May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Pilot Study to Assess the Acceptability and Reliability of Diagnostic Instruments for Glaucoma Case–Findings
Author Affiliations & Notes
  • R. Moosavi
    Glaucoma Research Unit, Moorfields Eye Hospital, London, United Kingdom
  • T.A. Ho
    Glaucoma Research Unit, Moorfields Eye Hospital, London, United Kingdom
  • G.M. Verdon–Roe
    Glaucoma Research Unit, Moorfields Eye Hospital, London, United Kingdom
    Visual Science,
    Institute Of Ophthalmology, London, United Kingdom
  • I.E. Murdoch
    Epidemiology/Int Eye Hlth,
    Institute Of Ophthalmology, London, United Kingdom
  • D.F. Garway–Heath
    Glaucoma Research Unit, Moorfields Eye Hospital, London, United Kingdom
  • Footnotes
    Commercial Relationships  R. Moosavi, None; T.A. Ho, None; G.M. Verdon–Roe, None; I.E. Murdoch, None; D.F. Garway–Heath, Heidelberg Engineering, F; Carl Zeiss Meditec, F; Carl Zeiss Meditec, C.
  • Footnotes
    Support  Unrestricted Grant from Pfizer
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 3425. doi:
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      R. Moosavi, T.A. Ho, G.M. Verdon–Roe, I.E. Murdoch, D.F. Garway–Heath; Pilot Study to Assess the Acceptability and Reliability of Diagnostic Instruments for Glaucoma Case–Findings . Invest. Ophthalmol. Vis. Sci. 2006;47(13):3425.

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

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Abstract
 
Purpose:
 

Diagnostic instruments have a potential role in case–finding for glaucoma. However, clinical studies rarely report the proportion of reliable/acceptable test results, especially in the case–finding environment. This was a pilot study to assess the performance of three diagnostic instruments in glaucoma case–finding.

 
Methods:
 

115 consecutive subjects attending an optometry practice for a regular sight test were recruited over a 3–month period. Subjects were tested with the Heidelberg Retina Tomograph II (HRTII), GDx VCC and Frequency Doubling Technology (FDT) Matrix Perimeter. The following indices were assessed: 1. Acceptability of the tests, assessed by asking two questions: (a) which was most acceptable test? (b) which was the least acceptable test? The answer options were one of the three instruments or undecided. 2. Performance of the instruments, assessed by examining the proportion of reliable images or fields produced. Assessment was made according to software–based established and recognised reliability criteria: (a) HRT II: reliable = mean pixel height standard deviation (MPHSD) <40 (b) GDx VCC: reliable = Numerical Quality Score ≥8 (c) FDT: a, reliable = fixation losses ≤20% and false–positive rate ≤15%; b, reliable = fixation losses ≤25% and false–positive rate ≤30%

 
Results:
 

62 subjects’ opinions sought for test acceptability; 115 subjects (45 male, 70 female; mean age: 66, range 50 to 93 years) recruited for instrument performance: HRT II (228 eyes tested); GDx VCC (226 eyes tested); FDT (229 eyes tested).  

 
Conclusions:
 

In this short series, the imaging device tests were found to be the most acceptable by the subjects. Test reliability, as judged by the criteria applied, was also highest with these devices, although there is no benchmark for comparing reliability between different devices. Supported by an unrestricted grant from Pfizer.

 
Keywords: detection • clinical (human) or epidemiologic studies: systems/equipment/techniques • imaging/image analysis: clinical 
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