The experience of 3 years of external quality assessment of preimplantation genetic diagnosis for cystic fibrosis

被引:9
作者
Deans, Zandra [1 ]
Fiorentino, Francesco [2 ]
Biricik, Anil [2 ]
Traeger-Synodinos, Joanne [3 ]
Moutou, Celine [4 ]
De Rycke, Martine [5 ]
Renwick, Pamela [6 ]
SenGupta, Sioban [7 ]
Goossens, Veerle [8 ]
Harton, Gary [9 ]
机构
[1] Royal Infirm Edinburgh NHS Trust, UK NEQAS Edinburgh, UK NEQAS Mol Genet, Dept Lab Med, Edinburgh EH16 4SA, Midlothian, Scotland
[2] Genoma Labs, Rome, Italy
[3] Univ Athens, St Sophias Childrens Hosp, Med Genet Lab, Athens, Greece
[4] SIHCUS CMCO, Serv Biol Reprod, Schiltigheim, France
[5] UZ Brussel, Ctr Med Genet, Brussels, Belgium
[6] Guys & St Thomas NHS Fdn Trust, Ctr Preimplantat Genet Diag, London, England
[7] UCL, Inst Womens Hlth, UCL Ctr PGD, London, England
[8] ESHRE Cent Off, Grimbergen, Belgium
[9] Reprogenetics, Livingston, NJ USA
关键词
external quality assessment; preimplantation genetic diagnosis; cystic fibrosis; ESHRE PGD CONSORTIUM; PRACTICE GUIDELINES; AMPLIFICATION;
D O I
10.1038/ejhg.2012.244
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Preimplantation genetic diagnosis (PGD) was first performed over 20 years ago and has become an accepted part of genetic testing and assisted reproduction worldwide. The techniques and protocols necessary to carry out genetic testing at the single-cell level can be difficult to master and have been developed independently by the laboratories worldwide offering preimplantation testing. These factors indicated the need for an external quality assessment (EQA) scheme for monogenic disease PGD. Toward this end, the European Society for Human Reproduction and Embryology came together with United Kingdom National External Quality Assessment Services for Molecular Genetics, to create a pilot EQA scheme followed by practical EQA schemes for all interested parties. Here, we detail the development of the pilot scheme as well as development and findings from the practical (clinical) schemes that have followed. Results were generally acceptable and there was marked improvement in results and laboratory scores for those labs that participated in multiple schemes. Data from the first three schemes indicate that the EQA scheme is working as planned and has helped laboratories improve their techniques and result reporting. The EQA scheme for monogenic PGD will continue to be developed to offer assessment for other monogenic disorders.
引用
收藏
页码:800 / 806
页数:7
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