Abstract
α1-Microglobulin (α1-m, protein HC), a relatively low molecular weight protein of about 31,000 daltons, was measured in urine of three groups of 34 preterm neonates: group A consisted of 9 healthy preterm neonates; groups B (n=13) and C (n=12) consisted of preterm neonates with suspected or confirmed bacterial infections. Immediately after birth, all group B neonates were treated with ampicillin and aztreonam in combination, and all group C neonates were treated with oxacillin and amikacin in combination. To optimize amikacin administration, computerized individually tailored doses were administered. Urine samples were obtained from a short collection in sterile bags on the 1 st, 4th, and 7th day after delivery in all infants. Urinary α1-m concentrations were measured by a turbidimetric method (latex agglutination photometric immunoassay) and results were expressed as a ratio to urinary creatinine. In group A, urinary α1-m concentrations were stable after birth. In group C, α1-m excretion increased immediately within the 1 st day of treatment, and over the 1st week of life urinary α1-m levels were significantly higher than in group A (P=0.033). These data support the conclusion that amikacin administration was the most important factor inducing renal tubular dysfunction in the neonates of group C.
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Fanos, V., Mussap, M., Verlato, G. et al. Evaluation of antibiotic-induced nephrotoxicity in preterm neonates by determining urinary α1-microglobulin. Pediatr Nephrol 10, 645–647 (1996). https://doi.org/10.1007/s004670050181
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DOI: https://doi.org/10.1007/s004670050181