Department of Cardiovascular Surgery, Methodist DeBakey Heart & Vascular Center, Houston, TX 77030, USA.
J Vasc Surg. 2011 Sep;54(3):754-9. doi: 10.1016/j.jvs.2011.03.260. Epub 2011 Jun 12.
Covered stents have been proposed as an endovascular option for recalcitrant cases of hemodialysis-related central venous occlusive disease (CVOD). This study evaluated the efficacy and durability of covered stents in treating CVOD to preserve a functional dialysis access circuit.
A retrospective review was performed of all patients with clinically significant CVOD who were treated by placement of covered stents from April 2007 to September 2010. Demographics, lesion locations and anatomic characteristics, stent graft, and access patency rates were determined. Complications, reinterventions, and factors influencing their outcomes were examined.
In 25 patients (56% men; mean age, 57 ± 29 years) with CVOD, covered stents were used in 20 to treat symptomatic venous hypertension or in 5 at the time of access creation to enable functionality. The target lesion was accessed via the dialysis access site or the common femoral vein. The Viabahn endoprosthesis (W. L. Gore and Associates, Flagstaff, Ariz) was used in 24 patients (average size and length, 11 mm × 5 cm) and a 13-mm × 5-cm Fluency covered stent (Bard Peripheral Vascular, Tempe, Ariz) was implanted in 1 patient. Technical success was 100%, and resolution of arm edema occurred after covered stent deployment in symptomatic patients. Two postprocedural cases (8%) of thrombosis occurred, one within 30 days and another at 3 months. Both required percutaneous thrombectomy and percutaneous transluminal angioplasty (PTA). Three additional patients (12%) required PTA due to restenosis in one of the ends of the device. Covered stent primary patency (PP), assisted primary patency (APP), and secondary patency (SP) were 56%, 86%, and 100% at 12 months, respectively. Access patency rates at 12 months were 29%, 85%, and 94% for PP, APP, and SP, respectively, in patients that received a covered stent for access salvage; patency rates were 74%, 85%, and 94% for PP, APP, and SP, respectively, in patients in whom the access was created after the venous outflow restoration.
Placement of covered stents for hemodialysis-related CVOD is safe, effective in relieving symptoms, and enabled functionality of new dialysis access circuits. Further prospective and randomized studies are necessary to determine whether covered stents provide superior long-term results to those achieved with PTA and bare metal stents.
带膜支架被提议作为治疗血液透析相关中心静脉阻塞性疾病(CVOD)的顽固病例的血管内选择。本研究评估了带膜支架在保留功能性透析通路方面治疗 CVOD 的疗效和持久性。
对 2007 年 4 月至 2010 年 9 月期间因带膜支架治疗的具有临床显著 CVOD 的所有患者进行回顾性分析。确定了人口统计学、病变部位和解剖学特征、支架移植物以及通路通畅率。检查了并发症、再次干预以及影响其结果的因素。
在 25 例 CVOD 患者(56%为男性;平均年龄 57±29 岁)中,20 例因症状性静脉高压而使用带膜支架,5 例在建立通路时使用带膜支架以保持功能。目标病变通过透析通路部位或股总静脉进入。24 例患者使用 Viabahn 血管内假体(戈尔公司,Flagstaff,Ariz)(平均大小和长度为 11mm×5cm),1 例患者植入 13mm×5cm Fluency 带膜支架(Bard 外周血管,Tempe,Ariz)。技术成功率为 100%,在有症状的患者中,带膜支架植入后手臂水肿得到缓解。2 例(8%)术后发生血栓形成,1 例发生在 30 天内,另 1 例发生在 3 个月时。两者均需要经皮血栓切除术和经皮腔内血管成形术(PTA)。另外 3 例(12%)由于器械的一端发生再狭窄而需要 PTA。带膜支架的初始通畅率(PP)、辅助性初始通畅率(APP)和继发性通畅率(SP)分别为 12 个月时的 56%、86%和 100%。在接受带膜支架进行通路挽救的患者中,12 个月时的通路通畅率分别为 PP、APP 和 SP 的 29%、85%和 94%;在静脉流出恢复后建立通路的患者中,12 个月时的通畅率分别为 PP、APP 和 SP 的 74%、85%和 94%。
带膜支架治疗血液透析相关 CVOD 是安全的,可有效缓解症状,并使新的透析通路具有功能。需要进一步的前瞻性和随机研究来确定带膜支架是否比 PTA 和裸金属支架提供更长期的结果。