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The Journal of Thoracic and Cardiovascular Surgery, Vol 101, 654-660, Copyright © 1991 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
V Videm, TE Mollnes, P Garred and JL Svennevig
Oxygenator/tubing sets coated with endpoint-attached heparin were compared
to uncoated sets in a dynamic model of extracorporeal circulation.
Biocompatibility was assessed by evaluations of complement activation and
platelet loss. The median concentration of C3 activation products increased
gradually from 12 AU/ml at baseline to 65 AU/ml after 120 minutes in the
uncoated sets and from 12 AU/ml to 19 AU/ml after 120 minutes in the coated
sets (p less than 0.002). The median concentration of the terminal
complement complex in the uncoated sets increased gradually from 3.1 AU/ml
at baseline to 18.2 AU/ml after 120 minutes. In the coated sets the
terminal complement complex reached a peak of 12.0 AU/ml at 15 minutes and
returned to baseline values at 60 minutes. Median platelet loss at 120
minutes was 166 x 10(9) in the uncoated and 21 x 10(9) in the coated sets
(p less than 0.01). Heparin coating thus improved biocompatibility by
reducing both complement activation and platelet loss.
ARTICLES
Biocompatibility of extracorporeal circulation. In vitro comparison of heparin-coated and uncoated oxygenator circuits
Institute for Experimental Medical Research, Ullevaal Hospital, Oslo, Norway.
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