nach oben

Journal of Genetic Counseling

Erschienen in:

15.12.2017 | Original Research

Implementing Group Prenatal Counseling for Expanded Noninvasive Screening Options

verfasst von: Betsy L. Gammon, Laura Otto, Myra Wick, Kristy Borowski, Megan Allyse

Erschienen in: Journal of Genetic Counseling | Ausgabe 4/2018

Einloggen, um Zugang zu erhalten

Abstract

Recently, practices have begun integrating cell-free DNA-based noninvasive prenatal screening as a screening option for a variety of genetic conditions. According to the National Society of Genetic Counselors, the integration of cfDNA screening into clinical prenatal practice may "significantly shift the paradigm of prenatal testing and screening for all women." The purpose of this study was to determine whether group information sessions can feasibly serve as an alternative to extended one-on-one genetic counseling for the increasing number of women making decisions about prenatal testing and screening. This study assessed the effect of group genetic information sessions coupled with abbreviated counseling on pregnant women’s knowledge about and attitudes toward prenatal testing and screening.

ACOG. (2016). ACOG practice bulletin no. 163: screening for fetal aneuploidy. ACOG.org.

ACOG and SMFM. (2016). Ob-Gyns release revised recommendations on screening and testing for genetic disorders. Press Release.

ACOG Committee on Practice Bulletins. (2007). ACOG practice bulletin no. 77: screening for fetal chromosomal abnormalities. Obstet Gynecol, 109(1), 217–227.

American Board of Genetic Counseling. (2016). About ABGC. Available From: www.abgc.net .

Benn, P., Cuckle, H., & Pergament, E. (2012). Non-invasive prenatal diagnosis for down syndrome: The paradigm will shift, but slowly. Ultrasound Obstet Gynecol, 39(2), 127–130. https://doi.org/10.1002/uog.11083.CrossRefPubMed

Bryant, A. S., Norton, M. E., Nakagawa, S., Bishop, J. T., Pena, S., Gregorich, S. E., & Kuppermann, M. (2015). Variation in women's understanding of prenatal testing. Obstetrics & Gynecology, 125(6), 1306–1312.

Bureau of Labor Statistics USDoL. (2015). Occupational outlook handbook, 2016–2017 edition 2015. Available From www.bls.gov .

Bureau USC. (2016). FFF: Women's history month: March 2016. Available From www.census.gov .

Chervenak, F. A., McCullough, L. B., Sharma, G., Davis, J., & Gross, S. (2008, 199). Enhancing patient autonomy with risk assessment and invasive diagnosis: an ethical solution to a clinical challenge. American Journal of Obstetrics and Gynecology, (1), 19–e1 Retrieved from Google Scholar.

Colicchia, L. C., Holland, C. L., Tarr, J. A., Rubio, D. M., Rothenberger, S. D., & Chang, J. C. (2016). Patient--Health care provider conversations about prenatal genetic screening: recommendation or personal choice. Obstetrics & Gynecology, 127(6), 1145–1152 Retrieved from Google Scholar.CrossRef

Constantine, M., Allyse, M., Rockwood, T., Wall, M., & De Vries, R. (2014). Imperfect informed consent for prenatal screening: lessons from the quad screen. Clinical Ethics, 9(1), 17–27.

Devers, P., Cronister, S., Ormond, K., Facio, F., Brasington, C., & Flodman. (2013). Noninvasive prenatal testing/noninvasive prenatal diagnosis: the position of the national society of genetic counselors. Journal of Genetic Counseling, 22(3), 291–295.CrossRefPubMed

Dondorp, W., de Wert, G., Bombard, Y., Bianchi, D. W., Bergmann, C., Borry, P., et al. (2015). Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Eur J Hum Genet. https://doi.org/10.1038/ejhg.2015.57.

Farrell, R. M., Nutter, B., & Agatisa, P. K. (2015). Patient-centered prenatal counseling: aligning obstetric healthcare professionals with needs of pregnant women. Women & Health 55(3):280–96. Retrieved from Google Scholar.

Farrell, R. M., Agatisa, P. K., Mercer, M. B., Mitchum, A., & Coleridge, M. (2016a). The use of noninvasive prenatal testing in obstetric care: educational resources, practice patterns, and barriers reported by a national sample of clinicians. Prenatal Diagnosis. https://doi.org/10.1002/pd.4812.

Farrell, R. M., Agatisa, P. K., Mercer, M. B., Mitchum, A., & Coleridge, M. (2016b). The use of noninvasive prenatal testing in obstetric care: educational resources, practice patterns, and barriers reported by a national sample of clinicians. Prenatal Diagnosis 36(6):499–506.

Gregg, A. R., Skotko, B. G., Benkendorf, J. L., Monaghan, K. G., Bajaj, K., Best, R. G., et al. (2016). Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the american college of medical genetics and genomics. Genet Med, 18(10), 1056–1065.

Harris, R. A., Washington, A. E., Feeny, D., & Kuppermann, M. (2001). Decision analysis of prenatal testing for chromosomal disorders: what do the preferences of pregnant women tell us? Genetic Testing, (5, 1), 23–32 Retrieved from Google Scholar.

Horsting, J. M., Dlouhy, S. R., Hanson, K., Quaid, K., Bai, S., & Hines, K. A. (2014). Genetic counselors' experience with cell-free fetal DNA testing as a prenatal screening option for aneuploidy. Journal of Genetic Counseling, 23, 377–400. https://doi.org/10.1007/s10897-013-9673-4.CrossRefPubMed

Hui, L., Teoh, M., da Silva Costa, F., Ramsay, P., Palma-Dias, R., Richmond, Z., et al. (2014). Clinical implementation of cell-free DNA based aneuploidy screening: perspectives from a national audit. Ultrasound Obstet Gynecol. https://doi.org/10.1002/uog.14699.

Hunter, A. G. W., Cappelli, M., Humphreys, L., Allanson, J. E., Chiu, T. T., Peeters, C., et al. (2005). A randomized trial comparing alternative approaches to prenatal diagnosis counseling in advanced maternal age patients. Clinical Genetics, 67(4), 303–313 Retrieved from Google Scholar.CrossRefPubMed

Knutzen, D. M., Stoll, K. A., McClellan, M. W., Deering, S. H., & Foglia, L. M. (2013). Improving knowledge about prenatal screening options: can group education make a difference? The Journal of Maternal-Fetal & Neonatal Medicine, 26(18), 1799–1803.CrossRef

Larion, S., Warsof, S. L., Romary, L., Mlynarczyk, M., Peleg, D., & Abuhamad, A. Z. (2014). Association of combined first-trimester screen and noninvasive prenatal testing on diagnostic procedures. Obstetrics & Gynecology, 123(6), 1303–1310 Retrieved from Google Scholar.CrossRef

Minkoff, H., & Berkowitz, R. (2014). The case for universal prenatal genetic counseling. Obstet Gynecol, 123(6), 1335–1338. https://doi.org/10.1097/AOG.0000000000000267.CrossRefPubMed

Musci, T. J., Fairbrother, G., Batey, A., Bruursema, J., Struble, C., & Song, K. (2013). Non-invasive prenatal testing with cell-free DNA: US physician attitudes toward implementation in clinical practice. Prenatal Diagnosis, 33(5), 424–428. https://doi.org/10.1002/pd.4091.CrossRefPubMed

Pain, E. (2016). Genetic counseling: A growing area of opportunity. Science. Jun. 13, 2016, http://www.sciencemag.org/careers/2016/06/genetic-counseling-growingarea-opportunity.

Pan, V., Yashar, B. M., Pothast, R., & Wicklund, C. (2016). Expanding the genetic counseling workforce: program directors’ views on increasing the size of genetic counseling graduate programs. Genetics in Medicine, 18(8), 842–849.

Roche, M. I., & Greb, A. E. (2016). It’s time to ramp up genetic counseling training. Genetics in Medicine, 18(8), 768–769.

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 Retrieved from Google Scholar.CrossRefPubMed

Shieh, C., Mays, R., McDaniel, A., & Yu. (2009). Health literacy and its association with the use of information sources and with barriers to information seeking in clinic-based pregnant women. Health Care for Women International, 30(11), 971–988.CrossRefPubMed

SMFM. (2014). Cell free DNA is not a simple blood test. SMFM.org - the Society for Maternal Fetal Medicine, Publications and Guidelines.

Suskin, E., Hercher, L., Aaron, K. E., & Bajaj, K. (2016). The integration of noninvasive prenatal screening into the existing prenatal paradigm: a survey of current genetic counseling practice. Journal of Genetic Counseling, 25(5), 1032–1043.

Thompson, S., Noblin, S. J., Lemons, J., Peterson, S. K., Carreno, C., & Harbison, A. (2015). Perceptions of latinas on the traditional prenatal genetic counseling model. Journal of Genetic Counseling, 24(4), 675–682 Retrieved from Google Scholar.CrossRefPubMed

Wax, J. R., Cartin, A., Chard, R., Lucas, F. L., & Pinette, M. G. (2015). Noninvasive prenatal testing: impact on genetic counseling, invasive prenatal diagnosis, and trisomy 21 detection. Journal of Clinical Ultrasound, 43(1), 1–6 Retrieved from Google Scholar.PubMed

Titel: Implementing Group Prenatal Counseling for Expanded Noninvasive Screening Options
verfasst von: Betsy L. Gammon
Laura Otto
Myra Wick
Kristy Borowski
Megan Allyse
Publikationsdatum: 15.12.2017
Verlag: Springer US
Erschienen in: Journal of Genetic Counseling / Ausgabe 4/2018
Print ISSN: 1059-7700
Elektronische ISSN: 1573-3599
DOI: https://doi.org/10.1007/s10897-017-0178-4

Neu im Fachgebiet Gynäkologie und Geburtshilfe

23.04.2024 | Medikamente in Schwangerschaft und Stillzeit | Nachrichten

Update Gynäkologie

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

Newsletter bestellen

Springer Medizin

Implementing Group Prenatal Counseling for Expanded Noninvasive Screening Options

Abstract

Neu im Fachgebiet Gynäkologie und Geburtshilfe

ICI-Therapie in der Schwangerschaft wird gut toleriert

Weniger postpartale Depressionen nach Esketamin-Einmalgabe

Bei RSV-Impfung vor 60. Lebensjahr über Off-Label-Gebrauch aufklären!

Harnwegsinfektprophylaxe: Es geht auch ohne Antibiotika

Update Gynäkologie

Springer Medizin

Abstract

Bitte loggen Sie sich ein, um Zugang zu diesem Inhalt zu erhalten

Weitere Artikel der Ausgabe 4/2018

Comparison of Practice Guidelines, BRCAPRO, and Genetic Counselor Estimates to Identify Germline BRCA1 and BRCA2 Mutations in Pancreatic Cancer

Time Costs for Genetic Counseling in Preconception Carrier Screening with Genome Sequencing

Genesurance Counseling: Genetic Counselors’ Roles and Responsibilities in Regards to Genetic Insurance and Financial Topics

“Second-Class Status?” Insight into Communication Patterns and Common Concerns Among Men with Hereditary Breast and Ovarian Cancer Syndrome

Perceived Changes to Obstetric Care and the Integration of Personal and Professional Life as a Pregnant Prenatal Genetic Counselor

Response to Costa, Lemos, and Paneque Letter to the Editor

Neu im Fachgebiet Gynäkologie und Geburtshilfe

ICI-Therapie in der Schwangerschaft wird gut toleriert

Weniger postpartale Depressionen nach Esketamin-Einmalgabe

Bei RSV-Impfung vor 60. Lebensjahr über Off-Label-Gebrauch aufklären!

Harnwegsinfektprophylaxe: Es geht auch ohne Antibiotika

Update Gynäkologie