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      Optical coherence tomography angiography

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          Abstract

          Optical coherence tomography (OCT) was one of the biggest advances in ophthalmic imaging. Building on that platform, OCT angiography (OCTA) provides depth resolved images of blood flow in the retina and choroid with levels of detail far exceeding that obtained with older forms of imaging. This new modality is challenging because of the need for new equipment and processing techniques, current limitations of imaging capability, and rapid advancements in both imaging and in our understanding of the imaging and applicable pathophysiology of the retina and choroid. These factors lead to a steep learning curve, even for those with a working understanding dye-based ocular angiography. All for a method of imaging that is a little more than 10 years old. This review begins with a historical account of the development of OCTA, and the methods used in OCTA, including signal processing, image generation, and display techniques. This forms the basis to understand what OCTA images show as well as how image artifacts arise. The anatomy and imaging of specific vascular layers of the eye are reviewed. The integration of OCTA in multimodal imaging in the evaluation of retinal vascular occlusive diseases, diabetic retinopathy, uveitis, inherited diseases, age-related macular degeneration, and disorders of the optic nerve is presented. OCTA is an exciting, disruptive technology. Its use is rapidly expanding in clinical practice as well as for research into the pathophysiology of diseases of the posterior pole.

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          Most cited references309

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          Optical coherence tomography.

          A technique called optical coherence tomography (OCT) has been developed for noninvasive cross-sectional imaging in biological systems. OCT uses low-coherence interferometry to produce a two-dimensional image of optical scattering from internal tissue microstructures in a way that is analogous to ultrasonic pulse-echo imaging. OCT has longitudinal and lateral spatial resolutions of a few micrometers and can detect reflected signals as small as approximately 10(-10) of the incident optical power. Tomographic imaging is demonstrated in vitro in the peripapillary area of the retina and in the coronary artery, two clinically relevant examples that are representative of transparent and turbid media, respectively.
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            Emergence of scaling in random networks

            Systems as diverse as genetic networks or the World Wide Web are best described as networks with complex topology. A common property of many large networks is that the vertex connectivities follow a scale-free power-law distribution. This feature was found to be a consequence of two generic mechanisms: (i) networks expand continuously by the addition of new vertices, and (ii) new vertices attach preferentially to sites that are already well connected. A model based on these two ingredients reproduces the observed stationary scale-free distributions, which indicates that the development of large networks is governed by robust self-organizing phenomena that go beyond the particulars of the individual systems.
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              Split-spectrum amplitude-decorrelation angiography with optical coherence tomography

              Amplitude decorrelation measurement is sensitive to transverse flow and immune to phase noise in comparison to Doppler and other phase-based approaches. However, the high axial resolution of OCT makes it very sensitive to the pulsatile bulk motion noise in the axial direction. To overcome this limitation, we developed split-spectrum amplitude-decorrelation angiography (SSADA) to improve the signal-to-noise ratio (SNR) of flow detection. The full OCT spectrum was split into several narrower bands. Inter-B-scan decorrelation was computed using the spectral bands separately and then averaged. The SSADA algorithm was tested on in vivo images of the human macula and optic nerve head. It significantly improved both SNR for flow detection and connectivity of microvascular network when compared to other amplitude-decorrelation algorithms.
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                Author and article information

                Journal
                9431859
                20937
                Prog Retin Eye Res
                Prog Retin Eye Res
                Progress in retinal and eye research
                1350-9462
                1873-1635
                1 February 2019
                08 December 2017
                May 2018
                07 March 2019
                : 64
                : 1-55
                Affiliations
                [a ] Vitreous, Retina, Macula Consultants of New York, New York, NY, United States
                [b ] Department of Electrical Engineering & Computer Science and Research Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge MA, United States
                [c ] The Department of Ophthalmology, Tufts University School of Medicine, Boston MA, United States
                [d ] Doheny Eye Institute, University of California – Los Angeles, Los Angeles, CA, United States
                [e ] Eye Clinic, Department of Biomedical and Clinical Sciences “Luigi Sacco”, Luigi Sacco Hospital, University of Milan, Milan, Italy
                Author notes
                [* ] Corresponding author. Vitreous, Retina, Macula Consultants of New York, 460 Park Ave., New York, NY 10022, United States. rickspaide@ 123456gmail.com (R.F. Spaide).
                Article
                NIHMS1006164
                10.1016/j.preteyeres.2017.11.003
                6404988
                29229445
                a214f037-fad0-46f5-8f24-eef193a1ad2e

                This is an open access article under the CC BY license ( http://creativecommons.org/licenses/BY/4.0/).

                History
                Categories
                Article

                Vision sciences
                multimodal imaging,optical coherence tomography,optical coherence tomography angiography

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