Evidence map›Paper›PMID 41810872›Full record

ArticleJournal of the Pediatric Infectious Diseases Society2026

Cerebrospinal Pharmacokinetic and Pharmacodynamic Evaluation of Sulbactam: Dosing Considerations for Acinetobacter baumannii Meningitis in Pediatric Patients.

Tetsushu Onita, Kazuro Ikawa

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Article in Journal of the Pediatric Infectious Diseases Society, 2026. 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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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Tetsushu OnitaDepartment of Pharmacy, Shimane University Hospital, 89-1 Enya, Izumo, Shimane 693-8501, Japan.ORCID 0000-0003-1174-0787
Kazuro IkawaGraduate School of Biomedical and Health Sciences, Hiroshima University, 1-2-3 Kasumi, Minami-ku, Hiroshima 734-8551, Japan.

Funding

JSPS KAKENHI 25K18652
6 · The paper itself

Abstract

backgroundEffective sulbactam dosing regimens for treating Acinetobacter baumannii meningitis in pediatric patients, considering the degree of cerebrospinal fluid (CSF) inflammation and its consequent effect on drug penetration, have not been thoroughly studied. This study aimed to describe a cerebrospinal pharmacokinetic (PK) model of sulbactam and propose a dosing strategy in pediatric patients based on pharmacodynamic (PD) evaluation with stochastic simulation.

methodsPublications were systematically extracted from MEDLINE for sulbactam CSF PK data collection. A cerebrospinal PK model was described using CSF samples and applied to estimate the probability of attaining the PK/PD target (60% time above the minimum inhibitory concentration [T > MIC] in CSF). The cerebrospinal PK/PD breakpoint was defined as the highest MIC at which the target attainment probability in CSF was ≥90% for each age group (infants [4 weeks to 11 months], children [1-6 years], and pediatrics [7-16 years]). RESULTS AND DISCUSSION: The study population included 21 pediatric patients aged 0.083-13.5 years. The CSF/serum concentration ratio at the various sampling points ranged 0.002-0.695. Based on the result of covariate analysis, CSF protein and CSF glucose levels were incorporated into the CSF-to-serum partition coefficient. The visual predictive check of CSF concentrations indicated no major bias. Regarding the cerebrospinal PK/PD evaluation, in infants and children groups with meningeal inflammation (eg, CSF protein > 100 mg/dL and CSF glucose < 40 mg/dL) a sulbactam dose of 200 mg/kg/day (as sulbactam component) with 0.5-h infusion was required to achieve 90% probability of CSF target attainment (60% T > MIC) up to an MIC of 4 μg/mL for A. baumanii.

conclusionsThis study identified effective dosing regimens for A. baumannii meningitis in pediatric patients in consideration of the degree of inflammation in CSF. High-dose sulbactam regimens can be considered to optimize CSF target attainment for A. baumannii meningitis in pediatric patients.

Indexed as

Acinetobacter baumanniiAcinetobacter InfectionsAnti-Bacterial AgentsMeningitis, BacterialSulbactamAdolescentChildChild, PreschoolFemaleHumansInfantInfant, NewbornMaleMicrobial Sensitivity TestsAnti-Bacterial AgentsSulbactamAcinetobacter baumanniicerebrospinal fluidmeningitispharmacokineticssulbactam

Identifiers

PMID41810872
PMCPMC13076937

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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.