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根据解剖学和生理学情况量身定制干预策略,可改善有症状的埃布斯坦畸形新生儿的治疗效果。

Tailored strategy to match anatomy and physiology with intervention can improve outcomes of symptomatic neonates with Ebstein anomaly.

作者信息

Pizarro Christian, Bhat Majeed A, Davis Deborah A, Duncan Daniel, Pelletier Glenn J, Baffa Gina

机构信息

Nemours Cardiac Center, Nemours/Alfred I. duPont Hospital for Children, Sidney Kimmel School of Medicine, Thomas Jefferson University, Wilmington, Del.

出版信息

JTCVS Open. 2022 Oct 6;12:344-354. doi: 10.1016/j.xjon.2022.09.007. eCollection 2022 Dec.

Abstract

OBJECTIVE

Neonatal presentation of Ebstein anomaly (EA) represents the most severe form of this condition. Despite significant advances, operative mortality remains high and management decisions represent a formidable challenge. We used a strategy aimed to match anatomy and physiology with type and time of intervention to increase survival.

METHODS

We performed a review of all patients with fetal or neonatal diagnosis of EA managed at a single center between 2007 and 2020.

RESULTS

Among 18 patients with EA, 8 underwent neonatal intervention. The most common indication included cyanosis and heart failure (8/8), end organ dysfunction (6/8), and maldistribution of cardiac output (6/8). Only 2/8 had antegrade pulmonary blood flow. Associated conditions included pulmonary regurgitation in 4/8, atrial tachyarrhythmia in 4, and a ventricular septal defect in 3. Three patients underwent initial stabilization with main pulmonary artery occlusion including bilateral pulmonary artery banding in 2. Five patients underwent biventricular repair with conversion to right ventricle exclusion in 2 cases. Three others underwent the Starnes procedure as initially planned. The median age at surgery was 10 days (range, 1-30) and median weight 2.6 kg (range, 1.9-4.0). The median duration of mechanical ventilation and intensive care unit stay were 9 days (range, 5-34) and 30 days (range, 15-100), respectively. Operative mortality was 1/8. At a median follow-up of 130 months (range, 5-146), there were no late deaths, and all survivors remain in functional class I and free of valvular reintervention.

CONCLUSIONS

Symptomatic neonates with EA can be effectively managed with good outcomes. Preoperative stabilization and choice of management pathway on the basis of anatomy and physiology can help reduce morbidity and mortality.

摘要

目的

新生儿期出现的埃布斯坦畸形(EA)是该病最严重的形式。尽管取得了重大进展,但手术死亡率仍然很高,管理决策是一项艰巨的挑战。我们采用了一种旨在使解剖结构和生理功能与干预类型和时间相匹配的策略,以提高生存率。

方法

我们对2007年至2020年在单一中心接受治疗的所有胎儿或新生儿期诊断为EA的患者进行了回顾。

结果

在18例EA患者中,8例接受了新生儿期干预。最常见的指征包括青紫和心力衰竭(8/8)、终末器官功能障碍(6/8)和心输出量分布异常(6/8)。只有2/8有顺行性肺血流。相关情况包括4/8有肺动脉反流、4例有心房快速性心律失常、3例有室间隔缺损。3例患者最初通过主肺动脉闭塞进行稳定治疗,其中2例包括双侧肺动脉环扎术。5例患者接受了双心室修复,其中2例转为右心室排除术。另外3例按最初计划进行了斯塔恩斯手术。手术时的中位年龄为10天(范围1 - 30天),中位体重2.6千克(范围1.9 - 4.0千克)。机械通气的中位持续时间和重症监护病房住院时间分别为9天(范围5 - 34天)和30天(范围15 - 100天)。手术死亡率为1/8。中位随访130个月(范围5 - 146个月)时,无晚期死亡病例,所有幸存者仍处于心功能I级,无需进行瓣膜再次干预。

结论

有症状的EA新生儿可以得到有效治疗,预后良好。术前稳定治疗以及根据解剖结构和生理功能选择管理途径有助于降低发病率和死亡率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4655/9801273/a453023be468/fx1.jpg

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