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71 Cards in this Set

  • Front
  • Back

Parietal lobe

Analyze sensory information


Awareness of body in space


Size and shape discrimination

Occipital lobe

Visual interpretation


Memory

Temporal lobe

Memory of sound


Understanding of language & music

Frontal lobe

Concentration


Memory


Motor function


Broca's Area


Affect


Personality


Judgement


Inhibitions

Seizures

Single event, of abnormal uncontrolled electrical discharge in the brain that disrupts a person's normal brain ability

Epilepsy

A chronic medical condition where there are many, unplanned, frequent, seizures

During the neurological assessment, the patient cooperates with the nurse's directions to grip with the hands and to move the feet but is unable to respond orally to the nurse's question. The nurse will suspect:



A) A brainstem lesion


B) Damage to the frontal lobe


C) A temporal lesion


D) Damage to the parietal lobe

Answer: B

Causes of seizures in people under 20 years old

Brain damage from birth


Congenital defects of CNS


Infection


Trauma


Genetic influences

Causes of seizures in people between 20 and 30 years old

Trauma


Vascular disease


Brain tumors

Causes of seizures in people greater than 50 years old

CVA


Brain tumor

Seizure phases

Prodromal Phase


Aural Phase


Ictal Phase


Postictal Phase


Prodromal Phase of a Seizure

Signs or activity which come before the seizure


Example: many have a "bad" feeling; a headache


Aural Phase of a Seizure

Sensory activity which precede a seizure


Example: smelling a burning smell; seeing halos

Ictal Phase of a Seizure

Full seizure; the patient is having the seizure NOW

Postictal Phase of a Seizure

Time of recovery after the seizure

Generalized Seizure

Every lobe in the brain is being shocked at one time


Can break down into probable altered consciousness and brief/possible altered consciousness


Includes generalized tonic-clonic seizures, absence seizures, myoclonic seizures, tonic seizures, clonic seizures, and atonic seizures

Partial Seizure

Localized at the beginning; starts in one area


Breaks down to Alert consciousness and altered consciousness


Includes simple partial seizures and complex partial seizures


Can develop into generalized seizures if not treated


Usually see the effects in the opposite side of the body

Probable altered consciousness in generalized seizures

Significant change of consciousness


Includes generalized tonic-clonic seizures and absence seizures


Worst types of seizures

Generalized Tonic-Clonic Seizures

Symptoms: loss of consciousness , falling to ground, incontinent, cyanosis, excessive salivation, bite tongue/cheek, Tightening and shaking


Postictal: sore muscles, fatigue, need sleep, pt can't recall seizure


Also know as Grand Mal seizures


A generalized probable altered consciousness seizures


The typical seizure you think of


DO NOT STICK ANYTHING IN MOUTH and Put them on their side

Absence Seizures

May see the patient drift away with fluttering of the eyes


Also known as Petty Mal seizures


A type of generalized probable altered consciousness seizure


Typically kids; usually stops by adolescence or changes to different type of seizure


Occur up to 100 times a day


May have a prodromal by hyperventilation & flashing lights


May see confusion/bizarre behavior and can affect kid's academic performance

Atonic Seizures

Muscles go flaccid


Type of brief/possible altered consciousness generalized seizures

Myoclonic Seizures

Quick tremor or jerk


Type of generalized brief/possible altered consciousness generalized seizures

Tonic Seizures

Tightening


A generalized brief/possible altered consciousness seizure

Clonic Seizures

Shaking


A generalized brief/possible altered consciousness seizure

Simple Partial Seizures

No loss of consciousness


Less than one minute


May involve simple motor, sensory (or combination)

Complex Partial Seizures

Alteration in consciousness or a clouding of consciousness


Greater than one minute


Confused postictally


Complex symptoms


Can involve behavioral, emotional, affective & cognitive functions

Complications of Seizures

Status Epilepticus


Psychosocial

Status epilepticus

Neuro emergency


It's when the seizure does not break


Seizure activity continues after 5 minutes


Give Valium or Adivan (slows activity), phenobarbital (helps break activity) IV

Seizure Dx

Accurate dx is critical


Accurate health hx & comprehensive description of seizure


EEG


MRI or CT
CBC, serum chemistries, LFT, kidney function tests, urine analysis

Tx of Seizures

Dilantin, Tegretol, Depakote, Keppra, Klonopin, Neurontin, Lamictal


Monitor serum blood levels with Dilantin


Surgery (Vagal Nerve Stimulator; surgically remove brain tissue)


Dilantin is drug of choice; therapeutic range is 10-20mcg

Nursing Care Post Seizure

Ensure physical safety


MAINTAIN AIRWAY


Assist in ventilation if pt respiratory arrests


NEVER PLACE ANYTHING IN MOUTH


Suction PRN
Loosen tight clothes


Establish IV


Administer phenobarbital, dilantin, benzodiazepines

Multiple Sclerosis


(Definition)

Chronic progressive degenerative disorder of the CNS characterized by disseminated demyelination of the nerve fibers of the brain and spinal cord

The nurse is called to the patient's room when the patient experiences a seizure. Upon finding the patient in a clonic reaction, the nurse should:



A) Turn the patient onto his side


B) Start oxygen by mask at 6L/min


C)Restrain the patient's arm and legs


D) Place tongue blade in the patient's mouth

ANSWER: A

Multiple Sclerosis


(Onset, etiology, characteristics)

Onset: 20-50 y/o; women > men; mainly caucasian


Etiology: Unclear


Characteristics: Activated T cells disrupt blood brain barrier


-->inflammatory response-->demyelination; Plaques form (sclerosis) on axon making it harder for nerve impulses to pass; eventually axons degenerate and no impulse can pass (late in disease)


Temporary myelin regeneration = remission


Clinical Course of MS

Relapsing Remitting


Primary Progressive


Secondary Progressive


Progressive Relapsing


Relapsing Remitting course of MS

85% of patients fall into ths


Remission for extended periods of time with flare-ups


25+ years prognosis before things debilitate them


Clear pattern of remission and of relapses

Primary Progressive course of MS

Progressive disease that may have plateaus but only temporary improvements


10% of patients


No remission


Prognosis is poor

Secondary Progressive course of MS

Begins like relapsing-remitting and then deteriorates

Progressive Relapsing course of MS

From onset, disease progression of disability with clear acute relapses after each remission with or without recovery

Signs and Symptoms of MS

Motor: weakness to paralysis; muscle spasticity


Sensory: numbness/tingling; partial blindness; decreased hearing; blurred vision; neuropathic pain


Cerebellar: nystagmus; dysphagia; ataxia


Others: fatigue; bowel and bladder changes; sexual disturbances


****S/s decrease during pregnancy but during postpartum women are at greater risk for disease exacerbation

Dx and Tx of MS

Dx: H&P, clinical manifestation, CSF analysis = increased immunoglobulin G; delayed evoked potential response; CT & MRI show sclerotic plaques


Tx: NO CURE; prednisone & ACTH to decrease inflammation; immunomodulator drugs (Betaseron); receptor modulators; muscle relaxants; surgery; avoid triggers



**triggers include heat, cold, stress and infections


**patients need to avoid crowds during flu season

MS Nursing Care

Promote optimal independence and functioning


Manage symptoms


Optimal nutrition


Prevent complications of limited mobility


Exercise helps (especially water sports) but NOT DURING AN ACUTE EXACERBATION

A 28 y/o woman who has MS asks the nurse about risks associated with pregnancy. Which response by the nurse is accurate?



A) "MS symptoms may be worse after the pregnancy."


B) "Women with MS frequently have premature labor."


C) "Symptoms of MS are likely to become worse during pregnancy."


D) "MS is associated with a slightly increased risk for congenital defects."

Answer: A

Parkinson's Disease Triad

Bradykinesia


Tremor


Rigidity

Parkinson's Disease


(Characterization and Cause)

Characterization: slowing down of the initiation and execution of movement (bradykinesia); muscle rigidity; tremor at rest; gait disturbance


Cause: decrease in Dopamine producing neurons


Parkinson's Disease


(Clinical manifestations)

Clinical Manifestations: Early--slight limp, slight tremor, dec. in arm swing


Late--tremor (pill roling, aggravated by stress and inc concentration, worse at rest); rigidity (resistance to passive movement through ROM, caused by sustained muscle contraction); bradykinesia (stooped shoulders, masked expression, little if any swing in arms, shuffling gait, drooling, slurred speech)

Treatment for PD

Medications: Dopamine Precursors (sinemet), Dopamine Receptor agonists (dec. amount of dopamine needed at the site), dopamine agonists (helps store it better)


Surgery: Deep brain stimulator implantation (current to brain, can change setting d/t symptoms and is reversible)

Nursing Care of PD

Promote optimal motor function: exercise


Promote self care


Promote optimal speech


Bowel regiment to prevent constipation


Nutriton (Aspiration risk, maintain body weight, eat with supervision/suction available, HOB eleveated, sitting upright)


Falls risk


Drooling (atropine 1% solution)


Speech therapy, physical therapy


Adequate fluids

Which of the following question should the home health nurse ask to determine if the meds are being given in appropriate dosages and times?



A) Is your weight remaining the same?


B) Do you experience any night sweats?


C)Can you see the television from a comfortable distance?
D) Are you having periods when walking is more difficult?

Answer: D

Myasthenia gravis


(Definition)

An autoimmune disease


Neuromuscular junction disease that causes varying degrees of weakness of particular skeletal muscles


Secondary to autoimmune process that decrease the number of ACh receptors


Typically thought to be started by a viral infection


Clinical Manifestations of MG

Easy muscle fatigue; restored after rest


Muscles affected--eyes, eyelids, chewing, swallowing, speaking and breathing


Typically, muscle weakness is worse by the end of the day


Major complications: Aspiration (#1 CONCERN), respiratory insufficiency, respiratory infection


**benefit greatly from short periods of rest

Dx tests for MG

Eyelids droop with exertion


Tensilon test: hand is electronically stimulated over and over, EMG shows muscle fatigue, tensilon is injected, if muscles improve then + for MG

Tx for MG

Drugs: Anticholinesterase drugs (free up receptor sites); alternate day corticosteroids, immunosuppressants


Plasmapheresis (often done for short term benefits or prior to surgery or for pts in a myasthenia crisis; removes plasma from blood to remove anti-ACh receptor antibodies)


Surgery: removal of thymus gland

Nursing Care of MG

Patient education regarding choking risk (secondary to weak gag and intercostal muscles)


Optimal nutrition secondary to impaired swallowing


Optimal communication


Self esteem (Secondary to pstosis, speech changes, role adjustment)


Give high caloric value b/c they may wear out half way through the meal

A nurse instructs a patient with MG about home care and the risk factors that can exacerbate the disease. Which of the following patient statements indicates a need for further teaching?



A) I ordered a med ID bracelet and will wear it every day


B)I have suction equipment at home in case I start to choke.


C) I will soak in the hot tub every day.


D)I should take my meds 45 minutes before breakfast, lunch, and dinner.

Answer: C

Dementia

Includes a plethora of disorders


8th leading cause of death in late life


Most common: Alzheimer's disease (60%)


Other forms: Vascular dementia (20%), Mixed types, fronto-temporal dementia, resulting from head trauma or anoxia

Alzheimer's Disease Manifestations

Loss of recent memory


Judgment problems


Personality changes


Deterioration of personal hygiene


Progressive to long term memory loss

Alzheimer's disease


(Characteristic and theories of causes)

Characteristc: high concentration of beta-amyloid plaques; neurofibrillary tangles seen on postmortem examination


Theories on causes: genetic mutations; environmental exposures, abnormalities in brain proteins or neurotransmitters

Alzheimer's Disease


(Dx and nursing implications)

Dx: by exclusion until the time of autopsy


Nursing implications: risk of injury and/or wandering; coping for the patient and later the family; self-esteem early on; self care issues; care giver burden

When teaching the children of a patient who is being evaluated for AD about the disorder the nurse explains that...


A) The most important risk factor for AD is a family hx of the disorder


B) A dx of AD can be made only when other causes of dementia have been ruled out


C)New drugs have been shown to reverse AD dramatically in some patients


D) The presence of brain atrophy detected by MRI confirms the dx of AD in pts with dementia


Answer: B

Consciousness

Continuum of brain wave activity


Can vary from : depression such as coma to hyperactivity such as a seizure

Determine Level of Consciousness

Behavior: Measure with Glasgow coma scale; range is 3-15; 8 and below is a coma



EEG

Glasgow Coma Scale


(Motor Response)

6--Obeys commands fully


5--Localizes to noxious stimuli


4--Withdraws from noxius stimuli


3--Abnormal flexion, i.e. decorticate posturing


2--Exensor response, i.ed. decerebrate posturing


1--No response

Glasgow Coma Scale


(Verbal Response)

5--Alert and oriented


4--Confused, yet coherent, speech


3--Inappropriate words and jumbled phrases consisting of words


2--incomprehensible sounds


1--no sounds

Glasgow Coma Scale


(Eye Opening)

4--Spontaneous eye opening


3--Eyes open to speech


2--Eyes open to pain


1--No eye opening

Intracranial Pressure (ICP)


(Definition and reasons for increased ICP)

Hydrostatic force measured in the brain CSF compartment


Reasons for Inc. ICP: hematoma, contusion, abscess, rapidly growing tumor, infection of the meninges

Increased ICP Complications

Complications: inadequate profusion-->brain damage; cerebral herniation-->brainstem compression-->respiratory arrest!!!


Cushing's Triad

Bradycardia with bounding pulse


Systolic HTN w/ widening pulse pressure


Irregular respiration pattern

Clinical Manifestations of Inc. ICP

Clinical Manifestations: Change in LOC (d/t dec blood flow); change in vital signs (subtle at first then cushing's triad); ocular signs (CN III compression --> dilation, NR, sluggish, inablilty to move eye upward and ptosis ipsilateral to lesion; fixed unilateral dilated pupil =hernation= NEURO EMERGENCY); dec motor function (coma when no response to pain); HA d/t pressure on arterial walls (occurs relentlessly but can worsen in AM and with straining); vomiting may not follow nausea; "unexpected vomiting" may also see projectile vomiting

Dx test fo inc ICP

CT & MRI to find cause


**lumbar puncture is not generally done on a person with increased ICP due to possible herniation b/c it could cause rapid pressure changes within the cranium

Inc ICP treatment

Tx underlying cause


Drug therapy: osmotic diuretic (Mannitol); corticosteroid (decadron)


Nursing care: respect of pt; HOB 30 degrees; maintain airway and adequate oxygenation; avoid anything that would inc. ICP; nutrition; skin integrity; infection