Ventilation/perfusion ratios measured by multiple inert gas elimination during experimental cardiopulmonary resuscitation

Acta Anaesthesiol Scand. 2014 Sep;58(8):1032-9. doi: 10.1111/aas.12378. Epub 2014 Jul 24.

Abstract

Background: During cardiopulmonary resuscitation (CPR) the ventilation/perfusion distribution (VA /Q) within the lung is difficult to assess. This experimental study examines the capability of multiple inert gas elimination (MIGET) to determine VA /Q under CPR conditions in a pig model.

Methods: Twenty-one anaesthetised pigs were randomised to three fractions of inspired oxygen (1.0, 0.7 or 0.21). VA/ Q by micropore membrane inlet mass spectrometry-derived MIGET was determined at baseline and during CPR following induction of ventricular fibrillation. Haemodynamics, blood gases, ventilation distribution by electrical impedance tomography and return of spontaneous circulation were assessed. Intergroup differences were analysed by non-parametric testing.

Results: MIGET measurements were feasible in all animals with an excellent correlation of measured and predicted arterial oxygen partial pressure (R(2) = 0.96, n = 21 for baseline; R(2) = 0.82, n = 21 for CPR). CPR induces a significant shift from normal VA /Q ratios to the high VA /Q range. Electrical impedance tomography indicates a dorsal to ventral shift of the ventilation distribution. Diverging pulmonary shunt fractions induced by the three inspired oxygen levels considerably increased during CPR and were traceable by MIGET, while 100% oxygen most negatively influenced the VA /Q. Return of spontaneous circulation were achieved in 52% of the animals.

Conclusions: VA /Q assessment by MIGET is feasible during CPR and provides a novel tool for experimental purposes. Changes in VA /Q caused by different oxygen fractions are traceable during CPR. Beyond pulmonary perfusion deficits, these data imply an influence of the inspired oxygen level on VA /Q. Higher oxygen levels significantly increase shunt fractions and impair the normal VA /Q ratio.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Validation Study

MeSH terms

  • Acetone / pharmacokinetics
  • Animals
  • Blood Circulation
  • Cardiac Pacing, Artificial
  • Cardiopulmonary Resuscitation*
  • Desflurane
  • Electric Impedance
  • Enflurane / pharmacokinetics
  • Ether / pharmacokinetics
  • Feasibility Studies
  • Hemodynamics
  • Isoflurane / analogs & derivatives
  • Isoflurane / pharmacokinetics
  • Krypton / pharmacokinetics
  • Mass Spectrometry / methods*
  • Noble Gases* / pharmacokinetics
  • Oxygen / blood
  • Random Allocation
  • Sulfur Hexafluoride / pharmacokinetics
  • Sus scrofa
  • Swine
  • Ventilation-Perfusion Ratio*
  • Ventricular Fibrillation / blood
  • Ventricular Fibrillation / physiopathology
  • Ventricular Fibrillation / therapy*

Substances

  • Noble Gases
  • Ether
  • Acetone
  • Krypton
  • Enflurane
  • Desflurane
  • Isoflurane
  • Oxygen
  • Sulfur Hexafluoride