PSY2004 SEMESTER 2 - WEEK 9 Flashcards
(41 cards)
what is life expectancy for williams syndrome
lacking research but expectation similar to neurotypicals
- shortened due to comorbid health conditions (heart problem, MHI)
what has life expectancy in DS rise from
from 12 in 1949, to 60 2018
why has DS life expectancy improved
- improvements in living conditions
- more than half of babies with DS have congenital heart conditions - improvement in treatment
what was original viewpoint on life expectancy of autistic individual
16yrs shorter than a neurotyp, 30yr shorter if also intellec dis
however, didn’t account for most people with diagnosis being young= skew age estimate of life expectancies
what is recent view of autism life expectancy
smaller differences in life-expectancy
why are autistic more shorter life expectancy?
- more likely co-occuring issue: epilepsy, hearing/vis impairment, cerebral palsy, MHI, immune condition, sleep disorder, obesity, heart disease
- communication barrier to healthcare:
- difficulty booking or talking to doctor, voicemail, anxiety, needing more time, expressing emotions differently
- sensory barriers: waiting room (noise, lighting, touching)
what are communicative recommendations to increase accessibility in autism healthcare
clear language
e-consult
instruction and written advice
signpost to directive resource
what are sensory processing recommendations to increase accessibility in autism healthcare
conduct sensory audit of premises
offer times facilitating attendences
allow time to process info
what are predictability recommendations to increase accessibility in autism healthcare
regular doctors
provide info on whats expect
advise on timings for procedure
compare adults/children who has williams syndrome
almost identical cog profile to children, sometimes increase visuospat ability
(Howlin & Udwin, 2006) parents quesionnar, mean age of child 36 - Williams syndrome, what % had health issue
79% heart problems
51% dep/anx
(Howlin & Udwin, 2006) parents quesionnar, mean age of child 36 - Williams syndrome, what % were independent
62% lived with families
16% lived independently
2% residential communities
(Howlin & Udwin, 2006) parents quesionnar, mean age of child 36 - Williams syndrome, what % education
71% attended college
33% attained formal qualification
(Howlin & Udwin, 2006) parents quesionnar, mean age of child 36 - Williams syndrome, what % works
20% full time educat
30% day centre
1.6% full-time employed
18% part-time
9% voluntary
6% stays at home
(Howlin & Udwin, 2006) parents quesionnar, mean age of child 36 - Williams syndrome, what % parents dissatisf with support
23% parents dissatisfied with ment/phys medical help
33% unhappy with educational provision
20% unhappy with workplace assistance
outline cognitive changes in adulthood DS
reach stage later, stays longer = developmental gap widens with age
hard to investigate cog -comorbid w/ early onset alzheim
memory and cog decline in-line with expectation for neurotyp indiv
outline physical changes in adulthood DS
accelerated ageing, skin/hair change, early-onset menopause, hearing impairments, diabetes, musculoskeletal problem
name key features of alzhiemer
excessive amounts of amyloid (form plaque) and tau (form tangle)
how does genetics mean more likely to have alzheimers DS
gene coding for amyloid precursor protein located on chromosome 21 - duplicated in DS, causing increased amyloid plaques and AD
how many DS individual have plaques assoc with alzheimer
up to 100% individuals 40+ years of age show plaques associated with AD (although don’t necessarily have AD)
how many DS age 30-39 show signs DS
33%
how many DS age 40-49 show signs DS
55%
how many DS age 60+ show signs DS
75%