Optical Coherence Tomography Artifacts Are Associated With Adaptive Optics Scanning Light Ophthalmoscopy Success in Achromatopsia.

achromatopsia adaptive optics inherited retinal disease optical coherence tomography

Journal

Translational vision science & technology
ISSN: 2164-2591
Titre abrégé: Transl Vis Sci Technol
Pays: United States
ID NLM: 101595919

Informations de publication

Date de publication:
01 2021
Historique:
received: 29 07 2020
accepted: 04 12 2020
entrez: 29 1 2021
pubmed: 30 1 2021
medline: 29 6 2021
Statut: epublish

Résumé

To determine whether artifacts in optical coherence tomography (OCT) images are associated with the success or failure of adaptive optics scanning light ophthalmoscopy (AOSLO) imaging in subjects with achromatopsia (ACHM). Previously acquired OCT and non-confocal, split-detector AOSLO images from one eye of 66 subjects with genetically confirmed achromatopsia (15 There was excellent agreement between the two observers for assessing OCT artifact severity category (weighted kappa = 0.88). Overall, AOSLO success was 47%. For subjects with OCT artifact severity category 1, AOSLO success was 65%; for category 2, 47%; for category 3, 11%; and for category 4, 0%. There was a significant association between OCT artifact severity category and AOSLO success ( Artifacts in OCT volumes are associated with AOSLO success in ACHM. Subjects with less severe OCT artifacts are more likely to be good candidates for AOSLO imaging, whereas AOSLO was successful in only 7% of subjects with category 3 or 4 OCT artifacts. These results may be useful in guiding patient selection for AOSLO imaging. Using OCT to prescreen patients could be a valuable tool for clinical trials that utilize AOSLO to reduce costs and decrease patient testing burden.

Identifiants

pubmed: 33510950
doi: 10.1167/tvst.10.1.11
pii: TVST-20-2893
pmc: PMC7804582
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

11

Subventions

Organisme : NEI NIH HHS
ID : R01 EY017607
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM080202
Pays : United States

Informations de copyright

Copyright 2021 The Authors.

Déclaration de conflit d'intérêts

Disclosure: K.M. Litts, None; E.N. Woertz, None; M. Georgiou, MeiraGTx (C); E.J. Patterson, None; B.L. Lam, AGTC (F), G.A. Fishman, AGTC (F); M.E. Pennesi, AGTC (F); C.N. Kay, AGTC (F); W.W. Hauswirth, AGTC (I, R); M. Michaelides, MeiraGTx (C); J. Carroll, MeiraGTx (C, F), OptoVue (F), AGTC (F), Translational Imaging Innovations (I)

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Auteurs

Katie M Litts (KM)

Department of Ophthalmology & Visual Sciences, Medical College of Wisconsin, Milwaukee, WI, USA.

Erica N Woertz (EN)

Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA.

Michalis Georgiou (M)

UCL Institute of Ophthalmology, University College London, London, UK.
Moorfields Eye Hospital NHS Foundation Trust, London, UK.

Emily J Patterson (EJ)

Department of Ophthalmology & Visual Sciences, Medical College of Wisconsin, Milwaukee, WI, USA.

Byron L Lam (BL)

Bascom Palmer Eye Institute, University of Miami, Miami, FL, USA.

Gerald A Fishman (GA)

Pangere Center for Inherited Retinal Diseases, The Chicago Lighthouse, Chicago, IL, USA.

Mark E Pennesi (ME)

Casey Eye Institute, Oregon Health & Science University, Portland, OR, USA.

Christine N Kay (CN)

Vitreoretinal Associates, Gainesville, FL, USA.

William W Hauswirth (WW)

Department of Ophthalmology, University of Florida, Gainesville, FL, USA.

Michel Michaelides (M)

UCL Institute of Ophthalmology, University College London, London, UK.
Moorfields Eye Hospital NHS Foundation Trust, London, UK.

Joseph Carroll (J)

Department of Ophthalmology & Visual Sciences, Medical College of Wisconsin, Milwaukee, WI, USA.
Department of Cell Biology, Neurobiology and Anatomy, Medical College of Wisconsin, Milwaukee, WI, USA.

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