Am J Perinatol 2007; 24(2): 141-146
DOI: 10.1055/s-2006-958159
Copyright © 2007 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA.

Efficacy and Renal Toxicity of One Daily Dose of Amikacin versus Conventional Dosage Regime

Ma. Guadalupe Vásquez-Mendoza1 , Arturo Vargas-Origel2 , Aurelia del Carmen Ramos-Jiménez1 , Gilberto Aguilar-Orozco3 , Gustavo Romero-Gutiérrez4
  • 1Department of Neonatology, Hospital de GinecoPediatria 48, Mexican Institute of Social Security, León, Guanajuato, México
  • 2School of Medicine, University of Guanajuato, León, Guanajuato, México
  • 3Clinical Laboratory, Hospital Aranda de la Parra, León, Guanajuato, México
  • 4Department of Perinatology, Hospital de GinecoPediatria 48, Mexican Institute of Social Security, León, Guanajuato, México
Further Information

Publication History

Publication Date:
15 February 2007 (online)

ABSTRACT

This study assessed the efficacy and renal toxicity of one daily dose of amikacin versus several doses in infected full-term newborns. A clinical trial was conducted with 120 patients who were divided into two groups: group A (n = 60), infants who received amikacin 20 mg/kg/d in one dose; and group B (n = 60), infants who received amikacin 10 mg/kg/d every 12 hours. Both groups also received ampicillin 100 mg/kg/day. Blood levels of amikacin, urinary β2-microglobulin (β2-m), serum creatinine (SCr), and glomerular filtration rate (GFR) were measured in each patient. No significant difference was found in demographic characteristics as well as in their β2-m, SCr, and GFR levels. Infection was resolved in 96% for infants of group A and 91% for group B (p = 0.254). Renal toxicity was present in 20 versus 31.6%, respectively (p = 0.211). In both groups no significant difference was found in peak amikacin levels, whereas trough levels were higher for group B (p = 0.004). No significant difference was found in efficacy or renal toxicity in either group. We recommend using amikacin in one daily dose. It could diminish the manipulation of intravenous access, reducing the risk of nosocomial infections.

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Arturo Vargas-OrigelM.D. 

San Javier 311, La Martinica CP 31500

León, Guanajuato, México

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