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Implementation of personalised medicine policies in mental healthcare: results from a stated preference study in the UK.
McMichael, Alan J; Kane, Joseph P M; Rolison, Jonathan J; O'Neill, Francis A; Boeri, Marco; Kee, Frank.
Affiliation
  • McMichael AJ; PhD, Health & Social Care Public Health Agency, Belfast, UK.
  • Kane JPM; PhD, Centre for Public Health, Queen's University Belfast, Belfast, UK.
  • Rolison JJ; PhD, Department of Psychology, University of Essex, Essex, UK.
  • O'Neill FA; MD, Centre for Public Health, Queen's University Belfast, Belfast, UK.
  • Boeri M; PhD, Health Preference Assessment, RTI Health Solutions, and School of Medicine, Dentistry and Biomedical Sciences, Queen's University Belfast, Belfast, UK.
  • Kee F; MD, Centre for Public Health, and UKCRC Centre of Excellence for Public Health Research (NI), Queen's University Belfast, Belfast, UK.
BJPsych Open ; 8(2): e40, 2022 Feb 03.
Article in En | MEDLINE | ID: mdl-35109949
ABSTRACT

BACKGROUND:

Public support for the implementation of personalised medicine policies (PMPs) within routine care is important owing to the high financial costs involved and the potential for redirection of resources from other services.

AIMS:

We aimed to determine the attributes of a PMP most likely to elicit public support for implementation. We also aimed to determine whether such support differed between a depression PMP and one for cystic fibrosis.

METHOD:

In a discrete-choice experiment, paired vignettes illustrating both the current model of care (CMoC) and a hypothetical PMP for either depression or cystic fibrosis were presented to a representative sample of the UK public (n = 2804). Each vignette integrated varying attributes, including anticipated therapeutic benefit over CMoC, and the annual cost to the taxpayer. Respondents were invited to express their preference for either the PMP or CMoC within each pair.

RESULTS:

The financial cost was the most important attribute influencing public support for PMPs. Respondents favoured PMP implementation where it benefited a higher proportion of patients or was anticipated to be more effective than CMoC. A reduction in services for non-eligible patients reduced the likelihood of support for PMPs. Respondents were more willing to fund PMPs for cystic fibrosis than for depression.

CONCLUSIONS:

Cost is a significant factor in the public's support for PMPs, but essential caveats, such as protection for services available to PMP-ineligible patients, may also apply. Further research should explore the factors contributing to condition-specific nuances in public support for PMPs.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Aspects: Implementation_research / Patient_preference Language: En Journal: BJPsych Open Year: 2022 Document type: Article Affiliation country: Reino Unido Country of publication: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Aspects: Implementation_research / Patient_preference Language: En Journal: BJPsych Open Year: 2022 Document type: Article Affiliation country: Reino Unido Country of publication: ENGLAND / ESCOCIA / GB / GREAT BRITAIN / INGLATERRA / REINO UNIDO / SCOTLAND / UK / UNITED KINGDOM