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Risk stratification and outcome of patients with hypertrophic cardiomyopathy ≥60 years of age

机译:≥60岁的肥厚型心肌病患者的风险分层和结局

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Objectives: The purpose of this study was to describe the clinical course and risk stratifyolder patients with hypertrophic cardiomyopathy (HCM)who were more than 60 years of age. Background: Two major problems associated with HCM are risk for sudden death and disease progression. These are relatively well defined in young patients. Whether patients of more advanced age harbour similar risks is unresolved and often creates clinical dilemmas, particularly in decisions for primary prevention of sudden death with implantable defibrillators. Methods: Patients for this study were selected from databases of 2 large HCM centers in USA. Consecutively presenting patients with HCM who were >=60 years of age at first presentation to these centers were selected for this study. These patients were followed up by hospital visit or telephone contact. Results: 428 consecutive older HCM patients were followed for 5.8+/-4.8 years. Of these, 279 (65%) survived to 73+/-7 years of age, most with no/mild symptoms including 135 with >=1 conventional sudden death risk factors and 50 (37%) with late gadolinium enhancement.On followup, 149 (35%) died at 80+/-8 years of age, mostly from nonHCMrelated causes(n=133, 31%), including a substantial proportion from non-cardiac disease (n=54). Sixteen patients (3.7%) had HCMrelatedmortality events (0.64%/year), including embolic stroke (n=6), progressive heart failure or transplantation (n=3),postoperative complications (n=2), and arrhythmic sudden death events (n=5, 1.2% [0.20%/year]). All-cause mortality wasincreased in HCM patients >=60 years of age compared with an age-matched US general population, predominantly as aresult of non-HCM-related diseases (P<0.001; standard mortality ratio, 1.5). Conclusions: HCM patients surviving into the seventh decade of life are at low risk for disease-related morbidity, mortality and sudden death, even in presence of conventional risk factors. Other cardiac or non-cardiac comorbidities have a greater impact on survival than HCM in older patients.
机译:目的:本研究的目的是描述年龄超过60岁的肥厚型心肌病(HCM)分层患者的临床病程和风险。背景:与HCM相关的两个主要问题是猝死和疾病发展的风险。这些在年轻患者中相对明确。年龄更大的患者是否具有相似的风险仍未解决,并常常造成临床难题,尤其是在采用植入式除纤颤器进行一级预防猝死的决策中。方法:本研究的患者选自美国2个大型HCM中心的数据库。首次向这些中心就诊的连续≥60岁的HCM患者被选入本研究。对这些患者进行了医院访问或电话联系。结果:连续428例年龄较大的HCM患者接受了5.8 +/- 4.8年的随访。其中279名(65%)存活至73 +/- 7岁,大多数无/轻度症状,其中135名常规猝死危险因子> = 1,而50名(37%)晚期enhancement增强。 149(35%)人在80 +/- 8岁时死亡,主要是由与非HCM相关的原因致死(n = 133,31%),其中很大一部分是由非心脏病引起的(n = 54)。 16名患者(3.7%)发生了HCM相关死亡事件(0.64%/年),包括栓塞性中风(n = 6),进行性心力衰竭或移植(n = 3),术后并发症(n = 2)和心律失常性猝死事件( n = 5,1.2%[0.20%/年])。与年龄相匹配的美国普通人群相比,年龄≥60岁的HCM患者的全因死亡率增加,主要是与非HCM相关疾病的结果有关(P <0.001;标准死亡率,1.5)。结论:即使存在常规危险因素,存活到第七十岁的HCM患者的疾病相关发病率,死亡率和猝死风险也较低。在老年患者中,其他心脏或非心脏合并症比HCM对生存的影响更大。

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