Comparative effects of cefoxitin and cefotetan on vitamin K metabolism

Author:

Sieradzan R R1,Bottner W A1,Fasco M J1,Bertino J S1

Affiliation:

1. Department of Pharmacy Services, Mary Imogene Bassett Hospital, Cooperstown, New York 13326.

Abstract

The effects of cefoxitin and cefotetan on vitamin K metabolism and clotting parameters in five healthy subjects were investigated. No changes in prothrombin time or in the formation of abnormal prothrombin were seen either during or following the cefoxitin or cefotetan phase. However, when phytonadione (10 mg) (vitamin K1) was administered at the completion of each course of antibiotics, formation of vitamin K 2,3-epoxide was observed only during the cefotetan phase. It is probable, therefore, that cefotetan, a cephamycin antibiotic containing the N-methylthiotetrazole side chain, inhibits hepatic vitamin K 2,3-epoxide reductase. While hypoprothrombinemia and formation of abnormal prothrombin were not seen in healthy subjects, the effect of cefotetan on the coagulation status of vitamin K-depleted patients may be adverse.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference14 articles.

1. Defects in vitamin K-dependent carboxylation associated with moxalactam therapy;Barza M.;J. Infect. Dis.,1986

2. Evidence for impaired hepatic vitamin K metabolism in patients treated with N-methyl-thiotetrazole cephalosporins;Bechtold H.;Thromb. Haemostasis,1984

3. Hypoprothrombinemia associated with cefamandole use in a rural teaching hospital;Bertino J. S.;Arch. Intern. Med.,1986

4. Immunoassays of human prothrombin species which correlate with functional coagulant activities;Blanchard R. A.;J. Lab. Clin. Med.,1983

5. R- and S-warfarin inhibition of vitamin K and vitamin K 2,3-epoxide reductase activities in the rat;Fasco M. J.;J. Biol. Chem.,1982

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