Thursday, October 20, 2022

cmecde 564

 



89Neurology

Station 34

Sensory system of the upper limbs examination

Before starting

Introduce yourself to the patient.

Confirm his name and date of birth.

Explain the examination and obtain his consent.

Position him so that he is comfortably seated and ask him to expose his arms and to position

them so that the palms are facing towards you.

Ask if he is currently experiencing any pain.

The examination

To examine the sensory system, test light touch, pain, vibration sense, and proprioception.

Do not forget to inspect the arms before you start. In particular, look for muscle wasting,

fasciculation, scars and other obvious signs.

Light touch (not light rub or stroke). Ask the patient to close his eyes and to say ‘yes’ each time he

is touched with a wisp of cotton wool. Apply the cotton wool to his sternum as a test. Then apply

it to each of the dermatomes of the arm, moving from the hand and up along the arm. Remember

to compare both sides against each other, asking, “Does it feel the same on both sides?”.

Pain. Ask the patient to close his eyes and apply a sharp object – ideally a neurological pin – to

the sternum and then to each of the dermatomes of the arm, as above. Compare both sides

against each other. If there is any loss of or difference in sensation, map out the area affected.

Figure 25. Dermatomes of the arm.

C4

C5

C5

POSTERIOR

ASPECT

ANTERIOR

ASPECT

C6

C8

C7

C4

C6

C7 C8

T3

T2

T1

T1

T3

T2


Clinical Skills for OSCEs

90 Station 34 Sensory system of the upper limbs examination

Vibration. Ask the patient to close his eyes and apply a vibrating 128 Hz tuning fork (not the

smaller 512 Hz tuning fork used in hearing tests) to the sternum and then over the bony prominences of the arm, starting with the interphalangeal joint of the thumb and moving up to the

wrist and then the elbow (only if not felt more distally). Compare both sides against each other,

asking the patient to tell you when he feels the vibration stop (you can hasten this by touching

the tuning fork).

Proprioception. Ensure that the patient does not suffer from arthritis or some other painful condition of the hand. Ask him to close his eyes. Hold the distal interphalangeal joint of his index

finger between the thumb and index finger of one hand. With the other hand, move the distal

phalanx up and down at the joint, asking him to identify the direction of each movement. Hold

the joint and phalanx from the sides, i.e. from their lateral and medial aspects. Tell the patient

something like, “I’m going to move your finger up and down. Is this up or down?” “What about this?

And that?” Again, compare both sides.

After the examination

Thank the patient.

Ensure that he is comfortable.

Ask to carry out a full neurological examination.

Summarise your findings and offer a differential diagnosis.

Conditions most likely to come up in a sensory system of the upper limbs examination station

Mononeuropathy:

lesion affecting a single nerve, e.g. ulnar, median, or radial nerve (see Station 33).

Polyneuropathy:

lesion affecting multiple nerves in a glove and stocking distribution, such as in diabetic

neuropathy.

Radiculopathy:

lesion affecting a single root nerve, e.g. C6.

Brown–Séquard syndrome:

numbness to touch and vibration and loss of proprioception (and weakness) on same side of

the lesion, and loss of pain and temperature sensation on the opposite side.

caused by lateral hemisection or injury of the spinal cord.

Syringomyelia:

loss of pain and temperature sensation but not of other sensory modalities.


91Neurology

Station 35

Motor system of the lower limbs examination

Before starting

Introduce yourself to the patient.

Confirm his name and date of birth.

Explain the examination and obtain his consent.

Position him and ask him to expose his legs.

Ask if he is currently experiencing any pain.

The examination

Inspection

Look for deformities of the foot.

Look for abnormal posturing.

Look for fasciculation.

Assess the muscles of the legs for size, shape, and symmetry. You can also measure the circumference of the quadriceps or calves.

Tone

Ensure that the patient is not in any pain.

Ask the patient to relax the muscles in his legs.

Test the tone in the legs by rolling the leg on the bed, by flexing and extending the knee, and/

or by abruptly lifting the leg at the knee.

Power

Test muscle strength for hip flexion, extension, abduction and adduction, knee flexion and extension, plantar flexion and dorsiflexion of the foot and big toe, and inversion and eversion of

the forefoot. Compare muscle strength on both sides, and grade it on the MRC scale for muscle

strength:

0 No movement.

1 Feeble contractions.

2 Movement, but not against gravity.

3 Movement against gravity, but not against resistance.

4 Movement against resistance, but not to full strength.

5 Full strength.

Table 15. Important root values in the lower limb – muscle strength

• Hip flexion (femoral nerve and iliopsoas muscle) L1, L2

• Hip extension (inferior gluteal nerve and gluteus maximus muscle) S1

• Hip adduction (obturator nerve and adductor muscles) L2

• Knee flexion (sciatic nerve and hamstrings) L5, S1

• Knee extension (femoral nerve and quadriceps) L3, L4

• Foot dorsiflexion (deep peroneal nerve and tibialis anterior muscle) L4, L5

• Foot plantar flexion (tibial nerve and gastrocnemius muscle) S1

• Big toe dorsiflexion (deep peroneal nerve and extensor hallucis longus) L5


Clinical Skills for OSCEs

92 Station 35 Motor system of the lower limbs examination

Reflexes

Test the knee jerk and ankle jerk with a tendon hammer (see Figure 26). Test the knee jerk by

raising and supporting the knee with one arm and striking the patellar tendon with the other.

To test the ankle jerk, abduct and externally rotate the hip and flex the knee and ankle. Then

strike at the Achilles’ tendon. Compare both sides. If a lower limb reflex cannot be elicited, ask

the patient to hook flexed fingers and pull apart while you re-test.

Figure 26. Testing the knee (A) and

ankle (B) reflexes.

Test for clonus by holding up the ankle and rapidly dorsiflexing the foot (2–3 beats is normal).

Test for the Babinsky sign (extensor plantar reflex) by scraping the side of the foot with your

thumbnail or, ideally, with an orange stick. The sign is positive if there is extension of the big

toe at the MTP joint, so-called ‘upgoing plantars’.

Table 16. Important root values

in the lower limb – reflexes

Knee jerk L3, L4

Ankle jerk S1

(A)

(B)


Neurology

Station 35 Motor system of the lower limbs examination 93

Cerebellar signs

Carry out the heel-to-shin test.

– lie the patient on a couch. Ask him to run the heel of one leg down the shin of the other,

and then to bring the heel back up to the knee and to start again. Ask him to repeat the test

with his other leg

Gait

If he can, ask the patient to walk to the end of the room and to turn around and walk back. (See

Station 37: Gait, co-ordination, and cerebellar function examination.)

After the examination

Thank the patient.

Ensure that he is comfortable.

Ask to carry out a full neurological examination.

If appropriate, indicate that you would order some key investigations, e.g. CT, MRI, nerve conduction studies, electromyography, etc.

Summarise your findings and offer a differential diagnosis.

[Note] An upper motor neuron lesion is suggested by spastic tone, reduced power, brisk reflexes, up-going plantars,

reduced co-ordination, and clonus. A lower motor neuron lesion is suggested by normal or reduced tone, reduced

power, reduced reflexes, down-going plantars, normal co-ordination, wasting, and fasciculations.

Figure 27. Testing for the Babinsky or extensor plantar sign.


Clinical Skills for OSCEs

94 Station 35 Motor system of the lower limbs examination

Conditions most likely to come up in a motor system of the lower limbs examination station

Mononeuropathy:

lesion affecting a single nerve, most commonly the

common peroneal nerve (resulting in foot drop).

Polyneuropathy:

lesion affecting multiple nerves in a glove and

stocking distribution as in diabetic neuropathy.

Radiculopathy:

lesion affecting a single root nerve (see Table 16).

Hemiplegia/hemiparesis:

paralysis or weakness on one side of the body

accompanied by decreased movement control,

spasticity, and hyperreflexia (upper motor neurone

syndrome).

Cauda equina lesion:

signs include unilateral or bilateral lower

limb motor and/or sensory deficits.

the ankle jerks are usually absent on both

sides.

upper motor neurone signs such as

Babinsky sign and clonus are absent.

Myopathy:

symmetrical weakness predominantly

affecting proximal muscle groups.

in contrast to neuropathy, in myopathy

muscle atrophy and hyporeflexia occur

very late.


95Neurology

Station 36

Sensory system of the lower limbs examination

Before starting

Introduce yourself to the patient.

Confirm his name and date of birth.

Explain the examination and ask for his permission to carry it out.

Position him on a couch and ask him to expose his legs.

Ask if he is currently experiencing any pain.

The examination

To examine the sensory system, test light touch, pain, vibration sense, and proprioception.

Do not forget to inspect the legs before you start. In particular, look for muscle wasting, fasciculation, scars, and any other obvious signs.

Light touch (not light rub). Ask the patient to close his eyes and to say ‘yes’ each time he is

touched with a wisp of cotton wool. Apply the cotton wool to his sternum as a test. Then apply

it to each of the dermatomes of the leg, moving from the foot and up along the leg. Remember

to compare both sides against each other, asking, “Does it feel the same on both sides?”.

Pain. Ask the patient to close his eyes and apply a sharp object – ideally a neurological pin – to

the sternum and then to each of the dermatomes of the leg, as above. Compare both sides

against each other. If there is any loss of or difference in sensation, map out the area affected.

Vibration. Ask the patient to close his eyes and apply a vibrating 128 Hz tuning fork (not the

smaller 512 Hz tuning fork used in hearing tests) to the sternum and then over the bony prominences of the leg, starting with the interphalangeal joint of the big toe (test more proximally

only if not felt distally). Compare both sides against each other, asking the patient to tell you

when he feels the vibration stop (you can hasten this by touching the tuning fork).

L3

POSTERIOR

ASPECT

ANTERIOR

S1 ASPECT

L3

L4

L5

L2

L2

L1

L3

S2

L5

L4

L5 S1

S3

Figure 28. Dermatomes of the leg.


Clinical Skills for OSCEs

96 Station 36 Sensory system of the lower limbs examination

Proprioception. Ensure that the patient does not suffer from arthritis, gout, or some other painful condition of the foot. Ask him to close his eyes. Hold the interphalangeal joint of his big toe

between the thumb and index finger of one hand. With the other hand, move the distal phalanx

up and down at the joint, asking him to identify the direction of each movement. Hold the joint

and phalanx from the sides i.e. from their lateral and medial aspects. Tell the patient something

like, “I’m going to move your toe up and down. Is this up or down?” “What about this? And that?”

Again, compare both sides. If the patient is able to stand, you can also perform Romberg’s test

(see Station 37: Gait, co-ordination, and cerebellar function examination).

After the examination

Thank the patient.

Ensure that he is comfortable.

Ask to carry out a full neurological examination.

If appropriate, indicate that you would order some key investigations, e.g. CT, MRI, nerve conduction studies, electromyography, etc.

Summarise your findings and offer a differential diagnosis.

Conditions most likely to come up in a sensory system of the lower limbs examination station

Mononeuropathy:

lesion affecting a single nerve.

Polyneuropathy:

lesion affecting multiple nerves as in alcoholic or diabetic neuropathy.

Radiculopathy:

lesion affecting a single root nerve (see Figure 28).

Cauda equina lesion:

signs include unilateral or bilateral lower limb motor and/or sensory deficits, including ‘saddle

anaesthesia’ (loss of sensation in the area of the buttocks and perineum).

Hemisensory loss:

loss of sensation including light, pain, temperature, vibration, and proprioception on one side

of the body.

normally accompanied by hemiplegia/hemiparesis with attendant spasticity and hyperreflexia (upper motor neurone syndrome).

Brown–Séquard syndrome:

numbness to touch and vibration and loss of proprioception (and weakness) on same side of

the lesion, and loss of pain and temperature sensation on the opposite side.

caused by lateral hemisection or injury of the spinal cord.

Posterior column disease:

loss of proprioception and vibration but not of other sensory modaliti


Station 37

Gait, co-ordination, and cerebellar function

examination

Before starting

Introduce yourself to the patient.

Confirm his name and date of birth.

Explain the examination and obtain his consent.

Ask if he is currently experiencing any pain.

Examination of gait

Inspection. Inspect the patient in the sitting position, noting any abnormalities of posture. Ask

him to stand up and ensure that he is steady on his feet. Truncal ataxis suggests a midline cerebellar lesion. Inspect posture from both front and side.

Gait and arm swing. Ask him to walk to the end of the room and to turn around and walk back.

If he normally uses a stick or frame, he should not be prevented from doing so. Note the gait

and also the arm swing and any difficulty in standing or turning.

Heel-to-toe test/tandem gait. Ask him to walk heel-to-toe, ‘as if on a tightrope’. Ataxia on a

narrow-based gait suggests a cerebellar or vestibular lesion.

Romberg’s test. Ask him to stand unaided with his feet together and his arms by his sides.

Assess with his eyes open and then with his eyes closed. If he sways and threatens to lose his

balance when his eyes are closed, the test is said to be positive, indicating posterior column

disease.

You must be in a position to steady the patient should he threaten to fall.

Examination of co-ordination

Resting tremor. Ask the patient to sit down, to rest his hands in his lap, and to close his eyes.

Resting tremor is a sign of Parkinson’s disease.

Intention tremor. Ask the patient to do something, e.g. remove his watch or write a sentence.

Muscle tone in the arms. Examine muscle tone in the elbow (flexion and extension) and wrist

(flexion and extension, abduction and adduction) joints. Compare both sides.

Dysdiadochokinesis. Ask the patient to clap and then show him how to clap by alternating the

palmar and dorsal surfaces of one hand. Once he is able to do this, ask him to do it as fast as he

can. Ask him to repeat the test with his other hand.

Finger-to-nose test. Place your index finger at about 2 feet from the patient’s face. Ask him to

touch the tip of his nose and then the tip of your finger with the tip of his index finger. Once he

is able to do this, ask him to do it as fast as he can. And remember that he has two hands! Look

for intention tremor and dysmetria (past-pointing), both signs of cerebellar disease.

Fine finger movements. Ask the patient to oppose his thumb with each of his other fingers in

turn. Once he is able to do this, ask him to do it as fast as he can. Again, remember that he has

two hands.

Muscle tone in the legs. Ask the patient to lie down on a couch and, if possible, to relax the

muscles in his legs. Test the tone in his legs by rolling the leg on the bed, by flexing and extending the knee, and/or by abruptly lifting the leg at the knee.

Heel-to-shin test. Ask the patient to run the heel of one leg down the shin of the other, and

then to bring the heel back up to the knee and to start again. Ask him to repeat the test with

his other leg.


Clinical Skills for OSCEs

98 Station 37 Gait, co-ordination, and cerebellar function examination

Assessment of cerebellar function

If you are specifically asked to assess cerebellar function, carry out the above plus test

eye movements (nystagmus) and ask the patient to say ‘baby hippopotamus’ (slurred/

staccato speech). If you are then asked to list cerebellar signs, remember the mnemonic

DANISH:

– Dysdiadochokinesis and dysmetria (finger overshoot)

– Ataxia

– Nystagmus – test eye movements

– Intention tremor

– Slurred/staccato speech – ask the patient to say ‘baby hippopotamus’ or ‘British constitution’

– Hypotonia/hyporeflexia

After the examination

Ask the patient if he has any questions or concerns.

Thank the patient.

Ensure that he is comfortable.

Ask to carry out a full neurological examination.

Summarise your findings and offer a differential diagnosis.

Conditions most likely to come up in a gait, co-ordination, and cerebellar function examination

station

Hemiplegic gait:

the pelvis tilts upwards, the hip is abducted, and the leg is swung forwards in a semi-circular

movement.

the leg is stiff and extended but the arm may be held in flexion and adduction with minimal

swing.

Scissor gait:

a spastic gait seen in cerebral palsy and resulting from muscle contractures.

the hips, knees, and ankles are flexed, producing a crouching and tiptoeing appearance.

in addition, the hips are adducted and internally rotated, such that the knees cross or hit each

other in a scissor-like movement.

Festinating gait:

seen in Parkinson’s disease.

short shuffling steps with stiff arms and legs and stooped posture; difficulty starting and

turning.

Ataxic gait:

seen in spinal and cerebellar lesions and in alcohol intoxication.

unsteady, broad-based gait with a lurching quality.

Neuropathic gait:

seen in peripheral neuropathies.

weak foot dorsiflexors result in a high-stepping gait with foot-slapping; the high-stepping is

an attempt to prevent the foot from dragging and being injured; also called ‘high-stepping

gait’ or ‘foot-slapping gait’.


Neurology

Station 37 Gait, co-ordination, and cerebellar function examination 99

Trendelenburg gait:

seen in weakness of the hip abductors or in an inability or reluctance to abduct the hip, e.g.

due to a fractured neck of femur or to arthritic pain.

the pelvis tilts to the unaffected side in the stance phase; as a result, the trunk lurches to the

affected side in an attempt to maintain a level pelvis.

bilateral Trendelenburg results in a typical waddling gait.

Antalgic gait:

seen in arthritis and trauma.

avoidance of motions that trigger pain.

often quick, short, and light footsteps.

not to be confused with a Trendelenburg gait.

Myopathic gait:

in muscular diseases the proximal pelvic girdle muscles are most affected, such that the

patient is unable to stabilise the pelvis in the stance phase.

the pelvis drops to the side of the leg being raised, and this results in a broad-based, waddling

gait.


Clinical Skills for OSCEs

100 Station 38

Speech assessment

The patient is likely to find the assessment difficult and distressing, so remember to be especially

empathetic. In particular, do not rush the examination or keep on interrupting the patient, but move

at a pace that feels comfortable for him.

Table 17. Definitions

Dysphonia Motor impairment of ability to vocalise speech

Dysarthria Motor impairment of ability to articulate speech

Dysphasia Cognitive impairment of ability to comprehend or express language

Aphasia Complete inability to comprehend or express language

Note: Expressive dysphasia (Broca’s area, in the inferolateral dominant frontal lobe) and receptive

dysphasia (Wernicke’s area, in the posterior superior dominant temporal lobe) often co-exist.

Before starting

Introduce yourself to the patient.

Confirm his name and date of birth.

Explain the assessment and obtain his consent.

Check that he speaks English and that he can hear you.

Ask him to try to describe his current problems.

The assessment

Orientation in time and place

Time

Name: (year) (season) (month) (date) (day)

Place

Name: (country) (county/region) (town) (hospital) (floor)

Dysphasia

Expressive

Assess whether the patient has difficulty in finding the right words whilst in conversation with you.

You could ask directly, “It seems like you know what you want to say but you’re struggling to get the

words out. Am I right?”

Nominal

Nominal dysphasia is a common form of expressive dysphasia. Ask the patient to name some common

objects such as a watch, pen, or badge; then to name the components of some of these objects, e.g.

hour hand, winder, strap, picture. If he is unable to name the object, ask him what it does: a correct

answer can help to distinguish nominal from receptive dysphasia.


Neurology

Station 38 Speech assessment 101

Receptive

Assess whether the patient has difficulty understanding you by asking him to carry out some simple

instructions such as ‘shut your eyes’, ‘touch your nose’, and ‘point to the door’. If appropriate, try out

a more complex three-stage command, for example, “Using your left hand, touch your nose and then

touch my finger.”

Conductive

Conductive aphasia is the inability to repeat words or phrases despite intact understanding. Ask the

patient to repeat, “No ifs, ands or buts.”

Dysarthria

Ask the patient to repeat some of the following: ‘British constitution’, ‘West Register Street’, ‘Baby

hippopotamus’, ‘Biblical criticism’, ‘Artillery’.

Assess the structures involved in phonation and articulation by asking the patient to repeat:

‘Me, me, me’ Lips.

‘La, la, la’ Tongue.

‘Ah’ Palate, larynx, and expiratory muscles.

Dysphonia

Make a note of the patient’s volume of speech, which may be low if there is weakness of the

vocal cords or respiratory muscles. Ask him to cough, and look out for ‘bovine’ cough, which

would suggest a lesion of cranial nerve X impairing the closure of the vocal cords.

Dyslexia

Correct the patient’s vision and ask him to read a short paragraph from a newspaper or magazine, and bear in mind that not all people who can’t read are dyslexic!

Dyscalculia

Ask the patient to carry out simple sums and subtractions.

Dysgraphia

Ask the patient to write a sentence.

After the assessment

Ask the patient if he has any questions or concerns.

Thank him.

Summarise your findings, offer a differential diagnosis, and state the probable area of the lesion.

Suggest a plan for further investigations and management, for example, mental state examination, full neurological examination, and speech and language therapy assessment (including an

assessment of swallowing).


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