• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/46

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

46 Cards in this Set

  • Front
  • Back
ICP complications
brain stem herniation
diabetes insipidus
syndrome of inappropriate antidiuretic hormone (SIADH).
ventricular catheter monitoring
complications
infection, meningitis, ventricular collapse, occlusion of the catheter by brain tissue or blood, and problems with the monitoring system
ICP
Nursing Interventions
Maintaining a Patent Airway
Achieving an Adequate Breathing Pattern
Optimizing Cerebral Tissue Perfusion
Monitoring Intracranial Pressure
Monitoring for Secondary Complications

Maintaining Negative Fluid Balance
Preventing Infection
Monitoring and Managing Potential Complications
Detecting Early Indications of Increasing Intracranial Pressure
Detecting Later Indications of Increasing ICP
Simple partial seizures
def
with elementary symptoms, generally without impairment of consciousness
With motor symptoms
With special sensory or somatosensory symptoms
With autonomic symptoms
Compound forms
Complex partial seizures
with complex symptoms generally with impairment of consciousness
With impairment of consciousness only
With cognitive symptoms
With affective symptoms
With psychosensory symptoms
With psychomotor symptoms (automatisms)
Compound forms
Generalized Seizures
convulsive or nonconvulsive, bilaterally symmetric, without local onset
Tonic-clonic seizures
Tonic seizures
Clonic seizures
Absence (petit mal) seizures
Atonic seizures
Myoclonic seizures (bilaterally massive epileptic)
Unclassified seizures
Causes of acquired seizures include:
Cerebrovascular disease
Hypoxemia of any cause, including vascular insufficiency
Fever (childhood)
Head injury
Hypertension
Central nervous system infections
Metabolic and toxic conditions (eg, renal failure, hyponatremia, hypocalcemia, hypoglycemia, pesticides)
Brain tumor
Drug and alcohol withdrawal
Allergies
A major responsibility of the nurse during a seizure is to .
observe and record the sequence of signs
Assessing Traumatic Brain Injury
Be on the alert for the following signs and symptoms:
Altered level of consciousness
Confusion
Pupillary abnormalities (changes in shape, size, and response to light)
Altered or absent gag reflex
Absent corneal reflex
Sudden onset of neurologic deficits
Changes in vital signs (altered respiratory pattern, widened pulse pressure, bradycardia, tachycardia, hypothermia or hyperthermia)
Vision and hearing impairment
Sensory dysfunction
Headache
Seizures
Concussion
If the brain tissue in the frontal lobe is affected
the patient may exhibit bizarre irrational behavior
Concussion
involvement of the temporal lobe
can produce temporary amnesia or disorientation.
Concussion
Familly teaching: following signs and symptoms and to notify the physician or clinic (or bring the patient to the emergency department) if they occur:
Difficulty in awakening
Difficulty in speaking
Confusion
Severe headache
Vomiting
Weakness of one side of the body
Most serious Brain injuries
Hematomas (collections of blood) that develop within the cranial vault
Nursing Interventions
brain Injury
Monitoring for Declining Neurologic Function
Level of Consciousness
Vital Signs
Motor Function
Maintaining the Airway
Monitoring Fluid and Electrolyte Balance
Promoting Adequate Nutrition
Preventing Injury
Maintaining Body Temperature
Maintaining Skin Integrity
Improve cognitive function
Preventing Sleep Pattern Disturbance
Support Family Coping
Adequate CPP
is greater than 70 mm Hg
Controlling Intracranial Pressure in Patients With Severe Brain Injury
Elevate the head of the bed as prescribed.
Maintain the patient's head and neck in neutral alignment (no twisting or flexing the neck).
Initiate measures to prevent the Valsalva maneuver (eg, stool softeners).
Maintain normal body temperature.
Administer O2 to maintain PaO2 >90 mm Hg.
Maintain fluid balance with normal saline solution.
Avoid noxious stimuli (eg, excessive suctioning, painful procedures).
Administer sedation to reduce agitation.
Maintain cerebral perfusion pressure >70 mm Hg.
The vertebrae most frequently involved in SCI
the 5th, 6th, and 7th cervical (neck) vertebrae (C5–C7), the 12th thoracic vertebra (T12), and the 1st lumbar vertebra (L1). These vertebrae are most susceptible because there is a greater range of mobility in the vertebral column in these areas
CENTRAL CORD SYNDROME
Characteristics: Motor deficits (in the upper extremities compared to the lower extremities; sensory loss varies but is more pronounced in the upper extremities); bowel/bladder dysfunction is variable, or function may be completely preserved.
Cause: Injury or edema of the central cord, usually of the cervical area. May be caused by hyperextension injuries.
ANTERIOR CORD SYNDROME
Characteristics: Loss of pain, temperature, and motor function is noted below the level of the lesion; light touch, position, and vibration sensation remain intact.
Cause: The syndrome may be caused by acute disk herniation or hyperflexion injuries associated with fracture-dislocation of vertebra. It also may occur as a result of injury to the anterior spinal artery, which supplies the anterior two thirds of the spinal cord
BROWN-SÉQUARD SYNDROME (LATERAL CORD SYNDROME)
Characteristics: Ipsilateral paralysis or paresis is noted, together with ipsilateral loss of touch, pressure, and vibration and contralateral loss of pain and temperature.
Cause: The lesion is caused by a transverse hemisection of the cord (half of the cord is transected from north to south), usually as a result of a knife or missile injury, fracture-dislocation of a unilateral articular process, or possibly an acute ruptured disk.
Injury at C1
Little or no sensation or control of head and neck; no diaphragm control; requires continuous ventilation
Injury at C2 to C3
Head and neck sensation; some neck control; independent of mechanical ventilation for short periods
Injury at C4
Good head and neck sensation and motor control; some shoulder elevation; diaphragm movement
Injury at C5
Full head and neck control; shoulder strength; elbow flexion
Injury at C6
Fully innervated shoulder; wrist extension or dorsiflexion
Injury at C7 to C8
Full elbow extension; wrist plantar flexion; some finger control
Injury at T1 to T5
Full hand and finger control; use of intercostal and thoracic muscles
Injury at T6 to T10
Abdominal muscle control, partial to good balance with trunk muscles
Injury at T11 to L5
Hip flexors, hip abductors (L1–L3); knee extension (L2–4); knee flexion and ankle dorsiflexion (L4–5
Injury at S1 to S5
Full leg, foot, and ankle control; innervation of perineal muscles for bowel, bladder, and sexual function (S2–4)
Brain Abscess
Clinical Manifestations
Headache, usually worse in the morning, is the most prevailing symptom. Fever, vomiting and focal neurologic deficits occur as well
MS
Clinical Manifestations
fatigue
depression
weakness
numbness
difficulty in coordination
loss of balance
pain
Visual disturbances due to lesions in the optic nerves or their connections may include blurring of vision
diplopia (double vision)
patchy blindness (scotoma)
total blindness
Nursing Interventions
MS
Promoting Physical Mobility
Exercises
Minimizing Spasticity and Contractures
Activity and Rest
Minimizing Effects of Immobility
Preventing Injury
Enhancing Bladder and Bowel Control
Enhancing Communication and Managing Swallowing Difficulties
Improving Sensory and Cognitive Function
Strengthening Coping Mechanisms
Improving Home Management
Promoting Sexual Functioning
Myasthenia gravis
Clincal manifestations
Diplopia (double vision) and ptosis (drooping of the eyelids)
weakness of the muscles of the face and throat
generalized weakness
dysphonia
Myasthenic Crisis
s/s
Respiratory distress
dysphagia (difficulty swallowing)
dysarthria (difficulty speaking), eyelid ptosis
diplopia
prominent muscle weakness
Guillain-Barré
clinical manifestations
muscle weakness
reflexes of the lower extremities
Hyporeflexia and weakness may progress to tetraplegia
paresthesias of the hands and feet
A motor cortex tumor
Clincal Manifestations
produces seizure-like movements localized on one side of the body, called Jacksonian seizures
An occipital lobe tumor
Clinical Manifestations
produces visual manifestations: contralateral homonymous hemianopsia (visual loss in half of the visual field on the opposite side of the tumor) and visual hallucinations.
A cerebellar tumor
Clinical Manifestations
causes dizziness, an ataxic or staggering gait with a tendency to fall toward the side of the lesion, marked muscle incoordination, and nystagmus (involuntary rhythmic eye movements), usually in the horizontal direction.
A frontal lobe tumor
clical manifestations
frequently produces personality disorders, changes in emotional state and behavior, and an apathetic mental attitude. The patient often becomes extremely untidy and careless and may use obscene language.
A cerebellopontine angle tumor
Tinnitus and vertigo appear first, soon followed by progressive nerve deafness (eighth cranial nerve dysfunction).
Numbness and tingling of the face and tongue occur (due to involvement of the fifth cranial nerve).
Later, weakness or paralysis of the face develops (seventh cranial nerve involvement). Finally, because the enlarging tumor presses on the cerebellum, abnormalities in motor function may be present.
Parkinson's Ds
Clinical manifestations
tremor
rigidity
bradykinesia (abnormally slow movements)
postural instability
Parkinson's Ds
Nursing Interventions
Improving Mobility
Enhancing Self-Care Activities
Improving Bowel Elimination
Improving Nutrition
Enhancing Swallowing
Encouraging the Use of AssiImproving Communication
stive Devices
Supporting Coping Abilities
Huntington's ds
Clinical Manifestations
Early
chorea
intellectual decline
emotional disturbance
Facial movements produce tics and grimaces
slurred expolisive speech
dosorganized gait
personality changes
Huntingtons's Ds
Clinical Manifestation's
Late
constant writhing
uncontrollable movement
unitelligible speech
impossible to ambulate
Dementia
ALS
clinical Manifestations
fatigue
progressive muscle weakness,
cramps
fasciculations (twitching) incoordination