Lecture 3: BSF Exam- Muscle Tone Flashcards

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
Q

What else is associated with hypotonia?

A

reduced deep tendon reflexes

26
Q

What does hypotonia result in?

A

poor posture, weakness, decreased function, pain

27
Q

What will hypertonia look like?

A

increased muscle bulk, well defined and will feel taught and hard

28
Q

What will hypo look like?

A

less definition, mushy feel

29
Q

How to examine muscle tone?

A

lie pt in supine and perform PROM, don’t hold muscle belly, make sure pt is relax and note ROM and end feels

30
Q

How do you check for spasticity?

A

stretch the limb at full motion at a fast speed, unidirectional

31
Q

What is important to remember when testing rigidity?

A

it is not velocity dependent and and is bi directional

32
Q

What is a 0 on the MAS?

A

no increase in muscle tone

33
Q

What is a 1 on the MAS?

A

slight increase in muscle tone, manifested by catch at end range of motion and minimal resistance after

34
Q

What is 1+ on the MAS?

A

slight increase in muscle tone, catch in mid range of motion followed by resistance

35
Q

What is 2 on MAS?

A

more marked increase in tone through ROM

36
Q

What is 3 on MAS?

A

considerable amount of tone throughout motion, passive movement difficult

37
Q

What is a 4 on MAS?

A

affected parts rigid in flexion or extension

38
Q

What is V1-3 on Tardieu?

A

v1- very slow movement of body part
v2- speed of limb falling at gravity
v3- as fast as possible

39
Q

How do you score a Tardeiu?

A

x/y

x is 0-5 rating scale
y is degree of angle where muscle reaction occurs

40
Q

What is a 0 on Tardieu?

A

no resistance throughout course of passive movement

41
Q

What is 1 on Tardieu?

A

slight resistance, no catch

42
Q

What is 2 on Tardeiu?

A

clear catch at precise angle, interrupts movement followed by release

43
Q

What is 3 on Tardeiu?

A

fatiguable clonus less than 10 seconds when maintaining pressure and at precise angle

44
Q

What is 4 on Tardeiu?

A

clonus for more than 10 seconds at precise angle

45
Q

What is 5 on Tardeiu?

A

joint is immovable

46
Q

What is Babinski’s sign?

A

when stimulus applied to bottom of foot the toes will extend instead of flex

47
Q

What is Hoffman’s sign?

A

flicking of middle finger

abnormal thumb and index finger will adduct and flex

indicative of hyper reflexia