Blood rheology changes during bezafibrate treatment

Br J Clin Pract. 1988 Nov;42(11):456-8.

Abstract

To evaluate the effect of bezafibrate on the haemorheological pattern, 30 atherosclerotic non-diabetic patients were enlisted in a double-blind, comparative, parallel group trial with bezafibrate (600 mg daily) or placebo being randomly assigned. The 45-day treatment period was preceded by a three week pharmacological wash-out. Haemorheological parameters such as whole-blood, plasma and serum viscosity, haematocrit, fibrinogen, fibrinogen/albumin ratio and erythrocyte filterability were evaluated before and at the end of treatment. The results showed no change in haemorheological determinants in the placebo-treated group but a significant reduction in whole-blood viscosity, in haematocrit, in fibrinogen and fibrinogen/albumin ratio was observed in the bezafibrate treated patients. No variation was present in the plasma and serum viscosity and in the erythrocyte filterability.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Aged
  • Arteriosclerosis / blood*
  • Arteriosclerosis / drug therapy
  • Bezafibrate / therapeutic use*
  • Blood Viscosity / drug effects*
  • Clinical Trials as Topic
  • Double-Blind Method
  • Fibrinogen / analysis
  • Hematocrit
  • Humans
  • Middle Aged
  • Random Allocation

Substances

  • Fibrinogen
  • Bezafibrate