Evidence map›Paper›PMID 41739775›Full record

ArticlePloS one2026

Multi-site bone marrow core biopsy improves diagnostic accuracy in dogs with hematologic disease.

Kristi M Smiley, Sara L Connolly, Rose Raskin, Michael F Rosser, Amy N Schnelle, Nicolas Lopez-Villalobos, Arnon Gal

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Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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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

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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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

7 authors.

Kristi M SmileyDepartment of Veterinary Clinical Medicine, University of Illinois Urbana-Champaign, Urbana, Illinois, United States of America.
Sara L ConnollyDepartment of Veterinary Clinical Medicine, University of Illinois Urbana-Champaign, Urbana, Illinois, United States of America.
Rose RaskinDepartment of Comparative Pathobiology, Purdue University, West Lafayette, Illinois, United States of America.
Michael F RosserDepartment of Veterinary Clinical Medicine, University of Illinois Urbana-Champaign, Urbana, Illinois, United States of America.
Amy N SchnelleDepartment of Veterinary Clinical Medicine, University of Illinois Urbana-Champaign, Urbana, Illinois, United States of America.
Nicolas Lopez-VillalobosSchool of Agriculture and Environment, Massey University, Private Bag 11 222, Palmerston North, New Zealand.
Arnon GalDepartment of Veterinary Clinical Medicine, University of Illinois Urbana-Champaign, Urbana, Illinois, United States of America.ORCID https://orcid.org/0000-0002-6449-2812

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSpatial heterogeneity within bone marrow significantly affects diagnostic accuracy in human and veterinary medicine, where single-site sampling may fail to detect focal disease processes. However, optimal bone marrow sampling strategies for canine hematologic disease diagnosis remain unclear, representing a critical knowledge gap in veterinary diagnostic pathology. We hypothesized that multi-site bone marrow core sampling would provide superior diagnostic accuracy compared to current single-site sampling standards in canine patients. The primary aim was to evaluate diagnostic capture probability of sampling one to four bone marrow sites in dogs with suspected hematologic disease. METHODS AND

findingsSixteen dogs with suspected hematologic disease underwent bone marrow trephine biopsies from four anatomical locations (bilateral proximal humerus and iliac crest) using the ARROW OnControl Powered Driver system. Two board-certified clinical pathologists independently evaluated 64 masked bone marrow samples. Diagnostic accuracy was assessed using truth set methodology, with statistical analysis including mixed-effects logistic regression and bootstrap confidence intervals. Multi-site core sampling significantly improved diagnostic capture probability. Moving from one to two sites increased diagnostic accuracy from 76.6% to 94.8% under the permissive rule (18.2% improvement, P < 0.0001), and from 28.1% to 47.9% when both pathologists agreed (19.8% improvement). Significant site-specific differences were observed in myeloid-to-erythroid ratios and megakaryocyte counts. Overall, 13.3% of samples were nondiagnostic, with modest inter-pathologist agreement (κ = 0.30, 42% agreement).

conclusionsMulti-site bone marrow core sampling provides clinically meaningful improvements in diagnostic accuracy for canine hematologic diseases, with the greatest benefit achieved by adding a second sampling site to current single-site protocols.

Identifiers

PMID41739775
PMCPMC12935199

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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.