3) Performing a Lower Extremity Neurological Exam Flashcards

1
Q

Neuropathic ulcers and neuropathic joints develop because of

A
  • Lack of pain perception

- Pain is a protective mechanism

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2
Q

When inspecting the motor system, the following points should be assessed

A
  • Resting posture (unusual rotation or posture of a joint)
  • Is the patient symmetrical
  • Muscle wasting or hypertrophy (focal or diffuse)
  • Involuntary movements (tremor, tics, myoclonic jerks, chorea or athetosis)
  • Muscle fasciculation (LMN disease)
  • Subcutaneous twitches over a muscle belly at rest (tapping the belly may stimulate fasciculation)
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3
Q

Sharp touch

A
  • Disposable pin
  • Sternal area to establish a baseline
  • Follow the same progression as with light touch, comparing both lower limbs
  • Ask the patient to report hypoaesthesia (feels blunter) or hyperesthesia (feels sharper)
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4
Q

Temperature

A
  • Compare the quality of temperature sensation on arms, face, trunk, hands, legs and feet
  • Containers of warm and cool water may be used for more accurate assessment
  • Ask the patient to distinguish between warm and cool on different areas of the skin with their eyes closed
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5
Q

Proprioception

A
  • Test at IPJ of the big toe
  • Hold the proximal phalanx with one thumb and finger and hold the medial and lateral sides of the distal phalanx with the other
  • Move the distal phalanx up and down
  • Ask the patient to tell you the direction of movement each time
  • Test on both feet
  • If there is an abnormality, move backwards to the MPJ and so on until joint position sense is normal
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6
Q

Vibration sense

A
  • 128 Hz tuning fork
  • Place it on the sternum to start with so that the patient can feel the sensation
  • Then place it on the big toe
  • No vibration? move backwards to the bony malleolus of the ankle, the tibial shaft and tuberosity and the anterior iliac crest
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7
Q

2-point discrimination

A
  • Calipers or areshaped paperclip
  • Alternate randomly between touching the patient with one point or with two points on the area being tested (finger, arm, leg, toe)
  • The patient is asked to report whether one or two points was felt
  • NOT usually performed on the soles of the feet because the distinguishing distance is usually much greater than that on the fingers
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8
Q

If there is a spinal cord lesion, there may not be equal diminution across all the sensory modalities

A
  • Light touch, vibration and joint position sense may remain intact while sharp touch and temperature are lost
  • This is because the lateral spinothalamic pathways may be damaged while the dorsal columns remain intact
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9
Q

Tone

A
  • The resistance felt when a joint is moved passively through its normal range of movement
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10
Q

Hypertonia vs. hypotonia

A
  • Hypertonia is found in upper motor neuron lesions

- Hypotonia is found in lower motor neuron lesions and cerebellar disorders

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11
Q

Clonus

A
  • Rhythmic and involuntary muscle contraction that can be provoked by stretching a group of muscles
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12
Q

Testing tone

A
  • Ask the patient to let their legs ‘go floppy’
  • Internally and externally rotate the ‘floppy’ leg
  • Assess for any increased or reduced tone
  • Then lift the knee off the bed with one of your hands
  • Note whether the ankle raises off the bed as well, signifying increased tone
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13
Q

Testing for ankle clonus

A
  • Flex the patient’s knee, resting the ankle on the bed
  • Dorsiflex the foot quickly and keep the pressure applied
  • You will be able to see the foot moving up and down if clonus is present
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14
Q

When assessing power, you must test the following

A
  • Hip flexion, extension, adduction and abduction
  • Knee flexion and extension
  • Foot dorsiflexion, plantar flexion, eversion and inversion
  • Toe plantar flexion and dorsiflexion
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15
Q

Deep tendon reflexes can be

A
  • Hyperactive (+++)
  • Normal (++)
  • Sluggish (+)
  • Absent (-)
  • (±) is used when the reflex is only present on reinforcement
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16
Q

Muscle stretch reflexes (deep tendon reflexes) grade scale

A
  • 0 = absent
  • 1 = present with reinforcement
  • 2 = normal
  • 3 = enhanced
  • 4 = unsustained clonus
  • 5 = sustained clonus
17
Q

Interpretation of DTR

A
  • Upper motor neuron lesions usually produce hyperreflexia

- Lower motor neuron lesions usually produce a diminished or absent response

18
Q

Superficial tendon reflexes

A
  • An extensor plantar response (upgoing big toe) is pathological (+ Babinski’s sign) and signifies an upper motor neuron lesion
19
Q

Babinski’s sign

A
  • Dorsiflexion of the big toe and abduction of the other toes
  • Physiologically, it is normally present in infants from birth to 12 months
  • After 12 months = non-specific upper motor neuron lesion
20
Q

Heel-shin test (cerebellar/coordination exam)

A
  • Ask the patient to lift one of their legs and flex it at the knee, keeping the other leg straight
  • They should then place the heel of the flexed leg on the knee of the other leg and run it down the shin towards the ankle and back again towards the knee
  • Ask them to repeat this several times
21
Q

Heel-toe test (coordination)

A
  • This tests balance mechanisms that rely on the cerebellar, vestibular and proprioceptive systems
  • The patient either needs to be barefoot or wearing flat shoes
  • Walk in a straight line so that the heel of the second foot touches the toes of the first foot, repeat
  • Look at how well they are able to perform this
  • Is there any staggering which would suggest a lesion of the cerebellum
22
Q

Romberg’s test (coordination)

A
  • This also tests balance mechanisms that rely on the cerebellar, vestibular and proprioceptive systems
  • Ask the patient to keep their eyes open and stand with their feet together, arms by their sides
  • Then ask them to maintain this position when they close their eyes
  • Patients who have cerebellar lesions often cannot stand in this position, even with their eyes open
  • If balance is only lost when the eyes are closed, this signifies a proprioceptive or vestibular lesion
  • Be ready to catch the patient by standing behind
23
Q

Examination of gait

A
  • Assess cerebellar function
  • Romberg’s test
  • Finger-nose pointing
  • Dysdiadochokinesia
  • Heel-to-shin testing
24
Q

Significant observations during gait exam

A
  • Shuffling gait
  • Balance
  • Postural sway
  • Rate of walking
  • Steppage gait
  • Difficulty turning
  • Widened base
  • Difficulty rising from chair
25
Q

Shuffling gait

A
  • May suggest Parkinsonism

- This is also associated with a flat foot strike in heel-to-toe testing with a reduced loading at the heel

26
Q

Balance

A
  • Do they veer off course?

- This suggests cerebellar dysfunction

27
Q

Postural sway

A
  • Feature of late-stage Parkinson’s disease and other conditions of poor balance
  • Balance cannot be maintained through standing, turning or walking
  • In Parkinson’s disease it relates to lack of flexibility in shifting postural responses
28
Q

Rate of walking

A
  • Do they start off slowly and then speed up (a Parkinsonian characteristic)
  • Is there general slowness (eg, joint degenerative disease, weakness)
29
Q

Steppage gait

A
  • Due to foot drop (loss of dorsiflexion)

- Needs to lift leg higher than normal

30
Q

Steppage gait is associate with conditions such as

A
  • Peroneal nerve injury
  • Fibular injury
  • Multiple sclerosis
  • Guillain-Barré syndrome
  • Prolapsed intervertebral disc
31
Q

Difficulty turning

A
  • Common with any gait disorder; turning is generally more difficult than walking
  • No balance or gait problems? about-face in one or two steps
  • Nonspecific problems? three or four steps
  • Five or more steps likely to have cerebral or basal ganglia dysfunction
32
Q

If a patient has less trouble turning than walking forwards

A
  • A psychogenic disturbance is likely
33
Q

Widened base

A
  • With frank ataxia, base width is about 12 inches
  • If base width approaches two feet, the likelihood of psychogenic gait disorder rises (unless the patient has morbid obesity or an obvious structural explanation)
34
Q

The assessment and examination of gait and balance need to be supplemented by

A
  • Appropriate history and examination of all systems

- Attention must be paid to speed of onset and rate of any deterioration

35
Q

Acute deterioration in gait

A
  • Feature of many serious conditions requiring urgent assessment and intervention
  • Vascular, infective, neoplastic, neurological, metabolic and toxicological conditions and acute confusional states