Abstract

BackgroundMyocarditis has been reported following the first two doses of Pfizer-BNT162b2 messenger RNA (mRNA) COVID-19 vaccination. Administration of a third dose (booster) of the vaccine was initiated recently in Israel.ObjectiveThe aim of this study was to describe the characteristics of patients referred for cardiac magnetic resonance (CMR) imaging with myocarditis following the booster.MethodsPatients referred for CMR imaging with a clinical diagnosis of myocarditis within 21 days following the booster, between July 13 and November 11, 2021, were analyzed.ResultsOverall, 4 patients were included, 3/4 (75%) were men, and the mean age was 27 ± 10 years. The time from booster administration to the onset of symptoms was 5.75 ± 4.8 days (range 2–14). Obstructive coronary artery disease was excluded in 3 of the patients (75%). CMR was performed 34 ± 15 days (range 8-47 days) following the 3rd vaccination. The mean left ventricular ejection fraction was 61 ± 7% (range 53–71%), and regional wall motion abnormalities were present in one of the patients. Global T1 was increased in one of the patients, while focal T1 values were increased in 3 of the patients. Global T2 was increased in one of the patients, while focal T2 values were increased in all the patients. Global ECV was increased in 3 of the patients, while focal ECV was increased in all the patients. Median late gadolinium enhancement (LGE) was 4 ± 3% (range 1–9%), with the inferolateral segment as the most common location (3 of the 4 patients). All the patients met the Updated Lake Louise Criteria.ConclusionsPatient characteristics and CMR imaging findings of myocarditis following the administration of the booster vaccine are relatively mild and consistent with those observed with the first two doses. Although larger-scale prospective studies are necessary, these initial findings are somewhat reassuring.

Highlights

  • Myocarditis has been reported to be a possible rare adverse event following the first or second dose of Pfizer-BNT162b2 messenger RNA COVID-19 vaccination [1–4]

  • Our aim in the current report was to describe the characteristics of patients referred for cardiovascular magnetic resonance (CMR) with myocarditis following the administration of the BNT162b2 messenger RNA (mRNA) COVID-19 vaccine

  • This study comprised consecutive patients who are members of Clalit Health Services (CHS), and who were referred for CMR at Mor Inside Ltd. (Kfar Saba, Israel), with a clinically suspected diagnosis of myocarditis within 21 days after receiving the third dose of the Pfizer-BNT162b2 mRNA COVID-19 vaccine between July 13, 2021, and November 11, 2021

Read more

Summary

Introduction

Myocarditis has been reported to be a possible rare adverse event following the first or second dose of Pfizer-BNT162b2 messenger RNA (mRNA) COVID-19 vaccination [1–4]. Following the resurgence of COVID-19 morbidity, the Israeli Ministry of Health announced a campaign to administer the third dose (i.e., booster) of the BNT162b2 mRNA COVID-19 vaccine (Pfizer–BioNTech) to individuals who received the second dose > 5 months earlier, starting on July 13 [9]. This third vaccine dose was reported to be effectively protected against severe COVID-19-related outcomes [9]. Administration of a third dose (booster) of the vaccine was initiated recently in Israel

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call