Manchester Heart Centre, Manchester Royal Infirmary, Manchester, UK.
Heart. 2012 Apr;98(8):631-6. doi: 10.1136/heartjnl-2011-300924.
Following national guidance on management of sudden unexplained death (SUD) in the young, inherited cardiac conditions (ICC) clinics were established to identify and treat relatives thought to be at increased risk. Studies have examined diagnostic yield of these clinics but outcome of clinical management has not been reported.
Observational outcome study of consecutively referred relatives of SUD victims.
Regional ICC clinic.
193 individuals (108 families) referred to a regional ICC clinic following SUD/aborted cardiac arrest of a young relative (mean follow-up 16.5 months, range 0.1-61).
All individuals underwent assessment by history, examination, ECG and echocardiography. Exercise electrocardiography, ajmaline provocation, further imaging techniques and genetic testing were performed in selected individuals. Implantable cardioverter-defibrillator (ICD) insertion based on national guidelines.
Forty-five patients (23%) from 38 families (35%) were diagnosed with an inheritable cause of sudden death. Eighteen had potentially prognostically important medication commenced and 4 had an ICD inserted on clinic recommendation (2 hypertrophic cardiomyopathy, 1 dilated cardiomyopathy, 1 arrhythmogenic right ventricular cardiomyopathy). Two other individuals had ICDs removed after negative testing for familial RYR2 mutations. No deaths have occurred during follow-up to date.
A diagnosis of an inheritable cause of sudden death was obtained in a significant minority of those with a family history of SUD/aborted cardiac arrest. The number of ICDs inserted as a result of specialist assessment was very small (2%). A major function of the clinic is reassurance of the clinically normal and cessation of treatment after exclusion of familial disease by genetic testing.
根据国家关于管理青年不明原因猝死(SUD)的指导意见,建立遗传性心脏病(ICC)诊所,以识别和治疗被认为风险增加的亲属。已有研究检查了这些诊所的诊断效果,但尚未报告临床管理的结果。
对 SUD/心搏骤停年轻亲属的连续转诊亲属进行观察性结局研究。
区域 ICC 诊所。
193 名个体(108 个家庭)在年轻亲属 SUD/心搏骤停/心搏骤停后被转诊至区域 ICC 诊所(平均随访 16.5 个月,范围 0.1-61 个月)。
所有个体均接受病史、检查、心电图和超声心动图评估。在选定的个体中进行运动心电图、阿马林激发试验、进一步的成像技术和基因检测。根据国家指南植入式心脏复律除颤器(ICD)。
38 个家庭(35%)的 45 名患者(23%)被诊断为突然死亡的遗传性病因。18 名患者开始服用潜在预后重要的药物,4 名患者根据诊所建议植入 ICD(2 名肥厚型心肌病、1 名扩张型心肌病、1 名致心律失常性右室心肌病)。另外 2 名个体在排除家族性 RYR2 突变后,ICD 被移除。迄今为止,在随访期间没有死亡发生。
在有 SUD/心搏骤停家族史的个体中,少数人被诊断为遗传性突发死亡病因。由于专科评估而植入 ICD 的数量非常少(2%)。诊所的主要功能是为临床正常的个体提供保证,并通过基因检测排除家族性疾病后停止治疗。