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Both tissue-type plasminogen activator and urokinase prevent intraabdominal abscess formation after surgical treatment of peritonitis in the rat.

Authors :
Buyne OR
van Goor H
Bleichrodt RP
Verweij PE
Hendriks T
Source :
Surgery [Surgery] 2008 Jul; Vol. 144 (1), pp. 66-73. Date of Electronic Publication: 2008 May 21.
Publication Year :
2008

Abstract

Background: Prevention of intraabdominal abscess formation constitutes an important goal in treatment of secondary peritonitis. Fibrinolytic therapy may be effective in this respect. The efficacy of recombinant tissue plasminogen activator (rtPA) and urokinase is compared in a preclinical model for surgical treatment of peritonitis.<br />Methods: Peritonitis was induced by intraperitoneal bacterial challenge in male Wistar rats. After 1 hour, surgery was performed. Four groups (n = 20) were treated with one of the following: rtPA, urokinase, streptokinase (a negative protein control), or saline. Blood cultures were taken at 6 and 24 hours; cell counts and cytokine measurements were performed in peritoneal fluid at 1, 3 and 5 days. After 5 days, animals were killed and intraperitoneal abscess formation was analyzed.<br />Results: Both rtPA and urokinase strongly (> 75%) and significantly (P < .05) reduced abscess formation without negative side effects. No bleeding complications were observed. Fibrinolytic therapy altered the intraperitoneal cellular distribution (less neutrophils and more macrophages) but did not essentially alter the courses of interleukin-6 and interleukin-10 (decreasing in time) or tumor necrosis factor-* (increasing in time) levels.<br />Conclusion: Both rtPA and urokinase effectively and safely reduce abscess formation in a rat model for treatment of secondary peritonitis. Fibrinolytic therapy should be further developed for clinical application.

Details

Language :
English
ISSN :
1532-7361
Volume :
144
Issue :
1
Database :
MEDLINE
Journal :
Surgery
Publication Type :
Academic Journal
Accession number :
18571586
Full Text :
https://doi.org/10.1016/j.surg.2008.03.025