June 2017
Volume 58, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2017
Using Delphi methodology in the development of a new patient reported outcome measure for stroke survivors with visual impairment
Author Affiliations & Notes
  • Lauren R Hepworth
    Health Services Research, University of Liverpool, Liverpool, United Kingdom
  • Fiona J Rowe
    Health Services Research, University of Liverpool, Liverpool, United Kingdom
  • Footnotes
    Commercial Relationships   Lauren Hepworth, None; Fiona Rowe, None
  • Footnotes
    Support  NIHR Career Development Fellowship (Dr Fiona Rowe)
Investigative Ophthalmology & Visual Science June 2017, Vol.58, 3303. doi:
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      Lauren R Hepworth, Fiona J Rowe; Using Delphi methodology in the development of a new patient reported outcome measure for stroke survivors with visual impairment. Invest. Ophthalmol. Vis. Sci. 2017;58(8):3303.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : To ascertain what items stroke survivors and stroke care professionals think are important when assessing quality of life in stroke survivors with visual impairment.

Methods : Items were sourced from a systematic review of instruments relevant to visual impairment caused by stroke. The number of items were reduced and adapted following a pilot of version one of the new instrument, leading to version two (62 items). Items from version two were evaluated in a Delphi survey. Stakeholders (stroke survivors/clinicians) were invited to take part in the process. The Delphi method involved three rounds of an electronic-based questionnaire. A consensus definition of ≥70% agreement was decided a priori. The survey asked participants to rank importance on a 9-point scale and also categorise the items by relevance to types of visual impairment following stroke or whether items were considered not relevant. Analysis of consensus (percentage response rate), stability (mean/SD) and agreement (weighted Kappa) were conducted.

Results : In total, 113 participants registered for the Delphi survey of which 47 (41.6%) completed all three rounds. Response rates to the three rounds were 78/113 (69.0%), 61/76 (81.3%) and 49/64 (76.6%) respectively. The participants included orthoptists (45.4%), occupational therapists (44.3%) and stroke survivors (10.3%). Consensus was reached on 56.5% (n=35) of items in the three round process, all for inclusion of the item. A consensus was reached for 83.8% (n=52) in the categorisation of items. The majority (82.6%) of the consensus were for relevant to ‘all visual impairment following stroke’; two (3.2%) items were deemed ‘not relevant’.

Conclusions : If this Delphi survey had been the primary method for further development of the new instrument, a reduction of two items would have been achieved. A further 27 items would require discussion at a consensus meeting. It was identified a hub and spoke model for the questionnaire based on the categorisation of items would not be possible due to a large number of core items (n=40) and few (n=13) additional items across four spokes. Psychometrics using Rasch analysis will be assessed prior to a consensus meeting. The consensus meeting will consider all data through facilitated clinical and patient input on the important items to assess quality of life with visual impairment following stroke.

This is an abstract that was submitted for the 2017 ARVO Annual Meeting, held in Baltimore, MD, May 7-11, 2017.

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