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首页> 外文期刊>Catheterization and cardiovascular interventions: Official journal of the Society for Cardiac Angiography & Interventions >Technical challenges of atrial septal stent placement in fetuses with hypoplastic left heart syndrome and intact atrial septum
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Technical challenges of atrial septal stent placement in fetuses with hypoplastic left heart syndrome and intact atrial septum

机译:发育不良左心综合征和完整房间隔的胎儿房间隔支架置入的技术挑战

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摘要

Objectives The objective of this study was to describe our single-institution experience with prenatal atrial septal stent placement for fetuses with hypoplastic left heart syndrome and an intact atrial septum (HLHS/IAS). Background Infants born with HLHS/IAS are at high risk for neonatal death, despite maximal postnatal therapy. Prenatal atrial septoplasty by static balloon dilation has been effective in decompressing the left atrium (LA) in utero, but several factors have limited the size of septal defects. We attempted to overcome the limitations of balloon septoplasty using transcatheter atrial septal stents. Methods All records from our institution of fetuses with HLHS/IAS that underwent prenatal atrial septal stent placement were reviewed, including operative notes and echocardiograms. Results Nine fetuses between 24 and 31 weeks gestation with HLHS/IAS underwent attempted fetal atrial septal stent placement. A stent was deployed across the atrial septum in five fetuses, with four fetuses demonstrating flow across the stent at the time of intervention. In four cases, stent placement failed due to malposition or embolization, but in three of the four cases, atrial balloon septoplasty at the same in-utero procedure successfully and acutely decompressed the LA. There were no maternal complications. There was one fetal demise. The remaining eight fetuses survived to delivery, but four died in the neonatal period (two of which had been stented). Conclusions Ultrasound-guided atrial septal stent placement is feasible in some fetuses with HLHS/IAS. Visualization of the septum and catheter tip is critical to technical success. Additional experience is necessary to determine the clinical impact of this intervention.
机译:目的这项研究的目的是描述我们的单机构经验,即对于发育不良的左心综合征和完整的房间隔(HLHS / IAS)的胎儿进行产前房间隔支架置入。背景尽管进行了最大程度的产后治疗,但出生于HLHS / IAS的婴儿仍处于新生儿死亡的高风险中。通过静态气囊扩张术进行产前房间隔成形术已经有效地减轻了子宫内左心房(LA)的压力,但是一些因素限制了间隔缺损的大小。我们试图克服使用经导管心房间隔支架进行球囊隔膜成形术的局限性。方法回顾了我院所有带HLHS / IAS的胎儿产前房间隔支架置入术的记录,包括手术记录和超声心动图。结果妊娠24至31周的HLHS / IAS胎儿中有9例尝试了胎儿房间隔支架置入术。在五个胎儿中,在整个房间隔中部署了一个支架,在干预时有四个胎儿展示了在支架中的流动。在4例中,由于位置不当或栓塞而导致支架置入失败,但在4例中的3例中,在相同的子宫内手术中成功进行了房室球囊造形术并急性减压了LA。没有产妇并发症。有一次胎儿死亡。其余8例胎儿存活下来,但4例在新生儿期死亡(其中2例已植入支架)。结论在某些HLHS / IAS胎儿中,超声引导房间隔支架置入术是可行的。隔垫和导管尖端的可视化对于技术成功至关重要。要确定此干预措施的临床影响,还需要其他经验。

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