大动脉转位和室间隔完整的婴儿从胎儿到新生儿的过渡:1例报告。

Biomedicine hub Pub Date : 2024-12-02 eCollection Date: 2025-01-01 DOI:10.1159/000542723
Jesse A Weeda, Arjan B Te Pas, Monique C Haak, Nico A Blom, Roel L F van der Palen
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引用次数: 0

摘要

简介:大动脉转位(TGA),特别是完整的室间隔(TGA- ivs),在胎儿到新生儿的过渡过程中提出了独特的挑战,这可能导致新生儿持续性肺动脉高压(PPHN)的发生。病例介绍:1例男婴TGA-IVS,经剖宫产分娩,出生后立即出现低氧血症和心动过速(产前SpO2: 50-60%,导管后SpO2: 70-75%)。超声心动图显示心房间隔松弛,两个心房连接双向分流。导管血流显示收缩期右至左分流,提示肺血管阻力高。出生后立即处理包括无创呼吸支持,在100%氧气下持续气道正压,并给予前列腺素E2以维持导管通畅。尽管最初的血氧饱和度较低,但基于对生命体征和超声心动图指标的持续趋势监测,强化治疗的升级被推迟。出生后2小时内氧合和循环逐渐改善至正常值,避免了插管、一氧化氮和/或球囊房间隔造口等强化干预措施的升级。出生后第3天动脉切换手术成功。结论:本病例强调了TGA-IVS胎儿-新生儿过渡可能对发生PPHN的贡献,PPHN可能在过渡后消退。此外,该病例强调了在出生后不需要早期侵入性干预的情况下提供温和血流动力学转变的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Fetal-to-Neonatal Transition of an Infant with Transposition of the Great Arteries and Intact Ventricular Septum: A Case Report.

Introduction: Transposition of the great arteries (TGA), especially with intact ventricular septum (TGA-IVS), presents unique challenges during fetal-to-neonatal transition, which can contribute to developing persistent pulmonary hypertension of the newborn (PPHN).

Case presentation: A male newborn with TGA-IVS, delivered via caesarean section, presented with hypoxemia and tachycardia immediately after birth (preductal SpO2: 50-60%, post-ductal SpO2: 70-75%). Echocardiography revealed a floppy interatrial septum and two interatrial connections with bidirectional shunting. Ductal flow showed systolic right-to-left shunting, suggesting high pulmonary vascular resistance. Immediate post-birth management included non-invasive respiratory support with continuous positive airway pressure at 100% oxygen and administration of prostaglandin E2 to maintain ductal patency. Despite initial low oxygen saturation levels, escalation of intensive treatments was deferred based on continuous trend monitoring of vital signs and echocardiographic indicators. Oxygenation and circulation gradually improved within the first 2 h after birth to normal values, obviating escalation of intensive interventions like intubation, nitric oxide and/or balloon atrial septostomy. Arterial switch operation at day 3 post-birth was successful.

Conclusion: This case highlights the possible contribution of fetal-to-neonatal transition in TGA-IVS to developing PPHN, which may subside after transition. Moreover, this case highlights the potential for providing a gentle hemodynamic transition without invariably needing early invasive interventions after birth.

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