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Delivery of a national prenatal exome sequencing service in England: a mixed methods study exploring healthcare professionals' views and experiences.
Peter, Michelle; Mellis, Rhiannon; McInnes-Dean, Hannah; Daniel, Morgan; Walton, Holly; Fisher, Jane; Leeson-Beevers, Kerry; Allen, Stephanie; Baple, Emma L; Beleza-Meireles, Ana; Bertoli, Marta; Campbell, Jennifer; Canham, Natalie; Cilliers, Deirdre; Cobben, Jan; Eason, Jacqueline; Harrison, Victoria; Holder-Espinasse, Muriel; Male, Alison; Mansour, Sahar; McEwan, Alec; Park, Soo-Mi; Smith, Audrey; Stewart, Alison; Tapon, Dagmar; Vasudevan, Pradeep; Williams, Denise; Wu, Wing Han; Chitty, Lyn S; Hill, Melissa.
Afiliação
  • Peter M; North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
  • Mellis R; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
  • McInnes-Dean H; North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
  • Daniel M; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
  • Walton H; North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
  • Fisher J; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
  • Leeson-Beevers K; Antenatal Results and Choices, London, United Kingdom.
  • Allen S; Department of Applied Health Research, University College London, London, United Kingdom.
  • Baple EL; Alström Syndrome UK, Torquay, United Kingdom.
  • Beleza-Meireles A; West Midlands Regional Genetics Laboratory, Central and South Genomic Laboratory Hub, Birmingham, United Kingdom.
  • Bertoli M; RILD Wellcome Wolfson Centre, University of Exeter Medical School, Royal Devon University Healthcare NHS Foundation Trust, Exeter, United Kingdom.
  • Campbell J; Peninsula Clinical Genetics Service, School, Royal Devon University Healthcare NHS Foundation Trust, Exeter, United Kingdom.
  • Canham N; Bristol Regional Genetics Service, St Michael's Hospital, Bristol, United Kingdom.
  • Cilliers D; Northern Genetics Service, International Centre for Life, Newcastle upon Tyne, United Kingdom.
  • Cobben J; Department of Clinical Genetics, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
  • Eason J; Liverpool Centre for Genomic Medicine, Liverpool Women's NHS Foundation Trust, Liverpool, United Kingdom.
  • Harrison V; Oxford Centre for Genomic Medicine, Oxford, United Kingdom.
  • Holder-Espinasse M; Faculty of Medicine, Imperial College & North West Thames Regional Genetics Service, London, United Kingdom.
  • Male A; Nottingham Regional Genetics Service, City Hospital Campus, Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.
  • Mansour S; Wessex Clinical Genetics Service, Princess Anne Hospital, Southampton, United Kingdom.
  • McEwan A; Clinical Genetics Department, Guy's Hospital, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.
  • Park SM; St George's University Hospitals NHS Foundation Trust, London, United Kingdom.
  • Smith A; Department of Obstetrics and Gynaecology, Nottingham University Hospitals, Nottingham, United Kingdom.
  • Stewart A; Department of Clinical Genetics, Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom.
  • Tapon D; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester, United Kingdom.
  • Vasudevan P; Sheffield Clinical Genomics Service, Sheffield, United Kingdom.
  • Williams D; Queen Charlotte's and Chelsea Hospital, Imperial College Healthcare NHS Trust, London, United Kingdom.
  • Wu WH; Department of Clinical Genetics, University Hospitals of Leicester NHS Trust, Leicester, United Kingdom.
  • Chitty LS; Clinical Genetics Unit, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, United Kingdom.
  • Hill M; North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom.
Front Genet ; 15: 1401705, 2024.
Article em En | MEDLINE | ID: mdl-38903755
ABSTRACT

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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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article