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Updated: May 5, 2026

Quantitative Fundus Autofluorescence for the Evaluation of Retinal Diseases
Published on: March 11, 2016
AI-based fluid quantification in neovascular age-related macular degeneration and diabetic macular edema treated with
Anna Theresa Lorenz1, André Marcio Messias1, Warda Darwisch1
1Eye Clinic Sulzbach, Knappschaftsklinikum Saar GmbH Krankenhaus Sulzbach, An d. Klinik 10, 66280, Sulzbach, Saar, Germany.
Purpose:
To assess faricimab treatment in neovascular age-related macular degeneration (nAMD) and diabetic macular edema (DME) with artificial intelligence-based fluid quantification on spectral-domain optical coherence tomography (SD-OCT).
Methods:
Retrospective patients with nAMD and DME; treatment-naïve, or on another intravitreal medication (switchers), loaded with 4 monthly intravitreal faricimab. SD-OCT (Heidelberg Engineering) at baseline and 16 weeks, then processed using the Fluid Monitor® (RetInSight). Sum of fluid volumes in the central 1 mm (pigment epithelial detachment, subretinal fluid, and intraretinal fluid) was computed (SF) and correlated with central subfield thickness (CST).
Results:
Thirty-four nAMD (25 switchers) and 21 DME (20 switchers) eyes were included. SF (nL) was 126.68 ± 17.24 and 37.84 ± 8.31 at baseline reduced to 80.78 ± 15.56 (p < 0.0001) and 15.28 ± 4.94 (p < 0.0001) for nAMD and DME, respectively. CST (µm) reduced from 405.12 ± 24.95 and 354.97 ± 15.89 to 320.33 ± 19.80 (p = 0.0001) and 302.41 ± 11.55 (p < 0.0001) in nAMD and DME, respectively. Mean intraindividual change between baseline and 16 weeks was larger using SF than with CST for nAMD (36.5% and 17.6%, respectively) and for DME (56.2% and 13.1%, respectively). A similar pattern was observed for each retinal compartment.
Conclusion:
When loaded with faricimab, total fluid decreased by 37% in nAMD and 56% in DME. Fluid volumetry appears more sensitive for retinal fluid.
Translational Relevance:
When AI-fluid volumetry is applied real-world nAMD and DME cases, then fluid volume offers a more sensitive and quantifiable measure of disease activity than CST.
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