The FINISH-3 Trial: A Phase 3, International, Randomized, Single-Blind, Controlled Trial of Topical Fibrocaps in Intraoperative Surgical Hemostasis

被引:23
作者
Bochicchio, Grant V. [1 ]
Gupta, Navyash [2 ]
Porte, Robert J. [3 ]
Renkens, Kenneth L. [4 ]
Pattyn, Piet [5 ]
Topal, Baki [7 ]
Troisi, Roberto Ivan [6 ]
Muir, William [8 ]
Chetter, Ian [9 ]
Gillen, Daniel L. [10 ]
Zuckerman, Linda A. [11 ,12 ]
Frohna, Paul A. [11 ,12 ]
机构
[1] Washington Univ, Sch Med, Dept Surg, Sect Acute & Crit Care Surg, St Louis, MO 63110 USA
[2] North Shore Univ Hlth Syst, Dept Vasc Surg, Skokie, IL USA
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Hepatopancreatobiliary Surg & Liver Transpla, Groningen, Netherlands
[4] Indiana Spine Grp, Indianapolis, IN USA
[5] Univ Hosp Ghent, Dept Surg, Ghent, Belgium
[6] UZ Ghent, Dept Gen & Hepatobiliary Surg, Ghent, Belgium
[7] Univ Hosp Gasthuisberg, Dept Abdominal Surg, Leuven, Belgium
[8] Spine Surg, Las Vegas, NV USA
[9] Univ Hull, Dept Vasc Surg, Kingston Upon Hull, East Yorkshire, England
[10] Univ Calif Irvine, Dept Stat, Irvine, CA USA
[11] ProFibrix Inc, Clin Dev, Seattle, WA USA
[12] Medicines Co, Seattle, WA 98109 USA
关键词
FIBRIN SEALANT; LIVER RESECTION; CLINICAL-TRIAL; EFFICACY; SAFETY; ADHESIVES;
D O I
10.1016/j.jamcollsurg.2014.09.019
中图分类号
R61 [外科手术学];
学科分类号
摘要
BACKGROUND: This Phase 3, international, randomized, single-blind, controlled trial (FINISH-3) compared the efficacy and safety of Fibrocaps, a ready-to-use, dry-powder fibrin sealant containing human plasma-derived thrombin and fibrinogen, vs gelatin sponge alone for use as a hemostat for surgical bleeding in 4 indications (ie, spinal, hepatic, vascular, soft tissue dissection). STUDY DESIGN: Adults with mild to moderate surgical bleeding (randomized 2: 1; Fibrocaps vs gelatin sponge) were treated at a single bleeding site (day 1). Time to hemostasis (TTH) during 5 minutes was compared (log-rank statistic) within each indication. Safety follow-up continued to day 29. RESULTS: Patients were treated (Fibrocaps, n = 480; gelatin sponge, n = 239) when undergoing spinal (n = 183), vascular (n = 175), hepatic (n = 180), or soft-tissue (n = 181) procedures. Fibrocaps was applied by spray device in 53% of all procedures (94% of hepatic and soft-tissue procedures). Fibrocaps significantly reduced TTH compared with gelatin sponge; estimated hazard ratios were 3.3, 2.1, 2.3, and 3.4 for the 4 surgical indications, respectively (each p < 0.001; primary end point). Fibrocaps significantly reduced median TTH for each indication (p < 0.001) and was superior for secondary efficacy end points of restricted mean TTH (p < 0.001) and probability of hemostasis at 3 (p < 0.001) and 5 (p <= 0.002) minutes. Adverse event incidences were generally similar between treatment arms. Non-neutralizing, anti-thrombin antibodies developed in 2% of Fibrocaps-treated and 3% of gelatin sponge-treated patients. CONCLUSIONS: Fibrocaps was well tolerated and significantly reduced TTH relative to gelatin sponge alone in all 4 surgical indications. These findings demonstrate the broad utility of Fibrocaps as a hemostatic agent for mild to moderate surgical bleeding. ((C) 2015 by the American College of Surgeons)
引用
收藏
页码:70 / 81
页数:12
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