Outcomes of extensive hemilaminectomy with durotomy on dogs with presumptive progressive myelomalacia: a retrospective study on 34 cases
BMC Veterinary Research volume 16, Article number: 476 (2020)
Progressive myelomalacia (PMM) is a fatal complication of progressive ascending and descending necrosis of the spinal cord after acute spinal cord injury. A recent study suggested that extensive hemilaminectomy with durotomy (EHLD) at the intramedullary T2-hyperintense region which performed immediately after magnetic resonance imaging (MRI) improved the survival rate in dogs with presumptive PMM. The objective of this retrospective study was to evaluate the effects of EHLD on halting the progression of PMM in dogs presumptively diagnosed with PMM which had the interval between MRI and surgery.
Thirty-four dogs with presumptive PMM which had undergone EHLD with the delay following MRI examination (range, 0 to 3 days) were included. The cranial side of EHLD was set depending on the delay time after MRI, MRI findings, neurological examination and intraoperative macroscopic appearance. Two weeks after surgery, the perioperative survival rate was 97% (33/34). During follow-up with a median time period of 82.5 weeks (range, 0-290 weeks), the postoperative survival rate was 91% (31/34). At the end of the follow-up period, 31 out of 34 dogs were alive without severe postoperative complications while the remaining 2 dogs died from causes not directly attributable to the surgery. There was no improvement in the pelvic limb function of all dogs.
EHLD appears to be effective in halting the progression of presumptive PMM and preventing morbidity even in dogs which had the interval between MRI and EHLD. Our algorithm of determining the range of EHLD may enable to set the appropriate ranges of EHLD in the cases which develop signs consistent with PMM after MRI examination.
Progressive myelomalacia (PMM) is a fatal disease characterized by progressive ascending and descending necrosis of the spinal cord after acute spinal cord injury [1, 2]. PMM is frequently observed following thoracolumbar intervertebral disk herniation (IVDH) with no deep pain perception (NDPP) in the pelvic limbs [1, 3]. The prevalence of PMM with IVDH has been estimated at 2%, ranging from 0–15% depending on clinical grade . In paraplegic dogs with NDPP, its prevalence ranges from 9 to 25% [2, 4,5,6,7,8].
The initial clinical signs of PMM are lower motor neuron signs in the pelvic limbs and cranial advancement of the caudal border of the cutaneous trunci muscle (CTM) reflex. CTM originates in the caudal gluteal region and runs cranially and ventrally to insert into the axillary region, where it connects with the latissimus dorsi muscle and the deep pectoral muscle . The CTM reflex is commonly used to localize thoracolumbar spinal lesions and its caudal movement is considered a reliable predictor of recovery in dogs affected by different pathologies including acute thoracolumbar myelopathies [10, 11].
Following the onset of PMM, loss of anal and abdominal tone, plegia of the thoracic limbs and respiratory muscles develop. Most dogs are euthanized before respiratory failure result in their deaths [1, 2]. The diagnosis is suspected by the course of clinical signs and corresponding magnetic resonance imaging (MRI) findings before confirmation with histology demonstrating necrosis of the spinal cord. An intramedullary hyperintense signal longer than 6 times the length of L2 vertebral body on T2-weighted images on MRI is suggestive of PMM . An extensive intramedullary hyperintensity has also been reported in dogs with IVDH that did not develop myelomalacia and with other myelopathies [1, 13, 14]. Since some dogs develop signs consistent with PMM after MRI examination, the absence of intramedullary T2 hyperintensity does not preclude the development of PMM .
Although the pathophysiological mechanism of PMM is poorly understood, it involves primary mechanical damage due to the spinal cord concussion and contusion caused by the disk herniation, and secondary damage caused by ischemia, edema, electrolyte shifts, oxidative stress, inflammation, and apoptosis [15,16,17]. A recent study showed elevated intramedullary pressure associated with hemorrhage further leads to the progression of spinal cord destruction .
Both durotomy and extended thoracolumbar durotomy were previously shown to improve the rate of regaining ambulation in dogs with IVDH and NDPP in the pelvic limbs [18, 19]. The improved outcome after durotomy or extensive durotomy seemed to result from physical decompression of the spinal cord [18, 19]. Additionally, performing durotomy seemed to prevent the development of PMM in dogs with IVDH and NDPP in the pelvic limbs . Another retrospective study also reported that prompt surgical decompression and treatment with corticosteroids were associated with lower odds of developing PMM in dogs with IVDH and NDPP .
Since several studies reported that elevated intramedullary pressure is involved in the pathophysiology of PMM [15, 21, 22], spinal decompression by surgery may be effective against the progression of PMM. A recent study suggested that the extensive hemilaminectomy with durotomy (EHLD) at the intramedullary T2-hyperintense region on MRI improved the survival rate of dogs with presumptive PMM compared with dogs underwent standard hemilaminectomy . In the study, EHLD was performed immediately after they underwent MRI under sustained anesthesia . However, it is unclear that EHLD can be applied in dogs with a delay after MRI because the myelomalacia progress over time in dogs with PMM. The purpose of the present study was to investigate the effectiveness and appropriate ranges of EHLD against the progression of PMM with a time lag after MRI.
Thirty-four dogs with presumptive PMM underwent EHLD (Table 1). Median age was 5.1 years (range, 2.8–13.8 years) at the time of surgery. There were 21 males (9 castrated) and 13 females (7 spayed). Breeds were 23 Miniature Dachshunds, 8 Toy Poodles, 2 French Bulldogs and 1 Chihuahua.
History and clinical signs
Clinical signs before surgery included paraplegia with NDPP (all dogs), plegia of the thoracic limbs (3 dogs) and paresis of the thoracic limbs (8 dogs). Mean duration from onset of non-ambulatory obtained through owner interviews to surgery was 3.8 days (range, 1 day to 9 days). Before referral for surgery, prednisone had been administered to 10 dogs. Medical treatment before surgery of 13 dogs was unknown.
Distribution of T-L IVDH site was T10-11 (1), T11-12 (3), T12-13 (5), T13-L1 (8), L1-2 (4), L2-3 (1), L3-4 (6), L4-5 (1), L5-6 (2) and multiple (3). Mean length of intramedullary hyperintense region was 13.9 (range, 6.7 to 21.7) times of the L2 vertebral body. No dogs underwent EHLD immediately after MRI. Mean duration from MRI to surgery was < 24 hours (19), 24–48 hours (12), 48–72 hours (1) and 72–96 hours (2).
Surgical details and histological findings
EHLD was performed in all dogs (Fig. 1). Extruded intervertebral disk material was present in all dogs and their spinal cords exhibited extensive gross softening and liquefaction macroscopically. In all dogs, a confirmed histological diagnosis of myelomalacia was made through biopsy in the softened spinal cord at the site of extruded intervertebral disc. The mean vertebral body-length window of the EHLD was 12 (range, 5 to 20). The cranial side of the EHLD was C7 (6), T1 (7), T2 (3), T3 (7), T4 (2), T5 (3), T7 (1), T8 (1), T9 (2), T10 (1), T13 (1). There were no intraoperative complications.
Two weeks after surgery, the perioperative survival rate was 97% (33/34, Table 2). One dog (No.23) which had tetraplegia died 3 days after surgery with respiratory failure (Tables 1 and 2). The dog belonged to the subgroup of cases which underwent EHLD within 24 hours after MRI examination (Table 2). Perioperatively, 15 dogs (44%) experienced fever (range, 39.1–40.2℃) between 1 day and 12 days after surgery. They were administered chloramphenicol and intravenous fluid infusion and recovered within a few days.
Postoperative outcome and follow-up
No dogs were lost to follow-up. During follow-up with a median time period of 82.5 weeks (range, 0-290 weeks), the postoperative survival rate was 91% (31/34, Table 2). Of the two dogs which died, one died 54 days after surgery (No. 6) from aspiration pneumonia, at home. The other dog died 56 days after surgery (No. 14) from renal failure secondary to pyelonephritis due to an ascending urinary tract infection at another hospital. Both dogs belonged to the subgroup of cases which had intact CP of the thoracic limbs, and the intervals were less than 24 hours between MRI and surgery (Table 2). All remaining dogs were alive during follow-up period. Although they had sporadic urinary tract infections, no serious postoperative complications occurred in this study. None of the dogs underwent spinal stabilization. No dogs had radiological evidence of spinal luxation or subluxation 2 weeks and 8 weeks after surgery (Fig. 2). In addition, 12 dogs were had radiographic evaluation at a median time period of 75.5 weeks after surgery (range, 13 to 204). Similarly, these dogs did not have radiological evidence of postoperative complications. None of the dogs experienced clinical improvement of pelvic limb function. In contrast, neurological function of the thoracic limbs was improved within 2 months after surgery in all 8 dogs with paresis of the forelimbs although it was not observed in the dogs with tetraplegia during follow-up period.
This study demonstrates EHLD as a potentially life-saving treatment for dogs with presumptive PMM, similar to a previous study . Additionally, the present study suggests that EHLD can apply to the cases with the delay following MRI examination. Typically, dogs diagnosed with PMM followed a fatal course [1, 3, 12]. According to the literature, the majority of dogs with presumptive and confirmed PMM are euthanized within 4 days following onset although delayed progression to euthanasia may take as long as 2 weeks . The perioperative survival rate in this study at 2 weeks after surgery was 97% (31/34), indicating high survival rate. It has been reported that elevated intramedullary pressure is involved in the pathophysiology of PMM [15, 21, 22]. More specifically, in PMM, spinal cord debris together with cerebrospinal fluid accumulating in the central canal are transported cranially and caudally due to the increased intramedullary pressure causing a broadening of the tissue necrosis and hemorrhagic lysis of the spinal cord segments. The dura mater plays an essential role in the function of the spinal cord. Representing the strongest structure of the meninges, it sustains the flow and pressure of the cerebral spinal fluid due to its stiffness in circumferential direction [22, 24, 25]. In an experimental edema model using the spinal cords of human cadavers, the pia mater was also showed to be involved in increasing intramedullary pressure . However, in the previous studies on human medicine, the physical therapy of incising the dura seems to achieve sufficient decompression effect on reducing intramedullary pressure [27, 28]. Therefore, we hypothesized that extensive incision of the dura mater and hemilaminectomy in dogs with PMM could reduce intramedullary pressure. It was already observed that decompression with durotomy is possibly an effective treatment for recovering ambulation in severe acute IVDH [18, 19]. These studies showed that durotomy in combination with decompression could potentially prevent the development of PMM in dogs with IVHD with NDPP of the pelvic limbs [18, 19]. The authors discussed that a durotomy might not prevent further progression in dogs advanced PMM . However, a recent study  and the present study indicate that spinal decompression with EHLD halts further progression of PMM even for cases with a presumptive diagnosis of advanced PMM.
The extend of hemilaminectomy and durotomy should be carefully considered. A previous study showed that the durotomy extending for four vertebral lengths improved functional outcome in dogs with severe spinal cord injury after acute IVDH . Selection of this length was based on previous studies on the length of spinal cord swelling estimated from imaging findings [14, 29]. In general, hyperintensity in T2-weighted images on MRI represents the liquid component. In dogs with presumptive and confirmed PMM, the T2-weighted images on MRI of the spinal cord frequently shows hyperintensity due to irreversible progressive necrosis of the parenchyma with or without intradural hemorrhage . Thus, EHLD should be performed with the hyperintense region on T2-weighted image taken as the affected portion of PMM. In a recent study, EHLD at the site of T2-hyperintense region was immediately performed after MRI examination in dogs with presumptive PMM following IVDH . All dogs enrolled in our study already underwent MRI at other referral centres before surgery, and the delay to surgery prompted hemilaminectomies and durotomies even longer than T2-hyperintense lengths on MRI. In cases operated on the day after MRI, the cranial side of the EHLD range was set to 1 additional vertebral body to the cranial side of the T2-weighted hyperintense region to take into account disease progression. In cases where several days have passed after MRI imaging, the rate of progression of myelomalacia could not be determined accurately. In dogs, musculocutaneous nerves originate from C7 and C8, the radial nerve from C8 and the median and ulnar nerves from C8 and T1 . Therefore, in cases operated more than 24 hours after MRI, the cranial extent of operation was set to T3 in cases with paresis of the thoracic limbs and set to T1 in cases with plegia of the thoracic limbs. Some dogs had abnormal macroscopic findings of swollen in the spinal cord at T3 or T1 during surgery, suggesting that intramedullary pressure was elevated due to progression of PMM. Accordingly, when swollen of the spinal cord at T3 or T1 was observed macroscopically after durotomy, an incision was extended to T2 or C7, respectively, of the anterior vertebral body. However, there is the possibility that this setting to cranial site of EHLD is too excessive. Further studies are necessary to evaluate minimal necessary extend of hemilaminectomy and durotomy.
One dog (No.23) which had tetraplegia died 3 days after surgery with respiratory failure. This finding suggests that cases with tetraplegia possibly have a higher risk of death after EHLD. According to the literature, the majority of dogs with presumptive and confirmed PMM are euthanized within 17 days of presentation . Similar to a previous study , although EHLD was shown to be effective as a life-saving treatment for presumptive PMM in this study, there was no improvement of pelvic limb function. It is necessary to recognize that EHLD is not a surgery aimed at reversing plegia but at stopping the progression of myelomalacia. Pre-operative informed consent with extensive counseling is important for the owner to understand the role of EHLD in PMM and the long-term care required after surgery.
EHLD is highly invasive to the spine and spinal cord, therefore the risk of postoperative complications was also expected to be high. However, no serious complications caused by EHLD occurred in this study. Two dogs died from causes unrelated to the surgery approximately 2 months after EHLD. Importantly, these dogs did not have plegia of the thoracic limbs before surgery and no cases with plegia of the thoracic limbs died during follow-up. Although limitations of this study include its small sample size, forelimb plegia is unlikely to be a risk factor in long-term postoperative survival. However, in cases with residual thoracic limb plegia, there is a concern of a decrease in postoperative quality of life. Conversely, without thoracic limb plegia, walking with a wheelchair is possible and the owner’s satisfaction is likely to be higher.
There are several limitations in our study due to its retrospective nature. A definitive diagnosis of PMM requires post-mortem examination [1, 31]. Instead, the diagnosis of presumptive PMM in this study was based on clinical signs that reflected the progressive myelopathy. Additionally, all dogs had histopathologic confirmation of focal myelomalacia at the site of extruded intervertebral disc. However, the lack of postmortem confirmation of PMM does not allow us to eliminate the cases of focal myelomalacia. Previous studies suggested that the presence of a cerebrospinal fluid (CSF): L2half − Fourier acquisition single−shot turbo spin−echo (HASTE) ≥ 7.4 times was higher sensitivity to diagnose presumptive and confirmed PMM than T2 hyperintensity used in the current study [1, 14]. Thus, CSF: L2HASTE may use as a more reliable MRI criterion for the suspicion of PMM although this finding was not specific to PMM as well as T2 hyperintensity [1, 14]. A second limitation relates to the lack of a control group in the present study. It was because there were few cases followed up without EHLD in our hospital. Previous studies demonstrated a fatal course in dogs with presumptive and confirmed PMM [12, 23]. However, in almost all previous reports, the dogs described as PMM were not able to confirm a fatal progression because most dogs were humanely euthanased before respiratory failure results in their spontaneous death [1, 3, 20]. Moreover, some dogs diagnosed with presumptive PMM showed halting further progression after initial progression , which is similar to the findings obtained from human patients with subacute posttraumatic ascending myelopathy . Thus, additional studies including control groups are necessary to address the presence of cases which did not have fatal progression even if untreated in our clinical setting.
In summary, EHLD appears to be a life-saving treatment for PMM. Our algorithm of determining the range of EHLD is likely to be useful for setting the appropriate ranges of EHLD in the cases which develop signs consistent with PMM after MRI examination. However, the pathophysiology of PMM is unknown in many ways and further studies are required to develop new treatment methods.
To evaluate the effects of EHLD on halting the progression of PMM in dogs diagnosed with presumptive PMM which had a time lag between MRI and surgery.
Design and setting
Retrospective review of 34 consecutive cases of presumptive PMM that have undergone EHLD at a private hospital.
The medical records of dogs diagnosed with IVDH at our referral and first opinion service from November 2014 through May 2020 were searched to identify cases with a presumptive diagnosis of PMM. According to the criteria of a previous study , a presumptive diagnosis of PMM was made based on neurological examination findings and the progression of clinical signs corroborated with MRI findings. All dogs presented with acute paraplegia and NDPP in both pelvic limbs and the tail. All dogs showed all the following additional clinical signs consistent with PMM: complete loss of pelvic limb reflexes, the loss of perineal and abdominal tones progressively, cranial advancement of the CTM reflex cut-off and a CTM reflex caudal border more than two vertebral levels cranial to the site of disc extrusion. All dogs had undergone MRI examination at multiple centres prior to surgery. MRI findings suggestive of PMM following IVDH were also taken into account as inclusion criteria. Extruded intervertebral disk material with spinal cord compression were detected by MRI in all dogs. The MRI findings of all dogs also showed intramedullary hyperintense region of the spinal cord > 6 times the length of L2 vertebral body on T2-weighted imaging . Since extensive intramedullary T2 hyperintensity on MRI is not specific findings of PMM, dogs were excluded if the progression of the signs stopped prior to surgery. Dogs with NDPP in the thoracic limbs were also excluded. Informed consent for the EHLD procedure and information collection for research purposes were obtained. The review of MRI was performed using an Osirix 64-bit imaging software workstation (Pixmeo, Bernex, Switzerland) by the author (RH).
The same anesthetic protocol was used for all dogs. Dogs were premedicated with 0.025 mg/kg atropine, subcutaneously. Anesthesia was induced using 0.5 mg/kg midazolam intravenously (IV), and Propofol (4 mg/ kg, IV, to effect). Anesthesia was maintained with isoflurane (1–2%) in 100% oxygen. Cefazolin sodium (25 mg/kg, IV) and 0.5 mg/kg morphine, were administered intramuscularly after induction.
Dogs were positioned in sternal recumbency. A dorsal approach was made to the T-L spine. At the beginning, hemilaminectomy was performed then the extruded disc material was removed. Subsequently, the dura mater of the spinal cord at the site was incised (Fig. 1a). After macroscopically verifying the presence of spinal softening and liquefaction at the IVDH site, EHLD was performed on the spinal cord (Fig. 1b). The hemilaminectomy and the durotomy were performed on the same vertebral body-length. In addition, the softened spinal cord at the site of extruded intervertebral disc was biopsied with a curette and fixed in formalin for histological diagnosis. A thin layer of subcutaneous fat graft was applied to the hemilaminectomy site before wound closure (Fig. 1c). The cranial side of the hemilaminectomy with durotomy range was set to 1 additional vertebral body to the cranial side of the T2-weighted hyperintense region as recognized by the MRI where the surgery was performed less than 24 hours after imaging (Fig. 3). In cases of more than 24 hours between MRI and surgery, the cranial site of the EHLD range was determined based on the neurological examination of the thoracic limbs and the macroscopic appearance during surgery (Fig. 3). The cranial site was set to T3 in cases with paresis of the thoracic limbs, and to T1 in those with plegia of the thoracic limbs (Fig. 3). If swollen of the spinal cord at T3 or T1 was seen macroscopically after durotomy, an incision was extended to T2 or C7, respectively, of the anterior vertebral body (Fig. 3).
Constant rate infusion of morphine (0.1–0.2 mg/kg/h, IV) was administered for the initial 48 hours after surgery. Prednisone (0.5 mg/kg, subcutaneously, 24 hours) was administered for 3–5 days after surgery. Cefazolin sodium (25 mg/kg, IV, every 12 hours) or Cephalexin (25 mg/kg, orally, every 12 hours) was administered for 10–14 days. Additionally, Chloramphenicol (25 mg/kg, IV, every 8 hours) was administered for 3–7 days to dogs with increased body temperature (> 39℃) . Dogs were discharged from the hospital 10–21 days after surgery.
Dogs were re-examined 2–4 weeks after discharge, and monthly re-examinations were conducted by the authors for 3–6 months to evaluate general health and neurologic signs. Dogs were also re-examined with radiographic evaluation of right lateral and dorsoventral views 2 weeks and 8 weeks after surgery by the author (RH) to evaluate a spinal luxation or subluxation. Subsequently, annual or biannual follow-up was performed by re-examination or telephone consultations.
Availability of data and materials
The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.
Cutaneous trunci muscle
No deep pain perception
Extensive hemilaminectomy with durotom
Half-Fourier acquisition single-shot turbo spin-echo
Thoracolumbar intervertebral disk herniation
Magnetic resonance imaging
Castel A, Olby NJ, Mariani CL, Munana KR, Early PJ. Clinical Characteristics of Dogs with Progressive Myelomalacia Following Acute Intervertebral Disc Extrusion. J Vet Intern Med. 2017;31(6):1782–9.
Olby N, Levine J, Harris T, Munana K, Skeen T, Sharp N. Long-term functional outcome of dogs with severe injuries of the thoracolumbar spinal cord: 87 cases (1996–2001). J Am Vet Med Assoc. 2003;222(6):762–9.
Balducci F, Canal S, Contiero B, Bernardini M. Prevalence and Risk Factors for Presumptive Ascending/Descending Myelomalacia in Dogs after Thoracolumbar Intervertebral Disk Herniation. J Vet Intern Med. 2017;31(2):498–504.
Scott HW, McKee WM. Laminectomy for 34 dogs with thoracolumbar intervertebral disc disease and loss of deep pain perception. J Small Anim Pract. 1999;40(9):417–22.
Stiffler KS, Stevenson MA, Sanchez S, Barsanti JA, Hofmeister E, Budsberg SC. Prevalence and characterization of urinary tract infections in dogs with surgically treated type 1 thoracolumbar intervertebral disc extrusion. Vet Surg. 2006;35(4):330–6.
Jeffery ND, Barker AK, Hu HZ, Alcott CJ, Kraus KH, Scanlin EM, Granger N, Levine JM. Factors associated with recovery from paraplegia in dogs with loss of pain perception in the pelvic limbs following intervertebral disk herniation. J Am Vet Med Assoc. 2016;248(4):386–94.
Olby NJ, Muguet-Chanoit AC, Lim JH, Davidian M, Mariani CL, Freeman AC, Platt SR, Humphrey J, Kent M, Giovanella C, et al. A Placebo-Controlled, Prospective, Randomized Clinical Trial of Polyethylene Glycol and Methylprednisolone Sodium Succinate in Dogs with Intervertebral Disk Herniation. J Vet Intern Med. 2016;30(1):206–14.
Fenn J, Ru H, Jeffery ND, Moore S, Tipold A, Soebbeler FJ, Wang-Leandro A, Mariani CL, Early PJ, Munana KR, et al. Association between anesthesia duration and outcome in dogs with surgically treated acute severe spinal cord injury caused by thoracolumbar intervertebral disk herniation. J Vet Intern Med. 2020;34(4):1507–13.
Slatter DH: Textbook of small animal surgery, vol. 1: Elsevier Health Sciences; 2003. p. 292–321.
Krogh JE, Denslow JS. The cutaneus trunci muscle in spinal reflexes. Electromyogr Clin Neurophysiol. 1979;19(1–2):157–64.
Muguet-Chanoit AC, Olby NJ, Lim JH, Gallagher R, Niman Z, Dillard S, Campbell J, Early P, Mariani CL, Munana KR, et al. The cutaneous trunci muscle reflex: a predictor of recovery in dogs with acute thoracolumbar myelopathies caused by intervertebral disc extrusions. Vet Surg. 2012;41(2):200–6.
Okada M, Kitagawa M, Ito D, Itou T, Kanayama K, Sakai T. Magnetic resonance imaging features and clinical signs associated with presumptive and confirmed progressive myelomalacia in dogs: 12 cases (1997–2008). J Am Vet Med Assoc. 2010;237(10):1160–5.
Wang-Leandro A, Hobert MK, Alisauskaite N, Dziallas P, Rohn K, Stein VM, Tipold A. Spontaneous acute and chronic spinal cord injuries in paraplegic dogs: a comparative study of in vivo diffusion tensor imaging. Spinal Cord. 2017;55(12):1108–16.
Gilmour LJ, Jeffery ND, Miles K, Riedesel E. Single-Shot Turbo Spin Echo Pulse Sequence Findings in Dogs with and without Progressive Myelomalacia. Vet Radiol Ultrasound. 2017;58(2):197–205.
Henke D, Gorgas D, Doherr MG, Howard J, Forterre F, Vandevelde M. Longitudinal extension of myelomalacia by intramedullary and subdural hemorrhage in a canine model of spinal cord injury. Spine J. 2016;16(1):82–90.
Marquis A, Packer RA, Borgens RB, Duerstock BS. Increase in oxidative stress biomarkers in dogs with ascending-descending myelomalacia following spinal cord injury. J Neurol Sci. 2015;353(1–2):63–9.
Mayer D, Oevermann A, Seuberlich T, Vandevelde M, Casanova-Nakayama A, Selimovic-Hamza S, Forterre F, Henke D. Endothelin-1 Immunoreactivity and its Association with Intramedullary Hemorrhage and Myelomalacia in Naturally Occurring Disk Extrusion in Dogs. J Vet Intern Med. 2016;30(4):1099–111.
Jeffery ND, Mankin JM, Ito D, Boudreau CE, Kerwin SC, Levine JM, Krasnow MS, Andruzzi MN, Alcott CJ, Granger N: Extended durotomy to treat severe spinal cord injury after acute thoracolumbar disc herniation in dogs. Vet Surg. 2020.
Takahashi F, Honnami A, Toki M, Dosaka A, Fujita Y, Hara Y, Yamaguchi S. Effect of durotomy in dogs with thoracolumbar disc herniation and without deep pain perception in the hind limbs. Vet Surg. 2020;49(5):860–9.
Castel A, Olby NJ, Ru H, Mariani CL, Munana KR, Early PJ. Risk factors associated with progressive myelomalacia in dogs with complete sensorimotor loss following intervertebral disc extrusion: a retrospective case-control study. BMC Vet Res. 2019;15(1):433.
Lu D, Lamb CR, Targett MP. Results of myelography in seven dogs with myelomalacia. Vet Radiol Ultrasound. 2002;43(4):326–30.
Shetye SS, Deault MM, Puttlitz CM. Biaxial response of ovine spinal cord dura mater. J Mech Behav Biomed Mater. 2014;34:146–53.
Nakamoto Y, Uemura T, Hasegawa H, Nakamoto M, Ozawa T: Outcomes of dogs with progressive myelomalacia treated with hemilaminectomy or with extensive hemilaminectomy and durotomy. Veterinary Surgery. 2020, in press.
Persson C, Evans S, Marsh R, Summers JL, Hall RM. Poisson’s ratio and strain rate dependency of the constitutive behavior of spinal dura mater. Ann Biomed Eng. 2010;38(3):975–83.
Wilcox RK, Bilston LE, Barton DC, Hall RM. Mathematical model for the viscoelastic properties of dura mater. J Orthop Sci. 2003;8(3):432–4.
Harwell DM, Gibson JL, Fessler RD, Holtz J, Pettigrew DB. Kuntz Ct: Pia Mater Significantly Contributes to Spinal Cord Intraparenchymal Pressure in a Simulated Model of Edema. Spine (Phila Pa 1976). 2016;41(9):E524–9.
Khaing ZZ, Cates LN, Fischedick AE, McClintic AM, Mourad PD, Hofstetter CP. Temporal and Spatial Evolution of Raised Intraspinal Pressure after Traumatic Spinal Cord Injury. J Neurotrauma. 2017;34(3):645–51.
Phang I, Werndle MC, Saadoun S, Varsos G, Czosnyka M, Zoumprouli A, Papadopoulos MC. Expansion duroplasty improves intraspinal pressure, spinal cord perfusion pressure, and vascular pressure reactivity index in patients with traumatic spinal cord injury: injured spinal cord pressure evaluation study. J Neurotrauma. 2015;32(12):865–74.
Duval J, Dewey C, Roberts R, Aron D. Spinal cord swelling as a myelographic indicator of prognosis: a retrospective study in dogs with intervertebral disc disease and loss of deep pain perception. Vet Surg. 1996;25(1):6–12.
Skelding A, Valverde A, Sinclair M, Thomason J, Moens N. Anatomical characterization of the brachial plexus in dog cadavers and comparison of three blind techniques for blockade. Vet Anaesth Analg. 2018;45(2):203–11.
Griffiths IR. The extensive myelopathy of intervertebral disc protrusions in dogs (‘the ascending syndrome’). J Small Anim Pract. 1972;13(8):425–38.
Miller BA, Ahmad FU. Subacute posttraumatic ascending myelopathy: a literature review. Spinal Cord Ser Cases. 2017;3:17012.
Sato J. Experimental and clinical studies on the time-dependent transit into cerebrospinal fluid of antibiotics administered systemically. Neurol Med Chir (Tokyo). 1978;18(10 2):753–63.
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This study was approved by the Institutional Review Board of Kyoto Animal Medical Center. Written informed consent was obtained from all owners.
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Ryuji Hirano and Ryota Asahina are joint first authors.
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Hirano, R., Asahina, R., Hirano, T. et al. Outcomes of extensive hemilaminectomy with durotomy on dogs with presumptive progressive myelomalacia: a retrospective study on 34 cases. BMC Vet Res 16, 476 (2020). https://doi.org/10.1186/s12917-020-02690-z