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  Vol. 125 No. 3, March 2007 TABLE OF CONTENTS
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Detecting Visual Function Abnormalities Using the Swedish Interactive Threshold Algorithm and Matrix Perimetry in Eyes With Glaucomatous Appearance of the Optic Disc

Lisandro M. Sakata, MD; Julio DeLeon-Ortega, MD, PhD; Stella N. Arthur, MD, MSPH; Blythe E. Monheit, MD; Christopher A. Girkin, MD, MSPH

Arch Ophthalmol. 2007;125(3):340-345.

Objective  To compare the ability of 24-2 frequency-doubling perimetry (FDP-Matrix) with standard automated perimetry with the Swedish interactive threshold algorithm (SAP-SITA) in detection of visual function abnormalities in patients with glaucomatous-appearing optic discs (GAOD).

Methods  This observational case-control study included 80 patients with GAOD and 54 control subjects diagnosed by masked assessment of optic disc stereoscopic photographs. Abnormal visual function at SAP-SITA and FDP-Matrix testing required consistent abnormalities in 2 visual field examinations, determined using the glaucoma hemifield test outside 99% normal limits, pattern standard deviation outside 95% normal limits, or 3 contiguous points in the pattern deviation probability plot outside 95% normal limits (at least 1 P<1%) within the same hemifield.

Results  The FDP-Matrix and SAP-SITA detected abnormal visual function in 51% and 44%, respectively, of GAOD eyes (P = .26), and both perimetry techniques identified 11% of healthy eyes as abnormal. Agreement between FDP-Matrix and SAP-SITA was moderate ({kappa} = 0.49), as only 35% of GAOD eyes and 2% of healthy eyes had both visual field test results flagged as abnormal.

Conclusions  The FDP-Matrix detected abnormal visual function in more eyes with GAOD than did SAP-SITA, although this difference was not significant. Each visual field test tended to identify different subsets of eyes with GAOD as abnormal. Combination of these perimetry techniques may improve the detection of visual function abnormalities in patients with glaucoma.


Author Affiliations: Department of Ophthalmology, School of Medicine, University of Alabama at Birmingham.







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