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Genetic screening in maternity care

Preventive Aims and Voluntary Choices

Bibliographic Data

ID2248599
AuthorsPiia Jallinoja (0000-0002-3889-2636, University of Helsinki, corresponding author)
Year2001
Volume23
Issue3
Pages286-307
Publication date2001-05-01
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueSociology of Health & Illness (JOURNAL)
Journal identifiersISSN: 0141-9889 • E-ISSN: 1467-9566
PublisherWiley (PUBLISHER • GB)
DOI10.1111/1467-9566.00253
OpenAlexW2073215034
LanguageEN
Citations received7
References cited13

This paper analyses a prenatal genetic screening programme for three gene defects, conducted at maternity care centres in Eastern Finland in 1995 and 1996. What is special in this case is that the screening ended sooner than was planned. This paper investigates how the genetic screening programme was launched, the problems it encountered and the circumstances of its closure. The present analysis focuses on the co-existence of, and tensions between, the two major objectives of the project: preventing disability and increasing mothers' choices. The tensions between these two objectives were highlighted at maternity care centres. The public health nurses working at these centres were confused about whether or not they should offer autonomous consumer choice or guidance to mothers to behave in responsible and health-conscious ways. The nurses' confusion was intensified because the goal of prevention was identified with financial savings for the municipality, which the nurses thought was an inappropriate reason for abortions

Closure (psychology) · Confusion · Economic growth · Economics · Eugenics · Health care · Maternity care · Political science · Turnover · BRCA gene mutations in cancer · Ethics and Legal Issues in Pediatric Healthcare · Foucault, Power, and Ethics · Medicine · Nursing · Psychology

  • ‘The alien baby’

    Sky Gross, Sky E Gross•Health Risk & Society•2010

  • Parental and professional agency in terminations for fetal anomalies

    Open Access•Katriina Koponen, Kaisa Laaksonen et al.•Scandinavian Journal of…•2012

  • Too Old to Become a Mother? Risk Constructions in 35+ Women's Experiences of Pregnancy, Child-Birth, and Postnatal Care

    Minna Kelhä•NORA - Nordic Journal of Feminist…•2009

  • Risk and anxiety

    Open Access•Ilpo Helén•Critical Public Health•2002

  • Ethics of clinical genetics

    Open Access•Piia Jallinoja, Piia T Jallinoja•Critical Public Health•2002

  • Innovative Health Technologies and the Social

    Open Access•Andrew Webster•Current Sociology•2002

  • Empty ethics

    Open Access•Owen Corrigan, Oonagh Corrigan•Sociology of Health & Illness•2003

  • Risk and Misfortune

    Judith Green•Risk and Misfortune•2013

  • Counselling the genetically ‘at risk’

    Alan Petersen•Health Risk & Society•1999

  • Genetics, choice and responsibility

    Ruth Chadwick•Health Risk & Society•1999

  • Managing genetic testing

    Open Access•Annemiek Nelis•New Genetics and Society•1999

  • The new genetics and the politics of public health

    Open Access•Alan Petersen•Critical Public Health•1998

  • Choices and Rights

    Tom Shakespeare•Disability & Society•1998

  • Eugenics and the New Genetics in Britain

    Open Access•Anne Kerr, Sarah Cunningham-Burley et al.•Science Technology & Human Values•1998

  • The sociology of entrenchment

    Open Access•Lene Koch, Dirk Stemerding•Social Science & Medicine•1994

  • The Molecular Biological Bandwagon in Cancer Research

    Joan H Fujimura•Social Problems•1988

  • Ontological Politics. A Word and Some Questions

    Open Access•A Mol•The Sociological Review•1998

  • Defining the 'social

    Open Access•Sarah Cunningham-Burley, Sarah Cunningham‐burley et al.•Sociology of Health & Illness•1999

  • Experts as 'storytellers' in reproductive genetics

    Open Access•E Ettorre•Sociology of Health & Illness•1999

Unique citing works7
Citations per year0,29
Citation span2002 - 2012 (11)
Citation velocityhistorical
Highly citedNo
Citation typesNeutral: 7

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