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Critical decision of operability in congenital heart disease patient with severe pulmonary hypertension

机译:先天性心脏病重度肺动脉高压患者可操作性的关键决策

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摘要

Repair of congenital heart disease in the presence of high pulmonary pressure has always been a contentious issue. Pulmonary vascular resistance (PVR) is considered important for establishing operability in these patients. However, PVR estimation is not always accurate and cannot solely be relied upon to make critical decision of operability. Clinical examination, chest X-ray, and echocardiography are also important indicators of pulmonary vascular disease. Knowledge of pits and falls of each investigation is important for appropriate management in these patients. We present a case report of successfully operated, 6-year-old child with anomalous origin of the right pulmonary artery from aorta, deemed inoperable on the basis of PVR estimation.
机译:在存在高肺压的情况下修复先天性心脏病一直是一个有争议的问题。肺血管阻力(PVR)被认为对于在这些患者中建立可操作性很重要。但是,PVR估算并不总是准确的,不能仅仅依靠它来做出可操作性的关键决定。临床检查,胸部X线检查和超声心动图检查也是肺血管疾病的重要指标。每次检查的坑坑洼洼的知识对于这些患者的适当管理很重要。我们提供了一个成功手术的6岁儿童的案例报告,该儿童来自主动脉右肺动脉异常,根据PVR估算被认为无法手术。

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