Atlantoaxial instability (AAI)/subluxation commonly occurs in small breed dogs. Ventral stabilization techniques using screws and/or pins and a plate or, more commonly, polymethylmethacrylate are considered to provide the most favorable outcome. However, the implantation of screws of sufficient sizes for long-term stability becomes challenging in toy breed dogs (e.g. <2 kg). We herein report the application of 3D printing technology to implant trajectory planning and implant designing for the surgical management of AAI in 18 dogs. The use of our patient-specific drill guide templates resulted in overall mean screw corridor deviations of less than 1 mm in the atlas and axis, which contributed to avoiding iatrogenic injury to the surrounding structures. The patient-specific titanium plate was effective for stabilizing the AA joint and provided clinical benefits to 83.3% of cases (15/18). Implant failure requiring revision surgery occurred in only one case, and the cause appeared to be related to the suboptimal screw-plate interface. Although further modifications are needed, our study demonstrated the potential of 3D printing technology to be effectively applied to spinal stabilization surgeries for small breed dogs, allowing for the accurate placement of screws and minimizing peri- and postoperative complications, particularly at anatomical locations at which screw corridors are narrow and technically demanding.

Immunohistochemistry was performed to assess whether oxidative stress and/or denatured proteins play roles in the pathogenesis of canine degenerative myelopathy (DM). Two Pembroke Welsh Corgi (PWC) dogs with a homozygous mutation (c.118G>A) in the canine superoxide dismutase 1 (SOD1) gene were examined. The pathological features of the dogs were consistent with those of previous cases of DM in PWC. In the spinal lesions, diffuse SOD1 expression was observed in the neurons while no inclusion-like aggregates had formed, which disagreed with the findings of a previous study. A unique inducible nitric oxide synthase (iNOS) staining pattern in reactive astrocytes and a significant increase in ubiquitin immunoreactivity in the spinal lesions were also observed. These findings indicate the involvement of oxidative stress and the accumulation of ubiquitinated proteins in the pathogenesis of canine DM, whereas the role of SOD1 remains unclear.

Objectives: To develop drill guide templates as an intraoperative guide, and to evaluate the accuracy and safety of screw placement in the lumbosacral junction. Samples: Canine cadaveric specimens of the lumbosacral junction (n = 6), and clinical cases of lumbosacral instability (n = 3). Procedures: Computed tomography data of the lumbosacral region of cadaveric specimens and clinical cases were obtained. The optimum screw trajectories were determined and drill guide templates were fabricated using a three-dimensional printing system. Drill holes were made using the templates in cadaveric specimens and clinical cases, and lumbosacral fixation was performed in clinical cases. Computed tomography images were obtained to compare the planned and postoperative drill hole trajectories, and the accuracy and safety of drilling and screw placement in the lumbosacral junction were evaluated. Results: Thirty-six drill holes were made in cadaveric specimens. The overall mean drill hole deviation was 2.05 ± 1.32 mm. A total of 12 screws were placed in the lumbosacral junctions of three clinical cases. The overall mean drill hole deviation was 2.43 ± 1.09 mm. Clinical signs improved within 2 weeks in the clinical cases. All drill holes were completely located within the bone in cadaveric specimens and clinical cases. Conclusion and Clinical Relevance: The surgical procedures using the drill guide templates were performed safely with good clinical outcomes. The drill guide template system provided useful surgical guidance to safely and precisely perform screw placement for lumbosacral fixation surgery in small dogs.

Canine degenerative myelopathy (DM) is characterized by progressive degeneration of the spinal cord. Although atrophic changes in the intercostal muscles were previously reported in the late stage of DM in Pembroke Welsh Corgis (PWCs), changes in respiratory function have not yet been examined. In the present study, we performed an arterial blood gas analysis and measured respiratory movements over progressive disease stages to document changes in respiratory function in DM-affected PWCs. We found that respiratory dysfunction progressed during the later stages of DM and correlated with a change in respiratory movement to the abdominal breathing pattern. These results suggested that hypoventilation occurred due to dysfunctional changes in the intercostal muscles and resulted in hypoxemia in the later stages of DM.