Multiple Sclerosis Flashcards

1
Q

what is MS

A

inflammatory demyelinating disorder of the CNS

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2
Q

what is meant by plauqes

A

areas of inflammation caused by T-cell mediated response

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3
Q

what are the 4 patterns of MS

A

Relapsing remitting
Secondary progressive
Progressive relapsing
Primary progressive

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4
Q

how does demyelination cause symptoms

A

acute relapses are caused by focal inflammatory demyelination – causes conduction block
severe damage causes permanent axonal destruction

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5
Q

how does MS normally present

A
monosymptomatic 
unilateral optic neuritis 
numbness/tingling in limbs
leg weakness
ataxia
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6
Q

what are signs of pyramidal dysfunction

A

increased tone
spasticity
weakness
affects extensors of upper limbs and flexors of lower limbs

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7
Q

what is Sx of optic neuritis

A

painful visual loss
lasts 1-2weeks
most improve (but not always)
associated with RAPD

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8
Q

what is RAPD

A

condition in which pupils respond differently to light stimuli shone in one eye at a time

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9
Q

what are sensory Sx of MS

A
pain
paraesthesia
numbness 
trigeminal neuralgia 
dorsal column loss
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10
Q

what is lost in dorsal column damage

A

proprioception and vibration loss

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11
Q

what are cerebellar dysfunction Sx

A

DANISH

  • Dysdiadokinesis
  • Ataxia
  • Nystagmus
  • Intention tremor
  • Slurred speech
  • Hypotonia
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12
Q

what are Sx of brain stem dysfunction

A

Diplopia = VI palsy

Facial weakness = VII palsy

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13
Q

what ophthalmic condition is almost seen exclusively in MS

A

Internuclear ophthalmoplegia

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14
Q

what is Internuclear ophthalmoplegia

A

caused by injury/dysfunction in the Medial longitudinal fasciculus

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15
Q

what are Sx of Internuclear ophthalmoplegia

A

Distortion of binocular vision
Failure of adduction- diplopia
Nystagmus in abducting eye
Lag

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16
Q

what are Sx of lower urinary tract dysfunction in MS

A
frequency
nocturia
urgency
urge incontinence
retention
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17
Q

what could Sx of lower urinary tract dysfunction in MS be confused with

A

BPH

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18
Q

what is used to treat fatigue in MS

A

amantadine

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19
Q

what is needed for a diagnosis of MS

A

At least 2 episodes suggestive of demyelination

Dissemination in time and place

20
Q

what would Ddx be in MS

A

Vasculitis
Granulomatous disorder e.g. sarcoidosis
Vascular disease e.g. stroke
Structural lesion e.g. mass pressing on spinal cord
Infection
Metabolic disorder e.g. folate deficiency

21
Q

what is the most sensitive test for MS

22
Q

why are blood tests done in suspected MS

A

don’t rule in MS but they rule out other differentials

23
Q

what blood tests should be done, and come back negative, to ensure it is MS

A

Plasma viscosity, FBC, CRP
Renal liver bone profile
Auto anti body screen - should be normal in MS
Borellia (lime disease), HIV, syphilis serology
B12 and folate

24
Q

what in the CSF suggests inflammation

A

oligoclonal bands of IgG on electrophoresis

25
what are the 3 categories of management of MS
acute exacerbation symptomatic treatment disease modifying treatment
26
what is the treatment of acute exacerbation of MS - Mild - Moderate - Severe
mild - symptomatic Tx moderate - oral steroids severe - admit/IV steroids
27
what are tx options for pyramidal dysfunction
physio occupational therapy anti spasmodic agents muscle relaxants - e.g. oral baclofen
28
what are anti spasmodic agents
baclofen tizanidine Botox
29
what can be given in severe cases of bed bound patients
Intrathecal baclofen / phenol
30
what Tx can be given for sensory symptoms
anti convulsant eg. gabapentin | anti depressant eg.amitriptyline
31
what causes lower urinary tract dysfunction in MS
increased tone at bladder neck | detruser hypersensitivity
32
Tx for lower urinary tract dysfunction
anti-cholinergics eg. oxybutynin desmopressin - stops urine production so only given for short period of time, i.e. they have to go on a plane journey catheterisation
33
what is the first line therapy for disease modifying treatment
Interferon Beta – Avonex, Rebif, Betaseron, Extavia Tecfedira
34
what is second line therapy for disease modifying
Monoclonal antibody – Tysabri, Lemtrada Fingolimod
35
what is third line therapy for disease modifying
Mitoxantrone
36
what treatment is first line in relapsing remitting MS
Tecfidera
37
when is monoclonal antibody drugs indicated in MS
highly active relapsing remitting multiple sclerosis
38
what is a deadly SE that needs to be looked for in Tysabri
Progressive multifocal leukoencephalopathy
39
what are SE of the interferons
flu Sx depression abortion
40
what is the most common pattern of MS
Relapsing-Remitting
41
what are features of RR MS
episodes of exacerbations/relapses i.e. clearly defined attacks of new or increasing neurologic symptoms followed by periods of partial or complete recovery (remissions) no progression of the disease during remission
42
what are features of Primary Progressive MS
worsening neurologic function from the onset of symptoms, without early relapses or remissions.
43
what are secondary progressive MS
initial relapsing-remitting course transition to a secondary progressive course in which there is a progressive worsening of neurologic function
44
what is progressive relapsing MS
pattern of relapses within primary progressive MS least common
45
risk factors for MS
smoking previous infectious mononucleosis genetics - HLA DRB1*15 carrier vit D deficiency