Effect of a single dose of tobramycin on systemic inflammatory response-induced acute kidney injury in a 6-hour porcine model * : Critical Care Medicine

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Laboratory Investigations

Effect of a single dose of tobramycin on systemic inflammatory response-induced acute kidney injury in a 6-hour porcine model *

Lipcsey, Miklós MD, PhD; Carlsson, Markus MD; Larsson, Anders MD, PhD; Algotsson, Lars MD, PhD; Eriksson, Mats MD, PhD; Lukinius, Agneta PhD; Sjölin, Jan MD, PhD

Author Information
Critical Care Medicine 37(10):p 2782-2790, October 2009.

Abstract

Objective: 

To evaluate whether the addition of tobramycin further compromises renal function in inflammatory response-induced acute kidney injury. Effective antibiotic treatment in septic shock is crucial for the outcome. The combination of aminoglycosides with different [beta]-lactam antibiotics offers a broad antimicrobial coverage, rapid bacterial killing, synergistic effects, and low antibiotic-induced endotoxin release. However, aminoglycosides have nephrotoxic effects that may aggravate sepsis-induced acute kidney injury.

Design: 

Prospective, randomized, placebo-controlled experimental study.

Setting: 

University research unit.

Subjects: 

Twenty-four healthy pigs.

Interventions: 

The animals were anesthetized and randomized to four groups. Groups I (n = 8) and II (n = 8) received endotoxin infusion for 6 hrs, whereas groups III (n = 4) and IV (n = 4) received saline. Groups I and III received 7 mg/kg of tobramycin 20 mins after the initiation of the protocol, whereas groups II and IV received saline.

Measurements and Main Results: 

The renal elimination rate of a bolus dose of cefuroxime was chosen as the primary end point. Renal function was also evaluated by urine output, creatinine clearance, plasma cystatin C, plasma urea, and urine NAG (N-acetyl-beta-D-glucoaminidase). After 3 hrs, there were significantly lower cefuroxime elimination rates in the two endotoxin groups than in the nonendotoxin groups. No difference in cefuroxime elimination rates between groups I and II could be detected at any time point. Similarly, there were changes indicating acute kidney injury in urine output, creatinine clearance, and plasma cystatin C in the endotoxin groups with no differences between groups I and II. Plasma urea and urine NAG did not differ between any of the groups.

Conclusions: 

The result of this study does not lend any support to the hypothesis that a single dose of tobramycin enhances the risk of acute renal failure in cases with systemic inflammatory response-induced acute kidney injury.

Copyright © by 2009 by the Society of Critical Care Medicine and Wolters Kluwer Health, Inc. All Rights Reserved.

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