Division of Cardiovascular-Thoracic Surgery, Children's Memorial Hospital, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60614, USA.
Ann Thorac Surg. 2011 Sep;92(3):986-91; discussion 991-2. doi: 10.1016/j.athoracsur.2011.04.112.
Anomalous aortic origin of a coronary artery (AAOCA) from the opposite sinus of Valsalva is a rare congenital anomaly with the potential for myocardial ischemia and sudden death. This review evaluated our series of AAOCA patients, who underwent coronary artery unroofing, to test our hypothesis that the intramural length of the anomalous coronary artery correlates with symptoms.
A retrospective analysis of symptoms, preoperative imaging (computed tomography and magnetic resonance imaging), intraoperative assessment, perioperative course, and follow-up were reviewed.
From 2005 to 2010, 27 patients (70% male) underwent surgical AAOCA repair. Mean age was 14.3±12 (range, 6 to 52) years. In 25 patients with right AAOCA, 14 had chest pain and 4 had syncope. Both patients with left AAOCA had chest pain. AAOCA unroofing was done in 25 and side-to-side anastomosis in 2. The intramural coronary artery length measured intraoperatively correlated with preoperative symptoms (symptoms=10±3.58 mm, no symptoms=5.2±1.5 mm, p<.002), as did preoperative imaging measurements (symptoms=7.8±2.8 mm, no symptoms=5.3±0.8 mm, p<.001). Preoperative imaging strongly predicted the intraoperative measurement (r=0.81, p=0.00001). There were no deaths, significant morbidity, or recurrence of symptoms.
Coronary unroofing for AAOCA is a safe method of enlarging the coronary orifice and eliminating the intramural course. Symptomatic patients had a longer intramural course than asymptomatic patients, as assessed by preoperative imaging and intraoperative measurements. These results may have important clinical implications in determining indications for operation.
起源于主动脉窦 opposite sinus of Valsalva 的异常冠状动脉(anomalous aortic origin of a coronary artery,AAOCA)是一种罕见的先天性异常,可能导致心肌缺血和猝死。本研究评估了接受冠状动脉开窗术的 AAOCA 患者,以验证我们的假设,即异常冠状动脉的壁内长度与症状相关。
回顾性分析了症状、术前影像学(计算机断层扫描和磁共振成像)、术中评估、围手术期过程和随访情况。
2005 年至 2010 年,27 例(70%为男性)患者接受了外科 AAOCA 修复。平均年龄为 14.3±12 岁(范围为 6 至 52 岁)。在 25 例右 AAOCA 患者中,14 例有胸痛,4 例有晕厥。2 例左 AAOCA 患者均有胸痛。25 例行冠状动脉开窗术,2 例行冠状动脉旁路吻合术。术中测量的壁内冠状动脉长度与术前症状相关(有症状=10±3.58mm,无症状=5.2±1.5mm,p<.002),术前影像学测量结果亦如此(有症状=7.8±2.8mm,无症状=5.3±0.8mm,p<.001)。术前影像学检查与术中测量结果具有高度相关性(r=0.81,p=0.00001)。无死亡、严重并发症或症状复发。
冠状动脉开窗术是一种安全的扩大冠状动脉口和消除壁内行程的方法。有症状的患者,无论是通过术前影像学检查还是术中测量,其壁内行程均长于无症状患者。这些结果可能对确定手术适应证具有重要的临床意义。