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Myocarditis and pericarditis associated with SARS-CoV-2 vaccines: A population-based descriptive cohort and a nested self-controlled risk interval study using electronic health care data from four European countries

  • Sophie H Bots
  • , Judit Riera-Arnau
  • , Svetlana V Belitser
  • , Davide Messina
  • , Maria Aragón
  • , Ema Alsina
  • , Ian J Douglas
  • , Carlos E Durán
  • , Patricia García-Poza
  • , Rosa Gini
  • , Ron M C Herings
  • , Consuelo Huerta
  • , Malede Mequanent Sisay
  • , Mar Martín-Pérez
  • , Ivonne Martin
  • , Jetty A Overbeek
  • , Olga Paoletti
  • , Meritxell Pallejà-Millán
  • , Anna Schultze
  • , Patrick Souverein
  • Karin M A Swart, Felipe Villalobos, Olaf H Klungel, Miriam C J M Sturkenboom
  • University Medical Center Utrecht
  • Agenzia Regionale di Sanitá
  • Fundació Institut Universitari per a la recerca a l'Atenció Primària de Salut Jordi Gol i Gurina (IDIAPJGol)
  • London School of Hygiene and Tropical Medicine
  • Spanish Agency of Medicines & Medical Devices
  • PHARMO Institute for Drug Outcomes Research
  • Unitat de Suport a la Recerca Tarragona-Reus

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Background: Estimates of the association between COVID-19 vaccines and myo-/pericarditis risk vary widely across studies due to scarcity of events, especially in age- and sex-stratified analyses. Methods: Population-based cohort study with nested self-controlled risk interval (SCRI) using healthcare data from five European databases. Individuals were followed from 01/01/2020 until end of data availability (31/12/2021 latest). Outcome was first myo-/pericarditis diagnosis. Exposures were first and second dose of Pfizer, AstraZeneca, Moderna, and Janssen COVID-19 vaccines. Baseline incidence rates (IRs), and vaccine- and dose-specific IRs and rate differences were calculated from the cohort The SCRI calculated calendar time-adjusted IR ratios (IRR), using a 60-day pre-vaccination control period and dose-specific 28-day risk windows. IRRs were pooled using random effects meta-analysis. Findings: Over 35 million individuals (49·2% women, median age 39-49 years) were included, of which 57·4% received at least one COVID-19 vaccine dose. Baseline incidence of myocarditis was low. Myocarditis IRRs were elevated after vaccination in those aged < 30 years, after both Pfizer vaccine doses (IRR = 3·3, 95%CI 1·2-9.4; 7·8, 95%CI 2·6-23·5, respectively) and Moderna vaccine dose 2 (IRR = 6·1, 95%CI 1·1-33·5). An effect of AstraZeneca vaccine dose 2 could not be excluded (IRR = 2·42, 95%CI 0·96-6·07). Pericarditis was not associated with vaccination. Interpretation: mRNA-based COVID-19 vaccines and potentially AstraZeneca are associated with increased myocarditis risk in younger individuals, although absolute incidence remains low. More data on children (≤ 11 years) are needed.

Original languageEnglish
Article number1038043
Pages (from-to)1-12
Number of pages12
JournalFrontiers in Pharmacology
Volume13
DOIs
Publication statusPublished - 24 Nov 2022

Bibliographical note

Funding Information:
The project received support from the European Medicines Agency (EMA/2018/23/PE).

Publisher Copyright:
Copyright © 2022 Bots, Riera-Arnau, Belitser, Messina, Aragón, Alsina, Douglas, Durán, García-Poza, Gini, Herings, Huerta, Sisay, Martín-Pérez, Martin, Overbeek, Paoletti, Pallejà-Millán, Schultze, Souverein, Swart, Villalobos, Klungel and Sturkenboom.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Adverse drug reaction
  • COVID-19 vaccine
  • Myocarditis
  • Pericarditis
  • Pharmacovigilance

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