TY - JOUR
T1 - How can contingent valuation inform the bioethics debate? Evidence from a survey on hereditary cancers in France
AU - Protière, Christel
AU - Chanel, Olivier
AU - Nogues, Catherine
AU - Coupier, Isabelle
AU - Mouret-Fourme, Emmanuelle
AU - Julian-Reynier, Claire
AU - Adenis, Claude
AU - Bignon, Yves Jean
AU - Bonadona, Valérie
AU - Chevrier, Annie
AU - Colas, Chrystelle
AU - Cohen-Haguenauer, Odile
AU - Demange, Liliane
AU - Dreyfus, Hélène
AU - Dugast, Catherine
AU - Eisinger, François
AU - Gauthiers-Villars, Marion
AU - Huiart, Laetitia
AU - Lasset, Christine
AU - Limacher, Jean Marc
AU - Longy, Michel
AU - Lortholary, Alain
AU - Luporsi, Élisabeth
AU - Olschwang, Sylviane
AU - Piot, Irwin
AU - Pujol, Pascal
AU - Stoppa-Lyonnet, Dominique
AU - Venat-Bouvet, Laurence
AU - Vennin, Philippe
AU - GENEPSO cohort investigators
PY - 2017
Y1 - 2017
N2 - BRCA1/2 carriers have a higher risk of developing breast and ovarian cancer at a younger age. Preimplantation genetic diagnosis (PGD) and prenatal diagnosis (PND) are two of the few options available to avoid transmitting the mutation. To inform the bioethics debate about authorization, a contingent valuation survey elicited preferences regarding access to PGD and PND from a sample of 460 respondents can be classified into three groups: one opposed to PGD/PND (28.3%), one strongly in favour of PGD/PND (45.8%), and one in an intermediate position (25.9%). We look for the determinants of these preferences, especially of the willingness to pay for PGD/PND. Overall, we find that BRCA1/2 carriers support access to PGD/PND, which has implications for recommendations to decision-makers. unaffected by cancer BRCA1/2 carriers (GENEPSO cohort). We find that the respondents can be classified into three groups: one opposed to PGD/PND (28.3%), one strongly in favour of PGD/PND (45.8%), and one in an intermediate position (25.9%). We look for the determinants of these preferences, especially of the willingness to pay for PGD/PND. Overall, we find that BRCA1/2 carriers support access to PGD/PND, which has implications for recommendations to decision-makers.
AB - BRCA1/2 carriers have a higher risk of developing breast and ovarian cancer at a younger age. Preimplantation genetic diagnosis (PGD) and prenatal diagnosis (PND) are two of the few options available to avoid transmitting the mutation. To inform the bioethics debate about authorization, a contingent valuation survey elicited preferences regarding access to PGD and PND from a sample of 460 respondents can be classified into three groups: one opposed to PGD/PND (28.3%), one strongly in favour of PGD/PND (45.8%), and one in an intermediate position (25.9%). We look for the determinants of these preferences, especially of the willingness to pay for PGD/PND. Overall, we find that BRCA1/2 carriers support access to PGD/PND, which has implications for recommendations to decision-makers. unaffected by cancer BRCA1/2 carriers (GENEPSO cohort). We find that the respondents can be classified into three groups: one opposed to PGD/PND (28.3%), one strongly in favour of PGD/PND (45.8%), and one in an intermediate position (25.9%). We look for the determinants of these preferences, especially of the willingness to pay for PGD/PND. Overall, we find that BRCA1/2 carriers support access to PGD/PND, which has implications for recommendations to decision-makers.
UR - http://www.scopus.com/inward/record.url?scp=85027259016&partnerID=8YFLogxK
U2 - 10.3917/reco.683.0379
DO - 10.3917/reco.683.0379
M3 - Article
AN - SCOPUS:85027259016
SN - 0035-2764
VL - 68
SP - 379
EP - 404
JO - Revue Economique
JF - Revue Economique
IS - 3
ER -