Heyligers Jan M M, Lisman Ton, Verhagen Hence J M, Weeterings Cees, de Groot Philip G, Moll Frans L
Department of Vascular Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
J Vasc Surg. 2008 Feb;47(2):324-9; discussion 329. doi: 10.1016/j.jvs.2007.10.005.
Almost a third of patients who undergo peripheral bypass procedures do not have suitable veins, making the use of prosthetic materials necessary. Prosthetic materials can cause platelet adhesion and activation of the coagulation cascade on the graft. One potential strategy to reduce this thrombogenicity is to covalently bind heparin to the endoluminal surface of grafts. This human in vivo study examined systemic effects of the endoluminal heparin and addressed whether graft implantation results in (1) a measurable reduction of systemic markers of hemostasis activation compared with control grafts and (2) antibody formation against heparin, potentially responsible for heparin-induced thrombocytopenia (HIT).
The study included 20 patients undergoing femoropopliteal bypass grafting, of whom 10 received a standard Gore-Tex Thin Walled Stretch Vascular Graft (W. L. Gore & Associates, Flagstaff, Ariz) and 10 received a heparin-bonded expanded polytetrafluoroethylene (ePTFE) graft (Gore-Tex Propaten Vascular Graft). Blood samples were drawn before and directly after the operation and at days 1, 3, 5, and week 6 after surgery. Established markers of in vivo activation of platelets and blood coagulation (prothrombin fragment 1+2, fibrinopeptide A, soluble glycoprotein V, thrombin-antithrombin complexes, and D-dimers) were measured using standard commercially available techniques. Antiplatelet factor 4/heparin antibody titers were measured using a commercially available enzyme-linked immunosorbent assay, and platelet counts were determined.
No statistical differences were observed in any of the markers of in vivo activation of platelets and blood coagulation between patients receiving Propaten or control ePTFE. Moreover, no antibodies against heparin could be demonstrated up to 6 weeks after implantation.
No measurable effect of heparin immobilization on systemic markers of hemostasis was found using a heparin-bonded ePTFE graft in vivo. Also, no antibodies against heparin could be detected up to 6 weeks after implantation.
近三分之一接受外周旁路手术的患者没有合适的静脉,因此必须使用人工血管材料。人工血管材料可导致血小板黏附并激活移植物上的凝血级联反应。一种降低这种血栓形成倾向的潜在策略是将肝素共价结合到移植物的腔内表面。这项人体体内研究考察了腔内肝素的全身效应,并探讨了移植物植入是否会导致:(1)与对照移植物相比,可测量的全身止血激活标志物减少;(2)产生针对肝素的抗体,这可能是肝素诱导的血小板减少症(HIT)的原因。
该研究纳入了20例行股腘动脉旁路移植术的患者,其中10例接受标准的戈尔特斯薄壁拉伸血管移植物(W.L.戈尔公司,亚利桑那州弗拉格斯塔夫),10例接受肝素结合的膨体聚四氟乙烯(ePTFE)移植物(戈尔特斯Propaten血管移植物)。在手术前、手术后即刻以及术后第1天、第3天、第5天和第6周采集血样。使用标准的商业可用技术测量已确定的体内血小板激活和血液凝固标志物(凝血酶原片段1+2、纤维蛋白肽A、可溶性糖蛋白V、凝血酶 - 抗凝血酶复合物和D - 二聚体)。使用市售的酶联免疫吸附测定法测量抗血小板因子4/肝素抗体滴度,并测定血小板计数。
接受Propaten移植物或对照ePTFE的患者之间,在任何体内血小板激活和血液凝固标志物方面均未观察到统计学差异。此外,植入后长达6周均未检测到针对肝素的抗体。
在体内使用肝素结合的ePTFE移植物未发现肝素固定对全身止血标志物有可测量的影响。此外,植入后长达6周未检测到针对肝素的抗体。