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      Risks of myocarditis, pericarditis, and cardiac arrhythmias associated with COVID-19 vaccination or SARS-CoV-2 infection

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          Abstract

          Although myocarditis and pericarditis were not observed as adverse events in coronavirus disease 2019 (COVID-19) vaccine trials, there have been numerous reports of suspected cases following vaccination in the general population. We undertook a self-controlled case series study of people aged 16 or older vaccinated for COVID-19 in England between 1 December 2020 and 24 August 2021 to investigate hospital admission or death from myocarditis, pericarditis and cardiac arrhythmias in the 1–28 days following adenovirus (ChAdOx1, n = 20,615,911) or messenger RNA-based (BNT162b2, n = 16,993,389; mRNA-1273, n = 1,006,191) vaccines or a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) positive test ( n = 3,028,867). We found increased risks of myocarditis associated with the first dose of ChAdOx1 and BNT162b2 vaccines and the first and second doses of the mRNA-1273 vaccine over the 1–28 days postvaccination period, and after a SARS-CoV-2 positive test. We estimated an extra two (95% confidence interval (CI) 0, 3), one (95% CI 0, 2) and six (95% CI 2, 8) myocarditis events per 1 million people vaccinated with ChAdOx1, BNT162b2 and mRNA-1273, respectively, in the 28 days following a first dose and an extra ten (95% CI 7, 11) myocarditis events per 1 million vaccinated in the 28 days after a second dose of mRNA-1273. This compares with an extra 40 (95% CI 38, 41) myocarditis events per 1 million patients in the 28 days following a SARS-CoV-2 positive test. We also observed increased risks of pericarditis and cardiac arrhythmias following a positive SARS-CoV-2 test. Similar associations were not observed with any of the COVID-19 vaccines, apart from an increased risk of arrhythmia following a second dose of mRNA-1273. Subgroup analyses by age showed the increased risk of myocarditis associated with the two mRNA vaccines was present only in those younger than 40.

          Abstract

          A self-controlled case series using individual-patient-level data from over 38 million people aged 16 years and over, reveals an increased risk of myocarditis within a week of receiving a first dose of ChAdOx1, BNT162b2 and mRNA-1273 vaccines, which was further increased after a second dose of either mRNA vaccine. SARS-CoV-2 infection was associated with even greater risk of myocarditis, as well as pericarditis and cardiac arrhythmia.

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          Cardiovascular Magnetic Resonance in Nonischemic Myocardial Inflammation

          This JACC Scientific Expert Panel provides consensus recommendations for an update of the cardiovascular magnetic resonance (CMR) diagnostic criteria for myocardial inflammation in patients with suspected acute or active myocardial inflammation (Lake Louise Criteria) that include options to use parametric mapping techniques. While each parameter may indicate myocardial inflammation, the authors propose that CMR provides strong evidence for myocardial inflammation, with increasing specificity, if the CMR scan demonstrates the combination of myocardial edema with other CMR markers of inflammatory myocardial injury. This is based on at least one T2-based criterion (global or regional increase of myocardial T2 relaxation time or an increased signal intensity in T2-weighted CMR images), with at least one T1-based criterion (increased myocardial T1, extracellular volume, or late gadolinium enhancement). While having both a positive T2-based marker and a T1-based marker will increase specificity for diagnosing acute myocardial inflammation, having only one (i.e., T2-based OR T1-based) marker may still support a diagnosis of acute myocardial inflammation in an appropriate clinical scenario, albeit with less specificity. The update is expected to improve the diagnostic accuracy of CMR further in detecting myocardial inflammation.
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            Safety of the BNT162b2 mRNA Covid-19 Vaccine in a Nationwide Setting

            Background Preapproval trials showed that messenger RNA (mRNA)–based vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) had a good safety profile, yet these trials were subject to size and patient-mix limitations. An evaluation of the safety of the BNT162b2 mRNA vaccine with respect to a broad range of potential adverse events is needed. Methods We used data from the largest health care organization in Israel to evaluate the safety of the BNT162b2 mRNA vaccine. For each potential adverse event, in a population of persons with no previous diagnosis of that event, we individually matched vaccinated persons to unvaccinated persons according to sociodemographic and clinical variables. Risk ratios and risk differences at 42 days after vaccination were derived with the use of the Kaplan–Meier estimator. To place these results in context, we performed a similar analysis involving SARS-CoV-2–infected persons matched to uninfected persons. The same adverse events were studied in the vaccination and SARS-CoV-2 infection analyses. Results In the vaccination analysis, the vaccinated and control groups each included a mean of 884,828 persons. Vaccination was most strongly associated with an elevated risk of myocarditis (risk ratio, 3.24; 95% confidence interval [CI], 1.55 to 12.44; risk difference, 2.7 events per 100,000 persons; 95% CI, 1.0 to 4.6), lymphadenopathy (risk ratio, 2.43; 95% CI, 2.05 to 2.78; risk difference, 78.4 events per 100,000 persons; 95% CI, 64.1 to 89.3), appendicitis (risk ratio, 1.40; 95% CI, 1.02 to 2.01; risk difference, 5.0 events per 100,000 persons; 95% CI, 0.3 to 9.9), and herpes zoster infection (risk ratio, 1.43; 95% CI, 1.20 to 1.73; risk difference, 15.8 events per 100,000 persons; 95% CI, 8.2 to 24.2). SARS-CoV-2 infection was associated with a substantially increased risk of myocarditis (risk ratio, 18.28; 95% CI, 3.95 to 25.12; risk difference, 11.0 events per 100,000 persons; 95% CI, 5.6 to 15.8) and of additional serious adverse events, including pericarditis, arrhythmia, deep-vein thrombosis, pulmonary embolism, myocardial infarction, intracranial hemorrhage, and thrombocytopenia. Conclusions In this study in a nationwide mass vaccination setting, the BNT162b2 vaccine was not associated with an elevated risk of most of the adverse events examined. The vaccine was associated with an excess risk of myocarditis (1 to 5 events per 100,000 persons). The risk of this potentially serious adverse event and of many other serious adverse events was substantially increased after SARS-CoV-2 infection. (Funded by the Ivan and Francesca Berkowitz Family Living Laboratory Collaboration at Harvard Medical School and Clalit Research Institute.)
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              Myocarditis With COVID-19 mRNA Vaccines

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                Author and article information

                Contributors
                julia.hippisley-cox@phc.ox.ac.uk
                Journal
                Nat Med
                Nat Med
                Nature Medicine
                Nature Publishing Group US (New York )
                1078-8956
                1546-170X
                14 December 2021
                14 December 2021
                2022
                : 28
                : 2
                : 410-422
                Affiliations
                [1 ]GRID grid.4991.5, ISNI 0000 0004 1936 8948, Nuffield Department of Primary Health Care Sciences, , University of Oxford, ; Oxford, UK
                [2 ]GRID grid.4991.5, ISNI 0000 0004 1936 8948, Wellcome Centre for Human Genetics, , University of Oxford, ; Oxford, UK
                [3 ]GRID grid.9918.9, ISNI 0000 0004 1936 8411, Leicester Real World Evidence Unit, , Diabetes Research Centre, University of Leicester, ; Leicester, UK
                [4 ]GRID grid.4305.2, ISNI 0000 0004 1936 7988, Usher Institute, , University of Edinburgh, ; Edinburgh, UK
                [5 ]GRID grid.4305.2, ISNI 0000 0004 1936 7988, Centre for Inflammation Research, , University of Edinburgh, ; Edinburgh, UK
                [6 ]GRID grid.13097.3c, ISNI 0000 0001 2322 6764, School of Immunology and Microbial Sciences, , King’s College London, ; London, UK
                [7 ]GRID grid.4991.5, ISNI 0000 0004 1936 8948, Nuffield Department of Clinical Neurosciences, , University of Oxford, ; Oxford, UK
                [8 ]GRID grid.410556.3, ISNI 0000 0001 0440 1440, NIHR Biomedical Research Centre, , Oxford University Hospitals NHS Trust, ; Oxford, UK
                [9 ]GRID grid.4563.4, ISNI 0000 0004 1936 8868, Division of Primary Care, , School of Medicine, University of Nottingham, ; Nottingham, UK
                [10 ]GRID grid.4991.5, ISNI 0000 0004 1936 8948, British Heart Foundation Centre of Research Excellence, , NIHR Oxford Biomedical Research Centre, University of Oxford, John Radcliffe Hospital, ; Oxford, UK
                [11 ]GRID grid.4305.2, ISNI 0000 0004 1936 7988, BHF/University Centre for Cardiovascular Science, , University of Edinburgh, ; Edinburgh, UK
                Author information
                http://orcid.org/0000-0002-6279-4884
                http://orcid.org/0000-0002-8242-3722
                http://orcid.org/0000-0002-5338-2538
                http://orcid.org/0000-0003-1023-3927
                http://orcid.org/0000-0002-2327-3306
                http://orcid.org/0000-0003-0533-7991
                http://orcid.org/0000-0001-7022-3056
                http://orcid.org/0000-0002-2479-7283
                Article
                1630
                10.1038/s41591-021-01630-0
                8863574
                34907393
                2b076c15-17f9-457b-92d1-866d75229a3d
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 15 October 2021
                : 15 November 2021
                Funding
                Funded by: UK Research and Innovation (grant ref 459 MC_PC_20029)
                Funded by: National Institute for Health Research (NIHR) Applied Research Collaboration East Midlands 451 (ARC-EM) and NIHR Lifestyle BRC
                Funded by: NIHR Oxford Biomedical Research Centre; the British Heart Foundation (Chair Awards CH/F/21/90010, CH/16/1/32013), Programme Grant (RG/20/10/34966) and Research Excellence Awards (RE/18/5/34216, RE18/3/34214).
                Funded by: Health Data Research UK BREATHE Hub
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                © The Author(s), under exclusive licence to Springer Nature America, Inc. 2022

                Medicine
                epidemiology,cardiovascular diseases
                Medicine
                epidemiology, cardiovascular diseases

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