Multiple sclerosis Flashcards

1
Q

what is multiple sclerosis?

A

inflammatory condition of the central nervous system

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2
Q

it is progressive demyelination of typical areas of ———— matter within the brain and spinal cord?

A

white

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3
Q

due to the limited capacity for re-myelination of axons this leads to defects in?

A

the rate and consistency of neuronal conduction

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4
Q

demyelination of white matter can occur

A

anywhere in the CNS

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5
Q

what is the most common phenotype of MS?

A

relapsing and remitting

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6
Q

what are plaques?

A

areas of demyelination

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7
Q

what is indicative of ongoing demyelination and inflammation?

A

active plaques

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8
Q

what is indicative or a burnt out active plaque?

A

inactive plaques

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9
Q

where are the common areas of demyelination? (4)

A

corpus callosum
optic nerve
periventricular white matter
cerebellar white matter

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10
Q

what are risk factors for developing MS? (5)

A
living in areas of higher latitude 
previous EBV infection 
1st degree relative with MS 
Presence of HLA DRB1 
common in young females
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11
Q

what is the presesntation of pyramidal dysfunction in mS?

A

features of upper motor neurone dysfunction

tonic spasms

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12
Q

what are examples of upper motor neurone dysfunction?

A

spasticity, weeakness, hyper-reflexia

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13
Q

where do upper motor neurone dysfunction tend to occur?

A

extensors of the upper limb and flexors of the lower limb

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14
Q

what type of tonic spasms are associated with MS?

A

frequent biref spasms of the lower limb

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15
Q

what is the preesentation of optic neuritis?

A

painful eye movements or visual loss

colour desaturation, loss of visual acuity

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16
Q

what is seeen in the swinging light test?

A

RAPD

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17
Q

what is seen on fundoscopy?

A

pale optic disc

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18
Q

what is a manifestation of brainstem demyelination affecting the medial longitudinal fasiculus on one or both sides?

A

internucleur ophtaahlmoplegia

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19
Q

what does INO cause?

A

horizontal diplopia

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20
Q

if you have a right INO

A

there is inability to adduct the right eye and a nystagmus of the left eye on attempted horizontal gaze to the left

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21
Q

what is pathognomonic of MS?

A

bilateral INO

22
Q

there is a sensaation of ——– trickling down one’s skin

23
Q

loss of sensation of DCLM tract manifested by?

A

clumsinesss due to loss of proprioception

24
Q

in regards to trigeminal neuralgia what is important to pay attention to?

A

bilateral attacks, on both sides of the face

25
what is Lhermitte's sign?
electric shock-like seensation down the upper limbs and trunk on neck flexion
26
what is Uhthoff's phenomenon?
exacerbation of current symptoms in hor environments - i.e. after a hot shower
27
electric shock-like seensation down the upper limbs and trunk on neck flexion
Lhermitte's sign
28
exacerbation of current symptoms in hor environments - i.e. after a hot shower
Uhthoff's phenomenon
29
what are the symptoms of cerebellar dysfunction?
``` dysdiodochokinesia ataxia nystagmus intention tremor slurred speech hypotonia ```
30
what type of incontinence is associated with MS?
urge incontinence , retention
31
how do you diagnose MS?
evidence of two distinct neurological deficits occuring at different tyimes implicating lesions of white matter which are spatially and functionally distinct
32
what two tools can be used to confirm MS?
MRI imaging and CSF analysis
33
what is seen on MRI imaging of MS?
multiple white matter plaques
34
what is seen in CSF of MS?
presence of IgG Oligoclonal bands
35
how do you manage mild acute relapse?
symptomatic treatment
36
how do you manage moderate acute relapse?
oral prednisolone
37
relapse rates may --------- during pregnancy and may -------------- 3–6 months after childbirth before returning to pre‑pregnancy rates
reduce | increase
38
there is a possible risk of ------------- following flu vaccination if they relapse and remitting MS?
the possible risk of relapse after flu vaccination
39
encourage people with ms to?
exercise
40
what is the 1st line DMARD for relapsing-remitting disease? (3)
Tecfidera, Beta-interferon or Glatiramer Acetate
41
where 1st line therapy with DMARD has failed to control disease activity the following can be used? (3)
Tysabri (Natalizumab) | Fingolimod
42
what is natalizumab?
monoclonal antibody
43
what is the risk of tysabri?
risk of progressive multifocal leukoencephalopathy via JC infection
44
what type of DMARD is fingolimod?
sphingosine-1-phosphate inhibitor
45
when is Ocrelizumab used?
1st line in early primary progressive MS only
46
how do you manage spasticity?
physiotherapy and oral baclofen/gabapentin
47
how do you manage neuropathic pain?
gabapentin
48
how do you maanage fatigue?
amantadine +/- modafinil if excessive daytime sleepiness
49
how do you manage bladder dysfunction?
bladder physiotherapy, cathterisation in cases of retention and anticholinergic drugs (oxybutynin) in cases of urgee incontinence
50
what type of hypersensitivity reaction is MS?
type IV mediated or cell mediated hypersensitivity
51
what is charcot's neurological triad?
Dysarthria intention tremor nystagmus