Cefpiramide kinetics and plasma protein binding in cholestasis

Br J Clin Pharmacol. 1994 Mar;37(3):295-7. doi: 10.1111/j.1365-2125.1994.tb04278.x.

Abstract

Cefpiramide is a new parenteral cephalosporin mainly excreted in the bile. Eight patients with cholestasis and 11 healthy subjects received a single 1 g i.v. dose. Cefpiramide concentrations in plasma and urine were measured by h.p.l.c. and plasma binding was determined by ultrafiltration. Total clearance of cefpiramide (mean +/- s.d.) was 15.5 +/- 7.1 ml min-1 in patients and 25.6 +/- 4.6 ml min-1 in healthy subjects. As a result, the terminal elimination half-life was longer in patients (12.0 +/- 2.9 h vs 5.3 +/- 0.9 h). Owing to impaired biliary elimination of cefpiramide in cholestasis, the urinary recovery of unchanged drug in patients was about five times greater than in healthy subjects (85.1 +/- 10.3% vs 16.2 +/- 3.9%). Plasma binding was significantly lower in cholestasis (fu = 0.23 +/- 0.13 vs 0.02 +/- 0.004 in healthy subjects). Accordingly, the dosage regimen of cefpiramide should be modified in patients with cholestasis.

Publication types

  • Comparative Study

MeSH terms

  • Aged
  • Aged, 80 and over
  • Blood Proteins / metabolism*
  • Cephalosporins / administration & dosage
  • Cephalosporins / blood
  • Cephalosporins / pharmacokinetics*
  • Cephalosporins / urine
  • Cholestasis / metabolism*
  • Chromatography, High Pressure Liquid
  • Female
  • Humans
  • Injections, Intravenous
  • Liver Function Tests
  • Male
  • Middle Aged
  • Protein Binding

Substances

  • Blood Proteins
  • Cephalosporins
  • cefpiramide