Neurological Examination Physical Diagnosis Learning Objectives

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Neurological Examination Physical Diagnosis

Transcript of Neurological Examination Physical Diagnosis Learning Objectives

Page 1: Neurological Examination Physical Diagnosis Learning Objectives

Neurological Examination

Physical Diagnosis

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Learning Objectives

• Select appropriate questions to elicit from the patient with a neurological complaint during a patient interview

• Differentiate “normal” from “abnormal” findings on neurological examination

• Identify common causes of various cranial nerve palsies

• Differentiate conductive hearing loss from sensorineural hearing loss

• Determine location of neurological lesion• Differentiate amongst the various movement

disorders

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Learning Objectives

• Differentiate atrophy, hypertrophy, and pseudohypertrophy.

• Differentiate between spasticity, rigidity, and flaccidity, and identify common causes of each.

• Differentiate upper motor neuron lesions from lower motor neuron lesions.

• Differentiate CNS disorders from PNS disorders, and identify location of the lesion & common causes.

• Compare and contrast the five clinical levels of consciousness.

• Given a case study perform the appropriate focused history and physical examination and formulate a differential diagnosis

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Purpose

• Determine if there is a neurological deficit– Sensory– Motor– Behavioral– Coordinative

• Localize the site of the problem

• Determine the etiology of the problem

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Terminology

• Paresis – slight or incomplete paralysis

• Paralysis (plegia) – loss or impairment of

motor function

• Hemiparesis

• Hemiplegia

• Paraplegia

• Quadriplegia

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Terminology

• Atrophy – a decrease in size

• Hypertrophy– enlargement of an organ or part due to an increase in size

of its constituent cells

• Pseudohypertrophy– increase in size without true hypertrophy

• Spasticity – hypertonicity with increased DTRs

• Rigidity – stiffness or inflexibility

• Flaccidity – loss of tone with diminished DTRs

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Focuses

• Mental status

• Cranial nerves

• Motor function

• Reflexes

• Sensory status

• Coordination and balance

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History

• Chief complaint• PQRST• Headache?• Vertigo?• Visual disturbance?• Tremors or dyskinesias?• Weakness?• Dysesthesias/Paresthesias?• Loss of consciousness?

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Key components of H&P

Complaint Hx P.E.

Altered mental status

Associated seizure activity; recent trauma or infection; illicit drug use; exposure to toxic substances

Mental status exam; pupillary reaction; corneal reflexes; gag reflexes; posturing/motor asymmetry; Babinski

Vertigo Differentiate between true vertigo and lightheadedness! Present at rest; affected by positional changes

CN VIII function; Dix-Hallpike maneuver; nystagmus

Headache Thorough hx; “worst headache ever?”; associated sx’s; neck pain/stiffness

CN function; pupillary reaction; fundoscopic exam; palpate temporal artery; Marcus-Gunn

Seizures Previous hx; frequency; motor activity; aura; LOC; post-ictal confusion; external etiology

Search for focal deficits; signs of trauma; hyperreflexia

Weakness Generalized or focal; loss of strength; pain; progressive or recurrent fatigue

Asymmetry7; atrophy; sensory deficits; fasciculations; DTRs

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Mental Status• Alertness• Attention• Orientation

– Person, Place, Time, & Situation• Cognitive function• Perception

– Illusions = misinterpretations of real external stimuli– Hallucinations = subjective sensory perceptions in the absence of stimuli

• Judgment• Memory

– Short-term & long-term• Speech

– Rate & rhythm– Spontaneity– Fluency– Simple vs. complex

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Levels of Consciousness

• Alert and Oriented• Disoriented• Obtunded

– Drowsy/somnolent– Clouded consciousness– Slow thought, movement, and speech

• Stuporous– Marked reduction in mental and physical activity– Vigorous stimuli needed to provoke a response

• Comatose– Completely unconscious– Cannot be aroused by painful stimuli– Absence of voluntary movement– +/- reflexes

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Glasgow Coma Scale

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Malingering (Nonorganic)

• Hand drop

• Blindness– EOM/I

• Unilateral diplopia

• Ammonia reaction (CN V vs. CN I)

• Absence of pain or weakness in different positions

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The “Difficult” Patient

• Observation is key!• Use ingenuity!• Be patient! • Agitated

– May be threatening or violent• Unresponsive

– Fail to participate• Unreliable

– Inattentive, preoccupied, inconsistent information• Hysterical

– Uncooperative

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Testing Cognitive Function

• Information & vocabulary– Common

• Calculating– Simple math– Word problems

• Abstract thinking– Proverbs– Similarities/differences

• Construction– Copy figures of increasing difficulty (i.e. circle, clock)

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Abnormalities of Thought Processes

Circumstaniality Indirection and delay in reaching a point because of unnecessary detail.

Loose Associations Person shifts from one unrelated subject to another.

Flight of Ideas Almost continuous flow of accelerated speech with abrupt topic changes.

Incoherence Incomprehensible because of illogic, lack of meaningful connections, abrupt topic changes, or disordered word use/grammar.

Confabulation Fabrication of facts or events to fill in gaps in impaired memory.

Perseveration Persistent repetition of words or ideas.

Echolalia Repetition of the words or phrases of others.

Neologisms Invented or distorted words.

Blocking Sudden interruption in mid-sentence or before completion of an idea.

Clanging Person chooses a word based on sound instead of meaning.

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Abnormalities of Thought Content

Obsessions Recurrent, uncontrollable thoughts, images, or impulses that a persons considers unacceptable or strange

Compulsions Repetitive acts that a person feels driven to perform to prevent or produce some unrealistic future state of affairs.

Delusions False, fixed, personal beliefs that are not shared by other members of the person’s culture.

Phobias Persistent, irrational fears; accompanied by a compelling desire to avoid the stimulus.

Anxieties Apprehensions, fears, or tensions that may be free-floating or focused (i.e. phobia).

Feelings of Unreality A sense that things in the environment are strange, unreal, or remote.

Feelings of Depersonalization

A sense that one’s self is different, changed, or unreal. Identity is lost.

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Delirium vs. Dementia• Although confusion and/or disorientation are signs of both Delirium and

Dementia, they are different• Delirium is an acute confusional state

– It is potentially reversible– Delirium usually occurs over a period of days to months

• Dementia is slow and insidious– It progresses slowly over months to years– Dementia is not reversible

Condition Onset Pattern Orientation Attention Memory Duration

Delirium Acute Fluctuating Usually impaired

Impaired/

Fluctuating

Impaired Hours or days

Dementia Insidious Progressive Normal or impaired

~Normal Impaired Months or years

Psychosis Variable Variable ~Normal Normal or impaired

Normal or impaired

Variable

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Visual disturbance

• Onset?

• Progression?

• TIA = brief, intermittent visual loss

• Migraine = “wavy”

• Retinal detachment = “drawn curtain”

• Acute glaucoma = “rainbows” or “halos”

• Digitalis toxicity = yellow hue

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Vertigo

• A sense of spinning– Person– Environment

• Suggests dysfunction of– Vestibular apparatus– Vestibular nerve

• Differentiate from “lightheadedness” and “faintness”– Results from impairment of brain oxygenation

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Dix-Hallpike maneuver

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Testing for AphasiaWord Comprehension

Comprehension of spoken language through recognition (“point to your nose”) or understanding (“Can dogs fly?”).

Repetition Repeat items of increasing complexity. Note the fluency and accuracy of the responses.

Naming Name a series of objects or colors. Gradually increase difficulty. Note the fluency and accuracy of the responses.

Reading Comprehension

Have the patient follow several simple written commands.

Writing Ask the patient to make up and write a sentence.

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Localization

• CNS vs. PNS– Brain/Brain stem– Spinal cord– Peripheral nerves

• Difficult when evaluating:– Radicular pain– Dysesthesia/paresthesia– Tremors– Incoordination

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Localization

• Cerebrum– Impaired intellect, memory, higher brain function

• Brain stem– unconsciousness

• LMN– paralysis with loss of DTRs– muscle atrophy with fasciculation

• LMN + anesthesia– peripheral nerve or spinal root

• UMN– involves whole muscle groups– increased or spastic muscle tone– +/- paralysis with DTR accentuation– Positive Babinski

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Organic Disease

• Asymmetric pupillary light reflex

• Abnormal fundus

• Ocular divergence

• Nystagmus

• Muscular atrophy

• Fasciculations

• Multiple complex signs/symptoms explained by a single lesion

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Headache

• 5th most common reason for OP visit

• Symptom! (not a disease)

• Most important diagnostic clue is a steady, bilateral, nonthrobbing pain that is worse in the a.m.– May awaken patient– Worse with VALSALVA

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Types of Headaches

• Tension

• Sinus

• Migraine– Classic– Common– Complicated– Cluster

• Post-traumatic

• Post-LP

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Types of Headaches

• Temporal Arteritis

• ICP

• Subarachnoid hemorrhage

• Infection

• Ocular

• Trigeminal neuralgia (Tic doloureaux)

• TMJ syndrome

• Toxic

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Headache History

• Location– Unilateral ~ migraine– Periorbital ~ glaucoma/uveitis– Parietal/Occipital ~ tension– Neck ~ meningitis or Subarachnoid hemorrhage

• Quality– “Throbbing” ~ vascular– “Intermittent jabbing” ~ Trigeminal neuralgia– “Pressure” ~ sinus

• Radiation?• Severity• Timing

– Constant vs. intermittent– Worse in a.m. or p.m.

• Worst headache ever?????

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Headache History

• Associated Sx’s– Visual disturbance– Vertigo– N/V– Dysesthesias– Aura

• Past medical history• Family history• Current medication/drug use• Suspect an extracranial etiology if pain is the

only symptom

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Physical Examination

• Appearance• Behavior/Mannerisms

– Gait and Posture– Motor behavior– Facial expressions

• Mood vs. Affect• MMSE• Test Cranial Nerves II through XII• Fundoscopic examination

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Physical Examination

• Test motor nerve function– Grip/SAR (Grade 0-5)– Station and gait – ambulate, turn, toes, heels, heel-to-toe, knee bend– Romberg

• Test sensory nerve function– Pain +/- Light touch– Two point discrimination (normally <5mm)– Proprioception/Stereognosis/Vibration

• Test deep tendon reflexes (0-4+)

• Test for meningeal irritation - Kernig’s & Brudzinski’s signs

• Straight leg raise– Used to identify potential discogenic injury and nerve root injury

• Test Coordination– Finger-to-nose– Rapid alternating movements of hands & feet

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Reflexes

• Corneal• Pharyngeal• Biceps• Triceps• Brachioradialis• Abdominal• Patellar (knee jerk)• Achilles (ankle jerk)• Babinski

– Positive suggests UMN lesion

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Cranial Nerves

• I - Olfactory• II - Optic• III - Oculomotor• IV - Trochlear• V - Trigeminal• VI - Abducens• VII - Facial• VIII - Vestibulocochlear (Acoustic)• IX - Glossopharyngeal• X - Vagus• XI - Accessory• XII - Hypoglossal

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Cranial Nerve I

• Responsible for sense of smell

• Receptors located in the upper 1/3 of the nasal septum.

• Test each nostril separately.

• Identify familiar odors.

• Avoid noxious substances

• Unilateral lesion = ipsilateral anosmia

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Cranial Nerve II

• Responsible for vision• Test visual acuity!!!!• Pupillary size

– Swinging-flashlight test

• Visual fields – Peripheral vision– Test by confrontation

• Fundoscopic examination– Papilledema

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Cranial Nerves III, IV, VI

• CN III involved in:– Pupillary reflex– Opening of the eyelids– Most extraocular movements

• CN IV– provides downward/inward eye movement

• CN VI– provides lateral eye movement

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Cranial Nerves III, IV, VI

• Check pupillary reaction/reflex– Direct & consensual

• Check eye movement through all six Cardinal fields– Unilateral complete paralysis is usually caused by increased ICP

or an aneurysm– Neither eye can move to the contralateral side

• Eyes “look toward the lesion”

– Injury may occur secondary to:• Infection• Orbital fracture• Internal carotid aneurysm• Mastoiditis• Increased ICP

• Look for nystagmus*

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Pupil Abnormalities

• Adie’s (Tonic) pupil– sluggish response

• Argyll Robertson pupil– irregular/unequal pupils– weak/absent reaction to light– exaggerated contraction to accommodation

• Marcus-Gunn pupil– results from reduced afferent input in the affected eye**– pupil fails to constrict fully– rapidly stimulate each eye in succession and observe the direct

and consensual light response in each• stimulation of the normal eye produces full constriction in both

pupils.• immediate subsequent stimulus of the affected eye produces an

apparent dilation in both pupils since the stimulus carried through that optic nerve is weaker

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Pupil Abnormalities

• Asymmetry of pupil size of >1mm suggests CN III compression

• Bilateral dilation suggests anoxia or drug affect• Unilateral constriction is seen with sympathetic

dysfunction (Horner syndrome) or carotid artery dissection

• Bilateral constriction is seen with:– Pontine hemorrhage– Drugs (opiates, Clonidine)– Toxins (organophosphates)

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Cranial Nerve V

• Sensory– Ophthalmic branch (sensory)

• Cornea, conjunctiva, ciliary body, nasal cavity, sinuses, skin of eyebrows/forehead/nose

– Maxillary branch (sensory)• Side of nose, lower eyelid, upper lip

– Mandibular branch (mixed)• Sensory – skin of temporal region, auricles, lower lip/face,

anterior 2/3 of tongue, mandibular gums/teeth• Motor - innervates the muscles of mastication

• Cerebral lesion causes contralateral paresthesia• Most lesions affect all 3 branches

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Cranial Nerve V Testing

• Inspect for tremor of the lips, involuntary chewing movements, and trismus

• Compare muscle tension bilaterally with teeth clenched

• Test tactile perception

• Test sharp-dull discrimination

• Test temperature perception

• Test corneal reflex– Tests V & VII directly and VII consensually

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Cranial Nerve VII

• Motor– Muscles of the face, scalp, and ears

• Autonomic– Vasodilation– Secretion of submaxillary/sublingual glands

• Sensory– Taste in anterior 2/3 of tongue– Ear canal/postauricular

• Palsies can occur secondary to:– Polio, ALS, MS, tumors, syphilis, Lyme disease,

Guillain-Barré Syndrome

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Cranial Nerve VII

• Inspect for flaccid paralysis• Differentiate UMN vs. LMN

– Elevate eyebrows– Close eyes– Show teeth– Whistle– Smile

• **Central lesions causes contralateral paralysis to lower half of face (below the eyes)

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Cranial Nerve VIII

• Responsible for sense of hearing and balance• Composed of the cochlear and vestibular nerves• Sensory• Test hearing

Conductive loss Sensorineural loss

Distortion of sound Minor Present with loss of upper tones

Noisy environment Hearing may seem to improve Hearing typically worsens

Patient’s voice Generally normal* Loud

Ear canal/TM Visible abnormality Normal

Weber Lateralizes to the impaired ear Lateralizes to the normal ear

Rinne BC > AC AC > BC

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Cranial Nerve VIII

• Look for spontaneous nystagmus• Romberg test/sign

– Functional test of position sense• Stand with feet together• Close eyes and maintain for 20-30 seconds

– Usually combined with a check for pronator drift• As above• Extend arms forward in supinated position• Briskly move arms downward (separately)• Arms should return smoothly to original position

• Lesion causes– Unilateral deafness– Imbalance

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Cranial Nerve IX

• Motor– Muscles of the pharynx

• Autonomic– Vasodilation

• Sensory– Taste in posterior 1/3 of tongue– Pharynx, tonsils, fauces, TM, posterior ear canal

• Test for– Elevation of the uvula– Gag reflex– Mucosal anesthesia

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Cranial Nerve X

• Motor, autonomic, and sensory functions– Palate, pharynx, larynx, neck, thorax, and abdomen

• Branches to:– Pharynx– Larynx– Esophagus– Heart– Bronchioles– Stomach– Liver– Celiac

• Perform indirect examination of the vocal cords• Lesion cause:

– Hoarseness/aphonia– Dyspnea/stridor

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Cranial Nerve XI

• Provides motor to– SCM– upper Trapezius

• Testing:– Have patient shrug against resistance– Head rotation and movement against

resistance

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Cranial Nerve XII

• Motor to tongue• Testing:

– Tongue movement• Midline• Tremors• Involuntary

– Atrophy– Lingual speech

• Paralysis causes deviation to the weak side

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Motor Function

• UMNs– Transmit impulses from cortical nerve bodies

to:• motor nuclei in brainstem (CNs)• Anterior horn cells of spinal cord

• LMNs– Transmit impulses from anterior horn cells

through anterior root into peripheral nerves– Terminate at the neuromuscular junction

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Motor Function• Inspection

– Symmetry– Muscle bulk; size and contours; flat or concave; unilateral or bilateral;

proximal or distal– Atrophy

• Palpation– Muscle tone

• Percussion– ? Fasciculations

• Check motor strength• Body position (during movement and at rest)• Involuntary movements

– Location, quality, rate, rhythm, amplitude and relation to posture, activity, fatigue, or emotions

• If an abnormality exists: – Identify muscle(s) involved– Central vs. peripheral?– Learn muscle innervations

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Motor Function

• Muscle tone– Slight residual tension in normal relaxed muscle– Feel muscle’s resistance to passive stretch

• Muscle strength– Wide variance - stronger dominant side– Test by asking patient to actively resist movement– If muscles too weak - test against gravity only or eliminate

gravity– If patient fails to move, watch or feel for weak contraction

• Suspect decreased resistance?– Hold forearm and shake hand loosely

• Resistance increased?– Varies or persists throughout movement

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Function and Innervations

Muscle(s) Function Primary Nerve OriginDELTOID Shoulder abduction Axillary C5-C6

BICEPS Elbow flexion Musculocutaneous C5, C6

TRICEPS Elbow extension Radial C6, C7, C8

WRIST EXTENSORS Radial C6, C7, C8

WRIST FLEXION Median C6, C7

HAND GRIP Grasp Fingers Median C7, C8, T1

FINGER ADDUCTION Median C7-T1

FINGER ABDUCTION Ulnar C8, T1

THUMB OPPOSITION Median C8, T1

HIP FLEXION Iliopsoas L2, L3, L4

HIP EXTENSION Gluteus maximus S1

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Function and Innervations

Motor Function Muscles Primary Nerve OriginKNEE EXTENSION Quadriceps L2, L3, L4

KNEE FLEXION Hamstrings L4, L5, S1, S2

FOOT DORSIFLEXION Tibialis Anterior Deep peroneal L4, L5

ANKLE PLANTAR FLEXION

Gastrocnemius mainly S1

EXTENSION OF GREAT TOE

Extensor hallicus longus

L5

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Motor function

• Always compare symmetry

• Note any atrophy

• Check muscle tone against resistance– Cogwheel rigidity = jerky, released in degrees– UMN paralysis = spasticity (increased tone)– LMN paralysis = hypotonia

• Test muscle strength– Grade 0 to 5

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Grading Muscular Response

Grade Muscular Response

0 No contraction detected

1 Barely detectable flicker or trace of contraction

2 Active movement with gravity eliminated

3 Active movement against gravity

4 Active movement against gravity and some resistance

5 Active movement against resistance without

evident fatigue - “Normal”

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Sensory Function

• Fatigues quickly– Efficiency – Special attention to areas of:

• Symptomology• Motor or reflex abnormalities• Trophic changes

– Confirm with repeat testing!! • Patterns of testing:

– Symmetrical– Distal vs. proximal: scattered stimuli– Vary pace

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Sensory Function Testing

• Look for abnormality– map out boundaries in detail

• Source of lesion

• Distribution of sensory abnormalities and kinds of sensations affected

• +/- motor/reflex abnormality

• Demonstrate to patient before testing

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Spinothalamic Tract

• Pain and temperature

• Crude touch (light touch without localization)

• Fibers cross & pass upward into thalamus

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Pain Sensation

• Sharp safety pin or other tool

• Demonstrate sharp & dull

• Test by:– Alternating sharp & dull w/ pt’s eyes closed

• Ask patient:– Sharp or dull?– Does this feel same as this?– Lightest pressure needed - do not draw blood

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Temperature

• Often omitted if pain sensation normal

• Two test tubes– filled with hot & cold water– or tuning fork heated or cooled by water

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Light Touch

• Wisp of cotton

• Touch lightly - avoid pressure

• Ask patient:– To respond

when touch is felt

– Compare one area with another

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Posterior Columns

• Position and vibration

• Fine touch

• Synapse in medulla, cross & continue on to thalamus

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Vibratory Sense

• 128 or 256 Hz Tuning fork

• If impaired, proceed proximally

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Proprioception

Grasp toe by sides - pull away from other toes

Demonstrate “up” & “down”

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Tactile Localization

• Have pt close eyes

• Touch pt on R cheek & L arm

• Ask patient where touch was felt

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Discriminative Sensations

• Stereognosis, graphesthesia, two-point discrimination

• Test ability of sensory cortex to correlate, analyze, & interpret sensations

• Dependent on touch & position sense

• Screen first with stereognosis - proceed to other methods if indicated

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Stereognosis• Ability to identify an

object by feeling it

• Place familiar object in patient’s hand & ask patient to identify it

• Normally patient manipulates it skillfully & identifies it correctly

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Graphesthesia

• Perform if inability to manipulate object

• Ability to identify numbers written in hand

• Use patient’s orientation

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Two-Point Discrimination

• Touch two places simultaneously

• Alternate stimuli

• Avoid pain

• Determine distance

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Spinal Reflexes: DTRs

• Segmental levels of DTRs:– Supinator reflex C5, 6– Biceps reflex C5, 6– Triceps reflex C6, 7– Abdominal reflexes - upper T8, 9, 10– - lower T 10, 11, 12– Knee (Patellar) L2, 3, 4– Plantar responses L5, S1– Achilles reflex S1 primarily

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Deep Tendon Reflexes: GradingGrade DTR Response

4+ Very brisk, hyperactive, with

clonus

3+ Brisker than average, slightly hyperreflexic

2+ Average, expected response;

normal

1+ Somewhat diminished, low

normal

0 No response, absent

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Reflex Hammer - Incorrect Usage

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Jendrassik’s Maneuver

• Reinforcement technique

• Upper extremities– clench teeth– squeeze thigh

• Lower extremities– lock fingers and

pull one against the other

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Biceps Reflex

C5,C6Elbow Flexion

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Triceps Reflex

C6, C7, C8Elbow Extension

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Brachioradialis Reflex

C5, C6Forearm semiflexion/semipronation

(NO wrist/hand flexion)

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Patellar Reflex

L2, L3, L4Knee Extension

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Achilles Reflex

S1, S2

Ankle Plantar Flexion

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Plantar Reflex

L5, S1, S2 Babinski Sign

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Abdominal Reflexes

T8, T9, T10:ABOVE umbilicusT10, T11, T12:BELOW umbilicus

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Anal Reflex

• Superficial reflex

• Loss of anal reflex suggests lesion of S2,3,4 reflex arc

• Possible lesion of cauda equina

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Clonus

• Rhythmic Oscillation

• Flexion/Extension

• UMN Lesion

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Cerebellar Function

• Requires integration of:– Motor system

– Cerebellar system

– Vestibular system

– Sensory system

• Assessed by:– Rapid alternating

movements

– Finger-to-Nose / Heel-to-Knee Test

– Romberg’s Test

– Gait

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Finger-to-Nose Test

• Finger-to-nose with moving target

• Stationary finger-to-nose with eyes closed

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Heel-to-Knee Test

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Rapid Alternating Movements

• First with hands• Repeat with feet• Diadochokinesia = ability to perform RAM• Dysdiadochokinesis = slow, irregular, clumsy

movements

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Station, Stance & Romberg’s Test

• Station & Stance– Pt stand with feet together– First, eyes open

• Romberg Test– Then, close eyes– If okay with eyes open, but

sways w/ eyes closed = + Romberg

– Mainly tests position sense• Vision can compensate for loss of

position sense

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Pronator Drift

• Often performed in conjunction with Romberg test

• Pronator drift– Muscular strength– Coordination– Position sense

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Gait

• Walk across room, turn and walk back

• Tandem walking

• Heel & toe walking

• Hop in place

• Shallow knee bend

• Rising from sitting position or stepping up on stool

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Meningeal Irritation

• Occur with meningitis & subarachnoid hemorrhage

• Brudzinski’s Sign– Flex the head– Marked pain in the neck– Patient flexes hip and BLE

• Kernig’s Sign– Pain when raising a straightened LE

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Lab/X-ray

• CBC, CMP, U/A• Specific drug levels• Plain films of the spine• CT of the brain & head• MRI of the brain & spine

– Greater resolution then CT for soft tissue/plaques• Angiography• CSF exam• EEG• EMG & NCT• PET/SPECT

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Spinal Studies

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Normal Skull Anatomy

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Normal L-Spine

MRI

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CSF

• Obtained through lumbar puncture• Indications:

– Suspected CNS infection (i.e. syphilis)– Suspected subarachnoid hemorrhage

• Contraindicated if cerebral mass/lesion is suspected

• Measure opening pressure• Obtain samples for cell counts, glucose,

protein level, and cultures

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Computed Tomography

• Gives adequate information about brain anatomy• Used primarily to detect hemorrhage & tumors• Can be performed with/without contrast• Indications:

– Focal neurologic deficits– Altered mental status– Head trauma– New-onset seizure– Increased ICP– Suspected mass lesion– Suspected subarachnoid hemorrhage– (with contrast) Abscess, intracranial tumor– (with contrast) Chronic subdural hematoma, infarct, vascular

malformation

Page 101: Neurological Examination Physical Diagnosis Learning Objectives

Review of Neurological Exam

• Six categories: – Mental status & speech– Cranial nerves– Motor function– Sensory function– Reflexes– Cerebellar function

• Carefully evaluate the hx of the CC

• CN assessment is essential!

Page 102: Neurological Examination Physical Diagnosis Learning Objectives

Summary• Select appropriate questions to elicit from the patient with a

neurological complaint during a patient interview• Differentiate “normal” from “abnormal” findings on neurological

examination– Identify common causes of various cranial nerve palsies– Differentiate conductive hearing loss from sensorineural hearing loss– Differentiate amongst the various movement disorders– Differentiate atrophy, hypertrophy, and pseudohypertrophy.– Differentiate between spasticity, rigidity, and flaccidity, and identify

common causes of each.• Determine location of neurological lesion

– Differentiate upper motor neuron lesions from lower motor neuron lesions

– Differentiate CNS disorders from PNS disorders, and identify location of the lesion & common causes.

• Compare and contrast the five clinical levels of consciousness.