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Achieving consensus on priority items for paediatric palliative care outcome measurement: Results from a modified Delphi survey, engagement with a children’s research involvement group and expert item generation

BACKGROUND: There is no validated outcome measure for use in children’s palliative care outside sub-Saharan Africa. Stakeholders must be involved in the development of such measures to ensure face and content validity. AIM: To gain expert stakeholder consensus on items for inclusion in a paediatric...

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Autores principales: Coombes, Lucy, Harðardóttir, Daney, Braybrook, Debbie, Scott, Hannah May, Bristowe, Katherine, Ellis-Smith, Clare, Fraser, Lorna K, Downing, Julia, Bluebond-Langner, Myra, Murtagh, Fliss EM, Harding, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657511/
https://www.ncbi.nlm.nih.gov/pubmed/37853579
http://dx.doi.org/10.1177/02692163231205126
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author Coombes, Lucy
Harðardóttir, Daney
Braybrook, Debbie
Scott, Hannah May
Bristowe, Katherine
Ellis-Smith, Clare
Fraser, Lorna K
Downing, Julia
Bluebond-Langner, Myra
Murtagh, Fliss EM
Harding, Richard
author_facet Coombes, Lucy
Harðardóttir, Daney
Braybrook, Debbie
Scott, Hannah May
Bristowe, Katherine
Ellis-Smith, Clare
Fraser, Lorna K
Downing, Julia
Bluebond-Langner, Myra
Murtagh, Fliss EM
Harding, Richard
author_sort Coombes, Lucy
collection PubMed
description BACKGROUND: There is no validated outcome measure for use in children’s palliative care outside sub-Saharan Africa. Stakeholders must be involved in the development of such measures to ensure face and content validity. AIM: To gain expert stakeholder consensus on items for inclusion in a paediatric palliative care outcome measure to establish face and content validity. DESIGN: This study was conducted in two phases following Rothrock and COSMIN guidance on patient-reported outcome measure development. Phase 1: Three-round modified Delphi survey to establish consensus on priority items. Phase 2: Item generation meeting with key stakeholders to develop initial measure versions. A young person’s advisory group was also consulted on priority outcomes. SETTING AND PARTICIPANTS: Delphi survey: Parents and professionals with experience of caring for a child with a life-limiting condition. Young person’s advisory group: young people age 10–20 years. Item generation meeting: bereaved parents, academics and clinicians. RESULTS: Phase 1: Delphi survey (n = 82). Agreement increased from Kendall’s W = 0.17 to W = 0.61, indicating movement towards consensus. Agreement between professional and parent ranking was poor (Cohen’s kappa 0.13). Professionals prioritised physical symptoms, whereas parents prioritised psychosocial and practical concerns. Advisory group: Children (n = 22) prioritised items related to living a ‘normal life’ in addition to items prioritised by adult participants. Phase 2: Five age/developmental stage appropriate child and proxy-reported versions of C-POS, containing 13 items, were drafted. CONCLUSIONS: This study highlights the importance and feasibility of involving key stakeholders in PROM item generation, as important differences were found in the priority outcomes identified by children, parents and professionals.
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spelling pubmed-106575112023-11-19 Achieving consensus on priority items for paediatric palliative care outcome measurement: Results from a modified Delphi survey, engagement with a children’s research involvement group and expert item generation Coombes, Lucy Harðardóttir, Daney Braybrook, Debbie Scott, Hannah May Bristowe, Katherine Ellis-Smith, Clare Fraser, Lorna K Downing, Julia Bluebond-Langner, Myra Murtagh, Fliss EM Harding, Richard Palliat Med Original Articles BACKGROUND: There is no validated outcome measure for use in children’s palliative care outside sub-Saharan Africa. Stakeholders must be involved in the development of such measures to ensure face and content validity. AIM: To gain expert stakeholder consensus on items for inclusion in a paediatric palliative care outcome measure to establish face and content validity. DESIGN: This study was conducted in two phases following Rothrock and COSMIN guidance on patient-reported outcome measure development. Phase 1: Three-round modified Delphi survey to establish consensus on priority items. Phase 2: Item generation meeting with key stakeholders to develop initial measure versions. A young person’s advisory group was also consulted on priority outcomes. SETTING AND PARTICIPANTS: Delphi survey: Parents and professionals with experience of caring for a child with a life-limiting condition. Young person’s advisory group: young people age 10–20 years. Item generation meeting: bereaved parents, academics and clinicians. RESULTS: Phase 1: Delphi survey (n = 82). Agreement increased from Kendall’s W = 0.17 to W = 0.61, indicating movement towards consensus. Agreement between professional and parent ranking was poor (Cohen’s kappa 0.13). Professionals prioritised physical symptoms, whereas parents prioritised psychosocial and practical concerns. Advisory group: Children (n = 22) prioritised items related to living a ‘normal life’ in addition to items prioritised by adult participants. Phase 2: Five age/developmental stage appropriate child and proxy-reported versions of C-POS, containing 13 items, were drafted. CONCLUSIONS: This study highlights the importance and feasibility of involving key stakeholders in PROM item generation, as important differences were found in the priority outcomes identified by children, parents and professionals. SAGE Publications 2023-10-18 2023-12 /pmc/articles/PMC10657511/ /pubmed/37853579 http://dx.doi.org/10.1177/02692163231205126 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Coombes, Lucy
Harðardóttir, Daney
Braybrook, Debbie
Scott, Hannah May
Bristowe, Katherine
Ellis-Smith, Clare
Fraser, Lorna K
Downing, Julia
Bluebond-Langner, Myra
Murtagh, Fliss EM
Harding, Richard
Achieving consensus on priority items for paediatric palliative care outcome measurement: Results from a modified Delphi survey, engagement with a children’s research involvement group and expert item generation
title Achieving consensus on priority items for paediatric palliative care outcome measurement: Results from a modified Delphi survey, engagement with a children’s research involvement group and expert item generation
title_full Achieving consensus on priority items for paediatric palliative care outcome measurement: Results from a modified Delphi survey, engagement with a children’s research involvement group and expert item generation
title_fullStr Achieving consensus on priority items for paediatric palliative care outcome measurement: Results from a modified Delphi survey, engagement with a children’s research involvement group and expert item generation
title_full_unstemmed Achieving consensus on priority items for paediatric palliative care outcome measurement: Results from a modified Delphi survey, engagement with a children’s research involvement group and expert item generation
title_short Achieving consensus on priority items for paediatric palliative care outcome measurement: Results from a modified Delphi survey, engagement with a children’s research involvement group and expert item generation
title_sort achieving consensus on priority items for paediatric palliative care outcome measurement: results from a modified delphi survey, engagement with a children’s research involvement group and expert item generation
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657511/
https://www.ncbi.nlm.nih.gov/pubmed/37853579
http://dx.doi.org/10.1177/02692163231205126
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