Division of Paediatric Cardiology, Institute of Clinical Sciences, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden.
Fundam Clin Pharmacol. 2010 Oct;24(5):637-52. doi: 10.1111/j.1472-8206.2010.00869.x. Epub 2010 Aug 19.
Clinically overt hypertrophic cardiomyopathy is the most common cause of sudden unexpected death in childhood and has significantly higher sudden death mortality in the 8- to 16-year age range than in the 17- to 30-year age range. A combination of electrocardiographic risk factors (a limb-lead ECG voltage sum >10 mV) and/or a septal wall thickness >190% of upper limit of normal for age (z-score > 3.72) defines a paediatric high-risk patient with great sensitivity. Syncope, blunted blood pressure response to exercise, non-sustained ventricular tachycardia and a malignant family history are additional risk factors. Of the medical treatments used, only beta-blocker therapy with lipophilic beta-blockers (i.e. propranolol, metoprolol or bisoprolol) have been shown to significantly reduce risk of sudden death, with doses ≥ 6 mg/kg BW in propranolol equivalents giving around a tenfold reduction in risk. Disopyramide therapy is a very useful adjunct to beta-blockers to improve prognosis in those patients that have dynamic outflow obstruction in spite of large doses of beta-blocker, and its use in patients with hypertrophic cardiomyopathy is not associated with significant pro-arrhythmia mortality. Calcium-channel blockers increase the risk of heart failure-associated death in hypertrophic cardiomyopathy (HCM) patients with severe generalized hypertrophy and should be avoided in such patients. Amiodarone does not protect against sudden death, and long-term use in children usually has to be terminated because of side effects. Therapy with internal cardioverter defibrillator implantation has high paediatric morbidity, 27% incidence of inappropriate shocks, and does not absolutely protect against mortality but is indicated as secondary prevention or in very high-risk patients.
临床上明显的肥厚型心肌病是儿童中最常见的猝死原因,8 至 16 岁年龄组的猝死死亡率明显高于 17 至 30 岁年龄组。心电图危险因素(肢体导联心电图电压总和>10 mV)和/或室间隔厚度大于年龄正常上限的 190%(z 评分>3.72)的组合定义了具有高度敏感性的儿科高危患者。晕厥、运动时血压反应迟钝、非持续性室性心动过速和恶性家族史是其他危险因素。在使用的治疗方法中,只有脂溶性β受体阻滞剂(即普萘洛尔、美托洛尔或比索洛尔)的β受体阻滞剂治疗已被证明可显著降低猝死风险,普萘洛尔等效剂量≥6mg/kgBW 可使风险降低约 10 倍。双异丙吡胺治疗是β受体阻滞剂的非常有用的辅助治疗,可改善尽管使用大剂量β受体阻滞剂仍存在动态流出道梗阻的患者的预后,其在肥厚型心肌病患者中的使用与明显的心律失常死亡率无关。钙通道阻滞剂增加肥厚型心肌病(HCM)患者伴严重弥漫性肥厚的心力衰竭相关死亡率,应避免在这些患者中使用。胺碘酮不能预防猝死,在儿童中长期使用通常因副作用而终止。植入式心律转复除颤器治疗的儿科发病率高,27%的不适当电击发生率,并且不能绝对预防死亡率,但适用于二级预防或极高危患者。