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5 Possible Scenarios
Please examine this patients..
1. Eyes 2. Cranial nerves excluding the eyes 3. Speech 4. Upper or Lower Limb 5. Cerebellar system
CRANIAL NERVES
SPINAL
CORD
SPINAL NERVES
N M J
LIMB MUSCLES
UMN
LMN
SCENARIO 1
Please examine this patients eyes
System
Inspection
Optic nerve (II) Eye movements (III, IV, VI)
Inspection
Clues by bed
Eyepatch: diplopia Magnifying glass: poor acuities
Face
Ptosis Pupil size / symmetry
TIP 1
Whenever you see asymmetrical pupils, look for ptosis
TIP 2
Whenever you see ptosis, look at pupil sizes
Usuallly Holmes Adie pupil (parasympathetic lesion) large at onset shrinks with age Think Myasthenia Gravis (levator palpebrae)
II
Acuity Fields Fundoscopy Pupillary reflexes
60
36 24 18 12 9 6 5
Visual Fields
L
ANTERIOR
Optic Nerve
2. Bitemporal hemianopia
Chiasm
3
POSTERIOR
Visual Fields
Normal
Optic Atrophy
Causes
1. MS
Papilloedema
Causes
1. Raised ICP 2. Hypertension
Pupil reflexes
Light (direct + consensual)
Normal pupil
constricts to light, dilates to dark
Accommodation
Failure suggests Holmes Adie or 3rd N palsy
III, IV, VI
Eye movements
Range Diplopia Nystagmus
3 6 3
R eye looking down +/- out So this is a (partial) right-sided 3rd (oculomotor) nerve palsy
Summary
II
III,VI Ptosis
Scenario 2
Please examine the cranial nerves excluding the eyes
System
Inspection I V VII VIII IX-X XI XII
I
Have you noticed any change in your sense of smell?
If yes, may be due to frontal lesions (eg tumour), or neurodegenerative conditions (Alzheimers, Parkinsons)
V
Sensory Motor Reflex
C2
Clench teeth
Feel masseter & temporalis
VII
Motor Distinguish between UMN & LMN
Inspection
VIII
Test with whispered numbers or finger rub Cover c/l ear
If u/l hearing loss, say I would like to perform Rinnes and Webers tests to distinguish between sensorineural and conductive deafness
Interpreting Rinnes
Normal
AC > BC
Sensorineural
AC > BC
Conductive
BC > AC
NB. Webers test just confirms conductive deafness
IX - X
IX
Sensory (gag)
X
Motor (uvula)
XI
Trapezius
Shoulder shrug
Sternocleidomastoid
Turn your head against my hand Remember you are testing muscle on opposite side
XII
Inspection (in mouth) Deviation Strength Speed
Tongue deviates to left Strong (R) side pushes weaker (L) side past the midline So this is a left-sided 12th (hypoglossal) palsy
Summary
I, IX,X,XI V VII very rare stroke; MS UMN: stroke LMN: Bells sensorineural: age, neuroma conductive: wax, otitis media stroke; MND
VIII
XII
Scenario 3
Please examine this patients speech
System
Easy question Free speech: Comprehension Naming Consonants Phrases (eg name, address) listen carefully! (increasing sophistication) (increasing sophistication) (p, t, k) (british constitution, baby hippopotamus, west register st)
Fluent
Comprehension intact
Normal Receptive dysphasia
Comprehension affected
Non-fluent
Naming problems
Expressive dysphasia Dysarthria
Articulation problems
Types of Dysarthria
Cerebellar
Explosive (poor control of volume) Staccatoed
Bulbar/Pseudobulbar
Nasal Strangled
Parkinsonian
Quiet Mumbled
Summary
Dysphasia
Dysarthria
Consonant Cerebellar
Bulbar/Pseudobulbar Parkinsonian
Stroke (CT)
VII, IX-X, XII (MRI) MS (MRI), tumour (CT), genetic (gene test) MND (EMG), Strokes (MRI) Myasthenia (Ach R ab, EMG) Parkinsons! (clinical)
Scenario 4
Please examine this patients upper / lower limbs
So you need an anatomical / structural overview of the nervous system And a list of 3-4 differentials for each site
Structure
MRI
Vascular (stroke) Tumour Central demyelination (multiple sclerosis) Infection (herpes encephalitis, zoster myelitis) Degenerative disease (Parkinsons, Alzheimers)
NCS/EMG
Structure
NCS/EMG
Peripheral nerve
Diabetes Alcohol/drugs Genetic (Charcot-Marie-Tooth) Peripheral demyelination (Guillain-Barre) Infection (syphilis)
NCS/EMG
Muscle
Genetic Muscular dystrophy Myotonic dystrophy Mitochondrial myopathy Myositis Gene test Gene test Muscle biopsy CK, ENA
Inspection
Bedside
Walking aids
Patient
Wasting & Fasciculations (LMN) Spotters
Parkinsons Myasthenia gravis Myotonic dystrophy
LMN
Wasting
Fasciculations
Parkinsons
Reduced facial expression
Rest tremor Bradykinesia ( if undertreated) Dyskinesia ( from treatment)
Myasthenia gravis
Ptosis (u/l or b/l) Difficulty rising from chair with arms folded
Myotonic dystrophy
Bilateral ptosis Grip myotonia Tent-shaped mouth
Tips 1 and 2
Best ways to start a limb examination
For UL exam
First test arms outstretched
For LL exam
First test gait
UL exam
Gross weakness
Subtle UMN weakness Cerebellar sign
Rebound
Pseudoathetosis
Proprioceptive loss
LL exam
Funny walks
Ataxic
Broad base
Shuffling
Waddling
Parkinsonian
Myopathic
Stamping
High stepping Circumduction Antalgic
Neuropathic
Foot drop UMN Non-neurological / functional
Tone
Upper Limbs
Elbow: flexion / extension, feel Wrist: flexion / extension & rotation, feel
Lower Limbs
Knee: Knee: Ankle: Ankle: flex hip quickly, observe for heel lift from bed flexion / extension, feel roll thigh, observe movement rapidly flex knee and ankle, observe for clonus
Tone
Abnormal tone
Reduced (Flaccid)
Difficult unless clear asymmetry
Increased
Clasp knife (Spastic) Lead Pipe / Cogwheel (Rigid)
Tone
Pyramidal
Sudden give/catch
Extrapyramidal
Even resistance
Power
Start proximally, work distally Compare R with L Isolate the joint when testing
UL SAB
EF/EE WE FAB Thumb abduction
LL
HF/HE KF/KE DF/PF
Power
MRC Grading
0 1 2 3 4 5 no muscle or joint movement muscle contraction only joint movement (gravity removed/aided) joint movement (despite gravity) joint movement (despite resistance) full power
Power
Tip 3
Interpreting power findings
Look for patterns of weakness
Patterns of Weakness
Focal v Diffuse
Proximal v Distal?
Muscle
Neuropathy
Neither
Pyramidal (UMN)
Non-specific
Patterns of Weakness
Focal weakness
Wrist drop
Radial nerve palsy C7 radiculopathy
Foot drop
Common peroneal nerve palsy L5 radiculopathy
Patterns of Weakness
Proximal v Distal
Proximal
Muscle / Neuromuscular junction EXCEPTION: Myotonic dystrophy
Distal
Peripheral Neuropathy AND Myotonic dystrophy
Patterns of Weakness
UMN
Posture
Flexed, Pronated arm
Reflexes
Hold Tendon hammer loosely
Compare sides Practice reinforcement Babinski
Scratch outside of foot and round below toes Observe the first movement of the big toe only
Reflexes
Root levels
(1 2 3 4 5 6 7)
Ankle Knee Biceps Supinator Triceps S1 L2,3,4 C5,6 C5,6 C7
Reflexes
Interpretation
Absent (after reinforcement)
LMN lesion Very helpful sign But remember acute UMN areflexia
Brisk
Normal: Young, anxious Abnormal: UMN
Especially if asymmetrical
Lower Limbs:
Heel-shin Tandem gait
Sensation
Difficult! This will be taken into account. Learn the dermatomes & practice them
Sensation
Tip 4
Once again, look for patterns!
Sensation
2. Dermatomal
root lesion cord lesion (sensory level)
T4 (nipples) T10 (umbilicus)
3. Romberg
Implies proprioceptive or vestibular failure, NOT cerebellar disease
Scenario 5
Please examine this patients cerebellar system
Cerebellum
System
Speech Eyes Arms Legs Gait
Cerebellum
Speech
How did you get here today Repetition
British Constitution West Register Street Baby hippopotamus
Cerebellum
Eyes
Nystagmus
Increases towards side of cerebellar lesion
Eye movements
Pursuit (slow tracking movements) Follow my finger
Broken, jerky
Cerebellum
Arms
Fingernose
Tip of nose to tip of finger as quickly and accurately as possible
Observe past-pointing, intention tremor (NB,. If tremor seen, check rest & postural components)
DDCK
Tap your hand like so (demonstrate) as fast as possible
Observe errors
Legs
Heel-shin
Place your heel onto your knee Then run it down your shin As quickly and accurately as possible Observe: overshooting
Cerebellum
Gait
First test truncal ataxia on bed
Ability to sit upright unsupported
Then stand them, observe base Then ask to walk normally, observe base Assess balance, especially on turns Ask to walk heel to toe (tandem), unless too unsteady
Cerebellum
Causes?
Same as for rest of brain: Stroke MS Tumour Infection Degenerative (genetic)
SUMMARY
Summary
Tip 5
Dont be too specific with the diagnosis
Identify the site of the lesion from the findings Then reel off your pre-prepared differential
Motor summary
UMN (Corticospinal) Inspection UL flexed LL extended Spasticity Pyramidal weakness Brisk Babinksi+ Ataxic Circumducts Festinant Reduced armswing Bradykinesia Soft voice Broad based Waddling Basal ganglia Cerebellar Anterior horn, root, nerve Wasting Fascics Reduced Distal weakness Absent Proximal weakness Proximal weakness Absent Neuromuscular junction Ptosis Muscle Rest tremor Mask-like face Lead pipe/ cogwheeling Titubation Ptosis Wasting
Additional Features
Pronator Drift
Dysarthria Nystagmus
Fatigueable
(with patient) (with examiner) (with examination) (with findings) (with diagnosis & DD) (with investigations)