Purchase this article with an account.
Luis de Sisternes, Michael F Marmor, Theodore Leng, Daniel Rubin; Automated Segmentation and Quantification of Retinal Layers in Patients with Hydroxychloroquine Toxicity. Invest. Ophthalmol. Vis. Sci. 2014;55(13):4799. doi: https://doi.org/.
Download citation file:
© ARVO (1962-2015); The Authors (2016-present)
To demonstrate a new automated method quantifying regional changes in retinal layers in spectral-domain optical coherence tomography (SD-OCT), to enhance detection of hydroxycholoroquine (HCQ) toxicity and its progression.
We studied clinical SD-OCT scans recorded on a Zeiss (Cirrus) instrument from 8 normal eyes, and 15 eyes previously classified as early, moderate or severe HCQ toxicity. We used gradient statistics to produce an initial estimation of 9 retinal layers visible on SD-OCT and a weighted median filtering iterative process to refine their location. The segmentation of layers was validated ophthalmologically by a retina specialist (MFM). Quantitative features describing 5 mean thickness measurements (nerve fiber layer, outer nuclear layer, inner, outer, and whole retina) were automatically generated for 9 macula regions (similar to ETDRS regions), together with en face maps showing regional thinning. Loss of the ellipsoid zone (EZ, also called IS/OS line) was recognized where signal strength of the line was too low to be located, and quantitative features were extracted describing its morphology.
Total retina thickness measurements were very similar (<5% difference) between our method and the Cirrus instrument. In normal eyes, the automated retinal layer outlines were accurately located, and en face maps showed no focal defects. Retinopathy patients showed progressive thinning of the outer retina, beginning in parafoveal areas but extending with more severe disease into the fovea and peripheral regions of the posterior retina. Small regions of thinning could be visualized more readily in the generated en face maps (showing the whole macula) than in routine cross-sectional scans. Our method could also show the morphology of EZ line damage as retinopathy increases.
We have developed methods to automatically measure a set of SD-OCT imaging features that may be helpful for recognizing and tracking HCQ toxicity with more precision than is presently possible. Preliminary results in patients with HCQ toxicity show a promising ability to follow changes in the EZ line, and to separate inner and outer retinal damage. Refinements may allow monitoring of patients for foveal cone damage and visual loss.
This PDF is available to Subscribers Only