Optimising exome prenatal sequencing services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS genomic medicine service

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Hill, Melissa, Ellard, Sian, Fisher, Jane, Fulop, Naomi, Knight, Marian, Kroese, Mark, Ledger, Jean, Leeson-Beevers, Kerry, McEwan, Alec, McMullan, Dominic, Mellis, Rhiannon, Morris, Stephen, Parker, Michael, Tapon, Dagmar, Baple, Emma, Blackburn, Laura, Choudry, Asya, Lafarge, Caroline ORCID: https://orcid.org/0000-0003-2148-078X, McInnes-Dean, Hannah, Peter, Michelle, Ramakrishnan, Rema, Roberts, Lauren, Searle, Beverly, Wynn, Sarah, Han Wu, Wing and Chitty, Lyn (2022) Optimising exome prenatal sequencing services (EXPRESS): a study protocol to evaluate rapid prenatal exome sequencing in the NHS genomic medicine service. NIHR Open Research, 2. p. 10. ISSN 2633-4402

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Official URL: https://doi.org/10.3310/nihropenres.13247.2

Abstract

Background: Prenatal exome sequencing (ES) for the diagnosis of fetal anomalies has been implemented nationally in England through the NHS Genomic Medicine Service that is based around seven regional Genomic Laboratory Hubs (GLHs). Prenatal ES has the potential to significantly improve NHS prenatal diagnostic services by increasing genetic diagnoses and informing prenatal decision-making. Prenatal ES has not previously been offered routinely in a national healthcare system and there are gaps in knowledge and guidance.
Methods: We are conducting a mixed-methods evaluation of the NHS prenatal ES service. Study design draws on a framework developed in previous studies of major system innovation and Normalisation Process Theory. There are five interrelated workstreams. Workstream-1 will use interviews and surveys with professionals, non-participant observations and documentary analysis to produce in-depth case studies at all GLHs. Data collection at multiple time points will track changes over time. In Workstream-2 qualitative interviews with parents offered prenatal ES or with previous experience of fetal anomalies will explore experiences and establish information and support needs. Workstream-3 will analyse data from all prenatal ES tests for nine-months to establish service outcomes (e.g. diagnostic yield, referral rates, referral sources). Comparisons between GLHs will identify factors (individual or service-related) associated with any variation in outcomes. Workstream-4 will identify and analyse practical ethical problems. Requirements for an effective ethics framework for an optimal and equitable service will be determined. Workstream-5 will assess costs and cost-effectiveness of prenatal ES versus standard tests and evaluate costs of implementing an optimal prenatal ES care pathway. Integration of findings will determine key features of an optimal care pathway from a service delivery, parent and professional perspective.
Discussion: The proposed formative and summative evaluation will inform the evolving prenatal ES service to ensure equity of access, high standards of care and benefits for parents across England.

Item Type:	Article
Identifier:	10.3310/nihropenres.13247.2
Keywords:	prenatal exome sequencing, genomic medicine service, ethics, counselling, study protocol, mixed methods
Subjects:	Medicine and health
Related URLs:	Publisher https://doi.org/10.3310/nihropenres.1324... https://openresearch.nihr.ac.uk/articles...
Depositing User:	Caroline Lafarge
Date Deposited:	12 Apr 2022 17:52
Last Modified:	04 Nov 2024 11:38
URI:	https://repository.uwl.ac.uk/id/eprint/8954