Johnson, Faye, Ulph, Fiona, MacLeod, Rhona and Southern, Kevin W 
ORCID: 0000-0001-6516-9083
(2022)
Receiving results of uncertain clinical relevance from population genetic screening: systematic review & meta-synthesis of qualitative research.
EUROPEAN JOURNAL OF HUMAN GENETICS, 30 (5).
pp. 520-531.
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Receiving results of uncertain clinical relevance from population genetic screening systematic review & meta-synthesis of qu.pdf - Published version Download (1MB) | Preview |
Abstract
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 qualitative research on experiences of receiving results of uncertain clinical relevance from population genetic screening. Eight databases were systematically searched for original qualitative research using the SPIDER framework, and checked against inclusion criteria by the research team and an independent researcher. Nine papers were included (from USA, Canada, UK, New Zealand). PRISMA, ENTREQ, and EMERGE guidance were used to report. Quality was appraised using criteria for qualitative research. All papers focused on parental responses to uncertain results from newborn screening. Data were synthesised using meta-ethnography and first- and second-order constructs. Findings suggest that results of uncertain clinical relevance are often experienced in the same way as a 'full-blown' diagnosis. This has significant emotional and behavioural impact, for example adoption of lifestyle-altering disease-focused behaviours. Analysis suggests this may be due to the results not fitting a common medical model, leading recipients to interpret the significance of the result maladaptively. Findings suggest scope for professionals to negotiate and reframe uncertain screening results. Clearer initial communication is needed to reassure recipients there is no immediate severe health risk from these types of results. Public understanding of an appropriate medical model, that accounts for uncertain genetic screening results in a non-threatening way, may be key to maximising the benefits of genomic medicine and minimising potential psychological harm.
| Item Type: | Article |
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| Uncontrolled Keywords: | Humans, Uncertainty, Parents, Genetics, Population, Qualitative Research, Genetic Testing |
| Divisions: | Faculty of Health and Life Sciences Faculty of Health and Life Sciences > Institute of Life Courses and Medical Sciences |
| Depositing User: | Symplectic Admin |
| Date Deposited: | 20 May 2022 13:31 |
| Last Modified: | 18 Jan 2023 21:01 |
| DOI: | 10.1038/s41431-022-01054-5 |
| Open Access URL: | https://www.nature.com/articles/s41431-022-01054-5 |
| Related URLs: | |
| URI: | https://livrepository.liverpool.ac.uk/id/eprint/3155218 |
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