Literature DB >> 18223471

Reduced vancomycin clearance despite unchanged creatinine clearance in patients treated with vancomycin for longer than 4 weeks.

Hirokazu Nakayama1, Hirotoshi Echizen, Masayo Tanaka, Mika Sato, Takao Orii.   

Abstract

Creatinine clearance-based nomograms are used routinely during the early phase of vancomycin therapy for individualizing doses. The authors studied whether such nomograms are also valid for patients receiving the drug for an extended period of longer than 4 weeks. A retrospective analysis was conducted on the therapeutic drug monitoring data obtained from 85 patients who received an intermittent intravenous infusion of vancomycin. The patients were allocated to one of five groups according to the length of drug exposure: Group 1 (4-7 days; n = 31), Group 2 (8-14 days; n = 22), Group 3 (15-21 days; n = 13), Group 4 (22-28 days; n = 8), and Group 5 (longer than 29 days; n = 11). Systemic clearance of vancomycin and estimated creatinine clearance calculated by Cockcroft & Gault's formula obtained from Groups 2 through 5 were compared with those from Group 1. Patients who had received vancomycin for longer than 4 weeks (Group 5) showed a significant (P < 0.05) reduction in systemic clearance of vancomycin by 50% compared with Group 1, whereas creatinine clearance remained unchanged. This study demonstrated that prolonged administration of vancomycin for over 4 weeks may result in a more pronounced reduction in systematic clearance of vancomycin than creatinine clearance. Our data suggest that creatinine clearance-based nomograms for individualizing vancomycin doses should be used with caution in patients who require substantially prolonged drug exposure such as those with infective endocarditis.

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Year:  2008        PMID: 18223471     DOI: 10.1097/FTD.0b013e318164f781

Source DB:  PubMed          Journal:  Ther Drug Monit        ISSN: 0163-4356            Impact factor:   3.681


  4 in total

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Review 2.  Use of vancomycin pharmacokinetic-pharmacodynamic properties in the treatment of MRSA infections.

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3.  Vancomycin therapeutic drug monitoring and population pharmacokinetic models in special patient subpopulations.

Authors:  Joaquim F Monteiro; Siomara R Hahn; Jorge Gonçalves; Paula Fresco
Journal:  Pharmacol Res Perspect       Date:  2018-07

4.  Time Course and Extent of Renal Function Changes in Patients Receiving Treatment for Staphylococcal Pneumonias: An Analysis Comparing Telavancin and Vancomycin from the ATTAIN Trials.

Authors:  Boris Nogid; Melinda K Lacy; Micah Jacobs; Jon Bruss; Jamie Dwyer
Journal:  Pharmacotherapy       Date:  2018-08-29       Impact factor: 4.705

  4 in total

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