Behavior and Dementia Flashcards

1
Q

Dementia

A

Impairment of 2/5 : Memory, Emotion, Visual/spatial, Executive language

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2
Q

Mild Cognitive Impairment

A

Impairment that does not meet the criteria for dementia because there is no impairment in function. - Risk factor for developing Alzheimer’s disease

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3
Q

Episodic Memory

A

memory of person experiences. Primarily affected in AD

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4
Q

Semantic Memory

A

memory of facts :

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5
Q

Declarative memory

A

semantic + episodic memory

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6
Q

Procedural memory

A

memory of how to do things. Less affected in AD.

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7
Q

Alzheimer’s Disease

A

Pts p/w atrophy of the mesial temporal lobe primarily (hippocampi) leading to diffuse brain atrophy over time.

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8
Q

Tx for alzheimer’s

A
  • Cholinesterase inhibitors : galantamine, donepezil (aricept).
  • NMDA receptor antagonist: Memantine ( Namenda)
  • They do not delay natural history just help symptoms .
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9
Q

What protein mutated in familial Alzheimer’s disease? ( younger than 60)

A

Amyloid precursor.

-Pathologically there are cortical neuritic plaques and neuronal loss in cerebral cortex.

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10
Q

What abnormality is likely to be associated with the underlying disease process of AD?

A
  • Presence of the e4 allele of apolipoprotein E.
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11
Q

Alzheimer’s disease is inevitable in which disease ?

A

Down syndrome

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12
Q

Difference between delirium and AD

A

Delirium has fluctuations in level of arousal

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13
Q

Evaluation of a patient with dementia

A
  • Look for reversible causes
  • Electrolyte panels ( Na/glucose)
  • renal function ( uremia)
  • hepatic function (encephalopathy)
  • TSH, serologic tests for syphilis, B12, UA ( UTI can cause delirium), tox screen HIV
  • Imaging
  • Meds: antiochole, benzos, and opiates.
  • pseudodementia
  • Lumbar puncture and eeg only when there are red flag : these included early onset or rapidly progressing dementia, immunocompromised pt, focal neurological findings, sign of systemic illness
  • dementia is distinguished from delirium by its lack of fluctuating course
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14
Q

Lewy body dementia

A
  • central feature: progressive cognitive decline, combined with :
  • pronouced fluctuation in alertness and attention ( differs from parkinsons because this isnt found in PD)
  • prominent visual hallucinations
  • Parkinsonism such as rigidity and braykinesia. Patients are hypersensitive to antopsychotics;
  • Sleep disturbance and orthostatic hypotension.
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15
Q

Charles Bonnet syndrome

A

Pts are mentally healthy, with often significant visual loss,
- typical hallucinations include small animals and people: they understand that the hallucinations are not real and are not typically bothered by it.

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16
Q

Frontal lobe damage

A
  • Apathy, abulia, mutism
  • poor judgement and inappropriate social behavior can occur with damage to frontal lobe but memory and general intelligence is often intact
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17
Q

Frontotemporal Degeneration ( Pick’s disease)

A
  • P/w different patterns of behavior
  • disinhibition: pt display inappropriate social behavior, lack of social tact , lack of empathy, distractibility loss of insight into behaviors of oneself and others. and increased interest in sex. agitation
  • Apathy: neglect of personal hygiene, repetitive or compulsive behavior and decreased energy and motivation
  • Language disturbance: patient develop global language difficulties termed primary progressive aphasia.
  • Occurs at younger age less than 65 and has more rapid progression than other dementias. memory is often relatively unaffected
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18
Q

requip

A

Dopamine agonist used to treat parkinson’s : side effect is increased impulsivity such as gambling or hypersexual behavior

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19
Q

Wernicke-korsakoff syndrome

A

Caused by a lack of thiamine/Vitamin B1
Triad of : Gait ataxia, encephalopathy (confabulation, dementia), and eye movement abnormalities (nystagmus)
- chronic alcoholics who received IV glucose in ER or in ICU patients or post gastric bypass.

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20
Q

Ganser’s syndrome

A
  • syndrome of approximate answers.
  • Seen in prisoners may represent attempt to manipulate legal situation.
  • form of malingering
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21
Q

Vascular dementia

A
  • Step-wise fashion: with focal neuro deficit
  • Risk factors; HTN, DM, smoking lipids
  • can present after a strategically placed lesion to hippocampus, medial thalamus or caudate.
  • often in conjunction with other dementing processes eg AD
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22
Q

Normal pressure hydrocephalus

A
  • Triad: Magnetic gait, dementia, urinary urgency/frequency.
  • Dx: continuous lumbar drain is most sensitive and specific
23
Q

Tx for NPH

A
  • VP shunt : leads to a risk of subdural hematoma
  • Ideal candidate for surg has evidence of ventriculomegaly +: one these: 1) presence of clearly identified etiology, gait difficulties more than cognitive, substantial improvement after CSF removal, lack of atrophy and white matter lesion onimaging
24
Q

Transient global amnesia

A

Complete and reversible anterograde and retrograde memory loss lasting up to 24 hrs.

  • Occurs in the context of emotional event or sexual activity.
  • might be migraine phenomenon
  • rarely occurs but must rule out vascular disease, epilepsy. no tx.
25
Q

Limbic encephalitis

A
  • Psychosis and memory loss
  • Seizures.
  • Hyperintesity of the mesial temporal lobe and frontal lobes b/l
  • CSF: anti-hu antibodies
  • Can be a paraneoplastic process in females associated with ovarian tumors
26
Q

CJD

A
  • prion disease
  • rapid onset change in mental status and myoclonus
  • sx: dementia, behavioral abnormalities : concentration, memory apathy depression
  • LP: 14-3-3 and phosphorylated tau
27
Q

Damage to b/l hippocampi would cause what?

A
  • Inability to make new memories
28
Q

Kluver-busy

A
  • caused by damage to b/l amygdala : Hypersexuality, placidity: diminished fear response
  • hyperphagia/ hyperorality: overeating
    Visual agnosia: difficulty recognizing familiar faces
29
Q

Wereneke’s Aphasia

A
  • receptive aphasia: able to speak with proper grammar but phrases are nonsensical, unable to repeat
  • due to damage of superior temporal gyrus
30
Q

Broca’s ( motor) aphasia

A
  • expressive aphasia
  • can understand speech but cannot speak fluently and are unable to repeat
  • damage to the inferior frontal gyrus
31
Q

Conduction aphasia

A
  • due to damage to arcuate fasciculus

- inability to repeat

32
Q

Prosody

A
  • The rhythmicity of speech usually in the non-dominant hemisphere.
  • can be due to damage to the inferior frontal or superior temporal gyri in the non dominant hemisphere.
33
Q

Pure word deafness

A
  • caused by b/l damage to posterior superior temporal lobes: primary auditory cortex
  • manifests as inability to comprehend meaning of speech but still being able to hear sounds, speak, read and write
34
Q

Akinetic mutism

A
  • damage to cingulate gyrus b/l-

- Pts can speak but chooses to do so only under extreme duress.

35
Q

Alexia without agraphia

A
  • Damage to left occipital lobe, splenium of corpus callosum

- Can be caused by infarction of the posterior cerebral artery

36
Q

Transcortical motor aphasia

A

Broca’s aphasia with intact repetition

37
Q

Transcortical sensory aphasia

A

Wernicke’s with intact repetitioin

38
Q

Global aphasia

A
  • Both broca and wernike’s
39
Q

Anomic aphasia

A
  • trouble naming objects
40
Q

Neologism

A
  • Made up words
41
Q

Semantic paraphasia

A
  • Substituted word is related to the intended word
42
Q

Phenomic paraphasia

A

syllables out of sequence

43
Q

Gerstmann’s syndrome

A
  • lesions in dominant parietal lobe ( angular gyrus

- Acalculia, agraphia, left/right confusion, finger agnosia

44
Q

Apraxia

A

a disorder of skilled movement not caused by weakness, akinesia, deafferentation, abnormal tone or posture, movement disorders intellectual deterioration poor comprehension or uncooperativeness.

45
Q

Neglect

A

Neglect of one half of patient’s world,

due to lesion in the non dominant parietal lobe

46
Q

prospagnosia

A
  • inability to recognize faces

- damage to fusiform gyrus of temporal lobe

47
Q

Astereoagnosia

A
  • inability to recognize objects when placed in her hand : localized to parietal lobe: primary somatosensory cortex.
48
Q

Anton’s syndrome

A

denial of blindness due to damage in b/l occipital lobes.

49
Q

Balint’s Syndrome

A
  • Due to damage to both posterior parietal lobes
  • Optic apraxia: incoordination of hand and eye movement
  • occulomotor apraxia: inability to voluntarily guide eye movements
  • Simultanagnosia: inability to perceive more than one object at a time in one’s visual field
50
Q

Posterior reversible encephalopathy syndrome (PRES)

A
  • A consequence of severe uncontrolled HTN especially if it is of rapid increase.
  • In women it is common in preeclampsia
  • P/w: seizures, visual disturbances, headaches and mental status changes
51
Q

Synesthesia

A

When activation of one sensor pathway leads to the involuntary activation of another

52
Q

Kleine-Levin syndrome

A

Sleeping Beauty:

  • Increased sleeping
  • Hyperphagia
  • Hypersexuality
53
Q

Pseudobulbar palsy

A
  • characterized by uncontrolled episodes of crying or laughing
  • tx: dextromethorphan/quinidine
54
Q

Alien hand syndrome

A

Associated with dementia occurs in corticobasal degeneration

  • can be consequence of surgery where corpus collosum is severed
  • hands have minds of their own