Division of Cardiology, Department of Internal Medicine, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Korea.
Department of Radiology, Chung-Ang University Hospital, Chung-Ang University College of Medicine, Seoul, Korea.
Yonsei Med J. 2024 Nov;65(11):629-635. doi: 10.3349/ymj.2023.0354.
The number of patients presenting with vaccination-related cardiovascular symptoms after receiving mRNA vaccines (mRNA-VRCS) is increasing. We investigated the incidence of vaccine-related adverse events (VAEs), including myocarditis and pericarditis, in patients with mRNA-VRCS after receiving BNT162b2-Pfizer-BioNTech and mRNA-1273-Moderna vaccines.
We retrospectively collected data on patients presenting with mRNA-VRCS who visited the outpatient clinic of two tertiary medical centers. Clinical characteristics, laboratory findings, echocardiographic findings, and electrocardiographic findings were evaluated. VAE was defined as myocarditis or pericarditis in patients after mRNA vaccination. Clinical outcomes during short-term follow-up, including emergency room (ER) visit, hospitalization, or death, were also assessed among the patients.
A total of 952 patients presenting with mRNA-VRCS were included in this study, with 89.7% receiving Pfizer-BioNTech and 10.3% receiving Moderna vaccines. The mean duration from vaccination to symptom was 5.6±7.5 days. VAEs, including acute myocarditis and acute pericarditis, were confirmed in 11 (1.2%) and 10 (1.1%) patients, respectively. The VAE group showed higher rates of dyspnea, echocardiography changes, and ST-T segment changes. During the short-term follow-up period of 3 months, the VAE group showed a higher hospitalization rate compared to the control group; there was no significant difference in ER visit (=0.320) or mortality rates (>0.999).
Amongst the patients who experienced mRNA-VRCS, the total incidence of VAEs, including acute myocarditis and pericarditis, was 2.2%. Patients with VAEs showed higher rates of dyspnea, echocardiographic changes, and ST-T segment changes compared to those without VAEs. With or without the cardiovascular events, the prognosis in patients with mRNA-VRCS was favorable.
越来越多的患者在接种 mRNA 疫苗(mRNA-VRCS)后出现与疫苗接种相关的心血管症状。我们调查了接受 BNT162b2-Pfizer-BioNTech 和 mRNA-1273-Moderna 疫苗后,mRNA-VRCS 患者疫苗相关不良事件(VAEs)的发生率,包括心肌炎和心包炎。
我们回顾性收集了在两家三级医疗中心门诊就诊的 mRNA-VRCS 患者的数据。评估了临床特征、实验室检查结果、超声心动图检查结果和心电图检查结果。mRNA 疫苗接种后患者的 VAEs 定义为心肌炎或心包炎。还评估了患者短期随访期间的临床结局,包括急诊就诊、住院或死亡。
本研究共纳入 952 例 mRNA-VRCS 患者,其中 89.7%接受了 Pfizer-BioNTech 疫苗,10.3%接受了 Moderna 疫苗。从接种到症状出现的平均时间为 5.6±7.5 天。VAEs,包括急性心肌炎和急性心包炎,分别在 11 例(1.2%)和 10 例(1.1%)患者中确诊。VAE 组呼吸困难、超声心动图改变和 ST-T 段改变的发生率更高。在 3 个月的短期随访期间,VAE 组的住院率高于对照组;急诊就诊率(=0.320)或死亡率(>0.999)无显著差异。
在经历 mRNA-VRCS 的患者中,VAEs(包括急性心肌炎和心包炎)的总发生率为 2.2%。与无 VAEs 患者相比,VAEs 患者呼吸困难、超声心动图改变和 ST-T 段改变的发生率更高。无论是否发生心血管事件,mRNA-VRCS 患者的预后良好。