Literature DB >> 14718937

Provision of genetic services in Europe: current practices and issues.

Béatrice Godard1, Helena Kääriäinen, Ulf Kristoffersson, Lisbeth Tranebjaerg, Domenico Coviello, Ségolène Aymé.   

Abstract

This paper examines the professional and scientific views on the social, ethical and legal issues that impact on the provision of genetic services in Europe. Many aspects have been considered, such as the definition and the aims of genetic services, their organization, the quality assessment, public education, as well as the partnership with patients support groups and the multicultural aspects. The methods was primarily the analysis of professional guidelines, legal frameworks and other documents related to the organization of genetic services, mainly from Europe, but also from USA and international organizations. Then, the method was to examine the background data emerging from an updated report produced by the Concerted Action on Genetic Services in Europe, as well as the issues debated by 43 experts from 17 European countries invited to an international workshop organized by the European Society of Human Genetics Public and Professional Policy Committee in Helsinki, Finland, 8 and 9 September 2000. Some conclusions were identified from the ESHG workshop to arrive at outlines for optimal genetic services. Participants were concerned about equal accessibility and effectiveness of clinical genetic services, quality assessment of services, professional education, multidisciplinarity and division of tasks as well as networking. Within European countries, adherence to the organizational principles of prioritization, regionalization and integration into related health services would maximize equal accessibility and effectiveness of genetic actions. There is a need for harmonization of the rules involved in financial coverage of DNA tests in order to make these available to all Europeans. Clear guidelines for the best practice will ensure that the provision of genetic services develops in a way that is beneficial to its customers, be they health professionals or the public, especially since the coordination of clinical, laboratory and research perspectives within a single organizational structure permits a degree of coherence not often found in other specialties.

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Year:  2003        PMID: 14718937     DOI: 10.1038/sj.ejhg.5201111

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  30 in total

1.  A profile of the genetic counsellor and genetic nurse profession in European countries.

Authors:  Cristophe Cordier; Debby Lambert; Marie-Antoinette Voelckel; Ulrika Hosterey-Ugander; Heather Skirton
Journal:  J Community Genet       Date:  2011-12-14

2.  The prediction of disease risk in genomic medicine.

Authors:  Wayne D Hall; Katherine I Morley; Jayne C Lucke
Journal:  EMBO Rep       Date:  2004-10       Impact factor: 8.807

Review 3.  Personal genetics: regulatory framework in Europe from a service provider's perspective.

Authors:  Keith A Grimaldi; Markus P Look; G Antonio Scioli; Juan Coll Clavero; Stathis Marinos; Tassos Tagaris
Journal:  Eur J Hum Genet       Date:  2010-12-01       Impact factor: 4.246

Review 4.  Clinical genetics in cardiology.

Authors:  Philippe Charron
Journal:  Heart       Date:  2006-08       Impact factor: 5.994

5.  EuroGentest standing up to scrutiny--first year demonstrates good progress harmonizing community approaches.

Authors:  Richard Hayhurst; Jean-Jacques Cassiman
Journal:  J Appl Genet       Date:  2006       Impact factor: 3.240

6.  Genetic testing in asymptomatic minors: background considerations towards ESHG Recommendations.

Authors:  Pascal Borry; Gerry Evers-Kiebooms; Martina C Cornel; Angus Clarke; Kris Dierickx
Journal:  Eur J Hum Genet       Date:  2009-03-11       Impact factor: 4.246

7.  Identifying outcomes of clinical genetic services: qualitative evidence and methodological considerations.

Authors:  Christalla Pithara
Journal:  J Genet Couns       Date:  2013-09-14       Impact factor: 2.537

Review 8.  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

9.  Recontacting in clinical genetics and genomic medicine? We need to talk about it.

Authors:  Daniele Carrieri; Sandi Dheensa; Shane Doheny; Angus J Clarke; Peter D Turnpenny; Anneke M Lucassen; Susan E Kelly
Journal:  Eur J Hum Genet       Date:  2017-02-08       Impact factor: 4.246

10.  Genetic professionals' views on genetic counsellors: a French survey.

Authors:  Christophe Cordier; Nicolas Taris; Ramona Moldovan; Hagay Sobol; Marie-Antoinette Voelckel
Journal:  J Community Genet       Date:  2015-08-18
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