Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1987 Apr;12(4):292-301.
doi: 10.2165/00003088-198712040-00003.

Teicoplanin pharmacokinetics in patients with chronic renal failure

Teicoplanin pharmacokinetics in patients with chronic renal failure

M Bonati et al. Clin Pharmacokinet. 1987 Apr.

Abstract

The pharmacokinetic profile of teicoplanin, a new glycopeptide antibiotic active against Gram-positive aerobic and anaerobic bacteria, was studied in 5 healthy male volunteers and 29 adult patients with various degrees of renal impairment, given a single 3 mg/kg intravenous dose. Teicoplanin was assayed in plasma and urine specimens by a microbiological method. Pharmacokinetic parameters for teicoplanin were estimated both by a 3-compartment open pharmacokinetic model and by non-compartmental analysis. Elimination half-life increased with the decrease in creatinine clearance and mean values ranged from 41 hours in volunteers to 163 hours in anuric patients. Renal failure did not affect either the volume of distribution of the central compartment (mean approximately 0.09 L/kg) or the steady-state volume of distribution (mean approximately 0.9 L/kg). Both total and renal clearance decreased with severity of disease, particularly the latter, while non-renal clearance was unaffected by renal failure. Average values were from 19 to 6 ml/min for total clearance and from 12 to 0.4 ml/min for renal clearance. There was a linear correlation between the total clearance of teicoplanin and creatinine clearance, as well as between renal clearance and creatinine clearance. The total urinary excretion of active teicoplanin averaged 65% of the administered dose in normal subjects, but was significantly reduced in the presence of renal insufficiency. Guidelines for administration of teicoplanin in patients with renal failure are given.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Clin Pharmacol Ther. 1982 Jul;32(1):113-21 - PubMed
    1. Antimicrob Agents Chemother. 1982 Mar;21(3):504-5 - PubMed
    1. Comput Programs Biomed. 1983 Feb-Apr;16(1-2):35-42 - PubMed
    1. Eur J Clin Pharmacol. 1986;31(4):501-4 - PubMed
    1. J Antimicrob Chemother. 1983 May;11(5):419-25 - PubMed

Publication types

LinkOut - more resources