Your browser doesn't support javascript.
loading
Exploring patient acceptability of emerging intravitreal therapies for geographic atrophy: A mixed-methods study.
Enoch, Jamie; Ghulakhszian, Arevik; Sekhon, Mandeep; Crabb, David P; Taylor, Deanna J; Dinah, Christiana.
Afiliación
  • Enoch J; Department of Optometry and Visual Sciences, City, University of London, London, UK.
  • Ghulakhszian A; Ophthalmology Department, London North West University Healthcare NHS Trust, Central Middlesex Hospital, London, UK.
  • Sekhon M; Population Health Research Institute, St George's, University of London, London, UK.
  • Crabb DP; Department of Optometry and Visual Sciences, City, University of London, London, UK.
  • Taylor DJ; Department of Optometry and Visual Sciences, City, University of London, London, UK.
  • Dinah C; Ophthalmology Department, London North West University Healthcare NHS Trust, Central Middlesex Hospital, London, UK. christiana.dinah@nhs.net.
Eye (Lond) ; 37(17): 3634-3642, 2023 12.
Article en En | MEDLINE | ID: mdl-37170013
BACKGROUND/OBJECTIVES: The acceptability of emerging intravitreal therapies for patients with Geographic Atrophy (GA) is currently unknown. This study therefore aimed to investigate the extent to which regular intravitreal injections may be acceptable to GA patients. SUBJECTS/METHODS: Thirty UK-based individuals with GA secondary to age-related macular degeneration (AMD), recruited from two London-based hospitals, were interviewed in April-October 2021 regarding acceptability of new GA treatments. Participants responded to a structured questionnaire, as well as open-ended questions in a semi-structured interview. The Theoretical Framework of Acceptability (TFA) informed framework analysis of the qualitative data. RESULTS: Twenty participants (67%) were female, and median (interquartile range (IQR)) age was 83 (78, 87) years. 37% of participants had foveal centre-involving GA, and better eye median (IQR) logMAR visual acuity was 0.30 (0.17, 0.58). Data suggested that 18 participants (60% (95% CI: 41-79%)) would accept the treatment, despite awareness of potential drawbacks. Eight participants (27% (95% CI: 10-43%) were ambivalent or undecided about treatment, and four (13%) (95% CI: 0-26%) would be unlikely to accept treatment. Reducing the frequency of injections from monthly to every other month increased the proportion of participants who considered the treatments acceptable. Conversely, factors limiting acceptability clustered around: the limited magnitude of treatment efficacy; concerns about side effects or the increased risk of neovascular AMD; and the logistical burden of regular clinic visits for intravitreal injections. Misunderstandings of potential benefits indicate the need for appropriately-designed patient education tools to support decision-making. CONCLUSIONS: Our study suggests a majority of participants would be positive about intravitreal treatment for GA, in spite of potential burdens.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Atrofia Geográfica / Degeneración Macular Húmeda Tipo de estudio: Prognostic_studies / Qualitative_research Idioma: En Revista: Eye (Lond) Asunto de la revista: OFTALMOLOGIA Año: 2023 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Atrofia Geográfica / Degeneración Macular Húmeda Tipo de estudio: Prognostic_studies / Qualitative_research Idioma: En Revista: Eye (Lond) Asunto de la revista: OFTALMOLOGIA Año: 2023 Tipo del documento: Article