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Lewis Sheiner


2020
Ljubljana, Slovenia



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Printable version

PAGE. Abstracts of the Annual Meeting of the Population Approach Group in Europe.
ISSN 1871-6032

Reference:
PAGE 16 (2007) Abstr 1134 [www.page-meeting.org/?abstract=1134]


PDF poster/presentation:
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Poster: Applications- Other topics


Catherine Sherwin A pharmacokinetic/pharmacodynamic model to determine optimal dosing targets for amikacin in neonatal sepsis

C.M.T. Sherwin (1, 2), S. Svahn (3), A.J. Van Der Linden (4), N.J. Medlicott (2), R. Broadbent (1), D.M. Reith (1)

(1) Department of Women’s and Child Health, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand; (2) School of Pharmacy, University of Otago, Dunedin, New Zealand; (3) University of Uppsala, Uppsala, Sweden; (4) Microbiology, Otago Diagnostic Laboratory, Dunedin Hospital, Dunedin, New Zealand

Objectives: To develop a PK/PD model to explore the determinants of treatment failure (TF) with the use of amikacin in neonates with suspected or proven sepsis.

Methods: A retrospective chart review was performed including all neonates treated with amikacin at Dunedin Hospital from Oct 2003 to Jan 2007. In these neonates, amikacin was commenced for treatment of suspected late onset neonatal sepsis. For those neonates with culture positive sepsis, TF was defined when an infant was diagnosised with a repeat infection caused by the same bacteria or a treatment switch to vancomycin due to no apparent clinical improvement. Amikacin E-tests were performed on the bacteria cultured from septic infants to determined amikacin minimum inhibitory concentrations (MIC). The population PK analysis included all the study subjects and was performed using NONMEM, version 5. The PD analysis included all the neonates with culture proven sepsis and used the posthoc estimates from the PK model, the MIC data and clinical characteristics in a logistic regression model using Stata, version 8.

Results: The PK model analysed 358 amikacin concentrations from 80 preterm and term neonates. A one-compartment first order elimination model was utilised. The median postmenstrual age (PMA) for the infants was 30.29 weeks, ranging (24.71 to 44.14). Median (range) current weight (CWT) was 1.06 kg (0.45 to 4.43). The final covariate model estimated clearance (CL) = 0.23 • 0.0746 (PMA) • 0.691 (CWT) and volume of distribution (V) = 0.957 •0.89(CWT). The PD model included 35 confirmed septic episodes from 26 infants. Fourteen episodes met the TF criteria. Median (range) amikacin peak concentration was 27.7 (17.1 to 36.8) mg/L, MIC was 3 (<0.5 to 12) mg/L and peak/MIC was 10.8 (2.3 to 71). In the PD model, two infants with peak/MIC <6 had TF, relative risk (RR) 2.86 (1.57–5.19). Three out of four patients with peak/MIC <8 had TF, RR 2.25 (0.95–5.34). There was no influence from area under the curve (AUC), gender, postnatal age (PNA) or peak and MIC as independent variables. Hence, other than peak/MIC <8, there were no independent predictors of TF.

Conclusions: The present study confirms the need for adequate amikacin peak concentrations to reduce the risk of TF. Therefore there is a need to develop a dosing regimen that reliably delivers a peak/MIC >8 for septic neonates.