Evidence map›Paper›PMID 39377581›Full record

ArticleAntimicrobial agents and chemotherapy2024

Population pharmacokinetic modeling of ceftriaxone in cerebrospinal fluid in children: should we be using once- or twice-daily dosing for meningitis?

A Boast, W Zhang, H Soeorg, G Gonis, A Di Carlo, A Daley, N Curtis, B McWhinney, J P J Ungerer, A Lei and 2 more

Abstract read
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Article in Antimicrobial agents and chemotherapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

A BoastDepartment of General Medicine and Laboratory Services, The Royal Children's Hospital Melbourne, Parkville, Australia.ORCID 0000-0002-9093-3992
W ZhangInfection, Immunity and Inflammation, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
H SoeorgInfection, Immunity and Inflammation, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
G GonisDepartment of General Medicine and Laboratory Services, The Royal Children's Hospital Melbourne, Parkville, Australia.
A Di CarloDepartment of General Medicine and Laboratory Services, The Royal Children's Hospital Melbourne, Parkville, Australia.
A DaleyDepartment of General Medicine and Laboratory Services, The Royal Children's Hospital Melbourne, Parkville, Australia.
N CurtisDepartment of General Medicine and Laboratory Services, The Royal Children's Hospital Melbourne, Parkville, Australia.
B McWhinneyDepartment of Chemical Pathology, Pathology Queensland, Brisbane, Australia.
J P J UngererDepartment of Chemical Pathology, Pathology Queensland, Brisbane, Australia.
A LeiAntimicrobials and Infectious Diseases Group, Murdoch Children's Research Institute, Melbourne, Australia.
J F StandingInfection, Immunity and Inflammation, Great Ormond Street Institute of Child Health, University College London, London, United Kingdom.
A GweeDepartment of General Medicine and Laboratory Services, The Royal Children's Hospital Melbourne, Parkville, Australia.ORCID 0000-0003-4016-8986

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Guidelines for bacterial meningitis in children recommend intravenous ceftriaxone 50 mg/kg (max 2 g) twice daily (BD) or 100 mg/kg (max 4 g) once daily (OD), leaving the decision regarding the dose frequency to the prescriber. We investigated the cerebrospinal fluid (CSF) penetration of ceftriaxone to evaluate whether one dosing regimen is superior. Unbound ceftriaxone concentrations were measured in serum and CSF samples from children aged 0-18 years treated with ceftriaxone if there was a sample remaining after clinical tests were performed. A serum-CSF population pharmacokinetic model was developed using non-linear mixed-effects modeling. The once- and twice-daily dosing regimens were simulated, and the probability of target attainment (PTA) was determined for maintaining a CSF concentration above a minimum inhibitory concentration (MIC) of 1 mg/L for common meningitis pathogens and 4 mg/L for

Indexed as

Anti-Bacterial AgentsCeftriaxoneMeningitis, BacterialMicrobial Sensitivity TestsAdolescentChildChild, PreschoolDrug Administration ScheduleFemaleHumansInfantInfant, NewbornMaleStaphylococcus aureusAnti-Bacterial AgentsCeftriaxonecephalosporinscerebrospinal fluid penetrationdosingmeningitispediatricspopulation pharmacokinetics

Identifiers

PMID39377581
PMCPMC11539224

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.