Pulmonary Atresia with Ventricular Septal Defect without Major Aorto-Pulmonary Collateral Arteries: Echocardiography and the Role of Computed Tomography and Magnetic Resonance Imaging.

Sarah Chambers Gurson
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Abstract

Pulmonary atresia with ventricular septal defect (PA-VSD) is usually diagnosed by transthoracic or fetal echocardiography, with the prenatal diagnosis being feasible and accurate if fetal cardiology services are available. The limitations of transthoracic echocardiography (TTE) in the evaluation of PA-VSD include the complete evaluation of the pulmonary arteries and patent ductus arteriosus, quantitative evaluation of the right ventricle size and function, and delineation of associated cardiac anomalies such as coronary artery anomalies, anomalies of systemic or pulmonary venous return, and complex arch anomalies. Echocardiography also has limitations in evaluating hemodynamics such as flow volumes, shunts, and regurgitant fraction. Despite these limitations, TTE remains the most widely available and the most cost-effective cardiac imaging modality for patients with PA-VSD and its accuracy in evaluating the sources of pulmonary blood flow and in selecting patients for systemic-to-pulmonary artery shunt palliation is well established. Cardiac computed tomography (CT) can answer many of the questions not answered by TTE, including demonstrating the PA anatomy and defining coronary artery, systemic and pulmonary venous, and aortic arch anatomies. The short acquisition time allows for the study to be performed without sedation/anesthesia in most patients. Cardiac CT is also useful in defining postoperative anatomy when there are non-magnetic resonance imaging (MRI) compatible devices or even MRI-compatible devices that cause a significant MRI artifact. Cardiac MRI/magnetic resonance angiography has emerged as an ideal modality to evaluate patients with PA-VSD as it allows for anatomic, functional, and hemodynamic assessment without exposure to ionizing radiation or iodinated contrast material. Both cardiac CT and cardiac MRI can be used to generate 3D imaging of the heart.

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肺动脉闭锁合并室间隔缺损无主动脉-肺动脉副支:超声心动图及计算机断层和磁共振成像的作用。
肺动脉闭锁合并室间隔缺损(PA-VSD)通常通过经胸或胎儿超声心动图诊断,如果有胎儿心脏病学服务,产前诊断是可行和准确的。经胸超声心动图(TTE)评估PA-VSD的局限性包括:不能全面评估肺动脉和动脉导管未闭,不能定量评估右心室大小和功能,不能描述相关心脏异常,如冠状动脉异常、全身或肺静脉回流异常、复杂弓异常等。超声心动图在评估血流动力学方面也有局限性,如血流容量、分流和返流分数。尽管存在这些局限性,TTE仍然是PA-VSD患者最广泛使用和最具成本效益的心脏成像方式,其在评估肺血流来源和选择进行全身-肺动脉分流姑息治疗的患者方面的准确性已得到证实。心脏计算机断层扫描(CT)可以回答许多TTE不能回答的问题,包括显示PA解剖结构,定义冠状动脉、全身和肺静脉以及主动脉弓解剖结构。较短的获取时间允许大多数患者在没有镇静/麻醉的情况下进行研究。当存在非磁共振成像(MRI)兼容设备或甚至MRI兼容设备导致显著MRI伪影时,心脏CT在定义术后解剖方面也很有用。心脏MRI/磁共振血管造影已成为评估PA-VSD患者的理想方式,因为它允许解剖、功能和血流动力学评估,而无需暴露于电离辐射或碘化造影剂。心脏CT和心脏MRI都可以用来生成心脏的3D成像。
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