What do people with Down Syndrome want from their cardiac team?

This research investigates the experiences of people with Down syndrome who have a congenital heart condition (CHC). While people with Down syndrome are at greater risk of CHC, little is known about their views on hospital treatment and healthcare. A review of the literature indicates the incidence...

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Main Author: Reilly, Deirdre Emer
Published: University of East London 2012
Subjects:
Online Access:https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559447
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spelling ndltd-bl.uk-oai-ethos.bl.uk-5594472019-01-15T03:18:27ZWhat do people with Down Syndrome want from their cardiac team?Reilly, Deirdre Emer2012This research investigates the experiences of people with Down syndrome who have a congenital heart condition (CHC). While people with Down syndrome are at greater risk of CHC, little is known about their views on hospital treatment and healthcare. A review of the literature indicates the incidence and implications of CHCs for people with Down syndrome including barriers accessing health care and higher mortality for this group. The research considered ethical issues pertinent to conducting research with people with a learning disability including the choice of research method, participant recruitment, data collection and analysis. A qualitative approach was adopted and involved semi-structured interviews with five individuals with Down syndrome and a CHC. The interview covered topics including in the impact of Down syndrome, the impact of a CHC, and involvement in healthcare decisions. Three themes resulted from a thematic analysis: Who is the Patient; Self-Care, Care from Others and Gaps in Care and Health and Fitness. The major implications of this research for people with Down syndrome, their families and healthcare professionals include the need for clarity regarding supported decision making and supporting those with Down syndrome who may not have family members to aid decisions. This research involved a small relatively homogenous group of individuals and the area could benefit from further research, for example those without parent carers to support healthcare decisions and medical procedures. The research highlighted difficulties inherent to carrying out research with vulnerable groups, such as those with a learning disability. Future research should consider the process of including vulnerable groups in research, such as how to balance the research agendas of the researchers and the researched.616.85University of East London10.15123/PUB.1439https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559447http://roar.uel.ac.uk/1439/Electronic Thesis or Dissertation
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topic 616.85
spellingShingle 616.85
Reilly, Deirdre Emer
What do people with Down Syndrome want from their cardiac team?
description This research investigates the experiences of people with Down syndrome who have a congenital heart condition (CHC). While people with Down syndrome are at greater risk of CHC, little is known about their views on hospital treatment and healthcare. A review of the literature indicates the incidence and implications of CHCs for people with Down syndrome including barriers accessing health care and higher mortality for this group. The research considered ethical issues pertinent to conducting research with people with a learning disability including the choice of research method, participant recruitment, data collection and analysis. A qualitative approach was adopted and involved semi-structured interviews with five individuals with Down syndrome and a CHC. The interview covered topics including in the impact of Down syndrome, the impact of a CHC, and involvement in healthcare decisions. Three themes resulted from a thematic analysis: Who is the Patient; Self-Care, Care from Others and Gaps in Care and Health and Fitness. The major implications of this research for people with Down syndrome, their families and healthcare professionals include the need for clarity regarding supported decision making and supporting those with Down syndrome who may not have family members to aid decisions. This research involved a small relatively homogenous group of individuals and the area could benefit from further research, for example those without parent carers to support healthcare decisions and medical procedures. The research highlighted difficulties inherent to carrying out research with vulnerable groups, such as those with a learning disability. Future research should consider the process of including vulnerable groups in research, such as how to balance the research agendas of the researchers and the researched.
author Reilly, Deirdre Emer
author_facet Reilly, Deirdre Emer
author_sort Reilly, Deirdre Emer
title What do people with Down Syndrome want from their cardiac team?
title_short What do people with Down Syndrome want from their cardiac team?
title_full What do people with Down Syndrome want from their cardiac team?
title_fullStr What do people with Down Syndrome want from their cardiac team?
title_full_unstemmed What do people with Down Syndrome want from their cardiac team?
title_sort what do people with down syndrome want from their cardiac team?
publisher University of East London
publishDate 2012
url https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.559447
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