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Improving follow up after predictive testing in Huntington’s disease: evaluating a genetic counselling narrative group session

Recently updated Huntington’s disease (HD) predictive testing guidelines emphasise clinicians’ responsibility to facilitate emotional support following testing, regardless of the result. Yet models of post-test counselling support are poorly defined. Moreover, it is unclear how these might be best d...

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Autores principales: Stopford, Cheryl, Ferrer-Duch, Mariangels, Moldovan, Ramona, MacLeod, Rhona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962407/
https://www.ncbi.nlm.nih.gov/pubmed/31001731
http://dx.doi.org/10.1007/s12687-019-00416-9
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author Stopford, Cheryl
Ferrer-Duch, Mariangels
Moldovan, Ramona
MacLeod, Rhona
author_facet Stopford, Cheryl
Ferrer-Duch, Mariangels
Moldovan, Ramona
MacLeod, Rhona
author_sort Stopford, Cheryl
collection PubMed
description Recently updated Huntington’s disease (HD) predictive testing guidelines emphasise clinicians’ responsibility to facilitate emotional support following testing, regardless of the result. Yet models of post-test counselling support are poorly defined. Moreover, it is unclear how these might be best delivered. In this project, a genetic counsellor and clinical psychologist developed standalone group sessions using collective narrative practices for individuals post-predictive testing. Here we present an evaluation of the experiences of one group of six people who have tested mutation positive for HD and remain pre-symptomatic. Two partners also attended the session. Observations, evaluation forms and telephone interviews were used in data collection. Interview data was available from five mutation-positive individuals and one partner. Qualitative data were analysed using a thematic framework approach. Responses were overwhelmingly positive, emphasising the importance of a specifically arranged time and space to share experiences in a structured way. This was typically the first time participants had spoken openly with someone in their situation. Narrative facilitation of discussion encouraged participants to re-discover their strengths and resiliences, with similar experiences being discovered through connections with others. The evaluation was successful in implementing group narrative interventions as part of the predictive test counselling support for Huntington’s disease. Participants suggested that the approach could be extended and adopted for other genetic conditions.
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spelling pubmed-69624072020-01-30 Improving follow up after predictive testing in Huntington’s disease: evaluating a genetic counselling narrative group session Stopford, Cheryl Ferrer-Duch, Mariangels Moldovan, Ramona MacLeod, Rhona J Community Genet Original Article Recently updated Huntington’s disease (HD) predictive testing guidelines emphasise clinicians’ responsibility to facilitate emotional support following testing, regardless of the result. Yet models of post-test counselling support are poorly defined. Moreover, it is unclear how these might be best delivered. In this project, a genetic counsellor and clinical psychologist developed standalone group sessions using collective narrative practices for individuals post-predictive testing. Here we present an evaluation of the experiences of one group of six people who have tested mutation positive for HD and remain pre-symptomatic. Two partners also attended the session. Observations, evaluation forms and telephone interviews were used in data collection. Interview data was available from five mutation-positive individuals and one partner. Qualitative data were analysed using a thematic framework approach. Responses were overwhelmingly positive, emphasising the importance of a specifically arranged time and space to share experiences in a structured way. This was typically the first time participants had spoken openly with someone in their situation. Narrative facilitation of discussion encouraged participants to re-discover their strengths and resiliences, with similar experiences being discovered through connections with others. The evaluation was successful in implementing group narrative interventions as part of the predictive test counselling support for Huntington’s disease. Participants suggested that the approach could be extended and adopted for other genetic conditions. Springer Berlin Heidelberg 2019-04-18 2020-01 /pmc/articles/PMC6962407/ /pubmed/31001731 http://dx.doi.org/10.1007/s12687-019-00416-9 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Stopford, Cheryl
Ferrer-Duch, Mariangels
Moldovan, Ramona
MacLeod, Rhona
Improving follow up after predictive testing in Huntington’s disease: evaluating a genetic counselling narrative group session
title Improving follow up after predictive testing in Huntington’s disease: evaluating a genetic counselling narrative group session
title_full Improving follow up after predictive testing in Huntington’s disease: evaluating a genetic counselling narrative group session
title_fullStr Improving follow up after predictive testing in Huntington’s disease: evaluating a genetic counselling narrative group session
title_full_unstemmed Improving follow up after predictive testing in Huntington’s disease: evaluating a genetic counselling narrative group session
title_short Improving follow up after predictive testing in Huntington’s disease: evaluating a genetic counselling narrative group session
title_sort improving follow up after predictive testing in huntington’s disease: evaluating a genetic counselling narrative group session
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6962407/
https://www.ncbi.nlm.nih.gov/pubmed/31001731
http://dx.doi.org/10.1007/s12687-019-00416-9
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