TY - JOUR
T1 - Non-invasive prenatal testing (NIPT) and pregnant women’s views on good motherhood
T2 - a qualitative study
AU - Garcia, Elisa
AU - Henneman, Lidewij
AU - Gitsels-van der Wal, Janneke T.
AU - Martin, Linda
AU - Koopmanschap, Isabel
AU - Bekker, Mireille N.
AU - Timmermans, Danielle R.M.
N1 - Funding Information:
We wish to thank all women and men who participated in this study. We thank the midwifery practices for their help with recruitment, and Elsbeth van Vliet-Lachotzki (VSOP Patient Alliance for Rare and Genetic Diseases) for her feedback on the interview guide and protocol. We thank all members of the Dutch NIPT Consortium (see Supplementary Appendix) for discussion and feedback on this study.
Funding Information:
Supported by a grant from the Netherlands Organization for Health Research and Development (ZonMw, No. 543002001).
Publisher Copyright:
© 2021, The Author(s), under exclusive licence to European Society of Human Genetics.
PY - 2022/6
Y1 - 2022/6
N2 - Women’s views on responsible motherhood influence decision-making regarding participation in prenatal screening. Previous studies showed that the probabilistic nature of the first-trimester combined test and the potential requirement for subsequent invasive diagnostics serve as legitimate reasons for women to exclude prenatal screening from their moral responsibilities. These moral barriers might now be less relevant with the introduction of the non-invasive prenatal test (NIPT) resulting in women feeling a moral duty to use NIPT screening as part of responsible motherhood. This qualitative study explores the impact of NIPT on women’s moral beliefs about the meaning of prenatal screening in relation to responsible motherhood. We performed semi-structured interviews with 29 pregnant women who were offered NIPT as a first-tier screening test within a Dutch nationwide study (TRIDENT-2). Results show that the inherent uncertainty about the fetus’s health despite improved accuracy and the lack of treatment for a detected disorder, combined with the possibility to obtain information about actionable anomalies through the fetal anomaly scan, support women’s perspectives that NIPT is not an obligation of responsible motherhood. Acceptance of NIPT is considered to be a free decision related to the information each woman needs to be a good mother for her child and her family. Women’s views may change when NIPT has expanded to include treatable or preventable conditions.
AB - Women’s views on responsible motherhood influence decision-making regarding participation in prenatal screening. Previous studies showed that the probabilistic nature of the first-trimester combined test and the potential requirement for subsequent invasive diagnostics serve as legitimate reasons for women to exclude prenatal screening from their moral responsibilities. These moral barriers might now be less relevant with the introduction of the non-invasive prenatal test (NIPT) resulting in women feeling a moral duty to use NIPT screening as part of responsible motherhood. This qualitative study explores the impact of NIPT on women’s moral beliefs about the meaning of prenatal screening in relation to responsible motherhood. We performed semi-structured interviews with 29 pregnant women who were offered NIPT as a first-tier screening test within a Dutch nationwide study (TRIDENT-2). Results show that the inherent uncertainty about the fetus’s health despite improved accuracy and the lack of treatment for a detected disorder, combined with the possibility to obtain information about actionable anomalies through the fetal anomaly scan, support women’s perspectives that NIPT is not an obligation of responsible motherhood. Acceptance of NIPT is considered to be a free decision related to the information each woman needs to be a good mother for her child and her family. Women’s views may change when NIPT has expanded to include treatable or preventable conditions.
UR - http://www.scopus.com/inward/record.url?scp=85112685403&partnerID=8YFLogxK
U2 - 10.1038/s41431-021-00945-3
DO - 10.1038/s41431-021-00945-3
M3 - Article
C2 - 34400811
AN - SCOPUS:85112685403
SN - 1018-4813
VL - 30
SP - 669
EP - 675
JO - European Journal of Human Genetics
JF - European Journal of Human Genetics
IS - 6
ER -