Animal Preparation and Procedure
The study was conducted after obtaining institutional approval for the use of animals by the Korea University Institutional Animal Care and Use Committee (Protocol No. KUIACUC-2011-151).
Twelve adult mongrel dogs with a mean weight of 21 ± 2.77 kg were used in this study. Every dog was cared for by well-trained men from the Laboratory Animal Program of the Korea University Medical Center. To prevent distress, experiments were performed in a quiet and comfortable environment; dogs were heavily sedated by intramuscular injection of 1 mg/kg xylazine hydrochloride (100 mg/mL; Rompun® Bayer, Seoul, Korea) and 3 mg/kg ketamine. Oxygen (100%) was supplied through a facial mask at a flow rate of 5 L/min. After sedation, the dog was placed in a sternal recumbency position during the epidural procedure and a lateral recumbency position during the intrathecal procedure for maximum flexion of the cervical spine. The cephalic or accessory cephalic veins were used for fluid administration and blood sampling. The procedures were performed after aseptic preparation.
Epidural Catheterization
Epidural catheterization was performed at the first thoracic (T1)-second thoracic (T2) intervertebral space with the C-arm fluoroscopy-guided midline approach. Before the procedure, the fur of the lower cervical and upper thoracic areas were shaved, and the skin disinfected. The needle entry point was confirmed by palpation of T1 and T2 spinous processes and by C-arm fluoroscopy. An 18-gauge, 90 mm Tuohy epidural needle (B. Braun Medical, Inc., PA, USA) was inserted in the line between T1 and T2 with the bevel facing cephalad. As the needle was advanced slowly through the supraspinous and interspinous ligaments and pierced the interarcuate ligament, a distinct popping sensation was felt. Then, the epidural space was confirmed by “loss of resistance” test (Fig. 1). A flexible epidural catheter (PerifixTM; B-Brown, Melsungen AG, Germany) was advanced cranially to the second cervical (C2)-third cervical (C3) level through the needle. The location of the catheter tip was verified fluoroscopically by injecting contrast medium into the catheter (Fig. 2). Once the correct position of the catheter was confirmed, it was fixed in place with sterile dressing. We measured the depth from the skin to the epidural space at the T1–T2 level every time. We also measured the length of the epidural catheter inserted at the C2–C3 level.
Intrathecal Catheterization
Intrathecal catheterization was performed through the cisterna magna (CM) in the sternal recumbency position with the neck slightly flexed. Before the procedure, the fur of the occipital and posterior neck was shaved, and the skin was disinfected. The needle entry point was the center of a virtual triangle comprising the external protuberance and the two tips of transverse processes of the first cervical vertebra (C1) (Fig. 3). After the bony landmarks were palpated, the 18-gauge Tuohy needle was inserted perpendicularly to the skin in the midline until resistance was no longer felt. After confirming cerebrospinal fluid (CSF) leakage without bleeding, a flexible intrathecal catheter (PerifixTM; B-Brown, Melsungen AG, Germany) was inserted and advanced caudally to the C2–C3 level so that the tip of the catheter was located immediately adjacent to the tip of the epidural catheter (Fig. 4-A, B, C). The location of the catheter tip was verified fluoroscopically by injecting contrast medium through the catheter (Fig. 5). Once the correct position was confirmed, the catheter was fixed on the occiput with sterile dressing. We measured the depth from the center of the virtual triangle to the intrathecal space (cm) each time. We also measured the length of the intrathecal catheter inserted at the C2–C3 level.
After acquiring the data, the dogs were euthanized with potassium chloride. After the intramuscular injection of 5 mg/kg ketamine and 1 mg/kg xylazine hydrochloride prior to the euthanasia, the dogs were confirmed to be unconscious. Potassium chloride was then intravascularly injected at a dose of 150 mg/kg. Fortunately, clonic spasm did not occur after the administration of potassium chloride. Death of dogs was confirmed by lack of pulse, breathing, corneal reflex, response to a firm toe pinch, and respiratory sounds and heartbeat with stethoscope and by the graying of the mucous membranes and rigor mortis. The euthanasia methods employed in this study followed the American Veterinary Medical Association (AVMA) guidelines for the euthanasia of dogs.