法洛四联症合并主动脉-肺主干支系修复后的连续肺灌注显像。

IF 1.1 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS World Journal for Pediatric and Congenital Heart Surgery Pub Date : 2023-05-01 DOI:10.1177/21501351231162959
Lisa Wise-Faberowski, Jin Long, Michael Ma, Helen R Nadel, Jennifer Shek, Jeffrey A Feinstein, Elisabeth Martin, Frank L Hanley, Doff B McElhinney
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引用次数: 2

摘要

背景:在法洛四联症和主要主动脉肺侧支(MAPCAs)患者中,肺血供是高度可变的。我们对这种情况的治疗方法强调肺循环的完全统一,包括所有肺段,并在肺段水平上解决狭窄。修复后,我们推荐连续肺灌注显像(LPS)来评估肺血流分布的短期变化。方法:我们回顾了修复后3年的出院后和随访LPS,分析了灌注的一系列变化、变化的危险因素以及LPS参数与肺动脉再介入的关系。结果:在543例术后LPS结果的患者中,317例(58%)只有出院前LPS可用于复查,而226例(20%)或更多(22%)在三年内随访扫描。总体而言,出院前的肺血流分布是平衡的,随着时间的推移变化很小;然而,这两个指标在患者之间存在相当大的差异。在多变量混合模型中,修复后的时间(P = 0.025),由动脉导管到一个肺的初始解剖(P = 0.014)与连续LPS的变化相关。随访LPS的患者更有可能进行肺动脉再干预,但在该队列中,LPS参数与再干预风险无关。结论:在MAPCAs修复后的第一年,连续LPS是一种非侵入性的方法,用于筛查发生在少数但重要的少数患者的明显修复后肺动脉狭窄。在围手术期后接受后续LPS治疗的患者中,随着时间的推移,总体人群的变化很小,但在一些患者中变化很大,而且存在相当大的可变性。LPS的发现与肺动脉再介入之间没有统计学关联。
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Serial Lung Perfusion Scintigraphy After Unifocalization and Repair of Tetralogy of Fallot With Major Aortopulmonary Collaterals.

Background: In patients with tetralogy of Fallot and major aortopulmonary collaterals (MAPCAs), pulmonary blood supply is highly variable. Our approach to this condition emphasizes complete unifocalization of the pulmonary circulation, incorporating all lung segments and addressing stenoses out to the segmental level. Post-repair, we recommend serial lung perfusion scintigraphy (LPS) to assess short-term changes in pulmonary blood flow distribution.

Methods: We reviewed post-discharge and follow-up LPS performed through three years post-repair and analyzed serial changes in perfusion, risk factors for change, and the relationship between LPS parameters and pulmonary artery reintervention.

Results: Of 543 patients who had postoperative LPS results in our system, 317 (58%) had only a predischarge LPS available for review, while 226 had 1 (20%) or more (22%) follow-up scans within three years. Overall, pulmonary flow distribution prior to discharge was balanced, and there was minimal change over time; however, there was considerable patient-to-patient variation in both metrics. On multivariable mixed modeling, time after repair (P = .025), initial anatomy consisting of a ductus arteriosus to one lung (P < .001), and age at repair (P = .014) were associated with changes on serial LPS. Patients who had follow-up LPS were more likely to undergo pulmonary artery reintervention, but within that cohort, LPS parameters were not associated with reintervention risk.

Conclusion: Serial LPS during the first year after MAPCAs repair is a noninvasive method of screening for significant post-repair pulmonary artery stenosis that occurs in a small but important minority of patients. In patients who received follow-up LPS beyond the perioperative period, there was minimal change over time in the population overall, but large changes in some patients and considerable variability. There was no statistical association between LPS findings and pulmonary artery reintervention.

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