Anesthesia Department, Memorial Hermann-Memorial City Medical Center, Houston, TX.
Grifols Bioscience Research Group, Grifols, Barcelona, Spain.
J Am Coll Surg. 2019 Nov;229(5):497-507.e1. doi: 10.1016/j.jamcollsurg.2019.07.008. Epub 2019 Jul 31.
Thrombin-based formulations have been used for topical hemostasis in surgery for decades. However, the number of randomized clinical trials comparing bovine vs human thrombin is limited.
A randomized, double-blind, non-inferiority phase II study evaluated the hemostatic efficacy and safety of plasma-derived topical thrombin (human) Grifols (TTH-Grifols; Instituto Grifols SA) vs bovine THROMBIN JMI (BT-JMI; GenTrac Inc) (2:1 ratio) in vascular, hepatic, soft tissue, and spinal operations. The primary efficacy end point was the percentage of patients achieving hemostasis at target bleeding sites with mild to moderate bleeding (response) within 5 minutes (T) of treatment application. Non-inferiority was met if the lower limit of the 95% CI of the response ratio of TTH-Grifols relative to BT-JMI by T exceeded 0.8. Secondary efficacy variables were the cumulative response by 3 and 4 minutes (T and T), and the number of treatment failures. Safety parameters were assessed.
Randomized patients in TTH-Grifols and BT-JMI groups were n = 137 and n = 68, respectively. In modified intention-to-treat population, rates of hemostasis by T were 78.3% (94 of 120) in TTH-Grifols and 80.3% (49 of 61) in BT-JMI (response ratio: 0.973; 95% CI 0.833 to 1.135). Rates of hemostasis in vascular, hepatic, soft tissue, and spinal operations ranged from 75.0% to 82.5% for TTH-Grifols and from 54.5% to 91.7% for BT-JMI. No significant differences in adverse events were observed between treatment groups. Antibodies to bovine factor V antigen were detected in 2 patients exposed to BT-JMI and in none exposed to TTH-Grifols.
The TTH-Grifols was safe and well tolerated as a local hemostatic agent and was non-inferior to BT-JMI. No antibodies to thrombin developed in TTH-Grifols-treated patients.
几十年来,基于凝血酶的制剂一直被用于手术中的局部止血。然而,比较牛源和人源凝血酶的随机临床试验数量有限。
一项随机、双盲、非劣效性 II 期研究评估了血浆来源的局部凝血酶(人源)Grifols(TTH-Grifols;Instituto Grifols SA)与牛源凝血酶 JMI(BT-JMI;GenTrac Inc)(2:1 比例)在血管、肝脏、软组织和脊柱手术中的止血效果和安全性。主要疗效终点是治疗应用后 5 分钟(T)内达到轻度至中度出血(有反应)的目标出血部位的患者比例(反应)。如果 TTH-Grifols 相对于 BT-JMI 的反应率的 95%CI 下限通过 T 超过 0.8,则符合非劣效性。次要疗效变量是 3 分钟和 4 分钟(T 和 T)的累积反应率,以及治疗失败的数量。评估了安全性参数。
TTH-Grifols 和 BT-JMI 组随机患者分别为 n=137 和 n=68。在改良意向治疗人群中,TTH-Grifols 的止血率为 78.3%(120 例中的 94 例),BT-JMI 的止血率为 80.3%(61 例中的 49 例)(反应比:0.973;95%CI 0.833 至 1.135)。TTH-Grifols 在血管、肝脏、软组织和脊柱手术中的止血率范围为 75.0%至 82.5%,BT-JMI 的止血率范围为 54.5%至 91.7%。两组间不良反应无显著差异。暴露于 BT-JMI 的 2 例患者和未暴露于 TTH-Grifols 的患者均检测到针对牛源因子 V 抗原的抗体。
TTH-Grifols 作为一种局部止血剂是安全且耐受良好的,并且不劣于 BT-JMI。在 TTH-Grifols 治疗的患者中未发现针对凝血酶的抗体。