Romp Robert L, Herlong J René, Landolfo Carolyn K, Sanders Stephen P, Miller Coleen E, Ungerleider Ross M, Jaggers James
Department of Pediatric Cardiovascular Surgery, Duke University Medical Center, Durham, North Carolina 27710, USA.
Ann Thorac Surg. 2003 Aug;76(2):589-95; discussion 595-6. doi: 10.1016/s0003-4975(03)00436-3.
Anomalous aortic origin of a coronary artery (AAOCA) from an incorrect sinus of Valsalva is a relatively rare congenital defect and is associated with sudden death. Several surgical techniques have been described to address this defect, but functional outcome has never been addressed. In this report we evaluate a consecutive series of patients treated with unroofing techniques using transthoracic echocardiography, graded exercise testing, and stress echocardiography to assess functional repair.
Nine consecutive patients (range 7 to 65 years) underwent surgical repair of AAOCA from 1995 to 2001. In all patients the intramural segment was at or below the level of the commissure. All patients underwent a modified unroofing procedure to move the coronary artery orifice to the appropriate sinus. In 2 patients, a new orifice was created without significant unroofing and disruption of the commissure. Patients were evaluated prospectively with exercise electrocardiography testing and by resting and stress echocardiography.
Of the 9 patients, 8 presented with symptoms suggestive of ischemia (chest pain, dyspnea on exertion, or syncope). Six patients had anomalous left main coronary artery arising from the right sinus of Valsalva, and 3 patients had anomalous right coronary artery from the left sinus of Valsalva. Transthoracic echocardiography and graded exercise testing was performed in all 9 patients (mean 29 months, range 4 to 85 months) after repair. Of the 9 patients, 8 also underwent stress echocardiography. In 8 of 9 patients the newly created coronary artery ostium was visualized by either two-dimensional echocardiography or color flow Doppler. All patients were symptom free at the time of follow-up. Exercise stress echocardiography was negative in all patients. Of the 8 patients, 7 had normal left ventricular shortening. No patients had regional wall motion abnormalities suggestive of ischemia. All patients were intervention free except 1 patient who developed severe aortic insufficiency and underwent a subsequent Ross procedure 44 months after his initial procedure.
Anomalous origin of a coronary artery from an incorrect sinus of Valsalva is known to be associated with increased risk of sudden death. Surgical correction can be carried out with minimal risk and good anatomic and functional results. Manipulation of the commissure can be avoided by creation of a neo-ostia without extensive unroofing of the intramural segment or manipulation of the intercoronary commissure. This may avoid aortic valve malfunction.
冠状动脉起源异常(AAOCA),即冠状动脉从错误的瓦尔萨尔瓦窦发出,是一种相对罕见的先天性缺陷,与猝死相关。已有多种手术技术用于处理该缺陷,但功能结局从未得到探讨。在本报告中,我们评估了一系列连续接受经胸壁超声心动图、分级运动试验和负荷超声心动图检查以评估功能修复情况的采用去顶技术治疗的患者。
1995年至2001年,9例连续患者(年龄7至65岁)接受了AAOCA的手术修复。所有患者的壁内段位于或低于瓣叶联合水平。所有患者均接受改良去顶手术,将冠状动脉开口移至合适的窦。2例患者在未进行明显去顶和瓣叶联合破坏的情况下创建了新开口。对患者进行前瞻性运动心电图测试以及静息和负荷超声心动图检查。
9例患者中,8例有提示缺血的症状(胸痛、劳力性呼吸困难或晕厥)。6例患者左冠状动脉主干起源于右瓦尔萨尔瓦窦,3例患者右冠状动脉起源于左瓦尔萨尔瓦窦。修复后所有9例患者(平均29个月,范围4至85个月)均进行了经胸壁超声心动图和分级运动试验。9例患者中的8例还接受了负荷超声心动图检查。9例患者中有8例通过二维超声心动图或彩色多普勒血流显像观察到新创建的冠状动脉开口。随访时所有患者均无症状。所有患者运动负荷超声心动图检查结果均为阴性。8例患者中,7例左心室缩短正常。无患者有提示缺血的节段性室壁运动异常。除1例患者在初次手术后44个月发生严重主动脉瓣关闭不全并接受了随后的罗斯手术外,所有患者均无需进一步干预。
已知冠状动脉从错误的瓦尔萨尔瓦窦发出与猝死风险增加相关。手术矫正风险极小,可获得良好的解剖和功能结果。通过创建新开口而不广泛去除壁内段或不操作冠状动脉间瓣叶联合,可避免对瓣叶联合的操作。这可能避免主动脉瓣功能障碍。