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Urinary excretion of adenosine deaminase binding protein in neonates treated with tobramycin
Authors:Nader Gordjani  Rainer Burghard  Dirk Müller  Helga Mathäi  Gunther Mergehenn  Jekabs U. Leititis  Matthias Brandis
Affiliation:(1) Children's Hospital, University of Freiburg, D-79106 Freiburg, Germany;(2) Children's Hospital Memmingen, D-87700 Memmingen, Germany;(3) Children's Hospital, University of Marburg, D-35037 Marburg, Germany;(4) Universitätskinderklinik, Mathildenstr. 1, D-79106 Freiburg, Germany
Abstract:The potential tubulotoxicity of tobramycin and cefotaxim were assessed in neonates by measuring the urinary level of adenosine deaminase binding protein (ABP) and urinary agr1-microglobulin and beta2-microglobulin. In a prospective study, 33 neonates who received tobramycin and cefotaxim for suspected neonatal sepsis were compared with 48 untreated newborns during the first 10 days of life. The urinary concentrations of ABP and its excretion rates, corrected for body weight and body surface area, were significantly increased from the 1st day of treatment. Urinary agr1-microglobulin and beta2-microglobulin were not elevated under tobramycin and cefotaxim during the first 2 days of treatment. We conclude that ABP may be a sensitive marker for the detection of proximal renal tubular injury during tobramycin and cefotaxim treatments of neonates. The increase in urinary ABP which occurs before an elevation of urinary agr1-microglobulin and beta2-microglobulin may reflect earlier structural than functional alterations. However, since none of the treated infants had signs of electrolyte disorders or glomerular dysfunction, the clinical relevance of ABP measurement should be reevaluated.
Keywords:Tobramycin  Cefotaxim  Nephrotoxicity  Adenosine deaminase binding protein  Neonates
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