Abstract

In 2004 prenatal risk assessment (PRA) was implemented as a routine offer to all pregnant women in Denmark. It was argued that primarily the new programme would give all pregnant women an informed choice about whether to undergo prenatal testing. On the basis of ethnographic fieldwork in an ultrasound clinic in Denmark and interviews with pregnant women and their partners, we call into question the assumption underlying the new guidelines that more choice and more objective information is a source of empowerment and control. We focus on one couple's experience of PRA. This case makes it evident how supposed choices in the context of PRA may not be experienced as such. Rather, they are experienced as complicated processes of meaning-making in the relational space between the clinical setting, professional authority and the social life of the couples. PRA users are reluctant to make choices and abandon health professionals as authoritative experts in the face of complex risk knowledge. When assumptions about autonomy and self-determination are inscribed into the social practice of PRA, authority is transferred to the couple undergoing PRA and a new configuration of responsibility evolves between the couple and their relationship to the foetus. It is argued that al-though the new programme of prenatal testing in Denmark presents itself in opposition to quasi-eugenic and paternalistic forms of governing couples' decisions it represents another form of government that works through the notion of choice. An ethics of a shared responsibility of PRA and its outcome would be more in agreement with how decisions are actually made.

Highlights

  • In 2004 prenatal risk assessment (PRA) was implemented as a routine offer to all pregnant women in Denmark

  • This paper reports from an ethnographic study of recent technology for prenatal risk assessment (PRA)

  • In Iceland every pregnant woman is informed about the possibility of undergoing PRA, but if she opts to undergo assessment she has to pay for the examination herself (Kristjánsdóttir 2008)

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Summary

New guidelines on prenatal risk assessment in Denmark

The implementation of prenatal risk assessment as a routine offer to all pregnant women in Denmark was primarily argued with the wish to give all pregnant women a choice as to whether to undergo prenatal testing (Sundhedsstyrelsen 2003a; 2003b; 2004). 1 2008 tive it may look as if the Danish Board of Health implicitly evaluates the prospect of a child being born with Down’s syndrome as more dangerous than the prospect of a healthy child being aborted through an invasive examination by installing a cut-off point which is lower than the risk of inducing a miscarriage by undergoing the test. This illustrates a conflict between achievements on a population level versus achievements on an individual level and indicates that the programme of prenatal testing in Denmark is built upon and shaped by preventive values (Koch 2003). Even though the Danish Board of Health does not characterise the new programme of prenatal testing in Denmark as a preventive screening programme, this study indicates that it is more effective in obtaining the goals of prevention that the previous programme

The study
Entering PRA
Communicating and receiving risk figures
Reflecting upon PRA and making complex risk figures meaningful
Findings
Literature
Full Text
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