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star whichever ones actually feel relevant, i didn't know which to filter out
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Cessation
Detoxification when over-drank
Reverses Wernicke’s Encephelopathy
High-dose vitamin B1 injections
Treatment for alcohol
inpatient or outpatient addiction services
Cure for Alzheimer’s
There is none.
Main diagnostic methods of Alzheimer’s
Neuropsychological assessment
Structural imaging
Drugs given for Alzheimer’s (2)
Cholinesterase inhibitors (stops loss of cholinergic neurons, improving communication between brain cells)
Memantine (increases glutamate)
2 treatments for aneurysms (vascular cognitive impairment)
Endovascular treatment: such as coiling or stent placement, which are inserted into the blood vessel through the groin
Neurosurgical intervention (clipping), where the aneurysm is closed with a metal clip
Cure for Parkinson’s
No cure !!
Drugs for Parkinson’s (5)
Levodopa
Dopamine agonists
Monoamine oxidase type-B inhibitors
Amantadine
Rivastigmine (for cognitive impairment)
Treatment for Parkinson’s (2)
→ deep brain stimulation (DBS) → implanting a thin wire with electrodes into the brain → high-frequency stimulation will alter the brain signals, leading to symptom improvement
→ levodopa-carbiodopa intestinal gel (LCIG, brand name Duodopa)
administered as a gel directly into the first part of the small intestine, to offer more continuous dopaminergic stimulation leading to more constant levodopa levels
Types of atypical parkinsonisms
Lewy body dementia (LBD)
Corticobasal degeneration (CBD)
Multiple system atrophy (MSA)
Progressive supranuclear palsy (PSP)
Lewy body dementia (LBD) characteristics
Early dementia
Cognitive impairment
Hallucinations
Rigidity
Bradykinesia
(very Parkinson’s like)
Corticobasal degeneration (CBD) characteristics
Asymmetric motor symptoms
Alien hand
Apraxia
Cognitive deficits
Multiple system atrophy (MSA) characteristics
Erectile dysfunction
Incontinence (pee self)
Orthostatic hypotension (BP suddenly drops)
Progressive supranuclear palsy (PSP) characteristics
Axial rigidity
Disinhibition
Emotional instability
6 first-generation epilepsy drugs
Luminal
Diphantoin
Ethymal
Depakine
Frisium
Tegretol
side effects: decrease info processing speed, attention, and executive functions
10 second- generation epilepsy drugs
Taloxa
Neurontin
Lamictal
Topamax
Keppra
Trileptal
Sabril
Zonegran
Diacomit
Lyrcia
varying side effects
4 third-generation epilepsy drugs
Fycompa
Briviact
Inovelon
Vimpat
no major side effects! :)
Epilepsy treatments (3)
→ Wada test
→ Grid surgery
→ stereo EEG
Genetic disorder detectors (2)
Non-invasive prenatal test (NIPT, through blood tests), or a combined test (blood test and nuchal scan), enabling genetic abnormalities to be detected
Whole-exome sequencing (WES) → examine entire genome for possible genetic variations
Glasgow Coma Scale
measure cognitive dysfunctions after brain injury
Elaborate drawing test
Rey Figure Test
Scale to determine the severity of Parkinson’s symptoms
Hoehn and Yahr Scale
Hyposmia
fked sense of smell (Parkinson’s)
Ischemic core
Spot on brain with critically low blood flow that WILL die
Penumbra
Brain area around ischemic core
Diaschisis
Brain area being functionally disconnected because of the affected brain tissue
Temporal confusion
Loss of sense of time (in Korsakoff’s, this affect how they consolidate (and sequence) their memories)
Simulating (ch3)
pretending non-existing complaints
Aggravating (ch3)
exaggerating complaints
Sensitivity (ch3)
identifying people with a disease
Specificity (ch3)
identifying people without a disease
Problematic alcohol use
Physical/psychological/social problems regardless of quantity
Alcohol Use Disorder (AUD)
Problematic use meeting the DSM criteria
Binge drinking
Took much in a short period, but with abstinence phases (>5 for men, >4 for women)
Alcohol intoxication
Excessive use causing disorientation, less of consciousness, etc. (‘being rlly drunk’, one-time thing, consistent intoxication can lead to others)
Alcohol withdrawal syndrome
Sudden withdrawal after long-term use
Status epilepticus
seizure activity lasting more than 5 minutes or recurrent seizures without recovery
Order from most common to least:
Lewy Body Dementia, Alzheimer’s Dementia, Frontotemporal Dementia, Vascular Dementia
Most common: Alzheimer’s Disease
Vascular Dementia
Lewy Body Dementia
Least common: Frontotemporal Dementia
Order from most common to least:
Noonan, Klinefelter, Neurofibromatosis 1, Turner, Prader-Willi
Klinefelter (1:600)
Noonan (1:1,000–1:2,500)
Turner (1:2,000)
Neurofibromatosis 1 (1:3,000)
Prader–Willi (1:15,000)
Type 1 error vs Type 2 error
Type I error is a false positive (rejecting a true null hypothesis)
Type II error is a false negative (failing to reject a false null hypothesis)
What are 7 types of validity’s
Face validity
Content validity
Concept validity
Criterion validity
Predictive validity
Concurrent validity
Ecological validity
Face validity
on the surface, how well does the test seem to be measuring what it’s meant to
Content validity
How representative is the test of all relevant content
Concept/construct validity
how well does it measure the theoretical concept
Criterion validity
to what extend can a test predict a patient’s performance on an external criterion
Predictive validity
how well does a test actually predict behaviour
Concurrent validity
comparison between a neuropsychological test and another instrument that measure the same construct
Ecological validity
the extent to which the test predicts how a patient will function in their own daily environment