Abstract
Objective: The introduction of non-invasive prenatal testing (NIPT) for Down syndrome (DS) has sparked social and ethical debates. To date, in-depth exploration of the voices of Australian mothers of a child with DS about NIPT has been lacking. The purpose of this study was to investigate the perspectives of Australian mothers of a child with DS towards the increasing availability of NIPT. Design and Setting: Fifteen mothers of children with DS aged 8 months–39 years participated in-depth interviews, conducted online via the software Zoom™. An inductive thematic analysis of interview data explored mothers’ perceptions of NIPT. Findings: Mothers perspectives were nuanced and personal to each woman's circumstance. All mothers highlighted the inevitable association between testing and termination, the importance of autonomy and respecting [m]others’ choices to test and to terminate, and that appropriate supports must be provided to ensure informed decision-making. These perspectives existed within an overarching theme of NIPT reflecting and reinforcing societal attitudes towards disability. Conclusion: Mothers of a child with DS viewed informed decision-making as crucial both prior to undertaking NIPT and following a positive test result. This study adds a unique Australian perspective to the necessary ongoing social and ethical debate.
Original language | English |
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Pages (from-to) | 118-124 |
Number of pages | 7 |
Journal | Midwifery |
Volume | 76 |
DOIs | |
Publication status | Published - 2019 |
Keywords
- Down syndrome
- counseling
- intellectual disability
- mothers
- prenatal diagnosis