Coronary Artery Anomalies Program, Texas Children's Hospital, Houston (T.T.D., S.S., C.B.-R., D.L.R.-O., P.M., Z.B., J.H.H., S.M.).
The Lillie Frank Abercrombie Section of Cardiology, Department of Pediatrics (T.T.D., S.S., D.L.R.-O., S.M.), Baylor College of Medicine, Texas Children's Hospital, Houston.
Circ Cardiovasc Interv. 2023 Apr;16(4):e012631. doi: 10.1161/CIRCINTERVENTIONS.122.012631. Epub 2023 Apr 18.
Anomalous aortic origin of a right coronary artery may cause myocardial ischemia and sudden death in the young. Data on myocardial ischemia or longitudinal outcomes are sparse in pediatric anomalous aortic origin of a right coronary artery population.
Patients <21 years with anomalous aortic origin of a right coronary artery were prospectively enrolled. Computerized tomography angiography defined morphology. Exercise stress test and stress perfusion imaging (sPI) were performed if >7 years or younger with concern for ischemia. High-risk features included intramural length, slit-like/hypoplastic ostium, exertional symptoms, or evidence of ischemia.
A total of 220 patients (60% males) were enrolled December 2012 to April 2020 at a median age 11.4 years (interquartile range, 6.1-14.5), including 168 (76%) with no/nonexertional symptoms (group 1) and 52 (24%) with exertional chest pain/syncope (group 2). Computerized tomography angiography was available in 189/220 (86%), exercise stress test in 164/220 (75%), and sPI in 169/220 (77%). Exercise stress test was positive in 2/164 (1.2%) patients in group 1, both had positive sPI. Inducible ischemia (sPI) was detected in 11/120 (9%) in group 1 and 9/49 (18%) in group 2 (=0.09). Intramural length was similar in patients with/without ischemia (5 [interquartile range, 4-7] versus 5 [interquartile range, 4-7] mm; =0.65). Surgery was recommended in 56/220 (26%) patients with high-risk features. In 52 surgical patients (38 unroofing, 14 reimplantation), all subjects were alive and have returned to exercise at last median follow-up of 4.6 (interquartile range, 2.3-6.5) years.
Anomalous aortic origin of a right coronary artery patients can present with inducible ischemia on sPI despite symptoms or intramural length. Exercise stress test is a poor predictor of ischemia and caution should be given to determine low-risk based solely on this assessment. All patients are alive at medium-term follow-up.
右冠状动脉异常起源可能导致年轻人心肌缺血和猝死。在儿科右冠状动脉异常起源人群中,关于心肌缺血或纵向结局的数据很少。
前瞻性纳入年龄<21 岁的右冠状动脉异常起源患者。计算机断层血管造影术定义形态。如果>7 岁或有缺血相关担忧,则进行运动应激试验和应激灌注成像(sPI)。高危特征包括壁内长度、缝隙样/发育不良的开口、用力症状或缺血证据。
2012 年 12 月至 2020 年 4 月,共纳入 220 例患者(60%为男性),中位年龄为 11.4 岁(四分位距,6.1-14.5),其中 168 例(76%)无/无用力症状(组 1),52 例(24%)有用力性胸痛/晕厥(组 2)。220 例患者中 189 例(86%)行计算机断层血管造影术,164 例行运动应激试验(75%),169 例行 sPI(77%)。运动应激试验阳性 2 例(1.2%),均行 sPI 阳性。组 1 中 11 例(9%)和组 2 中 9 例(18%)可诱发出缺血(sPI)(=0.09)。有缺血和无缺血患者的壁内长度相似(5[四分位距,4-7]与 5[四分位距,4-7]mm;=0.65)。56 例(26%)高危特征患者建议手术。52 例手术患者(38 例升主动脉切开术,14 例再植入术),所有患者均存活,最后一次中位随访时间为 4.6(四分位距,2.3-6.5)年,均恢复运动。
尽管有症状或壁内长度,右冠状动脉异常起源患者仍可通过 sPI 诱发出缺血。运动应激试验是缺血的不良预测指标,应谨慎判断仅根据该评估确定低危。所有患者在中期随访时均存活。