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The Journal of Thoracic and Cardiovascular Surgery, Vol 77, 119-126, Copyright © 1979 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
VP Addonizio Jr, JF Strauss 3d, RW Colman and LH Edmunds Jr
Temporary inhibition of platelet function with prostaglandin E1 (PGE1)
prevents platelets loss and functional alterations during extracorporeal
circulation with a membrane oxygenator. This study evaluated the ability of
PGE1 to prevent platelet injury in circuits containing a bubble oxygenator.
During in vitro recirculation of human blood, the circulating platelet
count, expressed as a percent of initial levels, decreased to 29%;
platelets became insensitive to adenosine diphosphate (ADP) and to
epinephrine; and plasma levels of low-affinity platelet factor 4 (LA-PF4)
progressively rose to 7.4 microgram per milliliter. With PGE1 (1.2 micron),
platelet counts remained stable at 92%; platelet reactivity remained normal
for 1 hour; and plasma levels of LA-PF4 rose to only 3.3 microgram per
milliliter. In rhesus monkeys that underwent cardiopulmonary bypass using a
bubble oxygenator without PGE1, platelet counts, expressed as a percent of
the prebypass platelet count, declined to 38%; platelets became insensitive
to ADP; plasma levels of LA-PF4 progressively rose to 8.4 microgram per
milliliter; and the mean postoperative bleeding time was 4.6 minutes. In
monkeys that received PGE1, platelet counts declined to only 65%; platelets
remained threefold more sensitive to ADP; platelets demonstrated delayed
release of LA-PF4 and the mean postoperative bleeding time was 2.7 minutes.
This report demonstrates that in a bubble oxygenator system, PGE1 reduces
platelet loss, mitigates platelet injury, and shortens postoperative
bleeding times following extracorporeal circulation.
ARTICLES
Effects of prostaglandin E1 on platelet loss during in vivo and in vitro extracorporeal circulation with a bubble oxygenator
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