Approach to Neuro Complaint Flashcards

(58 cards)

1
Q

What is the first thing you check within the neuro exam?

A

mental status, speech, and language

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2
Q

defective articulation with speech, usually caused by defect in motor control of speech apparatus

A

dysarthria

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3
Q

a disorder in producing or understanding language, usually caused by lesions in the dominant hemisphere (usually the left)

A

aphasia

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4
Q

How do you report mental status in soap note and what section does it belong in?

A
  • mental status: patient is alert and oriented x4 (to person, place, time, and event)
  • belongs in objective section
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5
Q

What is the difference between delirium and dementia?

What is the correlation between these two conditions and depression?

A
  • delirium is REVERSIBLE (common in older adults during hospitalization) while dementia is NOT REVERSIBLE (depression/delirium must be treated before dx, meds can slow progression)
  • depression can enchance symptoms of both delirium and dementia
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6
Q

CN I function?

A

olfactory nerve (smell)

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7
Q

CN II function?

A

visual acuity

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8
Q

CN III function?

A

raise eyelids, pupillary constriction, most extraocular movements

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9
Q

CN IV function?

A

downward, internal rotation of the eyes (looking toward nose)

*high yield*

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10
Q

CN V function?

A

sensory dermatomes (V1, V2, V3), motor function of mastication, corneal reflex (sensory)

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11
Q

CN VI function?

A

lateral deviation of the eye

*high yield*

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12
Q

CN VII function?

A

motor: facial movements (expression, closing eyes, mouth); sensory: taste of anterior 2/3 tongue

*high yield*

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13
Q

CN VIII function?

A

hearing (test using soft rub finger test, whisper test, or tuning fork)

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14
Q

CN IX function?

A

motor: phonation; sensory: posterior 1/3 taste, gag reflex arc

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15
Q

CN X function?

A

raise palate, motor function of pharynx

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16
Q

CN XI function?

A

shrug shoulders against resistance (traps), turn head L and R against resistance (SCM)

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17
Q

CN XII function?

A

motor function of tongue

(make sure it’s midline)

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18
Q

What are the cardinal gaze signs and their innervations?

A
  • inferior oblique (up and in), medial rectus (inward), superior rectus (up and out), inferior rectus (down and out): oculomotor N. (CN III)
  • superior oblique (down and in): trochlear N. (CN IV)
  • lateral rectus (outward): abducens N. (CN VI)
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19
Q

What are the associated symptoms and presentation of CN III lesions?

A
  • symptoms: ptosis (drooping of eyelid due to levator palpebrae weakness), pupillary dilation/asymmetry (due to disruption of ciliary plexus within parasympathetic innervation of pupil), ophthalmoplegia (denervation of extraocular muscles causing “down and out”)
  • presentation: sudden, unilat ptosis and ophthalmoplegia (diplopia can be masked by severe ptosis)
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20
Q

What are the symptoms and presentation associated with CN IV lesions?

A
  • symptoms: hypertropia (eye drifts medially), weakness of downward gaze (due to superior oblique, eye drifts upwards), vertical diplopia (dbl vision increases w/ downward gaze), head tilting (to oppo side of lesion)
  • presentation: vertical diplopia, difficulty reading/walking downstairs, torticollis secondary to head tilting
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21
Q

What are the associated symptoms of CN VI lesions?

A

(most common isolated CN palsy, seen often in subarachnoid hemorrhage, syphilis, trauma)

  • symptoms: convergent (medial) strabismus (esotropia) (inability to abduct eye due to lateral rectus weakness) and horizontal diplopia (esp when looking toward affected lateral rectus)
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22
Q

What are the symptoms and presentation a/w CN V lesions?

A
  • symptoms: decreased sensation, loss of corneal reflex, weakness of muscles of mastication, jaw deviation (toward weak side)
  • presentation: recurrent brief episodes of unilat shock-like pain, can be triggered by innocuous stim, can be reprod on exam by stroking dermatome w/ light touch

(90% of cases caused by aberrant vein or artery compression of N.)

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23
Q

What are the symptoms a/w CN VII lesions?

A
  • paralysis of muscles of facial expression of upper/lower facial portions: presents as widened palpebral fissure and increased nasolabial fold (Bell’s palsy)
  • loss of corneal reflex (efferent limb of CN VII)
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24
Q

What is the difference between Bell’s palsy and supranuclear (central) facial palsy?

A
  • Bell’s palsy (peripheral): etiology usually unknown, can be caused by trauma or infection
  • supranuclear facial palsy (central): spares upper face, usually a/w hemiplegia (important for determining if weakness is central or peripheral)
  • DIFFERENCE: Bell’s palsy is a peripheral nerve lesion on the unilat side of facial weakness, the entire affected side of the face shows weakness; supranuclear palsy is a central lesion on the contralat side of weakness, only affects lower muscles of face because unilat nerve fibers make up for lost innervation
25
What are the symptoms a/w CN VIII lesions?
- vestibular division: **disequilibrium** and **nystagmus** - cochlear division: **destructive** (sensorineural hearing loss) and **irritative** (can cause tinnitus)
26
What is nystagmus, what are the 3 types, and what are potential causes?
- **nystagmus**: rhythmic oscillation of eyes (2 phases, 1 is slow drift away from object, 2 is **saccade** phase quick rxn back), named for **saccade phase** - **types**: horizontal, vertical, rotatory - **causes**: vision impairment at early age, labyrinth or cerebellar disorder, drug tox (1-2 beats of nystagmus is nml physiologically, however sustained beats is abnormal/pathological)
27
What are symptoms a/w CN IX lesion?
- loss of gag reflex - loss of sensation in pharynx and posterior 1/3 of tongue - mild dysphagia
28
What are symptoms a/w CN X lesions?
- dysphonia (difficulty speaking) - dysphagia (difficulty swallowing) - dyspnea (difficulty breathing) - loss of gag or cough reflex
29
What are symptoms a/w CN XI lesions?
- **in SCM**: paralysis of muscle, difficulty turning head to opposite side of affected muscle - **in trap**: weakness results in unilat shoulder droop (testing for these is against mild resistance)
30
What are symptoms a/w CN XII lesions?
tongue **deviates** to **weak or affected side** and patient is unable to push tongue to opposite side (testing: patient protrudes tongue while physician applies mild resistance against cheeks)
31
How do you document that you tested cranial nerves?
- **never** just put "cranial nerves are intact" - if you did a **partial test**: "cranial nerves are grossly intact" - if you did a **thorough test**: "cranial nerves II-XII are intact to testing" (CN I is usually not tested unless in special circumstances)
32
dermatome of auricle of ear?
C2
33
dermatome of earlobe, ant/post neck?
C3
34
dermatome of superior shoulder?
C4
35
dermatome of radial aspect of forearm?
C6
36
dermatome of middle finger?
C7
37
dermatome of little finger?
C8
38
dermatome of nipple?
T4
39
dermatome of umbilicus?
T10
40
dermatome of inguinal region?
L1
41
dermatome of patella and medial calf?
L4 (this is what we test w/ the patellar reflex)
42
dermatome of anterolateral calf and great toe?
L5
43
dermatome of posterolateral calf and little toe?
S1 (this is what we test w/ Achilles reflex)
44
What are the primary sensations and how do we test them?
- **pain**: sharp object and gently touch patient (spinothalamic tract) - **temp**: often omitted if pain is nml, use cold metal object or test tubes w/ water (spinothalamic tract) - **vibration**: use tuning fork on bony prominence (posterior column) - **proprioception**: big toe positioning test w/ patient's eyes closed (posterior column)
45
What are the discriminative (cortical) sensations?
- **stereogenesis**: ability to identify shapes of objects - **graphesthesia**: ability to identify numbers/letters written on palm - **two-point discrimination** - **double simultaneous stimulation**
46
What are the 7 different patterns of sensory loss?
- **single nerve** - **root or roots**: loss in nerve distributions w/ single root (ex: C5-7 common in arms, L4, L5, S1 common in legs) - **spinal cord**: complete transection, hemi-section, posterior column, or anterior spinal syndrome - **brainstem**: crossed findings, ipsilat loss in face and contralat loss in body - **thalamic**: hemisensory loss of all modalities - **cortical**: intact primary sensations, loss of cortical sensations (i.e. graphesthesia and stereogenesis) - **functional**: non-anatomical (i.e. psychosomatic)
47
What are the different types of cerebellar/coordination testing?
- rapid alternating movements, finger-to-nose, heel-to-shin - gait: regular, heel-toe, toe-heel, hopping, shallow knee bend, get-up-and-go - stance: pronator drift test (ability to maintain body position w/ eyes closed)
48
- test that has patient stand with feet together and eyes closed - **(+) test**: patient is not able to stand upright - tests **proprioception, vestibular system**, and vision (you must have 2/3 of these functioning properly to stand upright, so this tests takes away vision and is focusing on proprioception and vestibular aspects) - best for testing **proprioception** b/c dysfunction w/ vestibular system presents more obviously w/ dizziness and loss of balance
**Romberg test** (did not include this w/ cerebellar testing b/c Dr. Pence said if you had an issue w/ cerebellar system you would not be able to stand w/ feet together even w/ eyes open)
49
What aspects of the motor system can you observe during a physical exam?
- gait - body position - involuntary movements - muscle bulk: hypertrophy or atrophy - muscle tone
50
How do you grade DTR's?
- 0-4/4 - 1-3 are not indicative of disease - 0/4: reflex absent - 4/4: issue w/ UMN
51
How do you grade strength?
0-5/5 | (see chart for further info)
52
Review of gait cycle:
53
- abnormal gait pattern - staggering, unsteady, feet wide apart, other cerebellar signs usually present - staggering will be toward side of lesion/damage
cerebellar ataxia
54
- abnormal gait pattern - unsteady, feet wide apart, feet thrown forward and slapped down first on heels then forefoot, patients watch ground when walking
sensory ataxia
55
- abnormal gait pattern - stooped forward, short steps commonly called "shuffling gait" w/ festination (involuntary hesitation), decreased arm swinging
Parkinsonian gait
56
What are the 3 common cutaneous or superficial reflexes?
- **abdominal reflex**: stroke skin of abd and look for involuntary reflex of abd muscles - **plantar response**: move from lateral portion of posterior foot and move anteriorly toward toes, intact reflex is toes curling down, non-intact reflex (**Babinski sign**) toes curl up which is nml in infants - **anal reflex**: stroke edge of anus w/ Q-tip, anus should wink, usually patients w/ non-intact reflex present w/ fecal incontinence
57
What are signs of meningeal infection? \*high yield\*
**nuchal rigidity**: neck stiffness w/ resistance to flexion - occurs in ~84% of patients w/ acute bacterial meningitis and 21-86% of patients w/ meningeal irritation due to subarachnoid hemorrhage - most reliable presentation in meningeal irritation (but diagnostic accuracy is low) - must be sure no concern for vertebral fx before testing - important to use imaging to r/o presence of trauma
58
What are the 2 physical exam tests for meningeal infection?
- **Brudsinski sign**: patient is supine while physician slowly flexes patient's neck; **(+) test** if patient involuntary flexes their hips and knees in response - **Kernig sign**: physician flexes patient's hip and knee then slowly extends knee straight keeping hip flexed; **(+) test**: pain or increased resistance to knee ext, also can cause passive flexion of neck