Computed tomography findings in a cohort of 169 dogs with elbow dysplasia - a retrospective study.


Journal

BMC veterinary research
ISSN: 1746-6148
Titre abrégé: BMC Vet Res
Pays: England
ID NLM: 101249759

Informations de publication

Date de publication:
06 Sep 2021
Historique:
received: 09 10 2020
accepted: 19 08 2021
entrez: 7 9 2021
pubmed: 8 9 2021
medline: 11 11 2021
Statut: epublish

Résumé

Canine elbow dysplasia (CED) is a complex developmental skeletal disorder associated with a number of pathological conditions within the cubital joint. Because CED is a heritable disease, it is important to identify and remove the affected animals from breeding. The first objective of this study was to describe the prevalence of medial coronoid process disease (MCPD) without (MCD) or with (FMCP) fragmented medial coronoid process, osteochondrosis (OC) and/or osteochondritis dissecans (OCD), ununited anconeal process (UAP), radio-ulnar incongruence (INC R-U) and humero-ulnar incongruence (INC H-U) in dogs with the use of CT imaging. The second aim was to determine the influence of demographics on the prevalence of investigated pathologies in dogs with clinical evidence of elbow dysplasia. In this retrospective study, CT data records of 169 dogs of different breeds presented to the small animal veterinary clinic from 2012 to 2018 were included. 69.23% of dogs diagnosed with CED were young (≤ 2 years old). The mean age of dogs presented with INC R-U was 1.68 ± 1.82 years, while in dogs without INC R-U the mean age was 2.64 ± 2.59 years. The mean age of dogs with INC H-U was 1.94 ± 2.06 years, while without INC H-U 3.29 ± 2.09 years. Labrador Retrievers, German Shepherd and Bernese Mountain dogs were most frequently presented with CED-associated lameness. In 122 dogs OA of varying severity was found. INC H-U, FMCP and MCD were among the most frequently found components of CED found in the present study. OCD and UAP were the least frequently diagnosed. Dogs presented with INC R-U and INC H-U were significantly younger than dogs without these CED components. Boxers, Dog de Bordeaux, American Staffordshire terriers and mixed-breed dogs were diagnosed later in life than the other breeds. OA of varying severity was found in 72.18% of dogs. Males accounted for more than 75% of the study population.

Sections du résumé

BACKGROUND BACKGROUND
Canine elbow dysplasia (CED) is a complex developmental skeletal disorder associated with a number of pathological conditions within the cubital joint. Because CED is a heritable disease, it is important to identify and remove the affected animals from breeding. The first objective of this study was to describe the prevalence of medial coronoid process disease (MCPD) without (MCD) or with (FMCP) fragmented medial coronoid process, osteochondrosis (OC) and/or osteochondritis dissecans (OCD), ununited anconeal process (UAP), radio-ulnar incongruence (INC R-U) and humero-ulnar incongruence (INC H-U) in dogs with the use of CT imaging. The second aim was to determine the influence of demographics on the prevalence of investigated pathologies in dogs with clinical evidence of elbow dysplasia.
RESULTS RESULTS
In this retrospective study, CT data records of 169 dogs of different breeds presented to the small animal veterinary clinic from 2012 to 2018 were included. 69.23% of dogs diagnosed with CED were young (≤ 2 years old). The mean age of dogs presented with INC R-U was 1.68 ± 1.82 years, while in dogs without INC R-U the mean age was 2.64 ± 2.59 years. The mean age of dogs with INC H-U was 1.94 ± 2.06 years, while without INC H-U 3.29 ± 2.09 years. Labrador Retrievers, German Shepherd and Bernese Mountain dogs were most frequently presented with CED-associated lameness. In 122 dogs OA of varying severity was found.
CONCLUSION CONCLUSIONS
INC H-U, FMCP and MCD were among the most frequently found components of CED found in the present study. OCD and UAP were the least frequently diagnosed. Dogs presented with INC R-U and INC H-U were significantly younger than dogs without these CED components. Boxers, Dog de Bordeaux, American Staffordshire terriers and mixed-breed dogs were diagnosed later in life than the other breeds. OA of varying severity was found in 72.18% of dogs. Males accounted for more than 75% of the study population.

Identifiants

pubmed: 34488762
doi: 10.1186/s12917-021-02997-5
pii: 10.1186/s12917-021-02997-5
pmc: PMC8419939
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

296

Subventions

Organisme : Ministerstwo Nauki i Szkolnictwa Wyższego
ID : 005/RID/2018/19

Informations de copyright

© 2021. The Author(s).

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Auteurs

Mateusz Hebel (M)

Department of Internal Diseases and Diagnostics, Poznan University of Life Sciences, ul. Wołyńska 35, 60-637, Poznań, Poland.

Wojciech K Panek (WK)

Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, 27607, USA.

Jakub J Ruszkowski (JJ)

Department of Animal Anatomy, Poznan University of Life Sciences, ul. Wojska Polskiego 71C, 60-625, Poznań, Poland. ruszkowskijj@gmail.com.
University Centre for Veterinary Medicine, Szydłowska 43, 60-656, Poznan, Poland. ruszkowskijj@gmail.com.

Maria Nabzdyk (M)

Department of Animal Anatomy, Poznan University of Life Sciences, ul. Wojska Polskiego 71C, 60-625, Poznań, Poland.

Dariusz Niedzielski (D)

Small Animal Veterinary Clinic, Klinika Psa i Kota, ul. Bolesława Krzywoustego 105/21, 51-166, Wrocław, Poland.

Katarzyna C Pituch (KC)

Department of Neurological Surgery, Feinberg School of Med, 676 N St. Clair, Suite 2210, Chicago, IL, 60611, USA.

Aaron M Jackson (AM)

Department of Small Animal Surgery, Medvet Chicago, 3123 N. Clybourn Ave, Chicago, IL, 60618, USA.

Maciej Kiełbowicz (M)

Department of Internal Diseases and Diagnostics, Poznan University of Life Sciences, ul. Wołyńska 35, 60-637, Poznań, Poland.

Małgorzata Pomorska-Mól (M)

Department of Preclinical Sciences and Infectious Diseases, Poznan University of Life Sciences, ul. Wołyńska 35, 60-637, Poznań, Poland.

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Classifications MeSH