Sudden cardiac death in myocarditis

Gennady G. Taradin, Grigoriy A. Ignatenko, Tatyana E. Kugler
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Abstract

According to statistics, myocarditis is one of the leading causes of sudden cardiac death (SCD) in children and young adults. The etiology of myocarditis includes infectious and non-infectious, including autoimmune diseases, as well as toxicities and hypersensitivity to various drugs or bites of insects, spiders, snakes, etc. The risk of myocarditis among patients with COVID-19 is 15.7-fold higher than that in the general population. The most common cause of death in myocarditis is heart arrhythmia, such as ventricular tachyarrhythmia, ventricular fibrillation, or severe bradycardia. Genetic predisposition, ion and metabolic disorders, mechanisms of autoimmune response, and direct cardiotoxic action in viral diseases play a role in the pathophysiology of inflammatory myocardial damage. While the majority of patients with myocarditis, who died suddenly, was asymptomatic or had few symptoms, a timely and accurate diagnosis of myocarditis seems to be an important challenge for prevention or minimization of SCD risk. Nonetheless, at present there is no convincing evidence of an association between laboratory and instrumental parameters and the SCD risk in such patients. Endomyocardial biopsy remains the "golden standard" in the diagnosis of myocarditis. Biomarkers (troponins or creatine phosphokinase) are not highly specific. The most common electrocardiographic findings in myocarditis are sinus tachycardia and nonspecific changes in the ST-T segment. The presence of Q wave, bundle branch block, Brugada syndrome, shortened or prolonged QT interval, and early ventricular repolarization are associated with an increased risk of SCD in myocarditis. Given the absence of specific echocardiographic signs of myocarditis, special attention is paid to the assessment of the size of the cardiac chambers, wall thicknesses, global and regional systolic and diastolic function of both the left and right ventricles, visualization of pericardial effusion and intracardiac thrombi. A combined cardiac magnetic resonance imaging using T2-weighted imaging and early and late gadolinium enhancement provides high diagnostic accuracy and seems to be a useful tool in the stratification of patients with suspected acute myocarditis. With the established etiology of myocarditis, specific therapy is necessary to eliminate the pathogen. It is necessary to take into account the likely arrhythmogenic effects of the drugs used in treatment. Non-steroidal anti-inflammatory drugs are generally not indicated in patients with myocarditis because they cause renal impairment and sodium retention, which can exacerbate left ventricular dysfunction and increase the risk of SCD. In the case of severe conduction disturbances and ventricular tachyarrhythmias, implantation of a pacemaker or cardioverter-defibrillator is necessary.
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心肌炎引起的心源性猝死
据统计,心肌炎是儿童和青少年心脏性猝死(SCD)的主要原因之一。心肌炎的病因包括感染性和非感染性,包括自身免疫性疾病,以及对各种药物的毒性和过敏或被昆虫、蜘蛛、蛇等咬伤。新冠肺炎患者发生心肌炎的风险是普通人群的15.7倍。心肌炎最常见的死亡原因是心律失常,如室性心动过速、室颤或严重心动过缓。遗传易感性、离子和代谢紊乱、自身免疫反应机制以及病毒性疾病中直接的心脏毒性作用在炎症性心肌损伤的病理生理中发挥作用。虽然大多数突然死亡的心肌炎患者无症状或几乎没有症状,但及时准确地诊断心肌炎似乎是预防或最小化SCD风险的重要挑战。尽管如此,目前还没有令人信服的证据表明实验室和仪器参数与此类患者的SCD风险之间存在关联。心肌炎内膜活检仍然是诊断心肌炎的“黄金标准”。生物标志物(肌钙蛋白或肌酸磷酸激酶)没有高度特异性。心肌炎最常见的心电图表现是窦性心动过速和ST-T段的非特异性改变。Q波、束支阻滞、Brugada综合征、QT间期缩短或延长、早期心室复极与心肌炎SCD风险增加相关。由于缺乏心肌炎的特殊超声心动图征象,因此特别注意评估心室的大小、壁厚、左右心室整体和局部收缩和舒张功能、心包积液和心内血栓的可视化。联合心脏磁共振成像使用t2加权成像和早期和晚期钆增强提供了很高的诊断准确性,似乎是一个有用的工具,在患者的分层疑似急性心肌炎。随着心肌炎病因的确定,有必要进行特异性治疗以消除病原体。有必要考虑到治疗中使用的药物可能产生的心律失常效应。非甾体类抗炎药一般不适用于心肌炎患者,因为它们会导致肾功能损害和钠潴留,加重左心室功能障碍,增加SCD的风险。在严重的传导障碍和室性心动过速的情况下,植入起搏器或心律转复除颤器是必要的。
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CiteScore
0.50
自引率
0.00%
发文量
42
审稿时长
8 weeks
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