Pfizer, Inc, Cary, NC, USA.
Clin Appl Thromb Hemost. 2011 Nov-Dec;17(6):620-32. doi: 10.1177/1076029611405187. Epub 2011 May 18.
Topical bovine thrombin has been associated with immune responses and anecdotal reports of coagulopathy. This open-label study assessed the impact on clinical hemostasis of human antibodies to bovine thrombin (aBT) or factor V/Va (aBV/Va) in response to topical bovine thrombin (THROMBIN-JMI) in patients both with and without preexisting anti-bovine antibodies. Noninferiority analysis assessed primary endpoint for mean shift from baseline activated partial thromboplastin time (aPTT) at 48 hours postsurgery; secondary endpoints included changes from baseline antibodies/titers and coagulation parameters through 8 weeks postsurgery. A total of 550 patients underwent surgery with THROMBIN-JMI utilized at investigator's discretion. Adjusted mean aPTT change in (+)aBT/(+)THROMBIN-JMI cohort was greater than (-)aBT/(-)THROMBIN-JMI cohort; 4.67-second upper confidence bound exceeded 4.5-second margin (based on assumed mean aPTT of 30 seconds) and noninferiority was not met. Post hoc analysis indicated noninferiority would have been met had noninferiority margin been set prior at relative 15% of actual baseline aPTT. Antibodies/titers were unchanged by THROMBIN-JMI exposure 48 hours postsurgery and unrelated to postsurgical changes in coagulation. Thus, THROMBIN-JMI exposure in patients with/without preexisting aBT or aBV/Va does not alter hemostasis.
局部牛凝血酶已与免疫反应和凝血病的传闻报告相关。这项开放性研究评估了在有或没有预先存在抗牛抗体的患者中,局部牛凝血酶(THROMBIN-JMI)引起的人抗牛凝血酶(aBT)或因子 V/Va(aBV/Va)抗体对临床止血的影响。非劣效性分析评估了术后 48 小时从基线激活部分凝血活酶时间(aPTT)的平均偏移的主要终点;次要终点包括术后 8 周从基线抗体/滴度和凝血参数的变化。共有 550 例患者接受了手术,研究者自行决定使用 THROMBIN-JMI。(+)aBT/(+)THROMBIN-JMI 队列中的调整后平均 aPTT 变化大于(-)aBT/(-)THROMBIN-JMI 队列;上限置信区间为 4.67 秒,超过 4.5 秒的边界(基于假设的平均 aPTT 为 30 秒),非劣效性未达到。事后分析表明,如果在术后 48 小时设定非劣效性边界为实际基线 aPTT 的相对 15%,则可以达到非劣效性。THROMBIN-JMI 暴露后 48 小时,抗体/滴度未发生变化,与术后凝血变化无关。因此,THROMBIN-JMI 暴露在有/无预先存在的 aBT 或 aBV/Va 的患者中不会改变止血。