Title
Acute renal insufficiency during telavancin therapy in clinical practice
Date Issued
01 March 2012
Access level
open access
Resource Type
journal article
Author(s)
Camins B.
Ritchie D.
Casabar E.
Warren D.
Washington University School of Medicine
Abstract
Objectives: To describe the tolerance to long-term telavancin therapy among inpatients as it relates to nephrotoxicity. Methods: Retrospective cohort study of adult patients who received telavancin at the Barnes-Jewish Hospital from 1 September 2009 to 1 December 2010. Patients who received less than three doses of telavancin, were on haemodialysis prior to telavancin administration or died within 48 h of initial telavancin administration were excluded. Results: Twenty-one patients received telavancin and met the inclusion criteria. Seven of 21 patients (33%) developed acute renal insufficiency during therapy. Patients who developed acute renal insufficiency had a mean glomerular filtration rate reduction of 56 mL/min/1.73 m 2. In the univariate analysis, high body mass index (P = 0.025), use of intravenous contrast dye (P = 0.017) and prior serum vancomycin trough levels >20 mg/L (P = 0.017) were associated with developing acute renal insufficiency. Two patients required haemodialysis; two had persistent renal insufficiency. Conclusions: Supratherapeutic vancomycin trough levels, high body mass index and receipt of intravenous contrast dye prior to telavancin therapy were associated with acute renal insufficiency. © The Author 2011. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved.
Start page
723
End page
726
Volume
67
Issue
3
Language
English
OCDE Knowledge area
Farmacología, Farmacia
Scopus EID
2-s2.0-84856967473
PubMed ID
Source
Journal of Antimicrobial Chemotherapy
ISSN of the container
03057453
Sponsor(s)
B. C. C. and D. J. R. are on the speaker’s bureau of Astellas Pharma US, Inc. B. C. C. has received research support from Astellas Pharma, US, Inc. D. K. W. has received research support from bioMérieux, Sage, Inc., Cubist Pharmaceuticals and 3M Healthcare, and has served as a consultant for 3M Healthcare and Bard, Inc. All other authors: none to declare.
Sources of information: Directorio de Producción Científica Scopus