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Ethnicity, bioethics, and prenatal diagnosis: The amniocentesis decisions of Mexican-origin women and their partners

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Listed:
  • Browner, C.H.
  • Preloran, H.M.
  • Cox, S.J.

Abstract

Bioethical standards and counseling techniques that regulate prenatal diagnosis in the United States were developed at a time when the principal constituency for fetal testing was a self-selected group of White, well- informed, middle-class women. The routine use of α-fetoprotein (AFP) testing, which has become widespread since the mid-1980s, introduced new constituencies to prenatal diagnosis. These new constituencies include ethnic minority women, who, with the exception of women from certain Asian groups, refuse amniocentesis at significantly higher rates than others. This study examines the considerations taken into account by a group of Mexican-origin women who had screened positive for AFP and were deciding whether to undergo amniocentesis. We reviewed 379 charts and interviewed 147 women and 120 partners to test a number of factors that might explain why some women accept amniocentesis and some refuse. A woman's attitudes toward doctors, medicine, and prenatal care and her assessment of the risk and uncertainty associated with the procedure were found to be most significant. Case summaries demonstrate the indeterminacy of the decision-making process. We concluded that established bioethical principles and counseling techniques need to be more sensitive to the way minority clients make their amniocentesis choices.

Suggested Citation

  • Browner, C.H. & Preloran, H.M. & Cox, S.J., 1999. "Ethnicity, bioethics, and prenatal diagnosis: The amniocentesis decisions of Mexican-origin women and their partners," American Journal of Public Health, American Public Health Association, vol. 89(11), pages 1658-1666.
  • Handle: RePEc:aph:ajpbhl:1999:89:11:1658-1666_1
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    Cited by:

    1. Gajdos, Thibault & Garrouste, Clémentine & Geoffard, Pierre-Yves, 2016. "The subjective value of a life with Down syndrome: Evidence from amniocentesis decision," Journal of Economic Behavior & Organization, Elsevier, vol. 127(C), pages 59-69.
    2. Shaw, Alison, 2011. "Risk and reproductive decisions: British Pakistani couples' responses to genetic counselling," Social Science & Medicine, Elsevier, vol. 73(1), pages 111-120, July.
    3. Wild, Kayli & Maypilama, Elaine Lawurrpa & Kildea, Sue & Boyle, Jacqueline & Barclay, Lesley & Rumbold, Alice, 2013. "‘Give us the full story’: Overcoming the challenges to achieving informed choice about fetal anomaly screening in Australian Aboriginal communities," Social Science & Medicine, Elsevier, vol. 98(C), pages 351-360.

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