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79 Cards in this Set

  • Front
  • Back
Causes of increased ICP
Most common with a head injury

Secondary:
–Brain tumor
–Subarachnoid hemorrhage
–Encephalopathies
Cushing’s response
the brain’s attempt to restore blood flow by increasing arterial pressure to overcome increased ICP
Cushing’s triad:
increased ICP)
1. Bradycardia
2. HTN
3. Respiratory changes (Cheyne-Stokes breathing)

----increased temp
Most important indicator for increased ICP
Change in level of responsiveness/consciousness

ex. Restlessness without cause, Confusion, ↑ drowsiness

This is a medical emergency
Give this to dehydrate the brain and reduce cerebral edema
Mannitol (osmotic diuretic)
Corticosteroids
Nursing diagnosis for increased ICP
• Ineffective airway clearance – most will be on the ventilator
• Ineffective breathing patterns
• Ineffective cerebral tissue perfusion
• Deficient fluid volume
• Risk for infection – screw in brain – don’t need to know
Management of ICP
• Foley catheter to monitor urinary output (monitor osmotic diuretics)
• Serum osmolality levels to assess hydration
• ****Corticosteriods to help reduce edema
• Maintain cerebral perfusion by using fluid volume & inotropic agents
• Reduce CSF & blood volume by draining CSF
• Control fever to ↓ rate at which cerebral edema forms
Primary head injury
initial damage to the brain (contusions, lacerations, torn bv due to impact, foreign object penetration)
Secondary head injury
evolves over hours & days after the injury - may not know for days!!!
Open skull fracture:

Closed skill fracture:
actual tear in the dura

dura is intact
Types of Fractures
Simple
Comminuted (actually splintered or multiple fracture line)
Depressed (bone fragments are embedded into the brain tissue-needs surgery - all others heal on their own)
Basilar (at the base of the skull) - battle sign is like a bruise behind the ear
rinorrhea:

otorrhea:
CSF coming out of the nose

CSF coming out of the ear
Open head injury:
-occurs with skull fracture or penetration of the skull; penetrates the dura
-brain exposed to the outside environment
Closed head injry:
Blunt trauma

****More serious than open
Concussion:
-Minor
-No structural damage
-Get over quickly
Contusion:
-Major
-Brain is bruised
-Can take several months to get over (H.A.s, vertigo, seizures)
S/sx of epidural hematoma
initial period of unconsciousness followed by a period of lucidness followed by a period of unconsciousness
Medical management of epidural hematoma
• MEDICAL EMERGENCY!!!!!
***Burr holes through skull to decrease the pressure
• Possible craniotomy
• Drain
Causes of subdural hematoma
Trauma - most common (acute)
Bleeding disorders
*Ruptured aneurisms

chronic - minor head injuries in elderly, take while to show up
Intracerebral hemorrhage
Causes:

S/sx:
missile, bullet, stab injuries


Systemic HTN
Nurse's Responsibilities for head injuries & increased ICP
LOC - Glasgow coma scale
VS - frequently
Motor function - monitor for spontaneous strength
Pupil size - NOT GOOD if one pupil is larger than the other one

Provide a stress free environment et group activities together
What does a thrombotic stroke result from?
****Narrowing of a blood vessel

DM & HTN at higher risk
What is an embolic stroke?
An emboli or clot (can come from endocardium)blocks circulation
Who's at risk for an embolic stroke?
Pts with:
mechanical heart valves
a-fib
What's the defining factor in determining if a pt had a TIA?
They will have COMPLETE recovery between attacks
Deficits and recovery with hemorrhagic stroke:
Deficits are severe
Recovery is long - we just have to wait until the blood is slowly slowly slowly reabsorbed
What's the window for thrombolytic therapy for a stroke?
3 HOURS from onset of s/sx

-have to make sure its not a hemorrhagic stroke
Nursing interventions for stroke pts:
***Need to be turned et monitored for skin breakdown due to hemiparesis or decreased mobility

Encourage to participate in ADLs as much as possible (ex. dress affected side first

Bladder training - may need to be on a schedule

Facilitate communication (speech therapy)
What kind of food does a stroke pt need?
Oatmeal consistency - avoid thin liquids, can use a thickener
Diff between primary & secondary brain tumors:
Primary: originate within the CNS

Secondary: Mets from somewhere outside the brain
Most common brain tumor:
Glioma - total removal causes considerable damage to vital structures
Most common type of glioma:
Astrocytoma
What type of brain tumor tends to recur?
Menigioma
Acoustic neuroma:
s/sx: hearing loss, tinnitus, dizziness

Usually on the 8th cranial nerve (responsible for hearing and balance)
Tx for brain tumors:
1) Surgery to get as much as possible (not the whole thing)
2) f/u surgery with radiation
3) corticosteroids - HAs

Chemo doesn't cross the BBB
Management for seizures:
prevention - enough meds to achive control w/ minimal side effects (drugs control-do not cure)

DO NOT restrain or put anything in their mouth - just make sure they are safe (ex. side rails up)
Who are most likely to develop seizures?
Older clients due to cerebrovascular disease, metabolic changes, and head trauma
Goals for managing status epilepticus (seizure activity longer than 30 minutes):
-stop the seizures ASAP
-ensure adequate cerebral oxygenation
-maintain a seizure-free state
Phases of migraines:
1) Prodrome
2) Aura
3) Headache
4) Recovery
Prodrome phase:
Hours to days before HA

Depression, irritability, feeling cold, food cravings, anorexia, activity level changes
Aura phase:
Lasts less than an hour

-scotomas (black spots)
-scitntillations (flashes of lights)
-parasthesias
-motor dysfunctions
HA phase:
4-72 hours
VASODILATION + decreased serotonin
-Throbbing, pounding, severe, incapacitating pain
-Photophobia
-N/V
Recovery phase:
-extended sleep
-muscle aches & tenderness
-exhaustion
Tx of migraines:
Abortive - must be taken during the ONSET (aura) or it will not work

Preventative - taking a med q day

All cause vasoconstriction (because a migraine is vasodilation)
Nursing care for migraines:
-educate on when to take meds
-educate on precipitating factors (cheese, wine, chocolate)
-provide quiet/dark room
-administer antiemetics
Who has the greatest incidence of cranial arteritis (temporal arteritis)?

Complication:
>70 y/o


blindness
What's the worst kind of meningitis?
Bacterial - can be deadly

dx'd w/ a spinal tap
S/sx of meningitis:
HA, fever
-Nuchal rigidity
-With bacterial; + Kernig's sign: when knee is flexed to stomach they cannot extend their leg
-With bacterial; + Brudzinski's sign: push their neck down and their hip & knee will flex
When is the meningitis vaccine recommended?
11 y/o well-check
What's MS:


How is MS characterized?
A disorder of the nervous system causing demyelinization

By periods of remission and exaccerbation
Most common type of MS
Relapsing-remitting: attack or series of attacks (exacerbations)
Early s/sx of MS:
***Blurred or double vision - almost always
-tingling/numbness
-loss of balance
-weakness in one or more limbs
Medical management of MS:
-tx is to delay progression
-manage chronic s/sx
-tx acute exacerbations

s/sx that need tx: spasticity, fatigue, bladder dysfunction, ataxia
Nursing interventions for MS:
Promote physical mobility
Prevent injury - due to bad coordination
Bladder/bowel training - Q2hours or teach straight cath

MS is aggravated by changes in temp - don't go outside to exercise
What's the cause of Myasthenia Gravis?
80-90% have ANTIBODIES to acetylcholine receptors and thymus gland problems
S/sx of MG
-Ptosis
-Bulbar symptoms - muscles that control speech, chewing, and swallowing (weakened)
-Hallmark sign**Waxing & waning s/sx: strong muscles in the morning and weak in the evening
What's the diff b/w myasthenic crisis and cholinergic crisis?
The difference is the response to the tensilon test

Myasthenic: acute exacerbation (mm weakness) - not enough meds

Cholinergic: OD of cholinergic drugs
Nursing & client education for MG:
-meds: take on time (BEFORE eating, so they can swallow)
-energy conservation strategies
-ptosis: wear a patch, use artificial tears, tape it shut
S/sx of Guillain-Barre Syndrome:
-ascending weakness (pks ~14th day)
-starts w/ muscle weakness and diminished reflexes of the lower extremities
What's generally the cause of mortality with Guillain-Barre?
Respiratory Failure

Usually go ahead and put them on the vent before this happens
Cause of Guillain-Barre:


Tx of Guillain-Barre
autoimmune attack on peripheral nerve myelin

IVIG (IV Immunoglobulins - removes circulating antibodies

Vent
Causes of peripheral neuropathies:
-systemic diseases (DM w/ poor control)
-Vit deficiency (B12)
-alcohol
What can trigger pain with Trigeminal Neuralgia (Tic Douloureux)?
cold
brushing teeth
What is Parkinsons associated with?
-decreased dopamine
-increase in excitatory neurotransmitters (more than inhibitory) - these effect voluntary movement
*****Classic triad for Parkinsons:
1) Tremor - first sign; pill-rolling
2) Rigidity - increase resistance to ROM
3) Bradykinesia - slowness of movement; losing ability of automatic motion, stooped posture, shuffled gain, *postural instability (propulsive gait)
Nursing dx for Parkinsons:

***focus on what you'd do to fix these
Risk for falls - fall precautions
Self-care deficit
Chronic confusion
Impaired physical mobility
Impaired verbal communication - speech therapy
Risk for imbalanced nutrition: less than body requirements - Feed them

Caregiver support/education
What is Huntington's Disease?
Chronic, progressive, disease of the nervous system that results in progressive involuntary choreiform (dance-like) movement and dementia
Can Huntington's be inherited?
YES, 50% risk of passing it onto their children
S/sx of Huntington's w/ nursing interventions:
-constant uncontrollable movement; maintain safety
-chorea, intellectual decline, emotional disturbance; treat physical symptoms
-ambulation becomes impossible, aparthy, suicidal; provide physical and emotional support to pt et family
-chewing/swallowing difficulty, CONSTANT movment; may need 4000-5000 calories/day to maintain body weight
Is alzheimers normal to develop as you grow older?
NO, it is NOT a normal part of aging
Is alzheimers genetic?
It can be - its very rare
Called familial alzheimers
Alzheimers stage 1
– Duration: 1 – 3 years
– Short-term memory loss
– Decreased attention span
– Subtle personality changes
– Mild cognitive deficits
– Difficulty with depth perception
Alzheimers stage 2
– Duration: 2 – 10 years
– Obvious memory loss
– Confusion
– Wandering behavior
– “Sundowning” – because they’ve been sleeping all day
– Irritability and agitation
– Decreased spatial orientation
– Impaired motor skills
– Impaired judgment
Alzheimers stage 3
– Duration: 8 – 10 years
– Absent cognitive abilities
– Disoriented to time and place
– Severely altered communication skills
– Impaired or absent motor skills
– Bowel and bladder incontinence
– Inability to recognize family & friends
– Disturbed sleep patterns/increased sleep time - bedridden
How's alzheimers dx'd?
Mostly s/sx et ruling out all other posibilities (depression, OD of meds, etc.)
CT/MRI show brain atrophy
Nursing for alzheimers
• Provide socialization – 1-2ppl at a time (not whole family)
• Promote adequate nutrition – make things very simple
• Promote balanced activity & rest – engage in activities during the day (don’t let them sleep)
• Educate on home & community based assistance
– Maintain safety – like baby-proofing the house
– Help maintain functional ability - ADLs
– Help meet personal needs - ADLs
ALS (AKA Lugarics Disease)
Body deteriorates, but the brain stays the same
– Atrophy of hands, forearms, and legs
– Paralysis
– Death (2-5yrs p onset of symptoms – due to respiratory failure)
How is ALS dx'd?
***Muscle biopsy
Based on s/sx
MRI
S/sx ALS:
• Tongue atrophy – tongue shrinks and have weakness of the soft palate (cannot laugh, speak)
• Dysphagia - risk for aspiration - impaired nutrition
• Dysarthria
• Muscle atrophy extending to flaccid quadriplegia
• Eventual respiratory muscle involvement - causes death