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Published on: April 19, 2011
Xenon and isoflurane improved biventricular function during right ventricular ischemia and reperfusion
M Hein1, A B Roehl, J H Baumert
1Department of Anesthesiology, University Hospital of Aachen, Aachen, Germany. mhein@ukaachen.de
Acta Anaesthesiologica Scandinavica
|October 21, 2009
Summary
Xenon and isoflurane equally protected against right ventricular ischemia complications. Xenon increased right ventricular contractility, while isoflurane improved left ventricular function.
Area of Science:
- Anesthesiology
- Cardiovascular Physiology
- Ischemic Heart Disease
Background:
- Anesthetics can offer cardioprotection but may impair myocardial contractility.
- Xenon lacks negative inotropic effects, suggesting potential hemodynamic benefits.
- Right ventricular ischemia presents a high risk of acute complications.
Purpose of the Study:
- To compare the effects of xenon and isoflurane on biventricular function during right ventricular ischemia and reperfusion.
- To evaluate xenon as a potentially superior anesthetic for maintaining global hemodynamics in this context.
Main Methods:
- A porcine model (n=36) was used to assess biventricular function via conductance catheter technique.
- Animals underwent 90 minutes of right ventricular ischemia followed by 120 minutes of reperfusion.
- Type B natriuretic peptide (BNP) gene expression was measured; a control group received barbiturate anesthesia.
Main Results:
- Cardiac output decreased significantly in unprotected animals during ischemia and reperfusion.
- Isoflurane improved left ventricular contractility and preload by reducing stiffness.
- Xenon increased right ventricular afterload, which was offset by enhanced contractility, with less pronounced diastolic effects.
Conclusions:
- Both xenon and isoflurane effectively prevented hemodynamic compromise during right ventricular ischemia-reperfusion.
- Equipotent hemodynamic protection was achieved through distinct inotropic and vasodilatory mechanisms.
- Both anesthetics inhibited upregulation of BNP mRNA in the remote left ventricle.
