首页> 外文期刊>The Annals of Thoracic Surgery: Official Journal of the Society of Thoracic Surgeons and the Southern Thoracic Surgical Association >Anomalous Origin of Left Coronary Artery From Pulmonary Artery in Older Children and Adults: Direct Aortic Implantation
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Anomalous Origin of Left Coronary Artery From Pulmonary Artery in Older Children and Adults: Direct Aortic Implantation

机译:年龄较大的儿童和成年人的肺动脉左冠状动脉异常起源:直接主动脉植入。

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Surgical TechniqueData Collection and Statistical AnalysisResultsAnomalous origin of the left coronary artery from the pulmonary artery (ALCAPA) presents rarely in adulthood and is treated by different surgical techniques with varying results. This study was undertaken to evaluate the feasibility of reestablishment of a dual coronary system in older children and adults with emphasis on direct aortic implantation.MethodsFrom 2002 to 2010, 10 patients aged 10 to 51 years (median age, 24 years) underwent surgical correction of ALCAPA. Median weight was 44.5 kg. All the patients except 2 were symptomatic. Two patients were in atrial fibrillation. Eight patients had varying degrees of mitral regurgitation, which was severe in 2. In all patients, the left coronary artery was arising from the facing sinus of the pulmonary artery. Direct left main coronary implantation into the aorta was feasible in all patients. Mitral valve replacement was done in 4 patients.ResultsAt a median follow-up of 5.5 years there was no new angina or infarction. One patient died 3 months postsurgery due to intracerebral bleed. Echocardiography demonstrated normal antegrade flow in the transferred left coronary artery, with 2 patients having persistent moderate mitral regurgitation. Coronary angiography done on follow-up in one patient revealed a patent transferred left coronary artery with distal development of new atherosclerotic lesion.ConclusionsDirect reimplantation of the ALCAPA is considered technically more difficult and hazardous in adults. With increased experience with coronary transfer technique, direct aortic implantation is feasible in adult cases. This provides a more physiologic correction and reestablishment of a dual coronary system with a better outcome.CTSNet classification:20Anomalous origin of the left coronary artery from the pulmonary artery is a rare congenital anomaly. It is usually seen as an isolated lesion and is present in one in 300,000 live births [
机译:手术技术数据收集和统计分析结果结果成年后很少出现左冠状动脉异常起源于肺动脉(ALCAPA),并通过不同的手术技术对其进行治疗,结果各不相同。这项研究旨在评估在较大的儿童和成年人中以直接主动脉植入为重点重建双冠状动脉系统的可行性。方法2002年至2010年,对10名年龄在10至51岁(中位年龄为24岁)的患者进行了手术矫正。阿尔卡帕中位数体重为44.5千克。除2例外,所有患者均出现症状。 2例患者发生房颤。 8例患者出现了不同程度的二尖瓣反流,其中2例严重。在所有患者中,左冠状动脉起源于面对的肺动脉窦。在所有患者中将左主冠状动脉直接植入主动脉是可行的。结果4例患者进行了二尖瓣置换术。结果在5.5年的中位随访中,未发现新的心绞痛或梗塞。一名患者在术后3个月因脑出血而死亡。超声心动图显示转移的左冠状动脉正常顺行血流,其中2例患者持续出现中度二尖瓣反流。对一名患者进行的冠状动脉造影检查显示,左冠状动脉已转移专利,远端出现新的动脉粥样硬化病变。结论从技术上讲,直接植入ALCAPA在成人中更加困难和危险。随着冠状动脉移植技术经验的增加,在成人病例中直接主动脉植入是可行的。 CTSNet分类:20左冠状动脉来自肺动脉的异常起源是一种罕见的先天性异常。它通常被视为孤立的病灶,并且在300,000例活产婴儿中有一个[

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