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292    CHAPTER 14  OCT fluid detection and quantification




                            Performance in exudative disease diagnosis and fluid detection has been shown to be
                         very high in a number of papers reviewed in this chapter. Interrater variability was also
                         demonstrated to be small and gold standards for training OCT classification methods
                         are generally available. This is important, as only a very high sensitivity and specificity
                         are clinically accepted for fluid detection. False negatives and false positives bring a
                         high risk of vision loss and an unnecessary increased treatment burden, respectively. By
                         contrast, the segmentation performance level required and most appropriate quantifica-
                         tion metric are currently unclear and likely depend on the particular clinical use case.
                         Fluid segmentation methods have shown lower performance, although approaching the
                         interrater variability. The large interrater variability reflects the difficulty of the annota-
                         tion task and produces a lower quality of the pixel-wise reference standard for training.
                         Thus, weakly supervised and unsupervised efforts are of special importance to support
                         the segmentation methods going beyond the limit of human annotator capabilities.
                            OCT is a relatively young imaging modality and is still rapidly evolving. In par-
                         ticular, the speed of acquisition is increasing and devices already operate at over
                         100,000 A-scans per second [81]. Thus, the next generation of OCT is expected to
                         have fewer artifacts and a higher SNR, facilitating the tasks of automated fluid de-
                         tection and segmentation. Clinically applicable automated fluid analysis is expected
                         to increase the set of readily available quantitative OCT biomarkers, which together
                         will enable personalized and predictive medicine in macular disease.



                           Acknowledgments

                         This work was supported by the Christian Doppler Research Association, the Austrian
                         Federal Ministry for Digital and Economic Affairs, and the National Foundation for
                         Research, Technology and Development.



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