Schild A Frederick, Schuman Earl S, Noicely Karlene, Kaufman Joyce, Gillaspie Erin, Fuller Joseph, Collier Patrick, Ronfeld Amy, Nair Ravikumaran
1Florida International University Herbert Wertheim College of Medicine, Miami, FL, USA.
J Vasc Access. 2011 Jul-Sep;12(3):248-52. doi: 10.5301/jva.2011.6351.
Preferred hemodialysis (HD) access is an autologous fistula. Vascular grafts are used in patients with vessels unsuitable to accomplish an arteriovenous fistula (AVF). It is recommended that most current grafts mature in situ for 2-3 weeks before being accessed. Graft complications occur because the structure was not designed for the trauma of repeated cannulation. This study graft has a different structure that enables early use. Its design minimizes weeping through the graft walls and is meant to endure repeated access, thus minimizing the use of HD catheters. The purpose of this study was to show that the Flixene™ graft can be safely placed in patients where fistulas have failed and can be cannulated in 24-72 hr, while maintaining patency rates similar to other polytetrafluoroethylene (PTFE) grafts on the market. Flixene™ configuration should also reduce the incidence of pseudoaneurysms and seromas.
A prospective two-center study placed 33 grafts in 33 patients; graft efficacy, post-operative complications, and patency were evaluated. Ease of cannulation and dialysis center complications related to early cannulation were documented. Six month follow-up data was analyzed.
Successful access was achieved in all 33 patients within 72 hr (29 patients within 24 hr). Overall primary patency at 6 months was 49%; primary-assisted patency at 6 months was 80%. No pseudoaneurysms or seromas were documented at 6 months. Complications were typical of graft access.
Early cannulation was successful in all patients. Primary and secondary patency rates at 6-months were equivalent to other data reported on PTFE grafts. Flixene™ successfully prevented pseudoaneurysm and seroma formation at 6 months of prospective follow-up. This graft is a better last-resort option for patients who cannot receive a fistula, compared to double-lumen cuffed catheters.
首选的血液透析(HD)通路是自体动静脉内瘘。血管移植物用于血管不适合建立动静脉内瘘(AVF)的患者。建议大多数现有移植物在原位成熟2至3周后再进行穿刺使用。移植物出现并发症是因为其结构并非为反复穿刺的创伤而设计。本研究的移植物具有不同的结构,能够早期使用。其设计可最大限度减少通过移植物壁的渗液,并旨在耐受反复穿刺,从而尽量减少HD导管的使用。本研究的目的是表明Flixene™移植物可安全地植入内瘘失败的患者体内,并可在24至72小时内进行穿刺,同时保持与市场上其他聚四氟乙烯(PTFE)移植物相似的通畅率。Flixene™的结构还应能降低假性动脉瘤和血清肿的发生率。
一项前瞻性双中心研究为33例患者植入了33个移植物;评估了移植物的疗效、术后并发症和通畅情况。记录了穿刺的难易程度以及与早期穿刺相关的透析中心并发症。分析了6个月的随访数据。
所有33例患者均在72小时内成功进行了穿刺(29例在24小时内)。6个月时的总体初级通畅率为49%;6个月时的初级辅助通畅率为80%。6个月时未记录到假性动脉瘤或血清肿。并发症为移植物穿刺的典型并发症。
所有患者早期穿刺均成功。6个月时的初级和次级通畅率与其他关于PTFE移植物报道的数据相当。在6个月的前瞻性随访中,Flixene™成功预防了假性动脉瘤和血清肿的形成。与双腔带 cuff 导管相比,对于无法接受内瘘的患者,这种移植物是更好的最后选择。