Abstract 99. Jahrestagung der DOG, 29. 9. - 2. 10. 01 im ICC, Berlin

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Impressum



Analysis of digital SLO-fundus autofluorescence images of geographic atrophy (GA) in AMD (FAM-Study).

1Schmitz-Valckenberg S., 1Jorzik J., 2Roider J., 3Weinberger A., 4Wolf S., 1Holz F. G. für die 1FAM-Studiengruppe

Departments of Ophthalmology, University of Heidelberg, INF 400, 69120 1Heidelberg, 2Regensburg, 3Aachen, 4Leipzig

Objective: Variations of fundus autofluorescence (AF) over time in the junctional zone of GA are recorded in the prospective fundus autofluorescence in age-related macula degeneration (FAM)-Study. Here, we evaluate a novel method for automated image analysis.
Methods: Until now, over 150 patients with GA due to ARMD have been included in the FAM-Study. AF images in vivo are recorded with a confocal SLO (exc. 488 nm, em. >500 nm; Heidelberg Retina Angiograph). The intensity of AF in atrophic areas is typically decreased. Two independent readers analysed these areas in 24 right eyes manually by outlining such areas using a mouse-driven arrow (A) and automatically by image analysis software (Global Lab Image/2) after subjective adjustement of thresholding (B). In the following, the Bland-Altman-test was performed.
Results: Larger areas were measured using A compared to B by both readers (agreement A/B: reader 1 1.04, 95%CI [0.66,1.42]; reader 2 0.62, 95%CI [0.43,0.81]). The agreement between the readers (intra-observer variability) was 0.39 (95%CI [0.02,0.76]) for A and -0.03 (95%CI [- 0.23;0.18]) for B. Features making the delineation of borders of GA difficult included large choroidal vessels with autofluorescent properties in the GA area and media opacities.
Conclusion: Fundus AF cSLO imaging provides a reliable means to delineate areas of GA. The automated image analysis allows more accurate detection and quantitation documentation of atrophic areas than the manually outlining. This method will be useful in longitudinal natural history studies and for monitoring effects of future therapeutic interventions to slow down progression in AMD-patients with GA. Support: DFG Ho 1926/2-1, DFG Priority Pogram AMD (SPP 1088), State of Baden-Wuerttemberg Research fund 500/2000




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