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"This lifetime commitment": Public conceptions of disability and noninvasive prenatal genetic screening
Rosemary J Steinbach1, Megan Allyse2, Marsha Michie3
1Stanford Center for Biomedical Ethics, Stanford, California.
American Journal of Medical Genetics. Part A
|November 15, 2015
Summary
New noninvasive prenatal genetic screening tests for Down syndrome are available. Most people support screening availability and continuing pregnancies with aneuploidy, regardless of their views on disability.
Area of Science:
- Genetics
- Bioethics
- Public Health
Background:
- Noninvasive prenatal genetic screening (NIPS) for conditions like Down syndrome is now widely available.
- These advancements raise ethical questions regarding prenatal testing for intellectual and developmental disabilities.
- Existing debates on prenatal testing are being re-examined in light of new technologies.
Purpose of the Study:
- To investigate public attitudes towards prenatal genetic screening.
- To understand how views on disability influence opinions on prenatal testing.
- To explore public perspectives on aneuploidy screening.
Main Methods:
- A web-based survey was conducted among a sample of the US public.
- The survey examined attitudes towards disability and prenatal testing.
- Qualitative analysis of responses was performed.
Main Results:
- The majority of respondents supported the availability of prenatal genetic screening.
- Most participants also supported continuing a pregnancy diagnosed with aneuploidy.
- Support for screening and continuation was observed across diverse opinions on disability.
Conclusions:
- Public opinion generally favors the availability of prenatal genetic screening.
- There is broad support for reproductive autonomy, including the decision to continue or terminate a pregnancy post-screening.
- Attitudes towards disability shape the reasoning behind these views, reflecting complex ethical considerations.
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