低体重儿童继发性室间隔缺损的血管内闭合术

I. Ditkivskyy, Denys L. Voloshyn, Y. V. Yermolovych, I. Perepeka, V. Lazoryshynets
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引用次数: 1

摘要

目标。评估在体重≤10kg的有症状儿童中使用封堵器经导管封堵继发性房间隔缺损(ASD)的有效性和安全性。材料和方法。在2014年11月至2021年6月期间,在乌克兰国家医学科学院国家阿莫索夫心血管外科研究所的基础上,对18名患者使用封堵器封堵继发性ASD,其中女性13例(72.2%),男性5例(27.8%),平均年龄18.94±9.44个月(最小12个月,最大4岁)。平均体重为9.294±1.170 kg(6.4 kg至10 kg),平均Z评分为-1.7±1.5(-4.6至0.46),平均身高为80 cm(71 cm至88 cm)。根据经食管超声心动图(TEE)的测量,缺陷的平均尺寸为13.7 mm±3.6 mm(最大18.0 mm,最小6.0 mm)。结果和讨论。在我们的出版物中,该方法的有效性为100%(18/18),而世界统计数据显示为94-95%。并发症发生率为5.6%(n=1)。我们建议这与使用尺寸气球和仔细选择设备有关。当为体重≤10 kg的有症状儿童选择治疗策略时,决定性因素是边缘的存在和缺陷的大小。根据TEE数据,当除主动脉边缘外,所有缺损边缘均≥4mm时,认为缺损适合闭合。尽管考虑了心房内膜的总长度,但它并不具有决定性的重要性,因为对于大多数具有所有边缘的封堵器来说,植入物的视野不会干扰心脏解剖结构的工作。为了确定缺陷的实际大小,我们建议在TEE控制下使用测量球囊。以下装置用于闭合缺损:MemoPart ASD封堵器、Amplatzer间隔封堵器,LifeTech HeartR封堵器和LifeTech Heart R多开窗心房间隔缺损(MF-ASD)封堵器。结论。经过研究,我们确信,血管内方法闭合血液动力学显著的继发性ASD治疗体重≤10 kg的儿童已被证明是一种有效的方法,100%的病例成功植入了封堵器。
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Endovascular Closure of Secondary Septal Defect in Children with Low Body Weight
The aim. To assess the effectiveness and safety of transcatheter closure of a secondary atrial septal defect (ASD) using an occluder in symptomatic children weighing ≤10 kg. Materials and methods. In the period from November 2014 to June 2021, on the basis of the National Amosov Institute of Cardiovascular Surgery of the National Academy of Medical Sciences of Ukraine, closure of secondary ASD using an occluder was performed in 18 patients, among them 13 women (72.2%) and 5 men (27.8%). Th e mean age of the patients was 18.94±9.44 months (the youngest patient was 12 months, the oldest was 4 years). The mean weight was 9.294±1.170 kg (6.4 kg to 10 kg), the mean Z-score was -1.7±1.5 (-4.6 to 0.46), the mean height was 80 cm (71 cm to 88 cm). According to the measurements by transesophageal echocardiography (TEE), the average size of the defects was 13.7 mm±3.6mm (the largest 18.0 mm, the smallest 6.0 mm). Results and discussion. In our publication, the effectiveness of the method was 100% (18/18), while the world statistics show 94-95%. Th e frequency of complications was 5.6% (n=1). We suggest that this is associated with the use of a sizing balloon and careful selection of the device. When choosing treatment tactics for symptomatic children weighing ≤10 kg, the decisive factor was the determination of the presence of edges and the size of the defect. Defects were considered suitable for closure, according to TEE data, when all margins of the defect were ≥4 mm, except for the aortic margin. Although the total length of the interatrial membrane was taken into account, it was not of decisive importance, since for most occluders with the presence of all edges, the fields of the implant could not interfere with the work of the anatomical structures of the heart. To determine the real size of the defect, we recommend a measuring balloon under TEE control. The following devices were used to close the defect: MemoPart ASD occluder, Amplatzer Septal Occluder, LifeTech HeartR Occluder, LifeTech HeartR Multi-Fenestrated Atrial Septal Defect (MF-ASD) Occluder.   Conclusion. After the study, we are convinced that the endovascular method of closing a hemodynamically significant secondary ASD for the treatment of children with a body weight of ≤10 kg has proven to be an effective method, with successful implantation of the occluder in 100% of cases.
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