Published July 2, 2018 | Version v.1
Journal article Open

A Prospective, Randomized, Phase III Study to Evaluate the Efficacy and Safety of Fibrin Sealant Grifols as an Adjunct to Hemostasis as Compared to Cellulose Sheets in Hepatic Surgery Resections

  • 1. Department for Minimally Invasive Upper Digestive Surgery, Clinical Center of Serbia, Hospital for Digestive Surgery - First Surgical Hospital, Dr Koste Todorovica Street No 66, Belgrade 11000, Serbia
  • 2. Bioscience Research Group, Grifols, Barcelona, Spain
  • 3. Division of Transplantation and Advanced Hepatobiliary Surgery, Department of Surgery, University of Utah School of Medicine, Salt Lake City, UT, USA
  • 4. HBP unit Clinical Center Niš, General Surgery Clinic, Niš, Serbia
  • 5. Department of Surgery, Medical School, University of Pécs, Pécs, Hungary
  • 6. Clinic of Surgical Oncology, Institute of Oncology and Radiology of Serbia, Belgrade, Serbia
  • 7. Department of Surgery, University of Wisconsin Hospital and Clinics, Madison, WI, USA
  • 8. Department of Surgery: Transplant&Immunology, Yale-NewHaven Hospital, New Haven, CT, USA
  • 9. Division of Multi-Organ Transplantation and Hepato-Pancreato-Biliary Surgery, Department of Surgery, Drexel University College of Medicine, Philadelphia, PA, USA

Description

Background Local hemostatic agents have a role in limiting bleeding complications associated with liver resection. Methods In this randomized, phase III study, we compared the efficacy and safety of Fibrin Sealant Grifols (FS Grifols) with oxidized cellulose sheets (Surgicel®) as adjuncts to hemostasis during hepatic resections. The primary efficacy endpoint was the proportion of patients achieving hemostasis at target bleeding sites (TBS) within 4 min (T4) of treatment application. Secondary efficacy variables were time to hemostasis (TTH) at a later time point if re-bleeding occurs and cumulative proportion of patients
achieving hemostasis by time points T2, T3, T5, T7, and T10. Results The rate of hemostasis by T4 was 92.8% in the FS Grifols group (n = 163) and 80.5% in the Surgicel® group (n = 162) (p = 0.01). The mean TTH was significantly shorter (p < 0.001) in the FS Grifols group (2.8 ± 0.14 vs. 3.8 ± 0.24 min). The rate of
hemostasis by T2, T5, and T7 was higher and statistically superior in the FS Grifols group compared to Surgicel®. No substantial differences in adverse events (AE) were noted between treatment groups. The most common AEs were procedural pain (36.2 vs. 37.7%), nausea (20.9 vs. 23.5%), and hypotension (14.1 vs 6.2%). Conclusions FS Grifols was safe and well-tolerated as a local hemostatic agent during liver resection surgeries. Overall, data demonstrate that the hemostatic efficacy of FS Grifols is superior to Surgicel® and support the use of FS Grifols as an effective local hemostatic agent in these surgical procedures.

Notes

The following centers of the Fibrin Sealant on Hepatic Resection Clinical Investigation Study Group that contributed with patients are acknowledged: Vanderbilt University Medical Center, Nashville, TN, USA; Thomas Jefferson University, Philadelphia, PA, USA; Washington University School of Medicine, St Louis, MO, USA; Scientific Research Institute of Oncology n.a. N.N. Petrov, Moscow, Russia; Columbia University Medical Center, Center for Liver Disease and Transplantation, New York, NY, USA; Georgia Regents University, Augusta, GA, USA; Ann and Robert Lurie Children's Hospital of Chicago, Chicago, Il, USA; University of Nevada School of Medicine, Las Vegas, NV, USA; Federal State Budgetary Scientific Institution Russian Oncological Scientific Center n.a. N.N. Blokhin, Moscow, Russia; Carolinas Medical Center, Charlotte, NC, USA; Milton S. Hershey Medical Center, Hershey, PA, USA; Medical University of South Carolina, Charleston, SC, USA; Methodist University Hospital, Memphis, TN, USA; Walter Reed National Military Medical Center, Bethesda, MD, USA; University Children's Hospital, Belgrade, Serbia; Institute for Health Protection of Children and Youth of Vojvodina, Vojvodina, Serbia; and Semmelweis University, Budapest, Hungary . Funding: Fibrin Sealant GRIFOLS

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