To describe parents'perceptions of familial hypercholesterolaemia (FH), an inherited predisposition to heart disease, following population-based neonatal screening.
A qualitative analysis of semi-structured interviews with the parents of 24 children who had received a positive screening test result informing them that their child was at-risk for having FH.
Responses to screening seemed to vary according to perceptions of the underlying cause of the positive screening test result.
When parents perceived the test as detecting raised cholesterol the condition was perceived as familiar, dietary in origin, controllable and less threatening.
When the test was seen as detecting a genetic problem, the condition was perceived as uncontrollable and, hence, more threatening.
These pilot data raise questions about the extent to which assessing disease risks by DNA analysis may result in a sense of fatalism, adversely affecting motivation to change behaviour and to reduce risks.
Mots-clés Pascal : Hypercholestérolémie, Maladie héréditaire, Génétique, Risque, Entretien, Parent, Perception sociale, Dépistage, Néonatal, Evaluation, Analyse qualitative, Nouveau né, Homme, Prévention, Royaume Uni, Europe, Lipide, Métabolisme pathologie, Dyslipémie, Hyperlipoprotéinémie
Mots-clés Pascal anglais : Hypercholesterolemia, Genetic disease, Genetics, Risk, Interview, Parent, Social perception, Medical screening, Neonatal, Evaluation, Qualitative analysis, Newborn, Human, Prevention, United Kingdom, Europe, Lipids, Metabolic diseases, Dyslipemia, Hyperlipoproteinemia
Notice produite par :
Inist-CNRS - Institut de l'Information Scientifique et Technique
Cote : 99-0312335
Code Inist : 002B22A. Création : 16/11/1999.