Multiple Sclerosis Flashcards

1
Q

What is the pathophysiology of multiple sclerosis?

A

Cell mediated autoimmune demyelination of the white matter CNS. This leads to reduced conduction velocity
Disseminated (over time and space)

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2
Q

What are some poor prognostic signs for MS?

A

Older patient
Motor signs at onset
Many MRI lesions

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3
Q

What are common first symptoms of MS?

A

Optic Neuritis - pain on eye movement with greying and blurring of vision
Odd sensations such as wetness or burning

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4
Q

What pathway does MS commonly involve?

A

Corticospinal path - motor pathway

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5
Q

How does heat affect MS symptoms?

A

Symptoms worsen

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6
Q

What sensory symptoms are seen in MS?

A
Dysaesthesia (abnormal unpleasant feeling when touched)
Pins and needles
Decreased vibration sense
Trigeminal neuralgia
Lhermitte's syndrome
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7
Q

What motor symptoms are seen in MS?

A

Spastic weakness
Myelitis
Hyper-reflexia

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8
Q

What GU symptoms are seen in MS?

A

Erectile dysfunction
Anorgasmia
Urinary frequency
Incontinence

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9
Q

What GI symptoms are seen in MS?

A

Swallowing difficulty

Constipation/diarrhoea

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10
Q

What eye symptoms are seen in MS?

A
Diplopia
Optic neuritis
Nystagmus
Opthalmoplegia
Uhthoff's Phenomenon
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11
Q

What cerebellar signs are seen in MS?

A

Trunk/limb ataxia
Intention tremor
Scanning speech (ataxic dysarthria)

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12
Q

What cognitive/visiospatial signs are seen in MS?

A

Amnesia
Executive dysfunction - emotional and behavioural difficulty
Depression/mood disorders
cognitive impairment

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13
Q

What are some subtypes of MS?

A

Relapsing-remitting (most common)
Secondary progressive disease
Primary progressive disease

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14
Q

What is relapsing-remitting MS like?

A

Acute 1-2 month attacks followed by periods of remission

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15
Q

What is secondary progressive disease?

A

R-R patients don’t fully remit and over time the disability accumulates (around 65% of R-R patients progress within 15 years)

See gait and bladder problems

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16
Q

What is primary progressive disease?

A

Progressive deterioration seen from the onset

17
Q

What is Lhermitte’s syndrome?

A

electric shocks in limbs on neck flexion

18
Q

What is Uhthoff’s phenomenon?

A

Worsening vision following rise in temperature

19
Q

What lifestyle advice is given for patients with MS?

A

Regular exercise
Stop smoking
Avoid stressful situations

20
Q

How are acute relapses managed?

A

High dose IV methylprednisolone

21
Q

What criteria have to be met for beta interferon to be used?

A

Not suitable for primary progressive.

Have to have had 2 relapses in past 2 years.

22
Q

What is the effect of beta interferon on MS?

A

Reduce number of relapses and MRI changes

No effect on disability

23
Q

What disease modifying drugs are used in MS

A
Interferon-B
Glatiramer acetate
Dimethyl fumerate
Alemtuzumab
Natalizumab
Fingolimod
24
Q

How is spasticity in MS controlled?

A

Baclofen and gabapentin

Physio

25
Q

How is tremor in MS controlled?

A

Botulinum toxin

Primidone

26
Q

How is bladder dysfunction managed?

A

If significant residual volume - self catheterise

Frequency symptoms - Anticholinergics

27
Q

How is oscillopsia (visual fields oscillating) managed?

A

Gabapentin

28
Q

How is fatigue managed?

A

Amantadine and CBT

29
Q

How is MS diagnosed? What are the results of these investigations?

A

MRI contrast: demyelination plaques (hyperintense plaques in the periventricular region)
Electrophoresis of CSF: oligoclonal bands of IgG
Evoked potentials: prolonged conduction

30
Q

Differentials for MS

A

Cervical spondylosis
Fibromyalgia
Stroke
B12 deficiency