Sevoflurane but Not Propofol Preserves Myocardial Function in Coronary Surgery Patients

Background Sevoflurane has been shown to protect against myocardial ischemia and reperfusion injury in animals. The present study investigated whether these effects were clinically relevant and would protect left ventricular (LV) function during coronary surgery. Methods Twenty coronary surgery patients were randomly assigned to receive either target-controlled infusion of propofol or inhalational anesthesia with sevoflurane. Except for this, anesthetic and surgical management was the same in all patients. A high-fidelity pressure catheter was positioned in the left ventricle and the left atrium. LV response to increased cardiac load, obtained by leg elevation, was assessed before and after cardiopulmonary bypass (CPB). Effects on contraction were evaluated by analysis of changes in dP/dtmax. Effects on relaxation were assessed by analysis of the load dependence of myocardial relaxation (R = slope of the relation between time constant &tgr; of isovolumic relaxation and end-systolic pressure). Postoperative concentrations of cardiac troponin I were followed during 36 h. Results Before CPB, leg elevation slightly increased dP/dtmax in the sevoflurane group (5 ± 3%), whereas it remained unchanged in the propofol group (1 ± 6%). After CPB, leg elevation resulted in a decrease in dP/dtmax in the propofol group (−5 ± 4%), whereas the response in the sevoflurane group was comparable to the response before CPB (5 ± 4%). Load dependence of LV pressure fall (R) was similar in both groups before CPB. After CPB, R was increased in the propofol group but not in the sevoflurane group. Troponin I concentrations were significantly lower in the sevoflurane than in the propofol group. Conclusions Sevoflurane preserved LV function after CPB with less evidence of myocardial damage in the first 36 h postoperatively. These data suggest a cardioprotective effect of sevoflurane during coronary artery surgery.

[1]  W. Schlack,et al.  One MAC of sevoflurane provides protection against reperfusion injury in the rat heart in vivo. , 2001, British journal of anaesthesia.

[2]  Sania T Haroun-Bizri,et al.  Does isoflurane optimize myocardial protection during cardiopulmonary bypass? , 2001, Journal of cardiothoracic and vascular anesthesia.

[3]  S. D. De Hert,et al.  The effects of the pericardium on length-dependent regulation of left ventricular function in coronary artery surgery patients. , 2001, Journal of cardiothoracic and vascular anesthesia.

[4]  M. Fukusaki,et al.  Sevoflurane Protects Stunned Myocardium Through Activation of Mitochondrial ATP-Sensitive Potassium Channels , 2001, Anesthesia and analgesia.

[5]  A. Lochner,et al.  Reduction of Postischemic Contractile Dysfunction of the Isolated Rat Heart by Sevoflurane: Comparison with Halothane , 2000, Anesthesia and analgesia.

[6]  I. Menown,et al.  Troponin T or troponin I as cardiac markers in ischaemic heart disease , 2000, Heart.

[7]  W. Schlack,et al.  Effect of propofol on reperfusion injury after regional ischaemia in the isolated rat heart. , 1999, British journal of anaesthesia.

[8]  P. Menasché,et al.  Evidence for preconditioning by isoflurane in coronary artery bypass graft surgery. , 1999, Circulation.

[9]  P. Pagel,et al.  Sevoflurane reduces myocardial infarct size and decreases the time threshold for ischemic preconditioning in dogs. , 1999, Anesthesiology.

[10]  J. Kampine,et al.  Sevoflurane mimics ischemic preconditioning effects on coronary flow and nitric oxide release in isolated hearts. , 1999, Anesthesiology.

[11]  S. Zahler,et al.  Sevoflurane and isoflurane protect the reperfused guinea pig heart by reducing postischemic adhesion of polymorphonuclear neutrophils. , 1999, Anesthesiology.

[12]  T. Gillebert,et al.  Length-dependent regulation of left ventricular function in coronary surgery patients. , 1999, Anesthesiology.

[13]  T. Gillebert,et al.  Contraction-relaxation coupling and impaired left ventricular performance in coronary surgery patients. , 1999, Anesthesiology.

[14]  W. Schlack,et al.  Effects of enflurane, isoflurane, sevoflurane and desflurane on reperfusion injury after regional myocardial ischaemia in the rabbit heart in vivo. , 1998, British journal of anaesthesia.

[15]  W. Schlack,et al.  Effects of halothane, enflurane, isoflurane, sevoflurane and desflurane on myocardial reperfusion injury in the isolated rat heart. , 1998, British journal of anaesthesia.

[16]  P. Noirhomme,et al.  Cardiac troponin I as an early marker of myocardial damage after coronary bypass surgery. , 1998, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

[17]  V. Piriou,et al.  A comparison of the effects of fentanyl and propofol on left ventricular contractility during myocardial stunning , 1998, Acta anaesthesiologica Scandinavica.

[18]  P. Pagel,et al.  Isoflurane Mimics Ischemic Preconditioning via Activation of KATP Channels: Reduction of Myocardial Infarct Size with An Acute Memory Phase , 1997, Anesthesiology.

[19]  P. Pagel,et al.  Role of Adenosine in Isoflurane‐induced Cardioprotection , 1997, Anesthesiology.

[20]  Michael V. Cohen,et al.  Volatile Anesthetics Protect the Ischemic Rabbit Myocardium from Infarction , 1997, Anesthesiology.

[21]  S. Zahler,et al.  Halothane, Isoflurane, and Sevoflurane Reduce Postischemic Adhesion of Neutrophils in the Coronary System , 1997, Anesthesiology.

[22]  T. Gillebert,et al.  Recovery of Systolic and Diastolic Left Ventricular Function Early after Cardiopulmonary Bypass , 1996, Anesthesiology.

[23]  P. Pagel,et al.  Mechanism of Myocardial Protection by Isoflurane: Role of Adenosine Triphosphate‐regulated Potassium (K sub ATP) Channels , 1996, Anesthesiology.

[24]  P. Pagel,et al.  Glyburide, a KATP Channel Antagonist, Attenuates the Cardioprotective Effects of Isoflurane in Stunned Myocardium , 1996, Anesthesia and analgesia.

[25]  A. Hsu,et al.  Morphine mimics the cardioprotective effect of ischemic preconditioning via a glibenclamide-sensitive mechanism in the rat heart. , 1996, Circulation research.

[26]  W. Schlack,et al.  Effect of halothane on myocardial reoxygenation injury in the isolated rat heart. , 1996, British journal of anaesthesia.

[27]  A. Hara,et al.  Propofol Attenuates Hydrogen Peroxide‐induced Mechanical and Metabolic Derangements in the Isolated Rat Heart , 1996, Anesthesiology.

[28]  K. Ichihara,et al.  Effects of sevoflurane on ischaemic myocardium in dogs , 1995, Acta anaesthesiologica Scandinavica.

[29]  G. Toubin,et al.  Use of cardiac troponin I as a marker of perioperative myocardial ischemia. , 1995, The Annals of thoracic surgery.

[30]  P. Grayburn,et al.  Are Contraction and Relaxation Coupled in Patients With and Without Congestive Heart Failure? , 1992, Circulation.

[31]  M. Davies,et al.  The antioxidant potential of propofol (2,6-diisopropylphenol). , 1992, British journal of anaesthesia.

[32]  J. Kampine,et al.  Recovery of Contractile Function of Stunned Myocardium in Chronically Instrumented Dogs is Enhanced by Halothane or Isoflurane , 1988, Anesthesiology.

[33]  V. Bhargava,et al.  Alteration of the Left Ventricular Diastolic Pressure-Segment Length Relation Produced by the Pericardium: Effects of Cardiac Distension and Afterload Reduction in Conscious Dogs , 1978, Circulation.

[34]  T. Etgen,et al.  Cardiac troponin I plasma levels for diagnosis and quantitation of perioperative myocardial damage in patients undergoing coronary artery bypass surgery. , 1998, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.