Suppr超能文献

儿童肺动脉吊带手术的长期预后

Long-term outcomes of surgery for pulmonary artery sling in children.

作者信息

Yong Matthew S, Zhu Michael Z L, Bell Douglas, Alphonso Nelson, Brink Johann, d'Udekem Yves, Konstantinov Igor E

机构信息

Department of Cardiac Surgery, Royal Children's Hospital, Melbourne, Australia.

Department of Paediatrics, University of Melbourne, Melbourne, Australia.

出版信息

Eur J Cardiothorac Surg. 2019 Jan 31. doi: 10.1093/ejcts/ezz012.

Abstract

OBJECTIVES

Pulmonary artery (PA) sling is a rare vascular anomaly often associated with congenital tracheal stenosis. We describe the long-term outcomes with repair of this condition.

METHODS

A retrospective study was conducted at 2 institutions. From 1984 to 2018, 33 patients with PA sling underwent repair.

RESULTS

The median age at the time of surgery was 5.9 months (quartile 1-3: 2.5-12 months). Concomitant tracheal surgery was required in 21 patients (64%) where slide tracheoplasty was used in 11 patients (52%). There were no early deaths in patients who did not require tracheal surgery (n = 12). Operative mortality was 22% (2 of 9 patients) between 1984 and 1993, 11% (1 of 9 patients) between 1994 and 2003 and 6.7% (1 of 15 patients) between 2004 and 2018. The 15-year probability of survival for patients who had PA sling repair alone was 100%, and for patients who required PA sling and tracheal repair was 76 ± 10% (95% confidence interval 51-89%) (P = 0.08). The mean follow-up for survivors was 14 ± 9.8 years (3 months-33 years). All survivors were in the New York Heart Association functional class I/II at the last follow-up. Spirometry performed at a median age of 10.4 years after PA sling and tracheal surgery demonstrated obstructive lung defects with median forced expiratory volume in 1 s of 1.0 l (48% predicted), forced vital capacity of 1.5 l (74% predicted) and forced expiratory volume in 1 s/forced vital capacity of 0.69 (78% predicted).

CONCLUSIONS

Early mortality after PA sling repair is determined by the need for tracheal surgery. Though late survival was excellent, and the majority of survivors remained asymptomatic, long-term respiratory assessment and follow-up is warranted for these patients.

摘要

目的

肺动脉吊带是一种罕见的血管异常,常与先天性气管狭窄相关。我们描述了修复这种疾病的长期结果。

方法

在两家机构进行了一项回顾性研究。1984年至2018年,33例肺动脉吊带患者接受了修复手术。

结果

手术时的中位年龄为5.9个月(四分位数1 - 3:2.5 - 12个月)。21例患者(64%)需要同时进行气管手术,其中11例(52%)采用了滑动气管成形术。不需要气管手术的患者(n = 12)无早期死亡。1984年至1993年手术死亡率为22%(9例中的2例),1994年至2003年为11%(9例中的1例),2004年至2018年为6.7%(15例中的1例)。单纯进行肺动脉吊带修复的患者15年生存率为100%,需要肺动脉吊带和气管修复的患者为76±10%(95%置信区间51 - 89%)(P = 0.08)。幸存者的平均随访时间为14±9.8年(3个月 - 33年)。所有幸存者在最后一次随访时纽约心脏协会心功能分级均为I/II级。在肺动脉吊带和气管手术后中位年龄10.4岁时进行的肺活量测定显示存在阻塞性肺缺陷,1秒用力呼气量中位数为1.0升(预测值的48%),用力肺活量为1.5升(预测值的74%),1秒用力呼气量/用力肺活量为0.69(预测值的78%)。

结论

肺动脉吊带修复后的早期死亡率取决于是否需要气管手术。尽管晚期生存率良好,且大多数幸存者无症状,但仍有必要对这些患者进行长期呼吸评估和随访。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验