PSY2004 SEMESTER 2 - WEEK 9 Flashcards

(41 cards)

1
Q

what is life expectancy for williams syndrome

A

lacking research but expectation similar to neurotypicals

  • shortened due to comorbid health conditions (heart problem, MHI)
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2
Q

what has life expectancy in DS rise from

A

from 12 in 1949, to 60 2018

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3
Q

why has DS life expectancy improved

A
  • improvements in living conditions
  • more than half of babies with DS have congenital heart conditions - improvement in treatment
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4
Q

what was original viewpoint on life expectancy of autistic individual

A

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

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5
Q

what is recent view of autism life expectancy

A

smaller differences in life-expectancy

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6
Q

why are autistic more shorter life expectancy?

A
  • 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)
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7
Q

what are communicative recommendations to increase accessibility in autism healthcare

A

clear language
e-consult
instruction and written advice
signpost to directive resource

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8
Q

what are sensory processing recommendations to increase accessibility in autism healthcare

A

conduct sensory audit of premises
offer times facilitating attendences
allow time to process info

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9
Q

what are predictability recommendations to increase accessibility in autism healthcare

A

regular doctors
provide info on whats expect
advise on timings for procedure

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10
Q

compare adults/children who has williams syndrome

A

almost identical cog profile to children, sometimes increase visuospat ability

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11
Q

(Howlin & Udwin, 2006) parents quesionnar, mean age of child 36 - Williams syndrome, what % had health issue

A

79% heart problems
51% dep/anx

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12
Q

(Howlin & Udwin, 2006) parents quesionnar, mean age of child 36 - Williams syndrome, what % were independent

A

62% lived with families
16% lived independently
2% residential communities

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13
Q

(Howlin & Udwin, 2006) parents quesionnar, mean age of child 36 - Williams syndrome, what % education

A

71% attended college
33% attained formal qualification

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14
Q

(Howlin & Udwin, 2006) parents quesionnar, mean age of child 36 - Williams syndrome, what % works

A

20% full time educat
30% day centre
1.6% full-time employed
18% part-time
9% voluntary
6% stays at home

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15
Q
A
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16
Q

(Howlin & Udwin, 2006) parents quesionnar, mean age of child 36 - Williams syndrome, what % parents dissatisf with support

A

23% parents dissatisfied with ment/phys medical help
33% unhappy with educational provision
20% unhappy with workplace assistance

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17
Q

outline cognitive changes in adulthood DS

A

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

18
Q

outline physical changes in adulthood DS

A

accelerated ageing, skin/hair change, early-onset menopause, hearing impairments, diabetes, musculoskeletal problem

19
Q

name key features of alzhiemer

A

excessive amounts of amyloid (form plaque) and tau (form tangle)

20
Q

how does genetics mean more likely to have alzheimers DS

A

gene coding for amyloid precursor protein located on chromosome 21 - duplicated in DS, causing increased amyloid plaques and AD

21
Q

how many DS individual have plaques assoc with alzheimer

A

up to 100% individuals 40+ years of age show plaques associated with AD (although don’t necessarily have AD)

22
Q

how many DS age 30-39 show signs DS

23
Q

how many DS age 40-49 show signs DS

24
Q

how many DS age 60+ show signs DS

25
what is usual age of onset of alzheimer for neurotyp
65+
26
summarise cognitive adult profile for autism
some areas of difficulty (ToM) improving w/ age however most model suggest no diff in age trajectory btw/ autistic/neurotyp or steeper declines
27
why is autism prevalence much lower for adult than childhood
diagnostic criteria changed over time, awareness of autism increased (seen in screening and medical record studies, community based case identification studies)
28
Grosvenor (2024) used electronic health records, insurance claim data, found what regarding ASD diagnosis
substant less adult diagnosed
29
O'Nions (2023) used population based retrospective cohort study of med record, found what regarding autism diagnosis
- substantially fewer adults diagnosed
30
why are there fewer autistic adults than children
- “grow-out of autism” - environmental factor - diagnostic criteria evolved, so autistic adults weren’t meeting criteria as a child - increased awareness
31
how can actual number autism be studied in community
use community based case identification study, via autisim screening, ie like Bruga (2011) using stratified sampling
32
what did Bruga (2011) find via Adult Psychiatric Morbidity Survey- overall prevalence
estimated autism prevalence 0.98%, none of identified cases had existing diagnosis of autism
33
what did Bruga (2011) find via Adult Psychiatric Morbidity Survey- gender splits
men= 1.82% women= 0.2%
34
what did Bruga (2011) find via Adult Psychiatric Morbidity Survey- time split
adult prev sim to children prevalence of 2007, suggesting that rate ASD not signif assoc with age, so cause of autism were "temporally constant"
35
what did Bruga (2011) find via Adult Psychiatric Morbidity Survey- whats autism associated with
reduced verbal IQ, lower educational attainment, male gender
36
what did Bruga (2011) find via Adult Psychiatric Morbidity Survey- who were excluded
care setting, moderate-severe intellctual disabil
37
what did Bruga (2011) find via Adult Psychiatric Morbidity Survey- follow up study focusing on intellc dis, what was prevalence
- autism prevalence higher in intellectual disabilities but gender differences reduced - prevalence of autism in combined reweighted sample was 1.1% - as moderate-profound intellectual disability makes up 0.3% population means overall association of autism with age and gender for population as whole unchanged by inclusion of rates for people with intellectual disability
38
what is AMPS
- given over several yrs, establish prevalence of psychiatric conditions in population - autism not psychiatric condition but q are included to study autism prevalence, designed as represent of households in England - data then is available for researcher secondary data analysis
39
what are challenges of autism diagnostics for adulthoods
not recog experience and dev coping strategy diagnosing usually require dev info, experiences, childhood milestone lack of dev norm to see diffic, harder to compare adult than child
40
when should assessment of autism be considered in adults
if show possible features (diffic obtaining/keeping job, education, init soc rel, contact with mental/LD serv, history of neurodev disab)
41
what mental health conditions can be difficult to identify for ASD adults
identifying depression in ASD is challenging: issues recognising and articulating feelings and emotions - rigid thought style and dichotmous thinking means more suicidal thoughts are actually done