Week 4- Head and Spinal Pain In Young Cats and Dogs Flashcards

1
Q

What are the three different types of spinal tumours?

A
  • Extradural
  • Intradural Extramedullary
  • Intramedullary
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2
Q

How would you do a vertebral column assesment?

A
  • Press on either side of the spinous processes.
  • Epaxial muscles: Pressing can help identify muscleassociated pain.
  • Articular or transverse processes: Squeezing these can
    confirm nerve root pain, especially in the caudal
    cervical and lumbar regions.
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3
Q

How would you do a neck evaluation?

A
  • Perform cautious flexion, extension, and lateral turning
    of the head and neck.
  • Place the palm on the side of the neck to detect
    resistance.
  • Encourage voluntary movement by tempting the animal
    with food moved side to side.
  • Dogs with neck pain may restrict head and ear shaking
    (less vigorous movement).
  • Cervical pain should be localised to the cranial, middle,
    or caudal cervical segments.
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4
Q

How might you do a thoracolumbar spine assesment?

A

Place a hand on the abdomen to detect muscle
tension as painful areas are approached.
* Press on the ribs to check for thoracic vertebral pain

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5
Q

How might you do a lumbosacral spine assesment?

A

Usually performed with the animal standing, but some
prefer lateral recumbency to minimise pressure
transfer to the hips.
* Hip extension may provoke a pain reaction in caudal
lumbar and lumbosacral disease

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6
Q

How might you do a tail manipulation?

A
  • Dorsiflexion of the tail may worsen lumbosacral joint
    pain by shifting the craniodorsal sacrum forward.
  • Important for assessing the lumbosacral,
    sacrococcygeal, and coccygeal intervertebral discs
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7
Q

How would you examine head and cranial structures?

A

Palpate the temporal muscles and mandible
* Open and close the mouth to assess for cranial
pain or TMJ involvement.

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8
Q

How would you do a peripheral nerve assesment?

A

Palpate the axilla to check for brachial plexus
involvement.
* Palpate the sciatic nerve where it passes caudal
to the greater trochanter, femur, and stifle.

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9
Q

What are the two most common immune-mediated diseases?

A

Meningoencephalitis of unknown origin (MUO) – 47.5%
* Steroid-responsive meningitis-arteritis (SRMA) – 30.7%

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10
Q

What are the two most common infectious conditions?

A

Discospondylitis – 9.3%
* Otogenic intracranial infection – 2.2%

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11
Q

What is SRMA?

A

Immune-mediated, non-infectious inflammatory disease of young to juvenile
dogs.
* Affects the meninges and blood vessels, leading to pain, fever, and neurological
deficits.

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12
Q

What is the pathogenesis of SRMA?

A

Immune dysregulation
Th2 and Th17-mediated immune response
Overproduction of IL-4 and IL-6 and IL-17
Neutrophil infiltration leads to severe inflammation in the
meninges.

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13
Q

What are the clinical signs of acute form SRMA?

A

Fever (pyrexia)
* Severe cervical pain (neck hyperesthesia)
* Reluctance to move (hunched posture)
* Depression and lethargy
* Mild neurological deficits (in some cases)

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14
Q

What are the clinical signs of chronic SRMA?

A

Occurs after insufficient treatment or relapses.
* Neurological deficits (ataxia, paresis).
* Spontaneous haemorrhage

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15
Q

What would be the laboratory findings for SRMA?

A

Elevated C-reactive protein (CRP) and
other acute phase proteins.
Neutrophilia with left shift.

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16
Q

What are the likely diagnostic findings in SRMA?

A

Associated immune
medicated polyarthritis
common
Can have cardiac
abnormalities

17
Q

What is the first-line therapy for SRMA?

A

Glucocorticoids (Prednisolone

Initial dose: 2–4 mg/kg q24h.
* Gradual tapering over 6+ months.

18
Q

What is the immunosuppressive therapy for SRMA?

A

Azathioprine (2 mg/kg q24h)
* Cytosine arabinoside (IV or SC protocols)
* Mycophenolate mofetil (20 mg/kg q24h)

19
Q

What is the supportive care for SRMA?

A

Pain management, monitoring CRP levels, periodic CSF analysis.

20
Q

What is the future research/ clinical implications on SRMA?

A

Need for prospective studies on new
immunomodulatory treatments.
* Monoclonal antibodies targeting IL17 as a potential therapy.
* Genetic research to improve
breeding strategies and reduce SRMA
prevalence.
* SRMA as a model for human
immune-mediated vasculitis (e.g.,
Kawasaki disease)

21
Q

Name 4 types of meningoencephalitis of unknown origin

A
  • Granulomatous meningoencephalomyelitis
  • Necrotising meningoencephalitis
  • Necrotising leukoencephalitis
  • Eosinophillic meningencephalomyelitis
22
Q

What is GME?

A

Angiocentric granulomatous inflammation, primarily
affecting the brainstem and cerebellum

23
Q

What is NME?

A

Necrotic lesions in the cortical grey matter, with T-cell infiltration.

24
Q

What are the clinical signs of MUO?

A

Spinal pain
* Seizures
* Ataxia and proprioceptive deficits
* Vestibular signs (head tilt, circling, loss of balance)
* Cranial nerve deficits
* Blindness

25
Q

What is MUA characterised by?

A

immune dysregulation

26
Q

What are the main treatments for MUO?

A

Glucocorticoid (prednisolone)
* Immunosuppression to reduce inflammation but does not cure
* Long terms use adverse effects
* Attempts to withdraw lead to disease relapse

27
Q

What are the additional immunosuppressive medications for MUO?

A

Cytarabine (Cytosine Arabinoside)
*A chemotherapy agent that suppresses immune cell proliferation.
*Often given as intermittent injections or continuous infusions.
*Cyclosporine
*Suppresses T-cell activation, potentially useful for T-cell-driven NME.
*Mycophenolate mofetil
*Inhibits lymphocyte function.
*Leflunomide
*Used for autoimmune diseases, but data on MUO is limited.
*Azathioprine
*A purine analog that inhibits DNA synthesis in rapidly dividing immune cells.

28
Q

What factors are associated with a poor MUO prognosis

A
  • Severe neurological signs (seizures, altered mentation, cranial nerve deficits).
  • Higher body weight and advanced age.
  • Elevated CSF cell counts and CSF hyperlactatemia.
  • Severe MRI abnormalities, including foramen magnum herniation and brainstem involvement
29
Q

What is canine chiari and syringomyelia?

A

brain is too big for the skull

30
Q

What are the clinical/ behavioural signs of Chiari pain?

A
  • activity change
  • sleep disruption
  • sleep with elevated head
  • change in behaviour to other people
31
Q

What is syringomyelia?

A

central spinal cord syndrome with central
neuropathic pain

presence of fluid filled cavity- syrinx

32
Q

What are the symptoms of syringomyelia?

A
  • Phantom scratching
  • Weakness
  • Thoracic limb muscle atrophy
    *Proprioceptive deficits
33
Q

What is discospondylitis?

A

Infection of IVD and vertebral endplate

34
Q

What animals is discospondylitis most common in?

A

Young and Old Large breed dogs- e.g great Danes

35
Q

What is the main source of discospondylitis infection?

A
  • UTI
  • Haematogenous
  • Migrating foreign body
36
Q

How might you diagnose a discospondylitis infection?

A
  • Diagnostic imaging
  • Culture
  • Brucellosis testing
37
Q

What is acute intervertebral disc extrusion?

A

sudden and severe herniation of the gel-like centre

38
Q

What dogs is atlantoaxial instability most common in?

A

Young toy dog breeds