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62 Cards in this Set

  • Front
  • Back
Tremor
-slow, unilateral resting tremor present in 75% at DX of Parkinson's. Disappears with purposeful movement. Rhythmic, slow turning motion. Present while at rest and increases when walking, concentrating or feeling anxious.
Rigidity-
resistance to passive limb movement. Passive movement may cause jerky movements (cogwheeling). Invol stiffness increases when another extremity is vol moving.(Parkinsons)
Bradykinesia-
most commonsymptom of Parkinson's. Refers to the overall slowing of active movement. Takes longer to complete activities and has difficulty initiating movement. (getting up)
Postural Instability
-loss of postural reflexes; stands with head bent forward and walks with a propulsive gait. Shuffling gait; walks faster/faster trying to move the feet forward. Difficulty pivoting causes loss of balance and a risk of falling.(Parkinsons)
Parkinsons
Complications
Risk for:
–Respiratory and Urinary tract infections
–Skin breakdown and injury from falls
•Side effects from Meds:
–Dyskinesia or orthostatic hypotension
Levodopa
-most effective and the mainstay of treatment. Levodopa is converted to dopamine in the basal ganglia, producing sym relief.
Anticholinergic:
Parkinson's tx
are effective in controlling tremor and rigidity. May be used in with Levodopa. Counteract the action of acetylcholine. Side effects: blurred vision, flushing, rash, constipation, urinary retention, & acute conf state. Poorly tol. Monitor pts with glaucoma and BPH.
Antiviral:
parkinsons tx
to reduce rigidity, tremor, bradykinesia and postural chgs. Acts by releasing dopamine from neuronal storage sites, exact mech is unknown. Side effects: low. Psych (mood chg, confusion, dep, hall), LE edema, nausea, epi distress, urinary retention, headache, & visual impairment.
Pergolide
is 10x more potent, no therapeutic advantage.
Used for post poning levodopa or after it loses effectiveness
–Side effects: nausea, vomiting, diarrhea, lightheadedness, hypotension, impotence and pshych effect.
Monoamine Oxidase Inhibitors:
Eldepryl (seleglinie) promising development. Inhibits dopamine breakdown and is thought to slow down the progression of disease. Currently used in combination with dopamine agonist to delay the use of carbidopa/levodopa. Side effects similar to Levodopa.
Catechol-O-methyltransferase Inhibitors:
clinical trials suggest little effect when given alone but can increase the duration of action of carbidopa or levodopa block and enzyme that metabolizes levodopa making more available for conversion to dopamine. Entacapone (Comtan) and Tolcapone (Tasmar). These meds reduce motor fluctuations in advanced disease.
Antidepressants:
tricyclics ex: Amitriptyline hcl (Elavil) typically prescribed because of its anticholinergic and antidepressant effects. Serotonin reuptake inhibitors (Prozac or Wellbutrin), are effective but may aggravate sym of parkinson’s.
Antihistamines:
Benadryl (diphenhydramine hcl), Banflex (orphenadrine citrate), and Neo-Synephrine (phenindamine hcl) have mild central anticholinergic and sedative effects and may reduce tremors.
Huntington’s Disease
def
•A chronic, progressive, hereditary disease of the nervous system that results in progressive involuntary choreiform movement and dementia.
Huntington’s Disease
Clinical Manifestations
•Most prominent chorea (abnormal invol movements), intellectual decline and often emotional disturbance.
•Progresses to a constant writhing, twisting, uncontrollable movement may involve entire body.
•Motions are devoid of purpose or rhythm.
•Face: tics and grimaces
•Speech: slurred, hesitant, explosive, to unintelligible.
•Chewing and swallowing difficulty; risk of choking and aspiration.
•Gait: disorganized to impossible
•Eventually w/c to bed bound
•Lost Bladder and Bowel control
•Cognitive: first personality changes to uncontrollable anger, profound depression to suicidal. Judgment and memory are impaired, eventual dementia.
Amyotrophic Lateral Sclerosis
Def
•Known as ALS or Lou Gehrig’s disease
•Unknown cause
•Loss of motor neurons in the anterior horns of the spinal cord and the lower brain stem.
•Motor neurons cells die, the muscle fibers they supply atrophy.
•Neuronal degeneration may occur in both the upper and lower motor neuron systems
ALS
Clincal Manifestations
Chief symptoms: fatigue, progressive muscle weakness, cramps, fasciculations, and incoordination of motor neurons in the anterior horns of the spinal cord results in progressive weakness and atrophy of the muscles of the arms, trunk or legs.
•Spasticity and the deep tendon stretch reflexes become brisk and overactive.
•Anal and bladder sphincters remain intact, spinal nerves are spared in this area.
ALS
Nusing Interventions
•Challenge to guide the patient in use of moderate intensity, endurance-type exercises for the trunk and limbs to help reduce spasticity.
•Facilitate communication
•Reduce risk of aspiration
•Decrease pain secondary to muscle weakness
•Decrease risk of injury related to falls
•Provide diversional activities such as reading and companionship.
•Family support
Menigitis
Clinical manifestations
Key: fever, severe headache, nausea, vomiting and nuchal rigidity
•Others: positive Kernig’s/brudzinski’s, photophobia, decreased LOC and signs of increased ICP.
Meningitis
Complications
•Increased ICP most common
•Residual neurologic dysfunction
•Hearing loss may be permanent; related to CN (VIII) irritation
•Hemiparesis, dysphasia and hemianopsia should resolve unless an ongoing infection is present.
•Waterhouse-Friderichsen syndrome: manifested by petechiae, DIC, adreanl hemorrhage and circulatory collapse. Associated with meningococcemia.
Meningitis
Management
Bedrest
•IV fluids
•Antibiotics IV; PCN/amp, cephalosporin
•Codeine for headache
•Dexamethasone
•Acetaminophen or asa for fever (T >100.4/38
•Hypothermia
•Phenytion IV
•Mannitol
•Clear liquids as desired or tolerated
•Vaccination preventative***
Viral Meningitis
s/s
Presents with a headache, fever, photophobia and nuchal rigidity.
–Moderate to high fever
Dx test: CSF exam by LP
Encephalitis
clincal manifestations
•Onset; usually nonspecific, with fever, headache, nausea and vomiting.
•Encephalitis can be acute or subacute.
•Onset day two or three and symptoms may vary.
•Minimal alterations in mental status to coma
•Virtually any CNS abnormality can occur including:
–Hemiparesis, tremors, seizures, cranial nerve palsies, personality changes, memory impairment, amnesia and dysphasia.
Assessing for Brain Abscesses
•Frontal Lobe s/s
–Hemiparesis
–Aphasia (expressive)
–Seizures
–Frontal headache
Assessing for Brain Absess
•Temporal Lobe s/s
–Localized headache
–Changes in vision
–Facial weakness
-Aphasia
Assessing for
Cerebellar Abscess s/s
–Occipital headache
–Ataxia (inability to coordinate movements)
–Nystagmus (rhythmic, involuntary movements of the eye)
Alzheimer’s disease and Dementia
Overview
•Alzheimer’s is a chronic, progressive, degenerative disease of the brain.
•Dementia is a syndrome characterized by dysfunction or loss of memory, orientation, attention, language, judgement, and resoning.
Warning signs AD
1.Memory loss that affects job skills
2.Difficulty performing familiar tasks
3.Problems with language
4.Disorientation to time and place
5.Poor or decreased judgment
6.Problems with abstract thinking
7.Misplacing things
8.Changes in mood or behavior
9.Changes in personality
10.Loss of initiative
Clinical manifestations-Dementia
•Depending on the cause the onset of symptoms may be insidious and gradual or more abrupt.
•Neurologic degeneration: gradual/progressive
•Vascular: abrupt
•Further classified as mild, moderate, severe
•Mild: forgetfulness beyond normal
•Mod: impaired ability to recognize family
•Sev: little memory, u/a to process new in
Spinal Cord Injury
A = Complete:
No motor or sensory function is preserved in the sacral segments S4-S5.
Spinal Cord Injury
B = Incomplete:
Sensory but not motor function is preserved below the neurologic level, and includes the sacral segments S4–S5.
Spinal Cord Injury
C = Incomplete:
Motor function is preserved below the neurologic level, and more than half of key muscles below the neurologic level have a muscle grade less than 3.
Spinal Cord Injury
D = Incomplete:
Motor function is preserved below the neurologic level, and at least half of key muscles below the neurologic level have a muscle grade of 3 or greater.
Spinal Cord Injury
E = Normal:
Motor and sensory function are normal.
Spinal Cord Injury
Injury above C4:
total loss of respiratory muscle function
Spinal Cord Injury
Below C4:
results in diaphragmatic if the phrenic nerve is functioning though edema or hemorrhage can affect function.
Cervical and thoracic injuries can cause paralysis of abdominal muscles and often intercostal inhibiting ability to cough.
Spinal Cord Injury
Any injury above T6;
decreases the influences of the sympathetic nervous sys
•Bradycardia, periph vasodilation results in hypotension. Reduces venous return and subsequently decreases cardiac output
•EKG monitoring essential
•RX: IV fluids, vasopressors
Spinal Cord Injury
Injury above T5:
ypomotility; paralytic ileus and gastric distension.
•Stress ulcers possible, if undiagnosed inability to diagnose due to lack of subjective symptoms.
•Less voluntary neurologic control over the bowel results in a neurogenic bowel. Need a good bowel regimen.
Spinal shock:
Def
represents a sudden depression of reflex activity in the spinal cord below the level of injury. Loss of sensation and motor.
Neurogenic shock:
due to loss of autonomic function below the level of injury. Vital organs affected; HR & B/P decrease. Loss of sympathetic causes a variety of other; decrease in CO, venous pooling in ext, and periph vasodilation.
spina bifida
overview
•Occurs during the 4thweek of gestation when ventral induction of the neural tube fails to occur.
•Degree of impairment corresponds to the level of the defect and size.
Spina Bifida
Results:
paralysis, partial paralysis, or varying sensory defects.
•Clubfeet, scoliosis and contracture and dislocation of the hips may also be associated with lesions
Cerebral palsy
overview
•Also known as; static encephalopathy
•Chronic, nonprogressive disorder of posture and movement.
Cerebral palsy
Characterized by
difficulty in controlling the muscles because of an abnomality in the extrapyramidal or pyramidal motor system (motor cortex, basal ganglia, cerebellum)
•Co-morbidities: cognitive, hearing, and visual impairments as well as seizures are common.
Hydrocephalus
•A result of an imbalance between the production and absorption of CSF
•Excess CSF accumulates in the ventricular system, causing dilation and compression of brain tissue against the skull
•Results in enlargement of the skull if sutures are open
•Results in s/s of increased ICP if sutures are fused.
Pedi Differences in neuro dysfunction
Papilledema rarely occurs because open fontanels and sutures can expand with ICP
•Primitive reflexes may reappear with neurologic disease. Ex: grasp, rooting (present @ birth then disappear by 5 months)
Clinical Manifestations of ICP
•Infant:
poor feeding, or vomiting
–Irritability or restlessness
–Lethargy
–Bulging fontanel
–High-pitched cry
–Increased head circumference
–Separation of cranial sutures
–Distended scalp veins
–Eyes deviated downward (“setting-sun” sign)
–Increased or decreased response to pain
Clinical Manifestations of ICP
Child:
headache
–Diplopia
–Mood swings
–Slurred speech
–Papilledema (after 48hrs)
–Altered level of consciousness
–Nausea and vomiting, especially in the morning
Papilledema
swelling of the optic disk
Postconcussion syndrome:
2 seeks to 2 months after the injury. Sym: persistent headache, lethargy, personality/behavioral changes, shortened attention span and memory, and changes in intellectual ability.
Myasthenia Gravis
Exacerbations
can be precipitated by emotional stress, pregnancy, trauma, various drugs; antibiotics, psychotropic's, beta blockers and neuromuscular blocers
Waterhouse-Friderichsen syndrome:
manifested by petechiae, DIC, adreanl hemorrhage and circulatory collapse. Associated with meningococcemia.
encephalitis
HSV encephalitis is the most common cause of acute non-epidemic viral encephalitis.
•Cytomegalovirus encephalitis is one of the most common complications in patients with AIDS.
Medulla Oblongata
Heart rate
Blood pressure
Respiration rate
reflexive digestive movements
Pons
a. Helps medulla in regulating respiration rate
b. Tracts between spinal cord and brain as well as brain to brain
Midbrain
a. Cranial somatic reflex for eye, head and neck muscles to visual stimuli
b. Cranial somatic reflex for trunk muscles to auditory stimuli
these are the so called "startle" responses
Thalamus -- functions
a. Sensory hub for incoming sensory impulses (except olfaction) to various regions of cerebral cortex
b. Interprets some sensory impulses (pain, light touch, pressure)
Hypothalamus -mostly gray matter
a. Controls body temperature
b. Thirst center (determines amount of water in blood)
c. Hunger centers (determines amount of glucose in blood)
d. Metabolism
e. Growth
f. Sex drive
g. Rage and aggression
. Pituitary gland
a. regulates metabolism, growth, osmotic pressure of blood, blood sugar (controlled by hormones from hypothalamus).
b. regulates body temperature, birth, lactation (controlled by nervous impulses from hypothalamus
Cerebellum
posture and coordination-allows smooth movements. Propioreception (muscle sense or position) comes from muscle spindle and tendon organ receptors to provide these functions.
Cerebral cortex (gray matter)
a. Sensory functions
prefrontal lobe
1) Memory
2) Judgement
3) Personality
4) Intelligence