key: cord-1003120-h22bzcnr
authors: Verma, Amanda K.; Lavine, Kory J.; Lin, Chieh-Yu
title: Myocarditis after Covid-19 mRNA Vaccination
date: 2021-08-18
journal: N Engl J Med
DOI: 10.1056/nejmc2109975
sha: 1c2e5c7ff232fdbf70fe0731b8362a84cc95468a
doc_id: 1003120
cord_uid: h22bzcnr

nan

To the Editor: The Centers for Disease Control and Prevention recently reported cases of myocarditis and pericarditis in the United States after coronavirus disease 2019 (Covid-19) messenger RNA (mRNA) vaccination. 1 In recently published reports, diagnosis of myocarditis was made with the use of noninvasive imaging and routine laboratory testing. [2] [3] [4] [5] Here, we report two cases of histologically confirmed myocarditis after Covid-19 mRNA vaccination. Patient 1, a 45-year-old woman without a viral prodrome, presented with dyspnea and dizziness 10 days after BNT162b2 vaccination (first dose). A nasopharyngeal viral panel was negative for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), influenza A and B, enteroviruses, and adenovirus (Table S1 in the Supplementary Appendix, available with the full text of this letter at NEJM.org). A serum polymerase-chainreaction (PCR) assay and serologic tests showed no evidence of active parvovirus, enterovirus, human immunodeficiency virus, or infection with SARS-CoV-2. At presentation, she had tachycardia; ST-segment depression detected on electrocardiography, which was most prominent in the lateral leads (Fig. S1 ); and a troponin I level of 6.14 ng per milliliter (reference range, 0 to 0.30). A transthoracic echocardiogram showed severe global left ventricular systolic dysfunction (ejection fraction, 15 to 20%) and normal left ventricular dimensions. Right heart catheterization revealed elevated right-and left-sided filling pressures and a cardiac index of 1.66 liters per minute per square meter of body-surface area as measured by the Fick method. Coronary angiography revealed no obstructive coronary artery Hematoxylin-eosin stains of heart-tissue specimens obtained by means of endomyocardial biopsy in patient 1 (Panel A) and autopsy in patient 2 (Panel B) showed myocarditis in both patients, with multifocal cardiomyocyte damage (arrows) associated with mixed inflammatory infiltration. Scattered eosinophils were noted (arrowheads). The images of the hematoxylin-eosin stains were obtained with 10× eyepieces and 40× or 60× objectives. Additional information is provided in the Supplementary Appendix. RV denotes right ventricle, and LV left ventricle. disease. An endomyocardial biopsy specimen showed an inflammatory infiltrate predominantly composed of T-cells and macrophages, admixed with eosinophils, B cells, and plasma cells (Fig. 1A and Figs. S2 through S4) . She received inotropic support, intravenous diuretics, methylprednisolone (1 g daily for 3 days), and, eventually, guideline-directed medical therapy for heart failure (lisinopril, spironolactone, and metoprolol succinate). Seven days after presentation, her ejection fraction was 60%, and she was discharged home. Patient 2, a 42-year-old man, presented with dyspnea and chest pain 2 weeks after mRNA-1273 vaccination (second dose). He did not report a viral prodrome, and a PCR test was negative for SARS-CoV-2 (Table S1 ). He had tachycardia and a fever, and his electrocardiogram showed diffuse ST-segment elevation (Fig. S1) . A transthoracic echocardiogram showed global biventricular dysfunction (ejection fraction, 15%), normal ventricular dimensions, and left ventricular hypertrophy. Coronary angiography revealed no coronary artery disease. Cardiogenic shock developed in the patient, and he died 3 days after presentation. An autopsy revealed biventricular myocarditis ( Fig. 1B and Figs. S5 and S6 ). An inflammatory infiltrate admixed with macrophages, T-cells, eosinophils, and B cells was observed, a finding similar to that in Patient 1.

In these two adult cases of histologically confirmed, fulminant myocarditis that had devel-oped within 2 weeks after Covid-19 vaccination, a direct causal relationship cannot be definitively established because we did not perform testing for viral genomes or autoantibodies in the tissue specimens. However, no other causes were identified by PCR assay or serologic examination.

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