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Living with an artificial eye: qualitative insights into patient and family member experiences.
Boele, Florien W; Kawalek, Jessica Charlotte; Nicklin, Emma; Gout, Taras; Watson, Judith M.
Afiliación
  • Boele FW; Leeds Institute of Medical Research at St James's, St James's University Hospital, University of Leeds, Leeds, LS9 7TF, UK. F.Boele@leeds.ac.uk.
  • Kawalek JC; Leeds Institute of Medical Research at St James's, St James's University Hospital, University of Leeds, Leeds, LS9 7TF, UK.
  • Nicklin E; Leeds Institute of Medical Research at St James's, St James's University Hospital, University of Leeds, Leeds, LS9 7TF, UK.
  • Gout T; Department of Ophthalmology, St James's University Teaching Hospital, Beckett St., Leeds, LS9 7TF, UK.
  • Watson JM; York Trials Unit, Department of Health Sciences, University of York, York, YO10 5DD, UK.
Int Ophthalmol ; 44(1): 227, 2024 May 22.
Article en En | MEDLINE | ID: mdl-38776029
ABSTRACT

PURPOSE:

Artificial eye users (AEUs) can experience a negative impact on psychological and emotional wellbeing, including reduced social functioning, which may be a consequence of living with one eye removed, and/or of having a prosthetic eye. This may have wider consequences for their families. We aimed to explore what it means to live with a prosthetic eye, for both AEUs and their families-and how any quality of life (QoL) issues impact on their day-to-day functioning.

METHODS:

A subset of AEUs and their family members taking part in a feasibility randomised controlled trial comparing hand-painted to digitally printed artificial eyes were invited for semi-structured interviews. Transcripts were analysed using reflexive thematic analysis. Qualitative results related to trial participation are covered elsewhere. Here, we focus on QoL and day-to-day functioning.

RESULTS:

Twelve AEUs (eight males) and five spouses (one male) who had worn artificial eyes for 2-65 years took part, and four themes were identified. (1) Impact on day-to-day life AEUs and their spouses have to adapt to (partial) sight loss, reduced levels of confidence, and social withdrawal. (2) Impact on psychological and emotional wellbeing distress among AEUs and their spouses can be severe and prolonged, highlight unmet support needs. (3) Challenges with treatment experiences AEUs experienced negative impact of fragmentation of care and long waiting times. (4) Worries about the future AEUs mentioned fragility of remaining sight, and concerns around potential need for further treatment.

CONCLUSION:

Patients and their family members experience negative impact of being an AEU on their everyday lives and quality of life. There is a potential role for psychosocial support services in supporting AEUs and their families even long after eye loss.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Calidad de Vida / Ojo Artificial Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Int Ophthalmol Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Calidad de Vida / Ojo Artificial Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Int Ophthalmol Año: 2024 Tipo del documento: Article