Your browser doesn't support javascript.
Acceptability of intravitreal injections in geographic atrophy: protocol for a mixed-methods pilot study.
Enoch, Jamie; Ghulakhszian, Arevik; Crabb, David P; Dinah, Christiana; Taylor, Deanna J.
  • Enoch J; 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.
  • Crabb DP; 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.
  • Taylor DJ; Optometry and Visual Sciences, City University of London, London, UK Deanna.Taylor.2@city.ac.uk.
BMJ Open ; 11(4): e049495, 2021 04 24.
Article in English | MEDLINE | ID: covidwho-1199793
ABSTRACT

INTRODUCTION:

Age-related macular degeneration (AMD) is a common cause of visual impairment, affecting central vision. Geographic atrophy (GA) is an advanced form of the non-neovascular (dry) type of AMD. Late-stage clinical trials suggest that intravitreal injections of novel therapeutics may slow down the rate of GA progression by up to 30% in 1 year, thus allowing people with GA to preserve central vision for a longer period. While intravitreal injections have become an established treatment modality for neovascular (wet) AMD, it is unknown whether patients with (more gradually progressing) GA would accept regular injections that slow down, but do not stop or reverse, vision loss. Therefore, this mixed-methods pilot study will aim to explore whether regular intravitreal injections will be acceptable as treatment for patients with GA, and the factors that may affect treatment acceptability. METHODS AND

ANALYSIS:

A mixed-methods survey has been designed in collaboration with a GA patient advisory group. The survey comprises of structured questionnaires, semi-structured interview questions regarding patients' perceptions of intravitreal injections and the burden of treatment, and a task eliciting preferences between different potential treatments. Due to COVID-19 restrictions, this study will be conducted remotely by telephone. Thirty individuals will be recruited from NHS Medical Retina clinics at Central Middlesex Hospital, London. Half of the participants will be naïve to intravitreal injections, while half will have previous experience of intravitreal injections for neovascular (wet) AMD. Qualitative data analysis will be conducted using the Framework Method of analysis to identify key themes from participants' accounts. ETHICS AND DISSEMINATION The study received Health Research Authority approval on 23 March 2021 (IRAS Project ID 287824). Findings will be disseminated through peer-reviewed publications and conference presentations to the medical retina community, as well as through dialogue with patients and macular disease charities.
Subject(s)
Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: Telemedicine / Geographic Atrophy / Wet Macular Degeneration Type of study: Observational study / Prognostic study / Qualitative research Limits: Humans Country/Region as subject: Europa Language: English Journal: BMJ Open Year: 2021 Document Type: Article Affiliation country: Bmjopen-2021-049495

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Main subject: Telemedicine / Geographic Atrophy / Wet Macular Degeneration Type of study: Observational study / Prognostic study / Qualitative research Limits: Humans Country/Region as subject: Europa Language: English Journal: BMJ Open Year: 2021 Document Type: Article Affiliation country: Bmjopen-2021-049495