Movement Considerations in Neuro Disorders Flashcards

1
Q

Signs Definition

A

Signs of neurologic dysfunction represent objective findings of pathology that can be determined by physical examination

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2
Q

Symptoms Definition

A

Symptoms are subjective reports associated with pathology that are perceived by the patient, but may not necessarily be objectively documented on examination

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3
Q

Definitions of Tone

A

Continuous state of mild contraction, thought to be due to low levels of spontaneous spike activity by alpha LMNs
Readiness of a muscle to work
Resistance by a muscle to passive stretch
Resting tension in a muscle

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4
Q

Tone Modifiers

A
UMN
Sensory input
LMN
Position
Ability to relax
State of alertness
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5
Q

Spasticity

A

Velocity dependent
implying response to external sensory stimulus
Tends to occur on one side of the joint (e.g., elbow flexors, not extensors)
Cannot be reduced just by cortical strategies
Typically occurs with cortical damage
‘Clasp knife’

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6
Q

Rigidity

A

Not velocity dependent
implying not a response to external sensory stimuli
Tends to occur on both sides of the joint (e.g., both flexors and extensors)
Can sometimes be reduced by cortical strategies
Typically occurs with BG damage
‘Cogwheel’

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7
Q

Spasticity and Function

A

No correlation between spasticity and degree of disability

We can strengthen individuals with UMN lesions (treating negative signs) without increasing spasticity - Guiliani, 1997

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8
Q

Modified Ashworth Scale - 0

A

No increase in muscle tone

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9
Q

Modified Ashworth Scale - 1

A

Slight increase in muscle tone, manifested by a catch and release or by minimal resistance at the end of the ROM when the affected part(s) is moved in flexion or extension

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10
Q

Modified Ashworth Scale - 1+

A

Slight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder (less than half) of the ROM

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11
Q

Modified Ashworth Scale - 2

A

More marked increase in muscle tone through most of the ROM, but affected part(s) easily moved

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12
Q

Modified Ashworth Scale - 3

A

Considerable increase in muscle tone, passive movement difficult

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13
Q

Modified Ashworth Scale - 4

A

Affected part(s) rigid in flexion or extension

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14
Q

Modified Tardieu Scale

A

Measures the point of resistance or “catch” to a rapid velocity stretch (R1 value)

Measures the point of mechanical resistance with slow stretch (R2 value)

A large difference between the initial catch and the point of mechanical resistance indicates a large reflexive component to motion limitation, and a small difference suggests a more fixed muscle contracture.

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15
Q

Abnormalities Resulting from Motor Cortex Dysfunction

A

Motor weakness (paresis)
Abnormal synergies
Co-activation
Abnormal muscle tone (usually hypertonia)

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16
Q

Abnormalities Resulting from BG Dysfunction

A

Hypokinetic disorders: bradykinesia and akinesia
Rigidity
Resting tremor
Hyperkinetic disorders: choreiform and athetoid movements, dystonia

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17
Q

Abnormalities Resulting from cerebellar Dysfunction

A

Hypotonia
Incoordination
Intention tremor
Impaired error correction affecting motor learning

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18
Q

Abnormal Synergistic Movements

A

After injury to the motor cortex – some suggestion that since there is a reduction in corticospinal control of movement, that abnormal synergies result from the recruitment of brainstem centers (rubrospinal)

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19
Q

Typical ‘abnormal’ limb synergies

A

Flexion synergy-flexion, abduction, and ER

Extension synergy-extension, adduction, IR

20
Q

Most Typical Abnormal Synergy

A
Flexion Synergy UE
Scapula: retraction & elevation
Shoulder: abduction & ER
Elbow: flexion
Forearm: supination
Wrist and finger: flexion
Extension Synergy LE
Hip: extension, adduction, IR
Knee: extension
Ankle: plantar flexion, inversion
Toe: extension
21
Q

Twitchell and recovery after stroke

A

Abnormal synergistic movement patterns in a stepwise sequence following stroke
Initial flaccidity and areflexia
Hyperreflexia, spasticity, stereotyped flexor and extensor voluntary movements
Voluntary movements out of abnormal synergies until normal movement is achieved.

Recovery is proximal to distal

Initial Flexor movements in UE and Extensor movements in LE

22
Q

Brunnstrom Assessment

A

Further defined 6 stages of recovery of motor function after stroke by asking individual to perform voluntary movements and observe the responses

Sitting - LE
Lift up hip and knee
Straighten knee
Tap your toes on the floor
Sitting - UE
Reach for my hand 
Standing
Lift hip and knee
Extend hip and flex knee
Tap toes
23
Q

Brunnstrom Stage 1

A

Flaccidity

No movement present (reflex or voluntary)

24
Q

Brunnstrom Stage 2

A

Weak associated reactions appear
Or minimal voluntary movement responses are present in limb synergies
Spasticity begins to develop

25
Q

Brunnstrom Stage 3

A

All movements are in synergy
Synergies may not be through full ROM
Spasticity peaks

26
Q

Brunnstrom Stage 4

A

Some movement combinations out of synergy
Mastered with difficulty
Spasticity now decreasing

27
Q

Brunnstrom Stage 5

A

Synergies lose their dominance
More difficult movement combinations can be mastered
Spasticity further decreases

28
Q

Brunnstrom Stage 6

A

No synergies; full isolated joint movement are possible

Decreased coordination

29
Q

Fugl Meyer Assessment Tool

A

Standardized test that includes joint ROM, pain, sensation, motor function and balance
Designed for individuals with CVA
Based on Brunnstrom’s stages of motor recovery
Includes specific voluntary movements the person attempts to perform
Scoring: 3 point scale for each item of motor function section (50 total movements)
0=item can not be performed
1=item can be partially performed
2=item performed faultlessly

Maximum scores: 
UE motor performance =66; 
LE motor performance = 34 
ULE TOTAL = 100
Motor scores < 50: severe motor impairment
50-84: marked motor impairment
85-95: moderate motor impairment
96-99: slight motor impairment
30
Q

Hypometria

A

Underestimation of the required force or range of movement

31
Q

Dysmetria

A

Traditionally, problems in judging the distance or range of a movement

32
Q

Hypermetria

A

Overestimation of the required force or range of movement

33
Q

Dysdiadochokinesia

A

Abnormal rapid movement

34
Q

Non-equilibrium tests

A

Finger to nose, heel to shin
Quality of movement
Subjectively graded 1-5

35
Q

Dystonia

A

Sustained muscle contractions, often twisting, repetitive and abnormal

36
Q

PT tx for tone

A

Rhythmic rotation in various positions

Can modulate tone, can’t reduce it

37
Q

Treatment (intervention) of involuntary movements

A

Reduced effort/increase efficiency
Weight bearing and approximation
Distal fixation
Limb weighting is controversial

38
Q

Define Positive Signs

A

Release of abnormal behaviors

ex: positive Babinski, tremor, hypertonicity

39
Q

Define Negative Signs

A

Loss of normal behaviors

ex: paresis, aphasia

40
Q

Primary impairments of body structure/function

A

Impairments that result from the original pathology/health condition
Ex: Paresis, paralysis, spasticity

41
Q

Secondary impairments of body structure/function

A

Result from primary impairments
Ex: contracture, adaptive changes to mechanical fiber properties, loss of ROM, deconditioning, skin breakdown, loss of strength

42
Q

Hypotonia

A

Less than normal tone, stiffness, tension

Little or no tension in response to passive stretch

43
Q

Hypertonia

A

Excessive tone, stiffness, tension in response to palpation of the muscle
Excessive tension in response to passive stretch

44
Q

Define these words:
Weakness
Paralysis/plegia
Paresis

A

Weakness: inability to generate adequate force, can be a musculoskeletal or neuro problem
Paralysis/plegia: total or severe loss
Paresis: mild or partial loss

45
Q

What is motor function?

A

The ability to learn and demonstrate the skillful and efficient assumption, maintenance, modification, and control of voluntary postures and movement patterns

Strength, power, and endurance

Coordinatiom and synergistic movements of agonists, antagonists, stabilizers