Outcomes After Stenting of Right Ventricular Outflow Tract for Tetralogy of Fallot and Its Variants.

IF 1.4 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Nisanth Selvam, Navaneetha Sasikumar, Raman Krishna Kumar
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引用次数: 0

Abstract

We reviewed our institutional database to examine the effect of right ventricular outflow tract (RVOT) stenting on branch pulmonary artery (PA) sizes and their outcomes. RVOT stenting was performed following standard technique. Since 2021, a conscious effort was made to spare the pulmonary valve (PV) whenever feasible. PA annulus and branch PA sizes were serially monitored by echocardiography. Sixty patients, (4.5 [1.75-24] months, weight 6.4 [3.5-9 kg]), were included (Time period:2012-2025). Commonest indications included cyanotic spell (65%) and hypoplastic branch PAs (30%). Pulmonary valve annulus measured 5.1 mm (4.0-7.7); Z score - 3.8 (- 5.1 to - 2.6), and MPA 4.35 mm (3.34-5.7); Z score - 4.9 (- 7.0 to [- 3.1]). At follow-up of 8(25-102) months, branch PAs grew in all, albeit at different paces. RPA z-scores improved from a baseline of - 2.48 (- 5.05 to [- 0.85]) to - 1.55 (- 3.07 to 0.46) and LPA z-scores from - 2.5 (- 4.38 to [- 0.78]) to - 1.08 (- 2.41 to 0.63) in hypoplastic PA group over 1-year period (p value < 0.001). Pulmonary valve was spared in 57% of patients in the cyanotic spell group and 22% of hypoplastic PA group. 29 (48%) patients underwent corrective surgery at 9 (6-14) months from RVOTS. Requirement of transannular patch (TAP) was 38% (11/29) and conduit was 34% (10/29). Valve sparing ICR was feasible in 67% (8/12) when the stent was placed below the valve. In addition to effective palliation, RVOT stenting promotes growth of branch pulmonary arteries even in those with inherently hypoplastic branch PAs. It is possible to effectively palliate selected patients without stenting across the pulmonary valve thereby potentially enabling valve-sparing TOF correction in those with suitable anatomy.

法洛四联症及其变异型右心室流出道支架置入术后的疗效。
我们回顾了我们的机构数据库,以检查右心室流出道(RVOT)支架置入对肺动脉分支(PA)大小及其结果的影响。RVOT支架置入按照标准技术进行。自2021年以来,在可行的情况下,有意识地努力避免使用肺动脉瓣(PV)。超声心动图连续监测肺动脉环和肺动脉分支的大小。纳入患者60例,年龄4.5[1.75-24]个月,体重6.4 [3.5-9 kg])(时间:2012-2025年)。最常见的适应症包括紫绀(65%)和发育不良分支PAs(30%)。肺动脉瓣环测量5.1 mm (4.0-7.7);Z得分- 3.8(2.6 - 5.1),和4.35 MPA mm (3.34 - -5.7);Z分数- 4.9(- 7.0到[- 3.1])。在8(25-102)个月的随访中,尽管速度不同,但分枝pa均有所增长。在1年的时间里,发育不良PA组的RPA z-评分从基线的- 2.48(- 5.05至[- 0.85])提高到- 1.55(- 3.07至0.46),LPA z-评分从- 2.5(- 4.38至[- 0.78])提高到- 1.08(- 2.41至0.63)(p值)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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