Multiple Sclerosis Flashcards

1
Q

Description: What is multiple sclerosis?

A
  • Demyelinating white matter disease of the central nervous system that follows a relapsing remitting course
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2
Q

Description: What are the types of MS?

A
  • Relapsing remitting MS
  • Primary progressive MS
  • Secondary progressive MS
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3
Q

Aetiology/ Risk Factors: MS is associates with what type of disease?

A
  • Autoimmune disease
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4
Q

Aetiology/ Risk factors: State 3 risk factors for MS. (3)

A
  • Temperate climates
  • Vitamin D
  • Epstein Barr virus
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5
Q

Pathology: Describe the pathology behind the demyelination in MS

A
  • Activated T cells cross the blood brain barrier
  • These T cells attack oligodendrocytes and myelin itself, leading to demyelination
  • Due to the lesion, there is increased number of inflammatory cells, leading to acute inflammation of the myelin sheath and loss of function
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6
Q

Symptoms: How does a patient with MS initially present?

A
  • A few days gradual onset of symptoms then it takes a few weeks to stabilise and eventually a partial or complete recovery
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7
Q

Symptoms/ signs: How many cases of MS present with a relapse and how does a relpase present? (1+^6)

A

80% of cases of MS present with a relapse

MS relapse presentation:

  • Limb weakness (motor)
  • Optic neuritis (inflammation of the optic nerve – almost always unilateral)
  • Brainstem diplopia, vertigo/ataxia
  • Bladder involvement (nerve signals to bladder delayed/ blocked due to demyelination)
  • Spinal cord (myelitis)
  • Sensory symptoms
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8
Q

Symptoms: In MS, what are the symptoms of optic neuritis? (3)

A

Optic neuritis symptoms:

  • Subacute vision loss
  • Reduced colour vision
  • Pain on moving the eye
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9
Q

Signs: In MS, what are the signs optic neuritis? (3)

A

Optic neuritis signs:

  • Relative afferent pupillary defect (RAPD) – patient’s pupil dilate when bright light is shone onto the unaffected/affected eye (LOOK UP!!!!)
  • Optic disc swelling initially, optic atrophy (death of the retinal ganglion cell axons) seen later
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10
Q

Signs: In MS, what are the signs associates with a brainstem relapse?

A

Signs of brainstem relapse:

  • Ophthalmoplegia (paralysis of the eye muscles due to lesions in CN III, IV, VI) (pons)
  • Vertigo, ataxia and nystagmus (abnormalities in the cerebellum)
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11
Q

Symptoms/ Signs: What are the types of myelitis and how does this present? (1+3)

A

Myelitis may be partial or transverse (complete):

  • Hyperaesthesia
  • Upper motor neurone changes below level of demyelination
  • Bladder and bowel involvement
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12
Q

Symptoms/ signs: How do further relapses of MS present?

A

AAA

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13
Q

Symptoms/ signs: As MS progresses, what symptoms and signs may present?

A

AAA

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14
Q

Signs: What signs can be seen on examination of a patinet with MS?

A

AAA

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15
Q

Invesitgations: What are the 2 types of ways to diagnose MS? (2)

A

Diagnosis may be

  • Clinical (Posers criteria)
  • MRI based (Macdonald criteria)
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16
Q

Investigations: What invesitgations do we perform for MS (5)

A
  • MRI of the brain (shows plaques which correspond with areas of demyelination, black holes may appear, FIRST LINE)
  • Analysis of CSF via lumbar puncture (look for oligoclonal bands on electrophoresis)
  • Delayed visual/ somatosensory evoked response (evoked potential)
  • Bloods (exclude other inflammatory conditions)
  • Chest x-ray
17
Q

Treatment: In MS, what are the different types of treaments?

A
  • Treatment of relapse
  • Disease modifying treatment
  • General health and diet
  • Symptomatic treatment

(Multi-disciplinary approach)

18
Q

Treatment: In MS, how do we treat?

(a) Treatment of relapse
(b) Disease modifying treatment
(c) General health and diet
(d) Symptomatic treatment

A

(a) Treatment of relapse:
- Oral prednisolone/ Methylprednisolone
- Rehabilitation
- Symptomatic treatment
(b) Disease modifying treatments (1st line treatments):
- Beta-interfons
- Glatiramer acetate
- Teriflunomide
- Dimethyl Fumarate

2nd line agents:

  • Fingolimod
  • Ocrelizumab
  • Cladribine
  • Alemtuzumab
  • Natalizumab
    (c) General lifestyle advice (health and diet)
    (d) Symptomatic treatment AAA
19
Q

Complications: How can MS progress (4)

A

MS progression:

  • Most patients develop progressive disability – axonal loss is important
  • ¼ of those with MS: activities of daily living (ADL) not affected
  • ¼ of those with MS: require a wheelchair
  • 15% severely disabled quickly
20
Q

Extra: In MS, who makes up the multi-disciplinary team? (8)

A

Members of the MS multidisciplinary team:

  • MS nurse
  • Physiotherapy
  • Occupational therapy
  • Speech and language therapy
  • Dietician
  • Rehabilitation specialist
  • Continence advisor
  • Psychology/ psychiatry