Midterm Flashcards
(155 cards)
2 types of Seizures
Generalized & Focal
Focal , pt is somewhat conscious & aware during the event
Common Causes of Seizures
- Very high fever (more common in children, Febrile seizure)
- CNS infection (bacterial meningitis)
- Hypoglycemia (severely low glucose level)
- Alcohol withdrawal (seizure precautions!)
- Epilepsy
- Acid-base imbalances (acidosis/hypoxia)
- Brain tumor
Epilepsy
A chronic condition.
Causes:
- severe brain trauma
- congenital birth defect
- Massive stroke
- Long lasting effects from an illness like bacterial meningitis
Stages of a Seizure - Prodromal
S&S appear days before big event like depression, anger, anxiety, GI & urinary issues
Stages of a Seizure - Aura
Happens prior to a seizure within seconds to mins!
Manifests as spots in vision, Deja vu, sudden weird smell or taste.
common with generalized tonic/clonic seizures (gran mal)
Stages of a Seizure - Ictus
The seizure itself, typically lasts 1-3mins.
Status Epilepticus lasts MORE than 5mins or 2 shorter seizures back to back
MUST TIME THE EVENT!!
For Status Epilepticus, pt needs to be medicated to STOP seizure! Usually IV push diazepam!
Stages of a Seizure - Post Ictus
Recovery of the brain post seizure. Tonic-Clonic seizures have the LONGEST recovery time, typically hours to days.
Absent seizures have immediate recovery!
Tonic-Clonic Seizure
aka Grand Mal
Most common type of generalized seizures!
Typically present w/ aura prior to it starting
Absent Seizure
Aka Petit Mal
More common in PEDIATRIC population!
Talking to someone & all of a sudden they go blank
They come back & don’t know what just happened
Seizure Precautions - Before Seizure
- assess risk factors
- seizure precautions in place:
- oxygen
- suction
- IV access
- Padded side rails
Seizure Precautions - During Seizure
- untie or loosen pt’s gown (choking risk)
- TURN PT TO THEIR LEFT SIDE TO ENSURE OPEN & PATENT AIRWAY
- Nothing in the mouth to prevent aspiration
- Time the seizure!! Important part of the assessment
- Assessing if there is bowel or bladder incontinence
- bed should be in lowest position & locked!
- how are the limbs moving? Assessing/documenting
- Did they cry out prior?
Seizure Precautions - After Seizure
- ensure pt is stable
- maintain airway
- neuro assessment
- vital signs
- blood draw to monitor drug levels/electrolytes
- Meds administered
- EEG , no caffeine, seizure meds, or stimulants prior!
Multiple Sclerosis (MS)
Autoimmune disorder that affects the myelin sheaths of neuron in the CNS
- affects women more than men, ages 20-40yo at highest risk
- can be relapsing or remitting, symptoms often appear & disappear in 85-90% of pts
- primary progressive type = progression of disability without relief
- cause unknown, no cure
Diagnosis of MS
- MRI to look for lesions (scarring/inflammation in brain & spinal cord)
- Lumbar puncture (look for oligoclonal bands signaling inflammation in CNS)
- Evoked potential study = electrode on scalp measuring how long it takes brain to process signals from nerves
S&S of MS
- muscle stiffness or spasms
- Ataxia
- pos Romberg sign = pt stands w/ eyes closed & feet together loses balance/sways
- Lhermet’s sign = pt moves their head in different ways & feels electric shock down their spine
- Uhthoff’s Sign = heat makes S&S worse (can also be heat from physical exertion)
- feel drained, depressed, mood swings
- Nystagmus (invol movements of the eyes)
- Optic neuritis (double or dull/gray vision)
- Overactive bowel/bladder or the opposite
Nursing Care & Management of MS
- Assistive devices for ADL like shower chair, commode, walker, Sara-steady
- Edu on what to avoid (heat, stress, infection prev)
- Clear understanding of bowel & bladder needs to Tx accordingly
- Exercise & PT
- connect w/ support groups
Myasthenia Gravis (MG)
Autoimmune condition that attacks muscle receptors that control VOLUNTARY muscles at the neuromuscular junction
Much more common in females.
Myasthenia Gravis S&S
- Hallmark sign is muscle weakness that gets worse w/ continued activity
- Initial S&S involve ocular muscles: diploid (double vision), Ptosis (drooping eyelid), strabismus (lazy eye)
- Weakness of facial muscles (mask face) mastication may become affected!
- Dysphonia (voice impairment)
- Generalized weakness of extremities
Resp failure in SEVERE cases
Myasthenic Crisis
Sudden, temporary exacerbation of symptoms of MG, commonly caused by INFECTION.
SEVERE RESP DISTRESS + Severe presentations of the normal S&S
- often caused by under medicating
- pt will likely require intubation & mech vent
- suctioning to prevent aspiration!
Cholinergic Crisis
Happens from OVER MEDICATING!
Too much ACh is hitting receptor sites, over stimulated receptors become desensitized.
Results in SLUDGEM:
Salivation
Lacrimation
Urination
Defecation
GI upset
Emesis
Miosis
Diagnosing MG
- Tensilon Test = Edrophonium chloride (ACh-esterase INHIBITOR) is administered , if immediate improvement in muscle strength , positive test for MG!
- CT scan showing enlargement of Thymus gland (thought to correlate to autoimmune pathology)
- Ice pack test = ice on eyes for 2min, if ptosis IMPROVES, MG is likely the culprit
Care & Management of MG
- Respiratory assessments!!!
- Assess swallowing (speech & swallow test)
- Risk for falls!
- No cure, just Tx S&S to improve quality of life
Guillain-Barre Syndrome (GBS)
Autoimmune attack on the peripheral nerve myelin causing paraesthesia (weakness) in the lower extremities THAT PROGRESSES FROM THE BOTTOM UP! TOE TO HEAD!
Most often a viral infection (usually resp or GI) proceeds clinical presentation of GBS by 2-6 weeks!!
Nursing care & Management of GBS
- As it ascends to torso, can cause RESP FAILURE! Monitor breathing
- Want to prev complications from potential to develop DVT & pressure injuries (think SCDs, repositioning, mepilex)
- High risk for paralytic ileus!!
-
Plasmaphoresis to try to rid body of autoimmune abs and replace with IVIG
can take up to 2 years to recover