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Exploring patient and family involvement in the lifecycle of an orphan drug: a scoping review
- Source :
- Orphanet Journal of Rare Diseases, Orphanet Journal of Rare Diseases, Vol 12, Iss 1, Pp 1-14 (2017)
- Publication Year :
- 2017
- Publisher :
- BioMed Central, 2017.
-
Abstract
- 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.
- Subjects :
- medicine.medical_specialty
Scoping review
Family involvement
Orphan Drug Production
Decision Making
lcsh:Medicine
Review
Orphan drug
03 medical and health sciences
0302 clinical medicine
Documentation
Rare Diseases
medicine
Orphan drugs
Humans
Pharmacology (medical)
030212 general & internal medicine
Medical diagnosis
Patient involvement
Genetics (clinical)
Reimbursement
business.industry
lcsh:R
General Medicine
Patient organization
3. Good health
Clinical trial
Family medicine
business
Delivery of Health Care
030217 neurology & neurosurgery
Subjects
Details
- Language :
- English
- ISSN :
- 17501172
- Volume :
- 12
- Database :
- OpenAIRE
- Journal :
- Orphanet Journal of Rare Diseases
- Accession number :
- edsair.doi.dedup.....94748cd9b56ece1edc96f70a5166019f