Ciccarelli Gian Paolo, Bruzzese Eugenia, Asile Gaetano, Vassallo Edoardo, Pierri Luca, De Lucia Vittoria, Guarino Alfredo, Lo Vecchio Andrea
Department of Translational Medical Sciences, Section of Pediatrics, University of Naples Federico II, Via S. Pansini, 5, 80131 Naples, Italy.
Department of Advanced Biomedical Sciences, Section of Cardiology, University of Naples Federico II, Via S. Pansini, 5, 80131 Naples, Italy.
Eur Heart J Case Rep. 2021 Oct 14;5(12):ytab405. doi: 10.1093/ehjcr/ytab405. eCollection 2021 Dec.
Multisystem inflammatory syndrome in children (MIS-C) is a rare life-threatening clinical condition that can develop in patients younger than 21 years of age with a history of infection/exposure to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The cardiovascular system is a main target of the inflammatory process that frequently causes myocardial dysfunction, myopericarditis, coronary artery dilation, hypotension, and shock. Multisystem inflammatory syndrome in children-associated myocarditis is usually characterized by fever, tachycardia, non-specific electrocardiogram abnormalities, and left ventricular dysfunction, but serious tachyarrhythmias may also occur. We report two cases of patients with MIS-C-associated myocarditis who developed severe bradycardia.
Two female adolescents with recent history of coronavirus disease 2019 (COVID-19) were initially hospitalized for long-lasting high-grade fever and severe gastrointestinal symptoms. Both patients were diagnosed with MIS-C-associated myocarditis for elevation of markers of myocardial injury (mean highly-sensitive cardiac troponin 2663 pg/mL, mean N-terminal-pro-brain natriuretic peptide 5097 pg/mL) and left ventricular dysfunction, which was subsequently confirmed by cardiac magnetic resonance. Both patients developed a severe sinus bradycardia (lowest heart rate 36 and 42, respectively), which appeared refractory to the treatment with intravenous Methylprednisolone and Immunoglobulins, despite a clinical and biochemical improvement. The use of Anakinra (a recombinant interleukin-1 receptor antagonist), was associated with a rapid improvement of cardiac rhythm and excellent clinical outcome at 6 months of follow-up.
In patients with MIS-C-associated myocarditis, a continuous cardiac monitoring is mandatory to promptly identify potential conduction abnormalities. Adolescents may present bradycardia as a rhythm complication. We experienced a rapid recovery after treatment with Anakinra, to be considered as add-on therapy in cases refractory to standard anti-inflammatory treatment.
儿童多系统炎症综合征(MIS-C)是一种罕见的危及生命的临床病症,可发生于21岁以下有感染/接触严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病史的患者。心血管系统是炎症过程的主要靶器官,常导致心肌功能障碍、心肌心包炎、冠状动脉扩张、低血压和休克。儿童多系统炎症综合征相关心肌炎通常表现为发热、心动过速、非特异性心电图异常和左心室功能障碍,但也可能发生严重的快速性心律失常。我们报告两例MIS-C相关心肌炎患者发生严重心动过缓的病例。
两名近期有2019冠状病毒病(COVID-19)病史的女性青少年最初因长期高热和严重胃肠道症状住院。两名患者均因心肌损伤标志物升高(平均高敏心肌肌钙蛋白2663 pg/mL,平均N末端脑钠肽前体5097 pg/mL)和左心室功能障碍而被诊断为MIS-C相关心肌炎,随后经心脏磁共振成像证实。两名患者均出现严重窦性心动过缓(最低心率分别为36次/分和42次/分),尽管临床和生化指标有所改善,但静脉注射甲泼尼龙和免疫球蛋白治疗无效。使用阿那白滞素(一种重组白细胞介素-1受体拮抗剂)后,心律迅速改善,随访6个月时临床结局良好。
对于MIS-C相关心肌炎患者,必须进行持续的心脏监测,以便及时发现潜在的传导异常。青少年可能出现心动过缓作为节律并发症。我们在使用阿那白滞素治疗后迅速康复,在标准抗炎治疗无效的情况下可考虑将其作为附加治疗。