
1.Surrey Biophotonics, Centre for Vision, Speech and Signal Processing and School of Biosciences and Medicine, The University of Surrey, Guildford, GU2 7XH, UK
2.NIHR Biomedical Research Centre at Moorfields Eye Hospital NHS Trust and UCL Institute of Ophthalmology, London, EC1V 2PD, UK
3.Centre for Ophthalmology and Visual Science (incorporating Lions Eye Institute), The University of Western Australia, Nedlands, Western Australia, 6009, Australia
4.Department of Ophthalmology, Royal Perth Hospital, Perth, Western Australia, 6000, Australia
5.Ophthalmology, Department of Surgery, University of Melbourne, Melbourne, Victoria, 3002, Australia
6.Department of Ophthalmology & Vision Science, University of California Davis, Sacramento, CA, 95817, USA
7.Surrey Biophotonics, Advanced Technology Institute, School of Physics and School of Biosciences and Medicine, University of Surrey, Guildford, Surrey, GU2 7XH, UK
Danuta M. Sampson (danuta.sampson@surrey.ac.uk)
Published:30 April 2022,
Published Online:18 March 2022,
Received:01 August 2021,
Revised:01 February 2022,
Accepted:14 February 2022
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Sampson, D. M. et al. Towards standardizing retinal optical coherence tomography angiography: a review. Light: Science & Applications, 11, 520-541 (2022).
Sampson, D. M. et al. Towards standardizing retinal optical coherence tomography angiography: a review. Light: Science & Applications, 11, 520-541 (2022). DOI: 10.1038/s41377-022-00740-9.
The visualization and assessment of retinal microvasculature are important in the study
diagnosis
monitoring
and guidance of treatment of ocular and systemic diseases. With the introduction of optical coherence tomography angiography (OCTA)
it has become possible to visualize the retinal microvasculature volumetrically and without a contrast agent. Many lab-based and commercial clinical instruments
imaging protocols and data analysis methods and metrics
have been applied
often inconsistently
resulting in a confusing picture that represents a major barrier to progress in applying OCTA to reduce the burden of disease. Open data and software sharing
and cross-comparison and pooling of data from different studies are rare. These inabilities have impeded building the large databases of annotated OCTA images of healthy and diseased retinas that are necessary to study and define characteristics of specific conditions. This paper addresses the steps needed to standardize OCTA imaging of the human retina to address these limitations. Through review of the OCTA literature
we identify issues and inconsistencies and propose minimum standards for imaging protocols
data analysis methods
metrics
reporting of findings
and clinical practice and
where this is not possible
we identify areas that require further investigation. We hope that this paper will encourage the unification of imaging protocols in OCTA
promote transparency in the process of data collection
analysis
and reporting
and facilitate increasing the impact of OCTA on retinal healthcare delivery and life science investigations.
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