MS, ALS, GBS, CNS tumors Flashcards

1
Q

HA red flags

A

+ interrupts sleep
+ worse with walking and improves throughout the day
+ elicited by postural changes, coughing, exercise
+ recent onset more severe or different than normal
+ new onset in older person
+ associated with nausea, vomiting, papilledema, or focal neuro signs

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2
Q

which structure is affected with MS?

A

oligodendrocytes (CNS myelin)

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3
Q

which type of MS does NOT have attacks?

A

primary progressive

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4
Q

which type of MS develops into secondary progressive?

A

relapsing-remitting

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5
Q

criteria for MS diagnosis

A

first attack sx must last 24 hr or more
one lesion on brain and:
+ increase in tone
+ Lhermitte’s sign
+ Uhthoff’s sign

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6
Q

pseudoexacerbation of MS last ___ hours

A

<24

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7
Q

what 2 key features does a MS diagnosis rely on?

A

dissemination of lesions in the CNS in SPACE AND TIME seen on MRI
(2 attacks and 2 brain lesions)

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8
Q

early S&S of MS

A

parasthesias progressing to numbness, weakness, and fatiguability**
visual disturbances (ex: diplopia)

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9
Q

primary fatigue with MS

A

due to location of plaques and hypometabolism

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10
Q

secondary fatigue with MS

A

due to increased energy required to perform activities (less efficient movements)

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11
Q

what S&S are unique to MS?

A
  1. Lhermitte’s sign
  2. Uhthoff’s phenomenon
  3. Charcot’s Triad
  4. Visual dysfunction
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12
Q

what is Charcot’s Triad?

A

when cerebellum is affected
1. scanning speech
2. intention tremor
3. nystagmus

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13
Q

what symptom of MS is a major concern for PT?

A

fatigue!

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14
Q

_____ neuralgia and ____ neuritis are secondary impairments of MS

A

trigeminal neuralgia and optic neuritis

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15
Q

what is a Marcus-Gunn pupil?

A

abnormal pupillary light reflex - seen with MS

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16
Q

a person with MS has a high score on the modified fatigue impact scale and fatigue severity scale, what does this mean?

A

greater fatigue severity
(physical, cognitive, psychosocial)

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17
Q

modified fatigue impact scale vs. fatigue severity scale

A

MFIS - 4 weeks
fatigue severity scale - last week

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18
Q

how may a person with MS present with gait?

A

extensor spasticity
scissoring
ataxia
uneven steps

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19
Q

what outcome measures assesses activity limitations with MS?

A

Expanded Disability Status Scale (EDSS)
12-Item MS Walking Scale (MSWS-12)*
MS Functional Composite (MSFC)

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20
Q

Expanded Disability Status Scale (EDSS)
fully ambulatory:
impaired ambulation:

A

fully ambulatory: 1-4.5
impaired ambulation: 5-9.5

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21
Q

a person with MS has a high score on the 12-Item MS Walking Scale (MSWS-12), what does this mean?

A

greater limitations with walking

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22
Q

3 components of MS Functional Composite (MSFC)

A
  1. timed 25-foot walk test
  2. 9-hole peg test
  3. 3-second version of paced auditory serial addition test
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23
Q

what outcome measures assesses participation with MS?

A

MS Impact Scale*

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24
Q

MS Impact Scale assesses impact within past ______

A

2 weeks

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25
Q

a person with MS has a high score on the MS Impact Scale, what does this mean?

A

higher impact of disease on daily function

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26
Q

which type of MS can reach near pre- exacerbation function?

A

relapsing remitting

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27
Q

which type of MS will have greater strength deficits?

A

progressive

28
Q

movement system impairment diagnoses (related to MS)

A
  1. movement pattern coordination deficit
  2. force production deficit
  3. fractionated movement deficit
  4. hypermetria
29
Q

movement pattern coordination deficit

A

Inability to coordinate an intersegmental task due to deficit of timing and sequencing between segments

30
Q

fractionated movement deficit

A

Inability to fractionate movement
Associated with hyperexcitability - associated reactions

31
Q

hypermetria

A

Inability to grade forces appropriately for the distance and speed aspects of a task

32
Q

exercise considerations for pts with MS

A

heat sensitivity
fatigue
energy conservation
equipment
time of day

33
Q

what is the most common form of motor neuron disease in adults?

34
Q

what structures are affected with ALS?

A

anterior horn cells (amyotrophic)
pyramidal cells (corticospinal and corticobulbar) in motor cortex (Lateral sclerosis)

35
Q

T/F: ONLY motor neurons are affected with ALS

36
Q

by the time most pts with ALS report weakness, they’ve lost about ___% of their motor neurons in the areas of weakenss

37
Q

which mm group is commonly weak with ALS?

A

neck extensors

38
Q

ALS Functional Rating Scale scoring

A

higher = better physical function

39
Q

what impairments are especially of concern with ALS?

A

respiratory and swallowing
postural control (neck extensors)

40
Q

life expectancy for ALS

41
Q

signs of overwork weakness (ALS)

A

+ post exercise fatigue interferes with activities
+ feeling weaker or pain >30 mins post exercise
+ excessive soreness 24-48 hrs post
+ severe muscle cramping, heaviness in extremities, prolonged SOB

42
Q

what structure is affected with GBS?

A

Schwann cells (LMN!!) of nerve roots and peripheral nerves (rapid loss!)

43
Q

ALS vs. GBS

A

ALS: motor only
GBS: can have sensory and ANS issues

44
Q

what is usually the 1st symptom of GBS?

A

weakness and NT in hands and feet, ascending limbs

45
Q

how do motor impairments with GBS present?

A

distal to proximal**
rapid and progressive
symmetrical
usually unilateral

46
Q

how do sensory impairments with GBS present?

A

glove and stocking

47
Q

_____ of patients with GBS require ventilation

48
Q

issues specific to acute stages of GBS

A

respiratory compromise (weakness)
dysautonomia (orthostatic hypotension, BP instability, cardiac arrythmias) (50%)

49
Q

a pt with GBS that has a single breath count test of ____ might require mechanical ventilation

50
Q

how long does acute stage of GBS last?

51
Q

when do peak motor symptoms for GBS present?

A

2-8 weeks post onset

52
Q

how long does plateau period of GBS last?

A

2-4 weeks
(80% w/i 3 weeks)

53
Q

improvement can begin about ___ post onset of GBS

A

2-3 months

54
Q

max paralysis for GBS occurs when?

A

1-2 days of onset

55
Q

when would pt with GBS be rediagnosed to CIDP?

A

if function continues to deteroriate or begin to deteriorate again after 8 weeks

56
Q

PT interventions for ascending phase of GBS

A

avoid overwork and eccentric***
gentle PROM, AAROM, AROM, positioning

57
Q

PT interventions for plateau phase of GBS

A

respiratory care (cough, breath)
AAROM & AROM
functional training and mobility
multi-joint and cross-plane work

58
Q

PT interventions for descending phase of GBS

A

desensitize dysthesias
contracture, ulcer, injury prevention
balance and postural control
strengthening (maybe eccentric)
aerobic & functional activities
DME (anticipate improvement)

59
Q

when can strength training begin for GBS? what are the guidelines?

A

limited reps low resistance once strength begins to return - plateau
can utilize rhythmic initiation
**if 3/5 or less avoid eccentric!!

60
Q

what 2 distinct age groups do CNS tumors typically occur in?

A

0-14
40-70

61
Q

what is the most common cause of death in children and adolescents 0-19?

A

primary CNS tumors

62
Q

secondary metastatic CNS tumors spread through ______

A

arterial circulation

63
Q

about ____% of pts with systemic cancer develop brain mets

64
Q

what is the most common type of non-malignant brain tumor?

A

meningioma

65
Q

what is the most common type of malignant brain tumor?

A

glioblastoma

66
Q

common S&S of CNS tumor

A

HA (50%)
seizures
AMS
papilledema
focal neuro signs

67
Q

what 2 main things need to be monitored for CNS tumor pt?

A

increased ICP (esp. acutely)**
AMS