Peer-reviewed veterinary case report
Effects of flexion and extension on the diameter of the caudal cervical vertebral canal in dogs.
- Journal:
- Veterinary surgery : VS
- Year:
- 2015
- Authors:
- Ramos, Renato M et al.
- Affiliation:
- Department of Veterinary Clinical Sciences · United States
- Species:
- dog
Abstract
OBJECTIVE: To quantify changes in the diameter of the vertebral canal with flexion and extension in the cervical vertebral column. STUDY DESIGN: Cadaveric biomechanical study. SAMPLE POPULATION: Cadaveric canine cervical vertebral column (n = 16 dogs). METHODS: All vertebral columns were evaluated with MRI. Group 1 consisted of 8 normal vertebral columns. Group 2 included 8 vertebral columns with intervertebral disc degeneration. Flexion, extension, compression, and tension were applied to the caudal cervical region (C4-5, C5-6, C6-7). Sagittal vertebral canal diameters (VCD) were obtained by measuring the distance between the ventral and dorsal aspects of vertebral canal. RESULTS: No differences were seen between groups, thus the results are for both groups. Comparison of VCD between flexion and extension with no load revealed a difference of 2.2 mm (28.9%; P < .001). Comparison between neutral position and extension revealed a reduction of 1.5 mm (16.5%; P < .001), whereas comparison between neutral and flexion showed an increase of 0.7 mm (7.7%; P = .001) in VCD. Comparison between neutral with no load and neutral with compression showed a difference of 0.5 mm, with reduction of 5.5% in the vertebral canal (P = .006). Comparison of extension with no load versus extension with tension revealed an increase of 0.7 mm (9.2%) in the vertebral canal (P < .001). CONCLUSIONS: Cervical vertebral canal diameter decreased significantly with extension and increased with flexion. The results support the presence of dynamic impingement possibly playing a role in diseases characterized by vertebral canal stenosis, such as cervical spondylomyelopathy.
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Search related cases →Original publication: https://pubmed.ncbi.nlm.nih.gov/25412567/