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1 OCT angiography features associated with exudation inclu
2 OCT angiography images centered at the fovea were obtain
3 OCT angiography measurements correlated with both radiat
4 OCT angiography provided a quantitative measurement of r
5 OCT B-scans show SLG as small, round, hyporeflective str
6 OCT demonstrated multiplane and longitudinal calcium fra
7 OCT did not improve the diagnostic accuracy of the TECS
8 OCT images were evaluated independently by 3 observers f
9 OCT images were graded for central macular thickness (CM
10 OCT measurements of GCC in healthy children show excelle
11 OCT measurements, taken at baseline and annually, were g
12 OCT offering 3-dimensional imaging of the retina is wide
13 OCT scans improved by 1 step in 10 patients in the PPV g
14 OCT scans improved by qualitative judgment in patients w
15 OCT showed significantly higher sensitivity, AUC and Kap
16 OCT thickness was symmetrical between each eye.
17 OCT was used to evaluate pigmented epithelial detachment
18 OCT-A images were analyzed from 310 eyes of 182 patients
19 Fluorescein angiography, a combination of 2 OCT protocols, and multicolor confocal scanning laser op
20 ) based on: (1) CFP only (2 parameters); (2) OCT biomarkers, minimal (3 parameters); (3) OCT biomarke
21 OCT biomarkers, minimal (3 parameters); (3) OCT biomarkers, extended (7 parameters); and (4) CFP and
24 e models based on CFP alone (model 1; 0.80), OCT alone (models 2 and 3; 0.82 for both), and when usin
25 gnosed with MINOCA, of whom 145 had adequate OCT image quality for analysis; 116 of these underwent C
28 ulation, the positive predictive value of an OCT scan showing complete PVD was 53%, whereas the negat
29 r and fluid features were extracted using an OCT machine-learning augmented segmentation platform.
31 between the retinal and choroidal anatomical OCT outcomes, rates of polyp closure and recurrences bet
32 Baseline fundus fluorescein angiograms and OCT images were graded for choroidal neovascularization
33 maging including fundus autofluorescence and OCT, electroretinography (ERG), and both microscopy and
36 logy, while clinical applications of IVM and OCT are revolutionizing cancer diagnosis and therapies.
37 important progress in the fields of IVM and OCT for cancer imaging in living subjects, highlighting
39 tes of change in SAP mean deviation (MD) and OCT RNFL thickness loss over time while adjusting for va
41 Clinical records, fundus photographs, and OCT imaging for patients with CLN2 disease collected dur
46 y, optical coherence tomography angiography (OCT-A) emerged as a non-invasive imaging technique allow
50 tive-optics optical coherence tomography (AO-OCT), spectral-domain OCT (SDOCT), and microperimetry (M
53 ior segment optical coherence tomography (AS OCT) is a helpful tool used to diagnose and manage many
55 on position 4 [TIP4]); anterior segment (AS) OCT tube parameters, including posterior cornea-to-tube
57 with significantly lower age, K-mean, and AS-OCT stages and higher pachymetric values (always P < .02
58 ination between bubble types, followed by AS-OCT stage, pachymetry, K-mean, and astigmatism (respecti
61 This study employed anterior segment OCT (AS-OCT) and slit-lamp (SL) photography to image the crystal
63 ior segment optical coherence tomography (AS-OCT) was performed in order to detect intrascleral hyper
66 d pupillometry examination using a binocular OCT system that presents a stimulus and simultaneously c
68 e optimal cutoff value for strut coverage by OCT which was defined as luminal endothelial cells with
70 fluid and intraretinal fluid as evaluated by OCT with respect to CNV type, total CNV, and leakage are
71 or possible culprit lesion was identified by OCT in 46.2% (67/145) of participants, most commonly pla
73 oherence tomography (OCT) technology, called OCT angiography (OCTA), capable of visualizing retina va
75 o evaluated using cross-polarization OCT (CP-OCT) during lesion dehydration to identify transparent s
78 gligible release in 0.1 N HCl, while the CTX-OCT was completely released after 300 min in phosphate b
84 owed weekly for 4 weeks with spectral-domain OCT (SD-OCT) assessing the time to maximal reduction of
85 le-layer sign" on structural spectral-domain OCT (SD-OCT) imaging, were used to identify characterist
87 herence tomography (AO-OCT), spectral-domain OCT (SDOCT), and microperimetry (MP) at 6 (baseline, BL)
93 of follow-up, 2 good quality spectral-domain OCT peripapillary retinal nerve fiber layer scans, and 2
95 n, in 47 distinct eyes, 4181 spectral-domain OCT slices were retrospectively reviewed to longitudinal
96 sed to monitor glaucoma, and spectral-domain OCT still has a relevant role in detecting fast progress
98 brosis was categorized using spectral-domain OCT with respect to retinal pigment epithelium (RPE) in
100 e present wide dynamic range en face Doppler OCT imaging with multiple time intervals ranging from 0.
107 average thickness (CAT) were collected from OCT images obtained at baseline and 3, 6, 9, and 12 mont
109 3 x 3-mm scan pattern SD-OCTA CIRRUS 5000 HD-OCT with AngioPlex (Carl Zeiss Meditec, Dublin, CA, USA)
112 he array's 60 electrodes using the Cirrus HD-OCT software in both the nasotemporal and superoinferior
113 luorescence imaging using the Spectralis HRA+OCT (Heidelberg Engineering, Inc., Heidelberg, Germany).
117 ng membrane (ILM) drape sign is an important OCT characteristic of Macular telangiectasia type 2 (Mac
122 e extent of retinal degeneration observed in OCT or fundus photographs; by using the fellow eye as a
123 vs. 8%; P = 0.01), and greater reduction in OCT-measured central subfield thickness (135 mum [SD, 15
126 of this study is to evaluate intraoperative OCT (iOCT) utility and outcomes during retinal detachmen
131 ith similar RNFL and macular damage, macular OCT-A shows less involvement of superficial and deep vas
134 or vitreous cortex are visualized on macular OCT, an accurate determination of attached vitreous can
135 tection of glaucoma progression with macular OCT imaging and propose ways to enhance its performance.
137 d by calibrated measurements across multiple OCT generations with corresponding visual fields (VFs).
138 n angiography (SSADA) software 7.1 to obtain OCT angiography (OCTA) images from fovea-centered 3 x 3-
141 Based on the pore network modeling (PNM) of OCT images, larger pores and connections were found in t
146 ographic atrophy (nGA) describes features on OCT imaging previously observed to precede the developme
147 of follow-up as well as anatomic features on OCT, including hole diameter and presence of vitreomacul
148 4% vs. 67.5%, P = 0.01), subretinal fluid on OCT (33.3% vs. 70.7%, P = 0.01), and greater extent of o
152 Outer retinal abnormalities persisted on OCT in patients after resolution of SRF and papilledema.
154 he 38 eyes graded as showing complete PVD on OCT, 20 eyes were found to have pre-existing PVD at the
158 eyes graded as showing attached vitreous on OCT, 129 eyes had attached vitreous at the time of surge
164 ch), macular integrity assessment perimetry, OCT, motion discrimination performance, and visual quali
165 were also evaluated using cross-polarization OCT (CP-OCT) during lesion dehydration to identify trans
173 oci (P < 0.001 and P = 0.045, respectively), OCT-reflective drusen substructures (P = 0.004 and P = 0
174 and average thickness on peripapillary RNFL OCT were associated significantly with LC and PLT thickn
175 act examination with and without a screening OCT was performed, evaluating for vitreoretinal diseases
177 ed study eyes in HARBOR with both FFA and SD OCT data were analyzed for (1) evidence of CNV activity
178 mits of agreement were between TD OCT and SD OCT were 26.64 to -22.95; between synthesized SD OCT and
180 to -22.95; between synthesized SD OCT and SD OCT were 8.11 to -6.73; and between SD OCT and SD OCT we
181 ts were imaged with color photography and SD OCT, and some were imaged with autofluorescence imaging,
184 tely predicting the severity of GFVD from SD OCT imaging can help clinicians more effectively individ
185 ndard, the sensitivity and specificity of SD OCT in detecting CNV activity was 91% (95% confidence in
186 lyzed for (1) evidence of CNV activity on SD OCT (presence of subretinal fluid, intraretinal fluid, a
188 h occult lesions that appear quiescent on SD OCT, as this type of lesion may show leakage on FFA.
191 were 26.64 to -22.95; between synthesized SD OCT and SD OCT were 8.11 to -6.73; and between SD OCT an
194 Deep learning models were trained to use SD OCT retinal nerve fiber layer (RNFL) thickness maps, RNF
197 l assessment of monthly spectral-domain (SD) OCT scans to determine MA prevalence, incidence, and pro
198 ect for axial length on spectral-domain (SD) OCT translates into lower signal strength and scan relia
200 erage of 4.8 SAP tests (range, 2-28), 3.6 SD-OCT tests (range, 2-10), and 8.3 HbA1c tests (range, 2-2
202 Qualitative structural AMD features and SD-OCT-based quantitative thickness changes of different re
204 ickening of the peripapillary vitreous by SD-OCT is useful in monitoring any vitreo-retinal change th
206 After 3 initial ranibizumab injections, SD-OCT detected nAMD activity in 89% of eyes when hemorrhag
207 l subjects underwent spectral domain OCT (SD-OCT) and qAF imaging with the Heidelberg HRA-Spectralis
208 kly for 4 weeks with spectral-domain OCT (SD-OCT) assessing the time to maximal reduction of central
209 sign" on structural spectral-domain OCT (SD-OCT) imaging, were used to identify characteristic featu
214 of follow-up and at least 2 good-quality SD-OCT scans and 2 clinical visits with Goldmann applanatio
215 scanning laser ophthalmoscopy (Spectralis SD-OCT; Heidelberg Engineering, Heidelberg, Germany) demons
216 y patient received visual acuity testing, SD-OCT and slit lamp examination prior to every injection.
217 e of GA was 1.6 (SD, 1.1) mm(2) using the SD-OCT cRORA criteria and 1.5 (SD, 1.0) mm(2) using the SD-
220 tral-domain optical coherence tomography (SD-OCT) (Spectralis) also measures the DFA (O-DFA) based on
221 tral domain optical coherence tomography (SD-OCT) demonstrated sub-retinal pigment epithelial nodular
222 tral-domain optical coherence tomography (SD-OCT) imaging and present a new classification scheme.
223 tral domain-optical coherence tomography (SD-OCT) revealed hyperreflective aberrations within photore
229 -sectional images (B-scans) obtained with SD-OCT showed that this dark band corresponds with an area
232 is study shows the potential value of serial OCT and tear cytokine measurements in the management of
234 ion rate enhancements of a difluorinated SNO-OCT derivative, as compared to the parent scaffold, were
235 ea were obtained on a prototype swept-source OCT device, and the VISTA algorithm was applied to visua
237 er (pRNFL) readings acquired with Spectralis OCT to distinguish between healthy and mild glaucoma pat
241 tinal thickness, distribution of fluid on SS OCT, and diameters and circuit of the foveal avascular z
243 known NE-MNV identified on swept-source (SS) OCT angiography (OCTA) and the "double-layer sign" on st
247 gh both imaging techniques are effective, SS-OCT appears to be at least comparable, or superior in sp
248 ity, specificity, and accuracy values for SS-OCT were 96.8% (95% confidence interval [CI] 83.81-99.43
254 The 95% limits of agreement were between TD OCT and SD OCT were 26.64 to -22.95; between synthesized
255 t significantly improved the agreement of TD OCT RNFLT measurements with SD OCT RNFLT measurements.
257 sed 284 newly diagnosed OAG patients with TD OCT images from a cohort of 516 recruited at 10 United K
258 een UKGTS treatment and placebo arms with TD OCT was 0.24 (P = 0.11) and with synthesized SD OCT was
260 Structural progression was measured by the OCT rate of thinning of the retinal nerve fiber layer (R
262 ocular information independently graded the OCT scans for the presence of ONH prelaminar schisis on
264 need to be considered while interpreting the OCT parameters in pathologic conditions such as glaucoma
265 ame misalignment, correct positioning of the OCT frames at the carina, lumen surface reconstruction,
266 d AXL, disc area, and signal strength of the OCT scan on retinal nerve fiber layer (RNFL) thickness,
268 es several technical novelties to tackle the OCT frame misalignment, correct positioning of the OCT f
270 pectral-domain optical coherence tomography (OCT) and 19,812 standard automated perimetry (SAP) tests
271 n advantage of Optical Coherence Tomography (OCT) and shown that the thickness of individual retinal
273 etry (UP), and optical coherence tomography (OCT) in diabetic eyes and compare the CCT values in pati
274 ing studies on optical coherence tomography (OCT) mainly focused on diabetic retinopathy and age-rela
275 r imaging with optical coherence tomography (OCT) measures the most critical retinal ganglion cells (
280 ystem based on Optical coherence tomography (OCT) technology, called OCT angiography (OCTA), capable
281 54,900 retinal optical coherence tomography (OCT) volume scans of 1094 patients with age-related macu
283 imaging (MRI), optical coherence tomography (OCT), VF, and optic disc photographs were reviewed.
284 aphy (QME), an optical coherence tomography (OCT)-based elastography technique that produces images o
285 symmetry using optical coherence tomography (OCT)-based measurements of the macular ganglion cell com
293 (SITA 24-2) tests (Zeiss, Dublin, CA), using OCT scans centered on MAC, ONH, or both (MAC + ONH) as i
295 9.0% sensitivity and 79.0% specificity using OCT images, versus 92.9% sensitivity and 96.4% specifici
296 he routine VA assessment and DFE while using OCT imaging through an undilated pupil followed by the i
301 Combining common clinical data points with OCT and OCTA data enhances the power of computer-aided d