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68 Cards in this Set
- Front
- Back
How long is MMSE
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30 questions
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Orientation questions
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5 pts: What is the (year) (season) (date) (day) (month)?
5 pts: Where are we (state) (country) (town) (hospital) (floor)? |
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Registration questions
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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 |
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attention and calculation questions
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o 5 pts: Serial 7’s. 1 point for each correct answer. Stop after 5 answers.
o Alternative: spell “world” backward. |
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recall questions
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o 3 pts: Ask for the 3 objects repeated above.
o Give 1 point for each correct answer. |
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Language questions
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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. |
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Normal MMSE
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>27
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MMSE suggesting dimentia?
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22, 24 in educated ppl
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mild dimentia
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• Scores of 20-26
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moderate dimentia
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10-19
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severe disease
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<10
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What is delirium
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– Alteration (fluctuating) level of consciousness
– Associated with altered attention and cognition – Rapid Onset – May be reversible – Always due to a medical/surgical cause |
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where is highest delirium
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surgical ICU then cardio ICU
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What is used to DX deliurium
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CAM-ICU worksheet
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most significant delirium elements of DX?
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inattention and broad fluctuations
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hyperactive delirium
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• Obvious deficits in focused attention and fluctuations of presentation
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quiet delirium
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• 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 |
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Motor SX w/delirium
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• Dysarthria
• Difficulty swallowing • Gait disturbances |
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Affective SX w/delirium
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• Dysphoria
• Lability • Anxiety |
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Life threatening causes of delirium? (WWHHHIMP)
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• 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 |
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what is Asterixis
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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.” |
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what is dimentia
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– Cognitive deficits and memory impairment
– Consciousness is NOT impaired as in delirium – Course is generally gradual and progressive – Very rarely is Dementia reversible |
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what must you have at least one of to have dimentia
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aphasia, apraxia, agnosia, Impaired executive functioning (planning, organizing, sequencing and abstraction).
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aphasia?
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disturbance in the comprehension or expression of language)
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what is apraxia
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impaired ability to perform a voluntary, purposeful motor activity despite intact motor ability. “Constructional apraxia” = cannot draw 2 or 3 dimensional forms).
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what is agnosia
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failure to recognize or identify objects despite intact sensory function).
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qualifiers for cognitive disorder
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• 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 |
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Neuro findings in alzheimers
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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 |
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Temporal lobe
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• Auditory
• Language comprehension (L) • Sensory prosody (R) • Memory and emotion |
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early stages of alzheimers
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loss ST memory, work finding difficulties (• Vague speech, Circumlocution, Use of clichés), develop apraxias (Affects dressing (motor apraxia), Affects eating)
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later alzheimers stages
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o Judgment becomes impaired
o May develop personality changes • Apathy • Hostility • Social withdrawal o Disturbed sleep-wake patterns |
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psych issues in dimentia
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depression, anxiety, dellutions, hallucinations, agitation
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MC pesonality change in dimentia
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apathy
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what is Capgras Syndrome
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misidentification syndrome: Belief that a friend, family member, or acquaintance been replaced by an identical-looking imposter
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Phantom boarder syndrome
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An unseen individual is living in the home
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What type of hallucinations are more common
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visual, in AA
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RF alzheimer
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o Increasing age
o Positive family history o History of head trauma o Down's Syndrome o Genetic component |
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What 3 chromosomes have been linked to alzheimers
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trisomy 21, chrom 14( presenilin 1 gene), chrom 1(presilin 2 gene)
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o Apo-E4 allele
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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 |
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What is vascular dimentia
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– Progression is “step-wise”
– Diffuse distribution – Formerly referred to as multi-infarct dementia |
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rf vascular dimentia
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o Vascular disease
o Vasculitis o Embolic disease (including atrial fibrillation) o Stroke yields a nine-fold increased risk of dementia |
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what is Creutzfeldt-Jakob Disease
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category of diseases called transmissible spongiform encephalopathies (TSEs).
rapidly progressing prion infection |
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What is spongiform
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• 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.
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MC CJD
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sporadic
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Most infrequent CJD?
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acquired
• Exposure to brain or nervous system tissue (medical procedures). • No evidence is contagious through casual contact with someone who has CJD |
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How can CJD be transmitted
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• The use of contaminated dura mater or corneal grafts
• By ingesting meat from cattle infected with bovine spongiform encephalopathy |
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First CJD signs
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– First signs may be vague somatic complaints or unspecified feeling of anxiety
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other CJD Si
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o Ataxia
o Extrapyramidal signs o Choreoathetosis o Dysarthria o Myoclonic jerks |
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other CJD SX
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o Emotional lability
o Anxiety o Euphoria o Depression o Delusions o Hallucinations |
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What gene is huntingtons on
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chrom 4
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onset of huntingtons
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o Onset in 30-40's (Patient usually has children by this time)
o Choreiform movements seen first and become more severe |
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dimentia in huntingtons
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o Dementia presents later- often with psychotic features.
o Dementia may first be described as a personality change |
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Describe Common dimentia of lewy dementia
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– Extreme sensitivity to antipsychotic drugs
– Visual hallucinations – More marked response to cholinesterase inhibitors |
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Clinical presentation of lewy dementia
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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 |
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DX criteria for Lewy Dementia
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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! |
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where is eosinophilic intraneuronal inclusion lewy body found
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cortex and subcortex
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Parkinsons symptoms
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(bradykinesia, resting tremor, pill-rolling tremor, mask-like faces (flat affect), shuffling gait, etc…)
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What is Pick's disease
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– Frontal lobe is predominately involved
– See frontal signs of disinhibition – Relative preservation of cognition |
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what may patients with picks disease have
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Kluver-Bucy Syndrome (hypersexuality, hyperorality – compulsion to examine objects by mouth, placidity/docility – low aggression, diminished fear response)
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What is pseudo dimentia
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– Depression that presents with cognitive and memory impairment that resembles dementia
– Treat with anti-depressant medication or ECT |
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What meds should you use for dementia
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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 |
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Cholinesterase acting meds
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tacrine, donepezil, revastigmine, galantamine
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MOA Memantine Hydrochloride (Namenda)
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• NMDA (N-methyl-D-aspartate) antagonist. Slows down the progression of the disease by blocking excessive stimulation of NMDA receptors
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MCC Amnestic disorder
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thiamine deficiency associated with alcohol dependency
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TRIAD SX for hydrocephalus that you should consider in dementia pts
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• Unsteadiness of gait
• Psychomotor retardation • Urinary incontinence • Wet, Wacky, and Wobbly |
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wht type of cognitive impairment do hydrocephalus pattients exhibit
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• Inattentive
• Easily sidetracked • Memory loss • Slow, but accurate recall |
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Hydrocephalus motor sx
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o Walk slowly
o Take shorter strides o Shuffle feet when walk |
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hydrocephalus outcomes
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• 1/3 significantly improve
• 1/3 stabilize or experience minor change • 1/3 continue to decline |