Evidence map›Paper›PMID 37996905›Full record

ReviewInternational journal of retina and vitreous2023

An update on visual prosthesis.

Kailyn A Ramirez, Laura E Drew-Bear, Maria Vega-Garces, Henry Betancourt-Belandria, J Fernando Arevalo

Open access · goldAbstract readReview
In one paragraph

Review in International journal of retina and vitreous, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
5.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 36 citations in OpenAlex.

  1. Trial
  2. Review
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  4. Article
  5. Article
  6. Neural Vision Restoration in Ophthalmology.Annals of biomedical engineering · 2026
    Review
  7. Article
  8. Motion perception with visual prostheses.Progress in biomedical engineering (Bristol, England) · 2026
    Review
  9. Article
  10. Review
  11. Article
  12. Review
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  15. Article
  16. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Kailyn A RamirezRutgers Robert Wood Johnson Medical School, New Brunswick, NJ, 08901, USA.
Laura E Drew-BearThe Wilmer Eye Institute, Johns Hopkins University School of Medicine, 600 N. Wolfe Street, Maumenee 713, Baltimore, MD, 21287, USA.
Maria Vega-GarcesRutgers New Jersey Medical School, Newark, NJ, 07107, USA.
Henry Betancourt-BelandriaUF Health Cardiovascular Center, University of Florida, Jacksonville, FL, 32209, USA.
J Fernando ArevaloThe Wilmer Eye Institute, Johns Hopkins University School of Medicine, 600 N. Wolfe Street, Maumenee 713, Baltimore, MD, 21287, USA. arevalojf@jhmi.edu.ORCID http://orcid.org/0000-0002-9290-1062
Johns Hopkins University · USRutgers, The State University of New Jersey · USUniversity of Florida Health · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo review the available evidence on the different retinal and visual prostheses for patients with retinitis pigmentosa and new implants for other indications including dry age-related macular degeneration.

methodsThe PubMed, GoogleScholar, ScienceDirect, and ClinicalTrials databases were the main resources used to conduct the medical literature search. An extensive search was performed to identify relevant articles concerning the worldwide advances in retinal prosthesis, clinical trials, status of devices and potential future directions up to December 2022.

resultsThirteen devices were found to be current and were ordered by stimulation location. Six have active clinical trials. Four have been discontinued, including the Alpha IMS, Alpha AMS, IRIS II, and ARGUS II which had FDA and CE mark approval. Future directions will be presented in the review.

conclusionThis review provides an update of retinal prosthetic devices, both current and discontinued. While some devices have achieved visual perception in animals and/or humans, the main issues impeding the commercialization of these devices include: increased length of time to observe outcomes, difficulties in finding validated meaures for use in studies, unknown long-term effects, lack of funding, and a low amount of patients simultaneously diagnosed with RP lacking other comorbid conditions. The ARGUS II did get FDA and CE mark approval so it was deemed safe and also effective. However, the company became more focused on a visual cortical implant. Future efforts are headed towards more biocompatible, safe, and efficacious devices.

Indexed as

Artificial visionRetinal prosthesesRetinitis pigmentosaStimulationVisual prostheses

Identifiers

PMID37996905
PMCPMC10668475
OpenAlexW4388938748

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.