2016
DOI: 10.1167/iovs.15-18694
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Automated Identification and Quantification of Subretinal Fibrosis in Neovascular Age-Related Macular Degeneration Using Polarization-Sensitive OCT

Abstract: Using PS-OCT, subretinal fibrosis can be identified as an intrinsically birefringent structure and can be segmented based solely on tissue-specific contrast. Polarization-sensitive OCT offers a unique method to identify clinically relevant components of SHRM (i.e., neovascular tissue versus fibrous tissue) and therefore allows for an optimized disease management and evaluation of therapeutic strategies.

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Cited by 41 publications
(40 citation statements)
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References 38 publications
(48 reference statements)
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“…Thus, these patterns do not match exactly and, especially in doubtful cases, can lead to misinterpretations. The occurrence of the patchy structures is similar to what has been reported earlier by Roberts et al 26 and could reflect an irregular pattern of inflammation and healing processes. The development of subretinal fibrosis is similar to that of fibrosis in other parts of the body; tissue inflammation causes the release of mediators recruiting inflammatory cells and fibroblasts.…”
Section: Discussionsupporting
confidence: 89%
See 2 more Smart Citations
“…Thus, these patterns do not match exactly and, especially in doubtful cases, can lead to misinterpretations. The occurrence of the patchy structures is similar to what has been reported earlier by Roberts et al 26 and could reflect an irregular pattern of inflammation and healing processes. The development of subretinal fibrosis is similar to that of fibrosis in other parts of the body; tissue inflammation causes the release of mediators recruiting inflammatory cells and fibroblasts.…”
Section: Discussionsupporting
confidence: 89%
“…PS-OCT makes use of the birefringent properties of fibrosis to establish its presence, offering an additional and potentially more reliable detection method. [25][26][27] In most cases with a birefringent signal, the fibrotic lesions showed a spatially heterogeneous patchy structure rather than a uniform birefringent layer. Those correlate with the occurrence of yellow-whitish lesions in the fundus images and formation of a hyperreflective layer in the structural images (in clear cases) but show more details of the local distribution of fibrotic tissue.…”
Section: Discussionmentioning
confidence: 99%
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“…A recent study using a PS-OCT system with an integrated retinal tracker [125] -which is important since the fixation capability of affected patients is usually poor, leading to heavy motion artifacts -demonstrated that fibrotic lesions can be readily identified and in the majority of cases also segmented by their characteristic birefringence patterns, showing column-like axis orientation patterns in PS-OCT B-scans (cf. Figure 18) [126]. The combination of PS-OCT with OCT angiography provides further insights into neovascular lesions in AMD patients [127].…”
Section: Imaging Of Macular Lesionsmentioning
confidence: 99%
“…In late stage non-exudative (dry) AMD, PS-OCT enables the assessment of atrophic areas lacking RPE (Figure 5a-d) [121,157,158]. In exudative diseases such as wet AMD, central serous chorioretinopathy, and diabetic macular edema, PS-OCT was demonstrated for imaging and identifying fibrotic scars, hard exudates, as well as pigment epithelial features [123,[159][160][161][162]. Finally, PS-OCT also proved useful to enhance contrast for imaging pathologic structures in less common retinal diseases such as macular telangiectasia and Stargardt disease [163,164].…”
Section: Ps-oct In the Eyementioning
confidence: 99%