EXAM 2 Flashcards
Cranial Nerve I: Olfactory Test
test sense of smell with familiar odor
Cranial Nerve II: Optic Test
test visual acuity and visual field with confrontation
Confrontation Test
gross measure of peripheral vision
-stand 2 fett from person
-have patient cover one eye, then cover your own eye opposite to the persons covered one
-hold finger as target midline between you and patient, slowly advance to periphery
-as person to say “now” as target is first seen
Confrontation Test: normal
50 degrees upward
90 degrees temporal
70 degrees down
60 degrees nasal
Cranial Nerve III, IV, VI: Oculomotor, Trochlear, Abducens Test
PERRLA
6 cardinal positions of gaze
PERRLA
pupils equal, round, reactive to light (direct and consensual) and accommodation
6 cardinal positions of gaze
right & up
right
right & down
left & up
left
left & down
nystagmus
back-and-forth oscillation of the eyes
nystagmus: amplitude
fine, medium or coarse movement
nystagmus: frequency
constant or fades after few beats
nystagmus: plane of movement
horizontal, vertical, rotary or combo
Cranial Nerve V: Trigeminal Test
Motor: asking the client to clench her teeth while you palpate the masseter (muscle of mastication)
Sensory- test light touch by having a client closer their eyes while you toucher her face gently with a wisp of cotton, patient identifies location
What does the corneal reflex test?
CN V sensory, CN VII motor
Corneal reflex test
-remove contacts, bring cotton wisp from side, lightly touch cornea
NORMALLY: patient blinks bilaterally
Cranial Nerve VII: Facial Test
Motor: have client smile, frown, puff out her cheeks, raise her eyebrows, close her eyes tightly
Sensory: anterior 2/3 taste (sugar, salt, lemon juice)
Cranial Nerve VIII: Vestibulocochlear Test
Whispered voice test
Cranial Nerve IX & X: Glossopharyngeal and Vagus Test
Motor: open mouth say “ahh” & gag reflex
NORMALLY: uvula and soft palate rise in midline
Sensory: CN IX does posterior 1/3 taste
Cranial Nerve XI: Accessory Test
shrug shoulders
Cranial Nerve XII: Hypoglossal Test
say “light, tight, dynamite”
screening neuro exam
perform on well persons who have no significant subjective findings
complete neuro exam
perform on person with neuro concerns
screening neuro exam
perform on well persons who have no significant subjective findings
neuro recheck exam
perform on person with demonstrated neuro defect, who requires period ic assessment
ansomia
Decrease or loss of smell occurs bilaterally
hemianopsia; hemianopia
Defective vision or blindness in one half of the visual field
ptosis
drooping eyelid
paresthesias
tingling, prickling, “pins & needles” (sensory loss)
diplopia
double vision
dysphagia
difficulty swallowing
What are the test to evaluate cerebellar function?
Balance Test (Gait)
Romberg Test
Rapid Alternating Movements (RAM)
Balance Test (Gait)
-observe as the person walks 10 to 20 feet, turns and returns to the starting point
NORMALLY: gait is smooth, rhythmic and effortless opposing arm swing is coordinating
Romberg test
-ask client to stand with feet at comfortable distance apart, arms at sides, and eyes closed for ~20 seconds
NORMALLY: patient can maintain posture and balance
Rapid Alternating Movements (RAM)
pat the knees with both hands, turn hands over, then faster
NORMALLY: done with equal turning and quick rhythmic pace
flaccidity
decreased muscle tone (hypotonia), muscle feels limp, soft, flabby
spasticity
increased muscle tone (hypertonia)
rigidity
constant state of resistance; resists passive movement in any direction (dystonia)
cogwheel rigidity
Increased tone is released by degrees during passive range of motion so it feels like small, regular jerks.
paralysis
decreased or loss of motor power
hemiplegia
Spastic or flaccid paralysis of one side of the body
paraplegia
symmetric paralysis of both lower extremities
quadriplegia
paralysis of all four extremities
paresis
weakness of muscles rather than paralysis
tic
involuntary, compulsive, repetitive twitching of a muscle group
myoclonus
Rapid, sudden jerk or a short series of jerks at fairly regular intervals. (ex: hiccup)
fasciculation
rapid continuous twitching of resting muscle without movement of limb
chorea
sudden, rapid, jerky, purposeless movement involving limbs, trunk, or face
irregular intervals, not rhythmic or repetitive
athetosis
slow, writhing involuntary movements
tremor
involuntary contraction of opposing muscle groups resulting in rhythmic movement of one or more joints
rest tremor
occurs when muscles are quiet and supported against gravity (hand in lap), coarse and slow, partly or completely disappears with voluntary movement
intention tremor
worse with voluntary movement (like reaching to a target)
spastic hemiparesis
Arm is immobile against the body, with flexion of the shoulder, elbow, wrist, and fingers and adduction of shoulder; does not swing freely. Leg is stiff and extended and circumducts with each step (drags toe in a semicircle).
cerebellar ataxia
staggering, wide-based gait; difficulty with turns; uncoordinated movement with positive Romberg sign
parkinsonian (festinating)
Posture is stooped; trunk is pitched forward; elbows, hips, and knees are flexed. Shuffling gait. Difficulty with any change in direction.
scissors
knees cross or are in contact, like holding an orange between the thighs.
steppage or foot drop
slapping quality, looks like walking up stairs with no stairs there
waddling
weak hip muscles- when the person takes a step, the opposite hip drops, which allows compensatory lateral movement of pelvis
short leg
Leg length discrepancy >2.5 cm (1 inch).
cerebral palsy
damage to cerebral cortex from a developmental defect (infancy and childhood), intrauterine meningitis or encephalitis, birth trauma, anoxia
muscular dystrophy
a chronic, progressive wasting of skeletal musculature producing weakness contracture and respiratory dysfunction or death
Parkinsonism
loss of dopamine-producing neurons causing motor tract disorder
symptoms: resting tremor, bradykinesia, cogwheel rigidity
cerebellar
A lesion in one hemisphere produces motor abnormalities on the ipsilateral side.
Multiple Sclerosis (MS)
chronic, progressive, immune mediated disease which axons experience inflammation, demyelination, degeneration and finally sclerosis
decorticate rigidity
upper: flexion of arm, wrist fingers, adduction of arms
lower: extension, internal rotation, plantar flexion
*tippy toes, puppy cry
decerebrate rigidity
Upper: stiffly extended, adducted, internal rotation, palms pronated.
Lower extremities: stiffly extended, plantar flexion; teeth clenched; hyperextended back
*tippy toes, sheet gripper, arched back, head back
flaccid quadriplegia
complete loss of muscle tone and paralysis of all four extremities (completely nonfunctional brainstem)
Opisthotonos
prolonged arching of back, with head and heels bent backward (meningeal irritation)
*doing the superman on stomach
stereognosis
Test the persons ability to recognize objects by feeling their forms, sizes and weights
position (kinesthesia)
test person’s ability to perceive passive movements of extremities
Tactile discrimination (fine touch)
measure the discrimination ability of the sensory cortex
Graphesthesia
ability to “read” a number by having it traced on the skin
two point discrimination
test ability to distinguish separation of two simultaneous pin points on skin
extinction
simultaneously touch both sides of body at the same time, both sensations should be felt
point location
touch skin and withdraw stimulus promptly; ask person to put finger where you touched
peripheral neuropathy
Loss of sensation involves all modalities; loss most severe distally at feet and hands
*complete loss at fingers and toes, diminished loss up to half forearm/half calf
individual nerves or roots
Decrease or loss of all sensory modalities; corresponds to distribution of involved nerve
*such as one entire arm
Spinal Cord Hemisection (Brown-Sequard Syndrome)
injury to one-half of the cord, causing contralateral loss of pain and temp
the ipsilateral side side of the lesion has paralysis and loss of vibration and touch sensation
*one leg has complete loss and the other has semi loss
Complete transection of spinal cord
Complete loss of all sensory modalities below level of lesion; associated with motor paralysis and loss of sphincter control
thalamus
loss of all sensory modality son the face, arm and leg on the side contrateral to lesion
cortex lesion
loss of discrimination on contralateral side; loss of graphesthesia, stereognosis, recognition of shapes and weights, finger findings
deep tendon reflexes (DTR)
measurement of stretch reflex reveals intactness of reflex arc at specific spinal levels and normal override on reflex of higher cortical levels