Literature DB >> 1929296

Pharmacokinetics of cefotaxime and desacetylcefotaxime in patients with liver disease.

R J Ko1, F R Sattler, S Nichols, E Akriviadis, B Runyon, M Appleman, J L Cohen, R T Koda.   

Abstract

The dispositions of cefotaxime and its metabolite desacetylcefotaxime were investigated in patients with different forms of chronic parenchymal liver disease (CPLD). A total of 31 subjects (27 patients and 4 controls) received a single 2-g dose of cefotaxime by infusion, and serial blood samples were drawn. The area under the concentration-time curve ranged from 176 to 241 micrograms.h/ml, the apparent half-life ranged from 1.49 to 2.42 h, and clearance ranged from 2.06 to 3.10 ml/min/kg in patients with four different forms of CPLD. The area under the concentration-time curve and the apparent half-life of desacetylcefotaxime ranged from 72 to 128 micrograms.h/ml and 7.1 to 13.4 h, respectively. Pharmacokinetic parameters were significantly different in patients with CPLD compared with those in control subjects and were related to clinical indices of hepatic impairment. Modest accumulation of cefotaxime in patients with severe hepatic impairment is unlikely to produce toxicity because of its high therapeutic index, and dosing modifications may not be required.

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Year:  1991        PMID: 1929296      PMCID: PMC245175          DOI: 10.1128/AAC.35.7.1376

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  21 in total

1.  Determination of cephalosporins and decomposition products by liquid chromatography with indirect electrochemical detection.

Authors:  H Fabre; W T Kok
Journal:  Anal Chem       Date:  1988-01-15       Impact factor: 6.986

2.  Spontaneous bacterial peritonitis: an explosion of information.

Authors:  B A Runyon
Journal:  Hepatology       Date:  1988 Jan-Feb       Impact factor: 17.425

3.  Comparison of in vitro activity of cefotaxime and desacetylcefotaxime alone and in combination against 320 gram-negative clinical isolates.

Authors:  G Piédrola; I Galan; A Leyva; M C Maroto
Journal:  Drugs       Date:  1988       Impact factor: 9.546

4.  Metabolism of cefotaxime in animals and man.

Authors:  J Chamberlain; J D Coombes; D Dell; J M Fromson; R J Ings; C M Macdonald; J McEwen
Journal:  J Antimicrob Chemother       Date:  1980-09       Impact factor: 5.790

5.  Pharmacokinetics of cefotaxime in subjects with normal and impaired renal function.

Authors:  J P Fillastre; A Leroy; G Humbert; M Godin
Journal:  J Antimicrob Chemother       Date:  1980-09       Impact factor: 5.790

6.  The human pharmacokinetics of cefotaxime and its metabolites and the role of renal tubular secretion on their elimination.

Authors:  R M Ings; D S Reeves; L O White; R P Bax; M J Bywater; H A Holt
Journal:  J Pharmacokinet Biopharm       Date:  1985-04

7.  The pharmacokinetics of cefotaxime and ceftriaxone in renal and hepatic dysfunction.

Authors:  R Wise; N Wright
Journal:  Infection       Date:  1985       Impact factor: 3.553

8.  Metabolism of cefotaxime: a review.

Authors:  H B Lassman; J D Coombes
Journal:  Diagn Microbiol Infect Dis       Date:  1984-06       Impact factor: 2.803

9.  Cefotaxime and desacetyl-cefotaxime blood levels in hepatic dysfunction.

Authors:  W Graninger; M Uihlein; P Ferenci; C Moser; A Georgopoulos
Journal:  J Antimicrob Chemother       Date:  1984-09       Impact factor: 5.790

10.  Cefotaxime and desacetyl cefotaxime kinetics in renal impairment.

Authors:  G R Matzke; P A Abraham; C E Halstenson; W F Keane
Journal:  Clin Pharmacol Ther       Date:  1985-07       Impact factor: 6.875

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  5 in total

Review 1.  Cefotaxime. A reappraisal of its antibacterial activity and pharmacokinetic properties, and a review of its therapeutic efficacy when administered twice daily for the treatment of mild to moderate infections.

Authors:  R N Brogden; C M Spencer
Journal:  Drugs       Date:  1997-03       Impact factor: 9.546

2.  Population pharmacokinetics of cefotaxime in intensive care patients.

Authors:  Maria Swartling; Anna-Karin Smekal; Mia Furebring; Miklos Lipcsey; Siv Jönsson; Elisabet I Nielsen
Journal:  Eur J Clin Pharmacol       Date:  2021-10-01       Impact factor: 2.953

3.  Clinical characteristics and outcomes of spontaneous bacterial peritonitis caused by Enterobacter species versus Escherichia coli: a matched case-control study.

Authors:  Seongman Bae; Taeeun Kim; Min-Chul Kim; Yong Pil Chong; Sung-Han Kim; Heungsup Sung; Young-Suk Lim; Sang-Oh Lee; Mi-Na Kim; Yang Soo Kim; Jun Hee Woo; Sang-Ho Choi
Journal:  BMC Infect Dis       Date:  2016-06-07       Impact factor: 3.090

4.  Variability in plasma concentration of cefotaxime in critically ill patients in an Intensive Care Unit of India and its pharmacodynamic outcome: A nonrandomized, prospective, open-label, analytical study.

Authors:  B Abhilash; Chakra Dhar Tripathi; Anoop Raj Gogia; Girish Gulab Meshram; Manu Kumar; B Suraj
Journal:  J Pharmacol Pharmacother       Date:  2016 Jan-Mar

Review 5.  Antibiotics and Liver Cirrhosis: What the Physicians Need to Know.

Authors:  Caterina Zoratti; Rita Moretti; Lisa Rebuzzi; Irma Valeria Albergati; Antonietta Di Somma; Giuliana Decorti; Stefano Di Bella; Lory Saveria Crocè; Mauro Giuffrè
Journal:  Antibiotics (Basel)       Date:  2021-12-28
  5 in total

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