Carer preferences of route of administration of transmucosal diamorphine and willingness to take part in a randomised controlled trial: an interview study (DIPPER).
Authors
Boyce, Katherine
Mitchell, Lorraine
Johnson, Margaret
Akinyooye, Victoria
Publication Date
2022-05-17Journal Title
BMC Palliat Care
ISSN
1472-684X
Publisher
Springer Science and Business Media LLC
Volume
21
Issue
1
Language
en
Type
Article
This Version
VoR
Metadata
Show full item recordCitation
Jamieson, L., Harrop, E., Liossi, C., Boyce, K., Mitchell, L., Johnson, M., Jani, Y., et al. (2022). Carer preferences of route of administration of transmucosal diamorphine and willingness to take part in a randomised controlled trial: an interview study (DIPPER).. BMC Palliat Care, 21 (1) https://doi.org/10.1186/s12904-022-00951-2
Abstract
BACKGROUND: Children and young people are usually given liquid morphine by mouth for breakthrough pain, which can take thirty minutes to work. A faster-acting, quickly absorbed, needle-free pain medicine, that is easy to administer is needed such as transmucosal (sublingual, buccal, intranasal) diamorphine. Research evidence relating to the administration of medication for breakthrough pain in children and young people is limited. This study aims to describe the experiences and preferences of parents and/or children and young people regarding the route of administration of diamorphine, barriers and facilitators comparative to oral morphine, and participation in a randomised controlled trial. METHODS: In-depth, semi-structured interviews with parents and/or children and young people at home or hospital/hospice. RESULTS: Thirteen interviews with: nine mothers, one father, and three sets of parents jointly. No interviews took place with a child/young person. Most families had experience of the buccal route which was effective in ease of administration and time to control pain. The intranasal route was preferred by parents irrespective of experience. Parents' willingness for their child to take part in a trial depended on the time commitment, their child's pain trajectory and the stability of analgesic requirements. CONCLUSION: A randomised controlled trial of oral morphine versus transmucosal diamorphine would need to consider trial logistics, especially time commitment. Parents felt that the trial should be introduced initially by the clinical team, with written information from the research team, and sufficient time to ask questions. Patients who had discontinued oral morphine because of side effects, or those with gastrointestinal failure, should be excluded. Maintaining stability in pain management was essential to families, so the timing of the trial is a potential issue.
Keywords
Research, Paediatrics, Palliative care, Terminal care, Opioids, Diamorphine, Breakthrough pain, Pain management
Sponsorship
Research for Patient Benefit Programme (PB-PG-0317-20036, PB-PG-0317-20036, PB-PG-0317-20036, PB-PG-0317-20036, PB-PG-0317-20036, PB-PG-0317-20036, PB-PG-0317-20036, PB-PG-0317-20036, PB-PG-0317-20036, PB-PG-0317-20036, PB-PG-0317-20036)
Identifiers
s12904-022-00951-2, 951
External DOI: https://doi.org/10.1186/s12904-022-00951-2
This record's URL: https://www.repository.cam.ac.uk/handle/1810/337240
Rights
Licence:
http://creativecommons.org/licenses/by/4.0/
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