Literature DB >> 8913452

Validation and nephrotoxicity of a simplified once-daily aminoglycoside dosing schedule and guidelines for monitoring therapy.

J M Prins1, G J Weverling, K de Blok, R J van Ketel, P Speelman.   

Abstract

There is no established dosing schedule for once-daily aminoglycoside dosing regimens, and accepted guidelines for monitoring therapy are lacking. We derived a simplified schedule from the Hull and Sarubbi (J. H. Hull and F. A. Sarubbi, Ann. Intern. Med. 85:183-189, 1976) nomogram, for which efficacy and safety in a once-daily dosing regimen were previously demonstrated, and prospectively followed serum aminoglycoside levels in patients. The standard treatment was gentamicin or tobramycin at 4 mg/kg of body weight given intravenously once daily. When the renal function was decreased, the daily dose was reduced, as follows: for an estimated creatinine clearance of between 50 and 80 ml/min, the daily dose was 3.25 mg/kg, for an estimated creatinine clearance of between 30 and 50 ml/min, the daily dose was 2.5 mg/kg, and for an estimated creatinine clearance of below 30 ml/min, the daily dose was 2 mg/kg. A total of 221 patients were studied (184 received gentamicin and 37 received tobramycin). First trough levels above 2 mg/liter were recorded in 11% of the patients, and they all had a baseline creatinine clearance below 50 ml/min, or a substantial decrease in clearance between enrollment and the day that the trough level was obtained. A peak level below 6 mg/liter was recorded in 6% of the patients, and half of them received the lowest daily dose. Twenty-five of the 179 evaluable patients (14%; 95% confidence interval, 9 to 19%) fulfilled the criteria for nephrotoxicity. In a multiple regression analysis, the duration of treatment and the use of other nephrotoxic antibiotics or high-dose furosemide, but not trough levels, were significant risk factors. Since the meaning of low peak levels is unclear and since most studies with multiple daily regimens confirm the lack of an association between trough levels and toxicity, we believe that monitoring of serum drug levels can be restricted to monitoring of trough levels in patients with a creatinine clearance below 50 ml/min or with a deteriorating renal function.

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Year:  1996        PMID: 8913452      PMCID: PMC163563     

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


  29 in total

1.  Prediction of creatinine clearance from serum creatinine.

Authors:  D W Cockcroft; M H Gault
Journal:  Nephron       Date:  1976       Impact factor: 2.847

2.  The association of aminoglycoside plasma levels with mortality in patients with gram-negative bacteremia.

Authors:  R D Moore; C R Smith; P S Lietman
Journal:  J Infect Dis       Date:  1984-03       Impact factor: 5.226

3.  Association of aminoglycoside plasma levels with therapeutic outcome in gram-negative pneumonia.

Authors:  R D Moore; C R Smith; P S Lietman
Journal:  Am J Med       Date:  1984-10       Impact factor: 4.965

4.  Double-blind comparison of the nephrotoxicity and auditory toxicity of gentamicin and tobramycin.

Authors:  C R Smith; J J Lipsky; O L Laskin; D B Hellmann; E D Mellits; J Longstreth; P S Lietman
Journal:  N Engl J Med       Date:  1980-05-15       Impact factor: 91.245

Review 5.  Aminoglycoside toxicity - a review of clinical studies published between 1975 and 1982.

Authors:  G Kahlmeter; J I Dahlager
Journal:  J Antimicrob Chemother       Date:  1984-01       Impact factor: 5.790

6.  Clinical and pharmacokinetic characteristics of aminoglycoside nephrotoxicity in 201 critically ill patients.

Authors:  J J Schentag; F B Cerra; M E Plaut
Journal:  Antimicrob Agents Chemother       Date:  1982-05       Impact factor: 5.191

7.  Gentamicin pharmacokinetics in 1,640 patients: method for control of serum concentrations.

Authors:  D E Zaske; R J Cipolle; J C Rotschafer; L D Solem; N R Mosier; R G Strate
Journal:  Antimicrob Agents Chemother       Date:  1982-03       Impact factor: 5.191

8.  Gentamicin dosing errors with four commonly used nomograms.

Authors:  T S Lesar; J C Rotschafer; L M Strand; L D Solem; D E Zaske
Journal:  JAMA       Date:  1982-09-10       Impact factor: 56.272

9.  Furosemide enhancement of experimental gentamicin nephrotoxicity: comparison of functional and morphological changes with activities of urinary enzymes.

Authors:  R D Adelman; W L Spangler; F Beasom; G Ishizaki; G M Conzelman
Journal:  J Infect Dis       Date:  1979-09       Impact factor: 5.226

10.  Single or multiple daily doses of aminoglycosides: a meta-analysis.

Authors:  M Barza; J P Ioannidis; J C Cappelleri; J Lau
Journal:  BMJ       Date:  1996-02-10
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Review 5.  Once daily aminoglycoside therapy. Is it less toxic than multiple daily doses and how should it be monitored?

Authors:  M L Barclay; C M Kirkpatrick; E J Begg
Journal:  Clin Pharmacokinet       Date:  1999-02       Impact factor: 6.447

6.  Ceftriaxone treatment of complicated urinary tract infections as a risk factor for enterococcal re-infection and prolonged hospitalization: A 6-year retrospective study.

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7.  Risk factors for acute kidney injury during aminoglycoside therapy in patients with cystic fibrosis.

Authors:  Kevin J Downes; Neha R Patil; Marepalli B Rao; Rajesh Koralkar; William T Harris; John P Clancy; Stuart L Goldstein; David J Askenazi
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8.  Risk factors for toxicity in elderly patients given aminoglycosides once daily.

Authors:  D L Paterson; J M Robson; M M Wagener
Journal:  J Gen Intern Med       Date:  1998-11       Impact factor: 5.128

9.  Protective effect of aminoguanidine against nephrotoxicity induced by amikacin in rats.

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Journal:  Urol Res       Date:  2004-07-20

10.  Quantitative justification for target concentration intervention--parameter variability and predictive performance using population pharmacokinetic models for aminoglycosides.

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Journal:  Br J Clin Pharmacol       Date:  2004-07       Impact factor: 4.335

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