Volatile anesthetics in oxygenators during cardiopulmonary bypass

  • Laura Gutiérrez-Soriano Cardiovascular Anesthesiology, Fundación Cardioinfantil. Bogotá, Colombia. https://orcid.org/0000-0002-3074-8146
  • Juan Carlos Kling-Gómez Cardiovascular Anesthesiology, Fundación Cardioinfantil. Bogotá, Colombia. https://orcid.org/0000-0002-5947-2884
  • Eduardo Becerra-Zapata Clinical Research, Department of Anesthesiology, Fundación Cardioinfantil. Bogotá, Colombia https://orcid.org/0000-0001-7225-6273
  • Olga Quintero Cardiovascular Anesthesiology, Fundación Santa Fe, Bogotá, Colombia.
  • Nicolás Maya-Trujillo Clinical Research, Department of Anesthesiology, Fundación Cardioinfantil. Bogotá, Colombia
  • Laura Peña-Blanco Clinical Research, Department of Anesthesiology, Fundación Cardioinfantil. Bogotá, Colombia https://orcid.org/0009-0002-8482-3794
Keywords: Cardiopulmonary bypass monitoring, Anesthesia during bypass, Membrane Oxygenator, Volatile anesthetics, Real-time monitoring

Abstract

Introduction: Continuous monitoring of exhaled concentrations and CO2 levels is often lacking during the administration of inhaled anesthetics in cardiopulmonary bypass (CPB), these levels often being adjusted intermittently based on blood gas values. This approach disregards variations in fresh gas and circulatory flows between blood samples.

Objective: To assess gas behavior during bypass circulation, evaluate data reliability, and analyze gradients through the membrane oxygenator.

Methods: Real-time monitoring of inhaled and exhaled volatile anesthetics, CO2, and oxygen was conducted at the oxygenator inlet and outlet ports during CPB. Seventy adult patients undergoing cardiac surgery on CPB were included in order to analyze the impact of circulatory flow across different oxygenators.

Results: A strong correlation was found between end-tidal CO2 and arterial blood gas CO2 (Spearman’s Rho = 0.74, p = 0.00). Isoflurane gradients differed significantly among the Affinity, Fusion, and Terumo oxygenators (p = 0.015). Equilibrium for Isoflurane was reached in 493.9 ± 164.98 seconds (95% CI: 454–532 seconds). When circulatory flow was reduced to 0.5 L/min, exhaled concentrations increased significantly (Fisher’s T, p = 0.07). Sevoflurane washout varied significantly across oxygenators at CPB initiation (mean: 117.5 s).

Conclusion: Continuous monitoring of inhaled and exhaled gases during CPB should be mandatory to optimize anesthetic delivery and achieve targeted plasma concentrations.

References

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How to Cite
1.
Gutiérrez-Soriano L, Kling-Gómez JC, Becerra-Zapata E, Quintero O, Maya-Trujillo N, Peña-Blanco L. Volatile anesthetics in oxygenators during cardiopulmonary bypass. Colomb. J. Anesthesiol. [Internet]. 2025 May 27 [cited 2025 Dec. 9];53(3). Available from: https://www.revcolanest.com.co/index.php/rca/article/view/1150

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Published
2025-05-27
How to Cite
1.
Gutiérrez-Soriano L, Kling-Gómez JC, Becerra-Zapata E, Quintero O, Maya-Trujillo N, Peña-Blanco L. Volatile anesthetics in oxygenators during cardiopulmonary bypass. Colomb. J. Anesthesiol. [Internet]. 2025 May 27 [cited 2025 Dec. 9];53(3). Available from: https://www.revcolanest.com.co/index.php/rca/article/view/1150
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