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采用标准和新颖方法对源于异常冠状窦的冠状动脉进行手术管理。

Surgical management of coronary artery arising from the wrong coronary sinus, using standard and novel approaches.

作者信息

Gulati Rajeev, Reddy Vadiyala Mohan, Culbertson Casey, Helton Gregory, Suleman Sam, Reinhartz Olaf, Silverman Norman, Hanley Frank L

机构信息

Department of Pediatric Cardiac Surgery, Stanford University Medical Center, Stanford, Calif, USA.

出版信息

J Thorac Cardiovasc Surg. 2007 Nov;134(5):1171-8. doi: 10.1016/j.jtcvs.2007.02.051. Epub 2007 Oct 4.

DOI:10.1016/j.jtcvs.2007.02.051
PMID:17976445
Abstract

OBJECTIVES

Patients with a coronary artery arising from the wrong sinus are susceptible to ischemia and sudden death. Risk is higher when the artery courses interarterially--between the pulmonary artery and aorta--has an intramural course, or has an abnormal orifice. In single coronary ostium without intramural course, unroofing and coronary reimplantation are inappropriate, and coronary artery bypass grafting is suboptimal. For this variant, we have devised pulmonary artery translocation.

METHODS

A retrospective review of 18 patients undergoing repair between January 1999 and March 2005 was performed. Mean age was 8.1 years (range 6 weeks-16 years). All anomalous arteries coursed interarterially. Ten patients had a right coronary artery from the left coronary sinus; 8 had a left coronary artery from the right sinus. Eleven had an intramural course, and 4 had a single coronary ostium without an intramural course. Ten (56%) patients had symptoms: chest pain (9/10), syncope (3/10), or dyspnea (2/10). Repair was implemented by unroofing (n = 11), reimplantation (n = 3), or pulmonary artery translocation (1 lateral, 3 anterior). All patients were followed up clinically and echocardiographically.

RESULTS

At a mean of 2.2 years (2 weeks-5 years), there was no mortality. Symptoms improved and function remained normal in all but 1 patient. He had sustained multiple infarcts in the anomalous artery's distribution and required transplantation despite repair.

CONCLUSIONS

Repair is indicated in all patients with coronary insufficiency and in asymptomatic patients with high-risk morphologic abnormalities. We recommend unroofing when an intramural component (or slit-like orifice) is present, reimplantation for separate ostia without an intramural course, and pulmonary artery translocation for single ostium without an intramural course. Coronary artery bypass grafting is thus avoided.

摘要

目的

起源于错误窦的冠状动脉患者易发生缺血和猝死。当动脉走行于动脉间(在肺动脉和主动脉之间)、有壁内走行或有异常开口时,风险更高。在无壁内走行的单一冠状动脉口时,开窗术和冠状动脉再植入术不合适,冠状动脉旁路移植术也不理想。针对这种变异,我们设计了肺动脉移位术。

方法

对1999年1月至2005年3月期间接受修复的18例患者进行回顾性研究。平均年龄为8.1岁(范围6周 - 16岁)。所有异常动脉均走行于动脉间。10例患者的右冠状动脉起源于左冠状窦;8例患者的左冠状动脉起源于右窦。11例有壁内走行,4例有无壁内走行的单一冠状动脉口。10例(56%)患者有症状:胸痛(9/10)、晕厥(3/10)或呼吸困难(2/10)。修复通过开窗术(n = 11)、再植入术(n = 3)或肺动脉移位术(1例外侧,3例前方)实施。所有患者均接受临床和超声心动图随访。

结果

平均随访2.2年(2周 - 5年),无死亡病例。除1例患者外,所有患者症状均改善且功能保持正常。该患者在异常动脉供血区域发生多处梗死,尽管进行了修复仍需要移植。

结论

所有冠状动脉供血不足的患者以及有高危形态学异常的无症状患者均应进行修复。当存在壁内成分(或裂隙样开口)时,我们建议采用开窗术;对于无壁内走行的单独开口采用再植入术;对于无壁内走行的单一开口采用肺动脉移位术。从而避免了冠状动脉旁路移植术。

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