AI Article Synopsis

  • The study aimed to validate a simplified high-dosage regimen for netilmicin in infants, analyzing 129 infants receiving 163 treatment courses based on factors like gestational and postnatal age.
  • Serum netilmicin concentrations were measured at different intervals, revealing significant differences in drug levels based on the infants' age and gestational age.
  • The findings suggest suitable dosing intervals of 48 hours for gestational ages under 29 weeks, 36 hours for 29-36 weeks, and 24 hours for full-term infants to balance safety and efficacy during the first week of life.

Article Abstract

The aim of this study was to validate a simplified high-dosage, extended-interval netilmicin dosage regimen for infants. A total of 129 infants receiving 163 treatment courses of netilmicin (6 mg kg every 24 or 36 h depending on gestational age (GA), postnatal age and postmenstrual age) was analysed. Serum netilmicin concentrations were monitored before (Cmin), 30 min (C0.5h) after and 7.5 h (C7.5h) after the third dose. In 110 patients during first week of life mean C0.5h was 10.5 mg/l. Mean C0.5h was significantly lower (9.0 mg/l) in 38 infants older than 1 week of age. 14 of 15 patients with Cmin levels > or = 2 mg/l receiving netilmicin every 36 h were < 28 weeks of gestation. In the first week of life significant correlations between GA and elimination half-life (p < 0.001) and between plasma creatinine and elevated Cmin (p < 0.002) were found, but no correlation between C0.5h and GA. In this high-dosage regimen a dosing interval of 48 h for GA < 29 weeks, 36 h for GA 29-36 weeks and 24 h for full term babies seems appropriate, during first week of life, to avoid the majority of elevated trough levels and still obtain maximal therapeutic efficacy.

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Source
http://dx.doi.org/10.1080/00365540410020613DOI Listing

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