MS Flashcards

1
Q

Multiple Sclerosis is

A

chronic inflammatory, autoimmune, demyelinating disease of CNS

An abnormality in the immune response thatresults in an attack on the individuals own neural tissue

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2
Q

Most common theory for MS

A

environmental trigger, probably a virus induces a delayed autoimmune attack on a genetically susceptible individual.

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3
Q

Relapsing –remitting (RRMS)

A

relapses with full recovery or some remaining neurological symptoms and residual deficits. Then New attack

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4
Q

MS New Attack

A

New symptoms must last at least 24 hours and be separate from other symptoms by at least 30 days to qualify as a new attack

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5
Q

Primary-progressive (PPMS)

A

progression from the onset without remission

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6
Q

Secondary-progressive ( SPMS)

A

initial relapsing-remitting course followed by progression at a variable rate.

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7
Q

Progressive-relapsing (PRMS)

A

progressive disease from onset but with clear acute relapses that may or may not have some recovery or remission.
Common in people who develop the disease after 40.

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8
Q

General clinical mainifestation of MS pt 1

A
Heat sensitivity
Fatigue
Gait disturbance
Weakness, mild paresis to total paralysis
Spasticity
Balance and coordination
Speech and swallowing dysfunction
BB dysfunctipon
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9
Q

General clinical manifestations of MS pt 2

A
Pain
Parenthesis and other sensory changes
Visual disturbances
Cog problems
Tremors
Depression
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10
Q

McDonald Criteria

A

For dx of MS

> /= 2 attacks and >/= 2 clinical evidence of lesion = MS

> /= 2 attacks and 1 clinical evidence of lesion and clear evidence of prior attack involving lesion in different location = MS

Other criteria gets more complicated. Just know big idea

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11
Q

McDonald- person who has 1 year steady disease progression needs

A

At least 2 of following:
>/= MS typical T2 lesion
>/= 2 T2 SC lesion
CSF oligioclonal bands

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12
Q

MS cure

A

None

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13
Q

MS treatment focused on

A

Immune modulation - slowing activated immune system from getting to central fibers slows the processes of demyelination in MS

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14
Q

Phase 1 MS treatment (acute)

A

Corticosteroids - reduce inflammation and shorten duration of flare ups

Plasma exchange - effective for people who have sudden, severe attacks of MS related disability but don’t benefit from high dose corticosteroid

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15
Q

Plasma exchange most helpful

A

In MS pts who had mild disability before attack

No proven benefit beyond 3 mo from onset of neuro symptoms

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16
Q

MS tx phase 2

A

Med used to modify the course of disease progression as well as ongoing management of symptoms of MS

17
Q

MS beta infernos - subacute

A

Approved only for people who have relapsing forms
Reduce frequency and severity of flare ups

Prevent disability
Recommended for people who have more than one MS attack/year and for those who dont recover well from flare ups

18
Q

MS - ABC drugs

A

A - interferon beta 1a (avonex)
B- interferon beta 1b (betaseron)
C - glatiramer acetate (copaxone)

19
Q

MS - corticosteroid plus ACTH

A

Shortened recovery period after acute attack

20
Q

MS - avonex and refib (interferon beta 1a)

A

Slow down immune response -> reduce inflammation, swelling, rapid proliferation of T and B cells, block activated T cells from crossing BBB and damaging myelin

21
Q

MS betaseron

A

Higher dose of interferon eliciting a movie potent reponse

22
Q

MS copaxone

A

Immunomodulator
Decoy to clot T cell receptors
Fools immune system to decrease attack on myelin

23
Q

MS Mitoxantrone

A

Immunosuppressant
Modify replacing and secondary progressive MS
Only drug approved for tx of secondary progressive MS

24
Q

Natalizumab

A

Monoclonal antibody that prevents immune cells from moving from blood into CNS

25
Q

MS Fingolimod

A

New oral immunomodulating agent under eval for tax of relapsing remitting MS

26
Q

MS depression

A

Meds and sleep aid

Clonazepam used at night to aid in sleep intation and decrease spasm

27
Q

Ms and botulism

A

Focal injections to decrease spastic uncles

28
Q

MS PT manage

A
Intervention  to manage - fatigue, weakness, spasticity, sensory loss
Balance and coordination training
Improve speech
Transfer and gait terminating
W/c training
Equipment/orthotic eval
Referral for psychological issues
29
Q

Average frequency of attacks of MS

A

1 a year

30
Q

MS attacks tend to be more frequent in

A

Early stages,

Become less frequent in later years

31
Q

MS strongest predictor of outcome

A

MRI
Scans w/ > 10 lesions - predict individuals will need cane w/in same time frame

Change in lesion load w/in first year is also a negative predictor of outcome

32
Q

MS onset at young age

A

May be more favorable than onset after 40 which is associated w/ PRMS

33
Q

MS one f the most important prognostic factors

A

Neuro findings at 5 years
Sig pyramidal and cerebellar signs w/ involvement of multiple sites associated w/ poorer prognosis and a more severe disability

34
Q

MS and life expectancy

A

Reduced by a modest amount

74% surviving after 25 yrs after onset
Only small percent able to work 10 years after dx
15 years, 50% need AD
20 yrs, 50% W/c

35
Q

MS Death rate in persons who are unable to walk or stand

A

More than 4x that in person same age w/out MS