 8 (3-21) vs. 3 (2-6) days, respectively (P = 0.001). Regarding myocarditis, an important disproportionate reporting was observed in adolescents (ROR, 22.3, 95% CI 19.2-25.9) and in 18-29 years old (ROR, 6.6, 95% CI 5.9-7.5) compared with older patients, as well as in male patients (ROR, 9.4, 95% CI 8.3-10.6). Reporting rate of myocarditis was increased in young adults and adolescents. Inflammatory heart reactions may rarely occur shortly following mRNA COVID-19 vaccination. Although an important disproportionate reporting of myocarditis was observed among adolescents and young adults, particularly in male patients, reporting rates support a very rare risk, that does not seem to compromise the largely positive benefit-risk balance of these vaccines. Furthermore, this study confirmed the value of disproportionality analyses for estimation of relative risks among subgroups of patients.

Identifiants

pubmed: 34860360
doi: 10.1002/cpt.2499
pmc: PMC9015432
doi:

Substances chimiques

COVID-19 Vaccines 0
Vaccines, Synthetic 0
mRNA Vaccines 0

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

605-613

Subventions

Organisme : CIHR
Pays : Canada
Organisme : Heart & Stroke Foundation of Canada
Organisme : Genome Canada
Organisme : University of Ottawa of Heart Institute
Organisme : CIHR
Pays : Canada

Informations de copyright

© 2021 The Authors. Clinical Pharmacology & Therapeutics published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.

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Auteurs

Laurent Chouchana (L)

Regional Center of Pharmacovigilance, Department of Pharmacology, Cochin Hospital, AP-HP.Centre - Université de Paris, Paris, France.

Alice Blet (A)

Departments of Medicine and Cellular & Molecular Medicine, University of Ottawa Heart Institute, University of Ottawa, Ottawa, ON, Canada.
Department of Anesthesiology, Critical Care and Burn Center, Lariboisière - Saint-Louis Hospitals, DMU Parabol, AP-HP Nord, University of Paris, Paris, France.
Inserm UMR-S 942, Cardiovascular Markers in Stress Conditions (MASCOT), University of Paris, Paris, France.

Mohammad Al-Khalaf (M)

Departments of Medicine and Cellular & Molecular Medicine, University of Ottawa Heart Institute, University of Ottawa, Ottawa, ON, Canada.

Tahir S Kafil (TS)

Departments of Medicine and Cellular & Molecular Medicine, University of Ottawa Heart Institute, University of Ottawa, Ottawa, ON, Canada.

Girish Nair (G)

Departments of Medicine and Cellular & Molecular Medicine, University of Ottawa Heart Institute, University of Ottawa, Ottawa, ON, Canada.

James Robblee (J)

Departments of Medicine and Cellular & Molecular Medicine, University of Ottawa Heart Institute, University of Ottawa, Ottawa, ON, Canada.

Milou-Daniel Drici (MD)

Regional Center of Pharmacovigilance, Department of Pharmacology, Nice University Hospital, Nice, France.

Marie-Blanche Valnet-Rabier (MB)

Regional Center of Pharmacovigilance, Department of Pharmacology, Besançon University Hospital, Besançon, France.

Joëlle Micallef (J)

UMR 1106, Inserm, Institute of Neurosciences System, Aix-Marseille University, Marseille, France.
Regional Center of Pharmacovigilance, Department of Clinical Pharmacology and Pharmacovigilance, University Hospitals of Marseille, Marseille, France.

Francesco Salvo (F)

INSERM, BPH, University of Bordeaux, Bordeaux, France.
CHU de Bordeaux, Pôle de Santé Publique, Service de Pharmacologie Médicale, Centre Régional de Pharmacovigilance, Bordeaux, France.

Jean-Marc Treluyer (JM)

Regional Center of Pharmacovigilance, Department of Pharmacology, Cochin Hospital, AP-HP.Centre - Université de Paris, Paris, France.
University of Paris, Paris, France.

Peter P Liu (PP)

Departments of Medicine and Cellular & Molecular Medicine, University of Ottawa Heart Institute, University of Ottawa, Ottawa, ON, Canada.

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