High-pressure fibrin sealant foam: an effective hemostatic agent for treating severe parenchymal hemorrhage
- PMID: 17583744
- DOI: 10.1016/j.jss.2007.02.012
High-pressure fibrin sealant foam: an effective hemostatic agent for treating severe parenchymal hemorrhage
Abstract
Background: The majority of early trauma deaths are related to uncontrolled, noncompressible, parenchymal hemorrhage from truncal injuries. The purpose of this study was to formulate a fibrin sealant foam (FSF) able to control severe parenchymal bleeding without compression or vascular control.
Materials and methods: FSF with high fibrinogen concentration (20 mg/mL) and low thrombin activity (5 U/mL) was prepared and pressurized by addition of liquid gas propellant. The efficacy of this foam was tested against a severe parenchymal hemorrhage, created by partial resection of liver lobes in anticoagulated rabbits (n = 7) and compared to untreated injury (n = 8) and placebo treatment (n = 7). The hemostatic efficacy of pressurized FSF (n = 8) was also compared to a commercially available liquid fibrin sealant (n = 8) and a developing dry powdered fibrin sealant product (n = 8) in the same model.
Results: The liver injury resulted in 122 +/- 11.5 mL blood loss and death of 75% of untreated rabbits (3.2-3.4 kg) within 1 h. Treatment with placebo foam had no effect on blood loss or mortality rate. Pressurized FSF significantly reduced bleeding, resulting in 56% (P < 0.05) and 66% (P < 0.01) reduction in blood loss as compared to untreated or placebo-treated animals, respectively, and 100% survival (P = 0.008). When pressurized FSF was compared with liquid and powdered forms of fibrin sealant, only foam significantly reduced blood loss (49%, P < 0.05) and mortality rate (54%, P < 0.05) of rabbits as compared to untreated control animals (n = 9).
Conclusion: Biological nature, rapid preparation, coverage of large wound areas, and effective hemostatic properties make pressurized FSF an ideal candidate for treating nonoperable parenchymal injuries in damage control procedures.
Similar articles
-
Development of an animal model for assessment of the hemostatic efficacy of fibrin sealant in vascular surgery.J Surg Res. 2001 Sep;100(1):84-92. doi: 10.1006/jsre.2001.6226. J Surg Res. 2001. PMID: 11516209
-
Comparison of a new hemostatic agent to current combat hemostatic agents in a Swine model of lethal extremity arterial hemorrhage.J Trauma. 2007 Aug;63(2):276-83; discussion 283-4. doi: 10.1097/TA.0b013e3180eea8a5. J Trauma. 2007. PMID: 17693824
-
A novel biologic hemostatic dressing (fibrin patch) reduces blood loss and resuscitation volume and improves survival in hypothermic, coagulopathic Swine with grade V liver injury.J Trauma. 2008 Jan;64(1):75-80. doi: 10.1097/TA.0b013e31815b843c. J Trauma. 2008. PMID: 18188102
-
Fibrin solutions to control hemorrhage in the trauma patient.J Long Term Eff Med Implants. 1998;8(2):161-73. J Long Term Eff Med Implants. 1998. PMID: 10181374 Review.
-
Fibrin sealant: current and potential clinical applications.Blood Coagul Fibrinolysis. 1996 Nov;7(8):737-46. Blood Coagul Fibrinolysis. 1996. PMID: 9034553 Review.
Cited by
-
Hemostatic Antimicrobial Hydrogels Based on Silicon, Iron, Zinc, and Boron Glycerolates for Wound Healing Applications.Gels. 2024 Dec 5;10(12):795. doi: 10.3390/gels10120795. Gels. 2024. PMID: 39727553 Free PMC article.
-
Biomaterials and Advanced Technologies for Hemostatic Management of Bleeding.Adv Mater. 2018 Jan;30(4):10.1002/adma.201700859. doi: 10.1002/adma.201700859. Epub 2017 Nov 22. Adv Mater. 2018. PMID: 29164804 Free PMC article. Review.
-
Development of a fatal noncompressible truncal hemorrhage model with combined hepatic and portal venous injury in normothermic normovolemic swine.PLoS One. 2014 Sep 24;9(9):e108293. doi: 10.1371/journal.pone.0108293. eCollection 2014. PLoS One. 2014. PMID: 25251401 Free PMC article.
-
Recent advances in biopolymer-based hemostatic materials.Regen Biomater. 2022 Sep 21;9:rbac063. doi: 10.1093/rb/rbac063. eCollection 2022. Regen Biomater. 2022. PMID: 36196294 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical