Mapelli Massimo, Amelotti Nicola, Andreini Daniele, Baggiano Andrea, Campodonico Jeness, Moltrasio Massimo, Majocchi Benedetta, Mantegazza Valentina, Vignati Carlo, Ribatti Valentina, Catto Valentina, Sicuso Rita, Moltrasio Marco, Pontone Gianluca, Agostoni Piergiuseppe
Heart Failure Unit, Centro Cardiologico Monzino, IRCCS, Via Parea 4, 20138 Milan, Italy.
Department of Clinical Sciences and Community Health, Cardiovascular Section, University of Milan, Via della Commenda 19, 20122 Milan, Italy.
Eur Heart J Suppl. 2022 May 18;24(Suppl C):C243-C247. doi: 10.1093/eurheartj/suac018. eCollection 2022 May.
The rate of post-vaccine myocarditis is being studied from the beginning of the massive vaccination campaign against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Although a direct cause-effect relationship has been described, in most cases, the vaccine pathophysiological role is doubtful. Moreover, it is not quite as clear as having had a previous myocarditis could be a risk factor for a post-vaccine disease relapse. A 27-year-old man presented to the emergency department for palpitations and pericardial chest pain radiated to the upper left limb, on the 4th day after the third dose of BNT162b2 vaccine. He experienced a previous myocarditis 3 years before, with full recovery and no other comorbidities. Electrocardiogram showed normal atrioventricular conduction, incomplete right bundle branch block, and diffuse ST-segment elevation. A cardiac echo showed lateral wall hypokinesis with preserved ejection fraction. Troponin-T was elevated (160 ng/L), chest X-ray was normal, and the SARS-CoV-2 molecular buffer was negative. High-dose anti-inflammatory therapy with ibuprofen and colchicine was started; in the 3rd day high-sensitivity Troponin I reached a peak of 23000 ng/L. No heart failure or arrhythmias were observed. A cardiac magnetic resonance was performed showing normal biventricular systolic function and abnormal tissue characterization suggestive for acute non-ischaemic myocardial injury (increased native T1 and T2 values, increased signal intensity at T2-weighted images and late gadolinium enhancement, all findings with matched subepicardial distribution) at the level of mid to apical septal, anterior, and anterolateral walls. A left ventricular electroanatomic voltage mapping was negative (both unipolar and bipolar), while the endomyocardial biopsy showed a picture consistent with active myocarditis. The patient was discharged in good clinical condition, on bisoprolol 1.25 mg, ramipril 2.5 mg, ibuprofen 600 mg three times a day, colchicine 0.5 mg twice a day. We presented the case of a young man with history of previous myocarditis, admitted with a non-complicated acute myopericarditis relapse occurred 4 days after SARS-CoV-2 vaccination (3rd dose). Despite the observed very low incidence of cardiac complications following BNT162b2 administration, and the lack of a clear proof of a direct cause-effect relationship, we think that in our patient this link can be more than likely. In the probable need for additional SARS-CoV-2 vaccine doses in the next future, studies addressing the risk-benefit balance of this subset of patient are warranted. We described a multidisciplinary management of a case of myocarditis recurrence after the third dose of SARS-CoV-2 BNT162b2 vaccine.
自针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的大规模疫苗接种运动开始以来,一直在研究疫苗接种后心肌炎的发生率。尽管已经描述了直接的因果关系,但在大多数情况下,疫苗的病理生理作用仍值得怀疑。此外,既往有心肌炎是否可能是疫苗接种后疾病复发的危险因素,目前尚不完全清楚。一名27岁男性在接种第三剂BNT162b2疫苗后第4天因心悸和放射至左上肢的心前区胸痛就诊于急诊科。他3年前曾患心肌炎,已完全康复,无其他合并症。心电图显示房室传导正常、不完全性右束支传导阻滞和弥漫性ST段抬高。心脏超声显示侧壁运动减弱,射血分数正常。肌钙蛋白-T升高(160 ng/L),胸部X线正常,SARS-CoV-2分子检测阴性。开始使用布洛芬和秋水仙碱进行大剂量抗炎治疗;第3天,高敏肌钙蛋白I达到峰值23000 ng/L。未观察到心力衰竭或心律失常。进行了心脏磁共振成像,显示双心室收缩功能正常,组织特征异常,提示中至心尖间隔、前壁和前侧壁水平存在急性非缺血性心肌损伤(固有T1和T2值增加、T2加权图像上信号强度增加以及钆延迟增强,所有发现均与心外膜下分布相匹配)。左心室电解剖电压标测为阴性(单极和双极均为阴性),而心内膜活检显示符合活动性心肌炎的表现。患者出院时临床状况良好,服用比索洛尔1.25 mg、雷米普利2.5 mg、布洛芬600 mg,每日3次,秋水仙碱0.5 mg,每日2次。我们报告了一例既往有心肌炎病史的年轻男性病例,该患者在接种SARS-CoV-2疫苗(第三剂)后4天出现无并发症的急性心肌心包炎复发。尽管观察到接种BNT162b2后心脏并发症的发生率非常低,且缺乏直接因果关系的确切证据,但我们认为在我们的患者中这种关联很可能存在。鉴于未来可能需要额外接种SARS-CoV-2疫苗,有必要开展针对这一患者亚组风险效益平衡的研究。我们描述了一例接种第三剂SARS-CoV-2 BNT162b2疫苗后心肌炎复发病例的多学科管理。