Cognitive Disorders Flashcards

1
Q

Cognitive Disorder

A

Significant change in cognition from a previous level of functioning. May effect memory, attn, language and judgement. May be associated with abnormalities of the central nervous system, general medical condition or substance abuse.

Typically described as either a Delirium or Dementia

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2
Q

Delirium

A

A waxing and waning change in a patients level of consciousness. Can be caused by virtually any medical disorder.

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3
Q

AEIOU TIPS

A
Alcohol/drug tox.
Electrolyte abs.
Iatrogenic causes (pharm)
Oxygen (hypoxia)
Uremia --> hepatic encephalopathy

Trauma
Infection
Poison
Seizure

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4
Q

Risk Factors for Delerium

A
Advanced Age
Pre-existing Brain Damage
Prior hx of delirium
Alcohol
Cancer
Diabetes
Sensory impairment
Malnutrition
Male Gender
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5
Q

Sx of Delerium

A
Short attn span
Visual Hallucination
Disorientation
Language disturbances
Disturbed psychomotor 
Emotional disturbance
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6
Q

Tx of Delerium

A

Fix the underlying cause

Agitation associated : psychotropics given such as Haloperidol.
Benzos rarely given unless delirium due to alcohol

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7
Q

Dementia

A

impairment of memory or other cognitive functions without alteration in the level of consciousness.

Most forms are progressive and irreversible
Most common is Alzheimers (15-25%)

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8
Q

DSM for Dementia

A

Multiple cognitive deficits manifested by Memory impairment and at least one of the following:
Aphasia, Apraxia, Agnosia, Disturbance of executive functioning.

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9
Q

MMSE

A

Orientation (date month year)
Registration (name three objects, repeat)
Attention and Calculation (count back for 100 by 7s)
Recall (repeat 3 items 5 mins later)
Language (Name a pen and clock, Say no if and’s or but’s)
Read and obey the following

Perfect : 30
Dysfunction: less than 25.

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10
Q

Etiology of Alzheimers

A

Decreased ACh due to loss of Noradrenergic neurons in the basal cereuleus and dec Choline Acetyltransferase.

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11
Q

Genes associated with Alzheimers

A

Presenilin 1 and 2.
Amyloid Precursor Protein
ApoE4 : If homozygous, 90% chance of getting alzheimers by 85. Heterozygous (45%)

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12
Q

Postmortem findings of Alzheimers

A

DIffuse atrophy with enlarged ventricles and flattened sulci.

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13
Q

Tx of Alzheimers

A

No Cure

Cholinesterase Inhibitors: Rivastigmine, Tacrine, Donepezil

NMDA Antagonists: Memantine (Namenda)

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14
Q

Vascular Dementia

A

2nd most common form of dementia

Produced by multiple small infarcts (lacunar)

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15
Q

Tx of Vascular Dementia

A

No effective treatment

Control of HTN may help overall.

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16
Q

Lewy Body Dementia

A

Due to aggregation of Alpha-synuclein –> Lewy Neurites and Lewy Bodies especially in the basal ganglia

Sx: Waxing and waning cognition is core feature
Visual hallucinations (well formed ideas of animals or people)
Paranoid delusions
Parkinsonism (tremor, bradykinesia, shuffling gait)
Sensitivity to neuroleptics
REM disorder is common.

17
Q

Dx of Lewy Body Dementia

A

Onset of dementia within 12 months of parkinsonism symptoms,

18
Q

Tx of Lewy Body Dementia`

A

Cholinesterase Inhibitors (help visual hallucinations)

Psychostimulants, levodopa/carbidopa, dopamine agonists.

Atypical neuroleptics

Clonazepam for REM sleep behavior

19
Q

Pick Disease (Fronto-Temporal Dementia)

A

Typically presents between the ages of 45-65

20-30% is familial and associated with the Progranulin and MAPT Genes

Mean duration is 4-6 years until death.

Marked atrophy of the frontal and temporal lobes
Neuronal loss, microvascularization and astrocytic gliosis in cortical layer II

20
Q

Pick Dx Sx

A

PROFOUND changes in personality and social conduct
Disinhibited verbal, physical and sexual behavior
Echolalia, overeating, ORAL EXPLORATION OF INNANIMATE OBJECTS
Poor insight about behavioral changes

21
Q

Pick Dx Tx

A

Anticholinergic and Antidepressants

22
Q

HIV Associated Dementia

A

Most common dementia caused by infectious disease

23
Q

Tx of HIV Associated Dimentia

A

HAART

Psychostimulants

24
Q

Huntington Disease

A

Autosomal Dominant. Onset between 35-50 (shows anticipation through generations).

Progressive dementia
Choreaform movements
Muscular hypertonicity
Psychiatric Manifestation
Increased rate of suicide.

MRI shows CAUDATE ATROPHY

25
Q

Genetics of HD

A

AD

Trinucleotide repeat on short arm of Chromosome 4

26
Q

Parkinson Disease

A

Progressive disease with neuronal loss in the Substantia Nigra –> decreased DA.

Occurs slightly more in men than in women

27
Q

Pathology of PD

A

Senile plaques and neurofibrillary tangles, loss of substantial nigra and thus DA

Tx: Levodopa/ Carbidopa

28
Q

Creutzfeld Jakob Disease

A

Rapidly progressive degenerative prion disease . May be inherited, sporadic or acquired

Rapidly progressive dementia in 6-12 months

Sx:
Myoclonus
Cerebellar/basal ganglia

29
Q

CJD Diagnosis

A

Spongiform changes of brain tissue

Generalized sharp waves on EEG

Myoclonus, Cortical Blindness, Ataxia, Pyramidal signs, Muscle Atrophy, Mutism

30
Q

Normal Pressure Hydrocephalus

A

Possible reversible cause of dementia
Have enlarged ventricles with Increased CSF pressure

WET: Often pee themselves
WOBBLY: Gait Disturbance
WACKY: Dementia

Tx is to relieve pressure.