Peripheral nerves Flashcards

1
Q

What makes up a peripheral nerve exam

A

General inspection
Gait
Myotomes
Tone
Deep tendon reflexes
UMNL Vs LMNL

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2
Q

General inspection

A

Scars: may provide clues regarding previous spinal, axillary or upper limb surgery.

Wasting of muscles: suggestive of lower motor neuron lesions or disuse atrophy.

Tremor: there are several subtypes including resting tremor and intention tremor.

Fasciculations: small, local, involuntary muscle contraction and relaxation which may be visible under the skin. Associated with lower motor neuron pathology (e.g. amyotrophic lateral sclerosis).

Myoclonus: brief, involuntary, irregular twitching of a muscle or group of muscles. All individuals experience benign myoclonus on occasion (e.g. whilst falling asleep) however persistent widespread myoclonus is associated with several specific forms of epilepsy (e.g. juvenile myoclonic epilepsy).

Hypomimia: a reduced degree of facial expression associated with Parkinson’s disease.

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3
Q

Gait

A
  • Gait and stance are reliant upon many factors: Vision, Sensation, Proprioception, Motor output.
  • Unsteadiness on standing with the eyes open is common in cerebellar disorders – Cerebellar Ataxia
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4
Q

Cerebellar Ataxia

A
  • Cerebellar dysfunction leads to a broad-based, unsteady (ataxic) gait, which usually makes tandem walking (walking heel to toe in a straight line) impossible
  • Instability which only occurs, or is markedly worse, on eye closure is indicative of proprioceptive sensory loss, referred to as Sensory Ataxia
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5
Q

Abnormal gait examples

A

Bilateral upper motor neuron damage causes a scissor-like gait due to spasticity. (Spasticity – incr muscle tone & spasm)

Propulsive gait – a stooped, stiff posture with the head and neck bent forward

Scissors gait – legs flexed slightly at the hips and knees like crouching, with the knees and thighs hitting or crossing in a scissors-like movement

Spastic gait – a stiff, foot-dragging walk caused by a long muscle contraction on one side

Steppage gait – foot drop where the foot hangs with the toes pointing down, causing the toes to scrape the ground while walking, requiring someone to lift the leg higher than normal when walking

Waddling gait – a duck-like walk that may appear in childhood or later in life

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6
Q

Gait and co-ordination tests

A

For cerebullum ataxia/Co-ordination impairment. Common in MS

Rombergs sign/pronator drift – stand with feet togther and arms out in front for 30secs the repat with eyes closed. Or in supination, observe if patients pronate involuntaily. +Ve if Pt cannot remain balenced

Finger-nose test – Pt touches nose then practintioners finger, which is moving left to rght & forward/backwards. +Ve if Pt over shoots and misses – issues with depth perception. False posative may by an optic injury.

Heel/shin test

Dysdiadochokinesis – Pt places palm ontop of palm in supination, then pronation, then repated again and again.

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7
Q

Myotomes

A

A group of muscles which is innervated by single spinal nerve root
Ranked from 1 to 5. 1 being no visible contraction, 3 movement against gravity and 5 normal power.
First ask Pt to do the movement first to check they can do the movement against gravity, tells you there are already a three.

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8
Q

Myotomes (lower)

A

L2-S2
* L2 Hip flexion, knee bent Pt drives knee to chest then down into
* L3 kick the door (Knee extension)
* L4 Dorsiflex and invert foot, resist Pt pulling back to neutral
* L5 - Big toes – Pt tries to extend
* S1 Plantar flex
* S2 Heel to bum (Knee flexion)

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9
Q

Myotomes (upper)

A

C1-T1 myotomes for the upper body
* C1 Chin Tuck
* C2 Head back
* C3 - CSP SB
* C4 – Shoulder elevation
* C5 – Shoulder Abduction
* C6 – Elbow extension
* C7 - Elbow flexion
* C8 – Thumb extension
* T1 Finger Abduction, adduction.

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10
Q

Assessing tone – test for hypertonia

A

Tone – passive resistance to stretch, common in Parkinson’s and MS

Wrist – flex/extend
Elbow - flex/extend
Shoulder – abduction, adduction hips (‘roll’)
Knee - flexion

Tone is graded from 0 -4 (No response, Hypotonia, Normal response, Mild-moderate hypertonia, Severe hypertonia)
Stiffness – compliance to deformation

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11
Q

Deep tendon Reflexes

A

Biceps C5
Brachioradialis C6
Triceps C7
Patella L4
Achilles S1

Use Jendrassik manoeuvre – smile/grit their teeth, grip hands and try to pull apart, distracts them from the reflex

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12
Q

Loss of deep tendon reflex implication

A

Peripheral neuropathies secondary to diabetes, alcohol abuse, or inflammation.

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13
Q

Superficial reflexes

A

Umbilical T8-12 – Absent with corticospinal tract lesion.
Babinskis L5-S1 – Usually accompanied with Hyperreflexia, Clonus and increased tone. ADULTS: Normal – digital flexion Abnormal – digital fanning pattern. INFANTS – Normal digital fanning Abnormal – digital flexion.

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14
Q

UMNL

A

Anything that effects the brain (Stroke, infection, SOL, Parkinsons, MS etc) prior to the anterior horn of the spinal cord.

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15
Q

LMNL

A

– Anything that effects the neuron from anterior horn to the muscle it innervates (Peripheral nerve injury, bells palsy, Myasthenia Gravis, Guilain Barre syndrome)

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16
Q

Spinal tracts

A

Spinothalamic
Spinocerebellar
Dorsal column

17
Q

Spinothalamic

A

Anterior: crude touch
Lateral: Pain & Temperature

18
Q

Spinocerebellar

A

Muscle spindle
Golgi tendon ORGAN

19
Q

Dorsal column

A

Conscious proprioception
Vibration
Fine touch

  • affected by diabetes. Leading to a loss of vibration sense.
20
Q

Spinal tracts (Descending)

A

PYRIMIDAL conscious control of muscles from the cerebral cortex to the muscles of the body and face

EXTRA-PYRIMIDAL: unconscious, reflexive or responsive control of muscles from various brainstem structures to postural or anti-gravity muscles

21
Q

Dermatomes

A

An area of skin in which sensory nerves derive from a single spinal nerve root

22
Q

Dermatone tests

A

Cotton wool
Sharp/Soft
Temperature
Vibration

Scored 0-2.
0 =Absent
1 = Altered sensation
2= Normal

23
Q

Cotten wool test

A

Light Touch – Dorsal Column (Medial Lemniscus)
With patient’s eyes closed use a soft piece of material (cotton wool)
Time stimuli irregularly
Use a dabbing motion rather than stroking

24
Q

Sharp/soft

A

Superficial Pain - Spinothalamic
Use a fresh neurological pin (or toothpick)
Explain that you are attempting to elicit a sharp sensation
Ask patient (eyes closed) to tell you when they feel sharp sensation
Assess each dermatome

25
Q

Temperature

A

Temperature- Spinothalamic
Place a cold metallic object on the patients skin at set sensory nerve testing points
Ask if it feels cold

26
Q

Vibration sense (dorsal column)

A

Place a tuning fork (128hz) over bony prominences working distally to proximal ask the patient to report when they can not feel the buzzing sensation.

Lower limb:tip of great toe, IP joint, medial malleolus,tibial tuberosity, ASIS

Upper limb: DIP of forefinger, radial styloid,olecronon,acromion

First sense affected in certain conditions e.g. Peripheral Neuropathy. But is often absent distally in healthy older people.

27
Q

Joint position sense

A

Joint Position Sense - Dorsal Column (Medial Lemniscus)
Demonstrate the procedure so pt can see
Ask pt to say up or down as you flex or extend the big toe from the side
Pt closes eyes, perform random movements of up or down

28
Q

Meningeal irritation testing 3 symptoms

A

The three cardinal symptoms are far more sensitive to meningitis. Pyrexia, Nuchal ridigity and headaches

29
Q

3 meningitis tests

A

L’hermittes – Passive CSP flexion – Positive sign is ‘electric’/radiating pain in the arms/legs

Kernigs – Flex the hip to 90 and slowly extend the knee. Resistance/Pain is positive Kernig’s

Brudzinski’s – L’hermittes (Passive or active) followed by knee/hip flexion is a positive Brudzinskis sign.