Titel: Non-Invasive Prenatal Testing: Implementation in England, France and Germany
Termin:
26.10.2022
Veranstaltungsort:
University of Oxford
Li Ka Shing Centre for Health Information and Discovery
Old Road Campus
Oxford OX3 7LF
United Kingdom
Referenten: Felicity Boardman, Hilary Bowman-Smart, Angus Clarke, Ruth Horn, Tamar Nov Klaiman, Caroline Lafarge, Laurence Lohmann, Adeline Perrot, Julia Perry, Christoph Rehmann-Sutter, Dagmar Schmitz, Heather Strange, Carine Vassy, Isabelle Ville
Weitere Informationen:
https://www.ethox.ox.ac.uk/files/research/nipt-workshop-2022
This comparative investigation takes non-invasive prenatal testing (NIPT) in England, France and Germany as a case study.
Non-invasive prenatal testing (NIPT) is a rapidly developing technology, which is constantly widening its scope in reproductive medicine. According to some authors, NIPT is at the 'vanguard of genomic medicine'. Since 2011, NIPT, which uses cell-free foetal DNA in the maternal blood, has been commercially available worldwide. NIPT can be done early in pregnancy - in the first trimester - and is considered highly reliable for detecting common chromosomal anomalies (e.g. trisomy 21, 18 or 13). NIPT for these anomalies is not used as a diagnostic test at present and so a positive NIPT test requires invasive testing for confirmation. Research is also being done to investigate the usefulness of the test for microdeletions (e.g. cri-du-chat syndrome) and for single gene disorders. Some researchers expect that, in the future, it could be used to sequence the whole-genome of a foetus.
In England, France and Germany, NIPT is, or will soon be, freely available to women with a chance of having a baby with a common chromosomal anomaly. Although all three healthcare systems agree that NIPT should be used as a second-tier test (i.e. following initial risk assessment), they differ with regard to: the risk thresholds they use, their public discourses about genomics, screening policies, professional regulations and laws regarding prenatal genetics/genomics.
The introduction of NIPT into routine antenatal care carries not only benefits but also raises important ethical questions about the meaning of health, risk, illness and disability, the scope of public health interventions, social inclusion and exclusion as well as reproductive choice. These issues require careful analysis within their specific contexts.
The aim of this project is to conduct an in-depth investigation of the ethical issues arising from NIPT in three different socio-cultural contexts within Europe (England, France and Germany).
To achieve this aim, our research team will investigate the values and socio-political particularities that shape the (future) use and regulation of NIPT within different socio-cultural contexts. This will involve a document analysis (of professional and ethics guidelines, policies, laws, bioethics and social sciences literature, media) and conceptual analysis (of the normative arguments) to examine the views and normative arguments presented in public debates on the ethical and social implications of NIPT in each country-site.
In addition, a comparative empirical research (observations, interviews, focus groups) will help to gain in-depth understanding of the experiences and practical-ethical problems the principal actors (patients, healthcare professionals, scientists, policy makers) encounter in practice and investigate how these are resolved in each country.
Finally, the project will provide a contextual understanding of the practical ethical issues raised by NIPT within their socio-cultural, legal and structural context. This will generate important elements for the development of models of good practice within Europe.
Kontakt:
Ruth Horn
Tel.:
+44 1865 287888
ruth.horn@ethox.ox.ac.uk
https://www.ethox.ox.ac.uk/Our-research/research-projects/nipt
Veranstalter: Ethox Centre
Schlagworte: Behinderung, Pränataldiagnostik, Schwangerschaftsabbruch