Neuro Flashcards

1
Q

What is MS?

A

Chronic auto-immune
demyelination of the white matter, brain and spinal cord
20-40
Women more common

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2
Q

ALS (Lou Gerigs)

A

Paralysis of voluntary muscles
40-60
Men more common
Tx is symptomatic, no cure

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3
Q

Guillain-Barre’

A

Reversible ascending paralysis that happens gradually
Acute inflammation disorder
Medications: steroids, plasmapheresis- immunoglobulin, analgesics

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4
Q

Myasthenia Gravis

A

Nerve impulses fail to cross the myoneural junction
Loss of acetylcholine (ACh) receptors
Autoimmune
Interventions: meds- anticholinesterases to increase amount of acetylcholine (pyridostigmine, nesternone), steroids,
Get things done in the morning bc fatigue gets worse throughout the day

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5
Q

Spinal shock

A

Temporary, sudden loss of reflex activity below the level of injury after spinal cord injury, temporary inflammatory response

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6
Q

Neurogenic shock

A

Massive vasodilation –> Above T6, venous pooling, extreme hypotension
All blood is going to extremities and not getting pumped back to the heart, causing hypotension
Treatment: fluids, vasoactive drugs to increase BP

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7
Q

Autonomic Dysreflexia

A

Exaggerated sympathetic response to noxious stimuli
It is characterized by paroxysmal HTN (the sudden onset of severe high blood pressure) associated with throbbing HEADACHE, profuse SWEATING, nasal stuffiness, flushing of the skin above the level of the lesion, BRADYCARDIA, anxiety, and sometimes by cognitive impairment
check bladder–>bladder scan
Autonomic dysreflexia is caused by an irritant below the level of injury, usually related to bladder or bowel

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8
Q

MS: clinical manifestations and Tx

A

Limited mobility, with fatigue, and visual disturbances, weakness, numbness, dysarthria (difficulty speaking), dysphagia, ataxia (unsteady gait) , sexual dysfunctions, nystagmus, spastic bladder
Tx: no cure or specific treatment - corticosteroids for symptomatic relief, immunosuppressants, baclofen for muscle spasticity

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9
Q

ALS: Clinical manifestations

A

Fatigue, cramps, twitching, loss of coordination
Slurred or nasal speech with dysarthria
Death occurs from failure of the respiratory system.

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10
Q

Myasthenia Gravis: Clinical manifestations

A

Drooping eye
Vision, breathing, swallowing, chewing, head control- most affected
Respiratory failure is the primary challenge.
fatigue increases as the day progresses
Tensilon test for diagnosis

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11
Q

Brain requirements

A

Glucose
O2
Blood (regulated by CO2)
Low ICP (

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12
Q

Migraine

A
chronic, throbbing
4-72 hours 
Auras may precede
Women
want to be in a dark room and not move
Triptan meds
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13
Q

Cluster headache

A
seasonal (4-12 weeks)
non-throbbing (usually around eye)
30 min-2 hours
Men 20-50 yrs old
Feels better with movement, oxygen and calcium channel blockers
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14
Q

What to note during a seizure

A

Order of activity, when it started, how long it lasted

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15
Q

Acute seizure meds

A

Lorazepam (IV) ativan
Diazepam (IV) valium
Diastat (Rectal)
Phenytoin (dilantin) or Fosphenytoin (IV)

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16
Q

Status epilepticus

A

Series of generalized seizures with no period of recovery.
Airway collapse→hypoxia→brain damage
Medical Management: stop seizures to promote adequate cerebral oxygenation
Nursing Management: monitor respiratory and cardiac function

17
Q

Meningitis

A

headache, stiff neck (nuchal rigidity), fever, nausea and vomiting, skin rash, photophobia, decreased LOC, confusion
Droplet precautions

18
Q

Encephalitis

A

Arboviruses (human transmission via mosquito/tick)
Enteroviruses (herpes zoster, mumps & chickenpox)
Herpes Simplex
Nursing management that of meningitis and Acyclovir (Zovirax)

19
Q

Parkinson Disease CM, Tx

A

decreased dopamine level causes loss of the ability to initiate and control voluntary movements
Micrographia, shuffled gait, bradykinesia, akathesia, stiff extremities, flexion contractures, mask, drooling, pain, pill rolling
Tx: levodopa, carbidopa, dopamine agonsit (parlodel), anticholinergic (benztropine),

20
Q

Alzheimer’s Disease

A

Chronic, progressive cognitive impairment
Aricept (donepezil) – slows progression
No cure
Safety is priority

21
Q

Huntington’s disease

A

Autosomal dominant
Progressive mental status deterioration
Choreiform (worm-like) movements that the p/t can’t control
30-50 year old