Literature DB >> 17926378

Excretion of cephaloridine and cephalothin in patients with renal impairment.

C M Kunin1, N Atuk.   

Abstract

Cephaloridine has been shown to possess certain favorable pharmacologic features while retaining the desirable antimicrobial properties of the parent compound, cephalothin. The major advantage of cephaloridine is its relatively greater resistance to metabolic degradation, presumably by the liver. This results in more prolonged blood levels in healthy subjects and a longer half-life in patients with severe renal disease. These features, together with reported enhanced antimicrobial activity and lack of inhibition by serum, suggest that it may replace or substitute for the parent compound, cephalothin, provided further clinical trials indicate that it proves to be an effective agent. Suggestions are given for a modified dosage schedule in uremic patients and during hemodialysis.

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Year:  1966        PMID: 17926378     DOI: 10.1056/NEJM196603242741205

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  14 in total

Review 1.  Critical compilation of terminal half-lives, percent excreted unchanged, and changes of half-life in renal and hepatic dysfunction for studies in humans with references.

Authors:  L A Pagliaro; L Z Benet
Journal:  J Pharmacokinet Biopharm       Date:  1975-10

2.  Clinical pharmacology of cefamandole as compared with cephalothin.

Authors:  I W Fong; E D Ralph; E R Engelking; W M Kirby
Journal:  Antimicrob Agents Chemother       Date:  1976-01       Impact factor: 5.191

3.  Pharmacokinetics of cefamandole in patients undergoing hemodialysis and peritoneal dialysis.

Authors:  M J Ahern; F O Finkelstein; V T Andriole
Journal:  Antimicrob Agents Chemother       Date:  1976-09       Impact factor: 5.191

4.  Drug kinetics and artificial kidneys.

Authors:  T B Gibson; H A Nelson
Journal:  Clin Pharmacokinet       Date:  1977 Nov-Dec       Impact factor: 6.447

5.  Hemodialysis-associated infections: treatment with cephapirin.

Authors:  S J Berman; W H Boughton; J G Sugihara; E G Wong; A W Siemsen
Journal:  Antimicrob Agents Chemother       Date:  1978-01       Impact factor: 5.191

6.  A pharmacokinetic slide rule for more accurate drug treatment.

Authors:  P Bättig; K Brune; H Schmitt; D Walz
Journal:  Eur J Clin Pharmacol       Date:  1974       Impact factor: 2.953

7.  Use and control of cephalosporins.

Authors:  S Eykyn
Journal:  J Clin Pathol       Date:  1971-07       Impact factor: 3.411

8.  Use of sodium cephalothin in the management of lung gangrene.

Authors:  B T le Roux
Journal:  Thorax       Date:  1971-09       Impact factor: 9.139

9.  Effect of hemodialysis and renal failure on serum and urine concentrations of cephapirin sodium.

Authors:  R V McCloskey; E E Terry; A W McCracken; M J Sweeney; M F Forland
Journal:  Antimicrob Agents Chemother       Date:  1972-02       Impact factor: 5.191

10.  Cephaloridine serum levels in patients on maintenance haemodialysis.

Authors:  J R Curtis; M J Marshall
Journal:  Br Med J       Date:  1970-04-18
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