右心室流出道支架治疗新生儿重度法洛四联症的首选方案

Ali Al-Akhfash
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引用次数: 0

摘要

背景:法洛四联症(TOF)新生儿可能是前列腺素依赖性的,除非完全矫正或缓解,否则不能出院。姑息可以通过改良的Blalock-Taussig分流(BTS)、导管支架术或右心室流出道(RVOT)支架术来实现。目的:本研究的目的是介绍我们通过RVOT支架术来缓解需要增加肺血流量的严重TOF新生儿的经验。方法:本研究对2016年8月至2019年12月在沙特阿拉伯卡西姆PSCC接受RVOT支架置入术的一系列患者进行。包括RVOT支架植入的病例。记录患者的临床数据、超声心动图、心导管插入术和随访数据。使用Microsoft Excel数据分析工具对数据进行分析。结果:在研究期间,连续四名被诊断为TOF并伴有严重发绀的患者接受了RVOT支架植入术。平均年龄和体重分别为2.8±1.7天和2.9±0.1公斤。所有患者在干预前均接受前列腺素输注。RVOT支架植入前后的平均饱和度分别为63%(±11%)和82%(±4%)(p=0.018)。一名患者在4个月后需要扩张RVOT支架。所有患者均存活,中位年龄6.5个月(6-12个月)时TOF完全修复。中位随访期为13个月。RVOT支架置入前和TOF完全修复前的中位分支PAs直径和Z评分分别为2.8 mm(Z评分:-2.5)和5.5 mm(Z得分:-0.5至-1.16)(p=0.001)。RVOT中的支架部署技术具有挑战性,需要进行干预前规划和讨论。使用软导管、冠状动脉导线和预安装的冠状动脉支架有助于RVOT和肺动脉瓣的交叉,然后进行支架部署
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Right Ventricular Outflow Tract Stenting as the First Option for Palliation of Neonates with Severe Tetralogy of Fallot
Background: Neonates with Tetralogy of Fallot (TOF) might be prostaglandin dependent and cannot be discharged from the hospital except after complete correction or palliation. Palliation could be achieved by modified Blalock-Taussig Shunt (BTS), ductal stenting, or right ventricular outflow tract (RVOT) stenting. Objective: The objective of this study was to present our experience of palliating neonates with severe TOF who require augmentation of the pulmonary blood flow by RVOT stenting. Methods: This study was conducted on a series of patients who had RVOT stenting in PSCC-Qassim, Saudi Arabia, from August 2016 till December 2019. Cases that had RVOT stenting are included. The patient's clinical data, echocardiography, cardiac catheterization, and follow-up data were recorded. Data were analyzed using The Microsoft Excel data analysis tool. Results: During the study period, four consecutive patients with a diagnosis of TOF with significant cyanosis underwent RVOT stenting. The mean age and weight were 2.8±1.7 days and 2.9±0.1 kg respectively. All were on prostaglandin infusion before the intervention. The mean saturation before and after RVOT stenting was 63% (±11%) and 82% (±4%) respectively (p = 0.018). One patient required RVOT stent dilatation after 4 months. All patients are alive and had complete TOF repair at a median age of 6.5 months (range 6 to 12 months). The median follow-up period is 13 months. The median branch PAs diameter and Z-score before RVOT stenting and immediately before complete TOF repair were 2.8 mm (Z score: -2.5) and 5.5 mm (Z score: -0.5 to -1.16) respectively (p = 0.001). Conclusion: RVOT stenting is a reasonable alternative palliation for patients with severe TOF. The technique of stent deployment in the RVOT is challenging and requires pre-intervention planning and discussion. Using soft catheters, coronary wires, and the premounted coronary stents facilitate crossing of the RVOT and pulmonary valve and then stent deploymen
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