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68 Cards in this Set

  • Front
  • Back
How long is MMSE
30 questions
Orientation questions
5 pts: What is the (year) (season) (date) (day) (month)?
5 pts: Where are we (state) (country) (town) (hospital) (floor)?
Registration questions
o 3 pts: Name 3 objects: 1 second to say each. Then ask the patient to name all 3 after you have said them. Give 1 point for each correct answer.
o Then repeat them until he/she learns all 3. Count trials and record
attention and calculation questions
o 5 pts: Serial 7’s. 1 point for each correct answer. Stop after 5 answers.
o Alternative: spell “world” backward.
recall questions
o 3 pts: Ask for the 3 objects repeated above.
o Give 1 point for each correct answer.
Language questions
o 2 ( ) Name a pencil and watch.
o 1 ( ) Repeat the following “No ifs, ands, or buts”
o 3 ( ) Follow a 3-stage command:
• “Take a paper in your hand, fold it in half, and put it on the floor.”
o 1 pt: Read and obey the following: “Close your eyes.”
o 1 pt: Write a sentence.
o 1 pt: Copy the design shown.
Normal MMSE
>27
MMSE suggesting dimentia?
22, 24 in educated ppl
mild dimentia
• Scores of 20-26
moderate dimentia
10-19
severe disease
<10
What is delirium
– Alteration (fluctuating) level of consciousness
– Associated with altered attention and cognition
– Rapid Onset
– May be reversible
– Always due to a medical/surgical cause
where is highest delirium
surgical ICU then cardio ICU
What is used to DX deliurium
CAM-ICU worksheet
most significant delirium elements of DX?
inattention and broad fluctuations
hyperactive delirium
• Obvious deficits in focused attention and fluctuations of presentation
quiet delirium
• State reflects inability to attend in sequential fashion to demands of environment

• Withdrawal
• Lack of involvement in or communication with environment
• Bland or flat affect
• Depressed level of consciousness that is short of frank stupor
Motor SX w/delirium
• Dysarthria
• Difficulty swallowing
• Gait disturbances
Affective SX w/delirium
• Dysphoria
• Lability
• Anxiety
Life threatening causes of delirium? (WWHHHIMP)
• Wernicke's encephalopathy: confusion + ataxia + ophthalmoplegia
• Withdrawal states after discontinuation of illicit or Rx drug use, even when small dosages used for short periods of time
• Hypertensive encephalopathy - assess using vital signs
• Hypoxia - assessed with arterial blood gases
• Hypoglycemia - assessed with a serum glucose level
• Intracranial bleeding suggested by headache and confirmed by neuroimaging
• Meningitis and encephalitis almost always produce focal neurological signs as well as headache, loss of consciousness, and seizures
• Poisons (including pesticides, solvents, or heavy metals) may lead to delirium
what is Asterixis
commonly associated with liver failure where it produces the flapping tremor of hepatic encephalopathy. (Then it is called liver flap).
• The flapping of the hand is sometimes said to resemble a “bird flapping its wings.”
what is dimentia
– Cognitive deficits and memory impairment
– Consciousness is NOT impaired as in delirium
– Course is generally gradual and progressive
– Very rarely is Dementia reversible
what must you have at least one of to have dimentia
aphasia, apraxia, agnosia, Impaired executive functioning (planning, organizing, sequencing and abstraction).
aphasia?
disturbance in the comprehension or expression of language)
what is apraxia
impaired ability to perform a voluntary, purposeful motor activity despite intact motor ability. “Constructional apraxia” = cannot draw 2 or 3 dimensional forms).
what is agnosia
failure to recognize or identify objects despite intact sensory function).
qualifiers for cognitive disorder
• Condition must represent a change from the baseline
• Deficits must be clinically significant- interfere with social or occupational functioning
• Deficits cannot occur exclusively during an episode of delirium
• Condition cannot be accounted for by another DSM IV diagnosis
Neuro findings in alzheimers
o Extracellular senile plaques
o Intracellular fibrillary tangles
o Synapse degeneration
o Loss of neurons in cortex and subcortex
o Neuron loss affects neurotransmitter system
• Decrease in acetylcholine in forebrain
Temporal lobe
• Auditory
• Language comprehension (L)
• Sensory prosody (R)
• Memory and emotion
early stages of alzheimers
loss ST memory, work finding difficulties (• Vague speech, Circumlocution, Use of clichés), develop apraxias (Affects dressing (motor apraxia), Affects eating)
later alzheimers stages
o Judgment becomes impaired
o May develop personality changes
• Apathy
• Hostility
• Social withdrawal
o Disturbed sleep-wake patterns
psych issues in dimentia
depression, anxiety, dellutions, hallucinations, agitation
MC pesonality change in dimentia
apathy
what is Capgras Syndrome
misidentification syndrome: Belief that a friend, family member, or acquaintance been replaced by an identical-looking imposter
Phantom boarder syndrome
An unseen individual is living in the home
What type of hallucinations are more common
visual, in AA
RF alzheimer
o Increasing age
o Positive family history
o History of head trauma
o Down's Syndrome
o Genetic component
What 3 chromosomes have been linked to alzheimers
trisomy 21, chrom 14( presenilin 1 gene), chrom 1(presilin 2 gene)
o Apo-E4 allele
earlier age of onset

• Alzheimer’s disease without and with Lewy bodies
• Pure Lewy body dementia
• Parkinson’s dementia without Alzheimer’s beta-amyloid plaques
What is vascular dimentia
– Progression is “step-wise”
– Diffuse distribution
– Formerly referred to as multi-infarct dementia
rf vascular dimentia
o Vascular disease
o Vasculitis
o Embolic disease (including atrial fibrillation)
o Stroke yields a nine-fold increased risk of dementia
what is Creutzfeldt-Jakob Disease
category of diseases called transmissible spongiform encephalopathies (TSEs).
rapidly progressing prion infection
What is spongiform
• Infected brains become filled with holes and begin to look like sponges when viewed under a microscope. CJD is the most common of the known human TSEs.
MC CJD
sporadic
Most infrequent CJD?
acquired
• Exposure to brain or nervous system tissue (medical procedures).
• No evidence is contagious through casual contact with someone who has CJD
How can CJD be transmitted
• The use of contaminated dura mater or corneal grafts
• By ingesting meat from cattle infected with bovine spongiform encephalopathy
First CJD signs
– First signs may be vague somatic complaints or unspecified feeling of anxiety
other CJD Si
o Ataxia
o Extrapyramidal signs
o Choreoathetosis
o Dysarthria
o Myoclonic jerks
other CJD SX
o Emotional lability
o Anxiety
o Euphoria
o Depression
o Delusions
o Hallucinations
What gene is huntingtons on
chrom 4
onset of huntingtons
o Onset in 30-40's (Patient usually has children by this time)
o Choreiform movements seen first and become more severe
dimentia in huntingtons
o Dementia presents later- often with psychotic features.
o Dementia may first be described as a personality change
Describe Common dimentia of lewy dementia
– Extreme sensitivity to antipsychotic drugs
– Visual hallucinations
– More marked response to cholinesterase inhibitors
Clinical presentation of lewy dementia
o Shares features of both Alzheimer's disease and Parkinson's disease
o May have repeated falls
o Unusually sensitive to adverse effects of neuroleptics
o Common psychiatric symptoms include depression and systematized delusions
DX criteria for Lewy Dementia
o Progressive cognitive decline
o At least two of the following for probable diagnosis
• Recurrent (well formed) visual hallucinations. May see auditory hallucinations
• Parkinsonism
• Fluctuating cognition (with variation in attention and alertness) – like dementia!
where is eosinophilic intraneuronal inclusion lewy body found
cortex and subcortex
Parkinsons symptoms
(bradykinesia, resting tremor, pill-rolling tremor, mask-like faces (flat affect), shuffling gait, etc…)
What is Pick's disease
– Frontal lobe is predominately involved
– See frontal signs of disinhibition
– Relative preservation of cognition
what may patients with picks disease have
Kluver-Bucy Syndrome (hypersexuality, hyperorality – compulsion to examine objects by mouth, placidity/docility – low aggression, diminished fear response)
What is pseudo dimentia
– Depression that presents with cognitive and memory impairment that resembles dementia
– Treat with anti-depressant medication or ECT
What meds should you use for dementia
increases the level of acetylcholine in the brain, enabling neurons to communicate with one another more effectively
– Meds used block the action of acetylcholinesterase- key enzyme involved in breakdown of acetylcholine in the synaptic cleft
– Drugs that enhance cognition
Cholinesterase acting meds
tacrine, donepezil, revastigmine, galantamine
MOA Memantine Hydrochloride (Namenda)
• NMDA (N-methyl-D-aspartate) antagonist. Slows down the progression of the disease by blocking excessive stimulation of NMDA receptors
MCC Amnestic disorder
thiamine deficiency associated with alcohol dependency
TRIAD SX for hydrocephalus that you should consider in dementia pts
• Unsteadiness of gait
• Psychomotor retardation
• Urinary incontinence
• Wet, Wacky, and Wobbly
wht type of cognitive impairment do hydrocephalus pattients exhibit
• Inattentive
• Easily sidetracked
• Memory loss
• Slow, but accurate recall
Hydrocephalus motor sx
o Walk slowly
o Take shorter strides
o Shuffle feet when walk
hydrocephalus outcomes
• 1/3 significantly improve
• 1/3 stabilize or experience minor change
• 1/3 continue to decline