Retinal imaging including optical coherence tomography angiography for detecting active choroidal neovascularization in pseudoxanthoma elasticum.


Journal

Clinical & experimental ophthalmology
ISSN: 1442-9071
Titre abrégé: Clin Exp Ophthalmol
Pays: Australia
ID NLM: 100896531

Informations de publication

Date de publication:
03 2019
Historique:
received: 18 06 2018
revised: 23 08 2018
accepted: 24 08 2018
pubmed: 1 9 2018
medline: 11 4 2020
entrez: 1 9 2018
Statut: ppublish

Résumé

The diagnostic accuracy of different retinal imaging modalities to detect active choroidal neovascularization (CNV) in pseudoxanthoma elasticum (PXE) is essential to enable a correct diagnosis but is currently poorly understood. Optical coherence tomography (OCT), fluorescein angiography (FA) and OCT angiography (OCT-A) are employed in daily practice, but a systematic comparison of these imaging techniques is lacking. Retrospective, observational study. Twenty patients (31 eyes) with PXE. OCT, FA and OCT-A imaging was performed in each eye and graded separately by independent readers. Diagnostic accuracy, sensitivity and specificity to detect CNV-activity of each modality and longitudinal change of CNV size measured by OCT-A. OCT showed the highest diagnostic accuracy (kappa = 0.57) in comparison to OCT-A or FA (kappa = 0.39 and 0.37, respectively). OCT-A, OCT and FA showed a diagnostic sensitivity of 0.9, 0.85 and 0.6, and a diagnostic specificity of 0.45, 0.72 and 0.82, respectively. Evaluation of longitudinal OCT recordings (24 eyes) resulted in optimal sensitivity and specificity (kappa = 1.0). Although median CNV size assessed using OCT-A remained stable on longitudinal measures of seven eyes, two eyes showed a distinct increase over time despite anti-vascular endothelial growth factor treatment. The systematic use of OCT, FA and OCT-A imaging can facilitate the diagnostic accuracy for detection and follow-up of CNV activity in PXE. While structural OCT is of high value, especially when longitudinal follow-up images are available, FA and OCT-A data might contribute to diagnostic accuracy in more complex cases.

Sections du résumé

IMPORTANCE
The diagnostic accuracy of different retinal imaging modalities to detect active choroidal neovascularization (CNV) in pseudoxanthoma elasticum (PXE) is essential to enable a correct diagnosis but is currently poorly understood.
BACKGROUND
Optical coherence tomography (OCT), fluorescein angiography (FA) and OCT angiography (OCT-A) are employed in daily practice, but a systematic comparison of these imaging techniques is lacking.
DESIGN
Retrospective, observational study.
PARTICIPANTS
Twenty patients (31 eyes) with PXE.
METHODS
OCT, FA and OCT-A imaging was performed in each eye and graded separately by independent readers.
MAIN OUTCOME MEASURES
Diagnostic accuracy, sensitivity and specificity to detect CNV-activity of each modality and longitudinal change of CNV size measured by OCT-A.
RESULTS
OCT showed the highest diagnostic accuracy (kappa = 0.57) in comparison to OCT-A or FA (kappa = 0.39 and 0.37, respectively). OCT-A, OCT and FA showed a diagnostic sensitivity of 0.9, 0.85 and 0.6, and a diagnostic specificity of 0.45, 0.72 and 0.82, respectively. Evaluation of longitudinal OCT recordings (24 eyes) resulted in optimal sensitivity and specificity (kappa = 1.0). Although median CNV size assessed using OCT-A remained stable on longitudinal measures of seven eyes, two eyes showed a distinct increase over time despite anti-vascular endothelial growth factor treatment.
CONCLUSIONS AND RELEVANCE
The systematic use of OCT, FA and OCT-A imaging can facilitate the diagnostic accuracy for detection and follow-up of CNV activity in PXE. While structural OCT is of high value, especially when longitudinal follow-up images are available, FA and OCT-A data might contribute to diagnostic accuracy in more complex cases.

Identifiants

pubmed: 30168640
doi: 10.1111/ceo.13385
doi:

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

240-249

Informations de copyright

© 2018 Royal Australian and New Zealand College of Ophthalmologists.

Auteurs

Johannes Birtel (J)

Department of Ophthalmology, University of Bonn, Bonn, Germany.

Moritz Lindner (M)

Department of Ophthalmology, University of Bonn, Bonn, Germany.
Nuffield Department of Clinical Neurosciences, University of Oxford, The Nuffield Laboratory of Ophthalmology, Sleep and Circadian Neuroscience Institute, Oxford, UK.
Department of Clinical Neurosciences, University of Oxford, Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, and Nuffield Laboratory of Ophthalmology, Oxford, UK.

Divyansh K Mishra (DK)

Department of Ophthalmology, University of Bonn, Bonn, Germany.

Philipp L Müller (PL)

Department of Ophthalmology, University of Bonn, Bonn, Germany.

Doris Hendig (D)

Institute for Laboratory and Transfusion Medicine, Heart and Diabetes, Center North Rhine-Westphalia, University Hospital of the Ruhr University of Bochum, Bad Oeynhausen, Germany.

Philipp Herrmann (P)

Department of Ophthalmology, University of Bonn, Bonn, Germany.

Frank G Holz (FG)

Department of Ophthalmology, University of Bonn, Bonn, Germany.

Monika Fleckenstein (M)

Department of Ophthalmology, University of Bonn, Bonn, Germany.

Martin Gliem (M)

Department of Ophthalmology, University of Bonn, Bonn, Germany.
Department of Clinical Neurosciences, University of Oxford, Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, and Nuffield Laboratory of Ophthalmology, Oxford, UK.

Peter Charbel Issa (P)

Department of Ophthalmology, University of Bonn, Bonn, Germany.
Department of Clinical Neurosciences, University of Oxford, Oxford Eye Hospital, Oxford University Hospitals NHS Foundation Trust, and Nuffield Laboratory of Ophthalmology, Oxford, UK.

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