Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio.
Department of Cardiovascular Medicine, Cleveland Clinic, Cleveland, Ohio.
Am J Cardiol. 2020 Aug 1;128:140-146. doi: 10.1016/j.amjcard.2020.05.021. Epub 2020 May 16.
Transthyretin cardiac amyloidosis (ATTR-CA) is an increasingly recognized infiltrative cardiomyopathy in which conduction system disease is common. The aim of our study was to define the incidence and prevalence of high-grade atrioventricular (AV) block requiring pacemaker implantation in our quaternary referral center. This was a single-center retrospective cohort study of 369 consecutive patients with ATTR-CA who underwent 12-lead electrocardiogram at the time of ATTR-CA diagnosis. During a mean follow-up of 28 months, serial ECGs and the electronic medical record were examined for the development of high-grade AV block and pacemaker implantation. Wild-type ATTR-CA (wtATTR-CA) was diagnosed in 261 patients and 108 had hereditary ATTR-CA (hATTR-CA). A total of 35 (9.5%) had high-grade AV block requiring pacemaker implantation at the time of diagnosis of ATTR-CA. The most common conduction abnormalities evident on the baseline ECG were a wide QRS complex, present in 51% with wtATTR-CA and 48% with hATTR-CA (p = 0.62), followed by first-degree AV block, which was present in 49% with wtATTR-CA and 43% with hATTR-CA (p = 0.31). During follow-up, high-grade AV block developed in 10% of those with hATTR-CA and 12% of patients with wtATTR-CA (p = 0.64). On multivariable models, high-grade AV block was not significantly associated with increased mortality. More advanced ATTR-CA stage and a history of obstructive coronary artery disease were associated with increased mortality on multivariable models. In conclusion, the incidence and prevalence of high-grade AV block is high in patients with ATTR-CA. Patients with ATTR-CA require close monitoring during follow-up for the development of conduction system disease.
转甲状腺素蛋白心脏淀粉样变(ATTR-CA)是一种日益被认识的浸润性心肌病,其传导系统疾病较为常见。我们的研究目的是在我们的四级转诊中心确定诊断为 ATTR-CA 的患者中需要植入起搏器的高级别房室(AV)阻滞的发生率和患病率。这是一项对 369 例连续接受 ATTR-CA 诊断时的 12 导联心电图检查的患者进行的单中心回顾性队列研究。在平均 28 个月的随访期间,对连续心电图和电子病历进行检查,以确定高级别 AV 阻滞和起搏器植入的发生情况。在 261 例患者中诊断为野生型 ATTR-CA(wtATTR-CA),108 例患者为遗传性 ATTR-CA(hATTR-CA)。共有 35 例(9.5%)在诊断为 ATTR-CA 时需要植入起搏器的高级别 AV 阻滞。在基线心电图上最常见的传导异常是宽 QRS 复合体,wtATTR-CA 患者中有 51%,hATTR-CA 患者中有 48%(p=0.62),其次是一度房室阻滞,wtATTR-CA 患者中有 49%,hATTR-CA 患者中有 43%(p=0.31)。在随访期间,hATTR-CA 患者中有 10%和 wtATTR-CA 患者中有 12%出现高级别 AV 阻滞(p=0.64)。在多变量模型中,高级别 AV 阻滞与死亡率增加无显著相关性。在多变量模型中,更高级别的 ATTR-CA 分期和阻塞性冠状动脉疾病史与死亡率增加相关。总之,ATTR-CA 患者的高级别 AV 阻滞发生率和患病率较高。ATTR-CA 患者在随访期间需要密切监测传导系统疾病的发生。