Skip to main navigation Skip to search Skip to main content

Comparison of poly-N-acetyl glucosamine with commercially available topical hemostats for achieving hemostasis in coagulopathic models of splenic hemorrhage

  • Steven D. Schwaitzberg
  • , Michele W. Chan
  • , David J. Cole
  • , Marjorie Read
  • , Timothy Nichols
  • , David Bellinger
  • , Raymond J. Connolly
  • Tufts-New England Medical Center
  • Medical University of South Carolina
  • University of North Carolina at Chapel Hill

Research output: Contribution to journalArticlepeer-review

45 Scopus citations

Abstract

Background: The hemostatic quality of the poly-N-acetyl glucosamine (p-GlcNAc) patch was compared with a fibrin sealant, fibrin bandage, and cellulose patch. Methods: A 2 × 2-cm capsular strip to a depth of 3 mm of the swine spleen was used as a source of bleeding. Splenic lacerations were created in hemophilia B dogs and treated with p-GlcNAc and Surgicel. Wounds were created in rabbits and treated with p-GlcNAc at 37°C and after keeping body core temperature at 29°C. Results: Poly-N-acetyl glucosamine was able to achieve hemostasis with greater efficacy than either of the fibrin-based bandages. In the hemophilia B dog study, p-GlcNAc significantly outperformed Surgicel, with p-GlcNAc achieving hemostasis in 75% of the treated wounds compared with 17% for the cellulose patch. The hypothermia study demonstrated that p-GlcNAc is equally effective at 29°C and at 37°C. Conclusion: Poly-N-acetyl glucosamine was effective at controlling bleeding in animals with experimentally induced or genetic coagulopathic disorders.

Original languageEnglish
Pages (from-to)S29-S32
JournalJournal of Trauma
Volume57
Issue number1 SUPPL.
DOIs
StatePublished - Jul 2004

Keywords

  • Cellulose patch
  • Fibrin bandage
  • Fibrin sealant
  • Hypothermia
  • Poly-N-acetyl glucosamine (p-GlcNAc) patch
  • Splenic laceration

Fingerprint

Dive into the research topics of 'Comparison of poly-N-acetyl glucosamine with commercially available topical hemostats for achieving hemostasis in coagulopathic models of splenic hemorrhage'. Together they form a unique fingerprint.

Cite this