# Perimetry of the Central Visual Field Using a Head-Mounted Open-Source Perimeter in Patients with Inherited Retinal Diseases

**Authors:** Cord Huchzermeyer, Friedrich Kruse, Jan Kremers

PMC · DOI: 10.3390/vision10010012 · Vision · 2026-02-14

## TL;DR

A low-cost head-mounted perimeter was tested for measuring vision in patients with inherited eye diseases, showing promise but with some limitations.

## Contribution

The study is the first to evaluate an open-source head-mounted perimeter for inherited retinal diseases.

## Key findings

- The Iowa-HMP showed typical visual field loss patterns in IRD patients.
- The device had a diagnostic sensitivity of 0.67 and specificity of 0.95 within its dynamic range.
- Open-source software facilitates research in perimetry for inherited retinal diseases.

## Abstract

Head-mounted (“virtual reality”) perimeters (HMPs), based on standard consumer electronic hardware, are a cheaper alternative to standard automated perimetry. They have not been validated in patients with inherited retinal disease (IRDs), yet. We evaluated the Iowa-HMP in a first pilot study. It consists of a legacy smartphone, a headset, and freely available, open-source software. We used the 10-2 grid, the ZEST algorithm, and a background of 10 cd/m2 to measure central visual fields in one normal subject, and in patients with occult macular dystrophy (n = 2), Stargardt’s disease (n = 3) and retinitis pigmentosa (n = 6). Results were compared with those from an Octopus 900 perimeter. The typical patterns of visual field loss were clearly discernible, but head-mounted perimeters generally have a limited dynamic range. Within the dynamic range of the Iowa-HMP (14 to 30 dB Octopus sensitivity), the Limits of Agreement (Bland-Altman) were ±7.5 dB. The Iowa-HMP had a diagnostic sensitivity of 0.67 for detecting locations with low perimetric sensitivity (<14 dB in the Octopus perimetry) with a diagnostic specificity of 0.95. Although the Iowa-HMP cannot be directly compared to standard perimetry in IRDs, open software greatly facilitates research in this area.

## Linked entities

- **Diseases:** occult macular dystrophy (MONDO:0013316), retinitis pigmentosa (MONDO:0008377)

## Full-text entities

- **Genes:** ABCA4 (ATP binding cassette subfamily A member 4) [NCBI Gene 24] {aka ABC10, ABCR, ARMD2, CORD3, FFM, RMP}, RP1L1 (RP1 like 1) [NCBI Gene 94137] {aka DCDC4B, OCMD, RP88}, SH2D1A (SH2 domain containing 1A) [NCBI Gene 4068] {aka DSHP, EBVS, IMD5, LYP, MTCP1, SAP}, RPGR (retinitis pigmentosa GTPase regulator) [NCBI Gene 6103] {aka COD1, CORDX1, CRD, PCDX, RP15, RP3}
- **Diseases:** toxic (MESH:D064420), macular dystrophies (MESH:D008268), Stargard's disease (MESH:D004194), injury to (MESH:D014947), central scotomas (MESH:D012607), Visual Field Loss (MESH:D014786), OMD (OMIM:613587), Bull's-Eye scotoma (MESH:C537833), STGD (MESH:D000080362), RP (MESH:D012174), associated (MESH:D018886), Inherited Retinal Diseases (MESH:D012164), glaucoma (MESH:D005901)
- **Chemicals:** Iowa-HMP (-), (hydroxy-)chloroquine (MESH:D006886), HMP (MESH:C009285), xenon (MESH:D014978)
- **Species:** Homo sapiens (human, species) [taxon 9606], Octopus (genus) [taxon 6643]

## Full text

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## Figures

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12921939/full.md

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Source: https://tomesphere.com/paper/PMC12921939