The Methodist Hospital and Weill Medical College of Cornell University, Houston, TX 77030, USA.
J Am Coll Surg. 2013 Sep;217(3):385-93. doi: 10.1016/j.jamcollsurg.2013.02.036.
This study evaluated the hemostatic effectiveness and safety of Fibrin Pad (Omrix Biopharmaceuticals Ltd.) vs absorbable hemostat in patients undergoing nonemergent surgery. Fibrin Pad is a topical absorbable hemostat designed to be effective in a variety of soft tissues and across multiple bleeding intensities.
Patients 18 years and older, requiring abdominal, retroperitoneal, pelvic, or thoracic (noncardiac) surgery and with an appropriate soft-tissue target bleeding site (TBS), were randomized to receive Fibrin Pad or absorbable hemostat (NCT00658723). Patients were stratified by bleeding severity at the TBS. Assessments included percentage of patients achieving hemostasis at 4 minutes after randomization with no rebleeding requiring treatment during the subsequent 6 minutes (primary endpoint), proportion of patients achieving hemostasis at 10 minutes, and incidence of treatment failure.
On the primary endpoint, 98.3% of patients with Fibrin Pad and 53.3% with absorbable hemostat achieved hemostasis at 4 minutes (p < 0.0001). The treatment differential was magnified (efficacy was maintained with Fibrin Pad but decreased with absorbable hemostat) with increasing bleeding intensity: in patients with mild bleeding, 100.0% vs 80.0% achieved hemostasis with Fibrin Pad and absorbable hemostat (p = 0.03), respectively; rates were 96.6% vs 26.7%, respectively (p < 0.0001) with moderate bleeding. Percentages of patients who achieved hemostasis at 10 minutes were: Fibrin Pad, 98.3% and absorbable hemostat, 73.3% (p < 0.0001). Incidences of adverse events were comparable between groups.
Fibrin Pad is superior to absorbable hemostat (SURGICEL Original Absorbable Hemostat [Ethicon]) in soft-tissue bleeding control and is safe and effective as an adjunct for rapidly and reliably achieving hemostasis for soft-tissue bleeding during surgery.
本研究评估了纤维蛋白敷贴(奥米瑞斯生物制药有限公司)与可吸收止血剂在非紧急手术患者中的止血效果和安全性。纤维蛋白敷贴是一种局部可吸收的止血剂,旨在有效应对各种软组织和多种出血强度。
年龄在 18 岁及以上、需要进行腹部、腹膜后、骨盆或胸部(非心脏)手术且有适当软组织靶出血部位(TBS)的患者,随机接受纤维蛋白敷贴或可吸收止血剂(NCT00658723)。患者根据 TBS 的出血严重程度进行分层。评估包括随机分组后 4 分钟时达到止血且随后 6 分钟内无再次出血需要治疗的患者比例(主要终点)、10 分钟时达到止血的患者比例以及治疗失败的发生率。
在主要终点方面,纤维蛋白敷贴组有 98.3%的患者和可吸收止血剂组有 53.3%的患者在 4 分钟时达到止血(p<0.0001)。随着出血强度的增加,治疗差异(纤维蛋白敷贴的疗效保持,而可吸收止血剂的疗效降低)变得更加显著:在轻度出血患者中,纤维蛋白敷贴组和可吸收止血剂组的止血率分别为 100.0%和 80.0%(p=0.03);中度出血患者的止血率分别为 96.6%和 26.7%(p<0.0001)。10 分钟时达到止血的患者比例为:纤维蛋白敷贴组为 98.3%,可吸收止血剂组为 73.3%(p<0.0001)。两组的不良事件发生率相当。
纤维蛋白敷贴在软组织出血控制方面优于可吸收止血剂(爱惜康 Original 可吸收止血剂),是一种安全有效的辅助手段,可快速可靠地实现手术中软组织出血的止血。