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评估可吸收氰基丙烯酸酯用于血管重建的前瞻性随机研究。

Prospective randomized study evaluating an absorbable cyanoacrylate for use in vascular reconstructions.

作者信息

Lumsden Alan B, Heyman Eugene R

机构信息

Division of Vascular Surgery, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

J Vasc Surg. 2006 Nov;44(5):1002-1009; discussion 1009. doi: 10.1016/j.jvs.2006.06.039. Epub 2006 Oct 3.

Abstract

BACKGROUND

An easy-to-use vascular sealant with good safety and efficacy is needed to prevent anastomotic bleeding in vascular surgery. This study evaluated the safety and efficacy of cyanoacrylate surgical sealant in establishing hemostasis of expanded polytetrafluoroethylene to arterial vascular anastomoses in arteriovenous (AV) grafts and femoral bypass grafts.

METHODS

This multicenter, randomized, controlled, open-label study was conducted in a hospital setting at 12 sites: 10 in the United States and 2 in Europe. A total of 151 patients undergoing femoral bypass procedures or AV shunt procedures for hemodialysis access using expanded polytetrafluoroethylene grafts were randomized 2:1 to receive cyanoacrylate surgical sealant or the control (oxidized cellulose) between April 26, 2004, and January 18, 2005. Randomization was stratified by clinical site and type of procedure. After the anastomosis, cyanoacrylate surgical sealant or the control was applied to all anastomosis sites for patients undergoing femoral bypass procedures and to only the arterial anastomosis sites for patients undergoing AV shunt procedures. The primary end point was the elapsed time from clamp release to hemostasis. Secondary end points were the proportion of patients achieving hemostasis at t = 0 (immediate), 1, 5, or 10 minutes after clamp release, use of additional adjunctive measures to achieve hemostasis, and occurrence of adverse events.

RESULTS

Baseline demographics and clinical characteristics showed that the two treatment groups were similar at baseline. The mean time from clamp release to hemostasis was 119.3 seconds with cyanoacrylate surgical sealant vs 403.8 seconds with the control (P < .001). Immediate hemostasis was achieved in 54.5% of patients receiving cyanoacrylate surgical sealant and in 10% of those receiving the control. The proportion of patients requiring additional adjunctive measures was lower with cyanoacrylate surgical sealant, and the occurrence of adverse events was similar in both groups.

CONCLUSIONS

This study demonstrates that cyanoacrylate surgical sealant is effective at reducing the time to hemostasis and achieving immediate hemostasis in AV shunt and femoral bypass procedures and that it is safe for internal use. Cyanoacrylate surgical sealant is an easy-to-use vascular sealant with good safety and efficacy that significantly decreases anastomotic bleeding in vascular surgery.

摘要

背景

血管外科手术中需要一种易于使用且安全性和有效性良好的血管密封剂来预防吻合口出血。本研究评估了氰基丙烯酸酯手术密封剂在建立动静脉(AV)移植物和股动脉旁路移植术中扩张聚四氟乙烯与动脉血管吻合口止血方面的安全性和有效性。

方法

这项多中心、随机、对照、开放标签研究在12个地点的医院环境中进行:美国10个,欧洲2个。2004年4月26日至2005年1月18日期间,共有151例使用扩张聚四氟乙烯移植物进行股动脉旁路手术或AV分流手术以建立血液透析通路的患者,按2:1随机分组,分别接受氰基丙烯酸酯手术密封剂或对照(氧化纤维素)治疗。随机分组按临床地点和手术类型进行分层。吻合术后,氰基丙烯酸酯手术密封剂或对照应用于接受股动脉旁路手术患者的所有吻合口部位,以及接受AV分流手术患者的仅动脉吻合口部位。主要终点是从松开血管夹到止血的时间。次要终点是在松开血管夹后t = 0(即时)、1、5或10分钟达到止血的患者比例、使用额外辅助措施来实现止血的情况以及不良事件的发生。

结果

基线人口统计学和临床特征表明,两个治疗组在基线时相似。使用氰基丙烯酸酯手术密封剂时,从松开血管夹到止血的平均时间为119.3秒,而对照组为403.8秒(P <.001)。接受氰基丙烯酸酯手术密封剂的患者中有54.5%实现了即时止血,而接受对照的患者中这一比例为10%。使用氰基丙烯酸酯手术密封剂的患者需要额外辅助措施的比例较低,两组不良事件的发生率相似。

结论

本研究表明,氰基丙烯酸酯手术密封剂在AV分流和股动脉旁路手术中可有效缩短止血时间并实现即时止血,且内部使用安全。氰基丙烯酸酯手术密封剂是一种易于使用且安全性和有效性良好的血管密封剂,可显著减少血管手术中的吻合口出血。

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