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Personalised colorectal cancer screening strategies: Information needs of the target population

Prior faecal Hemoglobin (f-Hb) concentrations of a negative fecal immunochemical test (FIT) can be used for risk stratification in colorectal cancer (CRC) screening. Individuals with higher f-Hb concentrations may benefit from a shorter screening interval (1 year), whereas individuals with undetecta...

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Autores principales: Toes-Zoutendijk, Esther, de Jonge, Lucie, Breekveldt, Emilie C.H., Korfage, Ida J., Usher-Smith, Juliet A., Lansdorp-Vogelaar, Iris, Dennison, Rebecca A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433032/
https://www.ncbi.nlm.nih.gov/pubmed/37601828
http://dx.doi.org/10.1016/j.pmedr.2023.102325
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author Toes-Zoutendijk, Esther
de Jonge, Lucie
Breekveldt, Emilie C.H.
Korfage, Ida J.
Usher-Smith, Juliet A.
Lansdorp-Vogelaar, Iris
Dennison, Rebecca A.
author_facet Toes-Zoutendijk, Esther
de Jonge, Lucie
Breekveldt, Emilie C.H.
Korfage, Ida J.
Usher-Smith, Juliet A.
Lansdorp-Vogelaar, Iris
Dennison, Rebecca A.
author_sort Toes-Zoutendijk, Esther
collection PubMed
description Prior faecal Hemoglobin (f-Hb) concentrations of a negative fecal immunochemical test (FIT) can be used for risk stratification in colorectal cancer (CRC) screening. Individuals with higher f-Hb concentrations may benefit from a shorter screening interval (1 year), whereas individuals with undetectable f-Hb concentrations could benefit from a longer screening interval (3 year). Individuals’ views on personalised CRC screening and information needed to make a well-informed decision is unknown. We conducted three semi-structured focus groups among individuals eligible for CRC screening (i.e. men and women aged 55 to 75) in the Netherlands. Thematic analysis was used to analyse participants’ information need on personalised CRC screening strategies. Fourteen individuals took part. The majority were positive about CRC screening and indicated that they would participate in personalised CRC screening. The rationale for a longer interval among those at lowest risk was, however, unclear for many. The preferred information on individual risk was variable: ranging from full information to only information on the personalised strategy without mentioning the risk. It was not possible to address everyone’s need with a single approach. Additional communications, e.g. public media campaigns, billboards, videos on social media, were also suggested as necessary. This study showed that preferences on receiving information on individual CRC risk varied substantially and no consensus was reached. Introducing a personalised screening programme will require careful communication, particularly around the rationale for the strategy, and a layered approach to deliver information.
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spelling pubmed-104330322023-08-18 Personalised colorectal cancer screening strategies: Information needs of the target population Toes-Zoutendijk, Esther de Jonge, Lucie Breekveldt, Emilie C.H. Korfage, Ida J. Usher-Smith, Juliet A. Lansdorp-Vogelaar, Iris Dennison, Rebecca A. Prev Med Rep Regular Article Prior faecal Hemoglobin (f-Hb) concentrations of a negative fecal immunochemical test (FIT) can be used for risk stratification in colorectal cancer (CRC) screening. Individuals with higher f-Hb concentrations may benefit from a shorter screening interval (1 year), whereas individuals with undetectable f-Hb concentrations could benefit from a longer screening interval (3 year). Individuals’ views on personalised CRC screening and information needed to make a well-informed decision is unknown. We conducted three semi-structured focus groups among individuals eligible for CRC screening (i.e. men and women aged 55 to 75) in the Netherlands. Thematic analysis was used to analyse participants’ information need on personalised CRC screening strategies. Fourteen individuals took part. The majority were positive about CRC screening and indicated that they would participate in personalised CRC screening. The rationale for a longer interval among those at lowest risk was, however, unclear for many. The preferred information on individual risk was variable: ranging from full information to only information on the personalised strategy without mentioning the risk. It was not possible to address everyone’s need with a single approach. Additional communications, e.g. public media campaigns, billboards, videos on social media, were also suggested as necessary. This study showed that preferences on receiving information on individual CRC risk varied substantially and no consensus was reached. Introducing a personalised screening programme will require careful communication, particularly around the rationale for the strategy, and a layered approach to deliver information. 2023-07-16 /pmc/articles/PMC10433032/ /pubmed/37601828 http://dx.doi.org/10.1016/j.pmedr.2023.102325 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular Article
Toes-Zoutendijk, Esther
de Jonge, Lucie
Breekveldt, Emilie C.H.
Korfage, Ida J.
Usher-Smith, Juliet A.
Lansdorp-Vogelaar, Iris
Dennison, Rebecca A.
Personalised colorectal cancer screening strategies: Information needs of the target population
title Personalised colorectal cancer screening strategies: Information needs of the target population
title_full Personalised colorectal cancer screening strategies: Information needs of the target population
title_fullStr Personalised colorectal cancer screening strategies: Information needs of the target population
title_full_unstemmed Personalised colorectal cancer screening strategies: Information needs of the target population
title_short Personalised colorectal cancer screening strategies: Information needs of the target population
title_sort personalised colorectal cancer screening strategies: information needs of the target population
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10433032/
https://www.ncbi.nlm.nih.gov/pubmed/37601828
http://dx.doi.org/10.1016/j.pmedr.2023.102325
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