Cephalosporin-induced hypoprothrombinemia: is the N-methylthiotetrazole side chain the culprit?
Author(s) -
G. Agnelli,
A. Del Favero,
Pasquale Parise,
Roberto Guerciolini,
B M Pasticci,
G.G. Nenci,
Frederick A. Ofosu
Publication year - 1986
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.29.6.1108
Subject(s) - hypoprothrombinemia , cefamandole , ceftazidime , cephalosporin , latamoxef , ceftriaxone , medicine , cefotaxime , moxalactam , incidence (geometry) , gastroenterology , pharmacology , microbiology and biotechnology , antibiotics , biology , mathematics , vitamin k , bacteria , genetics , pseudomonas aeruginosa , geometry
The reported high incidence of vitamin-K-reversible hypoprothrombinemia associated with the new beta-lactamase-stable cephalosporins prompted us to evaluate the effect on hemostasis of three cephalosporins (cefamandole, ceftriaxone, and ceftazidime) in 30 patients with serious infections. Cefamandole and ceftriaxone, both containing a sulfhydryl group, induced a significant and similar prolongation of prothrombin time and decrease in factor VII activity. Ceftazidime, in contrast, had no effect on these two parameters.
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