Pediatric Cardiology and GUCH Unit, Istituto Policlinico San Donato IRCCS, San Donato Milanese, Italy.
Catheter Cardiovasc Interv. 2011 Nov 15;78(6):933-9. doi: 10.1002/ccd.23239. Epub 2011 Aug 8.
Limited data exists in the literature concerning the percutaneous treatment of complete aortic isthmus atresia.
Between January 2007 and November 2010, 40 subjects underwent percutaneous treatment of aortic coarctation in our catheterization laboratory. Four out of 40 had aortic isthmus atresia with complete interruption. Median age at procedure was 48 years (range, 32-63 years). All subjects had history of arterial systemic hypertension refractory to medical treatment. Two subjects had a previous history of haemorrhagic stroke. All procedures were performed under general anesthesia and orotracheal intubation. In each case radial and femoral artery access was obtained. A radiofrequency (RF) system (Baylis MedComp Inc, Montreal, Canada) consisting of a Nykanen 0.024'' RFguidewire and coaxial microcatheter were used to perforate and cross the atretic segment. A guidewire was then snared and an artero-arterial circuit created. The area was predilated by using coronary angioplasty balloons. A 12 Fr Mullins long sheath was advanced and an E-PTFE covered 8Zig Cheatham-Platinum stent implanted. Patients were monitored in hospital for 48-72 hr. Follow-up was performed at 1, 3, 6, 12 months, and yearly thereafter.
Percutaneous recanalization of the atretic segment was performed successfully in all subjects. Mean fluoroscopy and procedure times were 30 ± 6 and 90 ± 15 min, respectively. After implantation, the gradient decreased significantly (prestent: mean value 52.25 mm Hg [range 33-70 mm Hg] versus post stent: mean value 3 mm Hg [range, 0-10 mm Hg] [P < 0.0001]). The stents were placed in the correct position in all subjects and no immediate complications occurred. During a mean follow-up of 19 months (2-41 months), there were no significant complication. All subjects had arterial systemic blood pressure within the normal range. In two out of four patients single agent antihypertensive drug therapy was needed. The first patient in our series was treated conservatively and needed further stent dilation with a second procedure approach, eight months after the initial stent implantation, performed without incident.
Our data show that use of radiofrequency energy perforation and covered CP stent implantation is a safe, effective, and promising tool for treatment of complete aortic isthmus atresia.
有关完全性主动脉峡部闭锁的经皮治疗,文献中仅有有限的数据。
2007 年 1 月至 2010 年 11 月期间,我们的导管室对 40 例主动脉缩窄患者进行了经皮治疗。其中 4 例患者为完全性主动脉峡部闭锁,中断完全。手术时的中位年龄为 48 岁(范围,32-63 岁)。所有患者均有动脉系统高血压病史,且药物治疗无效。2 例患者有出血性卒中史。所有手术均在全身麻醉和气管插管下进行。在每种情况下,均通过桡动脉和股动脉入路。使用射频(RF)系统(Baylis MedComp Inc,蒙特利尔,加拿大),该系统由 Nykanen 0.024''RF 导丝和同轴微导管组成,用于穿孔和穿过闭锁段。然后用圈套器套住导丝,并创建动静脉循环。使用冠状动脉扩张球囊对该区域进行预扩张。推进 12Fr Mullins 长鞘,并植入 E-PTFE 覆盖 8Zig Cheatham-Platinum 支架。患者在医院内监测 48-72 小时。此后每年进行随访,1、3、6、12 个月随访一次。
所有患者均成功地对闭锁段进行了经皮再通。平均透视和手术时间分别为 30 ± 6 和 90 ± 15 分钟。植入支架后,梯度明显降低(支架前:平均 52.25mmHg[范围 33-70mmHg];支架后:平均 3mmHg[范围 0-10mmHg] [P < 0.0001])。所有患者的支架均放置在正确位置,且无即刻并发症发生。在平均 19 个月(2-41 个月)的随访期间,无明显并发症。所有患者的动脉系统血压均在正常范围内。在 4 例患者中有 2 例需要单一降压药物治疗。我们系列中的第一位患者接受了保守治疗,需要进一步进行第二次支架扩张治疗,该患者在初始支架植入后 8 个月进行了治疗,过程顺利,无不良事件发生。
我们的数据表明,使用射频能量穿孔和覆盖 CP 支架植入术是一种安全、有效且有前途的治疗完全性主动脉峡部闭锁的方法。