Hyperoxic ventilation enables hemodilution beyond the critical myocardial hemoglobin concentration

Eur J Med Res. 2005 Nov 16;10(11):462-8.

Abstract

Background: When initiated in anemic hypoxia, hyperoxic ventilation (ventilation with pure O2, FiO2 1.0, HV) reverses hypoxia-induced ECG-changes and enables survival for several hours. The quantification of the HV-induced gain in anemia tolerance and particularly the Hb-equivalent of HV in this situation are unknown.

Methods: Nine anaesthetized pigs were hemodiluted under normoxia (FiO2 0.21) by exchange of whole blood for hydroxyethyl starch (HES) until predefined, ischemia associated ECG-changes occurred (timepoint Hb(crit)). From that time on all animals were ventilated with 100% O2 (FiO2 1.0). In the case of disappearance of the ECG changes with onset of HV, the animals were further hemodiluted until ECG changes reoccurred.

Results: HV initiated in anemic hypoxia (Hb 2.3 +/- 0.2 g/dl) improved ECG-readings of all animals, and allowed for a further exchange of 14 +/- 11 ml/kg blood until ECG-changes reoccurred at Hb 1.2 +/- 0.4 g/dl.

Conclusion: HV initiated in anemic hypoxia creates a margin of safety for myocardial tissue oxygenation and thus further increases anemia tolerance. The Hb equivalent of HV in this situation amounts to approximately 1g/dl.

MeSH terms

  • Animals
  • Blood Loss, Surgical / prevention & control
  • Blood Transfusion
  • Electrocardiography
  • Hematocrit
  • Hemodilution*
  • Hemodynamics
  • Hemoglobins / metabolism*
  • Hydroxyethyl Starch Derivatives / therapeutic use
  • Hyperoxia / physiopathology*
  • Myocardial Ischemia / physiopathology
  • Myocardium / metabolism
  • Oxygen / blood*
  • Oxygen Consumption / physiology
  • Plasma Substitutes / therapeutic use
  • Respiration, Artificial*
  • Sus scrofa / physiology*
  • Vascular Resistance / physiology

Substances

  • Hemoglobins
  • Hydroxyethyl Starch Derivatives
  • Plasma Substitutes
  • Oxygen