Eliciting parental preferences and values for the return of additional findings from genomic sequencing
- Author(s)
- Goranitis, I; Meng, Y; Martyn, M; Best, S; Bouffler, S; Bombard, Y; Gaff, C; Stark, Z;
- Details
- Publication Year 2024-02-14,Volume 9,Issue #1,Page 10
- Journal Title
- NPJ Genomic Medicine
- Publication Type
- Research article
- Abstract
- Health economic evidence is needed to inform the design of high-value and cost-effective processes for returning genomic results from analyses for additional findings (AF). This study reports the results of a discrete-choice experiment designed to elicit preferences for the process of returning AF results from the perspective of parents of children with rare conditions and to estimate the value placed on AF analysis. Overall, 94 parents recruited within the Australian Genomics and Melbourne Genomics programmes participated in the survey, providing preferences in a total of 1128 choice scenarios. Statistically significant preferences were identified for the opportunity to change the choices made about AF; receiving positive AF in person from a genetic counsellor; timely access to a medical specialist and high-quality online resources; receiving automatic updates through a secure online portal if new information becomes available; and lower costs. For AF uptake rates ranging between 50-95%, the mean per person value from AF analysis was estimated at AU$450-$1700 (US$300-$1140). The findings enable the design of a value-maximising process of analysis for AF in rare-disease genomic sequencing.
- Publisher
- Springer Nature
- Department(s)
- Health Services Research
- Publisher's Version
- https://doi.org/10.1038/s41525-024-00399-8
- Open Access at Publisher's Site
https://doi.org/10.1038/s41525-024-00399-8- Terms of Use/Rights Notice
- Refer to copyright notice on published article.
Creation Date: 2024-03-07 04:47:23
Last Modified: 2024-03-07 05:19:51