Background and objective: It has been demonstrated that volatile anaesthetics have cardioprotective properties during open‐heart procedures, especially when administered continuously. European Council Directive 93/42/EEC concerning medical devices bans the supplementary incorporation of anaesthetic vaporizers in the bypass circuit. Since the uptake of volatile anaesthetics via diffusion membrane oxygenators is severely reduced, it is hypothesized that clinically relevant concentrations of sevoflurane will remain in the patients' blood following saturation with a volatile agent before start of cardiopulmonary bypass. This study was designed to compare conventional and diffusion membrane oxygenators regarding their in vivo elimination of sevoflurane. Methods: Twenty patients undergoing elective coronary bypass surgery were randomly allocated to two groups, either using a conventional polypropylene membrane oxygenator or a plasma‐tight poly‐(4‐methyl‐1‐pentene) membrane oxygenator in a miniaturized extracorporeal circuit. Anaesthesia was maintained with sevoflurane, which was stopped at the start of cardiopulmonary bypass. During cardiopulmonary bypass, sevoflurane concentration was measured in blood and in the exhausted gas from the oxygenator. Results: The elimination of sevoflurane, expressed as the relative blood concentration, was significantly increased in polypropylene membrane oxygenators compared to poly‐(4‐methyl‐1‐pentene) membrane oxygenators. This resulted in an approximately threefold higher sevoflurane blood concentration in the poly‐(4‐methyl‐1‐pentene) group over the course of cardiopulmonary bypass. Conclusions: With the incorporation of a poly‐(4‐methyl‐1‐pentene) oxygenator in a miniaturized bypass circuit, relevant concentrations of a previously applied volatile agent can be maintained even without further supply throughout cardiopulmonary bypass. This might be an alternative approach to cardioprotection when sevoflurane cannot be administered through cardiopulmonary bypass.
[1]
S. D. De Hert,et al.
Cardioprotection with Volatile Anesthetics: Mechanisms and Clinical Implications
,
2005,
Anesthesia and analgesia.
[2]
T. Mashimo,et al.
Sorptive Loss of Volatile and Gaseous Anesthetics from In Vitro Drug Application Systems
,
2005,
Anesthesia and analgesia.
[3]
A. Liebold,et al.
Four years' experience with a miniaturized extracorporeal circulation system and its influence on clinical outcome.
,
2004,
Artificial organs.
[4]
S. D. De Hert,et al.
Cardioprotective Properties of Sevoflurane in Patients Undergoing Coronary Surgery with Cardiopulmonary Bypass Are Related to the Modalities of Its Administration
,
2004,
Anesthesiology.
[5]
M. Gruber,et al.
In Vivo Uptake and Elimination of Isoflurane by Different Membrane Oxygenators during Cardiopulmonary Bypass
,
2002,
Anesthesiology.
[6]
W. Schlack,et al.
Ketamine, but Not S (+)-ketamine, Blocks Ischemic Preconditioning in Rabbit Hearts In Vivo
,
2001,
Anesthesiology.
[7]
A. Mezzetti,et al.
Intermittent antegrade warm blood cardioplegia.
,
1995,
The Annals of thoracic surgery.