Clinical Approach to Multiple Sclerosis Flashcards
What are the 4 types of MS?
Relapsing remitting (45-50%)
Secondary progressive (20-25%), but begin in relasping and remitting type
Primary progressive (15-20%)
Benign (10-15%)
At what age are most patients diagnosed with MS?
In their 20s-30s.
What geographic “zone” has an increased incidence of MS?
Temperate zone; less common in the tropical zones.
What are a couple favorable prognostic clues about MS?
Women tend have a milder course
Earlier onset is associated with a better course
Which studies are used to help make a diagnosis of MS?
MRI of head, CT of spine: ovoid lesions of high signal on T2W1 in periventricular white matter and spinal cord. Acute lesions may enhance.
Multimodality evoked potentials (SSEPs, VEPs, BAER)
Lumbar puncture for CSF
What are common CSF findings in a patient with MS?
Oligoclonal bands and/or increased IgG synthesis rate.
In general, what form of is MS is treated with meds?
Which drug treats primary progressive MS (PPMS) in addition to relapsing forms?
Relapsing forms of MS
Ocrevus
What is used to treat acute exacerbation of CIS?
High dose corticosteroids
ACTH or IVIg can also be given on occasion
What is considered a Monofocal episode in CIS?
The person experiences a single neurologic sign or symptom that is caused by a single lesion.
What is considered a Multifocal episode (Acute Disseminated Encephalomyelitis (ADEM))?
The person experiences more than one sign or symptoms caused by lesions in more than one place.
What suggests a high risk of developing MS in a CIS patient?
When CIS patients have multiple demyelinating lesions on MRI, they have a 60-80% chance of developing MS in the next few years.
When CIS patients do not have multiple demyelinating lesions on MRI, they have a 20% risk of developing MS in the nest few years.
What are the major symptoms in MS?
Spasticity Intention tremor Urinary urgency (spastic bladder) Urinary retention/hesitancy Painful dysthesias Fatigue
What is Devic’s disease (Neuromyelitis Optica)?
What antibodies are found?
What is the treatment?
Inflammation and demyelination of optic nerves and spinal cord with relative sparing of the brain.
NMO (aquaporin) antibodies.
Steroids and plasma exchange followed by immunosuppression.