dc.contributor.advisor |
Farsiu, Sina |
|
dc.contributor.author |
Chiu, Stephanie Ja-Yi |
|
dc.date.accessioned |
2014-05-14T19:17:17Z |
|
dc.date.available |
2015-05-09T04:30:05Z |
|
dc.date.issued |
2014 |
|
dc.identifier.uri |
https://hdl.handle.net/10161/8688 |
|
dc.description.abstract |
<p>Accurate quantification of anatomical and pathological structures in the eye is
crucial for the study and diagnosis of potentially blinding diseases. Earlier and
faster detection of ophthalmic imaging biomarkers also leads to optimal treatment
and improved vision recovery. While modern optical imaging technologies such as optical
coherence tomography (OCT) and adaptive optics (AO) have facilitated in vivo visualization
of the eye at the cellular scale, the massive influx of data generated by these systems
is often too large to be fully analyzed by ophthalmic experts without extensive time
or resources. Furthermore, manual evaluation of images is inherently subjective and
prone to human error.</p><p>This dissertation describes the development and validation
of a framework called graph theory and dynamic programming (GTDP) to automatically
detect and quantify ophthalmic imaging biomarkers. The GTDP framework was validated
as an accurate technique for segmenting retinal layers on OCT images. The framework
was then extended through the development of the quasi-polar transform to segment
closed-contour structures including photoreceptors on AO scanning laser ophthalmoscopy
images and retinal pigment epithelial cells on confocal microscopy images. </p><p>The
GTDP framework was next applied in a clinical setting with pathologic images that
are often lower in quality. Algorithms were developed to delineate morphological structures
on OCT indicative of diseases such as age-related macular degeneration (AMD) and diabetic
macular edema (DME). The AMD algorithm was shown to be robust to poor image quality
and was capable of segmenting both drusen and geographic atrophy. To account for the
complex manifestations of DME, a novel kernel regression-based classification framework
was developed to identify retinal layers and fluid-filled regions as a guide for GTDP
segmentation.</p><p>The development of fast and accurate segmentation algorithms based
on the GTDP framework has significantly reduced the time and resources necessary to
conduct large-scale, multi-center clinical trials. This is one step closer towards
the long-term goal of improving vision outcomes for ocular disease patients through
personalized therapy.</p>
|
|
dc.subject |
Biomedical engineering |
|
dc.subject |
Computer science |
|
dc.subject |
Ophthalmology |
|
dc.subject |
graph theory and dynamic programming |
|
dc.subject |
GTDP |
|
dc.subject |
kernel regression-based classification |
|
dc.subject |
optical coherence tomography |
|
dc.subject |
quasi-polar transform |
|
dc.subject |
segmentation |
|
dc.title |
Graph Theory and Dynamic Programming Framework for Automated Segmentation of Ophthalmic
Imaging Biomarkers
|
|
dc.type |
Dissertation |
|
dc.department |
Biomedical Engineering |
|
duke.embargo.months |
12 |
|