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Equine veterinary journal2024; doi: 10.1111/evj.14088

Low-field magnetic resonance imaging of sagittal groove disease of the proximal phalanx in non-racing sport horses.

Abstract: Injuries of the sagittal groove of the proximal phalanx (P1) in equine athletes are considered to predominantly occur due to chronic bone stress overload. Objective: To describe the range of abnormalities that is present in the sagittal groove in a large group of horses diagnosed with sagittal groove disease (SGD) on low-field MRI. Methods: Retrospective, cross-sectional. Methods: Medical records were searched to identify initial MRI images of horses diagnosed with SGD and these were blindly evaluated using a semi-quantitative grading scheme and novel SGD MRI classification system reflecting potential pathways of pathological progression and severity of stress injury. Results: A total of 132 limbs from 111 horses were included in the study; predominantly warmbloods competing in showjumping (n = 83) and dressage (n = 18). SGD MRI classifications were: 0 (normal, n = 0), 1 (small subchondral defect, n = 2), 2 (osseous densification, n = 28), 3 (subchondral microfissure with osseous densification, n = 7), 4 (bone oedema-like signal within the subchondral ± trabecular bone and ± subchondral microfissure or demineralisation, n = 72), 5 (incomplete macrofissure/fracture, n = 23) and 6 (complete fracture, n = 0). Classification 4c (bone oedema-like signal with demineralisation) and 5 had higher proportions in the plantar third of hindlimbs (3% and 10%, respectively) compared with forelimbs (0% and 0%, respectively). SGD classification and extent of bone oedema-like signal were not significantly different between lame (n = 116) and non-lame limbs (n = 16) (both p > 0.05). Periosteal new bone and oedema-like signal were identified (either confidently or suspected) at the dorsoproximal aspect of P1 in 25% and 39% of limbs, respectively. Conclusions: Inclusion via diagnoses in original MRI reports, variable clinical history, small size of some classification groups. Conclusions: The presence or absence of lameness is not a dependable measure of the severity of SGD. The periosteal oedema-like signal of P1 has not previously been described in MRI of SGD and further supports the concept of bone stress injury.
Publication Date: 2024-04-02 PubMed ID: 38566459DOI: 10.1111/evj.14088Google Scholar: Lookup
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  • Journal Article

Summary

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The research paper presents a study on the use of low-field magnetic resonance imaging (MRI) in diagnosing sagittal groove disease (SGD), a bone stress injury, in non-racing sport horses, indicating that the presence or absence of lameness is not a reliable measure of SGD severity.

Objective and Methodology

The aim of this study was to describe the abnormalities present in the sagittal groove (a part of the bone structure in horse’s limb) of a large group of horses identified with SGD using low-field MRI. The data was collated retrospectively and used a cross-sectional method.

  • The researchers examined medical records to identify initial MRI images of horses diagnosed with SGD.
  • The images were evaluated blindly using a semi-quantitative grading system and a new SGD MRI classification system.
  • This classification system was aimed to show potential pathways of pathological progression and severity of this stress injury to the bone.

Results

The sample size covered 132 limbs from 111 horses, primarily warmbloods involved in showjumping and dressage.

  • Distinctions were made among the MRIs based on the novel SGD MRI classification system; each diagnosis ranged from small subchondral defects to complete fractures.
  • Higher proportions of certain classifications were found in the lower third of hindlimbs compared to forelimbs.
  • Interestingly, no significant differences were found between the extent of bone edema-like signals in lame and non-lame limbs.
  • The study also identified, either confidently or suspected, periosteal new bone and edema-like signal at the top front aspect of the proximal phalanx (P1) in 25% and 39% of limbs, respectively.

Conclusion

The study concluded that:

  • The presence or absence of lameness is not a reliable measure of the severity of SGD.
  • The detection of periosteal edema-like signals in P1, not previously described in MRIs of SGD, lends additional support to the concept of bone stress injury.
  • Further, diagnoses included in original MRI reports, variable clinical history, and the small size of some classification groups were identified as limitations to the study.

Cite This Article

APA
Faulkner JE, Joostens Z, Broeckx BJG, Hauspie S, Mariën T, Vanderperren K. (2024). Low-field magnetic resonance imaging of sagittal groove disease of the proximal phalanx in non-racing sport horses. Equine Vet J. https://doi.org/10.1111/evj.14088

Publication

ISSN: 2042-3306
NlmUniqueID: 0173320
Country: United States
Language: English

Researcher Affiliations

Faulkner, Josephine E
  • Department of Morphology, Imaging, Orthopaedics, Rehabilitation and Nutrition, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
Joostens, Zoë
  • Equitom Equine Clinic, Lummen, Belgium.
Broeckx, Bart J G
  • Department of Veterinary and Biosciences, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.
Hauspie, Stijn
  • Equitom Equine Clinic, Lummen, Belgium.
Mariën, Tom
  • Equitom Equine Clinic, Lummen, Belgium.
Vanderperren, Katrien
  • Department of Morphology, Imaging, Orthopaedics, Rehabilitation and Nutrition, Faculty of Veterinary Medicine, Ghent University, Merelbeke, Belgium.

References

This article includes 29 references
  1. Kuemmerle JM, Auer JA, Rademacher N, Lischer CJ, Bettschart‐Wolfensberger R, Fürst AE. Short incomplete sagittal fractures of the proximal phalanx in ten horses not used for racing.. Vet Surg 2008;37(2):193–200.
  2. Brünisholz HP, Hagen R, Fürst AE, Kuemmerle JM. Radiographic and computed tomographic configuration of incomplete proximal fractures of the proximal phalanx in horses not used for racing.. Vet Surg 2015;44(7):809–815.
    doi: 10.1111/vsu.12364google scholar: lookup
  3. Gold SJ, Werpy NM, Gutierrez‐Nibeyro SD. Injuries of the sagittal groove of the proximal phalanx in warmblood horses detected with low‐field magnetic resonance imaging: 19 cases (2007–2016).. Vet Radiol Ultrasound 2017;58(3):344–353.
    doi: 10.1111/vru.12488google scholar: lookup
  4. Mizobe F, Nomura M, Ueno T, Yamada K. Bone marrow oedema‐type signal in the proximal phalanx of thoroughbred racehorses.. J Vet Med Sci 2019;81(4):593–597.
    doi: 10.1292/jvms.18-0530google scholar: lookup
  5. Lipreri G, Bladon BM, Giorio ME, Singer ER. Conservative versus surgical treatment of 21 sports horses with osseous trauma in the proximal phalangeal sagittal groove diagnosed by low‐field MRI.. Vet Surg 2018;47(7):908–915.
    doi: 10.1111/vsu.12936google scholar: lookup
  6. Dyson S, Nagy A, Murray R. Clinical and diagnostic imaging findings in horses with subchondral bone trauma of the sagittal groove of the proximal phalanx.. Vet Radiol Ultrasound 2011;52(6):596–604.
  7. Curtiss AL, Ortved KF, Dallap‐Schaer B, Gouzeev S, Stefanovski D, Richardson DR. Validation of standing cone beam computed tomography for diagnosing subchondral fetlock pathology in the Thoroughbred racehorse.. Equine Vet J 2021;53(3):510–523.
    doi: 10.1111/evj.13414google scholar: lookup
  8. Smith MRW, Wright IM. Radiographic configuration and healing of 121 fractures of the proximal phalanx in 120 Thoroughbred racehorses (2007‐2011).. Equine Vet J 2014;46(1):81–87.
    doi: 10.1111/evj.12094google scholar: lookup
  9. Powell S. Low‐field standing magnetic resonance imaging findings of the metacarpo/metatarsophalangeal joint of racing Thoroughbreds with lameness localised to the region: a retrospective study of 131 horses.. Equine Vet J 2012;44(2):169–177.
  10. Markel MD, Richardson DW. Noncomminuted fractures of the proximal phalanx in 69 horses.. J Am Vet Med Assoc 1985;186(6):573–579.
  11. Smith MRW, Wright IM. Are there radiologically identifiable prodromal changes in Thoroughbred racehorses with parasagittal fractures of the proximal phalanx?. Equine Vet J 2014;46(1):88–91.
    doi: 10.1111/evj.12093google scholar: lookup
  12. Ramzan PHL, Powell SE. Clinical and imaging features of suspected prodromal fracture of the proximal phalanx in three Thoroughbred racehorses.. Equine Vet J 2010;42(2):164–169.
    doi: 10.2746/042516409x478695google scholar: lookup
  13. Holcombe S, Schneider R, Bramlage L, Gabel A, Bertone A, Beard W. Lag screw fixation of noncomminuted sagittal fractures of the proximal phalanx in racehorses: 59 cases (1973‐1991).. J Am Vet Med Assoc 1995;206(8):1195–1199.
  14. Noble P, Singer ER, Jeffery NS. Does subchondral bone of the equine proximal phalanx adapt to race training?. J Anat 2016;229(1):104–113.
    doi: 10.1111/joa.12478google scholar: lookup
  15. Singer E, Garcia T, Stover S. How does bone strain vary between the third metacarpal and the proximal phalangeal bones of the equine distal limb?. J Biomech 2021;123:1–9.
  16. Olive J, D'anjou MA, Alexander K, Laverty S, Theoret C. Comparison of magnetic resonance imaging, computed tomography, and radiography for assessment of noncartilaginous changes in equine metacarpophalangeal osteoarthritis.. Vet Radiol Ultrasound 2010;51(3):267–279.
  17. Fredericson M, Bergman AG, Hoffman KL, Dillingham MS. Tibial stress reaction in runners correlation of clinical symptoms and scintigraphy with a new magnetic resonance imaging grading system.. Am J Sports Med 1995;23(4):472–481.
  18. Kijowski R, Choi J, Shinki K, Del Rio AM, De Smet A. Validation of MRI classification system for tibial stress injuries.. Am J Roentgenol 2012;198(4):878–884.
    doi: 10.2214/ajr.11.6826google scholar: lookup
  19. Faulkner JE, Joostens Z, Broeckx BJG, Hauspie S, Mariën T, Vanderperren K. Follow‐up magnetic resonance imaging of sagittal groove disease of the equine proximal phalanx using a classification system in 29 non‐racing sports horses.. Animals 2023;14(1):34.
    doi: 10.3390/ani14010034google scholar: lookup
  20. Olive J, Serraud N, Vila T, Germain JP. Metacarpophalangeal joint injury patterns on magnetic resonance imaging: a comparison in racing Standardbreds and Thoroughbreds.. Vet Radiol Ultrasound 2017;58(5):588–597.
    doi: 10.1111/vru.12512google scholar: lookup
  21. Smith MA, Dyson SJ, Murray RC. Reliability of high‐ and low‐field magnetic resonance imaging systems for detection of cartilage and bone lesions in the equine cadaver fetlock.. Equine Vet J 2012;44(6):684–691.
  22. Ross MW. Scintigraphic and clinical findings in the Standardbred metatarsophalangeal joint: 114 cases (1993‐1995).. Equine Vet J 1998;30(2):131–138.
  23. Lin ST, Foote AK, Bolas NM, Peter VG, Pokora R, Patrick H. Three‐dimensional imaging and histopathological features of third metacarpal/tarsal parasagittal groove and proximal phalanx sagittal groove fissures in thoroughbred horses.. Animals 2023;13:2912.
    doi: 10.3390/ani13182912google scholar: lookup
  24. De Guio C, Ségard‐Weisse E, Thomas‐Cancian A, Schramme M. Bone marrow lesions of the distal condyles of the third metacarpal bone are common and not always related to lameness in sports and pleasure horses.. Vet Radiol Ultrasound 2019;60(2):167–175.
    doi: 10.1111/vru.12700google scholar: lookup
  25. Smith MA, Dyson SJ. Normal MRI anatomy: The fetlock region.. 2010. In: Murray R, editor. Equine MRI. Chichester, UK: John Wiley & Sons Ltd; p. 173–189.
    doi: 10.1002/9781118786574.ch6google scholar: lookup
  26. Murray R, Werpy N. Principles of MRI in horses: Image interpretation and artefacts.. 2010. In: Murray R, editor. Equine MRI. Chichester, UK: John Wiley & Sons Ltd; p. 101–145.
    doi: 10.1002/9781118786574.ch4google scholar: lookup
  27. Powell S. Pathology: The fetlock region.. 2010. In: Murray RC, editor. Equine MRI. Chichester, UK: John Wiley & Sons Ltd; p. 315–359.
  28. Nagy A, Malton R. Diffusion of radiodense contrast medium after perineural injection of the palmar digital nerves.. Equine Vet Educ 2015;27(12):648–654.
    doi: 10.1111/eve.12369google scholar: lookup
  29. Steverink JG, Oostinga D, van Tol FR, van Rijen MHP, Mackaaij C, Verlinde‐Schellekens SAMW. Sensory innervation of human bone: an immunohistochemical study to further understand bone pain.. J Pain 2021;22(11):1385–1395.

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