Transcatheter Recanalization of Atretic Pulmonary Veins in Infants and Children.

Jay D Patel, Mansi Mandhani, Rosemary Gray, Joelle Pettus, Courtney E McCracken, Amanda Thomas, Holly Bauser-Heaton, Dennis W Kim, Christopher J Petit
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引用次数: 2

Abstract

Background: Pulmonary vein stenosis is a progressive disease associated with a high rate of mortality in children. If left untreated, myofibroblastic proliferation can lead to pulmonary vein atresia (PVA). In our experience, transcatheter recanalization has emerged as a favorable interventional option. We sought to determine the acute success rate of recanalization of atretic pulmonary veins and mid-term outcomes of individual veins after recanalization.

Methods: We reviewed all patients with PVA at our institution between 2008 and 2020 diagnosed by either catheterization or cardiac computed tomography. All veins with successful recanalization were reviewed and procedural success rate and patency rate were noted. Competing risk analysis was performed to demonstrate outcomes of individual atretic veins longitudinally.

Results: Between 2008 and 2020, our institution diagnosed and treated 131 patients with pulmonary vein stenosis. Of these, 61 patients developed atresia of at least one pulmonary vein. In total, there were 97 atretic pulmonary veins within this group. Successful recanalization was accomplished in 47/97 (48.5%) atretic veins. No atretic pulmonary veins were successfully recanalized before 2012. The majority of veins were recanalized between 2017 and 2020-39/56 (70%). The most common intervention after recanalization was drug-eluting stent placement. At 2-year follow-up 42.6% of recanalized veins (20.6% of all atretic veins) remained patent with a median of 4 reinterventions per person.

Conclusions: Transcatheter recanalization of PVA can result in successful reestablishment of flow to affected pulmonary veins in many cases. Drug-eluting stent implantation was the most common intervention performed immediately post-recanalization. Vein patency was maintained in 42.6% of patients at 2-year follow-up from recanalization with appropriate surveillance and reintervention. Overall, only a small portion of atretic pulmonary veins underwent successful recanalization with maintained vessel patency at follow-up. Irrespective of successful recanalization, there was no detectable survival difference between the more recently treated PVA cohort and non-PVA cohort.

经导管肺静脉再通术在婴幼儿和儿童中的应用。
背景:肺静脉狭窄是一种进行性疾病,与儿童高死亡率相关。如果不及时治疗,肌成纤维细胞增生可导致肺静脉闭锁(PVA)。根据我们的经验,经导管再通已成为一种有利的介入治疗选择。我们试图确定闭锁肺静脉再通的急性成功率和再通后单个静脉的中期预后。方法:我们回顾了2008年至2020年在我们机构通过导管插入或心脏计算机断层扫描诊断的所有PVA患者。回顾所有成功再通的静脉,记录手术成功率和通畅率。进行竞争风险分析以纵向证明个体闭锁静脉的结果。结果:2008年至2020年,我院共诊治肺静脉狭窄131例。其中,61例患者出现至少一条肺静脉闭锁。本组共有97条闭锁肺静脉。47/97例锁静脉(48.5%)成功再通。2012年以前,没有一例闭锁肺静脉再通成功。大多数静脉在2017年至2020年之间重新通通-39/56(70%)。再通后最常见的干预措施是药物洗脱支架置入。在2年的随访中,42.6%的再通静脉(占所有锁静脉的20.6%)保持通畅,平均每人再干预4次。结论:经导管PVA再通术在许多病例中可以成功地重建受影响肺静脉的血流。药物洗脱支架植入是再通后立即进行的最常见的干预措施。通过适当的监测和再干预,42.6%的患者在再通后的2年随访中保持静脉通畅。总体而言,只有一小部分闭锁肺静脉在随访中成功再通并保持血管通畅。不管再通是否成功,最近治疗的PVA组和非PVA组之间没有可检测到的生存差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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