MS Flashcards

1
Q

Environmental associations?

A

Vit D/Sun exposure, smoking
 Viruses (Canine distemper, Herpes,
EBV)
 Changing sex incidence

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2
Q

Genetics associated?

A

HLA DRB1*1501

52 non HLA disease associated genes

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3
Q

T-helper differentiation?

A
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4
Q

patterns of disease course?

A

Bening (15%)

Relapsing (65%)

Primary Progressive (10-20%)

Secondary Progressive (50%)

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5
Q

Relapses?

A

Symptom or symptoms of neurological dysfunction with or without objective confirmation lasting more than 24hours
Exclude confounding causes of deterioration
Infection, menses, emotional stress, heat etc
In relapsing pattern disease rate = 1-.15 pa
Common sites
optic nerve, spinal cord, brainstem
Relapses decrease in frequency and severity with disease duration

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6
Q

Relapse frequency?

A

Clinical coroborated mean annualised relapse tates (MARR)

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7
Q

MS making the diagnosis?

A

History
Identify relapsing neurological dysfunction occurring at different sites.
Examination
Evidence for involvement of multiple sites within the central nervous system
Paraclinical evidence
MR, CSF, EPs
Exclude other causes

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8
Q

McDonald diagnostic criteria?

A

s

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9
Q

conditions ot be excluded?

A
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10
Q

disease heterogeneity?

A
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11
Q

Expanded disability scale status (EDSS)

A
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12
Q

assessment of disease activity?

A

Relapse frequency and severity
Rate of change in disability
Early fixed disability: esp motor, cerebellar, cognitive
MRI: T2 Lesion load, gadolinium enhancing lesions, atrophy

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13
Q

HCDMT treatment criteria?

A

Relapsing remitting disease
Independent mobility (preferably EDSS <5.5 ie 100m)
At least two clinically significant relapses in last 2 years
Secondary progressive disease
Able to walk >10m with or without assistance
At least two clinically significant relapses in last 2 years
Any increase in disability due to slow progression over the last two years has been minimal
All
Age >18 years
There are no contraindications

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14
Q

relapsing ms treatment?

A

Route 1
Symptomatic control, steroids during acute events
Route 2
Established DMTs
Tier 1 Interferon beta 1a/1b, Glatirimer acetate
Tier 2 Fingolimod
Tier 3 Natalizumab, Alemtuzumab
Route 3
Experimental treatments including, BG12, Laquinimod, Teriflunamide, Rituximab, Dacluzimab etc)

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15
Q

Consequences of treatment?

A
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16
Q

Symptomatic treatment?

A

Fatigue
•Vertigo
•Spasticity and muscle spasms
•Psychological difficulties
•Bladder and bowel dysfunction
•Sexual dysfunction
•Ataxia and tremor
•Cognitive impairment