O'Connor Mario, Hoyos Maria E, Fuentes Lee M, Martinez Hugo R, Fraser Charles D, Well Andrew
Department of Cardiovascular & Thoracic Surgery, Dell Medical School at The University of Texas at Austin, Austin, Tex.
Department of Cardiovascular & Thoracic Surgery, Dell Medical School at The University of Texas at Austin, Austin, Tex.
J Thorac Cardiovasc Surg. 2025 May 30. doi: 10.1016/j.jtcvs.2025.05.018.
Ebstein's anomaly is a rare condition that can be diagnosed at any age. Symptomatic neonatal Ebstein's anomaly represents a challenging clinical entity with high morbidity and mortality. This study aims to describe treatment modalities and outcomes in neonatal Ebstein's anomaly.
We performed a review of the Pediatric Health Information System from 2004 to 2023. Patients with an Ebstein's anomaly diagnosis who were admitted within the first 2 days of life and who underwent a surgical intervention during that admission were included.
A total of 330 patients were identified; 181 (55%) were female, 155 (47%) were non-Hispanic White, the median age at the initial Ebstein's anomaly surgery was 6 (interquartile range, 3-12) days, and the median birth weight was 2.9 (interquartile range, 2.5-3.2) kg. Median follow-up time was 1.8 (interquartile range, 0.1-6.8) years. Overall, 186 patients (56%) underwent isolated aortopulmonary shunt, 81 patients (25%) received the Starnes procedure, 58 patients (18%) received tricuspid valve repairs, and 5 patients (2%) received tricuspid valve replacements. Median length of stay was 38 (interquartile range, 24-74) days with no difference across procedures (P = .137). In-hospital mortality was 25% (n = 81), with tricuspid valve replacements (n = 4, 80%) having the highest. In multivariable Cox analysis, Black race (hazard ratio [HR], 2.7; 95% CI, 1.43-5.19; P = .002) and tricuspid valve replacements (HR, 8.2; 95% CI, 2.6-25.4; P < .001) had increased risk of mortality; older age at surgery (HR, 0.98; 95% CI, 0.97-0.99; P = .044) and higher birth weight (HR, 0.99; 95% CI, 0.99-0.99; P = .005) had a decreased risk for mortality. Overall survival at 10 years was 71% (95% CI, 66.0-76.3), and freedom from any cardiac reintervention at 10 years was 18% (95% CI, 12.7-25.8).
In a large multicenter dataset, surgery for neonatal Ebstein's anomaly is associated with significant mortality. Older age at surgery and higher birth weight are associated with decreased mortality. The initial approach does not dictate the need for a single ventricle pathway. These data can help counsel patients/families and help guide surveillance protocols and long-term management in this population.
埃布斯坦畸形是一种罕见疾病,可在任何年龄被诊断出来。有症状的新生儿埃布斯坦畸形是一个具有挑战性的临床实体,发病率和死亡率都很高。本研究旨在描述新生儿埃布斯坦畸形的治疗方式及治疗结果。
我们对2004年至2023年的儿科健康信息系统进行了回顾。纳入出生后2天内入院且在此次住院期间接受手术干预的埃布斯坦畸形确诊患者。
共识别出330例患者;181例(55%)为女性,155例(47%)为非西班牙裔白人,初次埃布斯坦畸形手术时的中位年龄为6(四分位间距,3 - 12)天,中位出生体重为2.9(四分位间距,2.5 - 3.2)kg。中位随访时间为1.8(四分位间距,0.1 - 6.8)年。总体而言,186例患者(56%)接受了单纯主肺动脉分流术,81例患者(25%)接受了斯塔内斯手术,58例患者(18%)接受了三尖瓣修复术,5例患者(2%)接受了三尖瓣置换术。中位住院时间为38(四分位间距,24 - 74)天,各手术方式之间无差异(P = 0.137)。住院死亡率为25%(n = 81),其中三尖瓣置换术(n = 4,80%)的死亡率最高。在多变量Cox分析中,黑人种族(风险比[HR],2.7;95%置信区间,1.43 - 5.19;P = 0.002)和三尖瓣置换术(HR,8.2;95%置信区间,2.6 - 25.4;P < 0.001)的死亡风险增加;手术时年龄较大(HR,0.98;95%置信区间,0.97 - 0.99;P = 0.044)和出生体重较高(HR,0.99;95%置信区间,0.99 - 0.99;P = 0.005)的死亡风险降低。10年时的总体生存率为71%(95%置信区间,66.0 - 76.3),10年时无任何心脏再次干预的比例为18%(95%置信区间,12.7 - 25.8)。
在一个大型多中心数据集中,新生儿埃布斯坦畸形手术的死亡率较高。手术时年龄较大和出生体重较高与死亡率降低相关。初始治疗方法并不决定是否需要采用单心室路径。这些数据有助于为患者/家属提供咨询,并有助于指导该人群的监测方案和长期管理。