Evidence map›Paper›PMID 40247665›Full record

SynthesisJournal of veterinary pharmacology and therapeutics2025

Pharmacokinetic-Pharmacodynamic Cutoff Values for Doxycycline in Pigs to Support the Establishment of Clinical Breakpoints for Antimicrobial Susceptibility Testing.

Pierre-Louis Toutain, Alain Bousquet-Melou, Aude A Ferran, Béatrice B Roques, Jérôme R E Del Castillo, Peter Lees, Siska Croubels, Eric Bousquet, Ludovic Pelligand

Abstract readMeta-Analysis
In one paragraph

Synthesis in Journal of veterinary pharmacology and therapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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.

Pierre-Louis ToutainINTHERES, Université de Toulouse, INRAE, ENVT, Toulouse, France.ORCID https://orcid.org/0000-0002-8846-8892
Alain Bousquet-MelouINTHERES, Université de Toulouse, INRAE, ENVT, Toulouse, France.ORCID https://orcid.org/0000-0002-7661-4311
Aude A FerranINTHERES, Université de Toulouse, INRAE, ENVT, Toulouse, France.ORCID https://orcid.org/0000-0002-6629-1088
Béatrice B RoquesINTHERES, Université de Toulouse, INRAE, ENVT, Toulouse, France.ORCID https://orcid.org/0000-0001-8229-437X
Jérôme R E Del CastilloDépartement de biomédecine vétérinaire, Faculté de médecine vétérinaire, Université de Montréal, Saint-Hyacinthe, Canada.ORCID https://orcid.org/0000-0001-5046-7926
Peter LeesDepartment of Comparative Biomedical Sciences, The Royal Veterinary College, University of London, London, UK.ORCID https://orcid.org/0000-0002-8966-3737
Siska CroubelsLaboratory of Pharmacology and Toxicology, Department of Pathobiology, Pharmacology and Zoological Medicine, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.ORCID https://orcid.org/0000-0001-6357-3517
Eric BousquetVirbac, France.
Ludovic PelligandDepartment of Comparative Biomedical Sciences, The Royal Veterinary College, University of London, London, UK.ORCID https://orcid.org/0000-0001-6005-1975

Funding

Ecole Nationale veterinaire de Toulouse and ENOVAT
6 · The paper itself

Abstract

This meta-analysis provides a population model of doxycycline (DOXY) disposition in pigs for computation of PK/PD cutoff values corresponding to differing modalities of DOXY administration orally in pigs. This analysis enables establishment of specific clinical breakpoints for the development of antimicrobial susceptibility testing of DOXY in pigs. The meta-analysis of 380 data sets, totaling 3295 plasma concentrations obtained from 300 pigs weighing 8.5-101 kg, was performed using a non-linear mixed effect model. The plasma clearance for a typical 50 kg BW pig was estimated to be 0.259 L/kg/h with a corresponding plasma half-life of 7.33 h. The bioavailability of DOXY administered in feed under field conditions was estimated to be 50%, with a large between-subject variability of 84.8%. The bioavailability of DOXY in solution in drinking water was significantly lower (30.7%) but much less variable, with a between-subject variability of 34.3%. Several dosing schedules (5 to 20 mg/kg per day) for two administration modalities (drinking water vs. food) were simulated to calculate the corresponding PK/PD cutoffs. The highest PK/PD cutoff of 0.50 mg/L was obtained for DOXY administered in feed at 20 mg/kg BW.

Indexed as

Anti-Bacterial AgentsDoxycyclineAnimalsBiological AvailabilityHalf-LifeMicrobial Sensitivity TestsModels, BiologicalSwineAnti-Bacterial AgentsDoxycyclineAntimicrobial susceptibility testingdoxycyclinepharmacokineticspigsPK/PD cutoff

Identifiers

PMID40247665
PMCPMC12257272

What OpenQuestion holds

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Registered trials

None linked

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.