Multiple Sclerosis Flashcards

1
Q

What is MS?

A

Inflammatory Demyelinating Disorder

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2
Q

Who is likely to get MS?

A

M:F - 1:3

30-40s

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3
Q

What is the usually pattern of presentation in MS?

A

Relapsing and remitting symptoms present then disappear.

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4
Q

What is the rarest form of MS?

A

Primary - no relapse

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5
Q

List clinical features of MS.

A
Pyramidal dysfunction 
Optic neuritis
Sensory symptoms 
Cognitive impairment 
Cerebellar dysfunction
Brain stem issues
Urinary incontinence
Fatigue
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6
Q

What pyramidal dysfunction is associated with MS?

A

Increased tone spasticity
Weakness
Flexor and extensor both affected the same.

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7
Q

What occurs in MS related optic neuritis?

A

Painful vision loss for 1-2 week
Most improve
Look for RAPD -Relative Afferent Pupillary Defect

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8
Q

What sensory symptoms are associated with MS?

A
Pain 
Paraethesia pins and needles
Proprioception and vibration
Numbness
Trigeminal Neuralgia
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9
Q

What cerebellar dysfunction is associated with MS?

A
Dysarthria 
Ataxia
Nystagmus - involuntary eye movement
Intention tremor
Pendular reflex
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10
Q

What brain stem issues are associated with MS?

A

Diplopia
VI palsy
Facial weakness VII

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11
Q

Why do some patients with MS present with Internuclear opthalmoplegia?

A

Disturbance of binocular vision
Failure of abducens due to VI palsy
Nystagmus in abduction eye

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12
Q

Why do MS patients present with urinary incontinence?

A

Increased tone at bladder neck and hypersensitivity

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13
Q

What is required for a diagnosis of MS?

A

At least 2 episodes suggestive of demyelination and alternative diagnosis excluded.
Either one on MRI and one clinical or both on MRI

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14
Q

What tests are undertaken in a suspected MS patient?

A

MRI CSF Neurophysiology Bloods

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15
Q

What are some differential diagnosis’s in a patient with MS like symptoms?

A
Vasculitis
Granulomatous
Structural lesions
Infection
Metabolic disorders
B12 deficiency
Folic acid deficiency
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16
Q

What are you looking for in the CSF of someone with MS?

A

Unmatched oligoclonal bands

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17
Q

If someone presents with acute mild MS what is the treatment?

A

Purely symptomatic

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18
Q

If someone presents with acute moderate MS what is the treatment?

A

Oral steroids

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19
Q

If someone presents with acute severe MS what is the treatment?

A

IV steroids and admission

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20
Q

Symptomatic pyramidal dysfunction is treated how?

A

Physiotherapy
Baclofen - spasticity
Tizanidine -spasticity
Botulinum Toxin - spasticity

21
Q

What treatment is given for the sensory symptoms of MS?

A

Anticonvulsant - Gabapentin
Antidepressant - Amitriptyline
Acupuncture
Lignocaine infusion

22
Q

What can be used for the treatment of urinary incompetence?

A

Anticholinergics
Catheterisation
Bladder training

23
Q

What is the first line disease modifying drug?

A

Tecfedira
Aubagia
INFβ IV

24
Q

What are second line disease modifying drugs used in MS?

A

Monoclonal antibodies i.e Lemtrada

Fingolimod

25
When are second line disease modifying drugs used?
In either resistant or severe early onset 2 episodes within a year.
26
What are the third line disease modifying drugs?
Mitoxantrone | Stem cell transplant
27
When are the third line disease modifying drugs used?
Very severe relapsing disease
28
What is Tecfidera ?
1st line Oral agent 44% reduction in symptoms
29
What is INFβ?
Interferron β SC or IM Decreases rate and severity of relapses Very few side effects
30
What is Fingolimod?
2nd line Oral agents Toxicity means not 1st line
31
What are some of the side effects of fingolimod?
Cardia toxicity Lower white cell count Hypertension
32
List some common monoclonal antibodies.
Rituximab | Natlilizumab
33
When is Rituximab used?
Highly active relapsing and remitting MS
34
How does Natilizumab work
Bings to α4 integrin Prevents binding of lymphocyte to the VCAM on blood vessel wall Prevent lymphocyte migration out of the blood vessel.
35
Describe plaques related to MS.
Well circumscribed and demarcated with an irregular shape often glassy and translucent. Massive variation in size
36
What does an active plaque appear like?
Perivascular inflammation Microglia Ongoing demyelination
37
What does an inactive plaque appear like?
Gliosis Few myelinated axons Reduced oligodendrocytes
38
What is the association of MS with latitude ?
Further from the equator there is an increase in prevalence of MS.
39
What is another primary cause of demyelination which isn't MS with a low mortality?
Acute disseminate Encephalomyelitis | Self limiting, full recovery with some defecits
40
What is another primary cause of demyelination which isn't MS with a high mortality?
Acute haemorrhage leukoencephalitis
41
What is a secondary cause of demyelination?
Central pontine myoclinosis
42
What causes Central Pontine myoclinosis?
Too fast correction of hyponatraemia
43
What virus can lead to. secondary form of demyelination?
JC virus
44
What can lead to a toxic secondary form of demyelination?
Organic solvents
45
List some environmental factors related to MS?
Vitamin D deficiency | Viral triggers e.g. EBV
46
List some genetic factors related to MS?
HLA DRB Polymorphism in Interleukins Familial link
47
What interleukins when mutated are linked to an increased risk of MS?
IL-2 | IL-7
48
What forms the oligoclonal bands found in the CSF of someone with MS?
IgG