On the determinants and the role of the payers in the uptake of genetic testing and data sharing in personalized health
Détails
Télécharger: fpubh-11-920286.pdf (916.47 [Ko])
Etat: Public
Version: de l'auteur⸱e
Licence: CC BY 4.0
Etat: Public
Version: de l'auteur⸱e
Licence: CC BY 4.0
ID Serval
serval:BIB_B2F74082561D
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
On the determinants and the role of the payers in the uptake of genetic testing and data sharing in personalized health
Périodique
Frontiers in Public Health - Health Economics
Statut éditorial
Publié
Date de publication
2023
Peer-reviewed
Oui
Volume
11
Pages
920286
Langue
anglais
Résumé
BACKGROUND
New health technologies and data offer tailored prevention and spot-on treatments, which can considerably reduce healthcare costs. In healthy individuals, insurers can participate in the creation of health capital through data and preventing the occurrence of a disease. In the onset of a disease, sequencing an individual's genome can provide information leading to the use of more efficient treatments. Both improvements are at the core of the ``personalized health'' paradigm. As a positive side-effect, a reduction in health care costs is expected. However, the integration of personalized health in insurance schemes starts with a closer understanding of the demand drivers. \newline
METHODS
Using novel data from a survey carried out in Switzerland, we determine the factors influencing the uptake and sharing of data from genetic tests. In our regression analyses, we use five sets of socioeconomic, lifestyle, health insurance, sentiment and political beliefs variables. Further, two framings assess the willingness to undertake a test and the readiness to share results with an insurer when the costs of the test are borne by the insurer or the individual. \newline
RESULTS
We find that socioeconomic, lifestyle or political belief variables have very little influence on the uptake of tests and the sharing of data. On the contrary, our results indicate that sentiment and insurance factors play a strong role. More precisely, if genetic tests are perceived as a mean to perform health prevention, this pushes individuals to take them. Further, using the insurer’s smartphone app leads to an increase of the likelihood to undergo a test and doubles the probability to share related data. Regarding insurance plans and deductible levels, there is no strong correlation neither with the willingness to take a test, nor to share the data. Finally, individuals with complementary health insurance plans are less likely to share results. From the framings for the payment of genetic tests, our results indicate a positive effect of the insurer as a payer on the willingness to undertake tests as well as on data sharing.\newline
CONCLUSION
Our results lay the ground for a deeper understanding of the role of payers on health decisions and sharing of health-related data. In particular, we find that it is relevant for health insurers to engage with their clients.
New health technologies and data offer tailored prevention and spot-on treatments, which can considerably reduce healthcare costs. In healthy individuals, insurers can participate in the creation of health capital through data and preventing the occurrence of a disease. In the onset of a disease, sequencing an individual's genome can provide information leading to the use of more efficient treatments. Both improvements are at the core of the ``personalized health'' paradigm. As a positive side-effect, a reduction in health care costs is expected. However, the integration of personalized health in insurance schemes starts with a closer understanding of the demand drivers. \newline
METHODS
Using novel data from a survey carried out in Switzerland, we determine the factors influencing the uptake and sharing of data from genetic tests. In our regression analyses, we use five sets of socioeconomic, lifestyle, health insurance, sentiment and political beliefs variables. Further, two framings assess the willingness to undertake a test and the readiness to share results with an insurer when the costs of the test are borne by the insurer or the individual. \newline
RESULTS
We find that socioeconomic, lifestyle or political belief variables have very little influence on the uptake of tests and the sharing of data. On the contrary, our results indicate that sentiment and insurance factors play a strong role. More precisely, if genetic tests are perceived as a mean to perform health prevention, this pushes individuals to take them. Further, using the insurer’s smartphone app leads to an increase of the likelihood to undergo a test and doubles the probability to share related data. Regarding insurance plans and deductible levels, there is no strong correlation neither with the willingness to take a test, nor to share the data. Finally, individuals with complementary health insurance plans are less likely to share results. From the framings for the payment of genetic tests, our results indicate a positive effect of the insurer as a payer on the willingness to undertake tests as well as on data sharing.\newline
CONCLUSION
Our results lay the ground for a deeper understanding of the role of payers on health decisions and sharing of health-related data. In particular, we find that it is relevant for health insurers to engage with their clients.
Mots-clé
personalized health, genetic testing, willingness to test, data sharing, preferences, survey study
Open Access
Oui
APC
3473 USD
Financement(s)
Fonds national suisse / Projets / CRSII5_180350
Création de la notice
02/02/2023 18:53
Dernière modification de la notice
03/03/2023 7:13