Evidence map›Paper›PMID 42675509›Full record

ReviewLaboratory animal research2026

Rabbit models of hip dysplasia: a narrative review.

Jessica E Goetz, Joshua Hockman, Michael C Willey

Abstract readReview
In one paragraph

Review in Laboratory animal research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Jessica E GoetzDepartment of Orthopedics & Rehabilitation, University of Iowa Healthcare Medical Center North Liberty, 701 Forevergreen Road, North Liberty, IA, 52317, United States.ORCID http://orcid.org/0000-0002-7197-5978
Joshua HockmanDepartment of Orthopedics & Rehabilitation, University of Iowa Healthcare Medical Center North Liberty, 701 Forevergreen Road, North Liberty, IA, 52317, United States.ORCID http://orcid.org/0009-0002-8394-8106
Michael C WilleyDepartment of Orthopedics & Rehabilitation, University of Iowa Healthcare Medical Center North Liberty, 701 Forevergreen Road, North Liberty, IA, 52317, United States. michael-willey@uiowa.edu.ORCID http://orcid.org/0000-0002-6922-8471

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The natural history of osteoarthritis development in individuals with hip dysplasia diagnosed after skeletal maturity is difficult to predict. While reorienting acetabular osteotomy improves pain and function for those with pre-arthritic hip dysplasia, the impact of dysplastic deformity correction on cartilage health and future cartilage degeneration remains unknown. The rabbit has been used as a preclinical model of hip dysplasia for investigation of joint degeneration and surgical treatment, but there is variability among protocols used to induce and characterize dysplastic deformity. The aim of this narrative review was to summarize techniques for inducing hip dysplasia, the associated morphologic and histopathologic changes, and the ability of surgical correction to mitigate joint degeneration in order to guide future research using the rabbit as a model of hip dysplasia. We identified 21 studies that induced dysplastic deformity in the rabbit hip. The most common method to induce dysplastic deformity was immobilization of the knee in extension in skeletally immature rabbits. Immobilization initiated at a younger age and for longer duration resulted in more severe dysplasia. In the few studies that assessed surgical treatment of the dysplastic hip, cartilage degeneration was reduced with correction of dysplastic deformity. We concluded that immobilizing skeletally immature rabbit knees in extension reliably causes dysplastic deformity of the hip, replicating a shallow and abnormally oriented acetabulum, which can progress to full dislocation more characteristic of hip dysplasia in infants and children, or be present without complete femoral head dislocation more characteristic of human hip dysplasia that presents in young adults. This model thereby offers the opportunity to assess the tissue level effects of hip dysplasia and the effects of surgical correction across the age spectrum.Clinical trials number : Not applicable.

Indexed as

Animal modelHipHip dysplasiaOsteoarthritisRabbit

Identifiers

PMID42675509
PMCPMC13527900

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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.