Evidence map›Paper›PMID 31103641›Full record

ArticleOphthalmology. Retina2019

Retinal Pathologic Features on OCT among Eyes of Older Adults Judged Healthy by Color Fundus Photography.

Jason N Crosson, Thomas A Swain, Mark E Clark, Carrie E Huisingh, Gerald McGwin, Cynthia Owsley, Christine A Curcio

Open access · greenAbstract read
In one paragraph

Article in Ophthalmology. Retina, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Observational
  3. Article
  4. Article
  5. Article
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

7 authors at 1 institution in 1 country.

Jason N CrossonRetina Consultants of Alabama, Birmingham, Alabama; Department of Ophthalmology, School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Thomas A SwainDepartment of Ophthalmology, School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama; Department of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham, Alabama.
Mark E ClarkDepartment of Ophthalmology, School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Carrie E HuisinghDepartment of Ophthalmology, School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Gerald McGwinDepartment of Ophthalmology, School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama; Department of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham, Alabama.
Cynthia OwsleyDepartment of Ophthalmology, School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama.
Christine A CurcioDepartment of Ophthalmology, School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama. Electronic address: christinecurcio@uabmc.edu.
University of Alabama at Birmingham · US

Funding

Functionally Validated Structural Endpoints for Early AMDR01EY029595 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI CURCIO, CHRISTINE A, OWSLEY, CYNTHIA · 2019 to 2023
$4.1M
A hyperspectral approach to RPE fluorophores in AMDR01EY027948 · NEI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI ACH, THOMAS, CURCIO, CHRISTINE A · 2017 to 2025
$3.8M
VISUAL DYSFUNCTION AND AGING--UNDERLYING MECHANISMSR01AG004212 · NIA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI OWSLEY, CYNTHIA · 1985 to 2012
$3.7M
NEI NIH HHS R01 EY027948NEI NIH HHS R01 EY029595NIA NIH HHS R01 AG004212
6 · The paper itself

Abstract

purposeOCT has revealed many details of retinal disease that were not available with older imaging technologies. In eyes of adults older than 60 years with healthy maculas as determined by color fundus photography (CFP) and a validated grading system, we screened for pathologic features using OCT. We also tested visual function to assess potential impact of the observed pathologic features on patients.

designCross-sectional study.

participantsPersons recruited from primary ophthalmology care clinics.

methodsColor fundus photographs were assessed by the 9-step Age-Related Eye Disease Study scale. OCT macular volumes of participants at step 1 on the Age-Related Eye Disease Study scale, considered healthy, were reviewed by a retina specialist masked to other participant characteristics. Participants were tested for 6 different cone- and rod-mediated visual functions.

main outcome measuresPercentage of participants with disorders detected on OCT review and visual function measures.

resultsIn 138 of 984 eyes (14%) considered healthy by CFP, pathologic features were detectable by OCT, with 8.4% having vitreomacular interface disorders. Among the low-prevalence disorders found, 5 eyes (0.5%) showed macular telangiectasia type 2. Relative to eyes lacking detectable chorioretinal pathologic features, eyes with any pathologic features were associated with poorer low-luminance visual acuity and rod-mediated dark adaptation. In eyes with epiretinal membranes, the largest single entity identified (n = 61 [6.2%]), significantly worse visual functions were best-corrected visual acuity (P = 0.0444), low-luminance visual acuity (P = 0.0151), and light sensitivity (central 3° and 9°; P = 0.0035 and P = 0.0097, respectively).

conclusionsMacular pathologic features with functional visual implications not identified by clinical examination or CFP are detectable with OCT. Vitreomacular interface disorders often are visually significant and treatable conditions that are visible on OCT, but are easily missed on CFP and clinical examination. Another such condition best seen on OCT is macular telangiectasia type 2, an untreatable disorder for which a clinical trial is in progress. OCT has a potential role in primary eye care clinics to screen for retinal pathologic features, especially in eyes with decreased visual acuity and otherwise normal examination results.

Indexed as

AgedAged, 80 and overCross-Sectional StudiesFemaleHumansMaleMiddle AgedOdds RatioPhotographyRetinaRetinal DiseasesTomography, Optical CoherenceVisual AcuityVitreous Body

Identifiers

PMID31103641
PMCPMC6718291
OpenAlexW2928318684

What OpenQuestion holds

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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.