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dc.contributor.authorBadaro, Emmerson
dc.contributor.authorKraus, Martin F.
dc.contributor.authorBaumal, Caroline R.
dc.contributor.authorWitkin, Andre J.
dc.contributor.authorHornegger, Joachim
dc.contributor.authorDuker, Jay S.
dc.contributor.authorWaheed, Nadia K.
dc.contributor.authorAdhi, Mehreen
dc.contributor.authorLiu, Jonathan Jaoshin
dc.contributor.authorFujimoto, James G
dc.date.accessioned2017-08-02T15:21:59Z
dc.date.available2017-08-02T15:21:59Z
dc.date.issued2015-11
dc.date.submitted2015-10
dc.identifier.issn0002-9394
dc.identifier.urihttp://hdl.handle.net/1721.1/110908
dc.description.abstractPurpose To analyze the vitreoretinal interface in diabetic eyes using 3-dimensional wide-field volumes acquired using high-speed, long-wavelength swept-source optical coherence tomography (SSOCT). Design Prospective cross-sectional study. Methods Fifty-six diabetic patients (88 eyes) and 11 healthy nondiabetic controls (22 eyes) were recruited. Up to 8 SSOCT volumes were acquired for each eye. A registration algorithm removed motion artifacts and merged multiple SSOCT volumes to improve signal. Vitreous visualization was enhanced using vitreous windowing method. Results Of 88 diabetic eyes, 20 eyes had no retinopathy, 21 eyes had nonproliferative diabetic retinopathy (NPDR) without macular edema, 20 eyes had proliferative diabetic retinopathy (PDR) without macular edema, and 27 eyes had diabetic macular edema (DME) with either NPDR or PDR. Thick posterior hyaloid relative to healthy nondiabetic controls was observed in 0 of 20 (0%) diabetic eyes without retinopathy, 4 of 21 (19%) eyes with NPDR, 11 of 20 (55%) eyes with PDR, and 11 of 27 (41%) eyes with DME (P = .0001). Vitreoschisis was observed in 6 of 22 (27%) healthy nondiabetic eyes, 9 of 20 (45%) diabetic eyes without retinopathy, 10 of 21 (48%) eyes with NPDR, 13 of 20 (65%) eyes with PDR, and 17 of 27 (63%) eyes with DME (P = .007). While no healthy nondiabetic controls and diabetic eyes without retinopathy had adhesions/pegs between detached posterior hyaloid and retina, 1 of 21 (4%), 11 of 20 (55%), and 11 of 27 (41%) eyes with NPDR, PDR, and DME, respectively, demonstrated this feature (P = .0001). Conclusion SSOCT with motion-correction and vitreous windowing provides wide-field 3-dimensional information of vitreoretinal interface in diabetic eyes. This may be useful in assessing progression of retinopathy, planning diabetic vitreous surgery, and predicting treatment outcomes.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (R01-EY011289-28)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (R01-EY013178-12)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (R01-CA075289-16)en_US
dc.description.sponsorshipUnited States. Air Force Office of Scientific Research (FA9550-10-1-0551)en_US
dc.description.sponsorshipUnited States. Air Force Office of Scientific Research (FA9550-12-1-0499)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.ajo.2015.10.025en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleThree-Dimensional Enhanced Imaging of Vitreoretinal Interface in Diabetic Retinopathy Using Swept-Source Optical Coherence Tomographyen_US
dc.typeArticleen_US
dc.identifier.citationAdhi, Mehreen; Badaro, Emmerson; Liu, Jonathan J. et al. “Three-Dimensional Enhanced Imaging of Vitreoretinal Interface in Diabetic Retinopathy Using Swept-Source Optical Coherence Tomography.” American Journal of Ophthalmology 162 (February 2016): 140–149 © 2016 Elsevier Incen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Research Laboratory of Electronicsen_US
dc.contributor.mitauthorAdhi, Mehreen
dc.contributor.mitauthorLiu, Jonathan Jaoshin
dc.contributor.mitauthorFujimoto, James G
dc.relation.journalAmerican Journal of Ophthalmologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsAdhi, Mehreen; Badaro, Emmerson; Liu, Jonathan J.; Kraus, Martin F.; Baumal, Caroline R.; Witkin, Andre J.; Hornegger, Joachim; Fujimoto, James G.; Duker, Jay S.; Waheed, Nadia K.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-0828-4357
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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