Evaluation of non-invasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal non-invasive diagnosis (RAPID) protocol

被引:61
作者
Hill, Melissa [1 ,2 ,3 ]
Wright, David [4 ]
Daley, Rebecca [1 ,5 ]
Lewis, Celine [1 ,2 ,3 ]
Mckay, Fiona [1 ]
Mason, Sarah [1 ]
Lench, Nicholas [1 ]
Howarth, Abigail [1 ]
Boustred, Christopher [1 ]
Lo, Kitty [6 ]
Plagnol, Vincent [6 ]
Spencer, Kevin [7 ]
Fisher, Jane [8 ]
Kroese, Mark [9 ]
Morris, Stephen [10 ]
Chitty, Lyn S. [1 ,2 ,3 ,5 ]
机构
[1] Children NHS Fdn Trust, Great Ormond St Hosp, North East Thames Reg Genet Serv, London WC1N 3BH, England
[2] Children NHS Fdn Trust, UCL Inst Child Hlth, London WC1N 3BH, England
[3] Children NHS Fdn Trust, Great Ormond St Hosp, London WC1N 3BH, England
[4] Univ Plymouth, Ctr Med Stat & Bioinformat, Plymouth PL4 8AA, Devon, England
[5] UCL, Hosp NHS Fdn Trust, Fetal Med Unit, London, England
[6] UCL Genet Inst, London, England
[7] Barking Havering & Redbridge Univ Hosp NHS Trust, Clin Biochem Dept, Romford, Essex, England
[8] Antenatal Results & Choices, London, England
[9] PHG Fdn, Cambridge, England
[10] UCL, Res Dept Appl Hlth Res, London, England
关键词
Non-invasive prenatal testing; Cell-free fetal DNA; Aneuploidy; Prenatal diagnosis; FETAL ANEUPLOIDY; DOWN-SYNDROME; HEALTH-PROFESSIONALS; 1ST TRIMESTER; DNA; WOMENS; VIEWS; PREFERENCES; TRISOMY-13; ATTITUDES;
D O I
10.1186/1471-2393-14-229
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background: Non-invasive prenatal testing (NIPT) for aneuploidies is now available through commercial companies in many countries, including through private practice in the United Kingdom (UK). Thorough evaluation of service delivery requirements are needed to facilitate NIPT being offered more widely within state funded healthcare systems such as the UK's National Health Service (NHS). Successful implementation will require the development of laboratory standards, consideration of stakeholder views, an analysis of costs and development of patient and health professional educational materials. Methods/Design: NIPT will be offered in an NHS setting as a contingent screening test. Pregnant woman will be recruited through six maternity units in England and Scotland. Women eligible for Down's syndrome screening (DSS) will be informed about the study at the time of booking. Women that choose routine DSS will be offered NIPT if they have a screening risk >= 1:1000. NIPT results for trisomy 21, 18, 13 will be reported within 7-10 working days. Data on DSS, NIPT and invasive testing uptake, pregnancy outcomes and test efficacy will be collected. Additional data will be gathered though questionnaires to a) determine acceptability to patients and health professionals, b) evaluate patient and health professional education, c) assess informed choice in women accepting or declining testing and d) gauge family expenses. Qualitative interviews will also be conducted with a sub-set of participating women and health professionals. Discussion: The results of this study will make a significant contribution to policy decisions around the implementation of NIPT for aneuploidies within the UK NHS. The laboratory standards for testing and reporting, education materials and counselling strategies developed as part of the study are likely to underpin the introduction of NIPT into NHS practice.
引用
收藏
页数:10
相关论文
共 51 条
[1]   Attitudes towards non-invasive prenatal testing for aneuploidy among US adults of reproductive age [J].
Allyse, M. ;
Sayres, L. C. ;
Goodspeed, T. A. ;
Cho, M. K. .
JOURNAL OF PERINATOLOGY, 2014, 34 (06) :429-434
[2]   Noninvasive Prenatal Testing for Fetal Aneuploidy [J].
不详 .
OBSTETRICS AND GYNECOLOGY, 2012, 120 (06) :1532-1534
[3]   Trisomy 13 detection in the first trimester of pregnancy using a chromosome-selective cell-free DNA analysis method [J].
Ashoor, G. ;
Syngelaki, A. ;
Wang, E. ;
Struble, C. ;
Oliphant, A. ;
Song, K. ;
Nicolaides, K. H. .
ULTRASOUND IN OBSTETRICS & GYNECOLOGY, 2013, 41 (01) :21-25
[4]   Chromosome-selective sequencing of maternal plasma cell-free DNA for first-trimester detection of trisomy 21 and trisomy 18 [J].
Ashoor, Ghalia ;
Syngelaki, Argyro ;
Wagner, Marion ;
Birdir, Cahit ;
Nicolaides, Kypros H. .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2012, 206 (04) :322.e1-322.e5
[5]   Prenatal Detection of Down Syndrome using Massively Parallel Sequencing (MPS): a rapid response statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, 24 October 2011 [J].
Benn, Peter ;
Borrell, Antoni ;
Cuckle, Howard ;
Dugoff, Lorraine ;
Gross, Susan ;
Johnson, Jo-ann ;
Maymon, Ron ;
Odibo, Anthony ;
Schielen, Peter ;
Spencer, Kevin ;
Wright, Dave ;
Yaron, Yuval .
PRENATAL DIAGNOSIS, 2012, 32 (01) :1-2
[6]   Genome-Wide Fetal Aneuploidy Detection by Maternal Plasma DNA Sequencing [J].
Bianchi, Diana W. ;
Platt, Lawrence D. ;
Goldberg, James D. ;
Abuhamad, Alfred Z. ;
Sehnert, Amy J. ;
Rava, Richard P. .
OBSTETRICS AND GYNECOLOGY, 2012, 119 (05) :890-901
[7]  
Braun V., 2006, Qualitative Research in Psychology, V3, P77, DOI 10.1191/1478088706qp063oa
[8]   Uptake of noninvasive prenatal testing (NIPT) in women following positive aneuploidy screening [J].
Chetty, Shilpa ;
Garabedian, Matthew J. ;
Norton, Mary E. .
PRENATAL DIAGNOSIS, 2013, 33 (06) :542-546
[9]   Noninvasive prenatal testing for aneuploidy-ready for prime time? [J].
Chitty, Lyn S. ;
Hill, Melissa ;
White, Helen ;
Wright, David ;
Morris, Stephen .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2012, 206 (04) :269-275
[10]   Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study [J].
Chiu, Rossa W. K. ;
Akolekar, Ranjit ;
Zheng, Yama W. L. ;
Leung, Tak Y. ;
Sun, Hao ;
Chan, K. C. Allen ;
Lun, Fiona M. F. ;
Go, Attie T. J. I. ;
Lau, Elizabeth T. ;
To, William W. K. ;
Leung, Wing C. ;
Tang, Rebecca Y. K. ;
Au-Yeung, Sidney K. C. ;
Lam, Helena ;
Kung, Yu Y. ;
Zhang, Xiuqing ;
van Vugt, John M. G. ;
Minekawa, Ryoko ;
Tang, Mary H. Y. ;
Wang, Jun ;
Oudejans, Cees B. M. ;
Lau, Tze K. ;
Nicolaides, Kypros H. ;
Lo, Y. M. Dennis .
BMJ-BRITISH MEDICAL JOURNAL, 2011, 342 :217