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910


Comparison of Trabectome Ab Interno Trabeculectomy to Baerveldt Glaucoma Implants using Propensity Score Matching [Meeting Abstract]

Wang, Steven Zhixie; Brown, Eric; Kaplowitz, Kevin; Kola, Sushma; Polat, Julia Kisin; Schuman, Joel S; Loewen, Nils A; Loewen Grp
ISI:000362882206262
ISSN: 0146-0404
CID: 1887462

Total Retinal Blood Flow Measurements with En Face Doppler Optical Coherence Tomography in Primary Open-Angle Glaucoma [Meeting Abstract]

Lee, ByungKun; Krishnan, Chandrasekharan; Choi, Woo Jhon; Adhi, Mehreen; de Carlo, Talisa; Chin, Adam T; Lu, Chen D; Duker, Jay S; Schuman, Joel S; Fujimoto, James G
ISI:000362882206316
ISSN: 0146-0404
CID: 1887472

Single Frame Virtual Averaging Improved Optical Coherence Tomography (OCT) Images Independent from Eye Movement Artifacts [Meeting Abstract]

Rangarajan, Anusha Alathur; Ishikawa, Hiroshi; Wollstein, Gadi; Kagemann, Larry; Sigal, Ian A; Bilonick, Richard Anthony; Sandrian, Michelle Gabriele; Schuman, Joel S
ISI:000362882206377
ISSN: 0146-0404
CID: 1887482

Induction of Adipose-derived Stem Cells to Trabecular Meshwork Cells for Glaucoma [Meeting Abstract]

Zhou, Yi; Yun, Hongmin; Yang, Enzhi; Schuman, Joel S; Du, Yiqin
ISI:000362891100150
ISSN: 0146-0404
CID: 1887492

Imaging of optic disc drusen: Swept-Source (SS)-OCT versus B-scan ultrasound [Meeting Abstract]

Ahn, Michelle; Eller, Andrew W; Wang, Bo; Mitchell, Ellen; Schuman, Joel S; Lu, Chen D; Grulkowski, Ireneusz; Fujimoto, James G; Wollstein, Gadi; Bonhomme, Gabrielle Rachelle
ISI:000362891102084
ISSN: 0146-0404
CID: 1887502

In-vivo 3D Deformation of Lamina Cribrosa Microstructure in Response to Acute Changes in Intraocular and Cerebrospinal Fluid Pressures [Meeting Abstract]

Wang, Bo; Sigal, Ian A; Smith, Matthew A; Kostanyan, Tigran; Bilonick, Richard Anthony; Tran, Huong; Kagemann, Larry; Tyler-Kabara, Elizabeth; Schuman, Joel S; Wollstein, Gadi
ISI:000362891102185
ISSN: 0146-0404
CID: 1887512

Longitudinal Profiles of Intraocular Pressure, Ocular Morphology and Visual Pathway Integrity in DBA/2J and C57BL/6J Mice [Meeting Abstract]

Yang, Xiaoling; Ho, Leon; van der Merwe, Yolandi; Conner, Ian; Kim, Seong-Gi; Wollstein, Gadi; Schuman, Joel S; Chan, Kevin C
ISI:000362891102190
ISSN: 0146-0404
CID: 1887522

Combining measurements from three anatomical areas for glaucoma diagnosis using Fourier-domain optical coherence tomography

Loewen, Nils A; Zhang, Xinbo; Tan, Ou; Francis, Brian A; Greenfield, David S; Schuman, Joel S; Varma, Rohit; Huang, David
AIMS: To improve the diagnostic power for glaucoma by combining measurements of peripapillary nerve fibre layer (NFL), macular ganglion cell complex (GCC) and disc variables obtained with Fourier-domain optical coherence tomography (FD-OCT) into the glaucoma structural diagnostic index (GSDI). METHODS: In this observational, cross-sectional study of subjects from the Advanced Imaging of Glaucoma Study, GCC and NFL of healthy and perimetrical glaucoma subjects from four major academic referral centres of the Advanced Imaging of Glaucoma Study were mapped with the RTVue FD-OCT. Global loss volume and focal loss volume parameters were defined using NFL and GCC normative reference maps. Optimal weights for NFL, GCC and disc variables were combined using multivariate logistic regression to build the GSDI. Glaucoma severity was classified using the Enhanced Glaucoma Staging System (GSS2). Diagnostic accuracy was assessed by sensitivity, specificity and the area under the receiver operator characteristic curve (AUC). RESULTS: We analysed 118 normal eyes of 60 subjects, 236 matched eyes of 166 subjects with perimetrical glaucoma, and 105 eyes from a healthy reference group of 61 subjects. The GSDI included composite overall thickness and focal loss volume with weighted NFL and GCC components, as well as the vertical cup-to-disc ratio. The AUC of 0.922 from leave-one-out cross validation was better than the best component variable alone (p=0.047). The partial AUC in the high specificity region was also better (p=0.01), with a sensitivity of 69% at 99% specificity, and a sensitivity of 80.3% at 95% specificity. For GSS2 stages 3-5 the sensitivity was 98% at 99% specificity, and 100% at 95% specificity. CONCLUSIONS: Combining structural measurements of GCC, NFL and disc variables from FD-OCT created a GSDI that improved the accuracy for glaucoma diagnosis. TRIAL REGISTRATION NUMBER: NCT01314326.
PMCID:5457797
PMID: 25795917
ISSN: 1468-2079
CID: 1884712

Psychophysical evaluation of haptic perception under augmentation by a handheld device

Wu, Bing; Klatzky, Roberta; Lee, Randy; Shivaprabhu, Vikas; Galeotti, John; Siegel, Mel; Schuman, Joel S; Hollis, Ralph; Stetten, George
OBJECTIVE: This study investigated the effectiveness of force augmentation in haptic perception tasks. BACKGROUND: Considerable engineering effort has been devoted to developing force augmented reality (AR) systems to assist users in delicate procedures like microsurgery. In contrast, far less has been done to characterize the behavioral outcomes of these systems, and no research has systematically examined the impact of sensory and perceptual processes on force augmentation effectiveness. METHOD: Using a handheld force magnifier as an exemplar haptic AR, we conducted three experiments to characterize its utility in the perception of force and stiffness. Experiments 1 and 2 measured, respectively, the user's ability to detect and differentiate weak force (<0.5 N) with or without the assistance of the device and compared it to direct perception. Experiment 3 examined the perception of stiffness through the force augmentation. RESULTS: The user's ability to detect and differentiate small forces was significantly improved by augmentation at both threshold and suprathreshold levels. The augmentation also enhanced stiffness perception. However, although perception of augmented forces matches that of the physical equivalent for weak forces, it falls off with increasing intensity. CONCLUSION: The loss in the effectiveness reflects the nature of sensory and perceptual processing. Such perceptual limitations should be taken into consideration in the design and development of haptic AR systems to maximize utility. APPLICATION: The findings provide useful information for building effective haptic AR systems, particularly for use in microsurgery.
PMCID:4480420
PMID: 25875439
ISSN: 0018-7208
CID: 1884782

Agreement among graders on Heidelberg retina tomograph (HRT) topographic change analysis (TCA) glaucoma progression interpretation

Iester, Michele M; Wollstein, Gadi; Bilonick, Richard A; Xu, Juan; Ishikawa, Hiroshi; Kagemann, Larry; Schuman, Joel S
PURPOSE: To evaluate agreement among experts of Heidelberg retina tomography's (HRT) topographic change analysis (TCA) printout interpretations of glaucoma progression and explore methods for improving agreement. METHODS: 109 eyes of glaucoma, glaucoma suspect and healthy subjects with >/=5 visits and 2 good quality HRT scans acquired at each visit were enrolled. TCA printouts were graded as progression or non-progression. Each grader was presented with 2 sets of tests: a randomly selected single test from each visit and both tests from each visit. Furthermore, the TCA printouts were classified with grader's individual criteria and with predefined criteria (reproducible changes within the optic nerve head, disregarding changes along blood vessels or at steep rim locations and signs of image distortion). Agreement among graders was modelled using common latent factor measurement error structural equation models for ordinal data. RESULTS: Assessment of two scans per visit without using the predefined criteria reduced overall agreement, as indicated by a reduction in the slope, reflecting the correlation with the common factor, for all graders with no effect on reducing the range of the intercepts between the graders. Using the predefined criteria improved grader agreement, as indicated by the narrower range of intercepts among the graders compared with assessment using individual grader's criteria. CONCLUSIONS: A simple set of predefined common criteria improves agreement between graders in assessing TCA progression. The inclusion of additional scans from each visit does not improve the agreement. We, therefore, recommend setting standardised criteria for TCA progression evaluation.
PMCID:4472474
PMID: 25336573
ISSN: 1468-2079
CID: 1884792