Maintaining long-term vessel patency in microvascular surgery using tissue-type plasminogen activator

J. E. Romano, Merrill A Biel

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

The primary cause of free flap failure remains vascular thrombosis at the microanastomosis site. Four-hour local infusion of tissue plasminogen activator (t-PA) has been proved to effectively lyse thromboses in microvascular studies of animals; however, rethrombosis occurs once the infusion of t-PA has been terminated. The present study was designed to examine the efficacy of 48 hours of a continous local t-PA infusion in maintaining long-term venous patency. Our previously described modified arterial inversion graft reanastomosed into the venous system was used in rabbits to form venous thrombi. Three mg of t-PA was infused over 48 hours in eleven rabbits. Seven of eleven grafts were patent at 48 hours and four remained patent at 1 week. In comparing the patency rates in this study with the overall patency rate using the modified arterial inversion graft model (1/22), there are statistically significant differences at both 48 hours (p < 0.001) and 7 days (p < 0.05). We conclude that lengthening the infusion time of t-PA may increase the long-term patency rate in this animal model.

Original languageEnglish (US)
Pages (from-to)391-395
Number of pages5
JournalOtolaryngology - Head and Neck Surgery
Volume105
Issue number3
DOIs
StatePublished - Jan 1 1991

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