Recommendations for OCT Angiography Reporting in Retinal Vascular Disease: A Delphi Approach by International Experts.


Journal

Ophthalmology. Retina
ISSN: 2468-6530
Titre abrégé: Ophthalmol Retina
Pays: United States
ID NLM: 101695048

Informations de publication

Date de publication:
09 2022
Historique:
received: 25 11 2021
revised: 12 02 2022
accepted: 15 02 2022
pubmed: 25 2 2022
medline: 14 9 2022
entrez: 24 2 2022
Statut: ppublish

Résumé

To develop a consensus nomenclature for reporting OCT angiography (OCTA) findings in retinal vascular disease (e.g., diabetic retinopathy, retinal vein occlusion) by international experts. Delphi-based survey. Twenty-five retinal vascular disease and OCTA imaging experts. A Delphi method of consensus development was used, comprising 2 rounds of online questionnaires, followed by a face-to-face meeting conducted virtually. Twenty-five experts in retinal vascular disease and retinal OCTA imaging were selected to constitute the OCTA Nomenclature in Delphi Study Group for retinal vascular disease. The 4 main areas of consensus were: definition of the parameters of "wide-field (WF)" OCTA, measurement of decreased vascular flow on conventional and WF-OCTA, nomenclature of OCTA findings, and OCTA in retinal vascular disease management and staging. The study end point was defined by the degree of consensus for each question: "strong consensus" was defined as ≥85% agreement, "consensus" as 80% to 84%, and "near consensus" as 70% to 79%. Consensus and near consensus on OCTA nomenclature in retinal vascular disease. A consensus was reached that a meaningful change in percentage of flow on WF-OCTA imaging should be an increase or decrease ≥30% of the absolute imaged area of flow signal and that a "large area" of WF-OCTA reduced flow signal should also be defined as ≥30% of the absolute imaged area. The presence of new vessels and intraretinal microvascular abnormalities, the foveal avascular zone parameters, the presence and amount of "no-flow areas," and the assessment of vessel density in various retinal layers should be added for the staging and classification of diabetic retinopathy. Decreased flow ≥30% of the absolute imaged area should define an ischemic central retinal vein occlusion. Several other items did not meet consensus requirements or were rejected in the final discussion round. This study provides international consensus recommendations for reporting OCTA findings in retinal vascular disease, which may help to improve the interpretability and description in clinic and clinical trials. Further validation in these settings is warranted and ongoing. Efforts are continuing to address unresolved questions.

Identifiants

pubmed: 35202889
pii: S2468-6530(22)00066-5
doi: 10.1016/j.oret.2022.02.007
pmc: PMC9393205
mid: NIHMS1796847
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

753-761

Subventions

Organisme : NEI NIH HHS
ID : R01 EY030564
Pays : United States
Organisme : NINDS NIH HHS
ID : UH3 NS100614
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.

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Auteurs

Marion R Munk (MR)

Department of Ophthalmology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland; Bern Photographic Reading Center, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland. Electronic address: marion.munk@insel.ch.

Amir H Kashani (AH)

Wilmer Eye Institute, Johns Hopkins Hospital, Baltimore, Maryland.

Ramin Tadayoni (R)

Ophthalmology Department, AP-HP, Hôpital Lariboisière, Hôpital Fondation Rothschild, and Université de Paris, Paris, France.

Jean-Francois Korobelnik (JF)

CHU Bordeaux, Service d'ophtalmologie, France; Univ. Bordeaux, INSERM, BPH, U1219, F-33000 Bordeaux, France.

Sebastian Wolf (S)

Department of Ophthalmology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland; Bern Photographic Reading Center, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Francesco Pichi (F)

Eye Institute, Cleveland Clinic Abu Dhabi, Abu Dhabi, United Arab Emirates; Cleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland.

Adrian Koh (A)

Eye & Retina Surgeons, Camden Medical, Singapore.

Akihiro Ishibazawa (A)

Department of Ophthalmology, Asahikawa Medical University, Hokkaido, Japan.

Alain Gaudric (A)

Ophthalmology Department, AP-HP, Hôpital Lariboisière, Université de Paris, 2 rue Ambroise Paré, 75010, Paris, France.

Anat Loewenstein (A)

Department of Ophthalmology, Tel Aviv Medical Center, Sackler Faculty of Medicine, Tel Aviv, Israel.

Bruno Lumbroso (B)

Centro Italiano Macula, Rome, Italy.

Daniela Ferrara (D)

New England Eye Center, Tufts Medical Center, Tufts University School of Medicine, Boston, Massachusetts.

David Sarraf (D)

Stein Eye Institute, Department of Ophthalmology, David Geffen School of Medicine at the University of California, Los Angeles, Los Angeles, California.

David T Wong (DT)

Department of Ophthalmology, Unity Health Toronto, University of Toronto, Canada.

Dimitra Skondra (D)

Department of Ophthalmology and Visual Sciences, The University of Chicago, Chicago, Illinois.

Francisco J Rodriguez (FJ)

Fundacion Oftalmologica Nacional, Universidad del Rosario, Bogota, DC, Colombia.

Giovanni Staurenghi (G)

Department of Biomedical and Clinical Science "Luigi Sacco" University of Milan Luigi Sacco Hospital Italy, Milan, Italy.

Ian Pearce (I)

St Paul's Eye Unit, Royal Liverpool University Hospital, Liverpool, United Kingdom.

Judy E Kim (JE)

Department of Ophthalmology, Medical College of Wisconsin, Milwaukee, Wisconsin.

K Bailey Freund (KB)

Vitreous Retina Macula Consultants of New York, New York; Department of Ophthalmology, New York University Grossman School of Medicine, New York, New York.

Maurizio Battaglia Parodi (MB)

Department of Ophthalmology, Scientific Institute San Raffaele Hospital, Milan, Italy.

Nadia K Waheed (NK)

Department of Ophthalmology, Tufts University School of Medicine, Boston, Massachusetts.

Richard Rosen (R)

Department of Ophthalmology, New York Eye and Ear Infirmary of Mount Sinai, New York City, New York.

Richard F Spaide (RF)

Department of Ophthalmology Vitreous Retina Macula Consultants of New York, New York; Department of Ophthalmology, New York University Grossman School of Medicine, New York, New York.

Shintaro Nakao (S)

Department of Ophthalmology, National Hospital Organization, Kyushu Medical Center, Fukuoka, Japan.

SriniVas Sadda (S)

Doheny Image Reading Center, Doheny Eye Institute, Los Angeles, California.

Stela Vujosevic (S)

Department of Biomedical, Surgical and Dental Sciences University of Milan, Milan, Italy; Eye Clinic IRCCS MultiMedica, Milan, Italy.

Tien Yin Wong (TY)

Department of Ophthalmology, Singapore Eye Research Institute, Singapore National Eye Center, Duke-NUS Medical School, National University of Singapore.

Toshinori Murata (T)

Department of Ophthalmology, Shinshu University School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano, 390-8621, Japan.

Usha Chakravarthy (U)

Ophthalmology and Vision Sciences, Queen's University, Belfast, United Kingdom.

Yuichiro Ogura (Y)

Department of Ophthalmology and Visual Science, Graduate School of Medical Sciences, Nagoya City University.

Wolfgang Huf (W)

Karl Landsteiner Institute for Clinical Risk Management, Vienna, Austria.

Meng Tian (M)

Department of Ophthalmology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland; Bern Photographic Reading Center, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland; Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing, China.

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Classifications MeSH