IDcare – a longitudinal register study of pre-pandemic and pandemic diagnostic profiles among people with intellectual disabilities: A cohort profile
(2024) The 17th IASSIDD World Congress- Abstract
- Background: There are few large register-based studies on people with intellectual disabilities (ID) that compare outcomes with the general population.
Methods: All people in Skåne, the southernmost part of Sweden the 1st of January 2014 was included. Data concerning demographics/vital events, healthcare utilization and service and support for people with ID or autism spectrum disorder (ASD) was collected from registers for 2014-2021. Data on COVID-19 vaccination, palliative care and intensive care were collected from registers for 2020-2021. Those with a registered diagnosis of ID (F7), Down Syndrome (Q90), or with service and support for people with ID or ASD, comprised the ID cohort (n=14716). People living in the same... (More) - Background: There are few large register-based studies on people with intellectual disabilities (ID) that compare outcomes with the general population.
Methods: All people in Skåne, the southernmost part of Sweden the 1st of January 2014 was included. Data concerning demographics/vital events, healthcare utilization and service and support for people with ID or autism spectrum disorder (ASD) was collected from registers for 2014-2021. Data on COVID-19 vaccination, palliative care and intensive care were collected from registers for 2020-2021. Those with a registered diagnosis of ID (F7), Down Syndrome (Q90), or with service and support for people with ID or ASD, comprised the ID cohort (n=14716). People living in the same household as someone in the ID cohort were excluded. The remaining comprised the general population cohort (gPop) (n=1226955). The cohorts were also divided into age groups (children: 0-12; adolescents: 13-18; Young adults: 19-24; Adults: 25-44; Lower middle-age:45-54; Upper middle-age:55-64; Older: 65-79; and Oldest old: 80 years and older).
Findings: The ID prevalence was 1.2%. Among those 77.9% had at least one measure of support for people with ID, 63.8% had at least one F7-diagnosis, and 5.8% a Q90 diagnosis. For those with F7-diagnosis 26.9% had mild, 7.4% moderate, 2.8% severe, 1.4% profound, and 25.4 other/unknown ID diagnosis. The proportion of people in the younger age groups were higher in the ID cohort compared to the gPop (children: 24 vs. 14%, adolescents: 14 vs. 6%, young adults: 16 vs. 8%, adults: 27 vs. 26%, lower middle-age: 8 vs. 13%, upper middle-age: 6 vs. 12%, older: 4 vs. 15% and oldest old: 1 vs. 6%).
Conclusions: The prevalence of ID was higher in younger age groups and in mild and other/unknown ID. A large proportion of people with ID had no registered/unknown diagnoses of ID severity during the study period. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/d060366e-f27b-4265-aa14-96de255e6d73
- author
- Sandberg, Magnus LU ; Kristensson, Jimmie LU ; Stroh, Emilie LU ; Edvardsson, David ; Edvardsson, Kristina and Axmon, Anna LU
- organization
- publishing date
- 2024-08-05
- type
- Contribution to conference
- publication status
- published
- subject
- conference name
- The 17th IASSIDD World Congress
- conference location
- Chicago, United States
- conference dates
- 2024-08-05 - 2024-08-08
- project
- Health care utilization in primary and specialist care among people with intellectual disability: A longitudinal register study
- Support, health care, end-of-life care, and causes of death among people with intellectual disability: Effects of the Covid-19 pandemic
- language
- English
- LU publication?
- yes
- id
- d060366e-f27b-4265-aa14-96de255e6d73
- alternative location
- https://www.lupop.lu.se/idcare_iassidd2024_cohort
- date added to LUP
- 2024-08-12 15:22:18
- date last changed
- 2024-08-13 07:33:14
@misc{d060366e-f27b-4265-aa14-96de255e6d73, abstract = {{Background: There are few large register-based studies on people with intellectual disabilities (ID) that compare outcomes with the general population. <br/><br/>Methods: All people in Skåne, the southernmost part of Sweden the 1st of January 2014 was included. Data concerning demographics/vital events, healthcare utilization and service and support for people with ID or autism spectrum disorder (ASD) was collected from registers for 2014-2021. Data on COVID-19 vaccination, palliative care and intensive care were collected from registers for 2020-2021. Those with a registered diagnosis of ID (F7), Down Syndrome (Q90), or with service and support for people with ID or ASD, comprised the ID cohort (n=14716). People living in the same household as someone in the ID cohort were excluded. The remaining comprised the general population cohort (gPop) (n=1226955). The cohorts were also divided into age groups (children: 0-12; adolescents: 13-18; Young adults: 19-24; Adults: 25-44; Lower middle-age:45-54; Upper middle-age:55-64; Older: 65-79; and Oldest old: 80 years and older). <br/><br/>Findings: The ID prevalence was 1.2%. Among those 77.9% had at least one measure of support for people with ID, 63.8% had at least one F7-diagnosis, and 5.8% a Q90 diagnosis. For those with F7-diagnosis 26.9% had mild, 7.4% moderate, 2.8% severe, 1.4% profound, and 25.4 other/unknown ID diagnosis. The proportion of people in the younger age groups were higher in the ID cohort compared to the gPop (children: 24 vs. 14%, adolescents: 14 vs. 6%, young adults: 16 vs. 8%, adults: 27 vs. 26%, lower middle-age: 8 vs. 13%, upper middle-age: 6 vs. 12%, older: 4 vs. 15% and oldest old: 1 vs. 6%). <br/><br/>Conclusions: The prevalence of ID was higher in younger age groups and in mild and other/unknown ID. A large proportion of people with ID had no registered/unknown diagnoses of ID severity during the study period.}}, author = {{Sandberg, Magnus and Kristensson, Jimmie and Stroh, Emilie and Edvardsson, David and Edvardsson, Kristina and Axmon, Anna}}, language = {{eng}}, month = {{08}}, title = {{IDcare – a longitudinal register study of pre-pandemic and pandemic diagnostic profiles among people with intellectual disabilities: A cohort profile}}, url = {{https://www.lupop.lu.se/idcare_iassidd2024_cohort}}, year = {{2024}}, }