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首页> 外文期刊>Pediatric Cardiology >Late Pulmonary Valve Replacement in Congenital Heart Disease Patients Without Original Congenital Pulmonary Valve Pathology
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Late Pulmonary Valve Replacement in Congenital Heart Disease Patients Without Original Congenital Pulmonary Valve Pathology

机译:无原发性先天性肺动脉瓣病理的先天性心脏病患者的晚期肺动脉瓣置换术

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Many congenital heart defects with pulmonary valve pathology are repaired or palliated in childhood. It is anticipated that these patients will need subsequent pulmonary valve replacement due to the pulmonary regurgitation or right ventricular dilation/failure that results from their original operation. Interestingly, some patients with prior congenital heart surgery and no congenital pulmonary valve pathology require pulmonary valve replacement in adulthood. The current study analyzed this subset of patients. The pediatric and adult congenital cardiac surgical databases at a large academic center were reviewed from 2001 to 2008 for pulmonary valve replacements. Patients without congenital pulmonary valve disease were identified. Preoperative, operative, and postoperative data were analyzed. Between 2001 and 2008, five patients with congenital heart disease but no pulmonary valve pathology underwent late pulmonary valve replacement. The initial congenital diagnoses were coarctation/ventricular septal defect (n = 3), complete atrioventricular septal defect (n = 1), and anomalous left coronary artery from the pulmonary artery (PA) (n = 1). All five patients had undergone main PA manipulation during their previous operations. Four of these patients had received PA banding and debanding, and one had received a Takeuchi tunnel repair and revision. All the patients underwent pulmonary valve replacement secondary to pulmonary regurgitation and right ventricular dilation. The average time from the last previous operation to the time of pulmonary valve replacement was 20.8 ± 9.1 years. Bioprosthetic valves were used for all the pulmonary valve replacements, and there were no mortalities. Patients who have undergone previous PA manipulation, regardless whether congenital pulmonary pathology is present, may be at risk for pulmonary valve replacement in adulthood. This report describes five cases of patients with a history of congenital heart surgery but no congenital pulmonary valve pathology who required pulmonary valve replacement due to the consequences of prolonged pulmonary regurgitation. Although pulmonary regurgitation may be well tolerated for many years, it is further evidence for the importance of close follow-up assessment and monitoring of young adults with congenital heart disease. Keywords Congenital heart disease - Pulmonary regurgitation - Pulmonary valve replacement
机译:在儿童期,许多具有肺动脉瓣病理的先天性心脏缺陷得以修复或缓解。可以预料的是,由于最初的手术导致肺返流或右心室扩张/衰竭,这些患者将需要随后的肺动脉瓣置换。有趣的是,一些先天性心脏手术且无先天性肺动脉瓣病变的患者在成年后需要更换肺动脉瓣。本研究分析了这部分患者。 2001年至2008年,对大型学术中心的儿科和成人先天性心脏外科手术数据库进行了回顾,以了解肺动脉瓣置换的情况。确定无先天性肺动脉瓣疾病的患者。分析了术前,术中和术后的数据。在2001年至2008年之间,有5例先天性心脏病但无肺动脉瓣病理的患者接受了晚期肺动脉瓣置换。最初的先天性诊断为缩窄/室间隔缺损(n = 3),完全房室间隔缺损(n = 1)和肺动脉左冠状动脉异常(n = 1)。所有五名患者在先前的手术中均接受了主要的PA操纵。这些患者中有四名接受了PA绑扎和解扎术,其中一名接受了竹内隧道的修复和翻修。所有患者均因肺返流和右心室扩张继发肺动脉瓣置换。从上一次手术到更换肺动脉瓣的平均时间为20.8±9.1年。生物人工瓣膜用于所有肺动脉瓣置换,并且没有死亡。先前接受过PA操作的患者,无论是否存在先天性肺病理,都可能在成年期有发生肺动脉瓣置换的风险。该报告描述了5例先天性心脏手术史但无先天性肺动脉瓣病变的患者,由于长期肺返流的后果而需要更换肺动脉瓣。尽管多年以来肺返流的耐受性良好,但这进一步证明了密切随访评估和监测患有先天性心脏病的年轻人的重要性。关键词先天性心脏病肺返流肺动脉瓣置换

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