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94 Cards in this Set

  • Front
  • Back
Aura
Peculiar sensation that proceeds a set of symptoms.
ex: seizure or Migraine headache
Contralateral
Opposite side
Decorticate
Abnormal posturing - flexing of upper extremities with extension of lower limbs, accompanied by elevated pressure on frontal lobe
Encephalitis
Inflammation of brain tissue
Hemiparesis
Weakness on one side of the body
Hemiplegia
Paralysis on one side of the body
Intracranial Pressure
Pressure within the cranium or skull
Ipsalateral
both sides of the body
Neuralgia
Nerve pain
Aura
Peculiar sensation that proceeds a set of symptoms.
ex: seizure or Migraine headache
Contralateral
Opposite side
Decerebrate
Abnormal extension of the upper extremities with extension of the lower extremities accompanies increased pressure on the entire cerebrum, the motor tract and the brain stem
Decorticate
Abnormal posturing - flexing of upper extremities with extension of lower limbs, accompanied by elevated pressure on frontal lobe
Encephalitis
Inflammation of brain tissue
Hemiparesis
Weakness on one side of the body
Hemiplegia
Paralysis on one side of the body
Intracranial Pressure
Pressure within the cranium or skull
Ipsalateral
same side of the body
Neuralgia
Nerve pain
Neurotransmitters
Biochemical messengers at nerve endings that activate receptors to stimulate or inhibit a response
Parathesia
abnormal sensation
Postical
after a seizure
Seizure
Convulsions, series of involuntary contractions of voluntary muscles
Neuron
Main cell body
Axons
Conduct impulses away from the cell body
Dendrites
Conduct impulses toward the cell body
Common neurotransmitters
Acetycholine, Norepinephrine, epinephrine, dopamine
CNS
Consist of brain and spinal cord
Peripheral nervous system
All nerves including spinal and cranial nerves
Sympathetic nervous system
Fight or flight response
Parasympathetic nervous system
Returns body to resting state
Brain stem and Diencephalon
Controls awareness and alertness through reticular activating system. composed of fibers scattered through the mid-brain,pons and medulla
Medulla
Links upper brain centers to other body parts through the spinal cord. Controls respiration, heart beat( partially) constricts blood vessels to raise the blood pressure
Pons
Relays messages from medulla to upper brain center, reflex center for some cranial nerves
Cerebellum
coordinates movement, balance, posture and spatial orientation
hypothalamus
controls pituitary, appetite, sleep and some emotions
Cerebrum ( forebrain)
Controls higher function and activity ( conscious mental processes, sensations, emotions and voluntary movement
Frontal Lobe
Voluntary muscle movement, verbal and written speech
Parietal Lobe
sensory reception areas, interprets pain, touch, temp, distances, size and shape
Temporal Lobe
auditory center for hearing and understanding spoken language, controls olfactory center
Occipital Lobe
visual center for seeing and reading
Neurological age related changes
decrease in # of nerve cells, Brain weight is reduced, Ventricles increase in size, Lipofuscin (age related pigment) deposited in nerve cells, amyloid ( a protein) is deposited in nerve cells, plaques and tangled fibers increased, Pupil size is smaller, eye tracking movements may be jerky, Achilles tendon jerk reflex is often absent, reaction time increases, tremors of hands, face and head are common
Migraine headaches
Thought to be caused by intracranial vasoconstriction followed by vasodilation . Patients may experience depression, irritablility, vision disturbances, nausea, and parathesias before onset of pain. Pain is usually unilateral, often begins in temple or eye area, is often intense, Tearing, nausea and vomiting may occur and patient may be hypersensitive to light and sound.
Cluster Headaches
Occur in series of episodes followed by a long period with no symptoms. Intensely painful seem to be related to stress and anxiety
Tension Headaches
Result from prolonged muscle contraction associated with anxiety, stress or external stimuli (brain tumor, abcessed tooth. Location of pain may vary, patient may have nausea and vomiting, dizziness, tinnitus, or tearing
Partial Seizures
abnormal electrical activity may be generated in localized areas of brain
Simple Seizures
Occurs in part of 1 central hemisphere - consciousness not impaired. May include motor, somatosensory, autonomic or psychic symptoms
Focal motor seizures
abnormal brain activity remains localized to a specific motor area, May or may not occur with "Jacksonian March"
Jacksonian March
Term for when an abnormal activity in one area "marches" (spreads) to adjacent areas
Complex Seizure
Pyschomotor or temporal lobe seizures.
Consciousness impaired - patient may exhibit bizarre, repetitive behaviors
Partial Seizure
can progress to involve entire brain = partial seizures with secondary generalization
Generalized Seizures
Involves entire brain from onset.
Consciousness is lost
Tonic -Clonic Seizure
(Grand Mal seizure)
tonic phase - Stiffening of muscles of extremities with loss of consciousness
Clonic phase - rhythmic movement of extremities occurs
Absence Seizure
( petit mal)
Brief period of loss of consciousness. Patient may appear to be daydreaming, May have automatisms
Automatisms
Lip-smacking, and eye blinking
Myoclonic Seizure
brief jerking or stiffening
Atonic Seizure
( drop attack)
sudden loss of muscle tone causes patient to collapse
Status ellipticus
medical emergency, continous seizure or repeated seizures in rapid succession for 30 minutes or more depriving the brain of oxygen and glucose (can lead to permanent brain damage)
Nursing interventions for seizures
protect patient from injury during and after seizures.
Teach patient and family about seizure disorders and treatments
Concussion
Head trauma with no visible sign of trauma, loss of consciousness for more than 5minutes
Contusion
More serious than concussion, causes actual bruising and bleeding of brain tissue. Can be very serious if brainstem is affected
hematoma
Collection of blood ( usually clotted)
Subdural Hematoma
Usually a result of tearing of veins that drain the blood , allows blood to accumulate in space beneath dura.
Acute subdural hematoma
develops within 24hrs of injury
Subacute subdural hematoma
develops 24hrs - 1 wk after initial injury
Chronic Subdural hematoma
develops weeks or months after initial injury. associated with low impact injuries causing slow, diffuse bleeding
Epidural Hematoma
forms in the space between inner surface of skull and outer most meningeal covering of brain. Results from arterial bleeding, secondary to laceration and tearing of meningeal arteries. Marked by -Momentary lapse of consciousness, Period of alertness, then rapid deterioration, and elevated Intracranial pressure. requires surgery to relieve pressure, remove clot, and stop bleeding
Intracerebral hemorrhage
results from lesions within tissue of brain, may be small or large and is accompanied by massive neurological deficits
penetrating injuries
result from sharp objects that penetrate the skull and brain tissue. Requires prompt surgical intervention
Meningitis
Inflammation of meningeal coverings of brain and spinal cord, caused by viruses and bacteria, signs and symptoms: headache, nuchal rigidity, irritablility, decrease in level of consciousness, Photophobia, hypersensitivity, seizures, Postive Kernigs sign. Positive Brudenski's sign
Kernig's sign
flex hip 90 degrees, then extend.
Positive result will produce pain in the hamstring
Brudzenski's sign
flexion of both hips when examiner flexes patients neck
Encephalitis
Inflammation of brain tissue caused by viruses. symptoms are directly related to area of brain affected and include fever, nuchal rigidity, headache, confusion, delirium, agitation, and restlessness
Gulliane Barre syndrome
( acute inflammatory polyneuropathy)
believed to be an autoimmune response to a viral infection. Myelin sheath is destroyed. signs and symptoms in 3 phases. 1. initial symmetric muscle weakness typically begining in lower extremities,and ascending to trunk and upper extremities, may affect cranial nerves resulting in vision & hearing problems and problems chewing and lack of facial expression, respiratory muscles may also be infected 2. Patient remains unchanged but there is no further deterioration in neurological function. 3. Muscle strength returns in a proximal-distal pattern and remylinization occurs.
4 types of Gulliane Barre syndrome
1. ascending
2. descending
3. Miller-Fisher syndrome
4. Pure motor GBS
Parkinson Disease
Progressive degenerative disorder of basal ganglia that results in eventual loss of coordination and control of involuntary motor movement. unknown cause but related to a deficiency of dopamine in the basal ganglia. Other types of Parkinson's is caused by atherosclerosis, use of phenothiazines and some toxins.
Parkinson's disease Major Triad
Tremors
Rigidity
Bradykinesia
Multiple Sclerosis
Chronic progressive degenerative disease. Thought to be autoimmune disorder. Attacks Myelin sheath around axons and disrupts conduction of nerve impulses through the CNS. can affect motor, sensory, cerebellar, and other pathways
Multiple Sclerosis Signs and Symptoms
vary from patient to patient.
Types of Multiple Sclerosis
Chronic Progressive - disease progresses steadily
Exacerbating-Remitting- marked by exacerbations and remissions
Relapsing-Progressive - less stable periods with fewer remissions
Stable - No active disease for at least 1 year
Amyotrophic Lateral Sclerosis (ALS, Lou Gerhig's disease)
Unknown cause viruses have been suspected. Degeneration of anterior horn cells and corticospinal tracts occur.
Signs and symptoms of Amyotrophic lateral Sclerosis
patients have both upper and lower motor neuron symptoms.
Upper motor neuron symptoms: spascity and hyperflexia
Lower motor neuron symptoms:weakness, atrophy, cramps, and muscle twitching.
Some patients have dysphagia and slurred speech. Intellect and sensory perception, vision and hearing are not affected
Huningtons's Disease
Inherited degenerative neurological disorder. Begins in Middle adulthood
Huningtons's Disease signs and symptoms
abnormal movements, emotional disturbances, and intellectual decline. symptoms progress steadily with increasing disability and death within 10 to 20 years
Myasthenia Gravis
Chronic progressive disease, Defect at neuromuscular junction where electrical impulses are transmitted to muscle tissue
Myasthenia Gravis signs and symptoms
weakness of voluntary muscle esp. muscles of chewing, swallowing and speaking. Partial improvements of strength with rest.
Dramatic improvement with anticholinergic drugs
Amyotrophic lateral sclerosis
Key signs and symptoms
awkwardness of fine finger movements
dysphagia
fatigue
Muscle weakness of hands and feet
fasciculations ( twitching)
Amyotrophic lateral sclerosis
Key Test Results
Creatinine kinase level elevated
Electromyography shows impaired impulse conduction in the muscles
Amyotrophic lateral sclerosis
Key Treatments
Symptomatic relief
Neuroprotective agents ( Rilutek)
Amyotrophic lateral sclerosis
Key Interventions
Monitor neurological and respiratory status
Evaluate swallow and gag reflexes
Monitor and record VS and I&O
Devise an alternate method of communication when necessary
Suction orapharynx PRN
Gulliane-Barre Syndrome
Key signs and treatments
Symmetrical Muscle weakness
(ascending from legs to arms)
Gulliane-Barre Syndrome
Key Test results
History of preceeding febrile illness( usually a respiratory tract infection)
CSF protein level begins to rise peaking at 4 to 6 weeks
CSF- WBC count remains normal
CSF Pressure - may rise above normal in severe cases
Gulliane-Barre Syndrome
Key Treatments
Anticoagulents
Corticosteroids
ET intubation, Tracheotomy or mechanical ventillation
IV fluid therapy
NG tube feedings or TPN
Plasmapheresis
Gulliane-Barre Syndrome
Key interventions
Watch for ascending sensory loss which precedes motor loss.
Monitor VS and LOC
Monitor and treat respiratory dysfunction
Maintain respiratory support
Reposition Patient every 2 hrs
Provide NG tube feedings as needed
Inspect clients legs for signs of thrombophlebitis, apply antiembolism stockings and sequential compression devices.
Encourage adequate fluid intake