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An assessment of health, social, communication, and daily living skills of adults with Down syndrome. | LitMetric

AI Article Synopsis

  • Adults with Down syndrome (DS) are living longer, but there is a lack of detailed information on their life skills and abilities, prompting the need for more quantitative data.
  • The study involved 157 caregivers of adults with DS aged 20 or older, who completed an online questionnaire assessing health, social, communication, and daily living skills to understand how age impacts functional abilities.
  • Results showed that more health issues were linked to lower independence and social engagement, while communication skills were mainly affected by current health problems; additionally, abilities declined after age 40, highlighting the importance of this data for caregivers and providers.

Article Abstract

Adults with Down syndrome (DS) are surviving longer, yet data delineating life skills are lacking. As providers are encouraged to provide a "balanced" description of DS to family members/caregivers, more quantitative data are required to accurately describe the abilities and potential of adults with DS. This study assessed health, social, communication, and daily living skills of adults with DS to describe the range of abilities and to show how increasing age contributes to functional abilities. Caregivers of an adult with DS 20 years of age or older participated in an online questionnaire. Descriptive statistics and scores from scales assessed relationships between the number of health issues reported and functional abilities, and how the abilities changed as age increased. Of 188 participants, 157 completed the survey with partial results included. Communication, independence, and social activity scores were compared to the number of congenital and non-congenital health issues reported. Linear regression results showed those with more health issues were significantly less likely to be independent and social. However, only current health issues affected communication skills. No significant correlation occurred between the number of congenital abnormalities and scores for independence/life skills as an adult. T-test by age group found decreasing abilities after 40 years of age. In conclusion, quantitative data and information from this study is beneficial for providers in order to describe the potential for an individual with DS and to assist caregivers to plan accordingly for the future of their adult with DS.

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Source
http://dx.doi.org/10.1002/ajmg.a.38721DOI Listing

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