Literature DB >> 1102452

Dosage adjustments of cefazolin according to the pharmacokinetics of this new cephalosporin.

J Lavillaureix, J M Brogard, M Pinget, F Ledoux.   

Abstract

Serum and urine levels of cefazolin were studied: 1. following a single 500mg intra-muscular dose of the drug in normal subjects (n = 10), in patients with renal impairment (n = 12) and in patients undergoing maintenance hemodialysis (n = 10); 2. following a single 500 mg intra-venous dose of the drug in normal subjects (n = 10). In normal subjects, serum half-lives averaged 1.75 hour after intravenous injection (Ke = 0.395) and 2.22 hours after intra-muscular injection (Ke = 0.312); urinary recovery of cefazolin over a six hours period amounted to 61% after intra-venous injection and to 47.5% after intra-muscular injection. The renal clearance of the drug approximated 40 ml/mn. A linear correlation (Ke = 0.022 + 0.0028 CrCl) was established between the overall elimination rate-constants and the creatinine clearances in the subjects under investigation. The various pharmacokinetic constants thus obtained can be used to calculate the maintenance doses, loading doses and dosage intervals adjusted according to creatinine clearances. These data actually yield dosage regimes adapted to each individual case according to the degree of renal function.

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Year:  1975        PMID: 1102452     DOI: 10.1007/bf01641051

Source DB:  PubMed          Journal:  Infection        ISSN: 0300-8126            Impact factor:   3.553


  14 in total

1.  Validity of values for glomerular filtration rate and extracellular fluid obtained from plasma concentration-time decay curves after single injections of mannitol in the dog.

Authors:  L A SAPIRSTEIN; M R HERROLD; M JANAKIS; E OGDEN
Journal:  Am J Physiol       Date:  1952-11

2.  Antibacterial activity and pharmacokinetic behavior of cefazolin as compared with five other cephalosporin antibiotics.

Authors:  P Naumann; E Reintjens
Journal:  Infection       Date:  1974       Impact factor: 3.553

3.  Cefazolin, a new semisynthetic cephalosporin antibiotic. II. In vitro and in vivo antimicrobial activity.

Authors:  M Nishida; T Matsubara; T Murakawa; Y Mine; Y Yokota
Journal:  J Antibiot (Tokyo)       Date:  1970-03       Impact factor: 2.649

4.  Pharmacology of cefazolin in human volunteers.

Authors:  P Nicholas; B R Meyers; S Z Hirschman
Journal:  J Clin Pharmacol       Date:  1973 Aug-Sep       Impact factor: 3.126

5.  Pharmacokinetics of cefazolin compared with four other cephalosporins.

Authors:  W M Kirby; C Regamey
Journal:  J Infect Dis       Date:  1973-10       Impact factor: 5.226

6.  Pharmacology of cefazolin and other cephalosporins in patients with renal insufficiency.

Authors:  W A Craig; P G Welling; T C Jackson; C M Kunin
Journal:  J Infect Dis       Date:  1973-10       Impact factor: 5.226

7.  Levels of cefazolin in human bile.

Authors:  M D Ram; S Watanatittan
Journal:  J Infect Dis       Date:  1973-10       Impact factor: 5.226

8.  Summary of symposium on cefazolin.

Authors:  D Kaye
Journal:  J Infect Dis       Date:  1973-10       Impact factor: 5.226

9.  Cefazolin vs cephalothin and cephaloridine. A comparison of their clinical pharmacology.

Authors:  C Regamey; R C Gordon; W M Kirby
Journal:  Arch Intern Med       Date:  1974-03

10.  Clinical and in vitro evaluation of cefazolin, a new cephalosporin antibiotic.

Authors:  K Ries; M E Levison; D Kaye
Journal:  Antimicrob Agents Chemother       Date:  1973-02       Impact factor: 5.191

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  1 in total

1.  Physiological modeling for indirect evaluation of drug tissular pharmacokinetics under non-steady-state conditions: an example of antimicrobial prophylaxis during liver surgery.

Authors:  Franck Lagneau; Jean Marty; Pascale Beyne; Michel Tod
Journal:  J Pharmacokinet Pharmacodyn       Date:  2005-02       Impact factor: 2.745

  1 in total

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