Autor: |
Kristin, O'Connor, Mark W, Davies, Pieter, Koorts, David W, Cartwright, Karen, Whitfield |
Rok vydání: |
2021 |
Předmět: |
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Zdroj: |
European journal of drug metabolism and pharmacokinetics. 46(5) |
ISSN: |
2107-0180 |
Popis: |
BACKGROUND AND OBJECTIVE: Gentamicin is commonly used in neonates, and it requires drug concentration monitoring. The objective of this study was to determine the extent of high trough (≥ 2 mg/l) and therapeutic peak serum gentamicin concentrations (5-12 mg/l) using our current gentamicin regimen and to adjust the dosing regimen accordingly and reassess.This was a prospective cohort study of neonates, with normal renal function, who were prescribed gentamicin. Group 1: March 2014-July 2017-gentamicin intravenous (IV) 2.5 mg/kg given every 36 h if30 weeks gestational age (GA) and every 24 h if ≥ 30 weeks GA; Group 2: August 2019-February 2020-gentamicin IV 3.5 mg/kg given every 36 h if30 weeks GA and every 24 h if ≥ 30 weeks GA. We assessed the number of neonates with aberrant trough and peak serum gentamicin concentrations.Forty-eight neonates30 weeks GA and 34 ≥ 30 weeks GA were given 2.5 mg/kg gentamicin. Eleven (23%) neonates30 weeks GA and four (13%) ≥ 30 weeks GA had subtherapeutic peak concentrations (5 mg/l); none had supratherapeutic (12 mg/l) or toxic trough concentrations (≥ 2 mg/l). Forty-four neonates30 weeks GA and 54 ≥ 30 weeks GA were given 3.5 mg/kg gentamicin. Eighty-four (86%) had non-toxic trough concentrations (2 mg/l). One (1%)30 weeks GA neonate had subtherapeutic (5 mg/l) and one (1%) neonate ≥ 30 weeks GA had supratherapeutic (12 mg/l) peak concentrations.Gentamicin regimen of 2.5 mg/kg given every 36 h for neonates30 weeks GA and every 24 h for neonates ≥ 30 weeks GA was suboptimal at achieving therapeutic gentamicin peak. Increasing the dosage to 3.5 mg/kg achieved therapeutic peak concentrations in 98% and non-toxic trough concentrations in 86% of all neonates (prior to dose interval adjustment). |
Databáze: |
OpenAIRE |
Externí odkaz: |
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