Sullivan Breanna, Desai Sanjay, Singh Tej M, Mitra Amit
1 The University of Chicago, Chicago, IL, USA.
2 MS Ramaiah Medical College, Bangalore, India.
J Vasc Access. 2019 Mar;20(2):146-152. doi: 10.1177/1129729818787717. Epub 2018 Aug 13.
: Radiocephalic fistulas are the preferred type of arteriovenous fistula due to their advantageous location. However, radiocephalic fistula maturation has historically been inferior to brachiocephalic fistulas. Research indicates that intermittent compression may aid in forearm vein dilation. Early use of a compression device may assist radiocephalic fistula maturation.
: This prospective, randomized, placebo controlled study evaluates device safety and the effect of intermittent compression on vein size of radiocephalic fistulas and brachiocephalic fistulas.
: This was an institutional review board-approved study. After fistula creation, a novel, intermittent pneumatic compression device (Fist Assist) was worn 15 cm proximal to fistulas 6 h daily for 30 days. Those in the treatment group (n = 43) wore Fist Assist (24 with brachiocephalic fistulas and 19 with radiocephalic fistulas). Clinical controls (n = 16) wore a sham device. Vein diameter was measured at 0 and 30 days by duplex measurement. Percentage increase was recorded and tested for significance.
: After 30 days, the mean percentage increase in vein diameter in the radiocephalic fistula treatment group was significantly larger than brachiocephalic fistulas in the treatment group at all proximal locations from the anastomosis. Increases in percentage vein dilation for those in the radiocephalic fistula treatment group were significantly larger than those in the control group. All fistulas treated with Fist Assist are still functional with no reported complications.
: Early application of the Fist Assist device may be more effective at helping radiocephalic fistula mature as compared to brachiocephalic fistulas. Successful radiocephalic fistula maturation may decrease vascular access costs, reduce complications, and preserve upper arm veins for future use in vascular access.
由于其有利的位置,桡动脉头静脉内瘘是动静脉内瘘的首选类型。然而,桡动脉头静脉内瘘的成熟度在历史上一直不如肱动脉头静脉内瘘。研究表明,间歇性压迫可能有助于前臂静脉扩张。早期使用压迫装置可能有助于桡动脉头静脉内瘘的成熟。
这项前瞻性、随机、安慰剂对照研究评估了一种装置的安全性以及间歇性压迫对桡动脉头静脉内瘘和肱动脉头静脉内瘘静脉大小的影响。
这是一项经机构审查委员会批准的研究。在建立内瘘后,一种新型的间歇性气动压迫装置(Fist Assist)在距离内瘘近端15厘米处佩戴,每天6小时,持续30天。治疗组(n = 43)佩戴Fist Assist(24例为肱动脉头静脉内瘘,19例为桡动脉头静脉内瘘)。临床对照组(n = 16)佩戴假装置。在第0天和第30天通过双功超声测量静脉直径。记录直径增加的百分比并进行显著性检验。
30天后,桡动脉头静脉内瘘治疗组在吻合口近端所有位置的静脉直径平均增加百分比均显著大于治疗组中的肱动脉头静脉内瘘。桡动脉头静脉内瘘治疗组的静脉扩张百分比增加显著大于对照组。所有接受Fist Assist治疗的内瘘仍在发挥功能,未报告并发症。
与肱动脉头静脉内瘘相比,早期应用Fist Assist装置可能更有效地帮助桡动脉头静脉内瘘成熟。成功的桡动脉头静脉内瘘成熟可能会降低血管通路成本,减少并发症,并保留上臂静脉以备将来用于血管通路。