Neonatal screening for cystic fibrosis: France rises to the challenge
- 72 Downloads
Summary: This paper describes the adjustments to the French neonatal screening programme required by the introduction of systematic screening for cystic fibrosis (CF), taking into account both the legal and statutory framework and the lessons of a pilot study carried out 10 years ago. The French association for the screening and prevention of infant handicaps (AFDPHE) has been mandated by its regulatory agencies to organize screening for CF in France (metropolitan and overseas territories). During the year 2001, expert groups (Technical Aspects, Information, Ethics and Genetics, Criteria for CF Centres, Protocol for the Care of a Newborn with CF) issued recommendations for the establishment of a national programme that would guarantee efficiency and adequate patient care from the time of diagnosis onward. The programme is based on a strategy combining immunoreactive trypsin (IRT) assay and the analysis of DNA mutations in dried blood samples obtained at 3 days of age. When an elevated IRT value is found, DNA analysis is performed on the same sample. Owing to the relative regional heterogeneity existing in France, 30 selected mutations are used, which provide 85% coverage. The Ethics and Genetics Committee recommended that, in order to avoid arousing anxiety by a recall, informed consent, according to the French legislation on bioethics, should be obtained for all neonates at birth by having the parents sign directly on the sampling paper. Information brochures for parents and health professionals have been designed. A new organization of patient care, involving the creation of CF centres recognized by the Ministry of Health, has been decided; all children diagnosed are to be referred to such centres, where they can be well cared for by a trained staff with sufficient means. The programme was implemented region by region in France, from the beginning of the year 2002 to early 2003. The expert groups still meet periodically to evaluate the implementation of the programme and to check that the terms of the agreement between the AFDPHE and the Social Security Agency are complied with.
KeywordsCystic Fibrosis Cystic Fibrosis Patient Congenital Adrenal Hyperplasia Neonatal Screening Sweat Test
Unable to display preview. Download preview PDF.
- Dhondt JL, Farriaux JP (1997) Impact of French legislation on neonatal screening. In Knoppers BM, ed. Human DNA: Law and Policy. The Hague: Kluwer Law International, 285–289.Google Scholar
- Duchassaing D, Dingeon B, Chalas J, Coude M, Coulhon M-P, Launay J-M (2002) Gentique mol6culaire: les 'bonnes pratiques' pré-et postanalytiques. Ann Biol Clin 60: 617–621.Google Scholar
- Feldmann D, Guittard C, Des Georges M, et al (2001) Diagnostic molculaire de la mucoviscidose: valuation de la trousse Elucigene® CF20 dans le sang et les cellules buccales. Ann Biol Clin 59: 277–283.Google Scholar
- Pollitt RJ, Green A, McCabe CJ, et al (1997) Neonatal screening for inborn errors of metabolism: cost, yield and outcome. Health Technology Assessment 1(7) (http: / /www.ncchta.org).Google Scholar
- Wilson JMG, Jungner G (1968) Principles of Screening for Disease. Geneva: World Health Organization, 26–39.Google Scholar