Coronary Anomalies Program, The Lillie Frank Abercrombie Section of Pediatric Cardiology (S.M., P.M., S.K.S.T., A.M.Q., S.P.J., E.D.M.), Texas Children's Hospital, Baylor College of Medicine, Houston.
Invasive Cardiac Imaging and Interventional Catheterization Laboratory, Le Bonheur Children's Hospital, The University of Tennessee Health Sciences Center, Memphis (H.A.).
Circ Cardiovasc Interv. 2020 Feb;13(2):e008445. doi: 10.1161/CIRCINTERVENTIONS.119.008445. Epub 2020 Feb 13.
Anomalous aortic origin of a coronary artery (CA) is the second leading cause of sudden cardiac death in young athletes. Management is controversial and longitudinal follow-up data are sparse. We aim to evaluate outcomes in a prospective study of anomalous aortic origin of CA patients following a standardized algorithm.
Patients with anomalous aortic origin of a CA were followed prospectively from December 2012 to April 2017. All patients were evaluated following a standardized algorithm, and data were reviewed by a dedicated multidisciplinary team. Assessment of myocardial perfusion was performed using stress imaging. High-risk patients (high-risk anatomy-anomalous left CA from the opposite sinus, presence of intramurality, abnormal ostium-and symptoms or evidence of myocardial ischemia) were offered surgery or exercise restriction (if deemed high risk for surgical intervention). Univariate and multivariable analyses were used to determine predictors of high risk.
Of 201 patients evaluated, 163 met inclusion criteria: 116 anomalous right CA (71%), 25 anomalous left CA (15%), 17 single CA (10%), and 5 anomalous circumflex CA (3%). Patients presented as an incidental finding (n=80, 49%), with exertional (n=31, 21%) and nonexertional (n=32, 20%) symptoms and following sudden cardiac arrest/shock (n=5, 3%). Eighty-two patients (50.3%) were considered high risk. Predictors of high risk were older age at diagnosis, black race, intramural course, and exertional syncope. Most patients (82%) are allowed unrestrictive sports activities. Forty-seven patients had surgery (11 anomalous left CA and 36 anomalous right CA), 3 (6.4%) remained restricted from sports activities. All patients are alive at a median follow-up of 1.6 (interquartile range, 0.7-2.8) years.
In this prospective cohort of patients with anomalous aortic origin of a CA, most have remained free of exercise restrictions. Development of a multidisciplinary team has allowed a consistent approach and may have implications in risk stratification and long-term prognosis.
冠状动脉(CA)异常起源是年轻运动员心脏性猝死的第二大主要原因。目前对该病的管理存在争议,且纵向随访数据较为缺乏。我们旨在通过一项针对 CA 异常起源患者的前瞻性研究,评估标准化算法治疗后的结果。
2012 年 12 月至 2017 年 4 月,前瞻性随访 CA 异常起源患者。所有患者均采用标准化算法进行评估,由专门的多学科团队进行数据审查。采用负荷成像评估心肌灌注情况。高危患者(高危解剖结构-来自对侧窦的异常左 CA、存在壁内走行、异常开口以及存在心肌缺血症状或证据)接受手术或运动限制(如果认为手术干预风险较高)。采用单变量和多变量分析来确定高危的预测因素。
在 201 名接受评估的患者中,163 名符合纳入标准:116 名异常右 CA(71%)、25 名异常左 CA(15%)、17 名单支 CA(10%)和 5 名异常回旋支 CA(3%)。患者因偶然发现(n=80,49%)、运动时(n=31,21%)和非运动时(n=32,20%)症状以及心脏骤停/电击(n=5,3%)就诊。82 名(50.3%)患者被认为存在高危因素。高危的预测因素为诊断时年龄较大、黑种人、壁内走行和运动性晕厥。大多数患者(82%)可以不受限制地进行体育活动。47 名患者接受了手术(11 例异常左 CA 和 36 例异常右 CA),3 名(6.4%)仍限制参加体育活动。所有患者的中位随访时间为 1.6 年(四分位间距 0.7-2.8),均存活。
在这项前瞻性 CA 异常起源患者队列中,大多数患者可不受限制地进行运动。多学科团队的建立可采用一致的方法,这可能对危险分层和长期预后具有重要意义。