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法洛四联症且无动脉导管时的胎儿特征及围产期结局

Fetal Characteristics and Perinatal Outcomes in Tetralogy of Fallot Without a Ductus Arteriosus.

作者信息

Issapour Azadeh, Dasgupta Minnie N, Zhang Amy, Tacy Theresa A, Maskatia Shiraz A, Collins R Thomas, Kaplinski Michelle

机构信息

Division of Cardiology, Department of Pediatrics, Stanford University School of Medicine, Lucile Packard Children's Hospital, Palo Alto, CA, USA.

Stanford Division of Pediatric Cardiology, 750 Welch Road Suite 325, Palo Alto, CA, 94304-1510, USA.

出版信息

Pediatr Cardiol. 2024 Dec 30. doi: 10.1007/s00246-024-03745-w.

Abstract

Absence of the ductus arteriosus (DA) is common in tetralogy of Fallot (TOF), occurring in up to 30% of cases. Yet, the clinical course and fetal echocardiographic features are not well described, limiting prenatal counseling. This study examines the fetal echocardiographic characteristics and perinatal outcomes in children with TOF absent DA (TOF/ADA), comparing them to those with a DA (TOF/DA). Fetal echocardiograms were retrospectively reviewed in children with TOF evaluated at our center between 12/1/2014 and 11/1/2022. Those with complete atrioventricular septal defect, pulmonary atresia or absent pulmonary valve were excluded. Diagnosis of TOF and absence of the DA were postnatally confirmed. Fetal echocardiographic indices, clinical characteristics, and perinatal course were compared between groups. The primary outcome was intervention (surgical or catheter-based) in the first 30 days of life. Among 58 fetuses with TOF, 23 (40%) had ADA, and 35 (60%) had a DA. The groups were similar in gestational age, with similar Apgar scores. Four neonates required interventions for cyanosis: 2 with TOF/ADA and 2 with TOF/DA. One TOF/ADA patient died within the first year of life, from non-cardiac causes. Those with TOF/ADA had smaller third trimester main pulmonary artery (MPA) z-scores (- 2.75 vs. - 2.18, p = 0.02) and smaller neonatal pulmonary valve, MPA, and branch pulmonary artery z-scores. A genetic diagnosis was more common with ADA, specifically 22q11.2 deletion (22%, p = 0.03). While there were differences observed across groups, including smaller fetal and neonatal right ventricular outflow tract size and more diagnoses of 22q11.2 in ADA, absence of the DA was not linked to poorer clinical outcomes. This study expands our understanding of fetal echocardiographic findings and clinical trajectory in TOF/ADA, offering crucial insights for consultation and postnatal planning.

摘要

动脉导管缺如(DA)在法洛四联症(TOF)中很常见,发生率高达30%。然而,其临床病程和胎儿超声心动图特征尚未得到充分描述,这限制了产前咨询。本研究探讨了无动脉导管的法洛四联症患儿(TOF/ADA)的胎儿超声心动图特征和围产期结局,并将其与有动脉导管的患儿(TOF/DA)进行比较。对2014年12月1日至2022年11月1日在本中心接受评估的TOF患儿的胎儿超声心动图进行回顾性分析。排除患有完全性房室间隔缺损、肺动脉闭锁或肺动脉瓣缺如的患儿。TOF和DA缺如的诊断在出生后得到证实。比较两组之间的胎儿超声心动图指标、临床特征和围产期病程。主要结局是出生后30天内的干预措施(手术或导管介入)。在58例TOF胎儿中,23例(40%)有ADA缺如,35例(60%)有DA。两组的孕周相似,阿氏评分也相似。4例新生儿因青紫需要干预:2例TOF/ADA患儿和2例TOF/DA患儿。1例TOF/ADA患儿在出生后第一年内死于非心脏原因。TOF/ADA患儿在孕晚期主肺动脉(MPA)的z评分较小(-2.75 vs.-2.18,p=0.02),新生儿肺动脉瓣、MPA和分支肺动脉的z评分也较小。ADA患儿更常进行基因诊断,特别是22q11.2缺失(22%,p=0.03)。虽然两组之间观察到一些差异,包括胎儿和新生儿右心室流出道尺寸较小,以及ADA患儿中22q11.2诊断较多,但DA缺如与较差的临床结局无关。本研究扩展了我们对TOF/ADA胎儿超声心动图表现和临床病程的理解,为咨询和产后规划提供了重要见解。

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