非ecmo中心先天性膈疝最佳手术时机:一项回顾性研究。

IF 0.8 4区 医学 Q4 PEDIATRICS World Journal of Pediatric Surgery Pub Date : 2024-12-24 eCollection Date: 2024-01-01 DOI:10.1136/wjps-2024-000807
Zhong Feng, Yan-Dong Wei, Ying Wang, Jing-Na Li, Chao Liu, Hui Zhang, Fei Wang, Tao Wu, Yu-Lin Jiang, Lishuang Ma
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引用次数: 0

摘要

背景:本研究旨在探讨不使用体外膜氧合(ECMO)的严重先天性膈疝(CDH)的修复时机,并确定早期干预的可行性,以避免不使用ECMO的患者因不修复而死亡。方法:对2013 ~ 2023年新生儿CDH进行单中心回顾性研究。结果:132例CDH患儿90天总生存率为81.8%(108/132),中位手术时间26.00(24.00,38.50)小时。三组患儿90天生存率差异有统计学意义:A组患儿60.5% (23/38),B组患儿91.3% (74/81),C组患儿84.6% (11/13)(log-rank p)。结论:患儿应在出生后至少24小时进行修复手术。非ecmo中心对CDH新生儿的最佳时机似乎是出生后24-48小时,这可以防止严重病例失去治疗机会。
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Optimal surgical timing for congenital diaphragmatic hernia in a non-ECMO center: a retrospective study.

Background: This study aims to address the timing of repair for severe congenital diaphragmatic hernia (CDH) without the use of extracorporeal membrane oxygenation (ECMO) and to determine the feasibility of an earlier intervention to avoid deaths associated with non-repair in patients who are more challenging to stabilize without ECMO.

Methods: This single-center retrospective study was conducted on neonates with CDH from 2013 to 2023. Based on the timing of surgery, the patients were classified into three groups: <24 hours (group A), 24-48 hours (group B) and ≥48 hours (group C). The 90-day survival rates were analyzed using Kaplan-Meier curves and compared among groups via log-rank tests. The independent factors related to survival assessed using the multivariate Cox regression model.

Results: Of 132 CDH infants, the overall 90-day survival rate was 81.8% (108/132), with a median operative time of 26.00 (24.00, 38.50) hours. A significant difference was observed in the 90-day survival rate among the three groups: 60.5% (23/38) in group A vs. 91.3% (74/81) in group B vs. 84.6% (11/13) in group C (log-rank p<0.001). In mild and severe cases and those with an oxygen index ≥7.5, group A resulted in significantly reduced survival rates. Multivariate Cox regression analysis indicated that surgical timing <24 hours remained an independent mortality-related risk factor in infants with CDH.

Conclusions: Repair surgery should be performed at least 24 hours after birth. The optimal timing for CDH neonates in non-ECMO centers appears to be 24-48 hours after birth, which can prevent the loss of treatment opportunities for severe cases.

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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
38
审稿时长
13 weeks
期刊最新文献
Surgical management of short-segment Hirschsprung disease. Delayed diagnosis of anorectal malformations: a call for standardization of the current definitions. Outcome of anatomical versus non-anatomical lung resection for necrotizing pneumonia in children. Methods families use to raise funds for anorectal malformation treatment at a single public referral hospital in Southwestern Uganda. Optimal surgical timing for congenital diaphragmatic hernia in a non-ECMO center: a retrospective study.
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