OPH Flashcards
Early onset alzheimer’s disease - 5% of all AD, genes
Amyloid precursor protein, presenilin 1&2
Autosomal dominant with almost complete penetrance
Frontotemporal dementia genes
Autosomal dominant variable pentrance
40% affected 1st degree relative
Late onset alzheimers genetics
Apo E contributes vascular
Dementia lifetime risk
20% women
10% men
Clinical diagnosis of dementia
Mostly history from patient and relatives
FHx, PMH, Drug history
HPc
How did it start?
* When did it start?
* How has it progressed?
* What can they NOT do now that they could do before?
* What do they DO now that you wish they didn’t do?
* What are they still doing that you think they shouldn’t
be doing?
* Visual hallucination ,delusions, failure to recognise
family members
Dementia investigations
tests for remediable causes - FBC, Us&Es, B12, Folate, TSH, CXR
Imaging - CT, MRi - early in course of dementia often completely normal, check for alt diagnosis
Dementia risk factors
Age, FHx, HTN, Cholesterol, DM, Smoking, mid-life obesity, alcohol, head injury
Lewy body dementia characteristics
Prominent visual hallucinations, visuospatial problems, fluctuating course, 70% neuroleptic sensitivity
Frontotemporal dementia characteristics
Personality & behaviour change, language problems, younger age groups
Alzheimer’s meds
Cholinesterase inhibitors - donepezil or rivastigmine may help some people with symptoms
Dementia management
Social support, driving, EPOA
Frontotemporal dementia cell changes
Pick Bodies
Alzheimers cell changes
Tau tangle and amyloid plaques in hippocampus
Lewy body dementia
Lewy bodies in substancia nigra (basal ganglia)
Cortex, brainstem, limbic system
Parkinson’s associated
Delirium if a patient is on a benzo it is better to keep it going than to stop it
True