Rao P S, Sideris E B, Hausdorf G, Rey C, Lloyd T R, Beekman R H, Worms A M, Bourlon F, Onorato E, Khalilullah M
University of Wisconsin Medical School.
Am Heart J. 1994 Nov;128(5):1022-35. doi: 10.1016/0002-8703(94)90602-5.
Several devices are available for transcatheter occlusion of atrial septal defect. This report describes the international experience with the buttoned device. During a 4.5-year period ending in February 1993, 180 transcatheter atrial septal defect occlusions were performed with the buttoned device. Patient age varied between 0.6 and 76 years and stretched atrial defect diameter between 5 and 25 mm. The defects were closed with 25 to 50 mm devices delivered through 8F (148 patients) or 9F (32 patients) sheaths. Twelve patients were adults whose defects were closed to prevent recurrence of cerebrovascular accidents caused by presumed paradoxic embolism. In the remaining patients the atrial defect was closed to treat the left-to-right shunt. The atrial septal defects were effectively occluded as demonstrated by (1) decrease in pulmonary-to-systemic flow ratio from 2.1 +/- 0.6 (mean +/- SD) to 1.05 +/- 0.1 (p < 0.01) by oximetry; (2) normalized S2 and disappearance of the diastolic murmur by auscultation; and (3) improvement in right ventricular volume overloading by echocardiogram. However, trivial to small shunts could be detected by color Doppler studies in 76 (45%) of 168 patients in whom such data are available. Complications included unbuttoning in 13 and whole-device embolization in 1. All patients remained stable, and retrieval of the device and surgical closure of the atrial septal defect were accomplished in 10 patients. Transcatheter retrieval was used in the remaining 4 patients. The incidence of unbuttoning, a major complication of the procedure, appeared to decrease with the increasing experience of the investigators and with device modification (third-generation). The follow-up duration varied between 1 month and 4 years. Six patients required surgery during the follow-up period. In the remaining patients (n = 160), clinical examination did not reveal signs of atrial shunts. Color Doppler studies revealed either complete disappearance of the previously demonstrated shunts or further diminution of their size. The results indicate that transcatheter occlusion of the atrial septal defects with buttoned devices is feasible, relatively safe, and effective, and it appears to be a viable alternative to surgery for some patients with secundum atrial septal defect. Complications are infrequent and should improve with experience.
有几种装置可用于经导管封堵房间隔缺损。本报告描述了纽扣式装置的国际应用经验。在截至1993年2月的4.5年期间,使用纽扣式装置进行了180例经导管房间隔缺损封堵术。患者年龄在0.6岁至76岁之间,房间隔缺损直径在5毫米至25毫米之间。使用通过8F(148例患者)或9F(32例患者)鞘管输送的25至50毫米装置封闭缺损。12例为成人患者,其缺损被封闭以预防由推测的反常栓塞引起的脑血管意外复发。在其余患者中,封闭房间隔缺损以治疗左向右分流。房间隔缺损被有效封堵,表现为:(1)通过血氧测定法,肺循环与体循环血流量之比从2.1±0.6(均值±标准差)降至1.05±0.1(p<0.01);(2)听诊时S2正常化且舒张期杂音消失;(3)超声心动图显示右心室容量超负荷改善。然而,在168例有此类数据的患者中,76例(45%)通过彩色多普勒研究可检测到轻微至小的分流。并发症包括13例纽扣松开和1例整个装置栓塞。所有患者病情保持稳定,10例患者进行了装置取出及房间隔缺损的外科闭合。其余4例患者采用经导管取出。纽扣松开是该手术的主要并发症,其发生率似乎随着研究者经验的增加以及装置改进(第三代)而降低。随访时间在1个月至4年之间。6例患者在随访期间需要手术。在其余患者(n = 160)中,临床检查未发现房间隔分流的迹象。彩色多普勒研究显示先前显示的分流完全消失或其大小进一步减小。结果表明,用纽扣式装置经导管封堵房间隔缺损是可行的、相对安全且有效的,对于一些继发孔型房间隔缺损患者而言,它似乎是一种可行的手术替代方法。并发症并不常见,且随着经验的积累应会有所改善。