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前瞻性、随机、二期、非劣效性研究,评估局部凝血酶(人)基立福作为血管、肝脏、软组织和脊柱开放手术中止血辅助剂的安全性和有效性。

Prospective, Randomized, Phase II, Non-Inferiority Study to Evaluate the Safety and Efficacy of Topical Thrombin (Human) Grifols as Adjunct to Hemostasis During Vascular, Hepatic, Soft Tissue, and Spinal Open Surgery.

机构信息

Anesthesia Department, Memorial Hermann-Memorial City Medical Center, Houston, TX.

Grifols Bioscience Research Group, Grifols, Barcelona, Spain.

出版信息

J Am Coll Surg. 2019 Nov;229(5):497-507.e1. doi: 10.1016/j.jamcollsurg.2019.07.008. Epub 2019 Jul 31.

Abstract

BACKGROUND

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.

STUDY DESIGN

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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。

研究设计

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。

结果

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。

结论

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。

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