UE function and Dementia Flashcards

1
Q

the process by which various brain ans spinal centers work cooperatively to accommodate the demands of intended movements

A

systems theory

Reaching, grasping and manipulating

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2
Q

sensory info on characteristics of object

A

Weight
Firmness
shape
slickness

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3
Q

timing problems
impaired inter-limb coordination
proximal weakness

A

reach dysfunction

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4
Q
anticipatory hand shape
grip force
precision grip
premature finger closure
slow release
A

grasp dysfunction

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5
Q
knowledge acquisition
comprehension
thinking
knowing
remembering
A

temporo-parietal areas

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6
Q

judgment
problems solving
imagination
planning

A

frontal areas

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7
Q

Types of memory

A

sensory
working memory
Long term memory

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8
Q

Sensory memory

A
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9
Q

Working memory

A
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10
Q

long term memory

A
Lifetime
explicit memory (conscious)
implicit memory (unconscious)
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11
Q

Explicit memory

A

Declarative memory

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12
Q

declarative memory

A

facts events
Episodic memory
Semantic memory

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13
Q

Episodic memory

A

autobiography

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14
Q

Semantic memory

A

facts

concepts

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15
Q

implicit memory

A

procedural memory

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16
Q

procedural memory

A

skills

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17
Q

what is it?

A

occipital lobes

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18
Q

How does it relate to me

A

temporal lobes

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19
Q

how do i feel about it

A

limbic system

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20
Q

what do i think about it

A

frontal lobe

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21
Q

brain aging begins between ages

A

20 and 30

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22
Q
disturbance of consciousness
change in cognition
acute onset (hours to days)
Fluctuating symptoms
evidence of medical etiology
Strong predictor of poor functional and cognitive status in the year following hospital admission
A

delirium

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23
Q

Confusion assessment method CAM

Diagnosis of delirium requires

A
  1. acute onset and fluctuating course
  2. altered level of consciousness
  3. inattention
  4. Disorganized thinking
    presence of both 1 and 2 and either 3 or 4
24
Q

impairments in thinking and memory that do not interfere with every day activities

A

Mild Cognitive Impairment (MCI)

25
MCI memory only
amnestic type
26
MCI judgment and or language
Multi-domain
27
``` forgets names loses objects forgets items on a list forgets multiple tasks forgets phone numbers unable to recall info after distraction Score >1 SD below mean on memory test ```
symptoms of MCI
28
``` Reaction time dual task performance word fluency category fluency delayed verbal recall narrative recall name face pair recall complex figure copying ```
detection of MCI
29
syndrome of impairment in memory and at least one other cognitive ability language visuospatial function executive funtion
dementia
30
coherent speech or ability to understand spoken or written language
language
31
recognition of common objects
visuospatial function
32
motor function, abstract and complex thought, and/or judgment
executive function
33
``` fogetfulness confusion weight loss sleep disturbance gait abnormalities ADL deficits ```
Early signs of dementia
34
protein accumulation outside the neurons
beta amyloid | plaques
35
accumulation inside the neurons
tau protien | tangles
36
disorientation, loss of insight loss of logical reasoning, poor judgement perceptual problems, inability to perform arithmetic inability to learn, loss of attention language impairment, apathy withdrawal, impaired ADLs
cognitive AD symptoms
37
``` paranoia, delusions sleep disturbance, hallucinations agitation/aggression, wandering/sundowning anxiety, depression hostility, fear, jealousy, insecurity ```
non cognitive AD symptoms
38
``` repeats questions anhedonia word finding problems frequently loses items personality changes ```
stage 1: 2-4 years
39
``` becomes lost easily confusion over recent events ADL impairments Argumentative Pacing Anxiety/depression delusions ```
stage 2: 2-10 years
40
unable to perform ADLs impaired speech/comprehension Unable to recognize family/friends Unable to recognize self
stage 3: 1-3 years
41
diagnostic criteria for AD
deficit in memory and at least one other cognitive domain decline from previous function that interferes with social or occupational functioning Gradual onset and continuous decline (>6 mo) Not due to other systemic, CNS, psychiatric, or drug induced condition Consciousness remains unaltered
42
``` Hemiparesis visual deficits incontinence pseudobulbar signs executive deficits psychomotor impairment personality/mood change hyperreflexia gait disturbance ```
Symptoms of VD
43
CADASIL
cerebral autosomal dominant arteriopathy with sub-cortical infarts and luekoencephalopathy
44
inherited genetic mutation strong association with migraines palliative treatment
CADASIL
45
clinical syndrome of varying pathologies
frototemporal dementias
46
monitoring
orbitofrontal area
47
motivation
anterior cingulate
48
executive functions
dorsolateral prefrontal areas
49
characterized by pick bodies and cells - abnormal formation and accumulation of tau protein in neurons selective for frontal and temporal lobes
Picks disease
50
``` aggressive, inappropriate behavior early onset of language pathology incontinence sociopathic, obsessive or steriotyped behaviors may occur with parkinsonianism ```
picks disease
51
associated with left temporal dysfunction loss of semantic memory and knowledge initial sparing of episodic memory and other cognitive functions impairment on language syntax, phonology
Semantic Dementia
52
Loss of expressive language | comprehension often spared, especially in early stages
primary progressive aphasia
53
accumulation of alpha-synuclein protein inside neural nuclei | close associations with parkinson's disease and AD
Lewy body Dementia
54
``` Striking fluctuations in cognition visual hallucinations Bradykinesia parkinsonian posture and gait tremor is less common, usually less severe ```
Lewy body dementia
55
People with cognitive impairment CANNOT
comprehend the environment adapt to the environment Cope with the environment