Acute spinal cord injury in the cat

Acute spinal cord injury in the cat

Journal of Feline Medicine and Surgery Acute Spinal Cord Injury in the Cat: Causes, Treatment and Prognosis Salih Eminaga, Vi...

24MB Sizes 5 Downloads 369 Views

Journal of Feline Medicine and Surgery

Acute Spinal Cord Injury in the Cat: Causes, Treatment and Prognosis Salih Eminaga, Viktor Palus and Giunio Bruto Cherubini Journal of Feline Medicine and Surgery 2011 13: 850 DOI: 10.1016/j.jfms.2011.09.006 The online version of this article can be found at:

Disclaimer The Journal of Feline Medicine and Surgery is an international journal and authors may discuss products and formulations that are not available or licensed in the individual reader's own country. Furthermore, drugs may be mentioned that are licensed for human use, and not for veterinary use. Readers need to bear this in mind and be aware of the prescribing laws pertaining to their own country. Likewise, in relation to advertising material, it is the responsibility of the reader to check that the product is authorised for use in their own country. The authors, editors, owners and publishers do not accept any responsibility for any loss or damage arising from actions or decisions based on information contained in this publication; ultimate responsibility for the treatment of animals and interpretation of published materials lies with the veterinary practitioner. The opinions expressed are those of the authors and the inclusion in this publication of material relating to a particular product, method or technique does not amount to an endorsement of its value or quality, or the claims made by its manufacturer.

Published by: International Society of Feline Medicine

American Association of Feline Practitioners


Additional services and information for Journal of Feline Medicine and Surgery can be found at: Email Alerts: Subscriptions: Reprints: Permissions:

>> Version of Record - Nov 1, 2011 What is This? Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

Journal of Feline Medicine and Surgery (2011) 13, 850–862 doi:10.1016/j.jfms.2011.09.006


ACUTE SPINAL CORD INJURY IN THE CAT Causes, treatment and prognosis Salih Eminaga, Viktor Palus and Giunio Bruto Cherubini Practical relevance Acute spinal conditions are a common emergency presentation in general veterinary practice and have the potential to cause devastating spinal cord injury (SCI) and consequent severe neurological deficits. SCI can be divided into two subgroups: exogenous SCI (vertebral fracture and/or luxation/subluxation) and endogenous SCI (intervertebral disc extrusion and ischaemic myelopathy). Clinical challenges The majority of cats with SCI have concurrent injuries. The clinician must perform a thorough physical examination and prioritise and then stabilise the life-threatening problems before focusing on the neurological examination. The possibility of multiple sites of SCI and spinal shock can make interpretation of the neurological examination challenging. While plain radiographs or myelography are usually diagnostic, they do not give direct information about the integrity of the spinal cord parenchyma or the severity of any damage. If facilities or experienced staff capable of performing the necessary surgery are not available, or advanced imaging is indicated, referral to a specialist veterinary institution should be considered. Audience This review is aimed at clinicians dealing with feline SCI in the emergency setting or at first-opinion level, and discusses causes, initial management, specific treatment and prognosis. Patient group While any cat may potentially be affected by SCI, there is a tendency for exogenous SCI to be more common in younger individuals and, in the authors’ experience, pure-breed cats are very rarely presented. Endogenous SCI can MULTIMEDIA be seen in any breed Six video recordings of feline SCI cases, both pre- and postoperative, are included and is typically a condition of adult cats. in the online version of this article doi:10.1016/j.jfms.2011.09.006


TRAUMA AND ITS CONSEQUENCES Spinal cord injury (SCI) is a common and devastating condition, both in humans and animals. Approximately 30,000 cases of SCI occur each year in the United States in humans. While there are no comparable figures in the veterinary field, in a retrospective post-mortem study exogenous SCI represented the third most common feline disorder; however, the actual figure is likely to be higher than even this suggests.1,2 Primary SCI is the direct effect of exogenous or endogenous trauma, which results in concussion, contusion and/or physical laceration of the spinal cord. The primary injury triggers a cascade of secondary events (vascular Early decompression changes, ion disturbances and excitotoxicity, free radical production and and stabilisation remain inflammation) with subsequent exacerbation of the original trauma.3 Vascular the most effective changes caused by the secondary injury treatment for SCI. impair the autoregulatory mechanisms of the spinal cord. When coupled with systemic hypotension, this results in significant changes to spinal cord perfusion.4 Most of the effort in the medical field is concentrated on reducing the cascade of secondary events. Unfortunately, no medical therapy has yet been definitively proven to be effective, either in humans or in animals.3,5 In humans, appropriate use of methylprednisolone sodium succinate (MPSS) has been shown to produce some degree of improvement in motor function at 6 weeks and 6 months.6 This benefit may not be evident in our patients because the level of improvement attributed to the use of MPSS may not be enough to produce a clinical improvement. Surgical decompression and stabilisation, with the aim of preventing further neural damage and relieving the compression from the spinal cord, still remains the main treatment protocol for the primary injury.3,7,8 The timing of surgery is controversial but there is increasing evidence that early decompression and stabilisation is associated with shorter hospitalisation times and can help to reduce the cascade of secondary events.5,9

Salih Eminaga DVM GPCert (SAS) MRCVS ECVN Resident in Neurology/Neurosurgery Viktor Palus DVM MRCVS ECVN Resident in Neurology/Neurosurgery Giunio Bruto Cherubini Hon Assoc Professor in Veterinary Neurology – University of Nottingham DVM DECVN MRCVS* Dick White Referrals, London Road, Six Mile Bottom, Cambridgeshire CB8 0UH, UK

Clinical Practice

*Corresponding author. Email: [email protected]


YJFMS_v13_i11_1103.indd 850

Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

1098-612X/11/110850+13 $36.00/0 © 2011 ISFM and AAFP. Published by Elsevier Ltd. All rights reserved.

11/4/2011 4:23:58 PM

R E V I E W / Acute spinal cord injury in the cat


Spinal trauma ABC

Vertebral trauma: fracture, luxation, subluxation


Exogenous trauma causing vertebral fracture, luxation and subluxation is an important cause of acute SCI in cats, representing 7% of spinal cord diseases according to one study.2 However, that study involved a referral, post-mortem population, and so the actual proportion is likely to be higher. Most cats, in fact, are not referred because of the perceived poor outcome or are not treated due to financial constraints. In most cases the trauma is caused by either a road traffic accident (RTA) or a fall from a height, but other causes such as gun shot wounds and bite wounds are also described.10–13 It is important to thoroughly evaluate any cat with suspected spinal trauma because of possible concomitant injuries and prioritise them accordingly. Between 30–83% of spine and spinal cord trauma cases have concomitant injuries (pulmonary contusions, pneumothorax, rib fractures, long bone fractures, pelvic fractures, abdominal organ injuries, haemoperitoneum and head trauma).10,13,14 It is also very important to recognise the possibility of vertebral fracture or luxation at an early stage to avoid any risk of further neural damage during examination of the cat.8 Even though SCI is rarely fatal, time is a key factor in terms of maximising the chances of a positive outcome. If practical, the cat can be secured to a flat board or a stretcher. Approximately 50% of all vertebral fractures and luxations/ subluxations involve the thoracolumbar junction (T10–L2); the lumbar region (31–67%) and sacrococcygeal junction (14–36%) are other commonly affected areas.10,13,14 Fractures involving the cervical vertebrae are comparatively uncommon in cats (2%).10 Approximately 20% of cats with traumatic spinal injuries also have acute intervertebral disc herniation secondary to trauma.11 The examination and management of a cat with suspected spinal trauma should focus first on systemic stabilisation (see ABC box). Hypovolaemia and hypoxaemia must be



Intubate if necessary AIRWAY

Be extra careful during intubation in cats with cervical trauma

Administer 100% oxygen Measure arterial blood gases



Insert large IV catheter and treat shock Run blood tests (PCV, TP, urea, creatinine, electrolytes) CIRCULATION Measure systemic blood pressure AVOID HYPOTENSION

Nonambulatory cats should be handled very carefully until an unstable spinal lesion has been ruled out.

Differentiation between upper (UMN) and lower motor neuron (LMN) signs

recognised and treated immediately, as they can exacerbate secondary SCI.3 It is paramount to assess ventilation, partial pressure of oxygen in arterial blood and systemic blood pressure in cats with SCI and to correct any deviation from normal.3 Packed cell volume, total protein level, urea, creatinine and electrolytes should be evaluated as a minimum as soon as possible. Once the immediately life-threatening problems have been addressed, neurological examination should take place to localise and assess the severity of the lesion (Tables 1 and 2). Non-ambulatory cats should be handled very carefully until an unstable spinal lesion has been ruled out. The absence


Neuroanatomical localisation by neurological examination

UMN signs

LMN signs

Fore limbs

Hind limbs Bladder

Lesion localisation

Motor function

Spastic paresis or paralysis

Flaccid paresis or paralysis





Spinal cord segmental reflexes

Normal to increased

Reduced to absent









Muscle tone

Normal to increased

Reduced to absent





Muscle atrophy

Late and disuse atrophy

Early and neurogenic atrophy





Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

YJFMS_v13_i11_1103.indd 851


851 11/4/2011 4:23:59 PM

Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

YJFMS_v13_i11_1103.indd 852

11/4/2011 4:24:00 PM

R E V I E W / Acute spinal cord injury in the cat




FIG 3 (a) Sagittal T2-weighted (T2W) MRI scan of a 3-year-old Oriental Shorthair cat with a T12 compression fracture (arrow) sustained during an RTA. (b) Transverse STIR MRI scan of the same cat; there is signal change within the spinal cord (arrow) and soft tissue swelling within the paraspinal muscles (arrow-head). (c) Scuffed nail and foot pad excoriation secondary to the trauma. A video clip of the cat, which was showing paraplegia (video 1), is available at doi:10.1016/j.jfms.2011.09.006



FIG 4 (a,b) Lateral and ventrodorsal radiographs showing a T8 fracture with displacement and spinal cord transection. Note the subtle change on the lateral projection compared with the gross spinal displacement visible on the ventrodorsal projection. (c) Lateral radiograph of a 2.5-year-old DSH cat showing an L6–L7 fracture with complete over-riding of L6 and L7 vertebrae; surgical exploration revealed spinal cord transection

Acute exogenous SCI Clinical decision making Acute exogenous SCI


Nociception absent

Nociception present

Radiographs (orthogonal views)

No spinal luxation MRI/CT (myelography)

MRI/CT (myelography) Spinal cord intact

The benefits of advanced imaging aside, a fundamental point is that lack of nociception associated with luxated/fractured vertebrae on survey spinal radiographs suggests a hopeless prognosis due to the functional transection of the spinal cord implied by complete sensory deficits (see clinical decision-making box and Fig 4).

Compressive lesion

Surgical decompression/ stabilisation

Spinal cord transected

Spinal instability

Surgical stabilisation

Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

YJFMS_v13_i11_1103.indd 853

Complete spinal luxation



853 11/4/2011 4:24:03 PM

R E V I E W / Acute spinal cord injury in the cat

Treatment should be aimed at controlling the pain (Table 3); preventing further neural damage by physically securing the patient to a flat board or a stretcher, thereby ensuring full body stabilisation; limiting the extent of secondary SCI; decompressing the spinal cord; and stabilising the fracture/luxation when indicated. Over the years a number of studies have investigated how to prevent and limit secondary injury. Many different therapeutic agents, including calcium channel antagonists, sodium channel antagonists, potassium channel blockers, polyethylene glycol and MPSS, have been investigated and some are under further investigation.3 However, the basics such as maintaining adequate blood pressure and tissue oxygenation and decompression of the spinal cord still constitute the most effective therapy for acute SCI.18,19 Use of glucocorticosteroids such as MPSS remains controversial and the beneficial effects are not fully proven in dogs and cats.


Analgesics commonly used in cats by the authors



Duration of effect


0.1–0.3 mg/kg IM or SC (may cause vomiting, so best to avoid in cats with suspected raised ICP)

4–6 h


0.1–0.3 mg/kg IV, IM or SC (does not cause vomiting)

4–6 h

Buprenorphine 0.01–0.02 mg/kg IV, IM, SC or sublingual 4 µg/kg as transdermal patch*

60 h*


1–4 mg/kg IV or SC†

24–36 h


0.1–0.3 mg/kg IV or SC, followed by 0.1 mg/kg PO q24h†

24 h


0.3 mg/kg IV as loading dose followed by 0.01 mg/kg/min IV (use is controversial in patients with suspected raised ICP)

Depends on infusion length

NB Where appropriate, if licensed products are available they should be used first or non-licensed drugs can be administered according to the cascade. * Therapeutic plasma concentration of fentanyl is reached within 12 h in cats and stays in the analgesic range for up to 72 h after application of the patch. † NSAIDs should be used with care in hypovolaemic patients or those receiving glucocorticosteroids. IM = intramuscularly, IV= intravenously, SC = subcutaneously, PO = by mouth, ICP = intracranial pressure

No clinical study has evaluated the efficacy and side effects of MPSS in traumatic spinal cord injury in cats. a


FIG 5 (a) Ventrodorsal radiograph of an L5–L6 fracture/subluxation in a 2-year-old DSH cat. (b) Ventrodorsal postoperative radiograph of the same cat



YJFMS_v13_i11_1103.indd 854

4–12 h


MPSS – the conflicting evidence MPSS has been shown to have some efficacy in human patients, but only when treatment was initiated within 3 h of trauma at 30 mg/kg followed by 5.4 mg/kg/h for 24 h; or, alternatively, initiated within 3–8 h of trauma at 30 mg/kg followed by 5.4 mg/kg/h for 48 h.6 However, as mentioned, the small degree of motor improvement attributed to this protocol in humans may not be significant in our patients. Thus, MPSS is contraindicated if more than 8 h have elapsed since the traumatic event, and in patients that have voluntary motor function.18 Moreover, one retrospective study reported a high incidence of adverse effects after dexamethasone administration in dogs with thoracolumbar disc herniation, and no difference in outcome was found compared with dogs treated with surgery alone.20

The treatment of choice in any cat with SCI and associated spinal instability and/or spinal cord compression is surgical (Fig 5). When compared with patients managed conservatively, early decompression and stabilisation is associated with a significant improvement in neurological status.7,14 In carefully selected rare cases with no spinal instability, conservative treatment has been reported to allow good outcomes.10,11,14 However, a consideration during the decisionmaking process is that it is often easier and less painful to care for animals with vertebral fracture/luxation soon after surgical stabilisation than it is to provide optimal nursing care for animals that must be rested or retain external coaptation devices for prolonged periods.8

Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

11/4/2011 4:24:06 PM

R E V I E W / Acute spinal cord injury in the cat

Sacrococcygeal and intercoccygeal vertebral luxations Sacrococcygeal and intercoccygeal vertebral luxations are well recognised and common injuries in cats that have suffered an RTA and are thought to result from traction on the tail (Fig 6).8,21 Typically there is devastating central nervous system (CNS) or peripheral nervous system (PNS) injury, which relates to the fact that, in cats, the spinal cord extends to the first sacral vertebra and the cauda equina to the first coccygeal vertebra.22 The clinical signs and prognosis depend on the extent of the injury to the spinal cord and PNS (nerve rootlets, cauda equina and peripheral nerve) and could range from a paralysed tail, and urinary and/or faecal incontinence to partial loss of sciatic nerve function or even

FIG 6 Tail traction injury with extensive soft tissue involvement in a 4-year-old DSH cat

FIG 7 Intercoccygeal luxation in a 4-year-old DSH cat. This cat subsequently made a full recovery; his perineal reflex and tail base sensation were intact on presentation. A video clip of a cat with sacrococcygeal luxation (video 2) is available at doi:10.1016/j.jfms.2011.09.006

complete pelvic plexus dysfunction (Fig 7).21 Fractures/luxation of sacrococcygeal vertebrae should be stabilised as soon as possible to prevent further traction injury to the cauda equina.21 Because of the size of the coccygeal vertebrae, amputating the tail immediately would provide a simpler and more viable option. Many affected cats present with difficulty in urination as a result of temporary or permanent damage to the pudendal and/or pelvic nerves (Fig 8). Although anatomically the lesion is affecting the LMN, the bladder may be difficult to express due to increased sympathetic tone secondary either to pain or to trauma at the level of the sympathetic sacral spinal chain.23 In these cases, and in cats that have developed reflex dyssynergia (detrusor contraction combined with inadequate urethral relaxation), it is mandatory to provide the necessary pharmacological aids during the recovery period. Various drug combinations can be used for this purpose (see box below). In animals in which there has been complete severance of the nerves (neurotmesis) that supply the bladder sphincter mechanism, the prognosis for recovery of bladder function is hopeless (Fig 9).24 Cats with tail base sensation on presentation are expected to regain urinary continence; reportedly, 60% of cats without tail base sensation on presentation could also regain their urinary continence.24 The prognosis for return of urinary continence is good if anal tone and perineal sensation are present on initial examination. Cats that do not become continent within 1 month usually fail to regain urinary function.25

UMN bladder Pharmacological intervention Smooth muscle relaxants ✜ Phenoxybenzamine (0.25–0.5 mg/kg PO q12h) ✜ Prazosin (0.25–0.5 mg/cat PO q8–12h) FIG 8 Neuroanatomy of the bladder. The hypogastric nerve originates from the L2–L5 spinal cord segments in cats and controls the relaxation of the detrusor muscle and contraction of the internal urethral sphincter during the urine storage phase. The pudendal nerve originates from the S1–S3 spinal cord segments and provides sensory and motor innervation to the external urethral sphincter. The pelvic nerve controls contraction of the detrusor muscle during voiding. The possible area of damage to the spinal cord in the case of traction injury secondary to sacrococcygeal luxation is shown in red. Intact spinal cord is shown in white

Striated muscle relaxants ✜ Dantrolene (0.5–2 mg/kg PO q8h) ✜ Diazepam (0.2–0.5 mg/kg PO q4–8h)

The prognosis for return of urinary continence is good if anal tone and perineal sensation are present on initial examination. Cats that do not become continent within 1 month usually fail to regain urinary function. Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

YJFMS_v13_i11_1103.indd 855


855 11/4/2011 4:24:08 PM

R E V I E W / Acute spinal cord injury in the cat



FIG 9 (a) Sagittal T2W MRI scan of an 8-year-old cat showing signal change, loss of integrity of the spinal cord at L7 level (arrow-head) and suspected severe spinal cord damage at the level of the origin of the sacral nerves (arrow). (b) Sagittal STIR image of the same cat showing transection at the level of the origin of the pelvic and pudendal nerves (arrow-head) and soft tissue damage (arrow) ventral to the tail


60% of dogs with grade 5 IVDE will recover successfully.36 This system has not yet been evaluated in cats; however, it can be used as a Intervertebral disc extrusion rough guide for the clinician dealing with a suspected case of feline IVDE (Table 4). Intervertebral disc disorder is not a common The investigation of a cat with suspected The most presentation in cats. Both acute intervertebral IVDE starts with the signalment and the colcommon disc extrusion (IVDE) and chronic intervertelection of a thorough history. Particular attenbral disc protrusion (Hansen type I and II, tion should be paid to any suspected trauma, intervertebral respectively) have long been reported to occur and other causes of spinal cord lesions should in cats.26 Because the incidence of feline IVDE also be considered during the investigation spaces has been reported to be as low as 0.09%,27 (ie, neoplastic, inflammatory, infectious or involved are many veterinarians are still not aware of the vascular diseases). Thorough neurological occurrence of IVDE in cats. It is certainly less examination will help localise the lesion to T13–L1 and common than it is in the canine population, in specific spinal cord segments and also helps in which the incidence has been reported to be as constructing working diagnoses and further L4–L5, high as 2%.28 The age of cats with IVDE is usudiagnostic plans (see box, page 857). The but L7–S1 and quality of the femoral pulses, pad temperaally about 8 years (range 1.5–17 years).29 There is no gender predilection and the majority of ture and colour of the nail beds should be cervical IVDE feline IVDE cases described in the literature assessed in a cat with acute-onset paraparesis have also been or paraplegia in order to rule out aortoiliac have been domestic shorthair cats.27,28,30 The onset of neurological signs is variable, but usuthromboembolism as a cause of the ischaemic reported. ally acute-progressive.27,29 The most common neuromyopathy. Haematology and biochemintervertebral spaces involved are T13–L1 and istry should be performed in order to assess L4–L5, but L7–S1 involvement and cervical the safety of general anaesthesia and surgery, IVDE have also been reported.29–33 if required. Jugular sampling should be perAs always the neurological signs depend formed with especial care in tetraparetic cats. on the neuroanatomical localisation. Signs Cerebrospinal fluid (CSF) analysis in cats include spinal hyperaesthesia, reluctance to with IVDE may be normal, or may reveal jump, urinary and faecal incontialbuminocytological dissociation nence, ataxia, and limb and tail or an elevated nucleated cell Clinical grading system for TABLE 4 SCI paresis (see video 3, doi:10.1016/ count, and therefore using this j.jfms.2011.09.006).27,30–38 A practical test without further imaging Grade Clinical status five-point system has been promight lead to an incorrect diagno0 Normal posed for grading IVDE in the sis and is not helpful in diagnos1 Spinal hyperaesthesia with no neurological thoracolumbar area in dogs ing IVDE in the cat.30 deficits After appropriate neuro(Table 4), and is particularly use2 Ataxia, paraparesis anatomical localisation, survey ful in trying to elicit information spinal radiographs of the area of about the expected outcome.36 3 Paraplegia with intact nociception Grades 1–4 have a very good interest may be useful in cases 4 Paraplegia with intact nociception and prognosis after decompressive of suspected trauma and acute urinary incontinence surgery, with more than 90% of onset of neurological signs.13 5 Paraplegia with loss of nociception Mineralised radiodense material dogs making a successful recovFrom Sharp and Wheeler36 inside the vertebral canal, with ery; in comparison only about



YJFMS_v13_i11_1103.indd 856

Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

11/4/2011 4:24:10 PM

R E V I E W / Acute spinal cord injury in the cat

Acute endogenous SCI Clinical decision making Acute paraparesis/plegia without external trauma

Spinal hyperaesthesia

No spinal hyperaesthesia

Normal peripheral femoral pulses

Survey radiographs

Pathological fractures

Normal or suspected intervertebral disc extrusion

Further treatment



Absent peripheral femoral pulses


Further investigation

Normal MRI/CT




associated narrowing of the intervertebral disc space, can be seen in some cases (Fig 10).27,34,35 Myelography has greater sensitivity in identifying the compressive extradural lesion of the spinal cord in dogs;37 however, feline data are lacking. Myelography is not always diagnostic, however,27,30 and further advanced imaging modalities should be considered in cats with suspected IVDE. In dogs, CT reportedly shows similar sensitivity


Consider CSF analysis

FIG 10 Survey radiographs of the lumbar vertebral column of a DSH cat; (a) lateral projection and (b) ventrodorsal projection. There is narrowing of the L5–L6 intervertebral space with calcified material in the L5–L6 intervertebral foramen (arrow). MRI scans from this cat are shown in Fig 11


Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

YJFMS_v13_i11_1103.indd 857



857 11/4/2011 4:24:11 PM

R E V I E W / Acute spinal cord injury in the cat



FIG 11 MRI scans of the DSH cat radiographed in Fig 10. (a) Sagittal T2W image showing the hypointense extradural material associated with the L5–L6 intervertebral space and compressing the spinal cord ventrally. (b) Transverse T2W image of the L5–L6 intervertebral space showing the hypointense extradural material displacing the spinal cord to the left side. Both images are characteristic of IVDE, which was also confirmed during surgery (Fig 12)

to myelography in diagnosing IVDE,38 but no large-scale studies have been published regarding CT sensitivity in cats. CT might reveal a hyperattenuating compressive lesion, especially in cases where the intervertebral disc is mineralised.27,33 MRI provides better contrast resolution than any of the above-mentioned imaging modalities and is therefore the ‘gold standard’ for imaging intervertebral discs.17 MRI usually reveals extradural material compressing the spinal cord above the affected intervertebral space (Fig 11).39 Intramedullary migration of the intervertebral disc and focal intramedullary oedema associated with extrusion of a small volume of intervertebral material have also been reported in cats.31,35 The only disadvantages of MRI and CT are accessibility and cost. However, the cost–benefits of these advanced imaging modalities outweigh other less expensive diagnostics by aiding assessment of the spinal cord and allowing more accurate planning of further therapy. The morbidity that often accompanies myelography is also avoided with CT/MRI.17 Conservative and surgical therapy are both recognised treatment options, as in dogs.36 The scattered information from published cases of feline IVDE seems to suggest that surgical treatment has better success,29 and it is also the authors’ treatment of choice for any cat with spinal cord compression and associated neurological deficits and/or persistent pain. Cats are more difficult to restrain for conservative treatment than dogs and thus early decompression might prevent further deterioration of neurological signs and improve the prognosis. However, in selected cases conservative management may also be an option to consider from the outset.31 The standard surgical techniques of hemilaminectomy (Fig 12), dorsal laminectomy and ventral slot are used, depending on the site of the lesion.27,30,32



YJFMS_v13_i11_1103.indd 858

FIG 12 Intraoperative view during right-sided hemilaminectomy for decompression of the spinal cord of the cat imaged in Figs 11 and 12. The arrow indicates the calcified nucleus pulposus compressing the spinal cord that appears to be swollen (*)

Post-surgical management is tailored to the patient’s needs and includes management of the urinary bladder, postoperative analgesia, nursing and physiotherapy. The prognosis is generally good for a full return to normal routine (see video 4, doi:10.1016/j.jfms.2011.09.006).

Feline ischaemic myelopathy

The most commonly affected site in cats with FIM seems to be the C6–T2 spinal cord segments.

Feline ischaemic myelopathy (FIM) has generally been considered to be a rare condition in cats. However, the reported occurrence has increased in recent years, probably due to increased accessibility to MRI and awareness of this condition among veterinary surgeons.29 As in dogs, FIM is suspected to be secondary to fibrocartilaginous embolism (FCE), but can only be definitively diagnosed on postmortem histological examination.40 There are several reports in the veterinary literature of cats and other non-domestic felids with suspected or confirmed FCE;40–47 however, the exact incidence of FCE has not yet been investigated in feline patients. Neurological signs occur due to obstruction of the spinal vessels by a small amount of nucleus pulposus from the intervertebral disc,

Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

11/4/2011 4:24:13 PM

R E V I E W / Acute spinal cord injury in the cat

Dorsolateral spinal artery

Radial artery

Radial artery

Irregular arterial ring Vertical artery

Ventral spinal artery



FIG 13 (a) Diagram of the spinal cord blood supply. The outer part of the spinal cord is supplied by the radial arteries and the inner part is supplied by the vertical artery. The middle part is supplied by both the radial and vertical arteries. Modified from King.57 (b) Transverse STIR image showing a hyperintense intramedullary lesion lateralised to the right side, suggesting infarction of the portion of the spinal cord supplied by the radial arteries on the right side (arrow)

causing an ischaemic necrotising myelopathy.41 Several mechanisms have been suggested to explain how the degenerated intervertebral disc material enters the bloodstream in humans48 and dogs.49 Affected cats are usually middle aged and

older, with no breed or gender predisposition.29 The most commonly affected site in cats seems to be the C6–T2 spinal cord segments; however, other sites can be affected.50 An explanation for this neuroanatomical localisation is currently lacking; however, an associa-

Nursing and supportive care for a cat with SCI ✜ Blood pressure Cats with mean arterial blood pressure ✜ ✜ ✜ ✜ ✜

below 60 mmHg (<80 mmHg systolic pressure, <50 mmHg diastolic pressure) should be treated. Fluids Isotonic crystalloids, hypertonic saline, colloids and/or blood component products (Table 5) should be used to effect as dictated by vital parameters and patient response. Oxygen administration Inspired oxygen fraction can be increased by oxygen ‘flow by’ or by mask using the appropriate flow rate/minute. Analgesia Pain management is very important in the case of spinal trauma and IVDE (Table 3). It is usually more difficult to assess nociception in cats than in dogs. Pressure ulcer prevention Appropriate nursing, such as regular turning and provision of suitable bedding, is important in preventing decubitus ulcers. Urinary bladder management An indwelling urinary catheter can be inserted (Fig 14) or regular manual expression (at least four times a day) performed. Diazepam (0.2–0.5 mg/kg IV q4–8h) can be used to facilitate manual expression (see box, page 855). Regular checking of urine culture and appropriate antibiotic therapy is recommended.

FIG 14 Nonambulatory cat with indwelling urinary catheter and closed urinary drainage system

TABLE 5 Fluid

Fluid therapy for hypovolaemic cats with trauma and SCI Dose

Isotonic 10–30 ml/kg boluses IV every 15–20 mins, to effect crystalloids (take care not to overload circulation; also take care with NaCl 0.9% not to cause dilutional acidosis) Hypertonic 2–4 ml/kg bolus over 15–30 mins IV (not appropriate in saline (7%) chronically dehydrated cats; check electrolytes after use) Colloids

2–5 ml/kg bolus to effect (take extreme care not to overload circulation)


2–5 ml/kg/h. Very useful if oxygen-carrying capacity is poor and/or blood products are not readiy available (do not exceed 10 ml/kg/h; take extreme care not to overload circulation)

NB All doses are recommended for use in cats without cardiopulmonary disease. Patient parameters and trends should be continuously monitored: heart rate, pulse quality, arterial blood pressure, oxygen saturation, temperature (core and extremities), ECG, capillary refill time, chest auscultation and urine production. IV = intravenous

✜ Nutrition Daily nutritional requirement has to be met. The following formula, where RER indicates the resting energy requirement, can be employed: RER (kcal) = (30 x Body weight) + 70 ✜ Nutritional support Appetite stimulants (eg, diazepam 0.05–0.1 mg/cat IV or mirtazapine 7.5 mg/cat) or feeding tube placement (eg, naso-oesophageal, gastric) must be considered if RER cannot be reached. ✜ Physiotherapy In non-ambulatory patients, physiotherapy is important to prevent muscle wastage and ligament contracture, and to improve recovery (see video 5, doi:10.1016/j.jfms.2011.09.006).

Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

YJFMS_v13_i11_1103.indd 859


859 11/4/2011 4:24:16 PM

R E V I E W / Acute spinal cord injury in the cat

FIM is very acute in onset and not progressive, which can differ from IVDE where owners usually report an acute onset, but often with progressive deterioration.

tion with protruded intervertebral discs frequently found in that area of the spinal cord has been proposed.51 The neurological signs vary according to the localisation,29 and are usually lateralised. This might be due to the particular vascularisation of the feline spinal cord: approximately half of the vertical arteries branch either to the left or to the right side, whereas the other half run centrally (Fig 13). Furthermore, it has been found that there are more unilateral arteries in the cervical area compared with the rest of the spinal cord.52 FIM is very acute in onset and not progressive, which can differ from IVDE where owners usually report an acute onset, but often with progressive deterioration. Moreover, ischaemic myelopathy usually presents as a hyperacute, non-painful myelopathy and is the main differential in those cats without spinal hyperaesthesia (see video 6, doi:10.1016/ j.jfms.2011.09.006). However, in some cases, cats, similar to dogs, can show discomfort or pain during the initial phase.45,49 In the absence of external trauma, ischaemic neuromyopathy caused by aortic or iliac thromboembolism is another mimic of acute-onset myelopathy that needs to be ruled out; paraparesis/paraplegia has been reported with this common feline condition and the neurological signs may deteriorate within the first 24 h, usually with gradual improvement thereafter.49 Reported clinical signs of thromboembolism include a weak or absent femoral pulse, cold limb extremities, cyanotic nail beds and painful muscles.53,54 MRI is the diagnostic imaging modality of choice when assessing a cat with non-painful myelopathy.17 Typically on MRI FIM presents as a focal well-defined T2-weighted and short-tau inversion recovery (STIR) hyperintense intramedullary lesion affecting either grey or white matter and often with obvious lateralisation (Figs 13 and 15).44,46 Contrast enhancement on T1-weighted images might be observed after 5–6 days.44 Treatment consists of supportive therapy, urinary bladder management, nursing and physiotherapy. In dogs, the prognosis depends on the severity of the neurological signs at the time of presentation and the extent of the lesion on MRI. The involvement of intumescences, presence of symmetrical clinical signs and decreased nociception have also been found to be associated with a poor prognosis.55,56 An equivalent study is, however, lacking for feline patients.



YJFMS_v13_i11_1103.indd 860



FIG 15 MRI scans of the cervical spinal cord of a cat. (a) Sagittal STIR image showing a hyperintense intramedullary lesion at the level of C5 (arrow). (b) Sagittal T2W image showing a hyperintense intramedullary lesion at the level of C2 (arrow). Both images are suggestive of ischaemic myelopathy in the light of a peracute presentation

KEY POINTS ✜ Always perform a thorough physical examination to assess concurrent injuries in a cat with spinal cord injury (SCI).

✜ ABC stabilisation is the first priority and duty. ✜ Neurological examination and localisation is mandatory prior to imaging.

✜ Securing the patient to a stretcher or flat board is necessary to avoid further neural damage in the case of an unstable fracture/luxation.

✜ Advanced imaging is irreplaceable for the appropriate treatment of SCI.

✜ Early decompression and stabilisation is paramount for spinal fracture/luxation.

✜ Analgesia is an important and ethical part of the management of SCI.

✜ Consider euthanasia only in the case of absent nociception in association with marked spinal displacement.

✜ Intervertebral disc extrusion and fibrocartilaginous embolism should be included as differential diagnoses in cats with SCI.

✜ Physiotherapy forms a significant part of rehabilitation after SCI.

Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

11/4/2011 4:24:17 PM

R E V I E W / Acute spinal cord injury in the cat

References 1
















Bagley Flanders AE, Croul SE. Spine trauma. In: Atlas SW, ed. Magnetic resonance imaging of the brain and spine. 3rd edn. Philadelphia: Lippincott, Williams and Wilkins, 2002: 1769–824. Marioni-Henry K, Vite CH, Newton AL, Van Winkle TJ. Prevalence of diseases of the spinal cord of cats. J Vet Intern Med 2004; 18: 851–58. Olby N. The pathogenesis and treatment of acute spinal cord injuries in dogs. Vet Clin North Am Small Anim Pract 2010; 40: 791–807. Olby NJ. Current concepts in the management of acute spinal cord injury. J Vet Intern Med 1999; 13: 399–407. Kube SA, Olby NJ. Managing acute spinal cord injuries. Compend Contin Educ Vet 2008; 30: 496–504. Bracken MB, Shepard MJ, Holford TR, et al. Administration of methylprednisolone for 24 or 48 hours or tirilazad mesylate for 48 hours in the treatment of acute spinal cord injury. Results of the Third National Acute Spinal Cord Injury Randomized Controlled Trial. J Am Med Assoc 1997; 277: 1597–604. Horlein BF. Acute trauma to the central nervous system. In: Horlein BF, ed. Canine neurology: diagnosis and treatment. 3rd edn. Philadelphia: WB Saunders, 1978: 381–405. Jeffery ND. Vertebral fracture and luxation in small animals. Vet Clin North Am Small Anim Pract 2010; 40: 809–28. Fehlings MG, Perrin RG. The timing of surgical intervention in the treatment of spinal cord injury: a systematic review of recent clinical evidence. Spine 2006; 31: 528–35. Besalti O, Ozak A, Tong S. Management of spinal trauma in 69 cats. Dtsch Tierarztl Wochenschr 2002; 109: 315–20. Grasmueck S, Steffen F. Survival rates and outcomes in cats with thoracic and lumbar spinal cord injuries due to external trauma. J Small Anim Pract 2004; 45: 284–88. Voss K, Montavon PM. Tension band stabilisation of fractures and luxations of the thoracolumbar vertebrae in dogs and cats: 38 cases (1993–2002). J Am Vet Med Assoc 2004; 225: 78–83. Bali MS, Lang J, Jaggy A, Spreng D, Doherr MG, Forterre F. Comparative study of vertebral fractures and luxations in dogs and cats. Vet Comp Orthop Traumatol 2009; 22: 47–53. Bruce CW, Barisson BA, Gyselinck K. Spinal fracture and luxation in dogs and cats. Vet Comp Orthop Traumatol 2008; 21: 280–84. 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: 1502–3. Kinns J, Mai W, Seiler G, et al. Radiographic sensitivity and negative predictive value for

















acute canine spinal trauma. Vet Radiol Ultrasound 2006; 47: 563–70. da Costa RC, Samii VF. Advanced imaging of the spine in small animals. Vet Clin North Am Small Anim Pract 2010; 40: 765–90. Platt SR, Olby N. Neurological emergencies. In: Platt SR, Olby N, eds. BSAVA manual of canine and feline neurology. 3rd edn. Gloucester: BSAVA, 2004: 320–36. Fletcher DJ, Dewey CW. Spinal trauma management. In: Dewey CW, ed. A practical guide to canine and feline neurology. 2nd edn. Iowa: Wiley-Blackwell, 2008: 405–17. Levine JM, Levine GJ, Boozer L, et al. Adverse effects and outcome associated with dexamethasone administration in dogs with acute thoracolumbar intervertebral disc herniation: 161 cases (2000–2006). J Am Vet Med Assoc 2008; 232: 411–17. Sturgess B, LeCouteur RA. Spinal fractures and luxations. In: Slatter D, ed. Textbook of small animal surgery. 3rd edn. Philadelphia: Elsevier Science, 2003: 1244–60. Nickel R, Schummer A, Seiferle E, eds. Midollo spinale. In: Trattato di anatomia degli animali domestici. Vol IV. Milano: Casa Editrice Ambrosiana, 1988: 27–52. Italian translation of: Lehrbuch der anatomie der haustiere. Berlin: Verlag, 1975. O’Brien D. Neurogenic disorders of micturition. Vet Clin North Am Small Anim Pract 1988; 18: 529–44. Tatton B, Jeffery N, Holmes M. Predicting recovery of urination control in cats after sacrocaudal injury: a prospective study. J Small Anim Pract 2009; 50: 593–96. Smeak DD, Olmstead ML. Fractures/luxations of the sacrococcygeal area in the cat: a retrospective study of 51 cases. Vet Surg 1985; 14: 319–24. King AS, Smith RN. Disc protrusions in the cat: distribution of dorsal protrusions along the vertebral column. Vet Rec 1960; 72: 335–37. Muñana KR, Olby NJ, Sharp NJH, Skeen TM. Intervertebral disk disease in 10 cats. J Am Anim Hosp Assoc 2001; 37: 384–89. Horlein BF. Intervertebral disks. In: Horlein BF, ed. Canine neurology: diagnosis and treatment. 3rd edn. Philadelphia: WB Saunders, 1978: 470–560. Marioni-Henry K. Feline spinal cord diseases. Vet Clin North Am Small Anim Pract 2010; 40: 1011–28. Knipe MF, Vernau KM, Hornof WJ, LeCouteur RA. Intervertebral disc extrusion in six cats. J Feline Med Surg 2001; 3: 161–68. Lu D, Lamb CR, Wesselingh K, Targett MP. Acute intervertebral disc extrusion in a cat: clinical and MRI findings. J Feline Med Surg 2002; 4: 65–68. Maritato KC, Colon JA, Mauterer JV. Acute nonambulatory tetraparesis attributable to cranial cervical intervertebral disc disease in a cat.

Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

YJFMS_v13_i11_1103.indd 861


861 11/4/2011 4:24:19 PM

R E V I E W / Acute spinal cord injury in the cat

J Feline Med Surg 2007; 9: 494–98. 33 Harris JE, Dhupa S. Lumbosacral intervertebral disk disease in six cats. J Am Anim Hosp Assoc 2008; 44: 109–15. 34 Kathmann I, Cizinauskas S, Rytz U, Lang J, Jaggy A. Spontaneous lumbar intervertebral disc protrusion in cats: literature review and case presentations. J Feline Med Surg 2000; 2: 207–212. 35 McConnell JF, Garosi LS. Intramedullary intervertebral disk extrusion in a cat. Vet Radiol Ultrasound 2004: 45: 327–330. 36 Sharp NHJ, Wheeler SJ. Small animal spinal cord disorders: diagnosis and surgery. 2nd edn. Philadelphia: Elsevier, 2005. 37 Olby NJ, Dyce J, Houlton JEF. Correlation of plain radiographic and lumbar myelographic findings with surgical findings in thoracolumbar disc disease. J Small Anim Pract 1994; 35: 345–50. 38 Israel SK, Levine MJ, Kerwin SC, Levine GJ, Fosgate GT. The relative sensitivity of computed tomography and myelography for identification of thoracolumbar intervertebral disk herniations in dogs. Vet Radiol Ultrasound 2009; 50: 247–52. 39 Smith PM, Jeffery ND. What is your diagnosis? A case of intervertebral disc protrusion in a cat. J Small Anim Pract 2006; 47: 104–6. 40 Cauzinille L, Kornegay JN. Fibrocartilaginous embolism of the spinal cord in dogs: review of 36 histologically confirmed cases and retrospective study of 26 suspected cases. J Vet Intern Med 1996; 10: 241–45. 41 Zaki FA, Prata RG, Werner LL. Necrotizing myelopathy in a cat. J Am Vet Med Assoc 1976; 169: 228–29. 42 Abramson CJ, Platt SR, Stedman NL. Tetraparesis in a cat with fibrocartilaginous emboli. J Am Anim Hosp Assoc 2002; 38: 153–56. 43 Adaska JM, Lynch S. Fibrocartilaginous embolic myelopathy in a Sumatran tiger (Panthera tigris sumatrae). J Zoo Wildl Med 2004; 35: 242–44. 44 MacKay AM, Rusbridge C, Sparkes AH, Platt SR. MRI characteristics of suspected acute spinal cord infarction in two cats, and a review of the literature. J Feline Med Surg 2005; 7: 101–7. 45 Coradini M, Johnstone I, Filippich LJ, Armit S.

Suspected fibrocartilaginous embolism in a cat. Aust Vet J 2005; 83: 550–51.

46 Mikszewski JS, Van Winkle TJ, Troxel MT. Fibrocartilaginous embolic myelopathy in five cats. J Am Anim Hosp Assoc 2006; 42: 226–33. 47 Ricci E, Cavicchio P, Cantile C. Fibrocartilaginous embolic myelopathy in a lion (Panthera leo). J Zoo Wildl Med 2010; 41: 339–42. 48 Han JJ, Massagli TL, Jaffe KM. Fibrocartilaginous embolism – an uncommon cause of spinal cord infarction: a case report and review of the literature. Arch Phys Med Rehabil 2004; 85: 153–57. 49 Cauzinille L. Fibrocartilaginous embolism in dogs. Vet Clin North Am Small Anim Pract 2000; 30: 155–67. 50 De Risio L, Platt SR. Fibrocartilaginous embolic myelopathy in small animals. Vet Clin North Am Small Anim Pract 2010; 40: 859–69. 51 King AS, Smith RN. Disc protrusions in the cat: distribution of dorsal protrusions along the vertebral column. Vet Rec 1960; 72: 335–37. 52 Caulkins SE, Purinton PT, Oliver JE. Arterial supply to the spinal cord of dogs and cats. Am J Vet Res 1989: 50: 425–30. 53 Smith SA, Tobias AH, Jacob KA, Fine DM, Grumbles PL. Arterial thromboembolism in cats: acute crisis in 127 cases (1992–2001) and long-term management with low-dose aspirin in 24 cases. J Vet Intern Med 2003; 17: 73–83. 54 Bowles BD, Coleman MG, Harvey CJ. Cardiogenic arterial thromboembolism causing non-ambulatory tetraparesis in a cat. J Feline Med Surg 2010; 12: 144–50. 55 Gandini G, Cizinauskas S, Lang J, Fatzer R, Jaggy A. Fibrocartilaginous embolism in 75 dogs: clinical findings and factors influencing the recovery rate. J Small Anim Pract 2003; 44: 76–80. 56 De Risio L, Adams V, Dennis R, McConnell FJ, Platt SR. Association of clinical and magnetic resonance imaging findings with outcome in dogs suspected to have ischemic myelopathy: 50 cases (2000–2006). J Am Vet Med Assoc 2008; 233: 129–35. 57 King AS. Physiological and clinical anatomy of the domestic mammals. Vol 1. Central nervous system. Oxford: Blackwell Science, 2005.

Available online at



YJFMS_v13_i11_1103.indd 862

Downloaded from at HUNTER COLLEGE LIB on May 25, 2014

11/4/2011 4:24:19 PM