multiple sclerosis Flashcards

1
Q

what is a MS

A

immune-mediated inflammatory, demyelinating, condition that affects both the brain and spinal cord

demyelination of the white matter of the CNS that tends to favour the optic nerves, brainstem, periventricular areas + spinal cord

demyelination decreases conduction velocity and some of the signal dissipates causing information to be lost

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2
Q

when does it start

A

MS is commoner in women than men and typically occurs in temporal regions. Symptoms typically commence in early life (20s and 30s) in the form of visual or sensory disturbances.

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3
Q

symptoms of MS

A

Visual

  • optic neuritis: common presenting feature
    optic atrophy, pale disc
  • Uhthoff’s phenomenon: worsening of vision following rise in body temperature
  • internuclear ophthalmoplegia

Sensory

  • paraesthesia - pins/needles
  • numbness
  • trigeminal neuralgia
  • Lhermitte’s syndrome: paraesthesiae in limbs on neck flexion
Motor
spastic weakness: most commonly seen in the legs
- horners
- bells
- incontinence

Cerebellar
ataxia: more often seen during an acute relapse than as a presenting symptom
tremor worst on movement

Others
urinary incontinence
sexual dysfunction
intellectual deterioration

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4
Q

what is bulbar palsy

A

9, 10, 11, 12

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5
Q

Ix for MS

A

neurological examination

  • Symptoms have to be progressive over a period of 1 year to diagnose primary progressive MS.
    1. MRI of brain or spinal cord - will demonstrate demyelination plaques
    2. Immunoelectrophoresis of CSF - will show oligoclonal bands of IgG

MRI - dorsum fingers
LP - elevated levels of IgG Oligoclonal bands
increase WBCs

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6
Q

3 main patterns of clinical presentation

A
  1. Relapsing remitting
  2. Secondary progressive
  3. Primary progressive
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7
Q

what is relapse remitting MS

A

they occur in different areas and different episodes

when you have attacks for at least 24 hours and then get better

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8
Q

what is secondary progressive

A

when you start off with remitting and then it gradually gets worse without relapses

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9
Q

what is primary progressive MS

A

it gets worse from the beginning

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10
Q

symptoms of optic neuritis

A
  • Central scotoma. This is an enlarged blind spot.
  • Pain on eye movement
  • Impaired colour vision
  • Relative afferent pupillary defect
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11
Q

McDonald criteria for MS

A
  1. Lesions consistent with an inflammatory process
  2. No alternative diagnosis
  3. Multiple lesions in time and space (Relapsing remitting MS)
  4. Progressive neurological deterioration for 1 year (Primary progressive MS)
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12
Q

how can a MS relpase be diagnosed

A
  1. Develops new symptoms
  2. Has rapid worsening of existing symptoms
  3. Symptoms last for more than 24 hours in the absence of infection or other cause after a stable period
    of one month or more
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13
Q

treatment for MS relapse

A

500mg 5 days course of ORAL steroids

OR

IV of steroids in hospital

METHYLPREDNISOLONE

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14
Q

fatigue treatment for MS

A

amantadine

other options include mindfulness training and CBT

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15
Q

spasticity treatment for MS

A

baclofen or gabapentin

Other options include diazepam, dantrolene and tizanidine
physiotherapy is important

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16
Q

oscillopisa?

A

when the eye moves side to side, up and down

images jump, hazy

17
Q

treatment for oscillopsia

A

gabapentin

18
Q

emotional lability treatment

A

amitryptilline

19
Q

Tx for neuropathic pain

A

amitryptilline
duloxetine
gabapentin
pregablin

20
Q

Tx for depression

A

citalopram
fluoxetine
paroxetine
sertraline.

21
Q

Tx for incontinence

A

ultrasound first to assess bladder emptying - anticholinergics may worsen symptoms in some patients

if significant residual volume → intermittent self-catheterisation
if no significant residual volume → anticholinergics may improve urinary frequency

1) behavioural management programme
2) antimuscarinic - oxybutinin

22
Q

reducing the frequency and duration of the relapses of MS

A

interferon beta or glatiramer acetate

active disease
Teriflunomide + dimethylfumerate

highly active disease
natalizumab + alemtuzumab

23
Q

planning to get pregnant what advise do u give for MS

A

fertility not affected

glatiramer acetate

stop DMTs 1 -12 months

24
Q

what is Uhthoff’s phenomenon

A

worsening of symptoms in higher temperatures

25
Q

factors influencing demyelination

A
Multiple genes
Epstein–Barr virus (EBV)
Low vitamin D
Smoking
Obesity
26
Q

what is internuclear opthalmoplegia

A

inability to move both your eyes together when looking to the side.
amage to the medial longitudinal fasciculus, a group of nerve cells leading to the brain. It’s common in young adults and older people.
diplopia

27
Q

poor prognosis

A

exhibiting nrainstem Sx such as tremor, nystagmus, ataxia as well as experiencing frequent attacks