Evidence map›Paper›PMID 42387116›Full record

ArticlePharmaceutical research2026

Impact of Febrile State on Vancomycin Clearance in Pediatric Patients: Insights From Population Pharmacokinetic Modeling.

Ryota Tanaka, Ayato Sawaguchi, Tomoyuki Mizuno, Kei Irie, Hiroyuki Ono, Erino Amano, Hironori Goto, Sho Tashiro, Ryosuke Tatsuta, Naoki Yoshikawa and 3 more

Abstract read
In one paragraph

Article in Pharmaceutical research, 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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0cells of the map it votes in
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

13 authors.

Ryota TanakaDepartment of Clinical Pharmacy, Oita University Hospital, 1-1 Idaigaoka, Hasama, Yufu, Oita, 879-5593, Japan. rtanaka@oita-u.ac.jp.ORCID http://orcid.org/0000-0002-8452-7971
Ayato SawaguchiDepartment of Clinical Pharmacy, Oita University Hospital, 1-1 Idaigaoka, Hasama, Yufu, Oita, 879-5593, Japan.
Tomoyuki MizunoDivision of Translational and Clinical Pharmacology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Kei IrieDivision of Translational and Clinical Pharmacology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Hiroyuki OnoDepartment of Clinical Pharmacy, Oita University Hospital, 1-1 Idaigaoka, Hasama, Yufu, Oita, 879-5593, Japan.
Erino AmanoDepartment of Clinical Pharmacy, Oita University Hospital, 1-1 Idaigaoka, Hasama, Yufu, Oita, 879-5593, Japan.
Hironori GotoDepartment of Pediatrics, Faculty of Medicine, Oita University, Yufu, Oita, Japan.
Sho TashiroDepartment of Clinical Pharmacy, Oita University Hospital, 1-1 Idaigaoka, Hasama, Yufu, Oita, 879-5593, Japan.
Ryosuke TatsutaDepartment of Clinical Pharmacy, Oita University Hospital, 1-1 Idaigaoka, Hasama, Yufu, Oita, 879-5593, Japan.
Naoki YoshikawaDepartment of Clinical Pharmacy, Oita University Hospital, 1-1 Idaigaoka, Hasama, Yufu, Oita, 879-5593, Japan.
Naoki HiranoDepartment of Pediatrics, Faculty of Medicine, Oita University, Yufu, Oita, Japan.
Kenji IharaDepartment of Pediatrics, Faculty of Medicine, Oita University, Yufu, Oita, Japan.
Hiroki ItohDepartment of Clinical Pharmacy, Oita University Hospital, 1-1 Idaigaoka, Hasama, Yufu, Oita, 879-5593, Japan.

Funding

Japan Society for the Promotion of Science 20H1029
6 · The paper itself

Abstract

objectiveAugmented renal clearance is increasingly recognized in pediatric patients with febrile neutropenia (FN), leading to enhanced elimination of renally cleared antimicrobials including vancomycin (VCM). Although fever‑associated hemodynamic changes may accelerate VCM clearance, their quantitative impact in the hospital-based general pediatric cohort remains unclear. The primary objective of this study was to quantify the effects of FN and infection-associated fever on VCM clearance in pediatric patients and to identify optimal dosing regimens across age and renal function strata.

methodsThis retrospective study included inpatients aged < 18 years receiving VCM with therapeutic drug monitoring. Population pharmacokinetic analysis was performed using a two‑compartment model with allometric scaling and maturation functions. Monte Carlo simulations were conducted to evaluate the probability of attaining a target area under the concentration-time curve (AUC

resultsA total of 129 patients and 214 VCM concentrations were analyzed. Estimated glomerular filtration rate and daily maximum body temperature (BT) ≥ 38°C were independently associated with increased VCM clearance. BT ≥ 38°C increased VCM clearance by 27%, and the final model showed robust predictive performance. Simulation analyses demonstrated that febrile patients required approximately 1.2-1.3‑fold higher daily VCM doses than those of afebrile patients across all age groups and renal function categories.

conclusionRenal function and BT ≥ 38°C significantly increase VCM clearance in pediatric patients. Standard dosing may be insufficient in febrile patients, and higher initial doses should be considered. Incorporating body temperature and renal function into dosing decisions may improve target exposure attainment.

Indexed as

Anti-Bacterial AgentsFebrile NeutropeniaFeverModels, BiologicalVancomycinAdolescentArea Under CurveBody TemperatureChildChild, PreschoolDrug MonitoringFemaleGlomerular Filtration RateHumansInfantMaleAnti-Bacterial AgentsVancomycinchildrenfebrile neutropeniainfection-associated feverpopulation pharmacokinetic modelingvancomycin

Identifiers

PMID42387116
PMCPMC13593700

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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.