oncologic or degenerative neurologic disorders Flashcards

1
Q

terminology

bradykinesia

A
  • abnormally slow voluntary movements
  • associated with parkinsons
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

terminology

dyskinesia

A
  • impaired ability to execute voluntary movements
  • associated with parkinsons and ALS
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

terminology

sciatica

A

pain and tenderness that radiates along the sciatic nerve that runs through the thigh and leg

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

terminology

spondylosis

A
  • degenerative changes occurring in a disc and adjacent vertebral bones
  • can occur in the cervical or lumbar vertebrae
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

name some different brain tumors

A
  • intercerebral tumors: gliomas (most common type of brain tumor)
  • meningiomas, neuromas, pituitary adenomas (all of these arise from a supporting structure)
  • angiomas (developmental tumor)
  • metastatic lesion
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

describe huntington disease

A
  • chronic progressive hereditary disease
  • progressive involuntary choreiform movement (jerking/twitching) and dementia
  • triad of sx: motor dysfunction, cognitive impairment, and behavioral features of apathy and blunted affect
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

describe parkinsons

A
  • slow progressive neurologic movement disorder
  • affects men more than women
  • symptoms generally appear in 50s, has appeared as early as 30s
  • idiopathic - most common form
  • secondary form being research (multifactorial combo of age, environment, and hereditary)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

describe the pathophysiology of parkinsons

A
  • decreased levels of dopamine
  • degeneration of dopamine storage cells
  • imbalance of acetylcholine (excitatory) and dopamine (inhibitory)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

does parkinsons have a gradual or super fast onset

A

gradual onset and slow progression

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what are the cardinal symptoms of parkinsons

A
  • Tremor
  • Rigidity, increased tone, stiffness
  • Bradykinesia / akinesia
  • Postural instability
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what are the two major subtypes of parkinsons

A
  • Tremor dominant (most other symptoms are absent)
  • Nontremor dominant (akinetic-rigid and postural instability)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

what are some psychological changes associated with parkinsons

A

Depression
Anxiety
Dementia (progressive)
Delirium
Mental deterioration

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what are some other symptoms associated with parkinsons

A

Sweating
Drooling
Paroxysmal flushing
Orthostatic hypotension
Gastric and urinary retention
Constipation and sexual dysfunction
Dysphagia

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

what are some complications of parkinsons

A

Respiratory and Urinary tract infections
Skin breakdown
Injuries from falls
Dyskinesia
Parkinsonian crisis – Emotional trauma or sudden medication withdrawal
Medication side effects
On/Off response – Rapid fluctuations in symptoms
Loss of medication effectiveness

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

whats used in the diagnosis of parkinsons

A
  • history
  • clinical presentation (think about the sx)
  • neurological exam (check grasp, posture, and gait)
  • other test may be done to rule out similar disorders
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

what meds may be used for parkinsons

A
  • carbidopa-levodopa (drug of choice): carbidopa stops levodopa from being metabolized
  • anticholinergics to control tremors
  • antiviral (amantadine) to reduce rigidity/tremors
17
Q

what are some nursing interventions for parkinsons

A
  • resp/cardiac support
  • quiet room
  • barbituates w/ antiparkinsonian drugs
  • need to shorten period between meds/increase doses
  • 2L fluid/day, increased fiber, stool softeners/laxatives, establish regular bowel routine (combat anticholinergic constipation)
  • encourage ROM
  • regular daytime rest
  • assist with ADLs
  • patient/family education
  • safety measures
  • emotional support
18
Q

describe ALS

A
  • unknown cause
  • most common of motor neuron diseases
  • loss of motor neurons -> muscle atrophy
  • risk factors: tend to be middle age (40-60) and male>female
  • survival rate varies (5-20yrs)
19
Q

what are the chief symptoms associated with ALS

A

Fatigue
Progressive muscle weakness
Cramps
Fasciculation (irregular twitching of muscles fibers)
Lack of coordination

20
Q

describe the damage to anterior horns associated with ALS

A

Progressive weakness
Atrophy of arms, legs, trunk
Spasticity
Hyperreflexia

21
Q

describe vocal effects associated with ALS

A

“thick” speech and difficulty projecting voice

22
Q

what are some later symptoms of ALS

A
  • Shortness of breath
  • Difficulty breathing
  • Dysphagia
  • Dysarthria
  • Progresses from upper extremities → shoulders → trunk → neck → throat
  • Lower extremities affected later
  • Some patients may experience cognitive impairment.
  • Bowel and bladder sphincters’ function is maintained
23
Q

whats included in the diagnosis of ALS

A
  • clinical presentation
  • EMG
  • muscle biopsy
  • MRI
24
Q

whats included in the treatment of ALS

A
  • supportive therpay only
  • therapy and rehab to maintain: quality of life, well-being, and function
  • feeding tube
  • mechanical vent
25
Q

what are some nursing interventions for ALS

A
  • supportive nursing care
  • ongiong assessment
  • suggest modifications as disease progresses
  • emotional support
  • conserving energy
  • avoid extreme cold/hot
  • prevent skin breakdown
  • encourage fluid intake
  • proper positioning
  • discuss advanced directives/end of life care