Documenti di Didattica
Documenti di Professioni
Documenti di Cultura
NEUROLOGY:
BATCH 2019 A/Y 2015-2016 MINI OSCE REVIEWER
Outline
I. Examination the cranial nerve: steps and how to report your findings
II. Pathway of the cranial nerve
III. Theoreticals
Legend
Blue – Demyers;
Red – asked/said during preceptorials
Table of Contents
Cranial nerve I ...................................................................................................................................................................................... 2
Cranial nerve II .................................................................................................................................................................................... 3
Cranial nerve III .................................................................................................................................................................................. 10
Cranial nerve IV ................................................................................................................................................................................. 19
Cranial nerve V ................................................................................................................................................................................... 20
Cranial nerve VI ................................................................................................................................................................................. 26
Cranial nerve VII ................................................................................................................................................................................. 28
Cranial nerve VIII ............................................................................................................................................................................... 32
Cranial nerve IX .................................................................................................................................................................................. 35
Cranial nerve X .................................................................................................................................................................................. 35
Cranial nerve XI .................................................................................................................................................................................. 39
Cranial nerve XII ................................................................................................................................................................................ 40
LEFT RIGHT
1. Ask patient first if he has a cold or any olfactory problem at the
moment.
2. Check the patency of both nostrils by placing a tissue against a
nostril and asking the patient to blow through his nose.
3. Ask the patient to close his eyes.
4. While one nostril is occluded, ask the patient to sniff and identify
the various odorants.
5. For the second trial, compress the opposite nostril and this time do
not present the stimulus.
6. The 3rd time, present the stimulus to the untested nostril.
How to report
The patient has patent nostrils with intact cranial nerve 1
II. Pathway
Olfactory bulb
Olfactory tract
III. Theoretical
I. Steps
DIRECT
1. Shine light in from the side of each eye to gauge pupil’s light reaction.
2. Observe for constriction.
CONSENSUAL
1. Watch the patient’s left eye while shining on the right.
2. Observe for constriction.
How to report
PERRLA as shorthand for “pupils equal, round and react to light and in accommodation”.
CN II – afferent and CN III – efferent (a2e3)
Direct and Consensual reflex are intact.
Damaged CN II of eye A
o When light shines on eye A: no response in either eye: “negative direct and consensual responses”
Damaged CN III of eye A
o When light shines on eye A: no response in A, but positive consensual response of B: “negative direct but
positive consensual response”
Example: Pupils 3 mm, equal, centered, react to light and in accommodation and dilate promptly in dim light.
VISUAL ACUITY
Snellen’s/Jaeger’s Test:
1. Allow the patient to use his/her glasses if available. (Although glasses
improve acuity by correcting for a refractive error, they do not improve
acuity impaired by opacities of the refracting media of the eye or retinal or
optic nerve lesions)
2. Let the Pt hold a Snellen’s chart at a 20 meter distance. (Jaeger’s chart at a 20/____ 20/____
14 inch ‘reading’ distance or arm’s length of the patient)
3. Have the patient cover one eye at a time.
4. Ask the Pt to read progressively smaller letters until they can go no
further.
5. Record the smallest line the patient read successfully. Repeat with the
other eye.
20/____ 20/____
If vision is not 20/20, do Pinhole Test
____/____ ____/____
If still not able to see letters, let the Pt move closer to the chart (10m away, 5m
away).
VISUAL ACUITY OF PARTIALLY BLIND
1. If still not able to see letters, check for Counting Fingers
How to report
Visual acuity is __/__ for the right and __/__ for the left.
A 20/30 vision means normal people could see from “30 meters away” what the Pt sees 20 meters away.
If the Pt is 10m or 5m away from the chart: A 10/30 vision means normal people could see from 30m away what the Pt
could see from 10m away.
CONFRONTATION TEST
1. Station yourself directly in front of Pt. Start with your left eye directly in 45: _____ 45: _____
line with the Pt’s right eye, at a distance of about 50 cm—eye to eye but
not breath to breath. The Pt covers the left eye with the left hand.
2. Hold up your left index finger just outside your own peripheral field, in the 135: ____ 135: ____
inferior temporal quadrant. Hold the finger about equidistant between
your eye and the Pt’s.
3. Move finger very slowly toward the central field. Request the Pt to say 225: ____ 225: ____
“now” as soon as the finger is seen. Try to match the perimeter of the Pt’s
visual field against your own. Test all quadrants of each eye separately,
each time starting at the limit of the field. 315: ____ 315: ____
4. After surveying the visual field by the wiggling finger, you can refine the
test by asking the Pt to count the number of fingers presented in each of
the four quadrants of the visual field of each eye. Then randomly hold up
one, two, or five digits (three or four is too complicated) in each quadrant
for the Pt to count.
5. Instruct the patient not to look at your nose. The Pt’s eyes will converge,
and your fields will not match.
How to report
On visual confrontation, ‘there are no visual field cuts’ or ‘there is bitemporal hemianopia’ or ‘there is left/right
homonomous hemianopia’
How to Test:
OPTIC DISC
Color (Pink/Pale): if pale → optic atrophy
Margins (Clear): if blurred margin or indistinct border (cannot see disc
well) → Optic disc swelling (pappilledema due to increased ICP)
State of Cup → Deep pale cup – Glaucoma
MACULA (located one disc size temporally/lateral; is avascular; larger than the
disc; and with indistinct margins)
Fovea Light Reflex (Note the pearl of light reflecting from the fovea
centralis, the center of the macula. This light reflection fades in older
persons.)
Bleeding, Exudate: (A fluid rich in protein and cellular elements that
oozes out of blood vessels due to inflammation and is deposited in
nearby tissues)
Edema, Drusen: (tiny yellow or white accumulations of extracellular
material)
How to report
The cup-to-disc ratio compares the diameter of the "cup" portion of the optic disc with the total diameter of the optic
disc. A good analogy to better understand the cup-to-disc ratio is the ratio of a donut hole to a donut. The hole represents
the cup and the surrounding area the disc. If the cup fills 1/10 of the disc, the ratio will be 0.1. If it fills 7/10 of the disc,
the ratio is 0.7. The normal cup-to-disc ratio is 0.2:0.5. A large cup-to-disc ratio may imply glaucoma or other
pathology.[2] However, cupping by itself is not indicative of glaucoma.
(-) Papilledema (means blurred or elevated optic papilla resulting from the edema fluid in the nerve fibers as they across
the disc to perforate the lamina cribosa and enter the optic nerve.
A-V ratio 3:2
First to be seen when doing ophthalmoscopy: media (liquid portion). If media is hazy, there is papilledema that may be
indicative of an increased intracranial pressure.
II. Pathway
Rods and cones Optic chiasm Mesencephalon Edinger-Westphal nucleus consensual pupillary constriction equals the
direct constriction
III. Theoretical
Two cranial nerves, II and V, convey afferents from the eye to the brain
1. The optic nerve, cranial nerve (CrN) II, conveys the afferent axons for two functions, the special sense of vision and
pupilloconstriction.
2. The trigeminal nerve, CrN V, conveys the afferents for general sensation: Ocular pain; Tearing reflex; Corneal reflex;
Proprioception from the extraocular muscles
The cone receptors of the macula mediate the two functions of the central field of vision:
i. Visual acuity
ii. Color vision
In the periphery of the retina, concentrically surrounding the macula, rod receptors mediate the two functions of the
peripheral field of vision:
i. Night vision
ii. Motion detection
I. Steps
How to report
(The pupils are symmetrical and measure _ mm, equally & briskly reactive to light/ there is photophobia, etc.)
EXTRAOCULAR MOVEMENTS
CARDINAL POINTS IN AN ‘H’ PATTERN
How to report
Patient was able to follow the finger without moving his head indicating intact cranial nerve 3,4, and 6.
How to report
How to report
Patient was able to look alternately with pupil constriction indicative of intact cranial nerve 3.
During the accommodation reflex for near vision, 3 distinct events occur. The visual axes converge onto the fixation point, the pupils
construct, and the lens thicken.
Convergence: medial recti (skeletal)
Pupilloconstriction: iris (smooth muscle;parasympathetic)
Lens thickening: ciliary muscle (smooth muscle;parasympathetic)
II. Pathway
III. Theoretical
HORIZONTAL GAZE
(Area colored green is the frontal eye field, or Brodmann Area 8.)
To understand how yoking of the eye muscles occur, study the following pathway:
III
Medial Longitudinal
PPRF Fasciculus
VI
LR MR
Right Left
Left!
VERTICAL GAZE
In contrast to horizontal gaze, vertical eye movements are generally under BILATERAL control of the cerebral cortex and the
upper brainstem.
The groups of nerve cells and fibers that govern upward and downward gaze are situated in the pretectal areas of the
midbrain and involve 3 integrated structures:
1. The rostral interstitial nucleus of the medial longitudinal fasciculus (riMLF)
2. Interstitial nucleus of Cajal (INC)
3. Nucleus and fibers of the posterior commissure
Projections for upgaze cross through the commissure before descending to innervate the third nerve nucleus while those
for downgaze may travel directly to the third nerve, thus accounting for the frequency of selective gaze palsies (for
example, upgaze may be paralyzed but downgaze may be preserved).
Clinical relevance
There are three main anatomical causes of an oculomotor nerve lesion:
1. Increasing intracranial pressure – this compresses the nerve against the temporal bone.
2. Aneurysm of the posterior cerebral artery.
3. Cavernous sinus infection or trauma.
Note: there are other pathological causes of oculomotor nerve palsy such as
1. diabetes,
2. multiple sclerosis,
3. myasthenia gravis
4. giant cell arteritis.
The oculomotor nerve is the major nerve supplying the ocular and extraocular muscles.
The clinical signs of CN III injury are all associated with the eye:
1. Ptosis (drooping upper eyelid) – due to paralysis of the levator palpabrae superioris.
2. Eyeball resting in the ‘down and out‘ location – due to the paralysis of the superior, inferior and medial rectus, and the
inferior oblique. The patient is unable to elevate, depress or adduct the eye.
3. Dilated pupil – due to the unopposed action of the dilator pupillae muscle.
Oculomotor nerve palsy. Note the ‘down and out’ position of the eye.
Neurological pathways governing ocular motility (i.e., how our eyes move) are independent of vision (i.e., what the eyes see)
although they are virtually inseparable.
The neural mechanisms that govern eye movements reside mainly in the midbrain and pons (where the nuclei of these cranial
nerves are) but are greatly influenced by centers in the medulla, cerebellum, basal ganglia, and the frontal, parietal and occipital
lobes of the brain.
Conjugate movement of the the eyes – symmetrical and synchronous movement of the eyes
VI VI
LR MR LR MR
PERIPHERAL DISORDER
A. OCULOMOTOR NERVE PALSY
CENTRAL DISORDERS
A. SUPRANUCLEAR – any lesion which can affect the frontal eye fields and the pathway down to the PPRF
B. INTERNUCLEAR – between the PPRF and cranial nerve nuclei
III
PPRF PPRF
VI VI
LR MR
R L
In medial longitudinal fasciculus syndrome, upon asking the patient to look to the RIGHT, the right eye abducts, while the LEFT eye
remains frozen (adduction failure of the LEFT eye)
Upon asking the patient to look to the LEFT, both eyes can look to the LEFT.
“One-and-a-half syndrome”
Left frontal eye field
III
PPRF PPRF
VI VI
LR MR
Upon asking the patient to look to the right, RIGHT eye abducts (with nystagmus), while LEFT eye remains midline.
Upon asking the patient to look to the left, both eyes are still.
Suppose one horizontal movement, say abduction, is ½; and adduction, ½. In this scenario, the only remaining movement is
abduction of one eye, and the other 1 ½ movements are affected, hence the name “one and a half syndrome.”
1. PARINAUD SYNDROME
Usually results from a mass lesion involving the region of the posterior third ventricle and upper dorsal midbrain
Also known as Sylvian aqueduct syndrome, dorsal midbrain syndrome, or the syndrome of the posterior commissure.
The pupils may have a poor, rarely absent, light response, and much better near response.
The pupils also tend to be large.
Consists of:
Paralysis of upward gaze
Failure of convergence
Retraction nystagmus
“Setting sun” sign
1. Spontaneous movements during ordinary Inspection while taking the history. Look for
behaviour and ordinary environmental stimuli malalignment, range and persistence of eye
movements, and for hyperkinesias such as
nystagmus.
2. Volitional fixation and volitional movements Examiner observes steadiness and range of eye
movements after commanding the patient to fixate
on a distant object straight ahead and then to move
the eyes to the right, left, up and down.
c. Reflex fixation The patient fixates straight ahead and the examiner
turns the patient’s head slowly to the right, left, up
and down.
a. Caloric nystagmus – study this and how to Irrigation of ears with hot or cold water.
interpret
c. Contraversive eye-turning test (Doll’s eye test, Quick turning of the patient’s head by the examiner’s
oculo-cephalic test) – study this, and interpretation hands; used in comatose patients
of the test
Pupillary defects
EXTRAOCULAR MOVEMENTS
1. During the history, the Ex judges the range of volitional eye
movements.
2. Start the formal examination with the Pt sitting. Gently press on
top of the Pt’s head with one hand and fix the head in position by
a “proprioceptive link” between yourself and the Pt, permitting
only the eyes to move. Mentally retarded or demented Pts have
difficulty separating eye and head movements.
3. Ask the Pt to fixate on your finger, which you hold up in the
midline, about 50 cm away
___ ___
4. Request the Pt to follow your finger with their head still, moving
___ ___
their eyes only.
___ ___
5. Move your index finger in an H shape in front of the patient so
___ ___
that the patients eyes are seen to move fully to right, left,
___ ___
superior, inferior and oblique.
___ ___
look for extra ocular palsy and nystagmus
ask the patient to tell you if they have any double vision
Avoid extremes of gaze as this can cause a physiological
nystagmus
How to report
“ Cranial neve 4 is intact”
II. Pathway
The trochlear nerve provides motor innervation to only one of the extraocular muscles of the eye, the superior oblique
muscle (a common mnemonic is SO4).
The nerve cell bodies of GSE neurons reside in the trochlear nucleus, which lies adjacent to the midline in the tegmentum of
the caudal midbrain.
Fibers arising from this nucleus initially descend for a short distance in the brainstem and then course dorsally in the
periaqueductal gray matter. The fibers decussate posteriorly and emerge from the brainstem at the junction of the pons
and midbrain, just below the inferior colliculus.
III. Theoretical
The superior oblique originates from the lesser wing of the sphenoid bone, just above the annulus of Zinn. Its tendon runs
through a trochlea (pulley) attached to the rim of the bony orbit
When the tendon runs to the eye, it inserts posteriorly to allow the superior oblique to have an effective pull when
contracting. In so attaching, the tendon runs somewhat medial to the vertical axis, like the superior and inferior recti.
Contraction of the superior oblique, when the eye starts in the primary position, causes:
CN IV Palsy
I. Steps
IPSILATERAL SIDE.
WEAK NORMAL REMARKS
RIGHT SIDE
LEFT SIDE
How to report
All muscles for mastication (Masseter, Temporalis and Pterygoids) are intact on both sides.
3. Then ask the patient to close his/her eyes. 2. Ngayon naman po, ipikit ninyo ang
4. Alternately touch the areas of the face (Opthalmic/ Maxillary/ mata ninyo at sabihin po ninyo kung
Mandibular) using your fingers as HOT and tuning fork as COLD, randomly. MAINIT o MALAMIG ang naramdaman
5. In touching the areas of the face, ask the patient if it is HOT or COLD. ninyo..”
How to report
Touch Sensation
Patient can/cannot able to detect light touch in all areas.
There is _____% deficit to light touch on R/L part of the face on V1/V2/V3 branches of the trigeminal nerve
Pain Sensation
Patient can/cannot able to detect pain in all areas.
Temperature Discrimination
Patient can/cannot able to discriminate hot and cold temperature in all areas.
Corneal Reflex
Positive/Negative corneal reflex.
Corneal Reflex of R/L eye is not responsive to touch.
II. Pathway
III. Theoretical
Sensory: Face
Motor: Muscles for Mastication
Temporal
Lateral and Medial Pterygoids
Masseter
trigeminal nerve is a mixed nerve. It has a larger component consisting of sensory fibers for the face and a smaller component
consisting of motor fibers for muscels of mastication
CN V conveys no efferents to glands or smooth muscle and no special afferents
Trigeminal Nerve three large branches:
V1- Opthalmic
V2- Maxillary
V3 - Mandibular
V1 and V2- Sensory
V3- Sensory and Motor
Tip of the nose – V1
Angle of the mandible- Not included sa
CN V kasi C2 na un.
o Mesencephalic nucleus
→ propioception of the face (feeling of position of the muscles)
→ The only structure in the CNS to contain the cell bodies of a primary afferent, which are usually contained within
ganglia
→ Peripheral processes of neurons in this nucleus receive impulses from peripheral receptors in the muscle spindles in
the muscles of mastication, and from other receptors that correspond to pressure
Clinical relevance
Lower motorneuron lesions (LMN)
Unilateral destruction of the axons of the CN V causes complete paralysis of all IPSILATERAL chewing muscles
Denervated muscles undergoes:
o atrophy and paralysis
The 2 most obvious sign of Lower motorneuron lesions (LMN)
Masseter - the most readily palpated muscle for atrophy
Right Side is Stimulated tapos ung Left Side ang nag blinked
Stimulation of one cornea causes contraction of the ipsilateral pterygoid muscle and a twitch of the jaw to the opposite
side.
o So kunwari stimulate mo ung right eye, ung magco contract ay ung RIGHT ipsilateral pterygoid muscle tapos ung
jaw mag ti twitch sa LEFT
It may indicate a UMN lesion more sensitively in amyotrophic lateral sclerosis than other UMN signs.
Consist of bilateral contraction of the orbicularis oculi muscle in response to percussion of the glabella with the fingertip or
a percussion hammer or to electrical stimulation of the supraorbital branch of the trigeminal nerve.
Trigeminal neuralgia
- The most common ailment affecting CN V (usually V1 and V2)
- Very painful when you chew or eat
I. Steps
Shape of pupils
Size of pupils
Ptosis
Lateral Rectus
Medial Rectus
Superior Rectus
Inferior Rectus
Superior Oblique
Inferior Oblique
Note
II. Pathway
Main Nucleus
The abducens nucleus is located in the pons, on the floor of the fourth ventricle, at the level of the facial colliculus.
Motor axons leaving the abducens nucleus run ventrally and caudally through the pons.
The abducens nerve leaves the brainstem at the junction of the pons and the medulla, medial to the facial nerve. In
order to reach the eye, it runs upward (superiorly) and then bends forward (anteriorly).
Remember!
Nuclei: Abducens Nerve
Origin: Junction of Pons and Medulla
Opening: Superior Orbital Fissure
Supplies: Motor and Lateral Rectus Muscle
III. Theoretical
Clinical relevance
Paralysis of the Lateral Rectus Muscle - Medial Strabismus and Horizontal Diplopia
A lesion in the abducens nerve result in paralysis of the lateral rectus muscle that normally ABDUCTS the eye. The
eye will then deviate medially as a result of the unopposed action of the medial rectus. The individual can turn the
ipsilateral eye from its medial position to the center (looking straight ahead), but not beyond it - Medial
strabismus (Convergent, internal strabismus, esotropia)
Eyes become misaligned, the individual experiences - Horizontal diplopia (Double Vision)
I. Steps
Inspect the face, both at rest and during conversation with the patient. Note any asymmetry (Asymmetry of Frontalis muscle,
Asymmetry of wrinkles for orbucularis oculi, asymmetry of nasolabial fold for Buccinator and asymmetry for Platysma), and observe
any tics or other abnormal movements.
NOTE: Asymmetry is the clue to unilateral weakness and is best perceived during conversation when the patient is unaware of being
observed.
How to report
Normal/abnormal nasolabial fold, eyelid sagging, mouth drooping
Intact cranial nerve 7 (if no significant findings)
How to report
Able/not able to do unilateral facial movements on (both) right and left side of the face
Do test for Taste - Cranial Nerve VII is responsible for taste sensation in the anterior 2/3 of the
tongue
Prepare:
Directions:
II. Pathway
III. Theoretical
All first-order sensory neurons are found in the geniculate ganglion within the temporal bone.
exits the brainstem in the cerebellopontine (CP) angle.
enters the internal auditory meatus and the facial canal.
exits the facial canal and skull via the stylomastoid foramen.
mediates facial movements, taste, salivation, and lacrimation.
***Remember the clinically important functions of CrN VII other than innervation of facial muscles, this will be one of the anticipated
questions during our OSCE according to our Preceptor
Functions of the facial muscles (Frontalis muscle, Orbicularis oculi, Buccinator and Platysma)
(1) Peripheral lesion of CN VII, the facial nerve, anywhere from its origin in the pons to its periphery in the face
(2) Central lesion involving the upper motor neuron system between the cortex and the pons.
These can be distinguished by their different effects on the upper part of the face. The lower part of the face normally is controlled
by upper motor neurons located on only one side of the cortex—the opposite side.
Left hemispheric damage to these pathways, as in a stroke, paralyzes the right lower face. The upper face, however, is controlled by
pathways from both sides of the cortex. Even though the upper motor neurons on the left are destroyed, others on the right remain,
and the right upper face continues to function fairly well.
A peripheral lesion of CN VII, exemplified here by a Bell’s palsy, is compared with a central lesion, exemplified by a left hemispheric
cerebrovascular accident:
I. Steps
2. Ask the patient about hearing deficits or has tinnitus. (abnormal sound perceived in the ear, hearing buzzing, clicking, ringing or
roaring sounds that only the patient can hear. Subjective tinnitus-arises not from real sounds but from auditory system disorder
eg. Presbyacusis, cochlear dse., or caused by drugs such as salicylates, loop diuretics, “mycin antibiotics, quinine , cysplastin.
Objective tinnitus is caused by real sound, audible to the Ex. Eg. Bruit from AV malformation, fistula.)
3. Do Otoscopy to ensure that the external auditory canals are open and that the eardrums are normal. (check for damaged
eardrums, wax, foreign bodies in EAC, etc.-mechanical impediment to sound conduction. )
How do you pull the ear for otoscopy? Pull the ear superiorly, posteriorly, laterally
Adult: up and out
Pedia: down and out
4. Rub your fingers together beside the patient’s ear and then the other.
5. Present a vibrating tuning fork prongs perpendicularly to each of the patient’s ears alternately and ask the patient to compare
loudness.
(forks with 512-2000 cps match frequencies most imp’t for speech perception.)
To semi quantitate the test, move the fork from one ear to the other and ask the Pt to compare the loudness of the sound in the
two ears. Also compare the distance from the ear at which you hear the sound with the distance at which the Pt hears it.
7. Air-Bone conduction test of Rinne compares the efficiency of the conduction of sound vibrations by bone and by air. (sensory
neural)
perform Rinne’s test with watch – usually sound is heard thru air conduction twice longer than bone conduction.
a. Hold a faintly vibrating tuning fork on the patient’s mastoid process until patient says that the sound can no longer be
heard.
b. Hold the same vibrating tuning fork to the patient’s ear.
c. Ask the patient to compare the sound with a tuning fork applied to the bone compared to that heard with the ear.
d. Report the findings on the Rinne test.
Analysis: Px hear better with tuning fork applied to his mastoid = conduction hearing loss.
*Conduction (mechanical) hearing loss- due to impediment of the conduction of sound vibration through the EAC or ossicles of the
middle ear.
If Px showed reduced hearing for air and for bone conduction = neurosensory loss.
*neurosensory hearing loss- reduction of hearing by a lesion of the organ of corti or of the auditory nerve- CN VIII.
If you press your fingertip in your ear completely occluding the ext. ear canal while holding a tuning fork against your mastoid, the
sound gets louder. This shows that even a mechanical obstruction of auditory canal decreases sound by air conduction, it causes
increase in bone conduction.
Bone mechanically transmits vibrations to the inner ear. It tests the integrity of the nerve. Neurosensory hearing loss impairs the
hearing of high frequencies by air conduction and decreases hearing via bone conduction. Nerve lesions block hearing by air and
bone, mechanical lesions block air conduction.
a. Place a vibrating tuning fork on the middle of the Pt’s forehead or on the vertex of the skull.
b. Ask the patient if sound is equally heard in both ears.
c. Report the findings of Weber’s test
***Normal person hears the vertex vibration equally in both ears. If a mechanical impediment blocks sound conduction in
one ear, the vertex sound localizes to the same ear. (R- heard louder, R ear impeded). If the Pt has auditory nerve lesion on
one side, the vertex vibration sounds loudest on the opposite side. Only a consistent lateralization to one side after several
trials is considered significant.
SBCM 2019 SECTION A Page 32 of 42
SAN BEDA COLLEGE OF MEDICINE
NEUROLOGY:
BATCH 2019 A/Y 2015-2016 MINI OSCE REVIEWER
9. Schwabach’s Test
a. Strike the tuning fork and place it on the mastoid area of the patient
b. Tell the patient to notify you if the sound is gone
c. If the patient says the sound is not already heard, put the tuning fork on your mastoid area to clarify
***Normally, wala ka na dapat marinig pag nilagay mo yung tuning fork sa mastoid mo. Pag nilagay mo sayo at may narinig
ka pa after the patient verbalized na wala na sya marinig, then there’s a problem.
a. Forewarn and position the Pt: Because of discomfort, the Ex should warn the Pt about the test, but mentioning the
expected symptoms voids the objectivity and validity of the test. Therefore, say this: “I will be rinsing your ear. It’s
somewhat uncomfortable, but I want you to pay attention to what you feel.” Because vertigo may cause the Pt to fall, place
the Pt in a sitting or reclining position.
b. Do otoscopy: Exclude a mechanical impediment such as wax, otitis, or a perforated eardrum that might allow water into
the middle ear, causing pain and infection. Remove excessive wax that may preclude adequate heat conduction.
c. Place spectacles on the Pt that have strong positive lenses (+10 to 30 diopters, Frenzel lenses). (You can buy them cheaply
in chain stores.) The lenses serve two purposes. They magnify the Pt’s eyes, making any nystagmus easier to see, and they
impair fixation by blurring vision. Fixation inhibits vestibular-induced nystagmus. Thus, the glasses increase the likelihood of
eliciting nystagmus, and make it easier to study if it occurs
d. Instruct the Pt to gaze ahead: Place an emesis basin or a towel next to the Pt’s ear to prevent wetting the Pt (and also for
emergency service should the Pt vomit).
e. Irrigate the ear with warm or cold water: Barber (1974) advocated instilling only 2 mL of ice water through a 14- to 16-
gauge needle. Tilt the Pt’s head to the opposite side and hold the water in the canal for a timed 20 seconds. After 20
seconds, place the horizontal canal vertical and watch for nystagmus. For a second method, fill a 50-mL syringe with water
at a temperature of 7°C above or below the normal 37°C of body temperature (30°C or 44°C). Gently instill the 50 mL of
water through a short rubber tube into the external auditory canal over a timed period of 40 seconds. Test both ears
because a consistent difference is required for significance. Wait about 5 minutes between each test.
f. Observe the Pt’s responses: At the end of irrigation, ask the Pt to direct the gaze more or less ahead and hold the arms
straight out. Inspect the Pt for the following:
g. Ask about symptoms: Ask whether the caloric irrigation reproduced the Pt’s usual sensation of movement, and ask about
the direction of any vertigo.
Patients with vertigo and postural deviations sometimes report confusing directionality, depending on whether
they are attending to their vertigo or their body tilt.
Normal individuals also respond somewhat variably to caloric irrigation.
Some Pts show little or no response from either ear. Determine whether irrigation of the two ears produces any
consistent difference.
a strong normal response from the right ear with little or no response from the left indicates a lesion of the
vestibular end organ, nerve, or immediate central connections on the left.
Hear whispering
[ ] Close [ ] Close
[ ] Close [ ] Close
Whisper
Air Conduction
Bone Conduction
Lateralization [ ] [ ] [ ]
II. Pathway
A. Upon penetrating the brainstem, the cochlear axons synapse at the cochlear nuclei.
B. These nuclei drape around the inferior/caudal cerebellar peduncle.
C. In the auditory pathway, the cochlear nuclei contain the secondary neurons.
D. In ascending through the brainstem, the auditory pathway disperses about equally ipsilaterally and bilaterally. Therefore, if
a Pt has a profound unilateral hearing loss, the lesion most likely would affect an auditory nerve.
E. The name of the auditory pathway that ascends through the brainstem is the lateral lemniscus through which axons run to
the inferior colliculus.
F. From the inferior colliculus, the pathway runs to the medial geniculate body.
G. Neurons of the medial geniculate body relay to the superior surface of the temporal lobe (transverse temporal gyri of
Heschl).
The cochlea senses and codes the vibrations, and nerve impulses are sent to the brain through the cochlear nerve.
From the external ear through the middle ear -conductive phase
Disorder: causes conductive hearing loss
From cochlea and the cochlear nerve - sensorineural phase
Disorder: causes sensorineural hearing loss
III. Theoretical
-Consists of Cochlear (auditory) and vestibular divisions. Cochlear division mediates hearing only and detects sound vibrations bet 20
and 20, 000 cps.
Cochlea contains receptor (organ of Corti) and the cochlear (Spiral) ganglion that originates from Cochlear division of CNVIII.
1. Receptor for hearing: The cochlea contains the receptor (the organ of Corti) and the cochlear (spiral) ganglion that originates the
cochlear division of VIII (see Fig. 9-6).
2. The cochlear ganglion contains the outside primary neurons for hearing.
3. Peripheral course of the cochlear nerve: The cochlear and vestibular divisions of VIII run through the internal auditory canal,
accompanied by CrN VII
4. CrNs VII and VIII attach to the brainstem at the pontomedullary sulcus.
Rinne test: AC>BC (Normal); BC>AC (Conductive hearing loss); AC>BC but not twice as long (Sensorineural)
Weber test: Sound equal in both ears (Normal); Sound lateralize to good ear (Sensorineural);
SPEECH
Test for articulation by the soft tissues, the soft palate, tongue, and lips, with the KLM test. Kuh, Kuh, Kuh tests the function of the
soft palate/velopharyngeal valve; La, La, La, tests the tongue/lingual; Mi, Mi, Mi tests the lips/labials.
La La La
Mi Mi Mi
SSS or Hisssss
V, V, V; Z, Z, Z; F, F, F
ABILITY TO SWALLOW/DYSPHAGIA
Ask the patient to swallow. To test for mild to moderate dysphagia, give the patient a glass containing 150 ml water. The patient
should swallow it a rate exceeding 10ml/s. any patient with dysphagia may aspirate food or fluids into the lung, causing aspiration
pneumonitis.
ABILITY TO SWALLOW
Ask the patient to say Ahh, inspect the tonsillar pillars for asymmetry as they arch upward and medially to form the palate.
Look at the arch, the arch above, not the uvula.
Ask the Pt to repeat: “We see three gray geese” to test palatal function. Traditionally, it was asking the Pt to say, Ahh… But
the vowel E requires tighter palatal closure, though the Pt can say Ah more easily with the mouth open to permit palatal
inspection.
If the palate fails to elevate when the Pt says ‘Ah’ but does elevate during the gag reflex, the Pt
would have a lesion of the UMN.
II. Pathway
The skeletal muscles supplied by CrNs IX and X originally came from branchial arches. The branchial efferent nucleus for IX and X, the
nucleus ambiguus, is in the medulla. CrN IX supplies only one muscle exclusively (stylopharyngeus). Because this muscle aids in
swallowing, its isolated function cannot be tested clinically. The remaining branchial efferent fibers of CrNs IX and X supply the
pharyngeal constrictors. Because they act as a unit in swallowing, the isolated function of the individual constrictors cannot be
tested at the bedside.
Cranial nerve IX innervate palate, tongue, and pharynx. Motor axons innervate the stylopharyngeus and middle pharyngeal
constrictor muscles. Sensory axons mediate taste from the tongue, the gag reflex, and the vasomotor, cardioinhibitory, and
respiratory reflexes of the carotid body and sinus
Normal Swallowing
Swallowing requires afferent information via CrNs V, IX, and X, and motor actions are mediated by CrNs V, VII, IX, X, and XII.
Connections in the region of the nucleus of the tractus solitarius in the medulla, in proximity to the respiratory center, act as a
swallowing center. It coordinates the actions of swallowing and breathing to avoid aspiration.
The levator veli palatini muscle, innervated via the pharyngeal plexus by CrN X, swings the soft palate upward and backward to
contact the posterior wall of the pharynx. This action seals off the naso pharynx from the oro pharynx. Unless the soft palate
elevates, there will be “nasal swallowing” and “nasal speech”.
Swallow
Whistle/ trumpet
Make certain speech sounds
The palate, pharynx, and vocal cords act with bilateral synchrony. By knowing this fact,you can predict that the number of crossed
and uncrossed UMN fibers from each cerebral hemisphere would be about equal. Because of the usual bilateral UMN innervation,
unilateral UMN lesions that cause hemiplegia only rarely cause unilateral weakness of the palate (Willoughby and Anderson, 1984),
but Pts with acute hemiplegia frequently show mild dysarthria (about 60%).
Articulation of Speech
Vowels require palatal elevation. The palate does not completely seal off the nasopharynx during most speech sounds. Instead, it
reduces the nasopharyngeal aperture, thereby detouring most of the air through the mouth, the path of least resistance. Only a few
sounds require complete palatal closure:
Plosive sounds require momentary impounding of air and sudden release (Puh, puh, puh and kuh, kuh, kuh).
Fricatives are high-frequency frictional or rustling sounds (V , V , V… ; Z , Z , Z… ; and F , F , F…) To produce sibilants and fricatives,
you must force a strong stream of air through a small aperture formed by lips, tongue, and teeth.
Removal of the adenoid tissue increases the distance the palate has to close to shut off the nasopharynx. A weak palate is now even
less capable of preventing nasal escape of air.
If the patient does not have any abnormal findings then you can say that “The cranial nerves 9 & 10 are intact”. Kapag naman may
abnormal findings halimbawa hindi sya nag-respond sa gag reflex pwede mong sabihin na “The patient has cranial nerves 9 and 10
deficit” since efferent arc ng gag reflex ang CN X at afferent naman ang CN IX. Tapos sa palate at larynx naman, kung saan magde-
deviate, nandun yung deficit so pwedeng pag sa left “The patient has a left CN X deficit”
V. Other
Electrical stimulation of the vagus nerve, called vagus nerve stimulation (VNS), is sometimes used to treat people with epilepsy or
depression.
The vagus nerve is involved in one of the most common causes of fainting, called vasovagal syncope.
I. Steps
Test for Sternocleidomastoid (SCM) - The sternocleidomastoid is a long muscle in the side of the neck that extends up from the
thorax to the base of the skull behind the ear. When the sternocleidomastoid on one side contracts, the face is turned to the
opposite side. When both muscles contract, the head is bent toward the chest.
LEFT RIGHT
Weakness Weakness
1. Inspect the SCM muscles for size and symmetry
Assymetry Assymetry
2. Palpate the muscles at rest and as they exert their actions.
Atrophy Atrophy
1. Facing the patient, place your right hand on the left check of the patient
and your left hand on his right shoulder to brace him.
2. Command the patient, “Turn your head to the left. Do not let me push it
back”
3. Examiner tries to force his head to the midline.
4. Repeat on the other side
* With the patient’s head turned to the left, you test the right SCM. (SCM
turns the head to the opposite side)
* The Patient’s head turns to the side of the lesion because of assumed
weakness of the SCM ipsilateral to the lesion
1. Ask the patient to tilt (as if touching the tip of shoulder with the ear)
Test for Trapezius Muscle - responsible for moving, rotating, and stabilizing the scapula (shoulder blade) and extending the head at
the neck. It is a wide, flat, superficial muscle that covers most of the upper back and the posterior of the neck. Like most other
muscles, there are two trapezius muscles – a left and a right trapezius – that are symmetrical and meet at the vertebral column.
Remarks
Weakness
1. Inspect the Trapezius muscles for size and symmetry.
Assymetry
2. Palpate the muscles at rest and as they exert their actions.
Atrophy
1. Place your hand on both patient’s shoulders and press down
II. Pathway
III. Theoretical
2 Parts:
Report that cranial nerve is intact without any evidence of Dysfunction upon assessment
Report patient was able to resist the strength that was applied if normal
Report any abnormalities: scapular winging, any weakness or atrophy on the side tested and muscle asymmetry.
I. Steps
III. Theoretical
3. Valves- regulate airflow between cavities. Airflow occurs when an air valve is open and there is a pressure difference
between the connecting cavities
FUNCTION:
Apex- originates from the apex of the mandible, (hard, unyielding and immobile)
Base: Fans out to insert into the base of the tongue (soft, fleshy, and mobile)
Symmetrical genioglossus contraction must pull the base of the tongue forward.
CLINICAL CORRELATION
Intrinsic Muscle – cause lateral movement of the tip of the non-protruded tongue
Interruption of CRN 12 causes muscle fiber of the ipsilateral tongue to undergo atrophy .
Ipsilateral deviation
V. Other
If the hypoglossal nerve is affected on one side, the tongue often deviates toward the side of the lesion on protrusion due
to imbalance of genioglossus contraction
When the hypoglossal nerve or its nucleus is damages, atrophy and fasciculation of the tongue are noted on the evaluation
The larynx may deviate towards the active side in swallowing due to unilateral paralysis of the hyoid depressors.
Lesions of the hypoglossal nerve may occur anywhere along its course and may result from tumor, demyelinating diseases,
syringomyelia and vascular accidents.
AUTHORS: