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Optimizing language for effective communication of gene therapy concepts with hemophilia patients: a qualitative study

BACKGROUND: For communities of people living with hemophilia and other genetic conditions, gene therapy could represent a paradigm shift in treatment strategies. As investigational therapeutic modalities such as gene therapy become more widely used and discussed, there is a critical need for all sta...

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Autores principales: Hart, Daniel P., Branchford, Brian R., Hendry, Sarah, Ledniczky, Robert, Sidonio, Robert F., Négrier, Claude, Kim, Michelle, Rice, Michelle, Minshall, Matthew, Arcé, Claire, Prince, Steve, Kelleher, Maria, Lee, Sharon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8082836/
https://www.ncbi.nlm.nih.gov/pubmed/33910590
http://dx.doi.org/10.1186/s13023-020-01555-w
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author Hart, Daniel P.
Branchford, Brian R.
Hendry, Sarah
Ledniczky, Robert
Sidonio, Robert F.
Négrier, Claude
Kim, Michelle
Rice, Michelle
Minshall, Matthew
Arcé, Claire
Prince, Steve
Kelleher, Maria
Lee, Sharon
author_facet Hart, Daniel P.
Branchford, Brian R.
Hendry, Sarah
Ledniczky, Robert
Sidonio, Robert F.
Négrier, Claude
Kim, Michelle
Rice, Michelle
Minshall, Matthew
Arcé, Claire
Prince, Steve
Kelleher, Maria
Lee, Sharon
author_sort Hart, Daniel P.
collection PubMed
description BACKGROUND: For communities of people living with hemophilia and other genetic conditions, gene therapy could represent a paradigm shift in treatment strategies. As investigational therapeutic modalities such as gene therapy become more widely used and discussed, there is a critical need for all stakeholders to communicate using a lexicon that is intelligible, accurate, consistent, and representative of novel treatments. In doing so, expectations can be more carefully managed and potential risks, benefits, and limitations better understood. In recognition of this need, a first-ever study of gene therapy lexicon was conducted using established methods of market research and linguistic analysis. METHODS: Ninety-four participants representing hematologists, nurses, caregivers, and people with hemophilia A, in six countries (US, UK, Spain, Germany, France, Italy) took part in a series of in-depth interviews, face-to-face focus groups, an advisory board meeting, and online group interviews to develop, refine, and test verbal, written, and pictorial language concepts through a three-phase iterative process. Sessions were conducted in local languages using detailed discussion guides. Feedback from participants was captured using real-time instant-response dial testing to measure moment-by-moment emotional responses to language stimuli. Semiquantitative analysis of the responses informed selection of preferred language concepts for final testing, and qualitative discussion explored preference rationale. Participants also completed polling and forced rank and choice written exercises. RESULTS: Study feedback showed that the hemophilia community has preferences around consistent lexicon to describe hemophilia and its management. Expert linguistic analysis of feedback from the three phases enabled agreement of a consensus lexicon of vocabulary and an optimized summary narrative for talking about gene therapy amongst people affected by hemophilia A. Preferences were largely consistent across audiences and countries, although some country-specific recommendations were made. A representative summary phrase was agreed: “Gene therapy is being studied in clinical trials with the aim to allow the body to produce factor VIII protein on its own”. CONCLUSIONS: The use of preferred language across different stakeholders increases understanding and comfort during discussions of novel and complex therapeutic modalities such as gene therapy. Consistent use of community-informed lexicon minimizes miscommunication and facilitates informed decision-making regarding potential future treatment opportunities.
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spelling pubmed-80828362021-04-29 Optimizing language for effective communication of gene therapy concepts with hemophilia patients: a qualitative study Hart, Daniel P. Branchford, Brian R. Hendry, Sarah Ledniczky, Robert Sidonio, Robert F. Négrier, Claude Kim, Michelle Rice, Michelle Minshall, Matthew Arcé, Claire Prince, Steve Kelleher, Maria Lee, Sharon Orphanet J Rare Dis Research BACKGROUND: For communities of people living with hemophilia and other genetic conditions, gene therapy could represent a paradigm shift in treatment strategies. As investigational therapeutic modalities such as gene therapy become more widely used and discussed, there is a critical need for all stakeholders to communicate using a lexicon that is intelligible, accurate, consistent, and representative of novel treatments. In doing so, expectations can be more carefully managed and potential risks, benefits, and limitations better understood. In recognition of this need, a first-ever study of gene therapy lexicon was conducted using established methods of market research and linguistic analysis. METHODS: Ninety-four participants representing hematologists, nurses, caregivers, and people with hemophilia A, in six countries (US, UK, Spain, Germany, France, Italy) took part in a series of in-depth interviews, face-to-face focus groups, an advisory board meeting, and online group interviews to develop, refine, and test verbal, written, and pictorial language concepts through a three-phase iterative process. Sessions were conducted in local languages using detailed discussion guides. Feedback from participants was captured using real-time instant-response dial testing to measure moment-by-moment emotional responses to language stimuli. Semiquantitative analysis of the responses informed selection of preferred language concepts for final testing, and qualitative discussion explored preference rationale. Participants also completed polling and forced rank and choice written exercises. RESULTS: Study feedback showed that the hemophilia community has preferences around consistent lexicon to describe hemophilia and its management. Expert linguistic analysis of feedback from the three phases enabled agreement of a consensus lexicon of vocabulary and an optimized summary narrative for talking about gene therapy amongst people affected by hemophilia A. Preferences were largely consistent across audiences and countries, although some country-specific recommendations were made. A representative summary phrase was agreed: “Gene therapy is being studied in clinical trials with the aim to allow the body to produce factor VIII protein on its own”. CONCLUSIONS: The use of preferred language across different stakeholders increases understanding and comfort during discussions of novel and complex therapeutic modalities such as gene therapy. Consistent use of community-informed lexicon minimizes miscommunication and facilitates informed decision-making regarding potential future treatment opportunities. BioMed Central 2021-04-28 /pmc/articles/PMC8082836/ /pubmed/33910590 http://dx.doi.org/10.1186/s13023-020-01555-w Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Hart, Daniel P.
Branchford, Brian R.
Hendry, Sarah
Ledniczky, Robert
Sidonio, Robert F.
Négrier, Claude
Kim, Michelle
Rice, Michelle
Minshall, Matthew
Arcé, Claire
Prince, Steve
Kelleher, Maria
Lee, Sharon
Optimizing language for effective communication of gene therapy concepts with hemophilia patients: a qualitative study
title Optimizing language for effective communication of gene therapy concepts with hemophilia patients: a qualitative study
title_full Optimizing language for effective communication of gene therapy concepts with hemophilia patients: a qualitative study
title_fullStr Optimizing language for effective communication of gene therapy concepts with hemophilia patients: a qualitative study
title_full_unstemmed Optimizing language for effective communication of gene therapy concepts with hemophilia patients: a qualitative study
title_short Optimizing language for effective communication of gene therapy concepts with hemophilia patients: a qualitative study
title_sort optimizing language for effective communication of gene therapy concepts with hemophilia patients: a qualitative study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8082836/
https://www.ncbi.nlm.nih.gov/pubmed/33910590
http://dx.doi.org/10.1186/s13023-020-01555-w
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