Parental experience of whole genome sequencing for children with sensorineural hearing lossShow others and affiliations
2026 (English)In: International Journal of Qualitative Studies on Health and Well-being, ISSN 1748-2623, E-ISSN 1748-2631, Vol. 21, no 1, article id 2641802
Article in journal (Refereed) Published
Abstract [en]
Purpose: The purpose of this in-depth interview study was to explore how parents of children with sensorineural hearing loss (SNHL) experienced genetic testing and whether they experienced risks and benefits.
Background: Most children with SNHL have a genetic etiology, which can be identified through genetic sequencing. A genetic test does not influence treatment, and whether patients and parents perceived genetic tests as valuable is unclear.
Methods: In this study, 10 parents of children with SNHL who underwent genetic testing were interviewed, and the content was analyzed using inductive thematic analysis.
Results: Three global themes were identified. In the first theme, (1) Limited knowledge creates uncertainty, parents described uncertainty related to the information provided, the test result itself and child-related factors. The second theme, (2) Genetic knowledge is considered important for the family and the future, explored the importance of knowledge. Parents wanted an explanation to make the future predictable, and the test had practical implications. In the last category, (3) Knowledge adds complexity and can be challenging, ethical considerations and risks associated with knowledge were highlighted.
Conclusion: The main conclusion was that parents experienced that genetic testing provided valuable personal information and had practical implications. However, a genetic diagnosis can cause concern and may affect family planning.
Place, publisher, year, edition, pages
Taylor & Francis, 2026. Vol. 21, no 1, article id 2641802
Keywords [en]
Sensorineural hearing loss, genetic sequencing, parental experiences, thematic analysis, interview study
National Category
Public Health, Global Health and Social Medicine
Research subject
Disability research
Identifiers
URN: urn:nbn:se:oru:diva-127950DOI: 10.1080/17482631.2026.2641802ISI: 001714011300001PubMedID: 41820818OAI: oai:DiVA.org:oru-127950DiVA, id: diva2:2045728
Funder
Hörselskadades Riksförbund, FA22- 00012026-03-132026-03-132026-03-20Bibliographically approved