产前诊断大动脉转位后的长期预后。

IF 1.5 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Peter Lillitos, Grace Moriarty, Thomas Witter, Conal Austin, Owen Miller, Gurleen K Sharland, John M Simpson, Vita Zidere, Trisha V Vigneswaran
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引用次数: 0

摘要

动脉转换手术(ASO)后的结果有很好的记录。被诊断为大动脉右旋转位(d-TGA)的胎儿的生存率和长期发病率报道较少。我们的目的是记录产前诊断的d-TGA的生存率、再干预和发病率,为产前咨询提供信息。我们回顾了1995年至2022年间在我们机构诊断的伴有或不伴有室间隔缺损(VSD)的d-TGA胎儿。将结果与同一时期接受干预的产后诊断患者进行比较。207名胎儿被诊断出有201例活产,2例宫内死亡,4例终止妊娠。分离性d-TGA 137例(68.2%),d-TGA- vsd 64例(31.8%)。中位出生体重3.21 kg (IQR 2.94-3.5 kg),中位出生妊娠38周(IQR 38-39)。术前房间隔气囊造口术(BAS) 126/201(62.7%)。在BAS之前没有患者死亡。其中三人在ASO前死亡。198/201例(98.5%)行ASO,其中45/198例(22.7%)合并室间隔关闭。ASO患者30天生存率为95.5%。研究期间的生存率为186/201(92.5%)。在同一时期,91名婴儿因产后诊断而接受手术,90名接受ASO手术。诊断时间不同,ASO术后30天生存率和长期生存率无显著差异。3例经产前诊断行ASO的患者未随访。再干预率无显著差异(产前:18/195 (9.2%);产后:12/86 (13.9%)p = 0.24)。产前诊断患者的发病率为心肌功能障碍3/195(1.5%)、肺动脉高压1/195(0.5%)、室上性心动过速3/195(1.5%)、神经系统发病率9/195(4.6%)、自闭症11/195(5.6%),与产后组比较无统计学差异。产前诊断d-TGA后生存率良好。在产前诊断的队列中,在BAS之前没有死亡。3例死于BAS,其中1例死于BAS与ASO之间新生儿缺氧。ASO后,大多数患者在产前诊断后存活到第三个十年。再干预发生率为9.2%。大约每20名患者中就有1名患有神经和行为疾病。产前诊断为d-TGA的患者的结果与产后诊断后接受ASO的患者相当,但这排除了未存活到心脏介入治疗的产后心焦患者。这些数据将有助于产前咨询。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-Term Outcome Following Prenatal Diagnosis of Transposition of the Great Arteries.

Outcomes following the arterial switch operation (ASO) are well documented. Survival and long-term morbidity for fetuses diagnosed with dextro-transposition of the great arteries (d-TGA) are less reported. We aimed to document survival, reinterventions and morbidity for prenatally diagnosed d-TGA to inform prenatal counseling. Fetuses with d-TGA with or without ventricular septal defect (VSD) diagnosed between 1995 and 2022 at our institution were reviewed. Outcomes were compared to postnatally diagnosed patients undergoing intervention during the same era. Two hundred and seven fetuses were diagnosed resulting in 201 livebirths, 2 intrauterine demise, and 4 pregnancy terminations. There were 137 (68.2%) with isolated d-TGA and 64 (31.8%) with d-TGA-VSD. Median birthweight 3.21 kg (IQR 2.94-3.5 kg), and median birth gestation 38 weeks (IQR 38-39). Preoperative balloon atrial septostomy (BAS) was performed in 126/201(62.7%). No patients died prior to BAS. Three died before ASO following BAS. ASO was performed in 198/201(98.5%) with 45/198(22.7%) having concomitant VSD closure. Thirty-day survival for ASO was 95.5%. Survival over the study period was 186/201(92.5%). During the same period, 91 infants were referred for surgery with postnatal diagnosis, and 90 underwent ASO. There was no significant difference in 30-day or long-term survival following ASO according to timing of diagnosis. Three prenatally diagnosed patients undergoing the ASO were lost to follow up. There was no significant difference in reintervention rates (prenatal: 18/195 (9.2%); postnatal: 12/86 (13.9%) p = 0.24). Morbidity in prenatally diagnosed patients included myocardial dysfunction 3/195(1.5%), pulmonary hypertension 1/195(0.5%), supraventricular tachycardia 3/195(1.5%), neurological morbidity 9/195(4.6%), and autism 11/195(5.6%), and none were statistically different to the postnatal group. Survival following prenatal diagnosis of d-TGA is good. In the prenatally diagnosed cohort there were no deaths prior to BAS. Three died after BAS, with one of these deaths attributable to newborn hypoxia between BAS and ASO. Following ASO, most patients survive into third decade following prenatal diagnosis. Reintervention occurred in 9.2%. Neurological and behavioral morbidity affected approximately 1 in 20 patients. Outcomes for those with prenatal diagnosis of d-TGA are comparable with the patients that undergo ASO following postnatal diagnosis, but this excludes patients with a postnatal diangosis who did not survive to cardiac intervention. This data will be helpful for prenatal counseling.

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来源期刊
Pediatric Cardiology
Pediatric Cardiology 医学-小儿科
CiteScore
3.30
自引率
6.20%
发文量
258
审稿时长
12 months
期刊介绍: The editor of Pediatric Cardiology welcomes original manuscripts concerning all aspects of heart disease in infants, children, and adolescents, including embryology and anatomy, physiology and pharmacology, biochemistry, pathology, genetics, radiology, clinical aspects, investigative cardiology, electrophysiology and echocardiography, and cardiac surgery. Articles which may include original articles, review articles, letters to the editor etc., must be written in English and must be submitted solely to Pediatric Cardiology.
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