Skip to main content
Erschienen in: Journal of Genetic Counseling 5/2018

17.03.2018 | Original Research

Talking Points: Women’s Information Needs for Informed Decision-Making About Noninvasive Prenatal Testing for Down Syndrome

verfasst von: Aimée C. Dane, Madelyn Peterson, Yvette D. Miller

Erschienen in: Journal of Genetic Counseling | Ausgabe 5/2018

Einloggen, um Zugang zu erhalten

Abstract

Adequate knowledge is a vital component of informed decision-making; however, we do not know what information women value when making decisions about noninvasive prenatal testing (NIPT). The current study aimed to identify women’s information needs for decision-making about NIPT as a first-tier, non-contingent test with out-of-pocket expense and, in turn, inform best practice by specifying the information that should be prioritized when providing pre-test counseling to women in a time-limited scenario or space-limited decision support tool. We asked women (N = 242) in Australia to indicate the importance of knowing 24 information items when making a decision about NIPT and to choose two information items they would most value. Our findings suggest that women value having complete information when making decisions about NIPT. Information about the accuracy of NIPT and the pros and cons of NIPT compared to other screening and invasive tests were perceived to be most important. The findings of this study can be used to maximize the usefulness of time-limited discussions or space-limited decision support tools, but should not be routinely relied upon as a replacement for provision of full and tailored information when feasible.
Literatur
Zurück zum Zitat ACOG. (2015). Cell-free DNA screening for fetal aneuploidy. Committee Opinion No. 640. Obstetrics & Gynecology, 126(3), e31–e37.CrossRef ACOG. (2015). Cell-free DNA screening for fetal aneuploidy. Committee Opinion No. 640. Obstetrics & Gynecology, 126(3), e31–e37.CrossRef
Zurück zum Zitat Allyse, M., Sayres, L., Havard, M., King, J., Greely, H., Hudgins, L., et al. (2013). Best ethical practices for clinicians and laboratories in the provision of non-invasive prenatal testing. Prenatal Diagnosis, 33(7), 656–661.CrossRefPubMedPubMedCentral Allyse, M., Sayres, L., Havard, M., King, J., Greely, H., Hudgins, L., et al. (2013). Best ethical practices for clinicians and laboratories in the provision of non-invasive prenatal testing. Prenatal Diagnosis, 33(7), 656–661.CrossRefPubMedPubMedCentral
Zurück zum Zitat Beulen, L., van den Berg, M., Faas, B. H., Feenstra, I., Hageman, M., van Vugt, J. M., & Bekker, M. N. (2016). The effect of a decision aid on informed decision-making in the era of non-invasive prenatal testing: a randomised controlled trial. European Journal of Human Genetics, 24(10), 1409–1416.CrossRefPubMedPubMedCentral Beulen, L., van den Berg, M., Faas, B. H., Feenstra, I., Hageman, M., van Vugt, J. M., & Bekker, M. N. (2016). The effect of a decision aid on informed decision-making in the era of non-invasive prenatal testing: a randomised controlled trial. European Journal of Human Genetics, 24(10), 1409–1416.CrossRefPubMedPubMedCentral
Zurück zum Zitat Braun, V., & Clarke, V. (2006). Using thematic analysis in psychology. Qualitative Research in Psychology, 3(2), 77–101.CrossRef Braun, V., & Clarke, V. (2006). Using thematic analysis in psychology. Qualitative Research in Psychology, 3(2), 77–101.CrossRef
Zurück zum Zitat Bryant, L. D., Green, J. M., & Hewison, J. (2010). The role of attitudes towards the targets of behaviour in predicting and informing prenatal testing choices. Psychology & Health, 25(10), 1175–1194.CrossRef Bryant, L. D., Green, J. M., & Hewison, J. (2010). The role of attitudes towards the targets of behaviour in predicting and informing prenatal testing choices. Psychology & Health, 25(10), 1175–1194.CrossRef
Zurück zum Zitat Drennan, J. (2003). Cognitive interviewing: verbal data in the design and pretesting of questionnaires. Journal of Advanced Nursing, 42(1), 57–63.CrossRefPubMed Drennan, J. (2003). Cognitive interviewing: verbal data in the design and pretesting of questionnaires. Journal of Advanced Nursing, 42(1), 57–63.CrossRefPubMed
Zurück zum Zitat Farrell, R. M., Agatisa, P. K., & Nutter, B. (2014a). What women want: lead considerations for current and future applications of noninvasive prenatal testing in prenatal care. Birth, 41(3), 276–282.CrossRefPubMedPubMedCentral Farrell, R. M., Agatisa, P. K., & Nutter, B. (2014a). What women want: lead considerations for current and future applications of noninvasive prenatal testing in prenatal care. Birth, 41(3), 276–282.CrossRefPubMedPubMedCentral
Zurück zum Zitat Farrell, R. M., Mercer, M. B., Agatisa, P. K., Smith, M. B., & Philipson, E. (2014b). It’s more than a blood test: patients’ perspectives on noninvasive prenatal testing. Journal of Clinical Medicine, 3(2), 614–631.CrossRefPubMedPubMedCentral Farrell, R. M., Mercer, M. B., Agatisa, P. K., Smith, M. B., & Philipson, E. (2014b). It’s more than a blood test: patients’ perspectives on noninvasive prenatal testing. Journal of Clinical Medicine, 3(2), 614–631.CrossRefPubMedPubMedCentral
Zurück zum Zitat Farrell, R. M., Nutter, B., & Agatisa, P. K. (2011). Meeting patients’ education and decision-making needs for first trimester prenatal aneuploidy screening. Prenatal Diagnosis, 31(13), 1222–1228.CrossRefPubMed Farrell, R. M., Nutter, B., & Agatisa, P. K. (2011). Meeting patients’ education and decision-making needs for first trimester prenatal aneuploidy screening. Prenatal Diagnosis, 31(13), 1222–1228.CrossRefPubMed
Zurück zum Zitat Hill, M., Wright, D., Daley, R., Lewis, C., McKay, F., Mason, S., Lench, N., Howarth, A., Boustred, C., Lo, K., Plagnol, V., Spencer, K., Fisher, J., Kroese, M., Morris, S., & Chitty, L. S. (2014). Evaluation of non-invasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal non-invasive diagnosis (RAPID) protocol. BMC Pregnancy and Childbirth, 14(229). https://doi.org/10.1186/1471-2393-14-229. Hill, M., Wright, D., Daley, R., Lewis, C., McKay, F., Mason, S., Lench, N., Howarth, A., Boustred, C., Lo, K., Plagnol, V., Spencer, K., Fisher, J., Kroese, M., Morris, S., & Chitty, L. S. (2014). Evaluation of non-invasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal non-invasive diagnosis (RAPID) protocol. BMC Pregnancy and Childbirth, 14(229). https://​doi.​org/​10.​1186/​1471-2393-14-229.
Zurück zum Zitat Kuppermann, M., Pena, S., Bishop, J. T., Nakagawa, S., Gregorich, S. E., Sit, A., Vargas, J., Caughey, A. B., Sykes, S., Pierce, L., & Norton, M. E. (2014). Effect of enhanced information, values clarification, and removal of financial barriers on use of prenatal genetic testing: a randomized clinical trial. JAMA, 312(12), 1210–1217.CrossRefPubMedPubMedCentral Kuppermann, M., Pena, S., Bishop, J. T., Nakagawa, S., Gregorich, S. E., Sit, A., Vargas, J., Caughey, A. B., Sykes, S., Pierce, L., & Norton, M. E. (2014). Effect of enhanced information, values clarification, and removal of financial barriers on use of prenatal genetic testing: a randomized clinical trial. JAMA, 312(12), 1210–1217.CrossRefPubMedPubMedCentral
Zurück zum Zitat Lewis, C., Hill, M., Skirton, H., & Chitty, L. S. (2016). Development and validation of a measure of informed choice for women undergoing non-invasive prenatal testing for aneuploidy. European Journal of Human Genetics, 24(6), 809–816.CrossRefPubMed Lewis, C., Hill, M., Skirton, H., & Chitty, L. S. (2016). Development and validation of a measure of informed choice for women undergoing non-invasive prenatal testing for aneuploidy. European Journal of Human Genetics, 24(6), 809–816.CrossRefPubMed
Zurück zum Zitat Lewis, C., Silcock, C., & Chitty, L. S. (2013). Non-invasive prenatal testing for Down’s syndrome: pregnant women’s views and likely uptake. Public Health Genomics, 16(5), 223–232.CrossRefPubMed Lewis, C., Silcock, C., & Chitty, L. S. (2013). Non-invasive prenatal testing for Down’s syndrome: pregnant women’s views and likely uptake. Public Health Genomics, 16(5), 223–232.CrossRefPubMed
Zurück zum Zitat Marteau, T. M., & Dormandy, E. (2001). Facilitating informed choice in prenatal testing: how well are we doing? American Journal of Medical Genetics, 106(3), 185–190.CrossRefPubMed Marteau, T. M., & Dormandy, E. (2001). Facilitating informed choice in prenatal testing: how well are we doing? American Journal of Medical Genetics, 106(3), 185–190.CrossRefPubMed
Zurück zum Zitat Michie, S., Dormandy, E., & Marteau, T. M. (2003). Informed choice: understanding knowledge in the context of screening uptake. Patient Education and Counseling, 50(3), 247–253.CrossRefPubMed Michie, S., Dormandy, E., & Marteau, T. M. (2003). Informed choice: understanding knowledge in the context of screening uptake. Patient Education and Counseling, 50(3), 247–253.CrossRefPubMed
Zurück zum Zitat Nagle, C., Gunn, J., Bell, R., Lewis, S., Meiser, B., Metcalfe, S., Ukoumunne, O. C., & Halliday, J. (2008). Use of a decision aid for prenatal testing of fetal abnormalities to improve women’s informed decision making: a cluster randomised controlled trial. BJOG, 115(3), 339–347.CrossRefPubMed Nagle, C., Gunn, J., Bell, R., Lewis, S., Meiser, B., Metcalfe, S., Ukoumunne, O. C., & Halliday, J. (2008). Use of a decision aid for prenatal testing of fetal abnormalities to improve women’s informed decision making: a cluster randomised controlled trial. BJOG, 115(3), 339–347.CrossRefPubMed
Zurück zum Zitat Nicolaides, K. H. (2004). Nuchal translucency and other first-trimester sonographic markers of chromosomal abnormalities. American Journal of Obstetrics & Gynecology, 191(1), 45–67.CrossRef Nicolaides, K. H. (2004). Nuchal translucency and other first-trimester sonographic markers of chromosomal abnormalities. American Journal of Obstetrics & Gynecology, 191(1), 45–67.CrossRef
Zurück zum Zitat Piechan, J. L., Hines, K. A., Koller, D. L., Stone, K., Quaid, K., Torres-Martinez, W., Wilson Mathews, D., Foroud, T., & Cook, L. (2016). NIPT and informed consent: an assessment of patient understanding of a negative NIPT result. Journal of Genetic Counseling, 25, 1127–1137.CrossRefPubMed Piechan, J. L., Hines, K. A., Koller, D. L., Stone, K., Quaid, K., Torres-Martinez, W., Wilson Mathews, D., Foroud, T., & Cook, L. (2016). NIPT and informed consent: an assessment of patient understanding of a negative NIPT result. Journal of Genetic Counseling, 25, 1127–1137.CrossRefPubMed
Zurück zum Zitat RANZCOG, College statement C-Obs 59: prenatal screening and diagnosis of chromosomal and genetic abnormalities in the fetus in pregnancy, 2015. RANZCOG, College statement C-Obs 59: prenatal screening and diagnosis of chromosomal and genetic abnormalities in the fetus in pregnancy, 2015.
Zurück zum Zitat Sachs, A., Blanchard, L., Buchanan, A., Norwitz, E., & Bianchi, D. W. (2015). Recommended pre-test counseling points for noninvasive prenatal testing using cell-free DNA: a 2015 perspective. Prenatal Diagnosis, 35(10), 968–971.CrossRefPubMed Sachs, A., Blanchard, L., Buchanan, A., Norwitz, E., & Bianchi, D. W. (2015). Recommended pre-test counseling points for noninvasive prenatal testing using cell-free DNA: a 2015 perspective. Prenatal Diagnosis, 35(10), 968–971.CrossRefPubMed
Zurück zum Zitat Schoonen, H. M., van Agt, H. M., Essink-Bot, M. L., Wildschut, H. I., Steegers, E. A., & de Koning, H. J. (2011). Informed decision-making in prenatal screening for Down’s syndrome: what knowledge is relevant? Patient Education and Counseling, 84(2), 265–270.CrossRefPubMed Schoonen, H. M., van Agt, H. M., Essink-Bot, M. L., Wildschut, H. I., Steegers, E. A., & de Koning, H. J. (2011). Informed decision-making in prenatal screening for Down’s syndrome: what knowledge is relevant? Patient Education and Counseling, 84(2), 265–270.CrossRefPubMed
Zurück zum Zitat Wilson, K. L., Czerwinski, J. L., Hoskovec, J. M., Noblin, S. J., Sullivan, C. M., Harbison, A., Campion, M. W., Devary, K., Devers, P., & Singletary, C. N. (2013). NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy. Journal of Genetic Counseling, 22(1), 4–15.CrossRefPubMed Wilson, K. L., Czerwinski, J. L., Hoskovec, J. M., Noblin, S. J., Sullivan, C. M., Harbison, A., Campion, M. W., Devary, K., Devers, P., & Singletary, C. N. (2013). NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy. Journal of Genetic Counseling, 22(1), 4–15.CrossRefPubMed
Metadaten
Titel
Talking Points: Women’s Information Needs for Informed Decision-Making About Noninvasive Prenatal Testing for Down Syndrome
verfasst von
Aimée C. Dane
Madelyn Peterson
Yvette D. Miller
Publikationsdatum
17.03.2018
Verlag
Springer US
Erschienen in
Journal of Genetic Counseling / Ausgabe 5/2018
Print ISSN: 1059-7700
Elektronische ISSN: 1573-3599
DOI
https://doi.org/10.1007/s10897-018-0250-8

Weitere Artikel der Ausgabe 5/2018

Journal of Genetic Counseling 5/2018 Zur Ausgabe

Update Gynäkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert – ganz bequem per eMail.