Evidence map›Paper›PMID 39439981›Full record

ArticleJournal of orthopaedics2025

A preclinical model for osteoarticular fracture fragment preservation for delayed re-implantation.

João Bourbon de Albuquerque, Gregory J Della Rocca, Aaron M Stoker, Chantelle C Bozynski, Anna Sullentrup, Tamara Gull, James L Cook, Julia A V Nuelle

Abstract read
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Article in Journal of orthopaedics, 2025. 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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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

0 citing papers in PubMed.

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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

8 authors.

João Bourbon de AlbuquerqueThompson Laboratory for Regenerative Orthopaedics & Missouri Orthopaedic Institute, University of Missouri, Columbia, MO, USA.
Gregory J Della RoccaThompson Laboratory for Regenerative Orthopaedics & Missouri Orthopaedic Institute, University of Missouri, Columbia, MO, USA.
Aaron M StokerThompson Laboratory for Regenerative Orthopaedics & Missouri Orthopaedic Institute, University of Missouri, Columbia, MO, USA.
Chantelle C BozynskiThompson Laboratory for Regenerative Orthopaedics & Missouri Orthopaedic Institute, University of Missouri, Columbia, MO, USA.
Anna SullentrupThompson Laboratory for Regenerative Orthopaedics & Missouri Orthopaedic Institute, University of Missouri, Columbia, MO, USA.
Tamara GullVeterinary Medical Diagnostic Laboratory, University of Missouri, Columbia, MO, USA.
James L CookThompson Laboratory for Regenerative Orthopaedics & Missouri Orthopaedic Institute, University of Missouri, Columbia, MO, USA.
Julia A V NuelleThompson Laboratory for Regenerative Orthopaedics & Missouri Orthopaedic Institute, University of Missouri, Columbia, MO, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Open articular fractures often include contaminated, devascularized osteoarticular fragments that are critical for joint reconstruction. Definitive treatment is often delayed such that decontamination and preservation of critical fragments for joint reconstruction is highly desirable. To validate decontamination and preservation protocols for safe and effective preservation of osteoarticular fragments for re-implantation, a preclinical animal model for inducing type 3 open articular fractures with contaminated, devascularized osteoarticular fragments was developed and validated. Materials and methods: With IACUC approval, purpose-bred hounds (n = 5) were humanely euthanized. Immediately following euthanasia, a penetrating captive bolt pistol with 1.25 grain cartridge centered on the cranial aspect of each distal humerus was discharged to create open fractures in 3 dogs (6 elbows). In 2 dogs, matched osteoarticular tissues from non-injured elbows (controls) were retrieved for comparison. Distal humerus, proximal radius, and proximal ulna osteoarticular fragments (n = 27) were immediately placed in Missouri Osteochondral Preservation System (MOPS) solution and stored at room temperature. Radiographic, chondrocyte viability, and quantitative microbial culture assessments were performed immediately (time-0) and at 7 and 14 days of storage. Results: This preclinical canine model reliably produced type 3 open distal humeral fractures characterized by devascularized and contaminated osteoarticular fracture fragments. All fragments produced extensive microbial growth through 14 days of storage. Without decontamination, viable chondrocyte density in the fragments decreased significantly within 7 days, likely attributable to the profound contamination. Conclusion: These data highlight the importance of developing a reliable method for point-of-care decontamination and preservation of osteoarticular fracture fragments for safe and effective reimplantation of articular fracture fragments for joint reconstruction.

Indexed as

Animal modelFracture fragmentsJoint reconstructionOpen articular fracturesViable chondrocyte density

Identifiers

PMID39439981
PMCPMC11491317

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