TY - JOUR
T1 - Psychological impact of additional findings detected by genome-wide Non-Invasive Prenatal Testing (NIPT)
T2 - TRIDENT-2 study
AU - Bakkeren, Iris M.
AU - Henneman, Lidewij
AU - van Vliet-Lachotzki, Elsbeth H.
AU - Martin, Linda
AU - Gitsels-van der Wal, Janneke T.
AU - Polak, Marike G.
AU - Bekker, Mireille N.
AU - Galjaard, Robert Jan H.
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to European Society of Human Genetics 2023.
PY - 2024/3
Y1 - 2024/3
N2 - In the Netherlands, genome-wide non-invasive prenatal testing (NIPT) is offered to all pregnant women as part of the nationwide TRIDENT-2 study. Findings other than trisomy 21, 18, or 13, which are called “additional findings”, are reported only on request of the pregnant woman. This study examined: (1) women’s pre-test perceptions and reasons to opt for additional findings and (2) women’s experiences with- and the psychological impact of being informed about an additional finding. A questionnaire, consisting of the anxiety measure State-Trait Anxiety Inventory (STAI), distress measure Impact of Event Scale (IES) and questions developed specifically for this study, was retrospectively administered to 402 women who received an additional finding. A total of 227 (56.5%) women completed the questionnaire. Most (60.2%) chose to know additional findings because they wanted as much information as possible about the health of their fetus. Almost all (92%) stated that receiving the additional finding was unexpected, a shock, and/or they were in disbelief, for 85% it caused a lot of worry. Post-test, high anxiety (STAI) levels were reported in 15.5% of women, and 7.5% reported severe distress (IES). Women who gave birth to an affected child (n = 10) experienced most psychological impact (STAI and IES). Eighty-six percent of women with a fetal aberration would opt for additional findings again, compared to 49.2% of women whose result was confined to the placenta. Pre-test counseling should focus on explaining the different results NIPT can generate. Post-test counseling should focus on guiding pregnant women through this uncertain and anxious time.
AB - In the Netherlands, genome-wide non-invasive prenatal testing (NIPT) is offered to all pregnant women as part of the nationwide TRIDENT-2 study. Findings other than trisomy 21, 18, or 13, which are called “additional findings”, are reported only on request of the pregnant woman. This study examined: (1) women’s pre-test perceptions and reasons to opt for additional findings and (2) women’s experiences with- and the psychological impact of being informed about an additional finding. A questionnaire, consisting of the anxiety measure State-Trait Anxiety Inventory (STAI), distress measure Impact of Event Scale (IES) and questions developed specifically for this study, was retrospectively administered to 402 women who received an additional finding. A total of 227 (56.5%) women completed the questionnaire. Most (60.2%) chose to know additional findings because they wanted as much information as possible about the health of their fetus. Almost all (92%) stated that receiving the additional finding was unexpected, a shock, and/or they were in disbelief, for 85% it caused a lot of worry. Post-test, high anxiety (STAI) levels were reported in 15.5% of women, and 7.5% reported severe distress (IES). Women who gave birth to an affected child (n = 10) experienced most psychological impact (STAI and IES). Eighty-six percent of women with a fetal aberration would opt for additional findings again, compared to 49.2% of women whose result was confined to the placenta. Pre-test counseling should focus on explaining the different results NIPT can generate. Post-test counseling should focus on guiding pregnant women through this uncertain and anxious time.
UR - http://www.scopus.com/inward/record.url?scp=85178909788&partnerID=8YFLogxK
U2 - 10.1038/s41431-023-01504-8
DO - 10.1038/s41431-023-01504-8
M3 - Article
C2 - 38057584
AN - SCOPUS:85178909788
SN - 1018-4813
VL - 32
SP - 302
EP - 308
JO - European Journal of Human Genetics
JF - European Journal of Human Genetics
IS - 3
ER -