Cargando…

Population Pharmacokinetic Characteristics of Amikacin in Suspected Cases of Neonatal Sepsis in a Low-Resource African Setting: A Prospective Nonrandomized Single-Site Study

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Amponsah, Seth K., Adjei, George O., Enweronu-Laryea, Christabel, Bugyei, Kwasi A., Hadji-Popovski, Kosta, Kurtzhals, Jorgen A.L., Kristensen, Kim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522970/
https://www.ncbi.nlm.nih.gov/pubmed/28761582
http://dx.doi.org/10.1016/j.curtheres.2017.01.001
_version_ 1783252253952442368
author Amponsah, Seth K.
Adjei, George O.
Enweronu-Laryea, Christabel
Bugyei, Kwasi A.
Hadji-Popovski, Kosta
Kurtzhals, Jorgen A.L.
Kristensen, Kim
author_facet Amponsah, Seth K.
Adjei, George O.
Enweronu-Laryea, Christabel
Bugyei, Kwasi A.
Hadji-Popovski, Kosta
Kurtzhals, Jorgen A.L.
Kristensen, Kim
author_sort Amponsah, Seth K.
collection PubMed
description 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.
format Online
Article
Text
id pubmed-5522970
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-55229702017-07-31 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 Curr Ther Res Clin Exp Article 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. Elsevier 2017-01-20 /pmc/articles/PMC5522970/ /pubmed/28761582 http://dx.doi.org/10.1016/j.curtheres.2017.01.001 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Amponsah, Seth K.
Adjei, George O.
Enweronu-Laryea, Christabel
Bugyei, Kwasi A.
Hadji-Popovski, Kosta
Kurtzhals, Jorgen A.L.
Kristensen, Kim
Population Pharmacokinetic Characteristics of Amikacin in Suspected Cases of Neonatal Sepsis in a Low-Resource African Setting: A Prospective Nonrandomized Single-Site Study
title Population Pharmacokinetic Characteristics of Amikacin in Suspected Cases of Neonatal Sepsis in a Low-Resource African Setting: A Prospective Nonrandomized Single-Site Study
title_full Population Pharmacokinetic Characteristics of Amikacin in Suspected Cases of Neonatal Sepsis in a Low-Resource African Setting: A Prospective Nonrandomized Single-Site Study
title_fullStr Population Pharmacokinetic Characteristics of Amikacin in Suspected Cases of Neonatal Sepsis in a Low-Resource African Setting: A Prospective Nonrandomized Single-Site Study
title_full_unstemmed Population Pharmacokinetic Characteristics of Amikacin in Suspected Cases of Neonatal Sepsis in a Low-Resource African Setting: A Prospective Nonrandomized Single-Site Study
title_short Population Pharmacokinetic Characteristics of Amikacin in Suspected Cases of Neonatal Sepsis in a Low-Resource African Setting: A Prospective Nonrandomized Single-Site Study
title_sort population pharmacokinetic characteristics of amikacin in suspected cases of neonatal sepsis in a low-resource african setting: a prospective nonrandomized single-site study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522970/
https://www.ncbi.nlm.nih.gov/pubmed/28761582
http://dx.doi.org/10.1016/j.curtheres.2017.01.001
work_keys_str_mv AT amponsahsethk populationpharmacokineticcharacteristicsofamikacininsuspectedcasesofneonatalsepsisinalowresourceafricansettingaprospectivenonrandomizedsinglesitestudy
AT adjeigeorgeo populationpharmacokineticcharacteristicsofamikacininsuspectedcasesofneonatalsepsisinalowresourceafricansettingaprospectivenonrandomizedsinglesitestudy
AT enweronularyeachristabel populationpharmacokineticcharacteristicsofamikacininsuspectedcasesofneonatalsepsisinalowresourceafricansettingaprospectivenonrandomizedsinglesitestudy
AT bugyeikwasia populationpharmacokineticcharacteristicsofamikacininsuspectedcasesofneonatalsepsisinalowresourceafricansettingaprospectivenonrandomizedsinglesitestudy
AT hadjipopovskikosta populationpharmacokineticcharacteristicsofamikacininsuspectedcasesofneonatalsepsisinalowresourceafricansettingaprospectivenonrandomizedsinglesitestudy
AT kurtzhalsjorgenal populationpharmacokineticcharacteristicsofamikacininsuspectedcasesofneonatalsepsisinalowresourceafricansettingaprospectivenonrandomizedsinglesitestudy
AT kristensenkim populationpharmacokineticcharacteristicsofamikacininsuspectedcasesofneonatalsepsisinalowresourceafricansettingaprospectivenonrandomizedsinglesitestudy