Guillain Barre Syndrome and MS Flashcards

1
Q

what part of the CNS does GB syndrome affect?

A

nerve roots and peripheral nerves

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what is the prognosis for GB syndrome?

A

it is good, most pts return return to PLOF within 1-2 yrs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what is the age risk factors for GB syndrome?

A

none, it can affect any age

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what gender risk factors are there for GB syndrome?

A

men are 2x more likely

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what is the significance of GB syndrome and infectious diseases?

A

2/3 of people who are diagnosed with GB had sxs of infectious disease 2 weeks prior to GB

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

explain the pathology of GBS

A

an infection activates an immune cascade that breaks up the myelin.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

what are 2 medical tests that help with the dx of GBS?

A

Examination of CSF for increased protein.
Nerve conduction test

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

what are some clinical signs that help the dx for GBS?

A

Progressive weakness of multiple nerve roots.
Symmetrical onset
Develops over a few days to weeks
Hyporeflexia or areflexia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what is a very common clinical presentation of pts with GBS?

A

severe fatigue

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

explain the 3 steps/progression of GBS using the correct terms

A

Nadir (peak) of motor impairments happens 2-8 weeks after onset.
Plateau occurs for 2-4 weeks
Improving occurs for 2 months to several years

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

talk about ventilation and GBS? How often is it required, what causes it and what are the implications of it?

A

it is required in ~40%. It is needed because of weakness of the intercostals, abdominals, diaphragm.
It increases risk of pneumonia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

how often is cranial nerve involvement in pts with GBS and what CNs are involved?

A

around 50%. CN 7, the facial nerve

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

how often do ANS sxs occur in pt with GBS and what are some ANS sxs that occur?

A

around 50%.
Orthostatic hypotension
cardiac dysrhythmias
BP fluctuations
ileus (lack of muscle contractions of intenstines)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

how would you educate a GBS pt if they asked whether they will be able to ambulate again or not?

A

I’d say it is highly likely, depending on their prognostic factors. 80% of GBS pts ambulate 6 months after onset.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what is the most common residual affect from GBS?

A

weak anterior tibialis

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what percentage of GBS pts die?

A

5-10%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

what are some factors associated with increased risk of mortality? (GBS)

A

severe weakness
bulbar dysfunction
ANS sxs
rapid onset
Age >60 y/o
Need for ventilation
Pulmonary infections

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

what is the sensation changes associated with GBS?

A

pain, hyperesthias

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

what can be done during a GBS pts recovery that will increase their chances of having recurring episodes of temporary loss of fx?

A

strenuous exercise and fatigue

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
20
Q

what exercises are recommended during the nadir and plateau stages?

A

AAROM and AROM

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
21
Q

describe MS in one sentence

A

It is an autoimmune disease that causes demyelination in the brain and SC

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
22
Q

what age range is associated with MS?

A

20-50

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
23
Q

in one sentence, what is a major difference between MS and GBS?

A

MS is UMN disorder and GBS is LMN

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
24
Q

what gender, ethnicity, and regions are associated with increased risk of MS?

A

women
caucasian
colder countries/areas

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
25
Does GBS, MS, or ALS have an increased risk if a family member has a hx?
MS and ALS
26
explain the signifigance of oligodendrocytes and astrocytes in MS
oligodendrocytes get attacked and can remyelinate but eventually die off. These dead areas are filled with astrocytes and become hardened/plaques
27
explain what the area of predilection is for MS
it is when MS prefers specific areas. It prefers optic nerve, white matter, and the cerebellar peducles
28
what areas in the spinal cord does MS prefer?
corticospinal tract and posterior column
29
Proteins found in CSF...explain how this is different between MS and GBS
They both protein in their CSF but there will be IgG present in MS but not in GBS
30
in order for a MS dx what criteria is required?
other dx to be r/o and one of the following... an MRI showing lesions in 2 different areas OR any new lesion seen on an MRI after the original scan
31
what are the 4 major subtypes of MS?
clinically isolated syndrome relapsing remitting MS primary-progressive MS secondary-progressive MS
32
what if the subtype of MS, clinically isolated syndrome is active?
it will become relapsing-remitting MS
33
what is the most common subtype of MS?
relapsing remitting
34
explain the difference between remission and relapse
relapse: brief episodes where sxs worsen then get better remission: when the disease doesn't progress and the pt has a complete or almost complete return to normal fx
35
explain the disease course of pts with primary-progressive MS
they progressively worsen without relapsing or remitting.
36
explain the disease course associated with secondary progressive MS
it begins as relapsing remitting MS but then the pt gets to a point where they stop really having relapses or remissions and they just progressively get worse.
37
explain what an exacerbation is and what qualifies as an exacerbation
an exacerbation has to last >24 hours. It is when new or recurrent sxs last >24 hrs and they aren't related to any other disease or injury
38
what can cause exacerbations?
infections, diseases of organs, stress
39
what is pseudo exacerbation?
an exacerbation but less than 24 hours
40
explain what Uthoff's symptom is
an adverse reaction to heat that is immediate and dramatic impact on fx.
41
what are some things you would educate a pt about if the suffer from Uthoff's symptom?
avoid enviroments or activities that increase body temp. If you feel these sxs come on then try to cool of and the sxs should resolve.
42
what is Lhemitte's sign?
when you cervical flex it causes a sharp pain
43
What occurs with Relative afferent pupillary defect (RAPD)?
shine a light into one eye and they both dilate
44
what 5 vision changes can be present in MS pts?
diplopia, RAPD/Marcus Gunn, scotoma, nystagmus, optic neuritis
45
what type of nystagmus would a pt with MS have?
vertical nystagmus
46
what are some sensory changes in pts with MS?
parasthesia and numbness pain: headaches, Lhemitte's sign, hyperpathia Tic douloureux
47
what tests can be used to test for cerebellar lesions?
heel to shin test dysdiadokinesia finger to nose gait
48
explain the relationship between MS and spasticity
75% of MS pts have it. Greater in LE. Fluctuates daily
49
what time of day should we schedule pts with MS, why?
In the morning, their fatigue worsens throughout the day
50
What factors can increase an MS pts fatigue? (6)
depression spasticity some medication exertion heat decreased sleep
51
what are 4 possible sxs of MS if the cerebellum is involved?
ataxia postural tremor intention tremor vestibular dysfunction
52
what impairments might a pt with MS have that lead to gait ataxia?
dysmetria dyssynergia dysdiadochokinesia
53
spasticity in what muscle may cause scissoring when walking?
abductors
54
how often does sxs of speech and swallowing affect MS pts? What are some sxs that they may experience?
40% Dysarthria Dysphonia Dysphagia
55
how often do patients with MS experience cognitive impairments?
50% of MS pts
56
what are 4 predictors of better prognosis in MS pts?
onset w/ only 1 sx Benign and RRMS <40 y/o Few overall lesions on brain scan
57
what affect can medications have on the relapses associated with MS?
can decrease relapse rate by 30% and reduce severity
58
what are 2 preventative and restorative interventions for MS during the early stages?
exercise and community classes
59
what are 2 preventative and restorative interventions for MS during the middle stages?
exercise and community classes
60
what are the parameters for aerobic conditioning in patients with MS? frequency, intensity, length
3-5 days a week, alternate days 60-85% HRmax 30 minutes a day or 3 10-minute sessions
61
what are some compensation ideas for gait ataxia?
light weights, weighted boots/jacket, weighted canes/walker/utensils
62
what is the scoring for the fatigue scale for motor and cognitive functions?
<43 mild <53 moderate <63 severe
63
explain the scoring for the 12-item MS walking scale?
it is 0-100 and the higher score indicates more disability
64
explain the scoring for the MSQOL-54
it is 0-100 and the higher the score the higher the QOL