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The Journal of Maternal-Fetal & Neonatal Medicine Volume 33, 2020 - Issue 8
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Original Articles

Decisional regret in women receiving high risk or inconclusive prenatal cell-free DNA screening results

Betsy L. GammonMayo Clinic, Biomedical Ethics Program, Rochester, MN, USA; ;University of Virginia School of Medicine, Charlottesville, VA, USA; View further author information
,
Carolina JaramilloMayo Clinic, Biomedical Ethics Program, Rochester, MN, USA; View further author information
,
Kirsten A. RigganMayo Clinic, Biomedical Ethics Program, Rochester, MN, USA; ORCID Iconhttp://orcid.org/0000-0002-0127-9555View further author information
ORCID Icon &
Megan AllyseMayo Clinic, Biomedical Ethics Program, Rochester, MN, USA; ;Obstetrics and Gynecology, Mayo Clinic, Rochester, MN, USACorrespondence[email protected]
ORCID Iconhttps://orcid.org/0000-0001-6136-9256View further author information
ORCID Icon
Pages 1412-1418 | Received 30 May 2018, Accepted 31 Aug 2018, Published online: 01 Oct 2018

Citations (8)

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Sidonie de Wergifosse, Elisa Bevilacqua, Iris Mezela, Sarah El Haddad, Caroline Gounongbe, Jérôme de Marchin, Valeria Maggi, Stéphanie Conotte, Dominique A. Badr, Jean-François Fils, Meriem Guizani & Jacques C. Jani. (2021) Cell-free DNA analysis in maternal blood: comparing genome-wide versus targeted approach as a first-line screening test. The Journal of Maternal-Fetal & Neonatal Medicine 34:21, pages 3552-3561.
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Articles from other publishers (7)

Marion Baldus. (2023) “Overestimated technology – underestimated consequences” – reflections on risks, ethical conflicts, and social disparities in the handling of non-invasive prenatal tests (NIPTs). Medicine, Health Care and Philosophy 26:2, pages 271-282.
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Molly Johnston, Chanelle Warton, Mark D. Pertile, Michelle Taylor‐Sands, Martin B. Delatycki, Lisa Hui, Julian Savulescu & Catherine Mills. (2022) Ethical issues associated with prenatal screening using non‐invasive prenatal testing for sex chromosome aneuploidy. Prenatal Diagnosis 43:2, pages 226-234.
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Miranda F. Lewit‐Mendes, Hazel Robson, Joanne Kelley, Justine Elliott, Erica Brown, Melody Menezes & Alison D. Archibald. (2022) Experiences of receiving an increased chance of sex chromosome aneuploidy result from non‐invasive prenatal testing in Australia: “A more complicated scenario than what I had ever realized”. Journal of Genetic Counseling 32:1, pages 213-223.
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J Whitehead, Josephine Hirsch, Ilina Rosoklija, Allison Goetsch Weisman, Jeffrey Dungan, Courtney Finlayson, Diane Chen & Emilie K. Johnson. (2022) Prenatal detection and evaluation of differences of sex development: A qualitative interview study of parental perspectives and unmet needs. Prenatal Diagnosis 42:10, pages 1332-1342.
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Tamra L. Shea. (2020) Informed Decision Making Regarding Prenatal Aneuploidy Screening. Journal of Obstetric, Gynecologic & Neonatal Nursing 49:1, pages 41-54.
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Karuna R.M. van der Meij, Erik A. Sistermans, Merryn V.E. Macville, Servi J.C. Stevens, Caroline J. Bax, Mireille N. Bekker, Caterina M. Bilardo, Elles M.J. Boon, Marjan Boter, Karin E.M. Diderich, Christine E.M. de Die-Smulders, Leonie K. Duin, Brigitte H.W. Faas, Ilse Feenstra, Monique C. Haak, Mariëtte J.V. Hoffer, Nicolette S. den Hollander, Iris H.I.M. Hollink, Fernanda S. Jehee, Maarten F.C.M. Knapen, Angelique J.A. Kooper, Irene M. van Langen, Klaske D. Lichtenbelt, Ingeborg H. Linskens, Merel C. van Maarle, Dick Oepkes, Mijntje J. Pieters, G. Heleen Schuring-Blom, Esther Sikkel, Birgit Sikkema-Raddatz, Dominique F.C.M. Smeets, Malgorzata I. Srebniak, Ron F. Suijkerbuijk, Gita M. Tan-Sindhunata, A. Jeanine E.M. van der Ven, Shama L. van Zelderen-Bhola, Lidewij Henneman, Robert-Jan H. Galjaard, Diane Van Opstal & Marjan M. Weiss. (2019) TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands. The American Journal of Human Genetics 105:6, pages 1091-1101.
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Lindsay Parham, Marsha Michie & Megan Allyse. (2017) Expanding Use of cfDNA Screening in Pregnancy: Current and Emerging Ethical, Legal, and Social Issues. Current Genetic Medicine Reports 5:1, pages 44-53.
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