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'Because of the risks': how US pregnant women account for refusing prenatal screening

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  • Markens, Susan
  • Browner, C. H.
  • Press, Nancy

Abstract

Most research on prenatal fetal testing in general, and maternal alpha-fetoprotein (AFP) screening in particular, has focused on women who accept and even actively seek prenatal diagnosis. Much of this work suggests that agreeing to prenatal diagnosis is inextricably linked to the processes associated with the 'medicalization' of reproduction and that most women do not see refusal as an option. In contrast, little attention has been paid to women who decline fetal diagnosis. Instead, it is generally assumed that women who do so are resisting this thrust toward medicalization and/or are opposed to abortion. Our research is designed to address this imbalance. We analyze how a group of US women who refused the offer of AFP screening account for their decisions and compare their explanations with those of women who took the test. Contrary to our expectations, we found that refusal did not signify rejection of and/or resistance to the offerings of science and technology. Rather, women who refused often employed biomedical categories, particularly the concept of 'risk', to reject its very offerings. Furthermore, refusers and acceptors were more alike than different in their views on abortion, medicalization and pregnancy. We conclude that the key difference between the two groups lies in their interpretation and application of biomedical concepts and modern risk-assessment.

Suggested Citation

  • Markens, Susan & Browner, C. H. & Press, Nancy, 1999. "'Because of the risks': how US pregnant women account for refusing prenatal screening," Social Science & Medicine, Elsevier, vol. 49(3), pages 359-369, August.
  • Handle: RePEc:eee:socmed:v:49:y:1999:i:3:p:359-369
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    Cited by:

    1. Raspberry, Kelly Amanda & Skinner, Debra, 2011. "Negotiating desires and options: How mothers who carry the fragile X gene experience reproductive decisions," Social Science & Medicine, Elsevier, vol. 72(6), pages 992-998, March.
    2. Gottfre[eth]sdóttir, Helga & Björnsdóttir, Kristín & Sandall, Jane, 2009. "How do prospective parents who decline prenatal screening account for their decision? A qualitative study," Social Science & Medicine, Elsevier, vol. 69(2), pages 274-277, July.
    3. Kissling, Alexandra, 2022. "“Thinking with my dad brain, not my man brain”: Understanding Men's and Women's sterilization risk narratives," Social Science & Medicine, Elsevier, vol. 292(C).
    4. Hammer, Raphaël P. & Burton-Jeangros, Claudine, 2013. "Tensions around risks in pregnancy: A typology of women's experiences of surveillance medicine," Social Science & Medicine, Elsevier, vol. 93(C), pages 55-63.
    5. Reid, Bernie & Sinclair, Marlene & Barr, Owen & Dobbs, Frank & Crealey, Grainne, 2009. "A meta-synthesis of pregnant women's decision-making processes with regard to antenatal screening for Down syndrome," Social Science & Medicine, Elsevier, vol. 69(11), pages 1561-1573, December.
    6. García, Elisa & Timmermans, Danielle R.M. & van Leeuwen, Evert, 2008. "The impact of ethical beliefs on decisions about prenatal screening tests: Searching for justification," Social Science & Medicine, Elsevier, vol. 66(3), pages 753-764, February.
    7. Ivry, Tsipy & Teman, Elly & Frumkin, Ayala, 2011. "God-sent ordeals and their discontents: Ultra-orthodox Jewish women negotiate prenatal testing," Social Science & Medicine, Elsevier, vol. 72(9), pages 1527-1533, May.
    8. Di Giacomo, Marina & Piacenza, Massimiliano & Siciliani, Luigi & Turati, Gilberto, 2022. "The effect of co-payments on the take-up of prenatal tests," Journal of Health Economics, Elsevier, vol. 81(C).
    9. 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.
    10. Armstrong, Natalie & Murphy, Elizabeth, 2008. "Weaving meaning? An exploration of the interplay between lay and professional understandings of cervical cancer risk," Social Science & Medicine, Elsevier, vol. 67(7), pages 1074-1082, October.
    11. Shostak, Sara & Zarhin, Dana & Ottman, Ruth, 2011. "What's at stake? Genetic information from the perspective of people with epilepsy and their family members," Social Science & Medicine, Elsevier, vol. 73(5), pages 645-654, September.

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