Durongpisitkul K, Soongswang J, Laohaprasitiporn D, Nana A
Department of Pediatrics, Siriraj Hospital, Mahidol University, Bangkok, Thailand.
J Med Assoc Thai. 2000 Sep;83(9):1045-53.
Surgical repair of secundum atrial septal defect (ASD) is a safe, widely accepted procedure with negligible mortality. However, it is associated with morbidity, discomfort and a thoracotomy scar. As an alternative to surgery, a variety of devices for transcatheter closure of ASD have been developed.
We report our clinical experience with transcatheter closure of ASD using the Amplatzer Septal Occluder, a new occlusion device with intermediate term follow-up.
PATIENTS & METHOD: Patients having ASD met established two-dimensional echocardiographic criteria for transcatheter closure were selected. ASD size was measured by transesophageal echocardiogram (TEE) and balloon occlusion catheter (stretched diameter). The Amplatzer's size was chosen to be equal to or 1 mm less than the stretched diameter. The device was advanced transvenously into a guiding sheath and deployed under fluoroscopic and TEE guidance. Once its position was optimal, it was released. TEE was undertaken to demonstrate the residual shunt.
There were 26 patients with a mean age of 17.2 +/- 15.9 years old (2 to 60) and a mean weight of 22 +/- 37.5 kg. (10.7 to 62.5). The mean ASD diameter measured by TEE was 18.3 +/- 5.2 mm. and by stretched diameter was 22 +/- 7.5 mm. Four patients who had ASD stretched diameter over 32 mm were excluded because a larger device was not available. Devices were deployed in 22 patients with sizes from 9 to 30 mm (median = 22mm). Immediately after closure a tiny residual shunt was observed at the core of the device in each case. At 24 hours only two patients had a small (< 2 mm) shunt. One patient with fenestrated ASD had a device embolized into the right ventricle with successful removal and surgical closure. Patients were followed-up for a mean duration of 8 +/- 3.5 months (from 3 to 12 months). Complete occlusion was found in 20 out of 21 patients (95%).
The Amplatzer Septal Occluder is a new device designed for closure of different sizes of ASD and can be easily and safely deployed. Our experience showed that this device could be used to close an ASD as large as 30 mm. The intermediate term follow-up also demonstrated an excellent closure result. Caution should be undertaken with patients who have a fenestrated atrial septal defect particularly at the septal rim.
继发孔型房间隔缺损(ASD)的外科修复是一种安全、广泛接受且死亡率可忽略不计的手术。然而,它会带来并发症、不适以及胸部手术疤痕。作为手术的替代方法,已开发出多种用于经导管封堵ASD的装置。
我们报告使用新型封堵装置Amplatzer房间隔封堵器经导管封堵ASD的中期随访临床经验。
选择符合经导管封堵既定二维超声心动图标准的ASD患者。通过经食管超声心动图(TEE)和球囊封堵导管测量ASD大小(伸展直径)。选择的Amplatzer封堵器大小等于或比伸展直径小1mm。该装置经静脉推进到引导鞘中,并在荧光透视和TEE引导下展开。一旦其位置最佳,即予以释放。进行TEE以显示残余分流。
有26例患者,平均年龄17.2±15.9岁(2至60岁),平均体重22±37.5kg(10.7至62.5kg)。通过TEE测量的ASD平均直径为18.3±5.2mm,伸展直径为22±7.5mm。4例ASD伸展直径超过32mm的患者被排除,因为没有更大尺寸的装置。22例患者使用了大小从9至30mm(中位数=22mm)的装置。封堵后立即在每个病例的装置核心处观察到微小的残余分流。24小时时仅有2例患者有小的(<2mm)分流。1例多孔型ASD患者的封堵器栓塞入右心室,成功取出并进行了外科手术闭合。患者平均随访8±3.5个月(3至12个月)。21例患者中有20例(95%)实现完全封堵。
Amplatzer房间隔封堵器是一种设计用于封堵不同大小ASD的新型装置,可轻松、安全地展开。我们的经验表明该装置可用于封堵最大达30mm的ASD。中期随访也显示出极佳的封堵效果。对于多孔型房间隔缺损患者,尤其是在房间隔边缘处,应谨慎操作。