A Comparison of Efficacy, Safety and Cost Between MANTATM and Proglide Vascular Closure Devices Following Transfemoral Transcatheter Aortic Valve Implantation

N. Ali, C. Dospinescu, M. Cunnington, C. Malkin, D. Blackman
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引用次数: 3

Abstract

Aims Access site vascular complications remain a recognised complication following transcatheter aortic valve implantation (TAVI). Suture-based vascular closure devices (VCDs) such as ProGlide® (Abbott Vascular Inc., Santa Clara, CA, USA) are widely used in order to achieve rapid haemostasis. The MANTATM (Essential Medical Inc., Malvern, PA, USA) is a collagen plug-based VCD which can be used as an alternative to traditional suture-based devices, but is significantly more expensive per-unit. We compare the efficacy, safety and total cost associated with the use of the MANTATM and ProGlide® VCDs. Methods This retrospective study included all consecutive patients who underwent transfemoral (TF) TAVI between November 2017-June 2018. The primary endpoints were primary access site-related VARC-2 vascular complications, VARC-2 bleeding and the overall per-patient cost incorporating treatment for complications or use of additional VCDs. Results A total of 136 patients were included in this study; 86 in the ProGlide® group and 50 in the MANTATM group. Baseline characteristics of the two groups were well-matched. Three patients in the ProGlide® group required surgical repair compared to none in the MANTATM group. However, no significant differences were observed with respect to overall primary access site-related VARC-2 vascular complications (10.5% vs. 10%; p=0.93) or VARC-2 bleeding (9.3% vs. 4.0%; p=0.25). There was no significant difference in the mean cost per patient when taking into consideration the use of additional VCDs and treatments for vascular complications (£568.79 vs. £599.95; p=0.90). Conclusion The use of the MANTATM VCD following TF TAVI is cost-neutral compared to ProGlide® VCDs, whilst being associated with no increase in VARC-2 vascular or bleeding complications.
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经股动脉主动脉瓣植入术后MANTATM与Proglide血管关闭装置的疗效、安全性和成本比较
目的经导管主动脉瓣植入术(TAVI)后,通路部位血管并发症仍然是公认的并发症。基于缝合的血管闭合装置(vcd),如ProGlide®(Abbott vascular Inc., Santa Clara, CA, USA)被广泛用于实现快速止血。MANTATM (Essential Medical Inc., Malvern, PA, USA)是一种基于胶原蛋白插入的VCD,可以作为传统基于缝合线的设备的替代品,但单位价格要贵得多。我们比较了使用MANTATM和ProGlide®vcd的有效性、安全性和总成本。方法:本回顾性研究纳入2017年11月至2018年6月期间所有连续接受经股(TF) TAVI的患者。主要终点是主要通路部位相关的VARC-2血管并发症、VARC-2出血和合并并发症治疗或使用额外vcd的每位患者总成本。结果本研究共纳入136例患者;ProGlide组86例,MANTATM组50例。两组患者的基线特征吻合良好。ProGlide组中有3例患者需要手术修复,而MANTATM组中没有患者需要手术修复。然而,在总体主要通路部位相关的VARC-2血管并发症方面,没有观察到显著差异(10.5% vs 10%;p=0.93)或VARC-2出血(9.3% vs. 4.0%;p = 0.25)。考虑到额外vcd的使用和血管并发症的治疗,每位患者的平均费用没有显著差异(568.79英镑vs 599.95英镑;p = 0.90)。结论:与ProGlide®VCD相比,在TF TAVI后使用MANTATM VCD是成本中性的,同时没有增加VARC-2血管或出血并发症。
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