MS Flashcards

1
Q

MS is caused my degradation of _____

A

myelin

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2
Q

How many MS patients are there in the US?

A

400k

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3
Q

What latitude is at high risk of MS?

A

northern/ cool climates (possible vitamin D link)

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4
Q

Genetic risk assc with MS

A

20-40x risk if 1st degree relative has MS

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5
Q

Acute treatment of optic neuritis

A

1 gram IV prednisone 3-5 days

for quicker improvement but no clear impact on longterm improvement

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6
Q

What is needed to diagnose MS in the absence of symptoms?

A

-positive brain MRI
-positive spinal cord MRI
-positive CSF
(2/3 needed)

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7
Q

CSF findings in MS

A

1) oligoclonal banding
2) high IgG/ albumin ratio
3) high IgG synthesis

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8
Q

What are traditional (platform) agents for treating MS?

A

1) interferons
2) glatiramer (copaxone)

  • *No evidence to combine the two
  • *Medicaid prefers copaxone first
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9
Q

Disadvantages to traditional agents for MS?

A

1) injections
2) incomplete efficacy
3) neutralizing Abs
4) ADRs/ adherence

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10
Q

What are three new MS oral therapies?

A

1) fingolimod (gilenya)
2) teriflunomide (augbagio)
3) dimethyl fumarate (tecfidera)

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11
Q

Gilenya/Fingolimod:

  • MC ADR
  • Most dangerous ADR
A

1) MC headache

2) dangerous: bradycardia, hypotension- first dose must be monitored

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12
Q

Teriflunomide:

compatible with pregnancy?

A
  • must be removed from system with cholestyramine if woman becomes pregnant
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13
Q

Common ADRs assc with Teriflunomide (auba-by-gio)

A
  • diarrhea
  • alopecia
  • hepatotoxic
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14
Q

Dimethyl fumarate (tecfidera) common side effects

A

flushing
diarrhea
nausea

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15
Q

Natalizumab is the most effective drug for MS but is second line why?

A

1/1000 risk of PML

*can test patients for PML Ab to predict risk before starting drug (2% risk conversion)

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16
Q

Transverse myelitis: define

A

demyelination of the spinal cord

17
Q

Variant of MS that fails to respond to DMARDs

A

Primary Progressive MS

18
Q

Neuromyelitis Optica:

aka

A

Devics Disease

19
Q

NMO: location of lesions

A

spinal cord+ optic nerves

loss of vision, loss of sensation, bladder dysfunction

20
Q

NMO Ab

A

IgG against aquaporin 4 (chloride channel)

21
Q

Tx NMO

A

Rituximab (CD20 Ab)

22
Q

Which is more severe: NMO or MS

A

NMO

23
Q

Classic MRI finding in NMO

A

very long central necrotic region in cord MRI

24
Q

NMO CSF findings

A

no bands

25
Q

Is co-existing autoimmune disease more common in NMO or MS?

A

NMO

26
Q

Treatment for spasticity

A

-baclofen
-benzos
-tizanidine
(all= fatigue)

27
Q

Treatment for neuropathic pain

A

1) amitryptiline (Elavil)
2) gabapentin (Neurontin)
3) pregabalin (lyrica)
4) carbamazepine (tegretol)
6) duloxetine (Cymbalta)

28
Q

Cognitive domain usually spared in MS

A

language and verbal skills

29
Q

What causes ^^ risk of cognitive dysfunction in MS

A
  • large T2 lesion area
  • large T1/2 lesion load
  • greater number of juxtacortical lesions
30
Q

What improves cognitive symptoms in MS?

A

stimulants, not alzheimers drugs

31
Q

How is urinary retention treated in MS?

A

alpha blockers

catheterization (intermittent)

32
Q

How is failure of bladder to store treated in MS?

A

1) scheduled voiding, limit fluids/diuretics
2) anticholinergics
3) botox in bladder