Lecture 3: BSF Exam- Muscle Tone Flashcards

(47 cards)

1
Q

Why is ROM important for a neuro exam?

A

will affect ACOM and affect activity

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2
Q

What is muscle tone?

A

resistance of muscle to passive elongation or stretch

neurological ready state of muscle to act

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3
Q

Why is muscle tone important?

A

supports posture, provides reflexive, energy efficient base for movement

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4
Q

What is muscle tone influenced by?

A

intrinsic mechanical or elastic properties of muscle fibers and connective tissue

and spinal reflex muscle contractions

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5
Q

What are two main types of muscle tone?

A

hypertonia- increase tone due to UMNL, hard resistance to passive stretch

hypotonia- decreased tone due to sometimes LMNL

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6
Q

Where does an UMNL occur?

A

injury or lesion to brain, brainstem, descending motor or pyramidal tract

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7
Q

Why does hypertonia happen?

A

increased excitability of alpha motor neurons (increased depolarization)

enhanced excitatory synaptic input (ms spindle or GTO)

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8
Q

What are two types of hypertonia?

A

spasticity and rigidity

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9
Q

What is spasticity?

A

an involuntary, velocity dependent, increased resistance to passive elongation

quick stretch results in increased resistance

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10
Q

What type of lesions usually cause spasticity?

A

pyramidal tract lesions in diseases like CP, CVA, MS, TBI

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11
Q

What is the clasp knife phenomenon?

A

strong resistance to initial passive movement followed by release of resistance

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12
Q

What is clonus?

A

cyclical, spasmodic alternating muscle contraction in response to sustained stretch

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13
Q

Why is spasticity a negative thing?

A

may lead to contracture, deformity, functional limitations, skin break down, weakness in both agonist and antagonist

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14
Q

Why might spasticity be helpful?

A

passive postural suport, may contribute to function in presence of reduced motor control

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15
Q

What factors will make spasticity worse?

A

infection, pressure sores, DVT, fatigue, bladder distention

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16
Q

What is PT management?

A

modalities, stretching, splinting, casting

but only temporary effect

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17
Q

What is rigidity?

A

increased resistance through range and not velocity dependent usually in both agonist and antagonist

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18
Q

What will rigidity look like in basal ganglia lesion?

A

cogwheel or leadpipe

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19
Q

What about brainstem lesions?

A

decerebrate or decorticate

20
Q

What is decorticate?

A

reflects loss of corticol control (lesion above red nucleus) with flexed UE and extended LE

21
Q

What is decerebrate?

A

reflects loss of inhibitory control of cortex and basal ganglia (below red nucleus) with full extension of all limbs and trunk

22
Q

What is dystonia?

A

involuntary painful muscle contraction or spasm causing repetitive twisting motions, abnormal posture

23
Q

What causes dystonia?

A

unknown currently, includes genetics, acquired, idiopathic

24
Q

What is hypotonia associated with?

A

LMNL- anterior horn or peripheral nerve damage

UMNL- spinal shock or cerebellar lesion

chromosmal abnormalities- downs, muscle disease- muscular dystrophy

25
What else is associated with hypotonia?
reduced deep tendon reflexes
26
What does hypotonia result in?
poor posture, weakness, decreased function, pain
27
What will hypertonia look like?
increased muscle bulk, well defined and will feel taught and hard
28
What will hypo look like?
less definition, mushy feel
29
How to examine muscle tone?
lie pt in supine and perform PROM, don't hold muscle belly, make sure pt is relax and note ROM and end feels
30
How do you check for spasticity?
stretch the limb at full motion at a fast speed, unidirectional
31
What is important to remember when testing rigidity?
it is not velocity dependent and and is bi directional
32
What is a 0 on the MAS?
no increase in muscle tone
33
What is a 1 on the MAS?
slight increase in muscle tone, manifested by catch at end range of motion and minimal resistance after
34
What is 1+ on the MAS?
slight increase in muscle tone, catch in mid range of motion followed by resistance
35
What is 2 on MAS?
more marked increase in tone through ROM
36
What is 3 on MAS?
considerable amount of tone throughout motion, passive movement difficult
37
What is a 4 on MAS?
affected parts rigid in flexion or extension
38
What is V1-3 on Tardieu?
v1- very slow movement of body part v2- speed of limb falling at gravity v3- as fast as possible
39
How do you score a Tardeiu?
x/y x is 0-5 rating scale y is degree of angle where muscle reaction occurs
40
What is a 0 on Tardieu?
no resistance throughout course of passive movement
41
What is 1 on Tardieu?
slight resistance, no catch
42
What is 2 on Tardeiu?
clear catch at precise angle, interrupts movement followed by release
43
What is 3 on Tardeiu?
fatiguable clonus less than 10 seconds when maintaining pressure and at precise angle
44
What is 4 on Tardeiu?
clonus for more than 10 seconds at precise angle
45
What is 5 on Tardeiu?
joint is immovable
46
What is Babinski's sign?
when stimulus applied to bottom of foot the toes will extend instead of flex
47
What is Hoffman's sign?
flicking of middle finger abnormal thumb and index finger will adduct and flex indicative of hyper reflexia