June 2013
Volume 54, Issue 15
Free
ARVO Annual Meeting Abstract  |   June 2013
Diagnostic accuracy of multifocal pupillographic objective perimetry in early age-related macular degeneration
Author Affiliations & Notes
  • Faran Sabeti
    Eccles Institute of Neuroscience, Australian National University, Canberra, ACT, Australia
    ARC Centre of Excellence in Vision Science, Canberra, ACT, Australia
  • Aiasha Saikal
    Eccles Institute of Neuroscience, Australian National University, Canberra, ACT, Australia
    ARC Centre of Excellence in Vision Science, Canberra, ACT, Australia
  • Maria Kolic
    Eccles Institute of Neuroscience, Australian National University, Canberra, ACT, Australia
    ARC Centre of Excellence in Vision Science, Canberra, ACT, Australia
  • Corinne Carle
    Eccles Institute of Neuroscience, Australian National University, Canberra, ACT, Australia
    ARC Centre of Excellence in Vision Science, Canberra, ACT, Australia
  • Rohan Essex
    Ophthalmology Department, The Canberra Hospital, Canberra, ACT, Australia
  • Andrew James
    Eccles Institute of Neuroscience, Australian National University, Canberra, ACT, Australia
    ARC Centre of Excellence in Vision Science, Canberra, ACT, Australia
  • Ted Maddess
    Eccles Institute of Neuroscience, Australian National University, Canberra, ACT, Australia
    ARC Centre of Excellence in Vision Science, Canberra, ACT, Australia
  • Footnotes
    Commercial Relationships Faran Sabeti, None; Aiasha Saikal, None; Maria Kolic, SeeingMachines Ltd (E); Corinne Carle, AU2012/905171 (P); Rohan Essex, None; Andrew James, Seeing Machines, Inc (P); Ted Maddess, Seeing Machines (F), Seeing Machines (P), EyeCo (I)
  • Footnotes
    Support None
Investigative Ophthalmology & Visual Science June 2013, Vol.54, 4164. doi:
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      Faran Sabeti, Aiasha Saikal, Maria Kolic, Corinne Carle, Rohan Essex, Andrew James, Ted Maddess; Diagnostic accuracy of multifocal pupillographic objective perimetry in early age-related macular degeneration. Invest. Ophthalmol. Vis. Sci. 2013;54(15):4164.

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

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Abstract
 
Purpose
 

To evaluate the diagnostic accuracy of multifocal pupillographic objective perimetry (mfPOP) in eyes with small (<63 µm), intermediate (≥63 to <125 µm) and large (>125µm) drusen using three different stimulus protocols.

 
Methods
 

Pupil responses were recorded from subjects with small (9 eyes, mean age 66.5 ± 14), intermediate (6 eyes, mean age 72.8 ± 5.2) and large (25 eyes, mean age 67.6 ± 11) drusen and compared with 20 normal controls (mean age 70.2 ± 9.88) using three 6 minute mfPOP stimulus protocols. Stimuli were presented dichoptically and both pupil responses were measured concurrently. All stimuli were yellow with a maximum luminance of 288 cd/m2 and background 10 cd/m2. A dart board layout having 44 independent test regions per eye extending from fixation to15° eccentricity, either using a sequence previously used in the lab with 33 ms flashes (OldStimuli), or using a new temporal sequence method was employed. Two protocols used the new temporal sequence method and on each presentation either flashed on for 33 ms (NewStimuli); or presented pedestal flicker for 266 ms at 15Hz (NewStimuliFlick). Diagnostic capacity was measured using areas under the curve (AUC) of receiver operator characteristic (ROC) plots for the two worst regions in each eye for the three mfPOP stimuli protocols.

 
Results
 

The absolute mean difference of AREDS scores between eyes was 0.48 ± 0.6 (mean ± SD). Response amplitudes for the NewStimuli achieved the best diagnostic accuracy with AUC values of 100% ± 0.0% (mean ± SE) for eyes containing small, intermediate and large drusen. In comparison NewStimuliFlick and OldStimuli were less diagnostic across all AREDS categories. In eyes containing small drusen NewStimuliFlick and OldStimuli achieved AUC values of 87.0% ± 6.8% and 92.6% ± 7.1% respectively for small drusen, 87.0% ± 8.1% and 65.8% ± 14.6% for intermediate drusen and 86.0% ± 5.3% and 82.0% ± 6.7% for large drusen. Utilizing time to peak response deviations reduced diagnostic accuracy across all stimulus protocols.

 
Conclusions
 

The new temporal sequence stimuli produced the best diagnostic accuracy for all AMD severities, in comparison to the old continuous sequence stimuli and the same stimuli containing flicker.

 
Keywords: 412 age-related macular degeneration • 667 pupil • 758 visual fields  
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