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Table of Contents - WOC 2012

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<strong>WOC</strong><strong>2012</strong> Abstract Book<br />

FP-IMG-SA 243 (3)<br />

Must know› About Magnetic Resonance Imaging for an<br />

Ophthalmologist<br />

Aggarwal Ekta (1) , Noronha Veena (2)<br />

1. Vasan Eye Care Hospitals<br />

2. VRR Scan<br />

Purpose: What an ophthalmologist should know about Magnetic Resonance<br />

Imaging. Methods: Magnetic Resonance Imaging is an indispensable<br />

investigative tool in the evaluation <strong>of</strong> orbital and neuro-ophthalmic lesions.<br />

Its superior s<strong>of</strong>t tissue contrast multiplanar capabilities and lack <strong>of</strong> ionizing<br />

radiations gives it an edge over Computed Tomography (CT). Besides basic<br />

technicalities, this paper shall address the imaging anatomy <strong>of</strong> the orbital<br />

and adjacent structures. The key MRI features <strong>of</strong> common cranio-orbital<br />

pathologies shall also be mentioned briefly. Result and Conclusion:<br />

The basic interpretation <strong>of</strong> MRI imaging for an ophthalmologist, especially the<br />

oculoplastics surgeon and neuro-ophthalomologist, shall be made simpler<br />

through this presentation.<br />

FP-IMG-SA 243 (4)<br />

DiOCTA : A Device Independent OCT Analysis<br />

Lorenz Birgit (1) , Zahn Steffen (1) , Pilch Mattheus (1) , Ehnes Alexander (1) ,<br />

Stieger Knut (1)<br />

1. Department <strong>of</strong> Ophthalmology, Justus-Liebig-University Giessen<br />

Aim: Current optical coherence tomography (OCT) technology generates vast<br />

amounts <strong>of</strong> data for disease identification and clinical studies <strong>of</strong> new<br />

therapeutics. Differences in the s<strong>of</strong>tware from devices <strong>of</strong> distinct generations<br />

and companies complicate the analysis in multicenter studies. The aim <strong>of</strong> this<br />

project is to generate a s<strong>of</strong>tware application for raw data analysis from different<br />

OCT devices. Method: Raw Data from currently available OCT devices<br />

can be imported into the new analysis s<strong>of</strong>tware and are processed in a three<br />

component operation, including automated layer segmentation, automated<br />

structure recognition and a disease advisory system based on Bayesian<br />

model systems. Results: The automated layer segmentation allows<br />

the segmentation <strong>of</strong> 11 intra-retinal layers and can be adjusted in diseased<br />

retinal images depending on the severity <strong>of</strong> layer reduction. Automated<br />

structure recognition can detect all vessels with their respective lumen and<br />

recognizes small dense particles and fluid containing compounds in a C-scan.<br />

The disease advisory system is currently set up for retinal degenerative<br />

disorders, in particular for LCA and RP pathology. Discussion: The device<br />

independent s<strong>of</strong>tware can be applied in multicenter studies to analyze the<br />

natural history <strong>of</strong> retinal pathologies over time and can evaluate the treatment<br />

benefit <strong>of</strong> new therapeutic applications.<br />

FP-IMG-SA 243 (5)<br />

Adaptive Optics-Like Quality SLO-OCT Fundus Imaging Using<br />

Compact Ultra High Resolution Confocal Microscopy and Ultra High<br />

Speed SD OCT<br />

Rosen Richard (1,2)<br />

1. New York Eye and Ear Infirmary<br />

2. New York Medical College<br />

PURPOSE: To develop an adaptive optics-like quality imaging system for<br />

clinical macular diagnosis,using combined Ultra High Resolution Confocal<br />

Microscopy and Ultra High Speed SD OCT. METHODS: Clinical subjects<br />

diagnosed with retinal disease were imaged using an enhanced commercial<br />

ultra high resolution confocal microscope/ ultra high speed SD OCT capable<br />

<strong>of</strong> magnifications revealing the photoreceptor matrix, nerve fiber layer fabric,<br />

and deep capillary beds . Clinical pathologic correlation was assessed on all<br />

images using conventional SD OCT/SLO imaging and fundus photography.<br />

RESULTS: Eyes <strong>of</strong> 20 patients with diabetic retinopathy, cystoid maculopathy,<br />

vascular occlusive disease, serous retinopathy, and macular degeneration<br />

were studied. Compared to current commercial OCT and SLO imaging devices<br />

the system was able to reveal cellular details and fine structure previously<br />

only available in larger adaptive optics systems which are cumbersome for<br />

the clinical environment. CONCLUSION: This system demonstrates the<br />

potential accessibility to microstructural imaging beyond current commercial<br />

standards to a level approaching adaptive optics resolution without its complex<br />

optical architecture. Its ability to detect subtle structural abnormalities may<br />

prove exceptionally valuable for detection<strong>of</strong> preclinical macular disease as<br />

pharmacological therapies focus on more subtle chronic changes.<br />

236<br />

FP-IMG-SA 243 (6)<br />

Does Ultrasound Bio-Microscopy Have a Role in the Diagnosis <strong>of</strong><br />

Temporal Arteritis?<br />

Mansour Magdi (1) , Deschenes Jean (2) , Khouqeer Zohair (1) , Al-Habbab<br />

Zainab (1)<br />

1. Saad Specialist Hospital<br />

2. Royal Victoria Hospital<br />

Objective: To evaluate the role <strong>of</strong> ultrasound biomicroscope (UBM) in the<br />

diagnosis <strong>of</strong> temporal arteritis. Method: Prospective case study, <strong>of</strong> twenty-six<br />

consecutive patients with clinical diagnosis <strong>of</strong> temporal arteritis was enrolled in<br />

this study. All patients were submitted to UBM before temporal artery biopsy.<br />

On UBM we searched for the presence <strong>of</strong> a hypoechoic effect surrounding the<br />

walls <strong>of</strong> the temporal arteries (halo sign), as well as an intra-arterial middle<br />

reflexive filling (intra-arterial filling affect). Results: The halo sign and the<br />

intra-arterial filling were simultaneously found in 5 (62.5%) <strong>of</strong> 8 patients with<br />

biopsy-proven temporal arteritis. However, only 6 (30%) <strong>of</strong> 18 patients with a<br />

negative biopsy presented both features simultaneously. On the other hand,<br />

the absence <strong>of</strong> these two parameters on the UBM <strong>of</strong> a patient with clinical<br />

suspicion <strong>of</strong> temporal arteritis strongly suggests that the temporal artery biopsy<br />

will be negative (negative predictive value=100%). Conclusion: This study<br />

suggests that the ultrasound biomicroscopy is a useful exam in predicting<br />

a negative result <strong>of</strong> the temporal artery biopsy in patients with suspicion <strong>of</strong><br />

temporal arteritis.<br />

FP-IMG-SA 243 (7)<br />

Spectral Domain Anterior Segment Optical Coherence Tomography<br />

in Microbial Keratitis<br />

Soliman Wael (1) , Fathalla Ahmed (1) , El-Sebaity Dalia M (1) ,<br />

Al-Hussaini Ashraf K (1)<br />

1. Ophthalmology Deparment, Assiut University Hospitals, Assiut University<br />

Purpose: To investigate the spectral domain anterior segment optical<br />

coherence tomography (SDAS-OCT) characteristics <strong>of</strong> microbial keratitis<br />

(fungal and bacterial keratitis). Methods: Twenty eyes <strong>of</strong> 20 patients with<br />

proved fungal and bacterial microbial keratitis, at different stages, underwent<br />

SDAS-OCT. Results: We examined 20 eyes <strong>of</strong> 20 patients. Eight<br />

eyes presented with proved bacterial keratitis and 12 eyes presented with<br />

proved fungal keratitis. Twelve different SDAS-OCT presentations <strong>of</strong> fungal<br />

and bacterial keratitis were explored in this study. These twelve presentations<br />

are hyper-reflective stromal lesions, epithelial defects, stromal edema, hyperreflective<br />

material (inflammatory plaque or mucous) over-lost epithelium or<br />

over the hyper-reflective stromal lesion, hyper-reflective lesion (inflammatory<br />

plaque attached to the endothelium), localized small stromal cystic spaces,<br />

full thickness large cystic spaces (necrotic stroma), localized stromal thinning<br />

with defective epithelium on top, loss <strong>of</strong> all layers <strong>of</strong> the cornea except the<br />

Descemet›s membrane (Descematocele), hyper-reflective stromal lesion(scar)<br />

with intact epithelium on top without stromal thinning, hyper-reflective stromal<br />

lesion(scar) with intact epithelium on top with localised stromal thinning, and<br />

diffuse stromal thinning with defective epithelium. Conclusions: SDAS-<br />

OCT imaging provides a range <strong>of</strong> characteristics that can be used in the<br />

future as an integral part in diagnosis and management <strong>of</strong> bacterial and fungal<br />

microbial keratitis.<br />

FP-IMG-SA 243 (8)<br />

Optical Quality and Wavefront Aberrations in Normal, Forme Fruste,<br />

and Manifest Keratoconus<br />

Dhawan Shikha (1) , Shetty Rohit (2) , K Shetty Bhujang (2) , Sasikumar Rajesh (2)<br />

1. Aditya Jyot Eye Hospital<br />

2. Narayana Netralaya<br />

Purpose: To evaluate optical quality and wavefront aberrations in normal,<br />

forme fruste and manifest keratoconus. Methods: A Prospective<br />

observational comparative study in 64 keratoconic eyes <strong>of</strong> 96 patients, 22<br />

forme fruste keratoconic eyes <strong>of</strong> 38 patients, and 100 healthy eyes <strong>of</strong> 168 age-<br />

and sex- matched subjects was performed. In the keratoconus group three<br />

further groups were differentiated according to the severity <strong>of</strong> keratoconus:<br />

mild (22 eyes), moderate (20 eyes) and severe keratoconus (22 eyes). Optical<br />

quality measurements were performed using the Optical Quality Analysis<br />

System (OQAS). Wavefront aberrations were measured and studied using<br />

Tscherning Aberrometer. Results: The difference in the mean values<br />

<strong>of</strong> the optical quality parameters between the normal and forme fruste group<br />

(p

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