Examining motor fxn Flashcards

1
Q

In what kind of brain lesions will you observe low tone?

A
LMN = nerve roots and peripheral injury
UMN = with initial spinal shock for SCI or stroke, but then transitions to high tone
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2
Q

A hyperactive tendon response indicates what lesion?

A

UMN

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3
Q

A score of 2 on the MAS means what?

A

2 = more marked increase in muscle tone through most of ROM, affected part easily moved

1 = slight increase in tone, minimal resistance at end of ROM
1+ = slight increase in muscle tone, minimal resistance through less than half ROM
3 = considerable increase in tone, passive movement difficult
4 = rigid
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4
Q

Is rigidity velocity dependent?

A

no

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5
Q

In SCI, what kind of DTRs would you expect?

A

hyperreflexic

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6
Q

What kind of CNS disorder has lead-pipe rigidity?

A

parkinsonism -> can be cogwheel or ratchet-like resistance to movement

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7
Q

If a patient is ataxic, what could the location of the lesion be?

A

cerebellum

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8
Q

Compare/contrast dysmetria/dysdiadochokinesia

A

dysdiadochokinesia = inability to perform rapidly alternating movements

dysmetria = unable to judge distance/range of a movement

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9
Q

How do you test dysmetria?

A

finger to nose then pencil

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10
Q

How do you test dysdiadochokinesia?

A

try to pronate/supinate quickly with one hand in the palm of another

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11
Q

Do people with a cerebrellar lesion/stroke have spasm?

A

no not typically

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12
Q

With stroke, what is the location of the lesion in the brain? (think cortex/tracts)

A

cerebral cortex corticospinal tracts

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13
Q

What do voluntary movements with stroke look like?

A

dyssynergic = abnormal timing/coactivation/activation, fatigueability

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14
Q

What do voluntary movements with parkinson’s look like?

A

bradykinesia/akinesia (lack of spontaneous and automatic movements)

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15
Q

Rigidity is associated with what CNS disorder?

A

parkinson’s

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16
Q

A patient you’re seeing has increased tone and sustained posturing in rigid extension of all four limbs and trunk/neck. What would you call this?

A

decerebrate

- for lesions between superior colliculus and vestibular nucleus

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17
Q

A patient has increased tone and has sustained posturing of the limbs in flexion and LEs in extension - what is this called?

A

decorticate

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18
Q

Your patient has prolonged, severe spasms of muscles during your session, causing them to throw their head, back, and heels into extension, while their arms and hands are rigidly flexed. What could be going on?

A

opisthotonos - seen in severe meningitis, tetanus, epilepsy

19
Q

Is Guillian-Barre a LMN or UMN issue?

A

LMN

20
Q

What kind of lesion produces rapid, focal, severe muscle wasting?

A

LMN (neurogenic atrophy)

- UMN is variable disuse atrophy

21
Q

What would a 2+ on the reflex scoring scale indicate?

A

2+ = visible movement of extremities

0 = absent
1+ = tone change, no visible movement of extr
3+ = exaggerated, full movement
4+ = oligatory and sustained movement, lasting for >30s
22
Q

Do we typically see proximal or distal muscle weakness with neuropathies?

A

distal (proximal with myopathies)

23
Q

What’s the typical pattern of spasticity at the hip?

A

extended, IR, adducted (scissoring)

24
Q

What type of sitting posture is associated with spasticity?

A

sacral sitting

25
Q

What type of ankle position is typically associated with spasticity, and what muscles are involved?

A

equinovarus (pf, inv)

  • gastroc
  • tib posterior
26
Q

Your patient with stroke has a lot of upper extremity spasticity noted in his chart, what do you expect his shoulder joint to look like? (assume extension)

A

adducted, IRed, depressed

27
Q

What does the STNR reflex look like?

A
  • flexion of the head produces flexion of the UEs with extension of the LEs
  • extension of the head produces extension of the UEs and flexion of the LEs

HEAD GOES WITH UPPERS

28
Q

Fatigue is present in many different neuro syndromes. Which ones are characteristic for fatigue d/t issues at the neural/myoneuronal junction?

A
  • MS
  • post polio
  • GBS
  • myasthenia gravis
29
Q

Depleted Ca2+ stores cause fatigue in what neurological disorder?

A

DMD

30
Q

Describe overwork weakness from post-polio or DMD.

A

prolonged decrease in absolute strength and endurance d/t excessive activity of partially denervated muscle

31
Q

When looking at voluntary movement control, describe what factors you should be watching for.

A

1) quality of movement patterns… synergistic?
2) timing and appropriateness of movement in response to stimulus
3) are movements symmetrical?
4) able to easily vary contraction type? eccentric/concentric/iso
5) adequate control of multiple body segments, postural stabilization?

32
Q

Intention tremor is commonly seen in what kind of disorders?

A

cerebellar disorders -> intention tremor when attempting voluntary movement

33
Q

Evidence of tics, athetosis, chorea, or resting tremors indicate damage to what part of the brain? What do all of these behaviors have in common?

A

extrapyramidal disorders, basal ganglia dysfunction

all of these are involuntary movements

34
Q

Your patient who has a L sided lesion CVA exhibits typical extension synergy in both his RUE and RLE. Describe what this looks like.

A

RUE extension = scap protracted, shoulder add*/IR, elbow ext, forearm pronation, wrist/finger flexion

RLE extension = hip ext/add/IR, knee ext, ankle PF*/inv

35
Q

Your patient with a R sided CVA exhibits typical flexion synergy in his LUE/LLE. Describe this.

A

LUE flexion = scap retract/elevated, shoulder abd, ER, elbow flexion, forearm sup, wrist/finger flex

LLE flexion = hip flex/abd/ER, knee flex, ankle DF/inv

36
Q

If a patient requires hand held assist to maintain balance, this automatically puts them in what balance rating category?

A

fair to poor

fair = min assist in static, can turn head and trunk without LOB with HHA
poor = mod-max assist static, can't turn or do anything
37
Q

Describe good from normal balance rating.

A
good = limited postural sway in static; can pick object off floor
normal = none; can shift weight easily in all directions
38
Q

What’s a typical TUG score?

A

normal intact adults: <10s

- 11-20s is normal for frail elderly

39
Q

What’s a high risk for falls score on the TUG?

A

> 30s = high risk

<20s = increased risk for falls

40
Q

What’s a score that indicates higher risk for falls on the Berg?

A

<45/56 = increased risk for falls

1 point drop indicates 6-8% increase in fall risk for those who score 54-46

41
Q

How is the tinetti scored? (aka POMA)

A

max score is 28, with <19/28 at high risk for falls, 19-24 = mod risk

  • looks at walking, sternal nudge, turn 360, bend over, timed rise, and a few others similar to berg
42
Q

What is an increased risk of falls score for the DGI?

A

<19/24

43
Q

What is a requirement to be able to take the HiMAT test?

A

HiMAT = high level mobility assessment tool

  • need to be independent walking for 20m without gait aids