Literature DB >> 17575456

Report of an international survey of molecular genetic testing laboratories.

Margaret M McGovern1, Rob Elles, Isabella Beretta, Martin J Somerville, Gerald Hoefler, Mauri Keinanen, David Barton, Nancy Carson, Elisabeth Dequeker, Radim Brdicka, Alena Blazkova, Ségolène Aymé, Birgit Schnieders, Clemens R Muller, Vibeke Dalen, Armando Albert Martinez, Ulf Kristoffersson, Meral Ozguc, Hansjakob Mueller, Joe Boone, Ira M Lubin, Jorge Sequeiros, Domenica Taruscio, Bob Williamson, Lynn Mainland, Hiroshi Yoshikura, Elettra Ronchi.   

Abstract

OBJECTIVE: To collect data on the practices of molecular genetic testing (MGT) laboratories for the development of national and international policies for quality assurance (QA).
METHODS: A web-based survey of MGT laboratory directors (n = 827; response rate 63%) in 18 countries on 3 continents. QA and reporting indices were developed and calculated for each responding laboratory.
RESULTS: Laboratory setting varied among and within countries, as did qualifications of the directors. Respondents in every country indicated that their laboratory receives specimens from outside their national borders (64%, n = 529). Pair-wise comparisons of the QA index revealed a significant association with the director having formal training in molecular genetics (p < 0.005), affiliation with a genetics unit (p = 0.003), accreditation of the laboratory (p < 0.005) and participation in proficiency testing (p < 0.005). Research labs had a lower mean report score compared to all other settings (p < 0.05) as did laboratories accessioning <150 samples per year.
CONCLUSION: MGT is provided under widely varying conditions and regulatory frameworks. The data provided here may be a useful guide for policy action at both governmental and professional levels. Copyright 2007 S. Karger AG, Basel.

Mesh:

Year:  2007        PMID: 17575456     DOI: 10.1159/000101753

Source DB:  PubMed          Journal:  Community Genet        ISSN: 1422-2795


  10 in total

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Authors:  Sarah Berwouts; Michael A Morris; Elisabeth Dequeker
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Review 3.  Regulatory issues for genetic testing in clinical practice.

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Authors:  Lisa V Kalman; Ira M Lubin; Shannon Barker; Desiree du Sart; Rob Elles; Wayne W Grody; Mario Pazzagli; Sue Richards; Iris Schrijver; Barbara Zehnbauer
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Review 5.  A review of consent practices and perspectives for pharmacogenetic testing.

Authors:  Susanne B Haga; Rachel Mills
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8.  Quality standards and samples in genetic testing.

Authors:  David Ravine; Graeme Suthers
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9.  Health care providers and direct-to-consumer access and advertising of genetic testing in the United States.

Authors:  Melanie F Myers
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  10 in total

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