Hausdorf G, Schulze-Neick I, Lange P E
Deutsches Herzzentrum Berlin, Abteilung Angeborene Herzfehler, Germany.
Br Heart J. 1993 Apr;69(4):343-6. doi: 10.1136/hrt.69.4.343.
A case of pulmonary atresia with ventricular septal defect is reported in which a communication was established between the right ventricle and the hypoplastic pulmonary artery by intervention, despite muscular atresia of the right ventricular outflow tract. The atresia was perforated with a special designed radiofrequency catheter (Osypka). After the creation of a canal within the muscular atresia, balloon dilatation (diameters 2, 3.5, and 7.2 mm) was performed. Arterial oxygen saturation increased from 64% to 78%. Lateral deviation of the radiofrequency catheter resulting in a lateral perforation of the atretic muscular infundibulum was well tolerated without later sequelae. Early restenosis within two weeks necessitated the implantation of a stent within the "recanalised" atresia resulting in an increased anterograde flow to the pulmonary artery. This case shows that "recanalisation" of muscular atresia of the pulmonary artery by radiofrequency is a promising technique. Additionally, stent implantation into the infundibulum to prevent restenosis is a first step to interventional right ventricular outflow tract reconstruction.
报道了一例室间隔缺损合并肺动脉闭锁的病例,尽管右心室流出道存在肌性闭锁,但通过介入治疗在右心室与发育不全的肺动脉之间建立了交通。使用特制的射频导管(奥西普卡)穿透闭锁处。在肌性闭锁处形成通道后,进行了球囊扩张(直径分别为2、3.5和7.2毫米)。动脉血氧饱和度从64%升至78%。射频导管的侧向偏移导致闭锁性肌性漏斗部出现侧向穿孔,但耐受性良好,未留下后遗症。两周内出现早期再狭窄,因此需要在“再通”的闭锁处植入支架,以增加肺动脉的顺行血流。该病例表明,通过射频对肺动脉肌性闭锁进行“再通”是一种有前景的技术。此外,在漏斗部植入支架以预防再狭窄是介入性右心室流出道重建的第一步。