May 2006
Volume 47, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2006
Optophysiology of the Human RetinaWith Functional Ultrahigh Resolution Optical Coherence Tomography
Author Affiliations & Notes
  • B. Hermann
    Medical University of Vienna, Vienna, Austria
    Center for Biomedical Engineering & Physics,
  • B. Povaay
    Medical University of Vienna, Vienna, Austria
    Center for Biomedical Engineering & Physics,
  • A. Unterhuber
    Medical University of Vienna, Vienna, Austria
    Center for Biomedical Engineering & Physics,
  • M. Lessel
    Medical University of Vienna, Vienna, Austria
    Department of Ophthalmology,
  • H. Sattmann
    Medical University of Vienna, Vienna, Austria
    Center for Biomedical Engineering & Physics,
  • U. Schmidt–Erfurth
    Medical University of Vienna, Vienna, Austria
    Department of Ophthalmology,
  • W. Drexler
    Medical University of Vienna, Vienna, Austria
    Center for Biomedical Engineering & Physics,
  • Footnotes
    Commercial Relationships  B. Hermann, None; B. Povaay, None; A. Unterhuber, None; M. Lessel, None; H. Sattmann, None; U. Schmidt–Erfurth, None; W. Drexler, Carl Zeiss Meditec, C.
  • Footnotes
    Support  FWF P14218 HIGHWIRE EXLINK_ID="47:5:1672:1" VALUE="P14218" TYPEGUESS="GEN, PIRDB, SPROT" /HIGHWIRE –PSY, FWF Y159–PAT, the Christian Doppler Society, EC Grant CORTIVIS QLRT–2001–00279, FEMTOLASERS Inc. and CARL ZEISS Meditec Inc.
Investigative Ophthalmology & Visual Science May 2006, Vol.47, 1672. doi:
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      B. Hermann, B. Povaay, A. Unterhuber, M. Lessel, H. Sattmann, U. Schmidt–Erfurth, W. Drexler; Optophysiology of the Human RetinaWith Functional Ultrahigh Resolution Optical Coherence Tomography . Invest. Ophthalmol. Vis. Sci. 2006;47(13):1672.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : To introduce a possible optical analogue to electrophysiology for non–invasive depth resolved optical mapping of retinal response in the living human retina.

Methods: : Time and frequency domain optical coherence tomography (OCT) technology using light centered at 1040 nm has been developed for high speed (up to 15000 A–scans per second) ultrahigh resolution retinal imaging. Utilizing a light source emitting spectrum centred at 1040 nm compared to longer wavelength has the advantages to significantly reduce power losses due to water absorption and furthermore avoids pre–stimulation of the retina due to the laser spectrum positioned far away from the spectral sensitivity range of the photoreceptors. High speed OCT technology enables not only three–dimensional imaging but also high time resolution of up to 50 µs for detection of fast physiological changes.

Results: : OCT technology using 1040 nm light and simultaneous ERG measurements have been used to perform preliminary in vivo optophysiology measurements in normal human subjects. Measurements were performed over 8 seconds with 3 seconds pre–stimulus period and different light stimuli (7 ms to 200 ms, at multiple intensities and wavelengths below 850 nm) foveal and parafoveal. Dark scans of the same duration with no light stimulation were also acquired for baseline measurements. Subjects were cyclopleged and dark adapted or light adapted respectively before the measurements. Pronounced changes in the retinal backscattering specifically in the depth of the photoreceptor layer were observed in the single flash M–scans as compared to the dark scan M–scans. Limitations and challenges of this technique due to eye motions for in vivo optophysiology will be discussed.

Conclusions: : Non–contact, optical probing of retinal response to visual stimulation with ∼5 µm axial and ∼20 µm transversal resolution, by functional ultrahigh resolution optical coherence tomography was demonstrated for the first time in vivo in normal healthy subjects and could be correlated to simultaneous ERG measurements.

Keywords: imaging methods (CT, FA, ICG, MRI, OCT, RTA, SLO, ultrasound) • retina • electroretinography: non-clinical 
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