Literature DB >> 17368860

Implementation of preconceptional carrier screening for cystic fibrosis and haemoglobinopathies: a sociotechnical analysis.

Roos Achterbergh1, Phillis Lakeman, Dirk Stemerding, Ellen H M Moors, Martina C Cornel.   

Abstract

OBJECTIVE: To obtain more insight into the process of potential implementation of a screening program, which aims to identify carriers of cystic fibrosis and haemoglobinopathies before pregnancy, in order to enable couples at high risk of having a child with these disorders, to make informed reproductive decisions.
METHODS: Use of sociotechnical analysis, based on a model of co-evolution between technology and society, and, for comparison, the study of the implementation processes of two already existing health care programs with similar aspects to the screening program at issue.
RESULTS: Factors important for success appeared to be the existence of sociotechnical niches, in which technological options can be developed and studied in an experimental setting; a structural approach of providing information to future parents; a party that can articulate demand; governmental involvement in the attunement between various stakeholders; and a screening infrastructure in which large-scale DNA diagnostic services are available.
CONCLUSIONS: Successful implementation of preconceptional carrier screening for cystic fibrosis and haemoglobinopathies will depend on changes at both regime and landscape level, including the establishment of a new preconceptional health care setting and a clearly visible public health authority which can coordinate, monitor and evaluate such an initiative in public health care.

Entities:  

Mesh:

Year:  2007        PMID: 17368860     DOI: 10.1016/j.healthpol.2007.02.007

Source DB:  PubMed          Journal:  Health Policy        ISSN: 0168-8510            Impact factor:   2.980


  16 in total

1.  Ethical, legal, and social issues in health technology assessment for prenatal/preconceptional and newborn screening: a workshop report.

Authors:  B K Potter; D Avard; V Entwistle; C Kennedy; P Chakraborty; M McGuire; B J Wilson
Journal:  Public Health Genomics       Date:  2008-09-03       Impact factor: 2.000

Review 2.  Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders.

Authors:  Frauke Becker; Carla G van El; Dolores Ibarreta; Eleni Zika; Stuart Hogarth; Pascal Borry; Anne Cambon-Thomsen; Jean Jacques Cassiman; Gerry Evers-Kiebooms; Shirley Hodgson; A Cécile J W Janssens; Helena Kaariainen; Michael Krawczak; Ulf Kristoffersson; Jan Lubinski; Christine Patch; Victor B Penchaszadeh; Andrew Read; Wolf Rogowski; Jorge Sequeiros; Lisbeth Tranebjaerg; Irene M van Langen; Helen Wallace; Ron Zimmern; Jörg Schmidtke; Martina C Cornel
Journal:  Eur J Hum Genet       Date:  2011-04       Impact factor: 4.246

3.  Developing a framework for implementation of genetic services: learning from examples of testing for monogenic forms of common diseases.

Authors:  Tessel Rigter; Lidewij Henneman; Jacqueline E W Broerse; Maggie Shepherd; Ignacio Blanco; Ulf Kristoffersson; Martina C Cornel
Journal:  J Community Genet       Date:  2014-06-04

Review 4.  Societal implications of expanded universal carrier screening: a scoping review.

Authors:  Lieke M van den Heuvel; Nina van den Berg; A Cecile J W Janssens; Erwin Birnie; Lidewij Henneman; Wybo J Dondorp; Mirjam Plantinga; Irene M van Langen
Journal:  Eur J Hum Genet       Date:  2022-09-12       Impact factor: 5.351

5.  Dynamics of reproductive genetic technologies: Perspectives of professional stakeholders.

Authors:  Ivy van Dijke; Carla G van El; Phillis Lakeman; Mariëtte Goddijn; Tessel Rigter; Martina C Cornel; Lidewij Henneman
Journal:  PLoS One       Date:  2022-06-21       Impact factor: 3.752

6.  Attitudes of general practitioners and midwives towards ethnicity-based haemoglobinopathy-carrier screening.

Authors:  Suze M P J Jans; Ank de Jonge; Lidewij Henneman; Martina C Cornel; Antoinette L M Lagro-Janssen
Journal:  Eur J Hum Genet       Date:  2012-05-02       Impact factor: 4.246

7.  A case study of haemoglobinopathy screening in the Netherlands: witnessing the past, lessons for the future.

Authors:  Suze M P J Jans; Carla G van El; Eddy S Houwaart; Marjan J Westerman; Rien J P A Janssens; Antoinette L M Lagro-Janssen; Anne Marie C Plass; Martina C Cornel
Journal:  Ethn Health       Date:  2011-08-08       Impact factor: 2.772

8.  Improving test properties for neonatal cystic fibrosis screening in the Netherlands before the nationwide start by May 1st 2011.

Authors:  Martina C Cornel; Johan J P Gille; J Gerard Loeber; Annette M M Vernooij-van Langen; Jeannette Dankert-Roelse; Piet A Bolhuis
Journal:  J Inherit Metab Dis       Date:  2012-07       Impact factor: 4.982

9.  The promises of genomic screening: building a governance infrastructure. Special issue: genetics and democracy.

Authors:  Martina C Cornel; Carla G van El; Wybo J Dondorp
Journal:  J Community Genet       Date:  2011-07-07

10.  Raising awareness of carrier testing for hereditary haemoglobinopathies in high-risk ethnic groups in the Netherlands: a pilot study among the general public and primary care providers.

Authors:  Stephanie S Weinreich; Elly Sm de Lange-de Klerk; Frank Rijmen; Martina C Cornel; Marja de Kinderen; Anne Marie C Plass
Journal:  BMC Public Health       Date:  2009-09-15       Impact factor: 3.295

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