Dirkmann Daniel, Britten Martin W, Pauling Henning, Weidle Juliane, Volbracht Lothar, Görlinger Klaus, Peters Jürgen
From the Klinik für Anästhesiologie und Intensivmedizin (D.D., M.W.B., H.P., J.W., K.G., J.P.) and Abteilung für Klinische Chemie (L.V.), Universität Duisburg-Essen and Universitätsklinikum Essen, Essen, Germany.
Anesthesiology. 2016 Jun;124(6):1277-85. doi: 10.1097/ALN.0000000000001076.
Sugammadex prolongs activated partial thromboplastin time (aPTT) and prothrombin time (PT) suggestive of anticoagulant effects. To pinpoint its presumed anticoagulant site of action, the authors assessed Sugammadex's impact on a panel of coagulation assays.
Sugammadex, Rocuronium, Sugammadex and Rocuronium combined, or saline were added to blood samples from healthy volunteers and analyzed using plasmatic (i.e., aPTT, thrombin time, and fibrinogen concentration) (n = 8 each), PT (quick), activities of plasmatic coagulation factors, and whole blood (extrinsically and intrinsically activated thromboelastometry) assays (n = 18 each). Furthermore, dose-dependent effects of Sugammadex were also assessed (n = 18 each) in diluted Russel viper venom time (DRVVT) assays with low (DRVVT1) and high (DRVVT2) phospholipid concentrations and in a highly phospholipid-sensitive aPTT assay.
Sugammadex increased PT (+9.1%; P < 0.0001), aPTT (+13.1%; P = 0.0002), and clotting time in extrinsically (+33.1%; P = 0.0021) and intrinsically (+22.4%; P < 0.0001) activated thromboelastometric assays. Furthermore, activities of factors VIII, IX, XI, and XII decreased (-7%, P = 0.009; -7.8%, P < 0.0001; -6.9%, P < 0.0001; and -4.3%, P = 0.011, respectively). Sugammadex dose-dependently prolonged both DRVVT1 and the highly phospholipid-sensitive aPTT assays, but additional phospholipids in the DRVVT2 assay almost abolished these prolongations. Thrombin time, a thromboelastometric thrombin generation assay, clot firmness, clot lysis, fibrinogen concentration, and activities of other coagulation factors were unaltered. Rocuronium, Sugammadex and Rocuronium combined, and saline exerted no effects.
Sugammadex significantly affects various coagulation assays, but this is explainable by an apparent phospholipid-binding effect, suggesting that Sugammadex`s anticoagulant effects are likely an in vitro artifact.
舒更葡糖可延长活化部分凝血活酶时间(aPTT)和凝血酶原时间(PT),提示有抗凝作用。为确定其假定的抗凝作用位点,作者评估了舒更葡糖对一组凝血试验的影响。
将舒更葡糖、罗库溴铵、舒更葡糖与罗库溴铵联合制剂或生理盐水加入健康志愿者的血样中,采用血浆检测法(即aPTT、凝血酶时间和纤维蛋白原浓度)(每组n = 8)、PT(快速法)、血浆凝血因子活性检测法以及全血检测法(外源性和内源性激活血栓弹力图法)(每组n = 18)进行分析。此外,还在低磷脂浓度(DRVVT1)和高磷脂浓度(DRVVT2)的稀释蝰蛇毒时间(DRVVT)试验以及高度磷脂敏感的aPTT试验中评估了舒更葡糖的剂量依赖性效应(每组n = 18)。
舒更葡糖使PT延长(+9.1%;P < 0.0001)、aPTT延长(+13.1%;P = 0.0002),外源性激活血栓弹力图法的凝血时间延长(+33.1%;P = 0.0021),内源性激活血栓弹力图法的凝血时间延长(+22.4%;P < 0.0001)。此外,凝血因子VIII、IX、XI和XII 的活性降低(分别为-7%,P = 0.009;-7.8%,P < 0.0001;-6.9%,P < 0.0001;-4.3%,P = 0.011)。舒更葡糖剂量依赖性地延长DRVVT1和高度磷脂敏感的aPTT试验时间,但在DRVVT2试验中添加额外磷脂几乎消除了这些延长作用。凝血酶时间、血栓弹力图凝血酶生成试验、血凝块硬度、血凝块溶解、纤维蛋白原浓度以及其他凝血因子的活性均未改变。罗库溴铵、舒更葡糖与罗库溴铵联合制剂以及生理盐水均无影响。
舒更葡糖对多种凝血试验有显著影响,但这可以通过明显的磷脂结合效应来解释,提示舒更葡糖的抗凝作用可能是体外假象。