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Population Pharmacokinetic Characteristics of Amikacin in Suspected Cases of Neonatal Sepsis in a Low-Resource African Setting: A Prospective Nonrandomized Single-Site Study.
Amponsah, Seth K; Adjei, George O; Enweronu-Laryea, Christabel; Bugyei, Kwasi A; Hadji-Popovski, Kosta; Kurtzhals, Jorgen A L; Kristensen, Kim.
Afiliação
  • Amponsah SK; Department of Pharmacology and Toxicology, School of Pharmacy, University of Ghana, Legon, Ghana.
  • Adjei GO; Centre for Tropical Clinical Pharmacology and Therapeutics, School of Medicine and Dentistry, College of Health Sciences, University of Ghana, Korle-Bu, Ghana.
  • Enweronu-Laryea C; Department of Child Health, School of Medicine and Dentistry, College of Health Sciences, University of Ghana, Korle-Bu, Ghana.
  • Bugyei KA; Department of Pharmacology and Toxicology, School of Pharmacy, University of Ghana, Legon, Ghana.
  • Hadji-Popovski K; INVIXO Consulting Group A/S, Copenhagen, Denmark.
  • Kurtzhals JAL; Centre for Medical Parasitology at Department of Clinical Microbiology, Copenhagen University Hospital, and Department of Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark.
  • Kristensen K; Development DMPK-PKPD, Novo Nordisk, Copenhagen, Denmark.
Curr Ther Res Clin Exp ; 84: e1-e6, 2017.
Article em En | MEDLINE | ID: mdl-28761582
BACKGROUND: Amikacin exhibits marked pharmacokinetic (PK) variability and is commonly used in combination with other drugs in the treatment of neonatal sepsis. There is a paucity of amikacin PK information in neonates from low-resource settings. OBJECTIVES: To determine the PK parameters of amikacin, and explore the influence of selected covariates, including coadministration with aminophylline, on amikacin disposition in neonates of African origin. METHODS: Neonates with suspected sepsis admitted to an intensive care unit in Accra, Ghana, and treated with amikacin (15 mg/kg loading followed by 7.5 mg/kg every 12 hours), were recruited. Serum amikacin concentration was measured at specified times after treatment initiation and analyzed using a population PK modeling approach. RESULTS: A total of 419 serum concentrations were available for 247 neonates. Mean (SD) trough amikacin concentration (from samples collected 30 minutes before the fourth dose) among term (n = 25), and preterm (<37 weeks' gestation n = 36) neonates were 6.2 (3.4) and 9.2 (5.7) µg/mL, respectively (P = 0.02). A 1-compartment model best fitted amikacin disposition, and birth weight was the most important predictor of amikacin clearance (CL) and distribution (V). The population CL and V of amikacin were related as CL (L/h) = 0.153 (birth weight/2.5)1.31, V (L) = 2.94 (birth weight/2.5)1.18. There was a high between-subject variability (58.9% and 50.7%) in CL and V, respectively. CL and V were 0.058 L/h/kg and 1.15 L/kg, respectively, for a mean birth weight of 2.1 kg, and the mean half-life (based on 1-compartment model), was 13.7 hours. CONCLUSIONS: The V and half-life of amikacin in this cohort varied from that reported in non-African populations, and the high trough and low peak amikacin concentrations in both term and preterm neonates suggest strategies to optimize amikacin dosing are required in this population.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2017 Tipo de documento: Article