Cargando…
Receiving results of uncertain clinical relevance from population genetic screening: systematic review & meta-synthesis of qualitative research
Genetic screening can be hugely beneficial, yet its expansion poses clinical and ethical challenges due to results of uncertain clinical relevance (such as ‘cystic fibrosis screen positive, inconclusive diagnosis’/CFSPID). This review systematically identifies, appraises, and synthesises the qualita...
Autores principales: | Johnson, Faye, Ulph, Fiona, MacLeod, Rhona, Southern, Kevin W. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9090782/ https://www.ncbi.nlm.nih.gov/pubmed/35256770 http://dx.doi.org/10.1038/s41431-022-01054-5 |
Ejemplares similares
-
Psychological Impact on Parents of an Inconclusive Diagnosis Following Newborn Bloodspot Screening for Cystic Fibrosis: A Qualitative Study
por: Johnson, Faye, et al.
Publicado: (2019) -
Processing of positive newborn screening results: a qualitative exploration of current practice in England
por: Chudleigh, Jane, et al.
Publicado: (2020) -
Qualitative exploration of health professionals’ experiences of communicating positive newborn bloodspot screening results for nine conditions in England
por: Chudleigh, Jane, et al.
Publicado: (2020) -
Parents' responses to receiving sickle cell or cystic fibrosis carrier results for their child following newborn screening
por: Ulph, Fiona, et al.
Publicado: (2015) -
Constructing a Bioethical Framework to Evaluate and Optimise Newborn Bloodspot Screening for Cystic Fibrosis
por: Armstrong, Rachael E., et al.
Publicado: (2020)