Long-term outcomes of individualised repair in patients with primary pulmonary vein stenosis.

IF 0.9 4区 医学 Q4 CARDIAC & CARDIOVASCULAR SYSTEMS
Zhangwei Wang, Yang Yang
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引用次数: 0

Abstract

Objectives: Primary pulmonary vein stenosis is a rare congenital heart condition and carries a poor prognosis. Various surgical techniques have been introduced to treat primary pulmonary vein stenosis. However, there is no consensus on the optimal approach. This study aimed to evaluate the outcomes of surgical treatment of primary pulmonary vein stenosis, identify the risk factors for pulmonary vein restenosis and reintervention, and determine the optimal strategy for primary pulmonary vein stenosis repair.

Methods: From December 2008 to December 2023, 64 patients with primary pulmonary vein stenosis undergoing surgical repair in our institution were included [non-sutureless group, n = 42; sutureless group, n = 22]. The Cox proportional hazard model was used to identify risk factors for pulmonary vein restenosis and pulmonary vein restenosis-related reintervention.

Results: There were three in-hospital deaths and one late death. The survival rates at 1, 5, and 15 years were 91.9%, 84.2%, and 69.8%, respectively, in the whole cohort. Compared with the non-sutureless group, the sutureless group did not significantly improve the long-term survival of primary pulmonary vein stenosis patients (P = 0.484). Pulmonary vein restenosis occurred in 15 patients. Multivariable analysis showed that Involvement of the left inferior pulmonary vein (P < 0.001) was the only independent risk factor for pulmonary vein restenosis, while sutureless repair (P = 0.037) was a protective factor. Pulmonary vein restenosis-related reintervention occurred in 12 patients. On multivariate analysis, three or four pulmonary veins involvement (P = 0.001) and preoperative severity score exceeding 5 (P = 0.050) were found to be independent risk factors associated with pulmonary vein restenosis-related reintervention; however, sutureless repair (P = 0.021) was a protective factor.

Conclusions: Management of infants with primary pulmonary vein stenosis is challenging. Surgical repair of primary pulmonary vein stenosis can be safely achieved using different techniques, with similar long-term mortality. Compared with non-sutureless repair, sutureless repair was significantly associated with decreased pulmonary vein restenosis and decreased pulmonary vein restenosis-related reintervention, respectively. Preoperative severity score exceeding 5, 3, or 4 pulmonary veins involvement, and left inferior pulmonary vein involvement are independent risk factors for adverse outcomes.

原发性肺静脉狭窄患者个体化修复的远期疗效。
目的:原发性肺静脉狭窄是一种罕见的先天性心脏病,预后较差。治疗原发性肺静脉狭窄的手术方法多种多样。然而,对于最佳方法并没有达成共识。本研究旨在评价原发性肺静脉狭窄的手术治疗效果,识别肺静脉再狭窄和再干预的危险因素,确定原发性肺静脉狭窄修复的最佳策略。方法:选取2008年12月至2023年12月在我院行手术修复的64例原发性肺静脉狭窄患者[非缝合组,n = 42;未缝合组,n = 22]。采用Cox比例风险模型确定肺静脉再狭窄及肺静脉再狭窄相关再干预的危险因素。结果:住院死亡3例,晚期死亡1例。整个队列的1年、5年和15年生存率分别为91.9%、84.2%和69.8%。与未缝合组相比,未缝合组未显著提高原发性肺静脉狭窄患者的长期生存率(P = 0.484)。15例发生肺静脉再狭窄。多变量分析显示,累及左下肺静脉(P < 0.001)是肺静脉再狭窄的唯一独立危险因素,无缝线修复(P = 0.037)是肺静脉再狭窄的保护因素。12例发生肺静脉再狭窄相关再干预。多因素分析发现,3条或4条肺静脉受累(P = 0.001)和术前严重程度评分超过5分(P = 0.050)是肺静脉再狭窄相关再干预的独立危险因素;然而,无缝线修复(P = 0.021)是保护因素。结论:婴儿原发性肺静脉狭窄的治疗具有挑战性。原发性肺静脉狭窄的手术修复可以使用不同的技术安全地实现,长期死亡率相似。与无缝线修复相比,无缝线修复分别与肺静脉再狭窄减少和肺静脉再狭窄相关再干预减少显著相关。术前严重程度评分超过5、3、4肺静脉受累和左下肺静脉受累是不良结局的独立危险因素。
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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来源期刊
Cardiology in the Young
Cardiology in the Young 医学-小儿科
CiteScore
1.70
自引率
10.00%
发文量
715
审稿时长
4-8 weeks
期刊介绍: Cardiology in the Young is devoted to cardiovascular issues affecting the young, and the older patient suffering the sequels of congenital heart disease, or other cardiac diseases acquired in childhood. The journal serves the interests of all professionals concerned with these topics. By design, the journal is international and multidisciplinary in its approach, and members of the editorial board take an active role in the its mission, helping to make it the essential journal in paediatric cardiology. All aspects of paediatric cardiology are covered within the journal. The content includes original articles, brief reports, editorials, reviews, and papers devoted to continuing professional development.
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