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95 Cards in this Set

  • Front
  • Back
What is Parkinson's disease?
Chronic, slowly progressive degenration of brains dopamine neuronal systems
What are the symptoms of Parkinson's disease?
Mask-like face
Trunk forward flexion
Muscle weakness/rigidity
Shuffling gait
Resting tremors
Pill-rolling
Bradykinesia
Complications of Levodopa therapy (SINEMET) for Parkinson's
Involuntary mvmts. (increase w/ higher doses, longer term therapy)
On-off phenomenon (mobility/immobility - unrelated to time of admin.)
Wearing-off phenomenon (before next dose due)

*Use of adjuncts may be necessary (Parlodel, Premax)
Assessment of client with Parkinson's
Tremors (lips, face, limbs, "temulous writing")
Posture (shuffling gait)
Equilibrium (festination - leaning trunk w/ each step)
Face (mask, no blink)
Speech (repetition)
Gradual dementia
Skin, urination, hypotsn.
Drooling, weight loss
Nsg. diagnoses & interventions for client with Parkinson's
Imp. physical mobility (assess rigidity/tremors, gait, bradykin. Q4H - give meds - acyive/passive ROM)
Nutrition (diet prefs., tremors/rigid. mouth/neckmeds should peak at meals, small, freq., hi-cal. semi-soft meals)
Injury r/t Gait dist. (armrests, handrails, clutter-free, wide-based stance, rails up)
Coping (express fear, encg. self-care/social activ.)
What's Amyotrophic Lateral Sclerosis (Lou Gehrig's Disease)?
Rapidly progressive degeneration of upper and lower motor neurons (atrophy of hands, forearms, legs, rest of body)
ALS nursing care
Impaired verbal (anticipate, use non-verbal, don't interrupt)
Impaired swallow (HOB 45-90, preferences, soft diet, mouth care, suction ready)
Impaired mobility (passive ROM, rest periods, mobility aids, musc. relaxants, reposit. Q2, relax. techniques)
Plasmapheresis is used for which conditions?
Myesthenia Gravis
Multiple sclerosis
Guillian-Barre Syndrome

*Diseases w/ a probable immunologic component
What's plasmapheresis?
Removal of plasma from the blood and replacemrnt with donor plasma/colliodial product
What are some potential complications with plasmapheresis?
HYPOCALCEMIA
HYPOKALEMIA
Vascular access
Bleeding
Anemia
Infection
Hypothermia
Air emboli
Nursing diagnosis and interventions for plasmapheresis
HYPOCALCEMIA/CITRATE TOX. (see: numbness, tingling, twitching, pos. Chvostek's & Trousseau's)
Give calcium gluconate
HYPOKALEMIA (see: leg cramps, confusion, malaise, dysrhythmias)
BLEEDING (anticoagulants, platelet count drop)
Monitor: CBC, PT, PTT, fibrinogen, platelets
Pressure Dressings
Observe sites Q30min.
FLUID VOL. DEFICIT
Monitor: HR, BP Urine output
Administer replacement fluids
What's multiple sclerosis?
Demylenation of nerve fibers (in brainstem, cerebellum, spinal cord, optic nerve, and cerebrum)
Decrease in nerve conduction velocity and impulse transmission (symptom remission when areas heal by sclerotic tissue)
In multiple sclerosis, some clinical manifestations of brainstem syndrome are:
Diplopia
Eye pain, Nystagmus

* Cranial nerves III - XII
In multiple sclerosis, some clinical manifestations of cerebral syndrome are:
Emotional lability - depression/euphoria

* Also optic neuritis (clouding, loss of field, pain), seizures, hemiparesis, hemi-sensory loss, dysphasia
In multiple sclerosis, some clinical manifestations of cerebellar syndrome are:
Charcot triad (dysarthria, intention tremor, nystagmus)

* Also ataxia, hypotonia, weakness
Nursing care of a client with MS
ALTERATION IN URINARY ELIMINATION
Assess pattern, palpate, offer bathroom Q2H, Kegel's, decrease eve. fluids, avoid caffeine, catheterize PRN, antispasmodics

* Also muscle fatigue (avoid increased body temp.), impaired mobility (teds, anticoags., T&P, splints/braces), impaired vision (alt. eye patch Q2H), impaired communication
What's myesthenia gravis?
Systemic autoimmune disease. Abnormal weakness of voluntary muscles that improve with rest and anticholinesterase drugs
Nursing assessment for myesthenia gravis
Facial Muscles: Mask-like, Drooping, Dysphagia, Choking, Drooling

Neck Muscles: Difficulty maintaining head position

Resp. Muscles: SOB, Weak cough, resp. failure
Differential diagnosis for myesthenia gravis
Recent history of anticholinesterase use and the Tensilon test
How is the edrophonium chloride (Tensilon) test done?
2 mg injected IV
No Symptoms?
Another 8mg
Observe for muscle tone improvement for 30 sec. - 1 min.

Tone improvement = positive for myesthenia gravis
Tone weakens = negative for MG (positive for cholinergic crisis)
Drug teaching & side effects of drugs for myesthenia gravis (increase acetylcholine concentration and inhibit acetylcholinesterase)
**Take drug exactly as prescibed and on time
**Schedule routine care activities one hr. after administration

Side effects: Blurred vision, difficulty with dark adaptation & far vision; urinary frequency, abdominal cramps, sweating
Nursing care of client with myesthenia gravis
Ineffective Breathing (severe musc. weakness) - administer anticholinesterase drugs, HOB 30-45, suction, O2, ABG's
Activity Intolerance - Schedule ADL's after rest or in AM
Altered nutrition (weak mastication/swallow) - antichol. meds 1 hr. before eating
Ocular weakness - alt. eye patch 1/2 hr.
What's Guillain-Barre syndrome?
Rapidly progressive, symmetrical, ascending, flaccid paralysis usually following a viral infection

**Hx of URI, gastric flu, mono or hepatitis common
Major worry with Guillain-Barre syndrome
When nerves innervating intercostal muscles and the diaphragm are compressed and demylenated - FATAL RESP. IMPAIRMENT
Nursing care of client with with Guillain-Barre syndrome
Impaired Mobility (assess cranial nerves QH, thrombo, teds, passive ROM, splints 2H on 2H off)
Ineffective Breathing (monitor rate, airway, ABG's, suction)
Autonomic Instability (BP, dysrhythmias, flushing, LOC)
Nursing assessment for spinal cord abscess
Hx. of boil on back (spread to CNS)
Local pain (radiates to legs)
Back spasms
Leg weakness
Numb/tingle (paraplegia 24-72 hrs)
Decreased urination/incont.
GI upset
Fever
Positive Kerning's or Brudzinski
CBC - Inc. neutrophils
CSF - yellow/cloudy, inc. protein
An infection in the paranasal sinuses may lead to an abscess where?
Frontal lobe
An ear infection may lead to an abscess where?
Temporal lobe
An infection in the middle ear or mastoid may lead to an abscess where?
Cerebellum
An staphylococcal skin infection may lead to an abscess where?
Epidural (Thorassic most common)
An systemic infection from lungs or GU system may lead to an abscess where?
Intramedullary
How to care for someone with AIDS dementia complex (ADC)
Provide orientation
Structured activity
Same provider
Verbal cues
Memory board
Nursing diagnoses and interventions for client with AIDS
Infection (r/t immunosupression) - assess: CBC /w differential, T4/T8 count, skin integ. invasive lines, gloves, gown, mask goggles w/ fluids, LOW MICROBIAL DIET, no plants, keep fever down
Alt. in thought - Neuro checks Q2H, nuchal rigidity,
Self care defecit
Altered nutrition
What's meningitis?
Inflamation of the brain and meninges covering spinal cord (via bacteria, fungi, viruses, parasites)

*Bacterial = greater severity
What do you see with bacterial meningitis?
Cloudy, turbid, yellow CSF
Headache
Elevated temp. (101-104)
Meningial Irritation (Nuchal rig., Pos. Kernig/Brudzinski, photophobia)
Rash w/ petechial hemorrhage
Cranial nerve defecits (ocular palsies, pupils, ptosis, diplopia, facial paresis, deafness, vertigo)
Progression = may see s/s of ICP
Seizures
What do you see with viral meningitis?
Headache
Nuchal rigidity
Photoohobia
General malaise
What can you expect to do for a client with bacterial meningitis?
Review lumbar puncture results - administer antinfectives for bacterial meningitis

(Spinal tap, ID organism, give antibiotics)
What's encephalitis?
Inflamation of brain parenchyma due to viral or bacterial infective agents
How do you get bacterial encephalitis?
Depressed skull fractures
Septic penetrating instruments
How do you get viral encephalitis?
Bite or sting
Secondary to viral infections
How do you get equine encephalitis? Area of concentration? Incidence? Symptoms?
Horse mosquito
Cerebrum/Brainstem
Adults >50, Horse workers
Sudden drowsiness -> coma
Convulsive seizures
Meningeal signs
Cranial nerve palsies
Hemiplegia, N/V
How do you get St. Louis encephalitis? Area of concentration? Incidence? Symptoms?
Mosquito
Blood vessels in thalamus and midbrain
Late summer
Recent "flu"
Meningeal signs
INTENTION TREMORS (fingers, lips, tongue)
Constricted pupils
ABSENT ABDOMINAL REFLEX
How do you get Rocky Mountain encephalitis? Area of concentration? Incidence? Symptoms?
Tick (resevoir in squirrels/rodents)
Diffuse CNS - localized in skin
Rural, mountainous terrain, late spring/early fall
Fever
Decreased consiousness
Measles like rash on 3rd or 4th day
Rash fades, replaces by MACULOPAPULAR RASH ON WRISTS AND ANKLES (spreading to legs, arms, trunk)
Tremors, Convulsions, Muscle rigidity
What's Subacute Sclerosing Panencephalitis (Dawson's Encephalitis) preceeded by
Rubeola (2-10 yrs. prior)

*Fatal Prognosis
What's Reye's syndrome?
Acute brain edema secondary to infiltration of liver

*3-7 days after URI, flu, chix pox, measels - Uses of ASA during infection implicated
What do you see with Reye's syndrome?
Vomiting (no nausea/diarrhea)
Behavior change
Staring
Alt. drowsiness/screaming
Musc. weakness
Light/sound/touch sensitivity
Seizures
ICP
Reye's syndrome Diagnostic tests
Increased:

SGOT
SGPT
BUN
Blood Ammonia

Decreased:

Blood Glucose
Whats Myelitis? What do we see with it?
Inflammation of the spinal cord secondary to an infectious process (viral/bacterial) elsewhere

**See: Rapid, flaccid paralysis, loss of urinary/fecal control, NO back pain
How do you get poliomyelitis?
Through oropharynx (droplet inhalation) or GI (fecally contaminated foods)

*Assess for recent resp./GI infection & subsequent rise in temp.
What do we see with poliomyelitis?
Weakness/malaise
Headache/stiff neck
Neck/back/leg musc. ache
Alt. irritability/drowsiness
Difficulty swallowing/breathing/speaking (hiccups)
Pos. Kernig's/Brudzinski's
Convulsions/seizures
Difficulty walking
Cerebellar ataxia
What's Herpes Zoster? Who's at risk?
Shingles (adults who haven't had chix pox)

*Viral infection of posterior root gamglion (spinal nerves)

40-50% have neuralgia for 1-2 yrs.
Interventions for herpes zoster
Quiet environment
Analgesics, topical antiinflammatory, antipruritics
Maintain skin/eye hygene
Eye patch for corneal abrasions
How do you get neurosyphilis?
CNS invasion of the spirochete Treponema pallidum (3-18 mos. after primary inoculation)
How is neurosyphilis diagnosed?
Positive flourescent treponemal antibody test (FTA) and VDRI
What's Bell's palsy?
Facial nerve paralysis (unilateral or bilateral) most recover within 4 wks.
Nursing care for Bell's palsy
Pain?
Electro. stim.
Facial sling
Facial exercises 4x daily
Inability to close eyes?
Nutrition?
Natalizumab (Tysabri) use
Relapsing MS, Reduces frequency of exacerbations
Natalizumab (Tysabri) general side effects
HYPERSENSITIVITY/anaphylaxis
Hives/rash/puritis
Dizziness/nausea
Fever/flushing
Hypotension
Dyspnea/chest pain
Natalizumab (Tysabri) GI side effects
Cholelithiasis
Gastroenteritis
Natalizumab (Tysabri) CNS side effects
Depression
Suicidal Ideation
Headache
Tremor
Natalizumab (Tysabri) respiratory side effects
Lower resp. infection
Tonsilitis
Natalizumab (Tysabri) GU side effects
UTI
Vaginitis
Urinary freq./urgency
Irregular mentstruation (amen., dysmen.)
Natalizumab (Tysabri) administration instructions
No IV push
Don't shake bag
Assess for hypersensitivity
300mg Q4wks.
Natalizumab (Tysabri) client/family teaching
Report s/s of allergic reaction
Depression, infections, gall stones possible
Assess for suicide
Glatiramer acetate (Copaxone) life threatening side effect
Vaginal hemorrhage
Glatiramer acetate (Copaxone) immediate post injection reaction
Flushing
CP
Palpitations
Anxiety
Dyspnea
Laryngeal constriction
Uticaria (Hives)
Mitoxanthrone (Novantrone) life time dose
140 mg
Mitoxanthrone (Novantrone) CV side effects
CHF
CP
Arrhythmias
Tachycardia
Hypotension (Cardiotoxicity)
Mitoxanthrone (Novantrone) patient/family teaching
Assess for cardiotoxicity

*Evaluate left ventricular ejection fraction on ECG
Pyrostigmine bromide (Mestinon) contraindications
Hypersensitivity
Intestinal or urogenital tract obstruction
Peritonitis
Pregnancy/Lactation
Use Pyrostigmine bromide (Mestinon) with caution in...
Asthma
Peptic Ulcer
Bradycardia
Arrhythmias
Coronary occlusion
Vagotonia
Hyperthyroidism
Epilepsy
Pyridostigmine bromide (Mestinon) administration
Slowly (.5mg over 1 min. IV push)
ATROPINE SULFATE on standby
DC & call MD for: Excessive salivation, emesis, urination, diarrhea
Decrease dose for excessive sweating/nausea

*Take exactly as pres. and ontime
*Schedule routine care 1hr. after admin.
Serious side effects of Sumatriptan (Imitrex)
(for migraines)
Acute MI
Dysrhythmias
Death w/in a few hrs. of use
Cerebral/subarach. hemorrhage
Stroke
Myocardial ischemia
Hypertensive crisis
Anaphylaxis
Nursing considerations when giving Sumatriptan (Imitrex)
(for migraines)
Single dose PO w/ fluids as soon as symptoms appear
NO second dose sooner than 2-4 hrs,
Must consult provider before 2nd dose.

*NO MAOI's, ergotamine, IV's (vasospasm), Hx of MI, stroke, TIA, CAD, angina
Onset and signs of fat emboli
Several hours to 3 days:

Temp elevated
Tachycardia
PO2 and PCO2 decrease
Serum lipase elevated
Petechial rash of neck shoulders, thorax, eyelids
Signs of respiratory fat emboli
Cough
CP
Cyanosis
Dyspnea
Rales
Signs of cerebral fat emboli
Confusion
Lethargy
Stupor
Coma
Seizures
Aphasia
Hemiplegia

More profound on second day
Challenges of a cervical spinal cord injury
Flaccid quadriplegia

Autonomic dysfunction:
Decreased BP
Absence of perspiration
Priapism
Gastric/Urinary/Fecal retention
**Respiratory distress/failure above C4 (nerves to diaphragm)
Challenges of a thoracic spinal cord injury
High paraplegia
(legs, trunk, urinary and rectal sphincters)

*after 3-4 wks. jerking reflex mvmts.
Challenges of a lumbar spinal cord injury
Persistant flaccid paraplegia of legs bladder and rectum
Does Horner's syndrome occur with complete or incomplete spinal transection?
Both
Signs of Horner's syndrome
Ipsilateral ptosis of eyelid and downward rotation of eyeball
Miotic pupil
Ipsilateral facial anhidrosis
What do we see with an incomplete transection?
Variable loss of motor and/or sensory function on the same side as the sectioning
What do we see with a complete transection?
Permanent loss of motor and sensory functionbelow the transection

SPINAL SHOCK
Initial signs of spinal shock
Decreased BP (syst <80)
Decreased pulse rate
Decreased resp. rate
Decreased temp.
Skin: pink warm dry
Areflexia, flaccid paralysis, loss of sensation below lesion
Signs of spinal shock 24-48 hrs after trauma
Paralytic ileus
Urinary retention
Signs of spinal shock 7-10 days after trauma
Stress ulcers (occult stool)
Decreased musc. tone/strength
Pulmonary/urinary infections
Some nursing challanges of spinal cord injury
Fecal impaction (glycerine suppositories)
Bladder distention/urine retention (intermittent catheterization)

UTI's, avoid colds/flus, promote independence
What's Brown-Sequard Syndrome? Signs?
Spinal cord injury where only one side of the cord is damaged

Signs:

Ipsilateral motor loss
Contralateral temp./sensation loss
What's autonomic Hyperreflexia? Signs? Interventions?
Increased autonomic nervous system activity due to noxious stimuli below the injury

S/s: Pounding headache, elevated BP, bradycardia, profuse sweating above injury, anxiety, visual disturbances

Intervention: Remove noxious cause, Raise HOB, Monitor BP, Give anti HTN med
Frequently, type of memory affected in Alzheimer's
Short term (long term largely intact)
Some features of Alzheimer's
Agitation
Wandering
Muscle rigidity over time

** Consistency/same HCP importent in care of these patients
Most significant factor in the development of CP
Anoxia (prenatal, perinatal & postnatal)

**Wide variety of impairmants r/t muscle and cognition
S/s of CP in an infant
Poor sucing
Persistent tongue thrust
Poor head control & failure to smile after 3mos.
Arching back
Extreme irritability/crying
Feeding difficulties (gagging/choking; tongue pushes out food)
Most common type of muscular dystrophy
Duchenne - regeneration and replacement of muscle tissue by connective tissue