Organ blood supply and tissue oxygenation after limited normovolemic hemodilution with 3% versus 6% Dextran-60

Infusionsther Transfusionsmed. 1993 Aug;20(4):130-9. doi: 10.1159/000222828.

Abstract

Background: The use of dextran solutions (DX) for hemodilution (HD) is considered being detrimental due to their effects on plasma viscosity.

Methods: 14 splenectomized beagles (12.7 +/- 1.3 kg) were anesthetized and randomly assigned to HD to 20 vol% hematocrit (hct) with either 3 or 6% DX-60. The effects of HD upon nutritional organ blood flow (radioisotope-labelled microspheres, phi 15 microns), local tissue oxygenation (pO2 multiwire surface electrode), plasma and blood volume (131I-labelled dog albumin distribution), and macrohemodynamics were evaluated with regard to actual changes in hct and plasma viscosity, respectively.

Results: Normovolemic HD with either solution resulted in equivalent changes in macrohemodynamics, and plasma and blood volume. Despite the increase in plasma viscosity associated with HD using 6% DX-60 (up to 1.45 +/- 0.10 mPa.s), blood flow rose in all organs studied (p < 0.05). After HD by means of 3% DX-60, plasma viscosity remained unchanged (1.09 +/- 0.04 mPa.s) but was not associated with higher organ blood flow as compared to 6% DX-60. In both groups, elevated pO2 values on the surface of liver and skeletal muscle (p < 0.01) as well as the shift in the pO2 histograms toward higher pO2 values indicated a more homogeneous tissue perfusion upon HD, independent of the diluent applied.

Conclusion: In comparison to 6% DX-60, the solution of 3% DX-60 is of equivalent efficacy as volume substitute and in the induction of normovolemic HD. The main advantage of 3% DX-60 solution, however, is the fact that twice as much volume can be administered before the recommended maximal daily dose of 1.5 g/kg DX is reached. Of the rheological factors influencing oxygen delivery, hematocrit thus plays the predominant role, while plasma viscosity is of minor importance.

MeSH terms

  • Animals
  • Blood Viscosity / drug effects*
  • Blood Viscosity / physiology
  • Dextrans / pharmacology*
  • Dogs
  • Dose-Response Relationship, Drug
  • Female
  • Hematocrit
  • Hemodilution / methods*
  • Hemodynamics / drug effects*
  • Hemodynamics / physiology
  • Liver / blood supply
  • Male
  • Muscles / blood supply
  • Oxygen / blood*
  • Oxygen Consumption / physiology
  • Regional Blood Flow / physiology

Substances

  • Dextrans
  • Oxygen