dementia Flashcards

(36 cards)

1
Q

what are the main risk factors

A

age and family history

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2
Q

what cognitive tests can you do

A

MMSE, ACE (Addenbrookes Cognitive Examination)

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3
Q

what does clock drawing test

A

parietal lobe

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4
Q

what reflexes should you check

A

primitive reflexes- grasp, pout

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5
Q

how can you test praxis

A

copying hand gestures, miming

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6
Q

investigations

A

FBC, ESR, B12, TFT, LFT, U&E, glucose. CT

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7
Q

what further investigations should be done in a younger patient

A

EEG, genetic testing HIV serology, metabolic tests, brain biopsy

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8
Q

what is the main cause of dementia

A

alzheimers

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9
Q

features of alzheimers

A

memory impairment, language impaired, apraxia- cant carry out skilled motor activities, agnosia, frontal executive function (organising, planning), anosognosia, visuospatial

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10
Q

what lobe is associated with visuospatial

A

parietal

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11
Q

what is anosognosia

A

lack of insight

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12
Q

what is agnosia

A

cant recognise objects, people

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13
Q

what are late non cognitive features AD

A

myoclonus, seizures, sleep wake cycle reversal, incontinence

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14
Q

what happens to personality in AD

A

stays relatively intact until late

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15
Q

what is the pathology in AD

A

B amyloid deposition in plaques, formation of tau containing intracellular neurofibrillary tangles

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16
Q

what does having a first degree relative do to your chance of having AD

A

doubles the lifetime risk

17
Q

what are the genes involved in AD

A

amyloid precursor protein, presenilin 1 and 2

18
Q

what other environmental risk factors AD

A

head trauma, vascular risk factors

19
Q

what are the degenerative causes dementia

A

AD, dementia with lewy bodies, frontotemporal dementia, huntingtons, parkinsons, prion

20
Q

what other causes for dementia

A

vascular, metabolic (uraemia, liver failure), toxic (alcohol, solvent abuse), vitamin (B12, thiamine), intracranial (tumour, haematoma, hydrocephalus), infections, psych

21
Q

what are the features of dementia with Lewy bodies

A

visual hallucinations (animals, people, sense of a presence- extracampine); fluctuating cognition, sleep disorders, Parkinsonism. memory loss may not occur at early stages. delusions, transient LOC

22
Q

what are there aggregations of in DLB

A

alpha-synuclein protein

23
Q

what happens in Parkinsons disease dementia

A

cognitive problems are a late feature- at least 1 year after onset and above 75.

24
Q

what may DLB and PDD respond to

A

cholinesterase inhibitors

25
what is vascular dementia course
can be progressive and similar to AD, can be a hx of TIAs or lots of cerebrovascular events. stepwise manner
26
additional signs in vascular dementia
apraxic gait disorders, pyramidal signs, urinary incontinence
27
what do you see on MRI in vascular dementia
widespread small vessel disease
28
what happens in frontotemporal dementia
frontal and temporal lob atrophy on MRI
29
when is the onset typically in frontotemp
30
what is the presentation frontotemporal dementia
frontal presentation- personality change, emotional blunting, apathy, disinhibition, carelessness, behavioural change. MEMORY IS PRESERVED. temporal presentation- progressive impairment language function
31
what is the incubation of prion disease
long- can be several years. but death happens soon after start getting symptoms
32
pathology prion disease
accumulation misfolded native prion protein PrPc
33
what is the commonest form of Creutzfeldt Jakob disease and what is the course
sporadic. spontaneous mutations. rapidly progressive dementia leads to death within 6months. myoclonus
34
what is iatrogenic CJD
from neurosurgical instruments as prion resistant to sterilisation; transplant material; cadaveric pituitary derived GH from pt with CJD
35
what is variant CJD
affects younger people. neuropsychiatric symptoms. ataxia and dementia with myoclonus/chorea. longer course- a few years
36
what drugs can be used in dementia
cholinesterase inhibitors (donezepil, rivastigmine), memantine (NMDA receptor antagonist)