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新生儿主动脉缩窄修复的有效性:长期经验。

Effectiveness of Repair of Aortic Coarctation in Neonates: A Long-Term experience.

机构信息

Pediatric Cardiology, Department of Women's and Children's Health, University of Padova, Via Giustiniani 2, 35128, Padova, Italy.

Department of Statistical Sciences, University of Padova, Padova, Italy.

出版信息

Pediatr Cardiol. 2022 Jan;43(1):17-26. doi: 10.1007/s00246-021-02685-z. Epub 2021 Aug 2.

DOI:10.1007/s00246-021-02685-z
PMID:34341850
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8766375/
Abstract

To evaluate early and long-term results of surgical treatment of aortic coarctation (CoAo) in neonates. This is a retrospective clinical review of neonates with CoAo, who underwent surgery between 1995 and 2019. Data were retrieved from our institutional database, to identify preoperative and postoperative characteristics. Statistical analysis was performed by means of relative risk ratio and Cox and logistic multivariate analysis. 218 consecutive neonates (M/F: 129/89, median age 11 days, IQR 7-17 days) were included; 202 (92.7%) had a left thoracotomy; 178 underwent extended end-to-end anastomosis (EEEA, 81.6%). Hypoplastic aortic arch (HAA) was present in 102 patients (46.8%); complex cardiac anomalies in 85 (39%). Significant postoperative complications occurred in 20 (9.2%). Thirty-day mortality was 2.3% (most in complex types). At a median follow-up of 10.4 years (IQR 5.6-15.0 years; FU completeness 95.9%), there were 8 late deaths (3.7%), all associated to complex CoAo. Among 196 survivors, 177 (93.2%) were in NYHA class I; re-interventions on aortic arch occurred in 9.2% (2.0% were surgical). Freedom from mortality and re-intervention on aorta at 10 years were 94.3% and 96.7%, respectively. Surgical repair of CoAo in newborns without CPB in our series was safe and low-risk, with excellent early and late outcomes.

摘要

目的

评估新生儿主动脉缩窄(CoAo)手术治疗的早期和长期结果。本研究回顾性分析了 1995 年至 2019 年期间接受手术治疗的 CoAo 新生儿的临床资料。从我们的机构数据库中检索数据,以确定术前和术后特征。采用相对风险比、Cox 和逻辑多元分析进行统计学分析。

方法

共纳入 218 例连续新生儿(男/女:129/89,中位年龄 11 天,IQR 7-17 天);202 例(92.7%)行左开胸术;178 例行延伸端对端吻合术(EEEA,81.6%)。102 例(46.8%)存在主动脉弓发育不良(HAA);85 例(39%)存在复杂心脏畸形。20 例(9.2%)发生严重术后并发症。30 天死亡率为 2.3%(大多数为复杂类型)。中位随访 10.4 年(IQR 5.6-15.0 年;FU 完整性 95.9%),有 8 例晚期死亡(3.7%),均与复杂 CoAo 相关。在 196 例存活者中,177 例(93.2%)NYHA 心功能分级为 I 级;主动脉弓再干预发生率为 9.2%(2.0%为手术)。10 年时死亡率和主动脉再干预的无事件生存率分别为 94.3%和 96.7%。

结论

在我们的系列中,无体外循环新生儿主动脉缩窄的手术治疗是安全的,风险低,具有极好的早期和晚期效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d4e/8766375/71489efa3b24/246_2021_2685_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d4e/8766375/3051f858a4aa/246_2021_2685_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d4e/8766375/71489efa3b24/246_2021_2685_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d4e/8766375/3051f858a4aa/246_2021_2685_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4d4e/8766375/71489efa3b24/246_2021_2685_Fig2_HTML.jpg

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World J Pediatr Congenit Heart Surg. 2019 Jul;10(4):469-474. doi: 10.1177/2150135119852329.
2
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3
Selective versus standard cerebro-myocardial perfusion in neonates undergoing aortic arch repair: A multi-center study.
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Kardiochir Torakochirurgia Pol. 2024 Dec;21(4):211-217. doi: 10.5114/kitp.2024.145904. Epub 2024 Dec 13.
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Sternotomy or thoracotomy for neonatal repair of coarctation of the aorta with aortic arch hypoplasia.胸骨切开术或开胸术用于新生儿主动脉缩窄合并主动脉弓发育不全的修复。
JTCVS Open. 2024 Oct 5;22:386-394. doi: 10.1016/j.xjon.2024.10.001. eCollection 2024 Dec.
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