Literature DB >> 2737232

High haemodialysis clearance of ornidazole in the presence of a negligible renal clearance.

F F Horber1, O Maurer, P J Probst, E Heizmann, F J Frey.   

Abstract

The pharmacokinetics of ornidazole was studied in 6 patients treated by haemodialysis and in 8 subjects with a creatinine clearance between 4 and 99 ml/min x 1.73 m2. Blood and urine collections were performed for 72 h after i.v. and oral administration of 1.0 g ornidazole. Total body clearance, half-life, volume of distribution and systemic availability were independent of renal function and did not differ from previously reported values in normal volunteers. The haemodialysis clearance of ornidazole was greater than 100% higher than the total body clearance. The renal clearance of ornidazole accounted for less than 7% of the total body clearance. The percentage of the dose of ornidazole recovered in urine as parent compound or as the biologically active metabolites [alpha-(chloromethyl)-2 hydroxymethyl-5 nitroimidazole-1 ethanol and 3-(2 methyl-5 nitroimidazole-1-yl)1,2 propanediol] decreased linearly with decreasing renal function. Although the sum of those three compounds recovered in urine accounted for less than 10% of the total dose of ornidazole administered, they yielded therapeutic concentrations (greater than 4 micrograms/ml) in urine over 24 h after dosing. Due to the peculiar pharmacokinetic behaviour of ornidazole, i.e. high haemodialysis clearance in the absence of significant renal clearance, no dosage adjustment is necessary while renal function declines, but an increased dose is mandatory while patients are on dialysis.

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Year:  1989        PMID: 2737232     DOI: 10.1007/bf00558301

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  15 in total

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Authors:  S J Powell; R Elsdon-Dew
Journal:  Am J Trop Med Hyg       Date:  1972-09       Impact factor: 2.345

2.  RO 7-0207 in amoebic liver abscess. Comparative study of the effects of RO 7-0207 and metronidazole.

Authors:  A Ruas; M H Correia; J C do Valle; J A Ribeiro
Journal:  Cent Afr J Med       Date:  1973-06

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Authors:  D E Schwartz; F Jeunet
Journal:  Chemotherapy       Date:  1976       Impact factor: 2.544

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Authors:  P R Sawyer; R N Brogden; R M Pinder; T M Speight; G S Avery
Journal:  Drugs       Date:  1976       Impact factor: 9.546

5.  Effect of hemodialysis and peritoneal dialysis on aztreonam pharmacokinetics.

Authors:  J S Gerig; N D Bolton; E A Swabb; W M Scheld; W K Bolton
Journal:  Kidney Int       Date:  1984-09       Impact factor: 10.612

6.  Metabolic studies of ornidazole in the rat, in the dog and in man.

Authors:  D E Schwartz; J C Jordan; W Vetter; G Oesterhelt
Journal:  Xenobiotica       Date:  1979-09       Impact factor: 1.908

7.  Pharmacokinetics of ornidazole in patients with renal insufficiency; influence of haemodialysis and peritoneal dialysis.

Authors:  H Merdjan; A Baumelou; B Diquet; O Chick; E Singlas
Journal:  Br J Clin Pharmacol       Date:  1985-02       Impact factor: 4.335

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Authors:  C S Lee; T C Marbury; L Z Benet
Journal:  J Pharmacokinet Biopharm       Date:  1980-02

9.  Differential effect of impaired renal function on the kinetics of clavulanic acid and amoxicillin.

Authors:  F F Horber; F J Frey; C Descoeudres; A T Murray; F C Reubi
Journal:  Antimicrob Agents Chemother       Date:  1986-04       Impact factor: 5.191

10.  Pharmacokinetics of carumonam in patients with renal insufficiency.

Authors:  F Horber; H J Egger; E Weidekamm; U C Dubach; F J Frey; P J Probst; K Stoeckel
Journal:  Antimicrob Agents Chemother       Date:  1986-01       Impact factor: 5.191

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  1 in total

Review 1.  Pharmacokinetics and pharmacodynamics of the nitroimidazole antimicrobials.

Authors:  K C Lamp; C D Freeman; N E Klutman; M K Lacy
Journal:  Clin Pharmacokinet       Date:  1999-05       Impact factor: 6.447

  1 in total

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