Department of Plastic Surgery, The First Affiliated Hospital of Sun Yat-sen University, Guangzhou, China.
Department of Burns, Plastics and Wound Repair Surgery, Nanxishan Hospital of Guangxi Zhuangzu Autonomous Region, Guilin, China.
Ren Fail. 2024 Dec;46(2):2371056. doi: 10.1080/0886022X.2024.2371056. Epub 2024 Jul 16.
Currently, three expanded polytetrafluoroethylene (ePTFE) prosthetic graft types are most commonly used for patients with end-stage kidney disease (ESKD) who require long-term vascular access for hemodialysis. However, studies comparing the three ePTFE grafts are limited. This study compared the clinical efficacy and postoperative complications of three ePTFE prosthetic graft types used for upper limb arteriovenous graft (AVG) surgery among patients with ESKD. Patients with ESKD requiring upper limb AVG surgery admitted to our center between January 2016 and September 2019 were enrolled. Overall, 282 patients who completed the 2-year follow-up were included and classified into the following three groups according to the ePTFE graft type: the GPVG group with the PROPATEN graft, the GAVG group with the straight-type GORE ACUSEAL, and the BVVG group with the VENAFLO II. The patency rate and incidence of access-related complications were analyzed and compared between groups. The patients were followed up postoperatively, and data were collected at 6, 12, 18, and 24 months postoperatively. Respective to these follow-up time points, in the GPVG group, the primary patency rates were 74.29%, 65.71%, 51.43%, and 42.86%; the assisted primary patency rates were 85.71%, 74.29%, 60.00%, and 48.57%; and the secondary patency rates were 85.71%, 80.00%, 71.43%, and 60.00%. In the GAVG group, the primary patency rates were 73.03%, 53.93%, 59.42%, and 38.20%; the assisted primary patency rates were 83.15%, 68.54%, 59.55%, and 53.93%; and the secondary patency rates were 85.39%, 77.53%, 68.54%, and 62.92%, respectively. In the BVVG group, the primary patency rates were 67.24%, 53.45%, 41.38%, and 29.31%; the assisted primary patency rates were 84.48%, 67.24%, 55.17%, and 44.83%; and the secondary patency rates were 86.21%, 81.03%, 68.97%, and 60.34%, respectively. The differences in patency rates across the three grafts were not statistically significant. Overall, 18, 4, and 12 patients in the GPVG, GAVG, and BVVG groups, respectively, experienced seroma. Among the three grafts, GORE ACUSEAL had the shortest anastomosis hemostatic time. The first cannulation times for the three grafts were GPVG at 16 (±8.2), GAVG at 4 (±4.9), and BVVG at 18 (±12.7) days. No significant difference was found in the postoperative swelling rate between the GPVG group and the other two groups. Furthermore, no statistically significant differences were found across the three graft types regarding postoperative vascular access stenosis and thrombosis, ischemic steal syndrome, pseudoaneurysm, or infection. In conclusion, no statistically significant differences in the postoperative primary, assisted primary, or secondary graft patency rates were observed among the three groups. A shorter anastomosis hemostatic time, first cannulation time, and seroma occurrence were observed with the ACUSEAL graft than with its counterparts. The incidence of upper extremity swelling postoperatively was greater with the PROPATEN graft than with the other grafts. No statistically significant differences were observed among the three grafts regarding the remaining complications.
目前,三种膨体聚四氟乙烯(ePTFE)人工移植物在需要长期血管通路进行血液透析的终末期肾病(ESKD)患者中最常用。然而,比较这三种 ePTFE 移植物的研究有限。本研究比较了三种 ePTFE 人工移植物在上肢动静脉内瘘(AVG)手术中治疗终末期肾病患者的临床疗效和术后并发症。
2016 年 1 月至 2019 年 9 月期间,我院收治的需要上肢 AVG 手术的终末期肾病患者被纳入研究。共有 282 例患者完成了 2 年随访,根据 ePTFE 移植物类型分为三组:GPVG 组采用 PROPATEN 移植物,GAVG 组采用直型 GORE ACUSEAL,BVVG 组采用 VENAFLO II。分析比较了各组的通畅率和与通路相关的并发症发生率。
术后对患者进行随访,术后 6、12、18 和 24 个月采集数据。在 GPVG 组中,相应的随访时间点的主要通畅率分别为 74.29%、65.71%、51.43%和 42.86%;辅助性主要通畅率分别为 85.71%、74.29%、60.00%和 48.57%;二级通畅率分别为 85.71%、80.00%、71.43%和 60.00%。在 GAVG 组中,相应的随访时间点的主要通畅率分别为 73.03%、53.93%、59.42%和 38.20%;辅助性主要通畅率分别为 83.15%、68.54%、59.55%和 53.93%;二级通畅率分别为 85.39%、77.53%、68.54%和 62.92%。在 BVVG 组中,相应的随访时间点的主要通畅率分别为 67.24%、53.45%、41.38%和 29.31%;辅助性主要通畅率分别为 84.48%、67.24%、55.17%和 44.83%;二级通畅率分别为 86.21%、81.03%、68.97%和 60.34%。三种移植物的通畅率差异无统计学意义。
总的来说,GPVG、GAVG 和 BVVG 组分别有 18、4 和 12 例患者发生血清肿。GORE ACUSEAL 移植物的吻合止血时间最短。三组移植物的首次穿刺时间分别为 GPVG 组 16(±8.2)天、GAVG 组 4(±4.9)天和 BVVG 组 18(±12.7)天。GPVG 组与其他两组的术后肿胀率无显著差异。此外,三组移植物的术后血管通路狭窄和血栓形成、缺血性盗血综合征、假性动脉瘤和感染发生率无统计学差异。
综上所述,三组患者术后的主要、辅助性和二级移植物通畅率无统计学差异。ACUSEAL 移植物的吻合止血时间、首次穿刺时间和血清肿发生率均低于其他移植物。PROPATEN 移植物术后上肢肿胀发生率高于其他移植物,但三组移植物的其余并发症发生率无统计学差异。