Q J Med 2002; 95: 291-297
© 2002 Association of Physicians
Risk factors for nephrotoxicity in elderly patients receiving once-daily aminoglycosides
1 From the Infectious Diseases Unit, 2 Department of Geriatrics, and 4 Clinical Microbiology Laboratory, Shaare Zedek Medical Center, Jerusalem, affiliated with the Faculty of Health Sciences, Ben Gurion University of the Negev, Be'er-Sheba, and 3 Department of Public Health, Hebrew University Hadassah Medical School, Jerusalem, Israel
Received 30 August 2001 and in revised form 28 January 2002
Background: There remain concerns about the safety of once-daily dosing of aminoglycosides (AGs) in the elderly.
Aim: To assess the safety of once-daily AGs in elderly patients and evaluate possible risk factors for nephrotoxicity.
Design: Prospective, non-interventional surveillance study.
Methods: All patients receiving AGs were monitored over 4 months. Clinicians determined the AG dose for each patient after estimating patient weight and calculating creatinine clearance (CrCl) using the Cockcroft-Gault formula. Parallel figures were calculated by the investigators using measured weight. Clinicians obtained an AG trough level 24 h after initiation of treatment, and, if non-toxic, every 57 days thereafter. AG toxicity was defined as an increase in serum creatinine of
50%.
Results: In the study period, 249 consecutive patients received an AG: 116 (47%) males, mean±SD age 75±16 years. Forty-two (17%) received amikacin and 207 (83%) gentamicin. An increase of
50% in serum creatinine was detected in 31/249 (12.4%); maximal creatinine was
177 µmol/l in 16/249 (6.4%), 186265 µmol/l in nine (3.6%), and >265 µmol/l in six (2.4%). None developed oliguric renal failure. Renal damage correlated with a high AG trough level (>1.1 µg/ml) (p<0.001); haemoglobin level <10 g/dl (p<0.05); hospital admission >7 days prior to AG treatment (p<0.005); and AG treatment
11 days (p<0.05). Mean CrCl based on estimated weight was 52±18 ml/min; that based on actual weight was 71±37 ml/min. Despite this, mean AG dose was 1.3±0.6 higher than optimal.
Conclusions: Oliguric and/or lasting renal toxicity is rare in elderly patients receiving once-daily aminoglycosides for <11 days, if regular trough drug levels are monitored.
Address correspondence to Dr A.M. Yinnon, Infectious Diseases Unit, Shaare Zedek Medical Center, PO Box 3235, Jerusalem 91031, Israel. e-mail: Yinnon{at}SZMC.org.il
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
L. Leibovici, L. Vidal, and M. Paul Aminoglycoside drugs in clinical practice: an evidence-based approach J. Antimicrob. Chemother., February 1, 2009; 63(2): 246 - 251. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Freundlich, R. W. Thomsen, L. Pedersen, H. West, and H. C. Schonheyder Aminoglycoside treatment and mortality after bacteraemia in patients given appropriate empirical therapy: a Danish hospital-based cohort study J. Antimicrob. Chemother., November 1, 2007; 60(5): 1115 - 1123. [Abstract] [Full Text] [PDF] |
||||
