Literature DB >> 33453057

Valuing genetic and genomic testing in France: current challenges and latest evidence.

Catherine Lejeune1, Ines F Amado2.   

Abstract

High-throughput next-generation sequencing technologies have seen an increase in use in most developed countries. The translation of genomic testing into clinical practice challenges the traditional model of medical care in France and raises numerous medical, legal, ethical, organizational, and financial issues. In order to allow the population to use this revolution to its advantage, France has conceived the French Plan for Genomic Medicine 2025. Its aim is to improve health and quality of life, to organize new pathways of care and counseling, and to make decisions about insurance coverage. It has also been designed to drive innovation and promote economic growth in France by incorporating genomic medicine into the French health care system. These issues can be addressed through evaluations developed to aid the decision-making process in the context of resource scarcity. Health economists can help to resolve these resource allocation challenges by measuring the impact of this technological revolution on patients, caregivers, providers, and the health care system. In this paper, we will review challenges associated with implementing genomic testing in France. One of the pilot studies of the French Plan for Genomic Medicine 2025 will be presented as an illustration of the role of health economists in overcoming some of the challenges of this technological revolution.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH, DE part of Springer Nature.

Entities:  

Keywords:  Economics; Genomics; Health care pathway; Public health

Year:  2021        PMID: 33453057      PMCID: PMC9530102          DOI: 10.1007/s12687-020-00503-2

Source DB:  PubMed          Journal:  J Community Genet        ISSN: 1868-310X


  18 in total

1.  Predictive genetic tests and health system costs.

Authors:  Steve Morgan; Jeremiah Hurley; Fiona Miller; Mita Giacomini
Journal:  CMAJ       Date:  2003-04-15       Impact factor: 8.262

Review 2.  Personal utility in genomic testing: a systematic literature review.

Authors:  Jennefer N Kohler; Erin Turbitt; Barbara B Biesecker
Journal:  Eur J Hum Genet       Date:  2017-03-15       Impact factor: 4.246

Review 3.  Ethical, Legal, and Social Implications of Personalized Genomic Medicine Research: Current Literature and Suggestions for the Future.

Authors:  Shawneequa L Callier; Rachel Abudu; Maxwell J Mehlman; Mendel E Singer; Duncan Neuhauser; Charlisse Caga-Anan; Georgia L Wiesner
Journal:  Bioethics       Date:  2016-11       Impact factor: 1.898

4.  Preference heterogeneity with respect to whole genome sequencing. A discrete choice experiment among parents of children with rare genetic diseases.

Authors:  Christine Peyron; Aurore Pélissier; Sophie Béjean
Journal:  Soc Sci Med       Date:  2018-08-21       Impact factor: 4.634

5.  A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorder.

Authors:  Kate Tsiplova; Richard M Zur; Christian R Marshall; Dimitri J Stavropoulos; Sergio L Pereira; Daniele Merico; Edwin J Young; Wilson W L Sung; Stephen W Scherer; Wendy J Ungar
Journal:  Genet Med       Date:  2017-05-04       Impact factor: 8.822

6.  Genome-Wide Sequencing for Unexplained Developmental Disabilities or Multiple Congenital Anomalies: A Health Technology Assessment.

Authors: 
Journal:  Ont Health Technol Assess Ser       Date:  2020-03-06

7.  Are whole-exome and whole-genome sequencing approaches cost-effective? A systematic review of the literature.

Authors:  Katharina Schwarze; James Buchanan; Jenny C Taylor; Sarah Wordsworth
Journal:  Genet Med       Date:  2018-02-15       Impact factor: 8.822

8.  Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability.

Authors:  Glen R Monroe; Gerardus W Frederix; Sanne M C Savelberg; Tamar I de Vries; Karen J Duran; Jasper J van der Smagt; Paulien A Terhal; Peter M van Hasselt; Hester Y Kroes; Nanda M Verhoeven-Duif; Isaäc J Nijman; Ellen C Carbo; Koen L van Gassen; Nine V Knoers; Anke M Hövels; Mieke M van Haelst; Gepke Visser; Gijs van Haaften
Journal:  Genet Med       Date:  2016-02-04       Impact factor: 8.822

9.  What is the clinical utility of genetic testing?

Authors:  Scott D Grosse; Muin J Khoury
Journal:  Genet Med       Date:  2006-07       Impact factor: 8.822

10.  Beyond clinical utility: The multiple values of DTC genetics.

Authors:  Mauro Turrini; Barbara Prainsack
Journal:  Appl Transl Genom       Date:  2016-02-01
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  2 in total

1.  Resource allocation in genetic and genomic medicine.

Authors:  J Buchanan; I Goranitis; I Slade; A Kerasidou; M Sheehan; K Sideri; S Wordsworth
Journal:  J Community Genet       Date:  2022-10

2.  Continuing the sequence? Towards an economic evaluation of whole genome sequencing for the diagnosis of rare diseases in Scotland.

Authors:  Michael Abbott; Lynda McKenzie; Blanca Viridiana Guizar Moran; Sebastian Heidenreich; Rodolfo Hernández; Lynne Hocking-Mennie; Caroline Clark; Joana Gomes; Anne Lampe; David Baty; Ruth McGowan; Zosia Miedzybrodzka; Mandy Ryan
Journal:  J Community Genet       Date:  2021-08-20
  2 in total

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