Literature DB >> 1929317

Gentamicin pharmacokinetics in patients with malignancies.

J S Bertino1, L A Booker, P Franck, B Rybicki.   

Abstract

The pharmacokinetics of gentamicin were investigated in 880 patients with leukemia (24 patients), other malignancies (211 patients), or no malignancies (645 patients) by using data collected by our Clinical Pharmacy Service. A significant difference was seen in the initial calculated creatinine clearance between the patients with leukemia and the other two groups. No differences in gentamicin pharmacokinetics were seen in patients with other malignancies versus those with no malignancies. Patients with leukemia had significantly faster drug clearance compared with those in the other two groups. A poor predictive value was found for total body clearance of gentamicin versus the initial calculated creatinine clearance in all groups. Multiple logistic regression analysis showed that only the initial calculated creatinine clearance differed in the leukemic group compared with those in the other patients. Our data suggest that no pharmacokinetic difference exists for gentamicin in patients with malignancies.

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Year:  1991        PMID: 1929317      PMCID: PMC245201          DOI: 10.1128/AAC.35.7.1501

Source DB:  PubMed          Journal:  Antimicrob Agents Chemother        ISSN: 0066-4804            Impact factor:   5.191


  14 in total

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Authors:  R D Moore; C R Smith; P S Lietman
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Authors:  R G Zeitany; N S El Saghir; C R Santhosh-Kumar; M A Sigmon
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Journal:  Arch Intern Med       Date:  1984-09

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Authors:  D E Zaske; R J Cipolle; R G Strate; W F Dickes
Journal:  Am J Obstet Gynecol       Date:  1981-04-15       Impact factor: 8.661

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  11 in total

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Authors:  J V Etzel; A N Nafziger; J S Bertino
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7.  Optimizing aminoglycoside therapy for nosocomial pneumonia caused by gram-negative bacteria.

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9.  Population pharmacokinetics of gentamicin in patients with cancer.

Authors:  M C Rosario; A H Thomson; D I Jodrell; C A Sharp; H L Elliott
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10.  Dosing of aminoglycosides to rapidly attain pharmacodynamic goals and hasten therapeutic response by using individualized pharmacokinetic monitoring of patients with pneumonia caused by gram-negative organisms.

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Journal:  Antimicrob Agents Chemother       Date:  1998-07       Impact factor: 5.191

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