Evidence map›Paper›PMID 34584904›Full record

ArticleBone reports2021

Developing a combat-relevant translatable large animal model of heterotopic ossification.

Richard T Epperson, Brad M Isaacson, David L Rothberg, Raymond E Olsen, Brooke Kawaguchi, John M Maxwell, Mary Dickerson, Paul F Pasquina, John Shero, Dustin L Williams

Open access · goldAbstract read
In one paragraph

Article in Bone reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
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

13 citing papers in PubMed, 16 citations in OpenAlex.

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  10. Biofilm · 2023
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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

10 authors at 3 institutions in 1 country.

Richard T EppersonUniversity of Utah, Bone & Biofilm Research Laboratory, Salt Lake City, UT, United States of America.
Brad M IsaacsonUniversity of Utah, Department of Orthopaedics, Salt Lake City, UT, United States of America.
David L RothbergUniversity of Utah, Bone & Biofilm Research Laboratory, Salt Lake City, UT, United States of America.
Raymond E OlsenUniversity of Utah, Department of Orthopaedics, Salt Lake City, UT, United States of America.
Brooke KawaguchiUniversity of Utah, Bone & Biofilm Research Laboratory, Salt Lake City, UT, United States of America.
John M MaxwellUniversity of Utah, Bone & Biofilm Research Laboratory, Salt Lake City, UT, United States of America.
Mary DickersonUniversity of Utah, Office of Comparative Medicine, Salt Lake City, UT, United States of America.
Paul F PasquinaThe Center for Rehabilitation Sciences Research, Uniformed Services University, Bethesda, MD, United States of America.
John SheroThe Center for Rehabilitation Sciences Research, Uniformed Services University, Bethesda, MD, United States of America.
Dustin L WilliamsUniversity of Utah, Bone & Biofilm Research Laboratory, Salt Lake City, UT, United States of America.
University of Utah · USUniformed Services University of the Health Sciences · USWalter Reed National Military Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heterotopic ossification (HO) refers to ectopic bone formation, typically in residual limbs following trauma and injury. A review of injuries from Operation Iraqi Freedom (OIF) and Operation Enduring Freedom (OEF) indicated that approximately 70% of war wounds involved the musculoskeletal system, largely in part from the use of improvised explosive devices (IED) and rocket-propelled grenades (RPG). HO is reported to occur in approximately 63%-65% of wounded warriors from OIF and OEF. Symptomatic HO may delay rehabilitation regimens since it often requires modifications to prosthetic limb componentry and socket size. There is limited evidence indicating a mechanism for preventing HO. This may be due to inadequate models, which do not produce HO bone structure that is morphologically similar to HO samples obtained from wounded warfighters injured in theatre. We hypothesized that using a high-power blast of air (shockwave) and simulated battlefield trauma (i.e. bone damage, tourniquet, bacteria, negative pressure wound therapy) in a large animal model, HO would form and have similar morphology to ectopic bone observed in clinical samples. Initial radiographic and micro-computed tomography (CT) data demonstrated ectopic bone growth in sheep 24 weeks post-procedure. Advanced histological and backscatter electron (BSE) analyses showed that 5 out of 8 (63%) sheep produced HO with similar morphology to clinical samples. We conclude that not all ectopic bone observed by radiograph or micro-CT in animal models is HO. Advanced histological and BSE analyses may improve confirmation of HO presence and morphology, which we demonstrated can be produced in a large animal model.

Indexed as

Ectopic boneHeterotopic ossificationHistologyLarge animal modelTraumatic HO

Identifiers

PMID34584904
PMCPMC8452791
OpenAlexW3201261068

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.