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Eur J Cardiothorac Surg ; 15(3): 346-52, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10333034

ABSTRACT

BACKGROUND: Acute pulmonary hypertension occurring after cardiopulmonary bypass can be a cause of post-operative morbidity and mortality. The purpose of this study was to investigate whether bosentan, a non-peptidic mixed endothelin antagonist affected the pulmonary hypertension induced by experimental cardiopulmonary bypass. METHODS: Pigs were anesthetized and instrumented to determine hemodynamic measurements. Pigs were randomized to receive either 3 mg/kg bolus + 7 mg/kg per h bosentan (n = 8) or saline (n = 7). All pigs underwent 90 min of cardiopulmonary bypass and were further observed for a 120-min period. RESULTS: In the control group, cardiopulmonary bypass induced a dramatic pulmonary hypertension (+78 +/- 13%, P < 0.005) and accompanied an increase of pulmonary vascular resistance (+228 +/- 50%, P < 0.005), whereas, in the treated group, bosentan completely prevented these deleterious effects of cardiopulmonary bypass with only a moderate decrease of systemic vascular resistance (-19 +/- 14.6%, P < 0.05). CONCLUSIONS: The present findings support the hypothesis that endogenous endothelin is a mediator of acute pulmonary hypertension occurring after cardiopulmonary bypass. Bosentan, a mixed endothelin antagonist completely prevented pulmonary hypertension after cardiopulmonary bypass and may, therefore, have therapeutic applications in the management of patients following cardiac surgery.


Subject(s)
Antihypertensive Agents/therapeutic use , Endothelin-1/physiology , Hypertension, Pulmonary/physiopathology , Sulfonamides/therapeutic use , Acute Disease , Animals , Antihypertensive Agents/pharmacology , Bosentan , Cardiopulmonary Bypass , Hemodynamics/drug effects , Hypertension, Pulmonary/drug therapy , Sulfonamides/pharmacology , Swine
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