neurologic function 2 Flashcards

1
Q

vascular neurologic disorders

A

-transient ischemic attack
-cerebrovascular accident
-cerebral aneurysm

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2
Q

transient ischemic attack (TIA)

A

“Mini Stroke”
A temporary episode of cerebral ischemia that results in symptoms of neurologic deficits, lasts 1-2 hours –> up to 24 hours
Begin suddenly and last for a short period
1 in 3 people experiencing a TIA eventually have a stroke
Manifestations are the same as for a stroke
Reflect the location of the ischemia

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3
Q

Ischemia can occur because of:

A

cerebral artery occlusion
(e.g., thrombus, or plaque),
cerebral artery narrowing
(e.g.,atherosclerosis or spasms),
cerebral artery injury
(e.g., inflammation or hypertension)

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4
Q

additional risk factors for transient ischemic attack

A

smoking, diabetes mellitus, advancing age, hypercholesterolemia, excessive alcohol consumption, and illicit drug use

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5
Q

cerebral vascular accident (CVA)

A

“Stroke”
An interruption of cerebral blood supply
Ischemic damage is permanent

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6
Q

ischemic strokes

A

-are the most common
-total vessel occlusion (e.g., thrombus, embolus, or plaque)

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7
Q

Hemorrhagic strokes

A

-the most fatal
-cerebral vessel rupture (e.g., cerebral aneurysm, arteriovenous malformation, or hypertension)

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8
Q

complications of cerebral vascular accident (CVA)

A

neurologic deficits and death

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9
Q

cerebral vascular accident (CVA) risk factors

A

smoking, diabetes mellitus, advancing age, hypercholesterolemia, excessive alcohol consumption, and illicit drug use

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10
Q

manifestations of TBI & CVA

A

-Muscle weakness or paralysis of the face, arm, or leg (usually unilateral)
-Aphasia or receptive aphasia
-Dysphagia
-Dysgraphia & Difficulty reading
-Vision issues (e.g., diplopia, nystagmus, and partial or complete loss of vision)
-Change in levels of consciousness
-Personality, mood, or emotional changes
-Confusion
-Agnosia (inability to recognize or identify sensory stimuli)
-Ataxia
-Vertigo or dizziness
-Incontinence of bowel or bladder

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11
Q

cerebral aneurysm

A

-A localized outpouching of a cerebral artery due to weakening of the artery wall
-Most frequently occur in on the circle of Willis
-Can put pressure on surrounding tissue as well as leak or rupture, causing a CVA or death
-Many are asymptomatic until they grow large enough to compress surrounding structures or rupture

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12
Q

cerebral aneurysm causes

A

congenital defects,
hypertension, diabetes mellitus, dyslipidemia,
connective tissue diseases (e.g., Marfan syndrome
traumatic brain injuries,
cigarette smoking, illicit drug use,

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13
Q

cerebral aneurysm manifestations

A

-vision issues headache, eye pain
-A sudden, severe headache is an indication that the aneurysm has ruptured;
-may also resemble symptoms of increased ICP and CVA

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14
Q

seizure disorders

A

epilepsy, focal seizures, generalized seizures

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15
Q

seizure

A

transient physical or behavior alteration that results from an abnormal electrical activity in the brain

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16
Q

epilepsy

A

seizure disorder resulting from spontaneous firing of abnormal neurons; characterized by recurrent seizures for which there is no underlying or correctable cause

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17
Q

causes for seizure disorders

A

-altered membrane ion channels, altered extracellular electrolytes, and imbalanced excitatory and inhibitory neurotransmitters
-Can occur secondary to trauma, cerebral ischemia, electrolyte disorders, acidosis, infection, fever, chemical ingestion (e.g., medications, illicit drugs, and alcohol)

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18
Q

two broad categories for seizure disorders

A

-focal and generalized
-not all can be easily defined as either focal or generalized

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19
Q

focal seizures

A

-“partial seizure”
-Occurs in just one part of the brain
-Usually lasts just a few seconds
-Some people may experience auras (unusual sensations just prior to an impending seizure)
-these are actually simple focal seizures in which the person maintains consciousness
-Seizure characteristics tend to be similar with every seizure

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20
Q

focal aware seizure

A

-individual remains conscious but expereiences unusual feelings or sensations that can take many forms (e.g., sudden and unexplainable feelings of joy, anger, sadness, or nausea; hear, smell, taste, see, or feel things that are not real)

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21
Q

complex focal seizure

A

-individual has changes in or loss of consciousness, producing a dreamlike experience; may display strange, repetitious behaviors (e.g., moving their mouth, walking in a circle) called automatisms

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22
Q

frontal lobe focal seizure manifestations

A

jacksonian seizure
-tingling feeling in hand or arm
-adversive seizures
-eyes or head both turn to one side

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23
Q

pariental lobe focal seizure manifestations

A

tingling in or jerking of leg, arm, face

24
Q

temporal lobe focal seizure manifestations

A

-strange smell or taste
-altered behavior
-feeling as if “i’ve been there before” or “ive seen that before” (deja vu)
-lip smacking or chewing movements

25
Q

occipital lobe focal seizure manifestations

A

flashing lights or spots
vomiting

26
Q

generalized seizures

A

-abnorm neuronal act on both sides of the brain
-may cause loss of consciousness, falls, or massive muscle spasms
-postictal period: just after the seizure, the individual may be confused, fatigued, and fall into a deep sleep

27
Q

(generalized) absence seizure

A

-individual may appear to be staring into space and/or have jerking or twitching muscles

28
Q

(generalized) tonic seizure

A

-causes stiffening of muscles of the body, generally those in the back and extremities

29
Q

(generalized) clonic seizure

A

-causes repeated jerking movements of muscles on both sides of the body

30
Q

(generalized) tonic-clonic seizure (previously called grand mal seizure)

A

-causes stiffening of the body and repeated jerks of the arms and/or legs as well as loss of consciousness

31
Q

chronic degenerative disorders

A

multiple sclerosis, parkinson’s disease, amyotrophic lateral sclerosis (ALS), Myasthenia gravis, Huntington’s Disease

32
Q

multiple sclerosis (MS)

A

-Debilitating autoimmune condition that involves a progressive and irreversible demyelination of brain, spinal cord, and cranial nerves
-Damage occurs in diffuse patches throughout the nervous system and slows or stops nerve impulses
-Symptom onset usually occurs between 20 and 40 years of age
-More common in females

33
Q

multiple sclerosis manifestations

A

-Vary depending on the degree of damage and the specific nerves affected
-Characterized by remissions and exacerbations: fatigue, ataxia, muscle spasms, paresthesia or abnormal sensation in any area, problems moving arms or legs, vision issues (e.g., diplopia and vision loss), diffuse neurological, dysfunctions

34
Q

parkinson’s disease

A

-progressive condition involving the destruction of the substantianigra in the brain
-Results in a lack of dopamine
-Causes movement issues that typically include tremors (involuntary shaking) of the hands and head
-Slowing or stopping of automatic movements (e.g., blinking)

35
Q

Parkinson’s disease manifestations

A

-Difficulty initiating or continuing movement (e.g., walking or getting out of a chair)
-Loss of fine hand movements (writing & eating can become difficult)
-Shuffling gait/Unsteady gait
-Slowed movements
-Dysphagia
-Masklike appearance to face
-Myalgia, Muscle cramps

36
Q

parkinson’s tremors

A

-Usually occur in the limbs at rest or when the limb is held out
-Go away during purposeful movement
-Eventually can be seen in the head, lips, tongue, and feet
-May be worse when tired, excited, or stressed
-Finger–thumb rubbing (“pill-rolling” tremor)

37
Q

amyotrophic lateral sclerosis

A

-“Lou Gehrig’s disease”
-Damage of the upper motor neurons of the cerebral cortex and lower motor neurons of the brain stem and spinal cord
-nerves lose their ability to trigger muscle movement, resulting in muscle weakness, disability, paralysis, and eventually death (usually w in 3 yrs of onset of symptoms)
-may also increase the risk for dementia

38
Q

amyotrophic lateral sclerosis

A

-manifestations become progressively worse as more motor neurons are damaged
-the loss of upper motor neurons results in spastic paralysis
-the loss of lower motor neurons results in flaccid paralysis

39
Q

early manifestations of amyotrophic lateral sclerosis

A

-footdrop
-lower extremity weakness or clumsiness,
-slurred speech, dysphagia
-muscle cramps and twitching in upper extremities and the tongue

40
Q

ALS manifestations

A

-freq begins in the upper or lower extremities and then spreads to other parts of the body
-as the disease advances, muscles become progressively weaker until they are paralyzed
-eventually affects chewing, swallowing, speaking, and breathing
-paralysis of the diaphragm
-aspiration - pneumonia

41
Q

myasthenia gravis

A

-autoimmune condition in which acetylcholine receptors are impaired or destroyed
-leading to a disruption of normal communication btwn the nerve and muscle at the neuromuscular junction
-This disruption causes weakness of the voluntary skeletal muscles because of inadequate nerve stimulation
-muscle weakness typically increases during periods of activity and improves after periods of rest

42
Q

myasthenia gravis manifestations

A

-muscles that control eye and eyelid movement, facial expression, chewing, talking, and swallowing are often, but not always, involved
-the muscles that control breathing and neck and limb movements may also be affected
-facial paralysis or weakness
-fatigue
-hoarseness or changing voice
-eye and vision issue (e.g., diplopia, ptosis, blurred vision, and difficulty maintaining gaze)
-breathing difficulty
-dysphagia

43
Q

factors that can worsen and cause a myasthenic crisis

A

-fatigue, illness, stress, extreme heat, alcohol consumption, and certain meds

44
Q

myasthenic crisis

A

potentially life-threatening complication that occurs when the muscles become too weak to maintain adequate ventilation
-diaphragm weakness/paralysis

45
Q

huntington’s disease

A

-condition caused by a genetically programmed degeneration of neurons in the brain
-autosomal dominant disorder involving a defect on chromosome 4
-offspring have 50% chance of inheriting
-leads to progressive atrophy of the brain, particularly in the basal ganglia and the frontal cortex
-no cure and no treatment
-universally fatal
-Most cases appear between 30 and 40 years of age, but may appear in childhood or adolescence
-Illness duration ranges from 10 to 30 years

46
Q

common causes of death by Huntington’s disease

A

-Most common causes of death are infection (most often pneumonia), injuries related to a fall, or other complications (e.g., suicide)

47
Q

huntington disease manifestations

A

behavioral changes:
-irritable, apatehtic
-antisocial
-paranoia & psychosis
-aggression and severe depression
cognitive changes:
-dementia
-loss of memory, muscle memory
-trouble focusing & decision making
motor deficiencies:
-rapid, jerky movements ‘chorea’
-tremors
-grimaces & twitching
-unsteady gait (increased fall risk)
-dysarthria & dysphagia

48
Q

dementia

A

-cortical function is decreased, impairing cognitive skills and motor coordination
-Issues with memory are common, short-term memory losses, confusion about historical events
-Behavioral and personality changes interfere with relationships, work, and activities of daily living

49
Q

dementia causecauses of dementia

A

vascular disease (e.g., atherosclerosis), infections, toxins, and genetic conditions

50
Q

types of dementia

A

-Alzheimer’s disease, vascular dementia, dementia with Lewy bodies, frontotemporal dementia, Creutzfeldt-Jakob disease, and AIDS dementia complex

51
Q

alzheimer’s disease

A

-most common form of dementia
-brain tissue degenerates and atrophies, causing a steady decline in memory and mental abilities
-not a part of norm aging, but risk increases w age

52
Q

three pathologic characteristics of alzheimer’s disease

A

-amyloid plaques mix w a collection of additional proteins, neuron remnants, and other nerve cell pieces
-neurofibrillary tangles: abnorm collections of a protein called tau that clumps together
-connections btwn neurons responsible for mem and learning are lost; neurons cannot survive when their connections to other neurons are lost

53
Q

alzheimer’s disease risk factors

A

Additional risk factors: family history, hypertension, hypercholesterolemia, diabetes mellitus, and history of traumatic brain injury

54
Q

alzheimer’s disease manifestations

A

-Include memory loss, problems with abstract thinking,
-difficulty finding the right word to express thoughts or even follow conversations,
-difficulty reading and writing
-disorientation (even in familiar surroundings)
-loss of judgment or social norms
-difficulty performing familiar tasks
-personality changes, hallucinations

55
Q

complications of alzheimer’s disease

A

infections (primarily pneumonia and urinary tract infections), injuries related to falls, malnutrition, dehydration, and decubitus ulcers

56
Q

brain tumors

A

-umbrella term for multiple forms of cancer
-may be malignant or benign
-may be primary, but most are secondary tumors (most commonly breast cancer, colon cancer, lung cancer, melanoma, and sarcoma)
-can be life-threatening due to increased ICP and difficulty accessing to surgically remove
-complications: neurologic deficits, seizures, personality changes, and death

57
Q

brain tumor manifestations

A

-vary depending on size and location
-Include:
Headaches of increasing frequency and severity
Unexplained nausea or vomiting
Vision problems
Gradual loss of sensation or movement in an extremity
Balance difficulties
Speech difficulties
Confusion
Hearing problems
Hormonal (endocrine) disorders