3. MS Flashcards

1
Q

What is Multiple Sclerosis?

A

Autoimmune demylination of the CNS (brain and SC) at multiple sites in the CNS over space and time that causes periods of exacerbations and remissions of symptoms.

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2
Q

Multiple Sclerosis

Symptoms (7)

A
  • Can cause any neurological sign. Common ones are
      1. Paresthesias (tingling)
      1. Optic neuritis (pain and vision loss)
      1. Urinary problems/ Bladder dysfunction: spastic bladder and overflow incontinence
      1. Gait disturbances
      1. Dysarthria (slow and slurred speech)
      1. Hemiparesis (weakness on 1 side of body)
    • Transverse myolitis?!?!
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3
Q

What are the 4 major types of MS?

In order from MC => LC

A
  1. Relapsing and remitting (45-50%)
  2. Secondary progressive (begin with relapsing and remitting type and still have some relapses)
  3. Primary progressive
  4. Benign
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4
Q

Secondary progressive MS patients begin their disease process as which form?

A

Relapsing remitting

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5
Q

When/who is MS most diagnosed in?

A

W 20-30; but often diagnosed from 15-50

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6
Q

How is M.S affected by geographic region?

A
  • ↑ risk depending on where you live before 14 YO:
  • More common in
    • Temperate regions (Minneapolis, NY)
      Less common in
    • Tropical regions (FL, Miami
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7
Q

The course of Multiple Sclerosis is most favorable in whom?

A
  1. Women
  2. Earlier onset (in 20s)
    1. *However, if really young (i.e., adolescent/early adult; 15YO) = unfavorable
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8
Q

Which test can confirm the diagnosis of MS?

A

No single test can be used. Many tests are done:

  1. MRI of the head and CT of the spine
  2. Multimodality evoked potentials (SSEPs, VEPs, BAER)
  3. Lumbar puncture of CSF
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9
Q

What do you see on MRI of the head and CT of spine in MS patient?

A
  1. MULTIPLE Ovoid lesions of high signal on T2WI in periventricular white matter and spinal cords
  2. Acute lesions may enhance
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10
Q

What do you see in CSF in MS patient?

A
  1. Oligoclonal bands
  2. ↑ IgG index/synthesis rate
  3. ↑ proteins
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11
Q

What causes M.S?

A
  • Unknown:
    • Genetic susceptability
    • Childhood event sensitizes immune system to attack CNS myelin ==> adult event triggers the disease (viral infection or post-partum period)
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12
Q

Only approved drug for patients with the Multiple Sclerosis: Primary Progressive type + relapsing forms of the disease?

A

Ocrevus

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13
Q

Disease modifying drugs for M.S (slow the progression and ↓ amount and severity of exacerbations

A
  1. IFN (interferons)
  2. Glatirimer Acetate
  3. Dimethyl Fumarate
    • mabs
    • mod
    • mide
  4. FINGOLAMOD?!
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14
Q

Treatment of acute exacerbation in MS?

How does this affect the exacerbation?

A
  • 1 gram of IV high-dose corticosteroid (methylprednisolone) for 3-5 days tapered with oral prednisolone
    • ↓ length of exacerbation, but does not change the outcome.
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15
Q

If patient has an acute exacerbation of M.S and cannot tolerate steroids, what is another treatment?

A
  1. ACTH (Acthar gel)
  2. IVIg
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16
Q

How is M.S diagnosed over space and time?

A

Multiple lesions over space and time

17
Q

What is a DDx of Multiple Sclerosis?

A

1. Clinicallly Isolated Syndrome (CIS): monofocal episode or multifocal episode

18
Q

What is a monofocal episode of Clinically Isolated Syndrome (CIS)?

A

Person experiences a single neurologic sign/symptom that’s caused by a single lesion (1 episode/1 time)

(i.e., optic neuritis in one eye)

19
Q

What is a multifocal episode of Clinically Isolated Syndrome (CIS)?

aka

A

Acute Disseminated Encephalomyelitis (ADEM)

  • Person experiences more than one sign/symptom caused by lesions in more than one place (i.e., optic neuritis in one eye plus hemiparesis) one time.
20
Q

When CIS patients have multiple demyelinating lesions on MRI, they have a __________% chance of developing MS within several years?

A
  • 60-80%
  • *High risk
21
Q

When CIS patients do not have multiple demyelinating lesions on MRI, they have a ______% chance of developing MS within several years

A
  • 20%
  • *Low risk
22
Q

What are some conditions which can mimic MS?

A
  1. Autoimmune disease: SLE w/ cerebritis or CNS vasculitis or Polyarteritis Nodosa w/ transverse myelitis
  2. Devic’s disease (neuromyelitis optica)
  3. B12 deficiency
  4. Lymphoma or leukemia w/ CNS involvement
  5. Spinocerebellar ataxias
  6. Infections: HIV, West Nile, HTLV-1, CMV, Lyme disease, Syphillis
  7. Granulomatous disease (sarcoidosis)
  8. Metachromatic leukodystrophy, adrenomyeloleukodystrophy
23
Q

tx for management of spasticity in patients with MS?

(symptom-management drugs, NOT disease-modifying)

A
  1. Baclofen (oral or intrathecal)
  2. Tizanadine
  3. Diazepam
  4. Carbamazepine
  5. Botox injections
  6. Dantrolene
24
Q

Tx of intention tremors in patients with MS?

(symptom-management drugs, NOT disease-modifying)

A
  1. Propanolol
  2. Promidone
  3. Clonazepam
25
Q

tx of urinary urgency (spastic bladder) in patients with MS?

(symptom-management drugs, NOT disease-modifying)

A
  1. Oxybutinin
  2. Detrol LA
26
Q

tx urinary retention/hesitency in patients with MS?

(symptom-management drugs, NOT disease-modifying)

A
  1. Bethanechol
27
Q

tx fatigue in patients with MS?

(symptom-management drugs, NOT disease-modifying)

A
  1. Amantadine
    • afinil
  2. Bupropion
  3. Methylphenidate
  4. Pemoline
  5. XRCISE
28
Q

What is Devic’s Disease (aka?)?

A
  • Devic’s Disease (NMO: Neuromyelitis Optica):
    • Variant/different entity of M.S that is characterized by inflammation and demyelination of the optic nerve and SC (often LONG segments of SC), but spares the brain
29
Q

Fairly sensitive and specific test to diagnose Devic’s disease (aka NMO)?

A

Aquaphorin 4 antibodies in blood and CSF

30
Q

What is the general treatment for Devic’s Disease (aka NMO)?

A
  1. Steroids and/or plasma exchange (plasmapheresis)
  2. Followed by: immunosupression (i.e., azothiaprine, mycophenolate mofetil, or rituxumab)
31
Q

Why is it important to differentiate if MS or Devic’s Disease?

A

More aggressive, but treatable