Clin: Multiple Sclerosis - Hon Flashcards

1
Q

disorder of the brain and spinal cord (CNS) characterized by a tendency for periods of increasing and decreasing symptoms and signs (exacerbations/remissions), which result from loss of nerve tract insulation (myelin) at multiple sites in the CNS

A

multiple sclerosis

  • most pts diagnosed in their 20’s-30’s (W>M)
  • no single test can confirm the diagnosis
  • unknown etiology, probably some genetic susceptibility (perhaps a childhood illness that sensitizes immune system to attack)
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2
Q

what are the most common symptoms of MS?

A
  • paresthesias
  • gait disturbances
  • weakness
  • visual loss (optic neuritis commonly seen)
  • urinary difficulty
  • dysarthria
  • hemiparesis
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3
Q
  • hemisection of cord
  • weakness in legs
  • sensory disturbance in legs
  • hyperreflexia
  • positive Babinski sign
A

Brown-Sequard syndrome

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4
Q

What are the 4 types of MS?

A
  • relapsing remitting (45-50%)
  • secondary progressive (20-25%)** these patients begin their disease process in the relapsing remitting category
  • primary progressive (15-20%)
  • benign (10-15%)
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5
Q

what is the geographic distribution of MS?

A
temperate zones (further from equator) see a higher incidence
- theory has to do with sunlight/vitamin D levels during pregnancy
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6
Q

what studies are used to make the diagnosis of MS?

A
  • MRI of the head, CT of spine

- lumbar puncture for CSF analysis

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7
Q

where would you see ovoid lesions in MS?

A

MRI of the spine

- in the periventricular white matter and in the spinal cord

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8
Q

what are the typical findings on lumbar puncture of MS patients?

A

presence of oligoclonal bands and/or increased IgG index/synthesis rate

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9
Q

how is MS diagosed?

A

BY MULTIPLE LESIONS OVER SPACE AND TIME - know this!

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10
Q

what are the main drugs used for “maintenance” in MS (to decrease the frequency and severity of exacerbations and slow the progression of the disease)

A
  • MAB’s
  • interferons
  • glatirimer acetate
  • dimethyl fumarate
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11
Q

what is the tx for an acute attack of MS (optic neuritis)?

A

high dose steroids (1g IV daily for 3-5 days)

- reduces the length of the exacerbation, but is not thought to change the overall outcome of it

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12
Q

what is the exception drug approved to treat primary progressive MS (PPMS) in addition to relapsing forms of the disease?

A

ocrevus

- is the ONLY drug available for PPMS!

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13
Q

what are the ddx of MS?

A
  • clinically isolated syndrome (CIS)
  • monofocal episode (single sign/sx caused by single lesion)
  • multifocal episode (aka acute disseminated ecephalomyelitis - ADEM) more than one sign/sx caused by lesions in more than one place
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14
Q

when CIS patients have multiple demyelinating lesions on MRI, what is the percent chance of developing MS?

A

60-80% within several years

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15
Q

when CIS patients do NOT have multiple demyelinating lesions on MRI, what is the percent chance of developing MS?

A

20%

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16
Q

what disease is known as a notorious mimicker of MS?

A

sarcoidosis

17
Q

what is the symptom management for spasticity?

A

baclofen (oral or intrathecal), tizanadine, diazepam, carbamazepine, botox, injections, dantrolene

18
Q

what is the symptom management for intention tremor?

A

propranolol, primidone, clonazepam

19
Q

what is the symptom management for urinary urgency (spastic bladder)?

A

oxybutininm, detrol LA

20
Q

what is the symptom management for urinary retention/hesitancy?

A

bethanechol

21
Q

what is the treatment management for painful dysesthesias (pins/needles)

A

carbamazepine, oxcarbazepine, gabapentin, phenytoin, baclofen

22
Q
  • *what is the treatment management for fatigue?**

- is really prominent in disease!

A

amantadine, modafinil, armodafinil, buproprion, methylphenidate, penoline, exercise

23
Q

aka neuromyelitis optica

  • sometime considered a “variant” of MS, but probably a different entity
  • characterized by inflammation and demyelination of optic nerves/spinal cord (often long segments) with relative sparing of brain
  • can use fairly sensitive and specific testing for NMO (Aquaphorin) antibodies in blood and CSF
A

Devic’s disease

  • order NMO to rule out this disease
  • is progressive, but can be stopped with right treatment (unlike MS)
24
Q

what is the tx for Devic’s disease?

A

steroids and/or plasma exchange

- followed by immunosuppression (azothiaprine, mycophenolate mofetil, rituxumab)