Tone Flashcards

(47 cards)

1
Q

resistance offered by muscles when passively lengthened “stiffness”

A

muscle tone

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2
Q

Diagnostic indicator of UMN problem

A

hypertonicity

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3
Q

UMN or LMN problem

A

Hypotonicity

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4
Q

Connective tissue capsuleintrafusal muscle fibersGamma motor axonsSensory axons

A

Muscle spindle

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5
Q

What fires the same time as the alpha motor neuron to contract the edges of the muscle spindle

A

gamma motor neuron

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6
Q

muscle spindles ending in central region of intrafusal fibers

A

Sensory axon

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7
Q

Types of sensory axons int he muscle spindles

A

Ia primaryII secondary

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8
Q

Sensitive to low amplitude, high velocity stretch inputsresult of activation is autogenic facilitation and reciprocal inhibition

A

Ia primary sensory ending

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9
Q

Sensitive to slow, sustained stretchactivation results less clear

A

II secondary sensory ending

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10
Q

Innervate intrafusal fibers (polar regions)Cell bodies in ventral horn of spinal cord (with alpha motor neuron)Not involved in stretch reflex pathway

A

Gamma motor neuron

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11
Q

Loss of normal alpha-gamma coactivationslack spindle, no input

A

hypotonia

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12
Q

a hypertonia condition that is velocity dependent and associated with hyperreflexia

A

Spasticity

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13
Q

Severe, constant hypertonia that is not velocity dependent

A

Rigidity

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14
Q

Alpha motor neurons are more sensitive to input due to net increase in excitatory synaptic input and or net decrease in inhibitory synaptic inputs

A

Neural causes of hypertonia

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15
Q

Immobilization has effect of changing visco-elastic propertiesChange in muscle fiber structure

A

Non neural causes of hypertonia

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16
Q

Types of tone

A

Clasp knifecog wheellead pipe

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17
Q

Most resistance at the beginning

A

clasp knife (swiss army knife)

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18
Q

Resistance throughout the range

A

Cog wheel

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19
Q

High level of resistance throughout

20
Q

modified ashworth scaleno increase in muscle tone

21
Q

modified ashworth scaleslight increase in muscle tone, manifested by a catch or by minimal resistance at the end of the range of motion when the affected part is moved in flexion or extension

22
Q

modified ashworth scaleSlight increase in muscle tone, manifested by a catch, followed by minimal resistance throughout the remainder of the ROM

23
Q

modified ashworth scalemore marked increase in muscle tone through most of the ROM, but affected part easily moved

24
Q

modified ashworth scaleConsiderable increase in muscle tone, passive movement difficult

25
modified ashworth scaleaffected parts rigid in flexion or extension
4
26
modified ashworth scaleUnable to test
9
27
x= spasticity angle (threshold)y= spasticity grade (gain)
Tardieu scale
28
Tardieu scaleno resistance
0
29
Tardieu scaleslight resistance
1
30
Tardieu scale clear catch, interrupting movement
2
31
Tardieu scaleFatigable clonus
3
32
Tardieu scaleUnfatigable clonus
4
33
pharmacological treatment for hypertonicity
baclofenvaliumbotox injection
34
multi muscle activation problems
Sequencing problemsAbnormal synergies
35
Coactivation across joint
sequencing problems
36
inability to move a single joint without simultaneous movement in other joints
Abnormal synergies
37
Brunnstrom stages after stroke
UE" flexor synergy is greater than extensorLE: extensor synergy is greater than flexor
38
Brunnstrom Stages of synergyno movement
stage 1
39
Brunnstrom Stages of synergyinvoluntary movement only
stage 2
40
Brunnstrom Stages of synergyabnormal synergy only
stage 3
41
Brunnstrom Stages of synergyisolate one joint
stage 4
42
Brunnstrom Stages of synergyisolate 2 joints
stage 5
43
Brunnstrom Stages of synergyisolate all joints
stage 6
44
Brunnstrom Stages of synergy normal movements
stage 7
45
activation problems in the LE
standing transfersgait
46
activation problems in the UE
manipulation and dexterity
47
tests for motor control or rehab assessment after stroke
Fugl meyerStreamS-Stream