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Exploring patient and family involvement in the lifecycle of an orphan drug: a scoping review
BACKGROUND: Patients and their families have become more active in healthcare systems and research. The value of patient involvement is particularly relevant in the area of rare diseases, where patients face delayed diagnoses and limited access to effective therapies due to the high level of uncerta...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741909/ https://www.ncbi.nlm.nih.gov/pubmed/29273068 http://dx.doi.org/10.1186/s13023-017-0738-6 |
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author | Young, Andrea Menon, Devidas Street, Jackie Al-Hertani, Walla Stafinski, Tania |
author_facet | Young, Andrea Menon, Devidas Street, Jackie Al-Hertani, Walla Stafinski, Tania |
author_sort | Young, Andrea |
collection | PubMed |
description | BACKGROUND: Patients and their families have become more active in healthcare systems and research. The value of patient involvement is particularly relevant in the area of rare diseases, where patients face delayed diagnoses and limited access to effective therapies due to the high level of uncertainty in market approval and reimbursement decisions. It has been suggested that patient involvement may help to reduce some of these uncertainties. This review explored existing and proposed roles for patients, families, and patient organizations at each stage of the lifecycle of therapies for rare diseases (i.e., orphan drug lifecycle). METHODS: A scoping review was conducted using methods outlined by Arksey and O’Malley. To validate the findings from the literature and identify any additional opportunities that were missed, a consultative webinar was conducted with members of the Patient and Caregiver Liaison Group of a Canadian research network. RESULTS: Existing and proposed opportunities for involving patients, families, and patient organizations were reported throughout the orphan drug lifecycle and fell into 12 themes: research outside of clinical trials; clinical trials; patient reported outcomes measures; patient registries and biorepositories; education; advocacy and awareness; conferences and workshops; patient care and support; patient organization development; regulatory decision-making; and reimbursement decision-making. Existing opportunities were not described in sufficient detail to allow for the level of involvement to be assessed. Additionally, no information on the impact of involvement within specific opportunities was found. Based on feedback from patients and families, documentation of existing opportunities within Canada is poor. CONCLUSIONS: Opportunities for patient, family, and patient organization involvement exist throughout the orphan drug lifecycle. However, based on the information found, it is not possible to determine which opportunities would be most effective at each stage. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-017-0738-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5741909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-57419092018-01-03 Exploring patient and family involvement in the lifecycle of an orphan drug: a scoping review Young, Andrea Menon, Devidas Street, Jackie Al-Hertani, Walla Stafinski, Tania Orphanet J Rare Dis Review BACKGROUND: Patients and their families have become more active in healthcare systems and research. The value of patient involvement is particularly relevant in the area of rare diseases, where patients face delayed diagnoses and limited access to effective therapies due to the high level of uncertainty in market approval and reimbursement decisions. It has been suggested that patient involvement may help to reduce some of these uncertainties. This review explored existing and proposed roles for patients, families, and patient organizations at each stage of the lifecycle of therapies for rare diseases (i.e., orphan drug lifecycle). METHODS: A scoping review was conducted using methods outlined by Arksey and O’Malley. To validate the findings from the literature and identify any additional opportunities that were missed, a consultative webinar was conducted with members of the Patient and Caregiver Liaison Group of a Canadian research network. RESULTS: Existing and proposed opportunities for involving patients, families, and patient organizations were reported throughout the orphan drug lifecycle and fell into 12 themes: research outside of clinical trials; clinical trials; patient reported outcomes measures; patient registries and biorepositories; education; advocacy and awareness; conferences and workshops; patient care and support; patient organization development; regulatory decision-making; and reimbursement decision-making. Existing opportunities were not described in sufficient detail to allow for the level of involvement to be assessed. Additionally, no information on the impact of involvement within specific opportunities was found. Based on feedback from patients and families, documentation of existing opportunities within Canada is poor. CONCLUSIONS: Opportunities for patient, family, and patient organization involvement exist throughout the orphan drug lifecycle. However, based on the information found, it is not possible to determine which opportunities would be most effective at each stage. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13023-017-0738-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-22 /pmc/articles/PMC5741909/ /pubmed/29273068 http://dx.doi.org/10.1186/s13023-017-0738-6 Text en © The Author(s). 2017 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Young, Andrea Menon, Devidas Street, Jackie Al-Hertani, Walla Stafinski, Tania Exploring patient and family involvement in the lifecycle of an orphan drug: a scoping review |
title | Exploring patient and family involvement in the lifecycle of an orphan drug: a scoping review |
title_full | Exploring patient and family involvement in the lifecycle of an orphan drug: a scoping review |
title_fullStr | Exploring patient and family involvement in the lifecycle of an orphan drug: a scoping review |
title_full_unstemmed | Exploring patient and family involvement in the lifecycle of an orphan drug: a scoping review |
title_short | Exploring patient and family involvement in the lifecycle of an orphan drug: a scoping review |
title_sort | exploring patient and family involvement in the lifecycle of an orphan drug: a scoping review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5741909/ https://www.ncbi.nlm.nih.gov/pubmed/29273068 http://dx.doi.org/10.1186/s13023-017-0738-6 |
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