Evidence map›Paper›PMID 41842728›Full record

ArticleJournal of veterinary pharmacology and therapeutics2026

Proposed Meropenem Breakpoints for Interpretation of Antimicrobial Susceptibility Testing of Bacteria Isolated From Dogs.

Mark G Papich, Marilyn N Martinez

Abstract read
In one paragraph

Article in Journal of veterinary pharmacology and therapeutics, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Mark G PapichCollege of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, USA.ORCID https://orcid.org/0000-0002-7591-7898
Marilyn N MartinezDepartment of Health and Human Services, Center for Veterinary Medicine, US Food and Drug Administration, Office of Generic Animal Drug, Center for Veterinary Medicine, Food and Drug Administration, College Park, Maryland, USA.ORCID https://orcid.org/0000-0002-4512-853X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Meropenem is a carbapenem antibiotic used infrequently in veterinary medicine. However, antimicrobial susceptibility testing standards are needed to monitor for resistance caused by carbapenem resistant Enterobacterales (CRE). The Clinical and Laboratory Standards Institute (CLSI) does not have veterinary-specific carbapenem breakpoints for testing bacteria isolated from animals. Our objective was to correct this deficiency and propose clinical antimicrobial susceptibility testing breakpoints for consideration by clinical laboratories, standard-setting organizations, and for monitoring and surveillance programs. We collected pharmacokinetic data from published studies, which were entered into a forecasting program to perform 10,000 Monte Carlo Simulation using a range of dosages considered for administration of meropenem to dogs. Our target for the simulations was a 90% Probability of Target Attainment (PTA) to reach a time-above-MIC for the unbound fraction of the drug (f T > MIC) for at least 40% of the dosing interval. Our results showed that this target can be met for a MIC of ≤ 1 μg/mL (Enterobacterales) with a dose of 20-30 mg/kg IV every 8 h or 10 mg/kg every 6 h. For a one-step higher dilution of ≤ 2 μg/mL (Pseudomonas aeruginosa), a dose of 20-30 mg/kg every 6 h is needed. Therefore, we propose new clinical MIC breakpoints for antimicrobial susceptibility testing these bacteria isolated from dogs of ≤ 1, 2, and ≥ 4 μg/mL for the Susceptible, Intermediate, and Resistant category, respectively, for testing bacteria of the Enterobacterales, and values of ≤ 2, 4, and ≥ 8 μg/mL, respectively, for testing P. aeruginosa.

Indexed as

Anti-Bacterial AgentsBacteriaDog DiseasesThienamycinsAnimalsDogsMeropenemMicrobial Sensitivity TestsMonte Carlo MethodAnti-Bacterial AgentsMeropenemThienamycins

Identifiers

PMID41842728
PMCPMC13371787

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