Multiple Sclerosis Flashcards

1
Q

Multiple Sclerosis

A
  • inflammatory dz of CNS

- many areas of brain and spinal cord affected by plaques or sclerosed areas

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2
Q

MS Pathophys

A
  • demyelination and inflammation leads to
  • plaques in brain and spinal cord which leads to
  • neurologic sxs reflective of affected areas
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3
Q

What are the 4 MS classifications?

A
  • relapsing/remitting (discrete attacks then recovery)
  • primary progressive (steady decline)
  • secondary progressive (starts RRMS then decline)
  • progressive relapsing (overlaps PPMS and SPMS)
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4
Q

MS Treatment Goals

A
  • decrease severity, intensity and duration of exacerbations
  • enhance exacerbation recovery
  • prevent relapse and onset of progressive dz
  • stop or reverse progressive MS
  • provide symptomatic relief
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5
Q

How are moderate and severe acute exacerbations treated?

A

corticosteroid

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6
Q

Corticosteroids MOA in PD

A
  • unclear

- may help preserve myelin and maintain BBB integrity

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7
Q

Why should corticosteroid use be reserved for PD exacerbations?

A

-effects are transient and tend to diminish w/ repeated use

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8
Q

Plasma Exchange

A

-tx option for pts w/ very severe attacks that do not respond to aggressive corticosteroid treatment

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9
Q

Interferons MOA

A
  • alter expression and response to surface antigens
  • can augment suppressor cell function
  • can suppress T-cell proliferation
  • may decrease BBB permeability
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10
Q

Name a couple interferon meds for MS.

A
  • beta 1a: Avonex and Rebif

- beta 1b: Betaseron and Extavia

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11
Q

Efficacy of Interferons

A
  • decrease frequency of exacerbations and delay disability

- early tx with interferon assoc with significant reduction in risk of MS progression

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12
Q

What is a contraindication of all interferon meds?

A

pregnancy and lactation

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13
Q

What are the most common adverse effects of interferon meds?

A

-HA, flu-like sxs, myalgia, injection site rxn

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14
Q

Interferon Monitoring

A
  • EDSS: kurtzke expanded disability status scale 0-10

- baseline CBC, plt, LFTs at 1 month then q3 months x1 year, then q6 months

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15
Q

Glatiramer/Copaxone Indication

A

relapsing remitting

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16
Q

Glatiramer/Copaxone Efficacy

A

decreases relapses and postpones relapses

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17
Q

Glatiramer/Copaxone AEs

A
  • vasodilation
  • arthralgia
  • chest pain
  • injection site reaction
18
Q

Fingolimond/Gilenya Indication

A
  • relapsing remitting

- progressive relapsing

19
Q

Fingolimond/Gilenya Efficacy

A

modestly better than avonex (interferon) at preventing relapse

20
Q

Fingolimond/Gilenya AEs

A
  • HA, increased LFTs
  • decrease HR, heart block
  • macular edema, bronchitis, pneumonia

-avoid in pts w/ recent MI, angina, stroke, TIA, severe HF

21
Q

What is unique about Fingolimond/Gilenya?

A

first ORAL disease modifying therapy for MS

22
Q

Teriflunomide/Aubagio Indication

A

relapsing forms of MS

23
Q

Teriflunomide/Aubagio AEs

A
  • N/D
  • hair loss
  • black box warning for hepatotoxicity
  • increased infx risk
  • teratogenic
24
Q

Teriflunomide/Aubagio Monitoring

A

-LFTs baseline, qmonth x6 months, then periodically

25
Dimethyl Fumarate/Tecfidera Indication
relapsing forms of MS
26
Dimethyl Fumarate/Tecfidera AEs
- flushing - N/D - decreased WBC - rare progressive multifocal leukoencephalopathy
27
Dimethyl Fumarate/Tecfidera Monitoring
-WBC baseline, q 3-6 months, then periodically
28
Mitoxantrone/Novantrone Indications
approved to decrease frequency of relapses and/or neurologic disability in adults w/ SPMS, PRMS or worsening RRMS
29
Mitoxantrone/Novantrone AEs
- decreased WBC and platelets, anemia - increased LFTs - decreased LVEF, HF - UTIs, N/V, mucositis - black box warning cardiotoxicity, acute myelogenous leukemia
30
Which pts should use Mitoxantrone/Novantrone?
-reserved for pts with worsening dz because of cardiotoxicity AEs
31
Natalizumab/Tysabri Indication
-monotherapy for relapsing forms of MS in pts who have documented inadequate response or intolerance to traditional MS therapies
32
Why should Natalizumab/Tysabri only be used as monotherapy?
fatalities reported w/ combination therapy
33
Natalizumab/Tysabri AEs
- rare progressive multifocal leukoencephalopathy - pts followed in ongoing safety registry - hepatotoxicity
34
Which pts should use Natalizumab/Tysabri?
reserved for pts who can't tolerate or don't respond to other therapies (due to risk of PML and hepatotoxicity)
35
How long should therapy be continued?
- continue indefinitely | - do not stop treatment during evaluation for continuing treatment
36
What medication should be prescribed as soon as possible following a definite MS diagnosis?
- interferon beta medication (Avonex, Rebif) | - or glatiramer acetate
37
Who should not use any of the MS medications?
pregnant or nursing mothers
38
Which drugs are considered first line disease modifying therapy for MS?
- interferon beta | - glatiramer/copaxone
39
Dalfampridine/Ampyra Efficacy
- increased walking speed in 35-45% of MS pts | - improved walking speed = improved ambulation
40
Dalfampridine/Ampyra AEs
- back pain, dizziness, insomnia, fatigue - nausea, balance disorder, UTI, falls, HA - rare seizure
41
Pt Education for MS
- educate about MS - community support - tx: injection techniques, adverse effects, symptomatic management