Spasticity Flashcards

1
Q

What is Spasticity?

A

Condition in which there is abnormal increase in muscle tone or stiffness of muscle

might interfere with movement, speech, or be associated with discomfort or pain

Velocity dependent

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2
Q

Cause(s) of Spasticity =

A

Usually damage to UMN pathways within the brain, brainstem, or spinal cord

Associated with SCI, MS, CP, CVA, TBI, ALS, hereditary spastic paraplegias, and some metabolic disorders

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3
Q

Symptoms of Spasticity =

A

Hypertonicity
Clonus
Exaggerated DTRs
Muscle spasms

Secondary:
> Scissoring (involuntary crossing of the legs)
> contractures

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4
Q

The amount of tension in resting muscle:
Contributing factors =

A

Assessed by PROM and normally minimal

Intrinsic and passive stiffness of the muscle provide normal muscle resting tone

Descending motor commands

Level of background excitability in spinal cord

Proprioceptive information

At rest, there are weak bonds between actin and myosin (without power stroke) - Immobility facilitates these bonds

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5
Q

Stretch following immobility =

A

feel increased resistance

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6
Q

Stretch following a prolonged contraction =

A

feel increased resistance

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7
Q

Slow, gentle stretch =

A

gentle detachment

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8
Q

Fast stretch =

A

remain attached contributing to increased stiffness

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9
Q

Titin =

A

Elastic properties provide mobility AND resistance

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10
Q

Joint resistance to movement =

A

elastic + contractile muscle forces

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11
Q

Cocontraction =

A

Simultaneous contraction of agonist and antagonist muscles

Frequently used for functional stability
> Wrist for distal movement
> LEs for standing
> Commonly see with new motor learning

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12
Q

Muscle Synergies =

A

Coordinated muscular action
> Normal function

Type II afferents (muscle spindles, joint receptors, cutaneous and subcutaneous touch and pressure)

Interneurons connect to motor neurons for muscles at other joints for spinal cord regulated coordinated function (frequently used patterns)

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13
Q

Pathologic synergies
Example: Patient post TBI or CVA

A

UMN lesion

Voluntary flexion of shoulder is accompanied by unwanted, simultaneous, obligatory flexion of the elbow

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14
Q

Associated Reactions =

A

Spontaneous movement = Involuntary movement when something else happens (yawn, strain, etc.)

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15
Q

Hypertonia =

A

Abnormal resistance to passive stretch

Occurs in UMN and some basal ganglia lesions

2 Types

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16
Q

2 types of hypertonia =

A

Spasticity
Rigidity

17
Q

Spasticity =

A

velocity dependent hypertonia

CVA or TBI (cerebrum injury)

May present with clasp-knife response

18
Q

Rigidity =

A

constant resistance/velocity independent hypertonia

Decerebrate and decorticate rigidity

Cogwheel or lead-pipe rigidity in basal ganglia lesion

19
Q

Hyperreflexia =

A

Exaggerated DTRs

Abnormal cutaneous reflexes

20
Q

Babinski Sign in Adults =

A

normal response (-)

abnormal response (+)
> normal in infants <7 months

21
Q

Clonus =

A

Involuntary, repeating, and rhythmic muscle contractions

22
Q

Unsustained clonus =

A

fades after a few beats, even with maintained muscle stretch

23
Q

Sustained clonus =

A

is always pathologic in origin and is produced when a lack of UMN modulation allows the activation of oscillating neural networks in the spinal cord

In people with chronic SCI or other MT lesions, sustained clonus of the soleus muscle may be triggered by placement of a foot on a wheelchair footrest

24
Q

Clinical Assessment of Spasticity =

A

Observation for posturing at rest

Resistance to PROM

Passive drop into gravity

Voluntary activation followed by passive drop into gravity

Easy movement
> ? Associated reaction

Challenging movement
> ? Associated reaction

Observation for impact on function

25
Q

Modified Tardieu Spasticity Scale - 0

A

no resistance throughout the course of passive movement

26
Q

Modified Tardieu Spasticity Scale - 1

A

slight resistance throughout the course of passive movement, with no clear catch at precise angle

27
Q

Modified Tardieu Spasticity Scale - 2

A

clear catch at precise angle, interrupting the passive movement, followed by release

28
Q

Modified Tardieu Spasticity Scale - 3

A

Fatigable clonus (<10 seconds when maintaining pressure) occurring at precise angle

29
Q

Modified Tardieu Spasticity Scale - 4

A

Infatigable clonus (>10 seconds when maintaining pressure) occurring at precise angle

30
Q

Modified Ashworth Scale - 0

A

no increase in muscle tone

31
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 range of motion when the affected part(s) is moved in flexion or extension

32
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

33
Q

Modified Ashworth Scale - 2

A

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

34
Q

Modified Ashworth Scale - 3

A

considerable increase in muscle tone, passive movement difficult

35
Q

Modified Ashworth Scale - 4

A

affected part(s) rigid in flexion or extension

36
Q

Modified Modified Ashworth Scale - 0

A

No increase in muscle tone

37
Q

Modified Modified Ashworth Scale

A

doesn’t have a 1+