Coronary Anomalies Program (T.T.D., P.M., D.L.R.-O., C.V.N., A.M.Q., S.K.S.-T., S.M.), Baylor College of Medicine, Houston.
Texas Children's Hospital and General Surgery Residency Program (R.Z.V.), Baylor College of Medicine, Houston.
Circ Cardiovasc Interv. 2020 Mar;13(3):e008375. doi: 10.1161/CIRCINTERVENTIONS.119.008375. Epub 2020 Feb 27.
Intraseptal anomalous aortic origin of a coronary artery is considered a benign condition. However, there have been case reports of patients with myocardial ischemia, arrhythmia, and sudden cardiac death. The purpose of this study was to determine the clinical presentation, myocardial perfusion on provocative stress testing, and management of children with anomalous aortic origin of a coronary artery with an intraseptal course in a prospective cohort.
Patients with anomalous aortic origin of a coronary artery and intraseptal course were prospectively enrolled from December 2012 to May 2019, evaluated, and managed following a standardized algorithm. Myocardial perfusion was assessed using stress imaging. Fractional flow reserve was performed in patients with myocardial hypoperfusion on noninvasive testing. Exercise restriction, β-blockers, and surgical intervention were discussed with the families.
Eighteen patients (female 6, 33.3%), who presented with no symptoms (10, 55.6%), nonexertional (4, 22.2%), and exertional symptoms (4, 22.2%), were enrolled at a median age of 12.4 years (0.3-15.9). Perfusion imaging was performed in 14/18 (77.8%) and was abnormal in 7/14 (50%); fractional flow reserve was positive in 5/8 (62.5%). All 4 patients with exertional symptoms and 3/10 (30%) with no or nonexertional symptoms had myocardial hypoperfusion. Coronary artery bypass grafting was performed in a 4-year-old patient; β-blocker and exercise restriction were recommended in 4 patients not suitable for surgery. One patient had nonexertional chest pain and 17 were symptom-free at median follow-up of 2.5 years (0.2-7.1).
Up to 50% of patients with intraseptal anomalous aortic origin of a coronary artery had inducible myocardial hypoperfusion during noninvasive provocative testing. Long-term follow-up is necessary to understand the natural history of this rare anomaly.
间隔内主动脉起源的冠状动脉异常通常被认为是良性的。然而,已有患者出现心肌缺血、心律失常和心源性猝死的病例报告。本研究的目的是在一个前瞻性队列中确定有间隔内行程的冠状动脉异常起源的患者的临床表现、激发性应激试验下的心肌灌注情况和治疗方法。
从 2012 年 12 月至 2019 年 5 月,前瞻性招募有间隔内行程的冠状动脉异常起源的患者,采用标准化算法进行评估和治疗。采用应激成像评估心肌灌注情况。对无创检查提示心肌灌注不足的患者进行血流储备分数检查。与患者家属讨论运动限制、β受体阻滞剂和手术干预。
18 例患者(女性 6 例,占 33.3%),其中无症状 10 例(占 55.6%),非运动性 4 例(占 22.2%)和运动性 4 例(占 22.2%),中位年龄 12.4 岁(0.3-15.9 岁)。18 例患者中有 14 例(77.8%)进行了灌注成像,其中 7 例(50%)异常;8 例中 5 例(62.5%)血流储备分数阳性。所有 4 例运动性症状患者和 10 例(30%)无症状或非运动性症状患者均有心肌灌注不足。一名 4 岁患者接受了冠状动脉旁路移植术;4 名不适合手术的患者建议使用β受体阻滞剂和运动限制。1 例患者出现非运动性胸痛,17 例患者在中位随访 2.5 年(0.2-7.1 年)时无症状。
在非侵入性激发性试验中,多达 50%的间隔内主动脉起源的冠状动脉异常患者存在可诱导性心肌灌注不足。需要长期随访以了解这种罕见异常的自然史。