Dementia and Delerium Flashcards

1
Q

Used up until the 19th century to mean various forms of mental derangement

-But, identified specifically with old age as early as the 1st or 2nd century CE by the poet Juvenal

A

Dementia

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2
Q

Used for both delusions and brain diseases (phrenitis) through the 19th century

A

Delerium

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3
Q

Two words to describe a break-down (failure) in brain function

A

Dementia and Delirium

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4
Q

A general term denoting the patient’s incapacity to think with customary speed, clarity, and coherence

A

Acute Confusional State

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5
Q

Its most conspicuous attributes are impaired attention and power of concentration, disorientation—which may be manifest or is demonstrated only by direct questioning, an inability to properly register immediate events and to recall them later, a diminution of all mental activity, including the normally constant inner ideation and sometimes by the appearance of bewilderment

A

Acute confusional state

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6
Q

Where “agitation, hallucinations, and sometimes convulsions and tremor accompany the core confusional state.”

A

Delerium

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7
Q

A disturbance in attention (i.e., reduced ability to direct, focus, sustain, and shift attention) and awareness (reduced orientation to the environment)

A

Delerium

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8
Q

The disturbance develops over a short period of time (usually hours to a few days), represents a change from baseline attention and awareness, and tends to fluctuate in severity during the course of a day

A

Delerium

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9
Q

DSM-5 classifies delirium as an additional disturbance in

A

Cognition

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10
Q

Delerium is a disturbance of

A

Arousal and/or attention

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11
Q

Subjective decline in functioning from baseline not normal for age affecting one or more cognitive domains

A

Mild Cognitive Impairment

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12
Q

Mild Cognitive Impairment is NOT associated with significant

A

Funcitonal Impairment

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13
Q

An acquired disturbance in cognition without impairment in daily functioning

A

Mild Cognitive Impairment (MCI)

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14
Q

Approximately what percentage of ED patients are delerious on presentation?

A

10-16%

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15
Q

Delerium patients over 65 have a 12 month mortality rate of?

A

40%

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16
Q

Failure of the cells of the brain to function appropriately generally due to failure in cerebral metabolism

A

Delirium

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17
Q

Failure in availability or distribution of necessary fuels for metabolism (i.e Glucose, Water, and Oxygen)

A

Failure of Cerebral Metabolism

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18
Q

Look for PE findings that might point to a particular etiology. For instance: asterixis and myoclonus for

A

Hepatic encephalopathy

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19
Q

Look for PE findings that might point to a particular etiology. For instance: Wide pupils, lack of sweating, increased HR, mumbling and picking for

A

Anticholinergic Delerium

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20
Q

A medical emergency (i.e. acute brian failure) that requires urgent medical care

A

Delirium

21
Q

Preferred over benzodiazepines and anticholinergics for agitation

A

Neuroepileptics

22
Q

Females are at a higher risk than males for

A

Dementia

23
Q

Decreased daily exercise or physical activities and decreased mental stimulation are risk factors for

A

Dementia

24
Q

Mainly functional, metabolic, infectious, or paraneoplastic/autoimmune causes

A

Reversible dementia

25
Q

Mainly due to structural lesions

A

Arrestable but non-reversible dementia

26
Q

What are the two types of cognitive enhancer medications?

A

Acetylcholinesterase inhibitors and NMDA receptor antagonists

27
Q

What are the three acetylcholinesterase inhibitors?

A

Donepazil, Rivastigmine, and Galantamine

28
Q

What is an example of an NMDA receptor antagonist?

A

Mementine

29
Q

Acute brain failute

A

Delirium

30
Q

Chronic brain failure

A

Dementia

31
Q

Cause an atypical Alzheimer’s syndrome

A

Lewy bodies

32
Q

Has the clinical characteristics of prominent motor symptoms (Parkinsonism) and behavioral symptoms (Visual Hallucinations and altered sensorium) early on

A

Lewy Body Dementia (LBD)

33
Q

Memory difficulties and language dysfunction are usually less severe then AD early in the disease. Relatively more visuo-spatial, attention, and executive dysfunction early compared to AD

A

LBD

34
Q

100% fatal. More rapid mortality and more functional difficulties relative to AD

A

LBD

35
Q

Deficits characterized by a loss of cholinergic neurons in the nucleus basalis of Meynert, decreased cortical choline acetyltransferase, and depletion of dopaminecontaining neurons

A

Lewy Body Dementia

36
Q

The main difference between LBD and PD is whether the dementia comes

A

Early (within 1st year) or later

37
Q

A dementia syndrome with prominent behavioral symptoms, featuring characteristic patterns of atrophy and later confirmed by Alzheimer to have an absence of plaques and tangles

A

Frontotemporal Dementia (Pick’s Disease)

38
Q

Characterized by left frontal degeneration and the development of primary language problems before rpogressing into a more typical dementia pattern

A

Primary Progressive Aphasia

39
Q

Characterised by anterior temporal atrophy and primary language and memory problems that differ from Mesulam’s PPA and typical AD

A

Semantic Dementia (SD)

40
Q

The primary deficit in SD is

A

Semantic knowledge

41
Q

Third most common degenerative dementia after AD and DLB

-Accounts for nearly 5-10% of all dementia

A

Frontotemporal Dementia (FTD)

42
Q

As common or more common than AD in patients in the 45-65 age group. Usually occurs at ages less then 65

A

FTD

43
Q

Varying degrees of argyrophilic Pick Bodies, Astrocytic plaques, Cytoplasmic inclusions, and Ballooned Neurons, depending on subtype

A

FTD

44
Q

Most cases of FTLD present with protein accumulations involving either:

A

TDP-43, Tau, or FUS

45
Q

40% of FTLD cases have a genetic heritability pattern with 10% being

A

Autosomal Dominant

46
Q

Mutations to microtubual-associated protein tau (MAPT) on chromosome 17 causes autosomal dominant syndrome called “FTDP-17” cause accumulations of

A

Tau

47
Q

Mutations to the Progranulin gene (PGRN) on chromosome 17 and C9orf72 on chromosome 9 have the highest association cause accumulation of

A

TDP-43

48
Q

Mutations to the FUS gene on chromosome 16 cause the accumulation of

A

FUS