PORT: Quality and Diagnostic Utility of Mydriatic Fundus Plenoptic Photography

Sponsor
Wills Eye (Other)
Overall Status
Withdrawn
CT.gov ID
NCT03037268
Collaborator
Mid Atlantic Retina (Other)
0
1
5
0

Study Details

Study Description

Brief Summary

  1. Establish the quality of fundus images produced by plenoptic ophthalmoscopy using the grading system proposed and utilized in the Fundus Photography versus Ophthalmoscopy Trials Outcomes in the Emergency Department (FOTO-ED) Study.

  2. Determine diagnostic utility of plenoptic ophthalmoscopy images by comparing masked image reviewers' quality measurements and findings to images obtained with a commercially available ocular fundus camera and documented exam findings

Condition or Disease Intervention/Treatment Phase
  • Device: Lytro Plenoptic Camera and 28D lens

Detailed Description

Visualization of the ocular fundus is considered an essential part of the physical examination, as abnormalities of the optic nerve, retinal vessels, and macula can reveal underlying systemic diseases and explain the etiology of visual complaints.

The Fundus Photography versus Ophthalmoscopy Trials Outcomes in the Emergency Department (FOTO-ED) Study demonstrated that only 14% of patients with complaints and conditions in which fundus examination is considered important had direct ophthalmoscopy performed by an ED physician .Greater than 80% of previously unknown fundus findings relevant to ED patient management were missed by ED physicians, but were identified by nonmydriatic digital fundus photography. Several of these cases resulted in recall of a discharged patient back to the ED for hospital admission once diagnostic fundus photos were reviewed.

In the search for an alternative to improve ease of use and fundus image quality, plenoptic technology provides a promising option for portable fundus imaging. Plenoptic, or light field, imaging has recently been introduced commercially with the release of the Lytro Plenoptic Camera (Mountain View, CA, USA). Utilizing an array of microlenses, the Lytro camera captures all available light in a scene from multiple vectors. By dividing up a scene as a whole with many individual microlenses, images can be refocused in post processing after acquisition, sharp focus can be attained in low light situations, and stereo images with perspective shifting can be attained.

To date there have been no published quantitative descriptions of the quality and reliability of plenoptic ophthalmoscopy using a commercially available, portable light field camera. Initial work from a pilot study using animal and human eyes was published in 2016. The purpose of the proposed prospective, cross sectional imaging study is to compare standard mydriatic fundus photography to a second generation camera developed with a Lytro plenoptic camera and customized light source, specifically analyzing diagnostic utility/sensitivity of detecting retinal pathology and overall image quality. If the image quality outcomes of the investigators proposed study are similar to those of the nonmydriatic fundus camera, the implications for physicians and the potential applications to ophthalmology related telemedicine are significant.

Study Design

Study Type:
Observational
Actual Enrollment :
0 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
Quality and Diagnostic Utility of Mydriatic Fundus Plenoptic Photography: The Plenoptic Ophthalmoscopy Reliability Trial
Anticipated Study Start Date :
Dec 1, 2018
Anticipated Primary Completion Date :
May 1, 2019
Anticipated Study Completion Date :
May 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Patients undergoing dilated examination

examined in the Retina Service of Wills Eye Hospital with and without visually significant posterior retinal or optic nerve pathology imaged with a Lytro Plenoptic Camera and 28D lens

Device: Lytro Plenoptic Camera and 28D lens
visual acuity measured, intraocular pressure obtained, eyes dilated as part of a standard exam for intended patient visit screened and consented for study subjected to bilateral plenoptic ophthalmoscopy mydriatic, single-field fundus images obtained images reviewed for quality and diagnostic utility by a masked grader

Outcome Measures

Primary Outcome Measures

  1. Image quality [through study completion, an average of 1 year]

    Image quality grade (1 - 5, with 1 being excellent and 5 being not diagnostically useful)

  2. Detection rate of "critical" retinal findings [through study completion, an average of 1 year]

    Sensitivity (%) of detection of "critical" retinal findings with plenoptic ophthalmoscopy. Critical retinal findings include retinal detachment, retinal vascular sheathing, retinal hemorrhage, retinal whitening, optic disc edema, optic disc pallor, optic disc cupping (> 0.5 cup-to disc ratio)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • With and without visually significant posterior retinal or optic nerve pathology,

  • Pregnant women if already dilated for reason other than study participation.

Exclusion Criteria:
  • Children,

  • Prisoners,

  • Poor view of posterior pole due to anterior segment pathology,

  • Poor view of posterior pole due to posterior media opacities that necessitate use of B-scan ultrasound to evaluate posterior pole.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mid Atlantic Retina- Wills Eye Institute Philadelphia Pennsylvania United States 19107

Sponsors and Collaborators

  • Wills Eye
  • Mid Atlantic Retina

Investigators

  • Principal Investigator: Jason Hsu, MD, Wills Eye Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Jason Hsu, MD, Dr., MD, Wills Eye
ClinicalTrials.gov Identifier:
NCT03037268
Other Study ID Numbers:
  • 14-447E
First Posted:
Jan 31, 2017
Last Update Posted:
Nov 13, 2019
Last Verified:
Nov 1, 2019
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided

Study Results

No Results Posted as of Nov 13, 2019