4.7 Article

Simultaneous pharmacokinetic/pharmacodynamic (PKPD) assessment of ampicillin and gentamicin in the treatment of neonatal sepsis

Journal

JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY
Volume 77, Issue 2, Pages 448-456

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jac/dkab413

Keywords

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Funding

  1. DNDi/GARDP
  2. German Federal Ministry of Education and Research (BMBF)
  3. German Ministry of Health
  4. South African Medical Research Council
  5. Department for International Development (DFID) UK
  6. Ministry of Health, Welfare and Sport of the Netherlands
  7. Medecins Sans Frontieres
  8. National Institute for Health Research Biomedical Research Centre (NIHR BRC) at Great Ormond Street Hospital for Children NHS Foundation Trust
  9. University College London
  10. United Kingdom MRC Fellowship [MR/M008665/1]
  11. MRC/DFID/Wellcome Joint Global Health Trials scheme [MR/M007367/1]
  12. Analytical Services International Ltd.

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This study investigated the pharmacokinetics of ampicillin and gentamicin, commonly used antibiotics for neonatal sepsis. The results showed that the combination therapy of ampicillin and gentamicin was insufficient to cover Enterobacterales, suggesting the need for alternative treatment options.
Objectives This study aimed to simultaneously investigate the pharmacokinetics of ampicillin and gentamicin, currently the WHO standard of care for treating neonatal sepsis. Methods Pharmacokinetic data were collected in 59 neonates receiving ampicillin and gentamicin for suspected or proven sepsis in the NeoFosfo trial (NCT03453177). A panel of 23 clinical Escherichia coli isolates from neonates with sepsis, resistant to either ampicillin, gentamicin or both, were tested for susceptibility using chequerboards. Pharmacokinetic/pharmacodynamic (PKPD) modelling and simulations were used to compare single-agent (EUCAST MIC) and combination (chequerboard MIC) target attainment with standard dosing regimens. Results A model was established that simultaneously estimated parameters of a one-compartment ampicillin model and a two-compartment gentamicin model. A common clearance for both drugs was used (6.89 L/h/70 kg) relating to glomerular filtration (CLGFR), with an additional clearance term added for ampicillin (5.3 L/h/70 kg). Covariate modelling included a priori allometric weight and post-menstrual age scaling of clearance. Further covariate relationships on renal clearance were postnatal age and serum creatinine. Simulation-based PKPD assessments suggest good Gram-positive (MIC <= 0.25 mg/L) cover. However, less than one-quarter of neonates were predicted to receive efficacious coverage against Enterobacterales (MIC <= 2 mg/L). The benefit of the ampicillin/gentamicin combination was limited, with only 2/23 E. coli clinical strains showing FIC index < 0.5 (synergy) and most in the range 0.5-1 (suggesting additivity). Simulations showed that feasible dosing strategies would be insufficient to cover resistant strains. Conclusions PKPD simulations showed ampicillin and gentamicin combination therapy was insufficient to cover Enterobacterales, suggesting the need for alternative empirical treatment options for neonatal sepsis.

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