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57 Cards in this Set

  • Front
  • Back
what is MS
chronic inflammatory demyelinating disease
what is the main characteristic of MS
demyelinating lesions, plaques, widely dispersed throughout CNS
what are plaques
demyelinating lesions in CNS in MS
____, ____, and ____ are present in the acute demyelination in MS
1) myelin breakdown products
2) edema
3) chemotaxis of lymphocytes
sometimes the myelin can be restored in MS patients, but if not what happens
microglial cells migrate to the lesion phagocytize the debris and produce fibrils that result in glial scar or plaque
what ultimately replaces the myelin sheath in MS patients
fibrous scarring--- Plaque
what do the lesions for MS typically look like
- symmetrical
- scattered throughout the white matter
lesions for MS are particularly found where
- cerebrum
- cerebellar peduncles
- brainstem
- corticospinal and dorsal spinal cord
what does MS do to the motor system
affects UMNs --> spasticity
does MS have sensory issues
yes- becasue affects CNS
how common is MS
50/ 100,000 (1:4,000)
what is the age for MS
20-40
what is the sex for MS
women to men = 2-3: 1
do men or women get the more progressive form of MS
men (but women more likely to get MS)
race for MS
- predominantly white populations
- blacks have 1/2 the risk
environment for MS
higher frequency the further you get from the equator
at what age does the risk with environment for MS stay the same
15 (doesn't matter where you travel after this point)
genetics for MS
slight correlation - but possibly also related to enviromnent
what is the etiology for MS
- actual cause unkown
what are the theories for causes for MS
- infectious origin (like GBD)
- immune-mediated pathogenesis
- some combo- genetic predisposition
what is a possible protective factor for MS
vitamin D--> may explain the equator factor
what could cause exacerbation of MS
- infiltrates of T cells and macrophages around acute lesions further interfering with conduction (gradually subside)
- abnormal response to common viruses
what are the types of MS
1) relapsing-remitting
2) primary-progressive
3) secondary-progressive
4) progressive-relapsing
what is relapsing-remitting MS
- clearly defined attacks of worsening neuro function
- relapses followed by partial or complete recovery periods during which no dz progression occurs
what is primary progressive MS
- slowly worsening neuro function from the beginning, no distiinct relapses or remissions
- rate of progression may vary with occasional plateaus and temporary minor improvements
what is secondary progressive MS
- initially presents as relapsing-remitting, but then begins to worsen more steadily with or without occasional flare-ups, remissions or plateaus
what is progressive relapsing MS
steadily worsening disease from the beginning, but with clear attacks of worsening fxn along the way
- may or may not experience some recovery following these periods but the disease continues to progress without remission
_____ is 85% of MS
relapsing remitting
______ is 10% of MS
primary progressive
______ is 5% of MS
progressive relapsing
____% of people with relapsing-remitting MS develop this form ______ within 10 years
50% ppl with relapsing remitting develop secondary-progressive within 10 years
_____ MS is followed by _____ MS
relapsing-remitting MS followed by secondary-progressive MS
what is the survival after onset of MS
35 years after onset
what is the prognosis for MS
death does not occur from the disease itself
74% of MS survive _____ post dx
25 years post dx
when do 50% of MS patients need a walker
15 years post dx
when do 50% of MS patients need a wheelchair
20 years post dx
at what point can most MS patients no longer work
10 years post dx
what gives a better prognosis for MS (6)
1) younger at onset
2) only 1 symptom during 1st year
3) sensory/visual symptoms at onset
4) acute onset of initial symptoms with complete and rapid remission
5) brief length of most recent exacerbation
6) minimal corticospinal and cerebellar signs after 5 years
if younger than _____ there is a better prognosis for MS because associated with milder strain
younger than 35
____ symptoms at onset give a better prognosis than if ____ symptoms at onset
sensory/visual symptoms have better prognosis than motor
minimal ____ and ____ signs after 5 years gives better prognosis
coritcospinal and cerebellar signs
what is McDonald Criteria
multiple signs of neurologic dysfunction involving dissemination in time/space (used for MS dx)
what results of McDonalt Criteria would be dx of MS
- 2 or more parts of CNS white matter affected
- 2 or more episodes, lasting more than 24 hours and seperated by more than 1 month
- slow or step-wise progression extending over at least 6 months
what diagnostic testing can be used for MS dx
- MRI
- visual evoked potential studies
- CSF analysis
- Blood tests
what is an MRI looking for in MS
plaques radiating away from ventricles
what is a VEP used for in dx MS
testing conduction of nerve, if demyelinated = slow
what is CSF analysis used for in dx MS
lumbar puncture looking for oligoclonal bands
what are the blood tests used for in dx of MS
not for MS, but can r/o other diseases/infections that decreases optic neuritis
what are the most common initial complaints of MS
- visual changes
- sensory symptoms
- urinary disturbances
what are the other S and S with MS
- fatigue
- movement disorders
- Lhermitte's sign
- trigeminal neuralgia
- dizziness/vertigo
- bowel, bladder and sex disturb.
- dysarthria, dysphagia
- mental disturbances
what is the medical management for acute relapses/exacerbations of MS
- corticosteroids
what are the corticosteroids used for tx MS
- mehtylprednisolone
- dexamethasone
- prednisone
what are the disease modifying therapies for MS
- immunomodulation for relapsing-remitting MS
- immunosuppressants
what are the immunomodulations used for MS
- interferon
- glatiramer acetate (copaxone)
- natilzumab (tysabril)
what are the immunosuppressants for MS
- thiopurines, methotrexate
- mitoxantrone (novantrone)
what are the other experimental approaches for MS
- plasmaphoresis
- HBO, BMT