Evidence map›Paper›PMID 42505488›Full record

ArticleBiomimetics (Basel, Switzerland)2026

Stress-Based Assessment of Bio-Inspired Phosphene Vision Encoding: Trade-Offs Among Performance, Residual Proxy Safety Burden, and Topology-Based Representation Metrics.

Youngseok Lee

Abstract read
In one paragraph

Article in Biomimetics (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

1 author.

Youngseok LeeDepartment of Electronics, Chungwoon University, Incheon 22100, Republic of Korea.ORCID 0009-0000-9873-0287

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phosphene-based visual neuroprostheses require encoding schemes that preserve task-relevant information while remaining feasible under safety-constrained stimulation. This study proposes a stress-based evaluation framework that reframes phosphene encoder assessment as a tri-objective operating-envelope problem rather than a single-metric comparison. Four representative encoders-rate, sparse, temporal, and optim-were evaluated under structured perturbations using two simulated prosthetic-vision(SPV) benchmarks: EMNIST Letters for symbolic recognition and a COCO-derived balanced subset for a reduced four-class COCO-derived image-level classification task. The final experimental configuration used 20,000/3000/3000 train/validation/test samples for EMNIST and 4000/1000/1000 for the COCO-derived benchmark. The framework combined structured stress sweeps, residual proxy safety-burden analysis, topology-based representation metrics, and stress-integrated utility summaries within a simulation-based evaluation setting. The results showed that clean-conditioning accuracy alone was insufficient to predict encoder behavior under stress. EMNIST exhibited broad operator-dependent degradation, whereas the COCO-derived benchmark showed a lower but more compressed performance regime. Residual proxy safety burden was only loosely aligned with performance, with moderate dissociation between performance and residual proxy safety burden in EMNIST and weaker alignment between these two axes in the COCO-derived benchmark. In the point-estimate utility summaries, the sparse encoder tended to yield comparatively favorable tri-objective utility values within the present single-run simulation-based framework, simplified SPV percept-synthesis operator, and fixed benchmark-specific decoder setting, primarily because it maintained an almost negligible residual proxy safety burden while preserving competitive performance and topology-based representation metrics. Topology-based analysis further indicated that topology-based representation metrics largely tracked task degradation in EMNIST, whereas topology-based representation metrics showed larger relative variation than decoder accuracy within the evaluated simulation setting under degraded COCO-derived conditions. Taken together, these findings provide an exploratory, benchmark-specific assessment suggesting that phosphene encoder evaluation may benefit from a multi-axis operating-envelope-oriented analysis that jointly considers stressed functional performance, residual proxy safety burden, and topology-based representation metrics within the present simplified SPV and fixed-decoder evaluation setting. These results should therefore be interpreted as simulation-level, configuration-dependent observations under a simplified SPV percept-synthesis operator, with safety-related quantities treated as residual proxy safety-burden summaries rather than as direct physiological, electrochemical, clinical, or implant-specific safety measurements.

Indexed as

multi-objective evaluationoperating-envelope characterizationphosphene visionresidual proxy safety burdensimulated prosthetic visionstress testingtopology-based analysisvisual neuroprosthesis

Identifiers

PMID42505488
PMCPMC13406808

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.