Delivery of a national prenatal exome sequencing service in England: a mixed methods study exploring healthcare professionals' views and experiences

被引:4
|
作者
Peter, Michelle [1 ,2 ]
Mellis, Rhiannon [1 ,2 ]
McInnes-Dean, Hannah
Daniel, Morgan [1 ,2 ]
Walton, Holly [4 ]
Fisher, Jane [3 ]
Leeson-Beevers, Kerry [5 ]
Allen, Stephanie [6 ]
Baple, Emma L. [7 ,8 ]
Beleza-Meireles, Ana [9 ]
Bertoli, Marta [10 ]
Campbell, Jennifer [11 ]
Canham, Natalie [12 ]
Cilliers, Deirdre [13 ]
Cobben, Jan [14 ,15 ]
Eason, Jacqueline [16 ]
Harrison, Victoria [17 ]
Holder-Espinasse, Muriel [18 ]
Male, Alison [1 ]
Mansour, Sahar [19 ]
McEwan, Alec [20 ]
Park, Soo-Mi [21 ]
Smith, Audrey [22 ]
Stewart, Alison [23 ]
Tapon, Dagmar [24 ]
Vasudevan, Pradeep [25 ]
Williams, Denise [26 ]
Wu, Wing Han [1 ,2 ]
Chitty, Lyn S. [1 ,2 ]
Hill, Melissa [1 ,2 ]
机构
[1] Great Ormond St Hosp Children NHS Fdn Trust, North Thames Genom Lab Hub, London, England
[2] UCL Great Ormond St Inst Child Hlth, Genet & Genom Med, London, England
[3] Antenatal Results & Cho, London, England
[4] UCL, Dept Appl Hlth Res, London, England
[5] Alstrom Syndrome UK, Torquay, England
[6] Cent & South Genom Lab Hub, West Midlands Reg Genet Lab, Birmingham, England
[7] Univ Exeter, Royal Devon Univ Healthcare NHS Fdn Trust, RILD Welcome Wolfson Ctr, Med Sch, Exeter, England
[8] Royal Devon Univ Healthcare NHS Fdn Trust, Peninsula Clin Genet Serv, Exeter, England
[9] St Michaels Hosp, Bristol Reg Genet Serv, Bristol, England
[10] Int Ctr Life, Northern Genet Serv, Newcastle Upon Tyne, England
[11] Leeds Teaching Hosp NHS Trust, Dept Clin Genet, Leeds, England
[12] Liverpool Womens NHS Fdn Trust, Liverpool Ctr Genom Med, Liverpool, England
[13] Oxford Ctr Genom Med, Oxford, England
[14] Imperial Coll, Fac Med, London, England
[15] North West Thames Reg Genet Serv, London, England
[16] Nottingham Univ Hosp NHS Trust, Nottingham Reg Genet Serv, City Hosp Campus, Nottingham, England
[17] Princess Anne Hosp, Wessex Clin Genet Serv, Southampton, England
[18] Guys & St Thomas NHS Fdn Trust, Guys Hosp, Clin Genet Dept, London, England
[19] St Georges Univ Hosp NHS Fdn Trust, London, England
[20] Nottingham Univ Hosp, Dept Obstet & Gynaecol, Nottingham, England
[21] Cambridge Univ Hosp NHS Fdn Trust, Dept Clin Genet, Cambridge, England
[22] St Marys Hosp, Manchester Ctr Genom Med, Manchester, England
[23] Sheffield Clin Genom Serv, Sheffield, England
[24] Imperial Coll Healthcare NHS Trust, Queen Charlottes & Chelsea Hosp, London, England
[25] Univ Hosp Leicester NHS Trust, Dept Clin Genet, Leicester, England
[26] Birmingham Womens & Childrens Hosp NHS Fdn Trust, Clin Genet Unit, Birmingham, England
基金
美国国家卫生研究院;
关键词
prenatal exome sequencing; prenatal diagnosis; genomic sequencing; healthcare professionals; genetic services; service evaluation; genomic medicine service; CHROMOSOMAL MICROARRAY; VARIANTS;
D O I
10.3389/fgene.2024.1401705
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Introduction In October 2020, rapid prenatal exome sequencing (pES) was introduced into routine National Health Service (NHS) care in England, requiring the coordination of care from specialist genetics, fetal medicine (FM) and laboratory services. This mixed methods study explored the experiences of professionals involved in delivering the pES service during the first 2 years of its delivery in the NHS.Methods A survey (n = 159) and semi-structured interviews (n = 63) with healthcare professionals, including clinical geneticists, FM specialists, and clinical scientists (interviews only) were used to address: 1) Views on the pES service; 2) Capacity and resources involved in offering pES; 3) Awareness, knowledge, and educational needs; and 4) Ambitions and goals for the future.Results Overall, professionals were positive about the pES service with 77% rating it as Good or Excellent. A number of benefits were reported, including the increased opportunity for receiving actionable results for parental decision-making, improving equity of access to genomic tests and fostering close relationships between FM and genetics departments. Nonetheless, there was evidence that the shift to offering pES in a clinical setting had brought some challenges, such as additional clinic time, administrative processes, perceived lack of autonomy in decision-making regarding pES eligibility and difficulty engaging with peripheral maternity units. Concerns were also raised about the lack of confidence and gaps in genomics knowledge amongst non-genetics professionals - especially midwives. However, the findings also highlighted value in both FM, obstetric and genetics professionals benefiting from further training with a focus on recognising and managing prenatally diagnosed genetic conditions.Conclusion Healthcare professionals are enthusiastic about the benefits of pES, and through multi-collaborative working, have developed relationships that have contributed to effective communication across specialisms. Although limitations on resources and variation in knowledge about pES have impacted service delivery, professionals were hopeful that improvements to infrastructure and the upskilling of all professionals involved in the pathway would optimise the benefits of pES for both parents and professionals.
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页数:14
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