Literature DB >> 11478531

Favorable attitudes toward testing for chromosomal abnormalities via analysis of fetal cells in maternal blood.

S T Zamerowski1, M A Lumley, R A Arreola, K Dukes, L Sullivan.   

Abstract

PURPOSE: The NICHD Fetal Cell Isolation Study (NIFTY) was a multicentered project to isolate fetal cells from maternal blood to detect fetal chromosomal abnormalities. The project included a psychosocial component, which is the basis of this article. We examined the attitudes of high-risk pregnant women toward the availability of a maternal blood test to identify fetal chromosomal abnormalities, how women would respond to hypothetical normal and abnormal maternal blood testing results, and the factors associated with a woman's preference to have an invasive procedure in response to a normal maternal blood test.
METHODS: High-risk pregnant women (N = 854) planning to have prenatal diagnostic invasive testing (amniocentesis or chorionic villus sampling) completed a survey.
RESULTS: The women highly favored maternal blood testing. Almost all women would seek invasive testing after an abnormal blood test. Only half of the women would seek invasive testing after a normal blood test; these women were older, more willing to terminate their pregnancy, and valued the increased accuracy of invasive testing more highly than women who would not have invasive testing after a normal maternal blood test.
CONCLUSIONS: Women having invasive diagnostic testing welcome a noninvasive procedure that uses fetal cells in maternal blood, and its availability would decrease invasive testing by approximately 50%. Research needs to examine the attitudes and anticipated responses of other risk groups as well as the effects of information about maternal blood test sensitivity and specificity on attitudes and responses.

Entities:  

Keywords:  Empirical Approach; Genetics and Reproduction

Mesh:

Year:  2001        PMID: 11478531     DOI: 10.1097/00125817-200107000-00006

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  5 in total

1.  Variables influencing pregnancy termination following prenatal diagnosis of fetal chromosome abnormalities.

Authors:  Anne Hawkins; Ana Stenzel; Joanne Taylor; Valerie Y Chock; Louanne Hudgins
Journal:  J Genet Couns       Date:  2012-09-23       Impact factor: 2.537

2.  Demographic and experiential correlates of public attitudes towards cell-free fetal DNA screening.

Authors:  Lauren C Sayres; Megan Allyse; Taylor A Goodspeed; Mildred K Cho
Journal:  J Genet Couns       Date:  2014-04-09       Impact factor: 2.537

3.  Non-invasive prenatal diagnosis for fetal sex determination: benefits and disadvantages from the service users' perspective.

Authors:  Celine Lewis; Melissa Hill; Heather Skirton; Lyn S Chitty
Journal:  Eur J Hum Genet       Date:  2012-03-28       Impact factor: 4.246

4.  Noninvasive prenatal diagnosis: pregnant women's interest and expected uptake.

Authors:  Reana Tischler; Louanne Hudgins; Yair J Blumenfeld; Henry T Greely; Kelly E Ormond
Journal:  Prenat Diagn       Date:  2011-10-26       Impact factor: 3.050

5.  Attitudes towards non-invasive prenatal testing for aneuploidy among US adults of reproductive age.

Authors:  M Allyse; L C Sayres; T A Goodspeed; M K Cho
Journal:  J Perinatol       Date:  2014-03-06       Impact factor: 2.521

  5 in total

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