gms | German Medical Science

7th International Symposium on AMD: Age-related Macular Degeneration – Understanding Pathogenetic Mechanisms of Disease

20.09. - 21.09.2019, Baden-Baden

Full-field OCT for imaging AMD progression

Meeting Abstract

  • Gereon Hüttmann - University of Lübeck/D; Medical Laser Center Lübeck/D
  • P. Koch - Medical Laser Center Lübeck/D
  • H. Sudkamp - Medical Laser Center Lübeck/D
  • M. Moltmann - Medical Laser Center Lübeck/D
  • D. Theisen-Kunde - Medical Laser Center Lübeck/D
  • C. Pfäffle - University of Lübeck/D
  • D. Hillmann - University of Lübeck/D; Thorlabs GmbH, Lübeck/D
  • C. von der Burchard - Kiel/D
  • J. Tode - Kiel/D
  • C. Ehlken - Kiel/D
  • T. Kepp - University of Lübeck/D
  • H. Handels - University of Lübeck/D
  • R. Birngruber - University of Lübeck/D
  • J. Roider - Kiel/D

7th International Symposium on AMD: Age-related Macular Degeneration - Understanding Pathogenetic Mechanisms of Disease. Baden-Baden, 20.-21.09.2019. Düsseldorf: German Medical Science GMS Publishing House; 2020. Doc19amd38

doi: 10.3205/19amd38, urn:nbn:de:0183-19amd381

Veröffentlicht: 5. Februar 2020

© 2020 Hüttmann et al.
Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung). Lizenz-Angaben siehe http://creativecommons.org/licenses/by/4.0/.


Gliederung

Text

Background: Optical coherence tomography (OCT) is indispensable for studying the progression of age-related macular degeneration (AMD), since it can show quantitatively morphological changes of the retina. However, current OCT devices can only be used in clinical settings and do not provide functional information. We developed a full-field (FF) technology for OCT which acquires all A-scans in parallel. This technology allows for very compact (shoe box size) low cost (5000 €) devices which can be used in point of care and home care settings. FF-OCT also allows invasive marker-free functional imaging of retinal function.

Methods: Two FF-OCT devices were evaluated. The low-cost version used the time domain (TD) principle and was tested with 39 patients with neovascular AMD for detection of relevant biomarkers. The device measured a field of 2 mm x 4 mm at 15 µm resolution within 10 seconds.

The second device used swept-source OCT for ultra-fast imaging of the retina with more than 100 volumes/s. Nanometer dynamic changes of the thickness of the photoreceptor and the ganglion cell layer were evaluated after optical stimulation in healthy subjects.

Results: With the low-cost version, patients were able to do unassisted OCT imaging of their retina with high success rate after only 5 to 10 min training. The most relevant biomarkers for AMD (i.e. intraretinal fluid, subretinal fluid and pigment epithelium detachment) were visible in the OCT volumes.

With the ultra-fast OCT, responses of photoreceptor and neuronal cells could be measured quantitatively.

Conclusions: FF-OCT opens new perspectives in imaging AMD progression by enabling daily self-surveillance by the patient at home. Continuous evaluation of the disease may become possible using automatic evaluation by artificial intelligence.

Functional imaging may enable an even earlier detection of disease progression.