neuro exam sensory and coord Flashcards

1
Q

somatic sensory pathways

A

Trigeminal lemniscus pathway(THALAMIC):
touch & pressure from the head (face) & neck region

Medial lemniscus pathway transmits (DORSAL COLUMN) :
touch & pressure, from rest of the body

Antero-lateral/ spinal lemniscus pathway:
pain & temperature from the body

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2
Q

hyper/hypoalgia

A
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2
Q

allodynia

A
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2
Q

testing light touch

A

LIGHT TOUCH:
Use a Wisp of cotton wool
Touch lightly – don’t drag
Compare both sides / symmetrical areas
Avoid calloused skin

call out dermatome after stimulation in osce

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3
Q

hyp/hypoanaest

A
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4
Q

Sensory testing – General points

A

patient co-operation is absolutely necessary
Always explain & demonstrate to the patient first
Patient close eyes during actual testing of sensation
Sensory testing quickly fatigues many patients & then may be unreliable

Pay special attention to areas with:
a) Symptoms such as numbness or pain
b) Motor or reflex abnormalities suggesting a lesion of the spinal cord or peripheral nerves
c) Trophic changes such as altered sweating, atrophy or ulceration

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5
Q

4 modalities are of sensory system examined

A

1) LIGHT TOUCH - Use a wisp of cotton wool

2) PAIN - Use a sharp straight (unused) pin (not an injection needle)

3) VIBRATION - Use a 128 Hz tuning fork

4) PROPRIORECEPTION - Joint position sense

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6
Q

testing sharp pain sensation

A

Use a new pin, & occasionally substitute the blunt end
(discard in sharps after use)
“ Is this sharp or blunt?”
“ Does this feel the same as this?”

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7
Q

single periph nerve pattern sense loss

A

due to periph nerve inj or entrapment if >2 isolated neuropathies

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7
Q

test for temp sensation

A

May be omitted if pain sensation is normal
Two test tubes - Hot & cold H2O

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8
Q

periph polyneuropathy

A

gloved or stocking distribution
length dependant

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8
Q

dermatomal pattern of sesniory loss

A

due to nerve root or spinal cord lesion

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9
Q

hemi sesnory pattern of loss

A

one side of the face or body has sesnory loss

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10
Q

stereogenssi

A

ability to id obj by feeling

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10
Q

finger gnosia

A

naming finger being rouched

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10
Q

two pt discrimination

A

<5mm on finger pads

11
Q

Finger agnosia

A

naming fingers touched

12
Q

Graphesthesia

A

number/letter identification

13
Q

test fir titubation

A

obs pt seated ask pt tp lift their head up if lyioong down
observe to head bobbing

14
Q

TEST FOR NYSTAGMUS

A

Involuntary “to & fro” movements of eyes
Jerk (quick & slow) or pendular
Test by asking patient to follow an object with the eyes
horizontal is main portiomn

14
Q

TEST SPEECH

A

Assess spontaneous speech
Speech may be slurred speech due to errors in timing, i.e.
incoordination of muscles controlling/involved in speech,
words broken down to individual syllables
Ask patient to say: (repetitively + fast)
ma…..ma…..ma….ma Labial
ta….ta…..ta….ta….ta Tongue
la….la….la….la….la Tongue
ga….ga….ga….ga Palate
Listen for: Slurring, scanning (separation of syllables), staccato Irregularities

15
Q

LOWER LIMB CO-ORDINATION

A

TONE & REFLEXES – refer motor examination for hpoton and pendular retglexes

HEEL-SHIN TEST for dysmetria & intention tremour

FOOT TAPPING (or HEEL TAPPING) TEST for dysdiadochokinesia

15
Q

UPPER LIMB CO-ORDINATION

A

TEST FOR ARM DRIFT –
due to various causes
TEST FOR REBOUND PHENOMENON
from hypotonia

FINGER-NOSE TEST -
look for intention tremor &
past-pointing or dysmetria

DYSDIADOCHOKINESIS –
difficulty with repetitively performed
alternating movements

16
Q

TEST TRUNCAL CO-ORDINATION & GAIT

A

Ask patient to fold his arms & sit up

Patient seated - observe if head/body are swaying - titubation/ truncal ataxia

Observe gait - ask patient to turn around suddenly - look for staggering/irregular gait

Heel to toe walking - observe for loss of balance/ does patient fall to one side?

17
Q

romberg test

A

Patient stands with feet together + eyes open
Examiner stands close to patient to support him if necessary,
then instructs patient to close eyes for 20-30 seconds
Note the ability to maintain an upright posture
(normally only minimal swaying occurs)
The Romberg test is positive
when unsteadiness increases with eye closure
(it indicates loss of proprioceptive sensation)

present in sensory ataxia
not cerebellar atxia

18
Q

Features of a Cerebellar Lesion

A

disease occur on the same side as the lesion (ipsilateral)
Speech – cerebellar speech is jerky, explosive & loud
Nystagmus – worse on looking towards lesion’s side
Upper limbs
Arm drift & Rebound due to hypotonia
Intention tremor
Past pointing or dysmetria
Dysdiadochokinesis
Trunk
Titubation
Truncal ataxia with midline lesions
Lower limbs
romberg negative
Hypotonia
Pendular knee jerks
Incoordination on heel-shin test
(note : if this is aggravated by eye closure, it suggests posterior column loss)
Loss of rhythmicity with foot tapping test
Gait
Broad-based ataxic gait
Unsteady with eyes open
Falls towards the side of the lesion
Difficulty with heel-toe walking
especially with midline lesion

19
Q

cerebellar lesion TA2R2NISH2D2

A

see slides