Evidence map›Paper›PMID 41742590›Full record

ArticleJournal of veterinary internal medicine2026

A population pharmacokinetic study of ampicillin therapy in hospitalized foals.

Anisa Bardhi, Julien Scala-Bertola, Ronette Gehring, Jole Mariella, Francesca Freccero, Raffaele Scarpellini, Carolina Castagnetti, Zoubir Djerada, Andrea Barbarossa

Abstract read
In one paragraph

Article in Journal of veterinary internal medicine, 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

9 authors.

Anisa BardhiDepartment of Veterinary Medical Sciences, University of Bologna, Via Tolara di Sopra 50, Ozzano Emilia I-40064, Bologna, Italy.ORCID 0000-0002-2012-2852
Julien Scala-BertolaLaboratoire de Pharmacologie, CHU de Reims, UR 3801 Pharmacologie et Pathologies Fragisilisantes, Université de Reims Champagne-Ardenne, 51 Rue Cognacq-Jay, Reims F-51000, France.ORCID 0000-0002-9863-9739
Ronette GehringDivision of Veterinary Pharmacotherapy and Pharmacy, Department of Population Health Sciences, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 104-106, 3584 CM Utrecht, the Netherlands.ORCID 0000-0002-1329-201X
Jole MariellaDepartment of Veterinary Medical Sciences, University of Bologna, Via Tolara di Sopra 50, Ozzano Emilia I-40064, Bologna, Italy.ORCID 0000-0003-4881-3898
Francesca FrecceroDepartment of Veterinary Medical Sciences, University of Bologna, Via Tolara di Sopra 50, Ozzano Emilia I-40064, Bologna, Italy.ORCID 0000-0002-1645-2111
Raffaele ScarpelliniDepartment of Veterinary Medical Sciences, University of Bologna, Via Tolara di Sopra 50, Ozzano Emilia I-40064, Bologna, Italy.ORCID 0000-0002-9727-941X
Carolina CastagnettiDepartment of Veterinary Medical Sciences, University of Bologna, Via Tolara di Sopra 50, Ozzano Emilia I-40064, Bologna, Italy.ORCID 0000-0001-5533-7637
Zoubir DjeradaLaboratoire de Pharmacologie, CHU de Reims, UR 3801 Pharmacologie et Pathologies Fragisilisantes, Université de Reims Champagne-Ardenne, 51 Rue Cognacq-Jay, Reims F-51000, France.ORCID 0000-0002-4022-7889
Andrea BarbarossaDepartment of Veterinary Medical Sciences, University of Bologna, Via Tolara di Sopra 50, Ozzano Emilia I-40064, Bologna, Italy.ORCID 0000-0002-7742-4229

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPharmacokinetic studies on ampicillin in foals are limited, underscoring a relevant gap in knowledge, particularly regarding the treatment of critically ill neonatal foals. HYPOTHESIS/

objectivesTo evaluate the adequacy of the ampicillin dosing regimen in hospitalized foals and, if necessary, suggest alternative dosing strategies to achieve effective ampicillin concentrations. ANIMALS: Data were collected from 12 hospitalized foals.

methodsFoals were treated with 20 mg/kg ampicillin intravenously every 6 h. Plasma samples were obtained within the first 48 h, and the minimum inhibitory concentration (MIC) was determined for pathogen-positive patients. Ampicillin concentrations were quantified using liquid chromatography-tandem mass spectrometry. A population pharmacokinetic model was developed using a nonlinear mixed-effects approach (stochastic approximation expectation-maximization or SAEM algorithm), and a pharmacodynamic evaluation of different dose regimens was conducted using Monte Carlo simulations.

resultsA 2-compartment model with first-order elimination was selected. Age significantly influenced peripheral compartment volume and clearance. The model demonstrated excellent internal validation, with 97% of observed values within prediction intervals and robust stability, as confirmed by bootstrap and visual predictive checks. Pharmacodynamic simulations indicated that a dosage regimen of 20 mg/kg every 6 h achieved optimal PTA (≥90%) for MICs of 0.06-0.25 mg/L with a 50% fT > MIC target. For higher MICs or a 100% fT > MIC target, more frequent dosing (q4h) and higher doses (30-40 mg/kg) were necessary. CONCLUSIONS AND CLINICAL IMPORTANCE: The results from the simulations highlight the clinical importance of adjusting dosing regimens based on foal characteristics and MIC to ensure effective treatment, especially in critically ill foals.

Indexed as

antibioticsdata modelingdosage simulationsequinetherapeutic drug monitoring

Identifiers

PMID41742590
PMCPMC12927874

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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.