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dc.contributor.authorHill, M
dc.contributor.authorWright, D
dc.contributor.authorDaley, R
dc.contributor.authorLewis, C
dc.contributor.authorMcKay, F
dc.contributor.authorMason, S
dc.contributor.authorLench, N
dc.contributor.authorHowarth, A
dc.contributor.authorBoustred, C
dc.contributor.authorLo, K
dc.contributor.authorPlagnol, V
dc.contributor.authorSpencer, K
dc.contributor.authorFisher, J
dc.contributor.authorKroese, M
dc.contributor.authorMorris, S
dc.contributor.authorChitty, LS
dc.date.accessioned2017-08-29T12:20:55Z
dc.date.issued2014-07-16
dc.description.abstractBACKGROUND: 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. NIHR PORTFOLIO NUMBER: 13865.en_GB
dc.description.sponsorshipThis manuscript presents independent research funded by the National Institute for Health Research (NIHR) under the Programme Grants for Applied Research programme (RP-PG-0707-10107) (the "RAPID" project). LSC is partially funded by the Great Ormond Street Hospital Children’s Charity and the NIHR Biomedical Research Centre at Great Ormond Street Hospital. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health.en_GB
dc.identifier.citationVol. 14, article. 229en_GB
dc.identifier.doi10.1186/1471-2393-14-229
dc.identifier.urihttp://hdl.handle.net/10871/29101
dc.language.isoenen_GB
dc.publisherBioMed Centralen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/25027965en_GB
dc.rights© Hill et al.; licensee BioMed Central Ltd. 2014. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.en_GB
dc.subjectBiomarkersen_GB
dc.subjectChromosome Disordersen_GB
dc.subjectChromosomes, Human, Pair 13en_GB
dc.subjectChromosomes, Human, Pair 18en_GB
dc.subjectDNAen_GB
dc.subjectDown Syndromeen_GB
dc.subjectEnglanden_GB
dc.subjectFees and Chargesen_GB
dc.subjectFemaleen_GB
dc.subjectGenetic Testingen_GB
dc.subjectHumansen_GB
dc.subjectPatient Acceptance of Health Careen_GB
dc.subjectPatient Education as Topicen_GB
dc.subjectPregnancyen_GB
dc.subjectPrenatal Diagnosisen_GB
dc.subjectResearch Designen_GB
dc.subjectScotlanden_GB
dc.subjectState Medicineen_GB
dc.subjectTrisomyen_GB
dc.titleEvaluation of non-invasive prenatal testing (NIPT) for aneuploidy in an NHS setting: a reliable accurate prenatal non-invasive diagnosis (RAPID) protocolen_GB
dc.typeArticleen_GB
dc.date.available2017-08-29T12:20:55Z
exeter.place-of-publicationEnglanden_GB
dc.descriptionThis is the final version of the article. Available from BioMed Central via the DOI in this record.en_GB
dc.identifier.journalBMC Pregnancy and Childbirthen_GB
dc.rights.urihttp://creativecommons.org/licenses/by/4.0


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© Hill et al.; licensee BioMed Central Ltd. 2014. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Except where otherwise noted, this item's licence is described as © Hill et al.; licensee BioMed Central Ltd. 2014. This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.