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Cardiac device implantation in Fabry disease: A retrospective monocentric study

机译:法布里疾病中的心脏病植入:回顾性单眼性研究

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摘要

The incidence and predictive factors of arrhythmias and/or conduction abnormalities (ACAs) requiring cardiac device (CD) implantation are poorly characterized in Fabry disease (FD). The aim of our retrospective study was to determine the prevalence, incidence, and factors associated with ACA requiring CD implantation in a monocentric cohort of patients with confirmed FD who were followed up in a department of internal medicine and reference center for FD.Forty-nine patients (20M, 29F) were included. Nine patients (4M, 5F; 18%) had at least one episode of ACA leading to device therapy. Six patients (4M/2F) required a pacemaker (PM) for sinus node dysfunction (n=4) or atrioventricular disease (n=2). One female patient required an internal cardioverter-defibrillator (ICD) to prevent sudden cardiac death because of nonsustained ventricular tachycardia (nSVT). One female patient required PM-ICD for sinus node dysfunction and nSVT. One patient underwent CD implantation before the diagnosis of FD. The annual rate of CD implantation was estimated at 1.90 per 100 person years. On univariate analysis at the end of the follow-up period, the factors associated with ACAs requiring CD implantation were as follows: delayed diagnosis of FD, delayed initiation of enzyme replacement therapy, age at the last follow-up visit, and severe multiorgan phenotype (hypertrophic cardiomyopathy, chronic kidney disease, and/or sensorineural hearing loss). On multivariate analysis, age at diagnosis of FD and age at the last follow-up visit were independently associated with an increased risk of ACAs requiring CD (P<0.05).Considering the high frequency of ACAs requiring CD implantation and the risk of sudden death in patients with FD, regular monitoring is mandatory, especially in patients with a late diagnosis of FD and/or with a severe phenotype. Regular Holter ECGs, therapeutic education of patients, and deliverance of an emergency card including a phenotype summary are crucial in the care of FD patients.Available guidelines for device therapy and the efficacy of enzyme replacement therapy for arrhythmias or conduction abnormalities are discussed.
机译:需要心脏装置(CD)植入的心律失常和/或传导异常(ACA)的发病率和预测因素在法布里疾病(FD)中具有较差的特征。我们的回顾性研究的目的是确定与ACA相关的患病率,发病率和因素,需要在一名内科医学部门的确认FD患者中的单眼群组中的CD植入植入患者中的CD植入。包括患者(20M,29F)。九名患者(4M,5F; 18%)至少有一集ACA导致装置治疗。六名患者(4M / 2F)需要鼻窦功能障碍(N = 4)或房室疾病的起搏器(PM)(n = 2)。一名女性患者需要内部心脏病患者 - 除颤器(ICD),以防止由于不良心室性心动过速(NSVT)突然死亡。一个女性患者需要PM-ICD用于窦节节功能障碍和NSVT。一名患者在诊断FD之前接受了CD植入。年度CD植入率估计为每100人的1.90岁。在短暂性分析在随访期结束时,需要CD植入的ACAS相关的因素如下:延迟诊断FD,酶替代疗法的延迟开始,最后的后续访问和严重的多功能表型(肥厚性心肌病,慢性肾脏疾病和/或感官听力损失)。关于多变量分析,最后一次后续访问的FD和年龄诊断的年龄与需要CD的ACA的风险增加(P <0.05)。考虑需要CD植入的ACA的高频和猝死的风险在FD患者中,经常监测是强制性的,特别是在患者诊断FD和/或具有严重表型的患者中。常规的HOLTER ECG,患者治疗教育以及包括表型概述的急诊卡在FD患者的护理中至关重要。讨论了可利用的装置治疗准则和对心律失常或传导异常的酶替代治疗的疗效。

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