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

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

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

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

Tone Modifiers

A
UMN
Sensory input
LMN
Position
Ability to relax
State of alertness
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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’

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

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

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

Modified Ashworth Scale - 0

A

No increase in muscle tone

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

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

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

Modified Ashworth Scale - 2

A

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

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

Modified Ashworth Scale - 3

A

Considerable increase in muscle tone, passive movement difficult

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

Modified Ashworth Scale - 4

A

Affected part(s) rigid in flexion or extension

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

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

Abnormalities Resulting from Motor Cortex Dysfunction

A

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

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

Abnormalities Resulting from BG Dysfunction

A

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

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

Abnormalities Resulting from cerebellar Dysfunction

A

Hypotonia
Incoordination
Intention tremor
Impaired error correction affecting motor learning

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
Brunnstrom Stage 3
All movements are in synergy Synergies may not be through full ROM Spasticity peaks
26
Brunnstrom Stage 4
Some movement combinations out of synergy Mastered with difficulty Spasticity now decreasing
27
Brunnstrom Stage 5
Synergies lose their dominance More difficult movement combinations can be mastered Spasticity further decreases
28
Brunnstrom Stage 6
No synergies; full isolated joint movement are possible | Decreased coordination
29
Fugl Meyer Assessment Tool
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
Hypometria
Underestimation of the required force or range of movement
31
Dysmetria
Traditionally, problems in judging the distance or range of a movement
32
Hypermetria
Overestimation of the required force or range of movement
33
Dysdiadochokinesia
Abnormal rapid movement
34
Non-equilibrium tests
Finger to nose, heel to shin Quality of movement Subjectively graded 1-5
35
Dystonia
Sustained muscle contractions, often twisting, repetitive and abnormal
36
PT tx for tone
Rhythmic rotation in various positions | Can modulate tone, can't reduce it
37
Treatment (intervention) of involuntary movements
Reduced effort/increase efficiency Weight bearing and approximation Distal fixation Limb weighting is controversial
38
Define Positive Signs
Release of abnormal behaviors | ex: positive Babinski, tremor, hypertonicity
39
Define Negative Signs
Loss of normal behaviors | ex: paresis, aphasia
40
Primary impairments of body structure/function
Impairments that result from the original pathology/health condition Ex: Paresis, paralysis, spasticity
41
Secondary impairments of body structure/function
Result from primary impairments Ex: contracture, adaptive changes to mechanical fiber properties, loss of ROM, deconditioning, skin breakdown, loss of strength
42
Hypotonia
Less than normal tone, stiffness, tension | Little or no tension in response to passive stretch
43
Hypertonia
Excessive tone, stiffness, tension in response to palpation of the muscle Excessive tension in response to passive stretch
44
Define these words: Weakness Paralysis/plegia Paresis
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
What is motor function?
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