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96 Cards in this Set

  • Front
  • Back
NAME & DEFINE:

3 major features of Parkinson's
1. Bradykinesia - slowed movement
2. Hypokinesia - reduced amplitude
3. Dysrhythmia - loss of rhythm
HOW:

Could one enhance a Parkinsonian rest tremor?
By distracting the patient (making them subtract 3s, for example)
NAME:

The 4th cardinal component of Parkinsonism
"Loss of Postural Reflexes" = postural instability not caused by issues with cerebellum, vision, vestibular system, etc .... can use a "pull test" to assess
NAME:

A possible consequence of levodopa treatment in advanced Parkinson's patients
Can develop a levodopa induced dyskinesia ... which is choreiformic in nature
WHERE:

Would you place an implant for DBS?
Subthalamic nucleus (STN) implant
NAME:

Events favoring an Epileptic Seizure vs. a Psychogenic Non-Epileptic Seizure (PNES)
EPILEPTIC SEIZURES
--aura
--brief duration (1-2 mins)
--post-ictal confusion
--abnormal posturing
--amnesia for the event
--incontinence
--events arising from sleep
--self injury (lateral tongue biting)
--eyes open at the onset of the event

PNES
--specific nontraditional triggers (aka not photic stimulation or hyperventilation)
--event occurs in waiting or examination room
--histrionic behavior during exam
--rapid cognitive post-ictal recovery
--ability to induce seizure
--presence of fibromyalgia, chronic pain, chronic fatigue
EXPLAIN:

When light is shined on the left eye, that eye constricts. When the light is swung to the right eye, the right eye dilates.
Indicates a right afferent pupillary defect
WHAT:

Causes obstructive sleep apnea
Narrowing of the airway leading to obstruction of air flow during sleep
HOW:

Does the modified Mallampati 2 Classification System predict risk of sleep apnea
By relating tongue size to pharyngeal size
NAME:

3+/5 medical associations with sleep apnea
1. Increased age
2. Obesity
3. Craniofacial/soft tissue abnormalities
4. Endocrine Disorders
5. Hypothyroidism
NAME:

Possible hypersomnias to consider in a patient if sleep disordered breathing is not present
Idiopathic hypersomnia
Narcolepsy
WHAT:

Scores on an Epworth Sleepiness Scale indicate excessive daytime sleepiness?
10+ = excessive sleepiness
18+ = severe sleepiness

Test is out of 24 (8 situations rated 0-3)
NAME:

Current gold standard for evaluating sleep fragmentation and determining etiology
Polysomnography (PSG)
WHAT:

Is a normal Apnea/Hypopnea index
<5/hour
NAME:

Things to question a patient about when he/she present with sleep compaints
--Sleep hygiene (bedtime, rise, caffeine, meds, exercise, distractions)
--h/o insomnia
--head trauma
--hallucinations
--sleep paralysis
--cataplexy
WHAT:

Parts of sleep does patients with restless leg syndrome have difficulty with
Both initiating sleep and maintaining sleep
NAME:

Conditions known to make restless leg syndrome worse
Iron Deficiency!
Kidney disease
Pregnancy

**patients with RLS are associated with an increased risk of depression/anxiety which is relevant as >>>most anti-depressants make RLS worse<<<
STATE:

Prevalence/Demographics of restless leg syndrome
2.5-10% in western industrialized countries

Equal rates between boys and girls

More common post-puberty in women (potentially due to increased risk of iron deficiency
STATE:

How the following causes of leg discomfort would present differently from RLS
1. Nocturnal leg cramps
2. Peripheral neuropathy
3. Arthritic or muscle pains
4. Peripheral vascular disease
1. unilateral, sudden onset
2. no relieved by movement, accompanied by additional neuropathic sx like numbness/tingling/pain
3. tends to be stiffness brought on by immobility, so can be relieved by movement, but would be seen at any time of day and particularly worse in the morning
4. discomfort made worse by movement
WHAT:

Are the following tests best used for:
1. PSG
2. MSLT
3. MWT
1. Sleep apnea
2. Diagnose excessive sleepiness or REM problems
3. Used to determine the success of therapy helping excessive daytime sleepiness
HOW:

Long does it take to realign the circadian rhythm to night shift work
5-6 days (~90 minutes per day)
DEFINE:

Zeitgebers
Factor in the environment with a periodicity capable of synchronizing the endogenous circadian rhythm into a 24-hour cycle
HOW:

Much less sleep do night-shift workers get compared to daytime working peers
10 hours less per week
WHAT:

Percentage of patients admitted to the EMU have both PNES and epileptic seizures
5-15%
WHAT:

Is the effect of stress on the following:
1. MS
2. Memory
3. Cortisol
1. Sometimes linked to exacerbations (additionally stress management has shown significant reduction in enhancing lesions)
2. Negatively affects consolidation of short/long term memory, spatial memory, navigation
3. Increases corisol
WHAT:

Brain volume changes are observed in stress and under what situations do they reverse
Stress assocaited with decreased volume of hippocampus and amygdala

--> decrease in cortisol levels reverses hippocampal atrophy

--> whereas adding cortisone decreases recall
WHAT:

Percentage of medical students experience
1. burnout
2. SI
1. 50%
2. 10%
WHAT:

Do the following tests assess
1. Life Orientation Test
2. Pearlin's Personal Mastery Scale
3. Rosenberg Self-Esteem Scale
1. optimism - favorable expectations
2. mastery - belief in bringing about desired outcomes
3. self-esteem - evaluation of self-worth
HOW:

Can one increase optimism
Best Possible Scenario mental imaging
WHAT:

Genetic factor is related to increased psychological resources
Oxytocin receptor gene (OXTR)
DEFINE:

Eustress
A positive/adaptive response to a stressor
HOW:

1. Many deaths per year are the result of misdiagnosis?

2. Much does one's risk of death increase with a misdiagnosis
1. 40-80k

2. 2-5 times
WHAT:

Percentage misdiagnosis rate is consistently found at necropsy
50%
STATE:

With regards to mental status changes, what is the differential for a (1) Chronic/Slowly Progressive Course vs. (2) an Acute/Subacute Progression
1. think neurodegenerative disorders (dementia)

2. consider toxic vs. metabolic vs. infectious vs. medications
DESCRIBE:

The two major types of aphasia and what region of the brain is responsible for each
1. Expressive aphasia = Broca's (think broken speech, can't get words outs) ... also described as a nonfluent aphasia >>>> FRONTAL LOBE <<<<

2. Receptive aphasia = Wernicke's (think word salad, lots of random words) ... also described as fluent aphasia >>>> PARIETAL LOBE <<<<
DEFINE:

Dysarthria
Motor dysfunction leading to aphasia (thus is a "secondary aphasia")
DEFINE:

Apraxia
Inability to follow a motor command (not due to primary motor disorder or language impairment)
NAME & DEFINE:

Frontal Release Signs
Are patterned behavior reflexes present in infancy that are normally inhibited in adulthood by the frontal lobe ... but reappear after damage

Include: snout reflex, root reflex, palmomental reflex
LOCALIZE:

CN abnormality
= above spinal chord
LOCALIZE:

CN + ipsilateral deficit
= supranuclear (eg stroke)
LOCALIZE:

CN + contralateral deficit
= brainstem (eg stroke, tumor)
LOCALIZE:

CN V-VIII + contralateral deficit
= cerebellopontine angle (eg tumor)
LOCALIZE:

Unilateral CN IX-XI abnormality
= jugular foramen (tumor)
LOCALIZE:

Unilateral CN III, IV, V, VI abnormality
= cavernous sinus
NAME:

Disorders associated with hyposmia
Dementia, Parkinson's dz, B12 deficiency
HOW:

Would you diagnose conversion disorder in a patient with anosmia
Anosmia to ammonia is due exclusively to CN V
DIAGNOSE:

Unilateral anosmia
Suspect subfrontal tumor
LOCALIZE:

Tunnel Vision (pt reports the same size area of perception regardless of how far from the testing screen the examination is performed)
Conversion Disorder
LOCALIZE:

Bitemporal loss
Lesion at chiasm
LOCALIZE:

Bilateral Visual Field loss
= AT or POSTERIOR to chiasm
LOCALIZE:

Unilateral Visual Field loss
= ocular, retinal, optic nerve, or conversion
LOCALIZE:

Afferent pupillary defect
= optic nerve lesion anterior to chiasm
LOCALIZE:

Bilateral small pupils that reduce in size when the patient focuses on a near object, but do not constrict when exposed to bright light
-- accomodate but do not react

AKA Argyll Robertson (prostitute's) pupil

= midbrain lesion, specific for neurosyphilis (also diabetes???)
DIAGNOSE:

32 yo otherwise healthy female with one abnormally dilated pupil which does not constrict in response to light, loss of deep tendon reflexes, and abnormalities of sweating
= Adie's Syndrome

Thought to be the result of a viral or bacterial infection that causes inflammation and damage to neurons in the ciliary ganglion, an area of the brain that provides parasympathetic control of eye constriction
DIAGNOSE:

Upgaze difficulties on EOM exam
= stroke, or progressive supranuclear palsy

Latter = Progressive supranuclear palsy (PSP) is a rare brain disorder that causes serious and progressive problems with control of gait and balance, along with complex eye movement and thinking problems. One of the classic signs of the disease is an inability to aim the eyes properly
DIAGNOSE:

Ptosis, EOM fatigue on EOM exam
= neuromuscular
DIAGNOSE:

EOM difficulties, optic neuritis on EOM exam
= MS
DIAGNOSE:

CN III Palsy
= potentially ...
--aneurysm
--diabetic ophthalmoplegia
--ophthalmoplegic migraine
NAME:

Roles of each CN V branch
V1 = ophthalmic = forehead and corneal sensation/reflex

V2 = maxillary = infraorbital, palatal and upper teeth sensation

V3 = mandibular = chin, lower teeth, tongue sensation

Also facial sensation/muscles of mastication
DISTINGUISH:

CN IV vs. X lesion
CN IV = asymmetric palate elevation

CN X = asymmetric uvula deviation
DISTINGUISH:

CN XII UMN vs. LMN lesion
UMN = tongue away from lesion, weak, hyper gag reflex

LMN = tongue towards lesions, weak, fasculations
DISTINGUISH:

Spasticity
Rigidity
Cogwheeling
Myotonia
Dystonia
Spasticity = increased tone w/ sudden release
Rigidity = increased tone throughout range
Cogwheeling = intermittent catch
Myotonia = delay in muscle relaxation after activation
Dystonia = simultaneous activation of against/antagonist
WHEN:

Would one see hypotonia
With a LMN insult
WHEN:

Would one see spasticity
With UMN lesion
WHEN:

Would one see dystonia
With extrapyramidal abnormalities
WHEN:

Would one see myotonia
With myotonic muscular dystrophy
WHEN:

Would one see rigidity
With abnormalities to the extrapyramidal pathways, basal ganglia
WHAT:

Is suggested by proximal vs. distal weakness
Proximal = myopathy
Distal = peripheral neuropathy
NAME:

Signs consistent with an UMN vs. LMN lesion
UMN = weakness, NO acute atrophy, NO fasiculations, INCREASED reflexes, INCREASED tone

LMN = weakness, YES atrophy, YES fasiculations, DECREASED reflexes, DECREASED tone
NAME:

Nerve and Dorsal Root of deltoid muscle
axillary nerve, C5
NAME:

Nerve and Dorsal Root of biceps muscle
musculoskeletal nerve, C6
NAME:

Nerve and Dorsal Root of triceps muscle
radial nerve, C7
NAME:

Nerve and Dorsal Root of brachioradialis muscle
radial nerve, C6
NAME:

Nerve and Dorsal Root of extensor carpi ulnaris muscle
posterior interosseous nerve (branch of radial), C7
NAME:

Nerve and Dorsal Root of extensor digitorium muscle
radial nerve, C7
NAME:

Nerve and Dorsal Root of dorsal interosseous muscle
ulnar nerve, T1
NAME:

Nerve and Dorsal Root of abductor pollicus brevis muscle
median nerve, T1
NAME:

Nerve and Dorsal Root of iliopsoas muscle
lumbosacral plexus/femoral nerve, L1 L2
NAME:

Nerve and Dorsal Root of hamstrings muscle
sciatic nerve, S1
NAME:

Nerve and Dorsal Root of tibialis anterior muscle
deep peroneal nerve, L4 L5
NAME:

Nerve and Dorsal Root of gastrocnemius muscle
tibial nerve, S1
NAME:

The dermatome corresponding to the following
Deltoid
Thumb
Index Finger
Small Finger
Nipple
Umbilicus
Great Toe
Lateral Foot
Deltoid = C5
Thumb = C6
Index Finger = C7
Small Finger = C8
Nipple = T4/5
Umbilicus = T10
Great Toe = L5
Lateral Foot = S1
DESCRIBE & DIAGNOSE:

Apraxic gait
Ataxic gait
Short steps w/ reduced arm swings
Spastic gait
Steppage gait
Waddling gait
Apraxia = difficulty initiating gait = NPH
Ataxia = broad based and uncoordinated = cerebellar
Short steps = Parkinson's
Spastic = scissor like = bilateral UMN
Steppage = high knees, slap foot = peroneal palsy, L5 lesion
Waddling = pelvic/shoulder rotation = myopathy or muscular dystrophy
WHAT:

Does no response to an attempt to elicit a plantar reflex indicate
Unfortunately nothing ... patient could be normal, or could have super severe neuropathy or could have severe weakness
NAME:

Functions controlled by the cerebellar midline vs. hemispheres
Midline = tandem walking, hammer toe, shin scrape

Hemispheres = rapidly alternating movements, finger-nose-finger, limb ataxia
NAME:

Focus areas of Physical Therapy
transfers, gait, balance, wheelchair management, strengthening, functional mobility

also coma stimulation?
NAME:

Inappropriate physical therapy consults
--if patients are already focusing at baseline/premorbid level
--if pt is medically unstable
--if patient is sedated
--if pt is scheduled for OR within a few days
NAME:

Focus areas of Occupational Therapy
Maximize independence in ADLs and instrumental ADLs including interventions like splinting, self-care, home management training, cognitive retraining, adaptive equipment training
WHEN:

Would the following be indicated
Helmet
Resting Hand Splint
Multipodus Boot
Elbow Extension Splint
Helmet = hemicraniectomy
Resting Hand Splint = prolonged flaccidity, or increased tone, or hemiplegia/neglect
Multipodus Boot = flaccidity >1wk, or increased tone
Elbow Extension Splint = increased tone
NAME:

Inappropriate OT consults
--patient unable to participate because they are ... medically unstable ... on bedrest w/out splinting needs ... in coma without splinting needs
--patient scheduled for surgery soon
--patient already independent
NAME:

The types of conditions evaluated by Speech Language Pathology
many! swallowing, speech, language, cognitive, tracheostomy, alternative communication, voice disorders
NAME:

Phases of a swallow
oral phase --- pharyngeal phase --- esophageal phase
NAME:

Most likely origins of dysphagia
71% = brainstem lesions
14% = unilateral hemisphere lesions
NAME:

Slippery slope consequences of dysphagia
Upper airway obstruction
Aspiration pneumonia (NOTE: 20-50% mortality rate)
Dehydration
Death
STATE:

What should happen to CVA pts with regards to SLP
ALL CVA pts --> need swallow screen before initiating PO diet/meds

3 oz screen administered by doctors/nurses

Consult SLP as appropriate
NAME:

The gold standard for evaluating swallowing function
Videofluoroscopic Swallow Study ... AKA Modified Barium Swallow