MS Flashcards

1
Q

what is MS

A

progressive, ronic infalmmation degeration of the myelin of the CNS

destruction of the mylein sheath and the axons

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2
Q

what are the contributing factors to MS

A

inflammation

autoimmune

infection

enviromental

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3
Q

what is the peak age for MS

A

20 - 50

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4
Q

is MS more prevalent in men or women

A

women - white women

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5
Q

what is the life expectancy of someone with MS

A

normal

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6
Q

Increased risk for MS

A

affected family member

viral agents

vit D def

smoking

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7
Q

what are the three factors that contribute mostly to MS

A

genes

environment

autoimmune response

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8
Q

what is the pathophysiology of MS

A

abnormal autoimmune responses that attacks - inflammatory cascade

myelin

oligodendrytes

CNS nerve fibers

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9
Q

what does demyelination do

A

this slow the neural transmission and causes rapid nerve fatigue

I can also cuase a a conduction block

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10
Q

what patho factor contribute to the relapsing-remitting forms of the disease

A

the decrease in the inflammatory attack

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11
Q

what happens with chronic disease and myelination

A

there is less remyleination between the attacks that results in axon and cell death

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12
Q

what Certain areas are susceptible to demyelination

A

optic nerve

periventricular white matter

spinal cord - corticospinal and DCML

cerebellar peducles

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13
Q

where is periventricular white matter located

A

white matter located immediately adjacent to the CFS filled ventricles of the brain

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14
Q

what is the most common disease course for MS

A

Relapsing-Remitting

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15
Q

how is Relapsing-Remitting MS characterized

A

attacks with period of remission

active - replase period
not active - remission period

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16
Q

what kind of MS will those intially with Relapsing-Remitting transition to

A

Secondary Progressive

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17
Q

what does Secondary Progressive look like

A

starts off with relapsing remitting disease form and then progresses to irreversible worsening of neurological function

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18
Q

who do we characterize secondary progressiev MS

A

as ‘active’ or ‘not active’ or ‘with progression’ or ‘without progression’

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19
Q

what is the least common type of MS

A

primary progressive

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20
Q

primary progressive characterized as

A

continuous worsening of disease without distinct attacks

progressive disablity from onset

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21
Q

what is the Clinically Isolated Syndrome

A

he first episode of inflammatory demyelination

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22
Q

when will Clinically Isolated Syndrome be diagnosed as MS

A

when the secound episode occurs

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23
Q

active - Clinically Isolated Syndrome

A

if a anothere episode occurs

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24
Q

no active - Clinically Isolated Syndrome

A

if there are no other episode after the first instance

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25
what are some factors that are associated with relapse
viral of bacterial infections disease of major organ system major of minor stresses Pseudo exacerbation
26
what are Pseudo exacerbation
temporary worsening of MS symptoms lasting 24 hours or less can be brought on by heat
27
what is Uthoff’s symptom
when MS is brought on my heat
28
how do we diagnose MS
neuro exam labs and test to rule out mimics of MS - MRI, lumbar puncture
29
how good is MRI for looking at MS
90-95 sensitive
30
key feature of MRI and MS imaging
Dissemination in space Dissemination in time
31
what does dissemination mean
to spread out
32
where are MS lesion normally
Characteristic lesions are periventricular, often ovoid and perpendicular to ventricle
33
what are Dawson’s fingers
demyelinating plaques through the corpus callosum can help to differentiate MS from other demyelinating conditions
34
what do we find in the CSF for MS
Elevated total immunoglobulin (IgG) in CSF Presence of oligoclonal IgG bands in response to inflammatory demyelinating lesions
35
what do we find in the CSF for MS - primary progressive
will have higher levesl of CFS then other types of MS
36
what are Evoked potentials
the electrical activity in areas of your brain and spinal cord in response to stimulation.
37
Evoked potentials and MS
Up to 90% of individuals have abnormal evoked potentials
38
what Evoked potentials are the most helpful in diagnosing MS
visual Evoked potentials
39
what are the signs and symptoms of MS
Fatigue Temperature intolerance Visual symptoms Gait Dysfunction Changes in sensation Motor symptoms Imbalance/dizziness Pain Urinary and sexual dysfunction Cognitive deficits Anxiety/depression Speech and swallowing changes
40
is fatigue common in those with MS
yes
41
how does fatigue impact the individual with MS
impact on physical functioning and ability to participate in activity and life roles
42
what are the central factor the contribute to increase fatigue in those with MS
Neurochemical change Inflammation Reduced axonal conduction velocity Decreased cerebral glucose metabolism
43
is pain common in those with MS
yes
44
how is pain with MS described
intense, sharp, shooting, shock-like, or burning
45
common type of pain see with MS
Trigeminal neuralgia Lhermitte’s sign (flexion of the neck) Paroxysmal limb pain Headache Neuropathic pain
46
what is Trigeminal neuralgia
chronic pain disorder that involves sudden attacks of severe facial pain.
47
what is Lhermitte’s sign
an electric shock-like sensation that occurs on flexion of the neck.
48
what is Paroxysmal limb pain
come on very suddenly, last only a few seconds or minutes and then disappear just as quickly.
49
what is Neuropathic pain
sponataneous nerve pain
50
what is the secondary pain seen with MS
MSK pain
51
do we see visual changes with MS
yes
52
what kind of visual chnages do we see with MS
optic neuritis nys diplopia Internuclear Ophthalmoplegia
53
what are the symptoms of optic neuritis
eye pain blurring or blindness central scotoma, abnormal pupillary light reflex, usually unilateral
54
what is central scotoma
a blind spot in the middle of your vision
55
what is Internuclear Ophthalmoplegia
the failure of the effect eye to add (convergence is intact) nys in the abd eye lesion of the medial long fasiculus
56
what motor systems impairment do we see with MS
issue in the corticospinal tract UMN - weakness and spac
57
why do we see balance, dizzyness, and coordination issues with MS
lesions in the BS (vest pahways, visual pathways), cere
58
what balance issue do we see with MS
tremor balance, dizzyness coordination - ataxia
59
what moevment system issues do we see with MS
Weakness Fatigue Spasticity Impaired postural control Impaired sensation Visual changes Ataxia
60
do we see cog impairment with MS
yes 70%
61
what kind of cog deficts do we see
Processing speed, selective attention, executive functioning, visuospatial function
62
Bowel/bladder dysfunction
Bladder dysfunction in up to 80% of persons with MS Constipation
63
why do we see consipation issues for those with MS
lesions to the gastrocolic reflex inactivity, spasticity in pelvic floor muscles
64
what Speech/Swallowing dysfunction do we see with MS
Muscle weakness, spasticity, tremor, ataxia Slurred speech, changes to vocal quality Difficulty chewing, inability to swallow, coughing after meals
65
is depression an issue in those with MS
yes rection to the stress of the disease
66
sexual function is this impacted
yes
67
what are the features for a better progonosis in those with MS
monofocal onset Onset with Optic Neuritis or isolated sensory symptoms low replease rate (2-5 years) low disablility at 5 years low MRI lesion load
68
what does monofocal mean
only affect one area of the central nervous system
69
what are the feature of a poor prognosis
multifocal onset
70
what does multifocal mean
multiple areas of the CNS is impacted short intervals between attacks disability at 5yrs high MRI lesion load first: brainstem, cere, bowel/bladder symptoms
71
what is the goal for managing MS
Modify or slow disease course Treat relapses (exacerbations) Manage symptoms Improve function and safety Address emotional health
72
Acute relapses - meds
Corticosteroid therapy (methylprednisolone) Plasmapheresis may be used failure to respond to steroids
73
Disease Modifying Therapeutic Agents (MS Coalition) - goal
prevent future disease activity Early and successful control of disease is important for reducing disability
74
what do Injectable synthetic interferon drugs do
Slow down immune system response by reducing inflammation, swelling, and proliferation of T and B cells
75
examples of Injectable synthetic interferon drugs
Avonex Rebif Betaseron Extavia Plegridy
76
pain meds
SSNRIs antiinflammatory medications
77
MS is a diagnosis of what
exclusion
78
what are the most common MS symptoms - IMPORTANT
fatigue, pain, visual changes, motor symptoms, sensory changes, and mobility limitations
79
exposure ot heat and stress can do what to MS symptoms
exacerbate MS symptoms
80
when do we start PT in those with MS
As soon as possible after diagnosis!
81
what is the role of the PT in MS
Preventative interventions Compensatory interventions Maintenance interventions
82
what are Maintenance interventions
intermittent visits to maintain current level of function/ability
83
what are Compensatory interventions
modifying task, activity, or environment to allow for optimal function
84
what are Preventative interventions
minimize complications, early detection of impairments, activity limitations, reduce degree of disability
85
what should be prioritized in the neuro PT exam
CN sensation motor coordination balance functional
86
do you include the mental exam
depends on the pt presentation
87
what are the common CN deficts that we see with MS
Optic pain and visual changes (optic neuritis) Diplopia or disconjugate gaze Facial sensation changes, complaints of facial pain & paresthesia (trigeminal neuralgia) Dizziness Dysphagia, impaired gag reflex
88
what is MS Hug
crawling, electric shock, heavy, lead-like, tightness around rib
89
what is L’Hermittes Sign
Stabbing electric shock running down spine with cervical flexion
90
why do we see weakness with MS -primary
due to demyelination of axons, loss of recruitment and firing rate of motor neurons
91
why do we see weakness with MS - secoundary
deconditioning, compensatory movements, mechanical tightness, pain, poor proprioception
92
what is a test for func motor movement
9-hole peg test
93
how do we see balance issue in those with MS
Cerebellar or Brain Stem lesion Sensory dysfunction Change in vision Change in Posture Comorbid conditions
94
Core Outcome Measures for balance and gait
5xSTS Berg ABC 10MWT 6MWT FGA
95
when to schedule PT sessions
early
96
should you do PT if indivdual in on replase
no pause until remission
97
managing Somatosensory deficits
Sensory reorganization training Resistance exercise Loading limb through exercise Education on skin care, pressure relief, maintaining skin integrity
98
PT Management of Spasticity
Stretching & ROM exercise Strengthening & functional activities Orthoses or splinting for contracture prevention Topical ice can provide short-term effects edu
99
Strength Training for those with MS - why might force production be low
reduced ability to activate muscles, reduced muscle metabolic responses, muscle weakness due to muscle fiber atrophy, spasticity, and disuse
100
strength training in those with MS
Alternate with endurance/aerobic training days Circuit training may be helpful, alternate UE and LE exercises Optimal time for individual to rest in between sets
101
modes of exercise for MS strength training
weight machines, resistance bands, free weights, functional strength training, group exercise
102
for Aerobic Conditioning what HR do we want to work at
60-80 of max
103
what to consider with Aerobic Conditioning for those with MS
prevent overheating consider mornings Consider alternating days with aerobic conditioning and strength training
104
what type of aerobic conditioning should
treadmill or overground walking, elliptical, stationary or recumbent bike, swimming, water aerobics, upper body ergometer Continuous or intermittent - work up to 30 minutes
105
what balance training - treatment types
include interventions for improving stability during static and/or dynamic tasks
106
Static balance actives
sitting, quadruped, standing
107
what commonly leads to gait dysfunctions
Weakness in hip musculature and ankle DF sensory changes, ataxia, spasticity
108
what should locomotion training include
Targeted strengthening Tone management, stretching Task-specific training incorporating motor leaning principles to enhance skill acquisition Functional training activities
109
when are orthotic needed
when walking skill declines
110
are KFAO used often
not used due to increased energy expenditure
111
are Wheeled devices often use
in advanced disease
112
Education - for fatigue
energy conservation importance of exercises activity pacing sleep stress management
113
what kind of training in included in the PT session
strength aerobic balance locomotion