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How 'Micro' is Microperimetry? - Characterizing the Effect of Fundus Tracking on the Psychometric Function

Lipsky, T.; Ehrenzeller, C.; Ansari, G.; Pfau, K.; Harmening, W.; Wu, Z.; Pfau, M.

2026-03-27 ophthalmology
10.64898/2026.03.25.26349170 medRxiv
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Purpose: To quantify whether fundus tracking in microperimetry improves psychometric parameter estimation (in vivo demonstration of improved stimulus-delivery precision), and to derive a psychometrically grounded criterion intensity for suprathreshold (defect-mapping) microperimetry. Methods: Twenty-five healthy volunteers underwent MAIA2-microperimetry at five loci: three outside and two inside the blind spot. Frequency-of-seeing (FoS) functions were measured in four blocks (2 tracking on; 2 tracking off). FoS-data were fit using cumulative-Gaussian psychometric functions estimating sensitivity parameters. Mixed-effect models assessed tracking effects, and posterior simulations defined the optimal criterion intensity for separating 'seeing' from 'non-seeing' loci. Results: Tracking had little effect on threshold estimates at loci outside the blind spot, but lowered threshold estimates within the blind spot (posterior median difference PMD [95% CrI] of -1.46 dB [-2.30, -0.62] at locus 4, and -1.02 dB [-1.94, -0.08] at locus 5). Tracking was associated with steeper psychometric slope parameters at loci 1-3 (PMD of -0.14 dB [-0.29, 0.01], -0.27 dB [-0.43, -0.12], and -0.22 dB [-0.40, -0.04]). Without tracking, false-positive responses were more frequent when fixation shifts displaced stimuli toward the 'seeing' retina. Simulation-based analysis identified 13 dB as nominally optimal criterion for suprathreshold microperimetry (Youden index: 0.76 [0.74, 0.79], comparable to 10 dB (0.74 [0.72, 0.76]). Conclusions: Even in healthy volunteers with stable fixation, fundus tracking measurably reduced sensitivity estimates at 'non-seeing' loci and sharpened FoS curves in the 'seeing' retina. A criterion intensity of 10 to 13 dB is a defensible choice for separating 'seeing' and 'non-seeing' retina in suprathreshold (defect-mapping) perimetry paradigms.

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