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The Journal of Thoracic and Cardiovascular Surgery, Vol 93, 120-126, Copyright © 1987 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
KH Teoh, SE Fremes, RD Weisel, GT Christakis, SJ Teasdale, MM Madonik, J Ivanov, AV Mee and PY Wong
Cardiac surgery stimulates the systemic synthesis of prostacyclin and
thromboxane A2, but the cardiac release of these prostanoids has been
reported infrequently. Fifty-four patients undergoing elective coronary
artery bypass had coronary sinus catheters inserted to evaluate the cardiac
release of the stable metabolites of prostacyclin (6-keto- prostaglandin F1
alpha) and thromboxane A2 (thromboxane B2). Arterial concentrations of
6-keto-prostaglandin F1 alpha and thromboxane B2 were elevated after
cardiac cannulation and during cardiopulmonary bypass. The cardiac release
of 6-keto-prostaglandin F1 alpha was observed after cannulation and during,
but not after, cardiopulmonary bypass. Cardiac thromboxane B2 release was
detected after cross-clamp release and persisted during the early
postoperative period when cardiac 6-keto- prostaglandin F1 alpha release
was no longer detectable. Cardiopulmonary bypass stimulated the systemic
production of thromboxane and prostacyclin. The cardiac release of
thromboxane was unopposed by cardiac prostacyclin production in the early
postoperative period and may contribute to reperfusion injury.
ARTICLES
Cardiac release of prostacyclin and thromboxane A2 during coronary revascularization
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