Krishnamurthy Rajesh, Golriz Farahnaz, Toole Benjamin J, Qureshi Athar M, Crystal Matthew A
Department of Radiology, Nationwide Children's Hospital, Columbus, OH, USA.
Department of Radiology, Baylor College of Medicine, Houston, TX, USA.
Ann Pediatr Cardiol. 2020 Apr-Jun;13(2):117-122. doi: 10.4103/apc.APC_94_19. Epub 2020 Apr 21.
Pulmonary atresia with the ventricular septal defect is a rare congenital heart defect with high anatomic variability. The most important management question relates to the sources of pulmonary blood flow. The ability to differentiate between ductal dependence and major aortopulmonary collateral arteries is critical to achieving good outcomes and avoiding life-threatening hypoxia in the postneonatal period. Having accurate information about pulmonary arteries, major aortopulmonary collateral arteries, and sources of blood supply to each pulmonary segment is crucial for choosing the optimal surgical strategy. The purpose of this study is to compare computed tomography angiography (CTA) with cardiac catheterization for anatomic delineation of surgically relevant anatomy in pulmonary atresia with ventricular septal defect with major aortopulmonary collateral arteries.
Retrospective review of all children with pulmonary atresia with ventricular septal defect with major aortopulmonary collateral arteries cared for at a large tertiary children's hospital who underwent cardiac catheterization with angiography and CTA close to each other without interval therapy. All studies were performed between 2007 and 2011.
There were 9 patients who met the inclusion criteria. Pulmonary artery anatomy (confluent vs. nonconfluent) was correctly identified in 9 patients by CTA and 8 patients by catheterization. There were no significant differences between CTA and catheterization in the identification of major aortopulmonary collateral arteries (mean = 3.4 collaterals/study via catheterization; mean = 3.1 collaterals/study via CTA; = 0.67). CTA was superior to catheterization in the delineation of segmental pulmonary blood flow ( = 0.006).
CTA and catheterization are equivalent in their ability to delineate pulmonary artery anatomy and major aortopulmonary collateral arteries.
室间隔缺损合并肺动脉闭锁是一种罕见的先天性心脏缺陷,具有高度的解剖学变异性。最重要的治疗问题涉及肺血流的来源。区分导管依赖性和主要体肺侧支动脉对于获得良好预后以及避免新生儿期后危及生命的低氧血症至关重要。掌握有关肺动脉、主要体肺侧支动脉以及每个肺段血液供应来源的准确信息对于选择最佳手术策略至关重要。本研究的目的是比较计算机断层血管造影(CTA)与心导管检查在室间隔缺损合并主要体肺侧支动脉的肺动脉闭锁患者中对手术相关解剖结构的解剖学描绘。
回顾性分析在一家大型三级儿童医院接受治疗的所有室间隔缺损合并主要体肺侧支动脉的肺动脉闭锁患儿,这些患儿在短时间内先后接受了心导管血管造影和CTA检查,且期间未接受间隔治疗。所有研究均在2007年至2011年期间进行。
有9例患者符合纳入标准。CTA正确识别了9例患者的肺动脉解剖结构(融合型与非融合型),心导管检查正确识别了8例。在识别主要体肺侧支动脉方面,CTA与心导管检查无显著差异(心导管检查平均每例研究发现3.4条侧支;CTA平均每例研究发现3.1条侧支;P = 0.67)。在描绘肺段血流方面,CTA优于心导管检查(P = 0.006)。
CTA和心导管检查在描绘肺动脉解剖结构和主要体肺侧支动脉方面能力相当。