Stability of fibrin sealant in cerebrospinal fluid: an in vitro study.

Published

Journal Article

OBJECTIVE: The in vitro stability of fibrin sealant in cerebrospinal fluid (CSF) was investigated to verify the efficacy of intracranial application of fibrin sealant. METHODS: Human CSF was collected from 11 patients. Fibrin glue spheres (diameter, 5 mm) were incubated in CSF specimens at 37 degrees C. At 2, 4, 8, 24, and 48 hours, the diameter of the spheres was measured and the ultrastructure was evaluated by transmission electron microscopy. A control group consisted of sealant spheres in physiological saline (n = 2). RESULTS: In all CSF samples, the fibrin sealant did not degrade with time. The size, consistency, color, and shape of the sealant remained unchanged, even 48 hours after placement in the CSF. Transmission electron microscopic analysis of the fibrin sealant revealed an amorphous, fibrinous meshwork. No morphological differences existed between fibrin sealant complex placed in the CSF for different time periods and sealant placed in physiological saline. CONCLUSION: Within the limitations of this in vitro study, human CSF has no adverse effects on fibrin sealant in terms of alteration of structure and morphology. Fibrin sealant is stable in a CSF environment and can be effectively used in the cisternal or subarachnoidal space.

Full Text

Duke Authors

Cited Authors

  • Menovsky, T; de Vries, J; van den Bergh Weerman, M; Grotenhuis, JA

Published Date

  • December 2002

Published In

Volume / Issue

  • 51 / 6

Start / End Page

  • 1453 - 1455

PubMed ID

  • 12445351

Pubmed Central ID

  • 12445351

International Standard Serial Number (ISSN)

  • 0148-396X

Language

  • eng

Conference Location

  • United States