Brothers Julie A, McBride Michael G, Seliem Mohamed A, Marino Bradley S, Tomlinson Ryan S, Pampaloni Miguel H, Gaynor J William, Spray Thomas L, Paridon Stephen M
Division of Cardiology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.
J Am Coll Cardiol. 2007 Nov 20;50(21):2078-82. doi: 10.1016/j.jacc.2007.06.055. Epub 2007 Nov 5.
We sought to prospectively evaluate evidence of myocardial ischemia after surgical repair of anomalous aortic origin of a coronary artery with an interarterial course (AAOCA).
An AAOCA is a rare anomaly associated with increased myocardial ischemia and sudden death risk in children. Data evaluating ischemia after AAOCA repair are limited.
We included children who underwent AAOCA surgery between October 2001 and December 2006. They were prospectively assessed with exercise stress test (EST), stress echocardiogram (SE), and stress myocardial perfusion scan (MPS).
Of 24 participating children, 15 (63%) were male, 16 (67%) had anomalous right coronary (ARCA), and 7 (29%) were asymptomatic. Median age was 12 (5 to 18) years; follow-up was 15 (2 to 48) months. All had unobstructed neo-coronary ostia by echocardiogram and were asymptomatic. One anomalous origin of left main coronary artery (ALCA) patient and 8 ARCA patients had post-operative evaluations suggestive of ischemia. The ALCA patient had reversible apical septal and mid-anteroseptal hypokinesis on SE. Of the ARCA patients, 2 had inferior ST-segment depression on EST; subsequently, 1 had normal tests, but the other developed anterolateral Q waves. Two patients had blunted blood pressure response with EST, 1 had fixed apical inferior hypokinesis on SE, 2 had reversible perfusion defects on MPS, and 1 had a fixed perfusion defect on MPS.
Subclinical changes suggestive of ischemia might occur despite patent neo-coronary ostia, notably after ARCA repair. The implication of these results on indication for surgery and subsequent sudden death risk is unknown. Serial EST, SE, and MPS are essential in evaluating ongoing ischemia risk after AAOCA repair.
我们旨在前瞻性评估经动脉走行的冠状动脉异常起源(AAOCA)手术修复后心肌缺血的证据。
AAOCA是一种罕见的异常情况,与儿童心肌缺血增加和猝死风险相关。评估AAOCA修复后缺血情况的数据有限。
我们纳入了2001年10月至2006年12月期间接受AAOCA手术的儿童。对他们进行了运动负荷试验(EST)、负荷超声心动图(SE)和负荷心肌灌注扫描(MPS)的前瞻性评估。
24名参与研究的儿童中,15名(63%)为男性,16名(67%)有右冠状动脉异常(ARCA),7名(29%)无症状。中位年龄为12(5至18)岁;随访时间为15(2至48)个月。所有患者经超声心动图检查显示新冠状动脉开口通畅且无症状。1例左主冠状动脉异常起源(ALCA)患者和8例ARCA患者术后评估提示有缺血。ALCA患者在SE上有可逆性心尖间隔和中前间隔运动减弱。在ARCA患者中,2例在EST时有下壁ST段压低;随后,1例检查结果正常,但另1例出现前侧壁Q波。2例患者在EST时血压反应减弱,1例在SE上有固定的心尖下壁运动减弱,2例在MPS上有可逆性灌注缺损,1例在MPS上有固定性灌注缺损。
尽管新冠状动脉开口通畅,但仍可能出现提示缺血的亚临床变化,尤其是在ARCA修复后。这些结果对手术指征和随后猝死风险的影响尚不清楚。连续的EST、SE和MPS对于评估AAOCA修复后持续的缺血风险至关重要。