Although the current OCT imaging system was designed to examine the retinal structures, a novel application in imaging the anterior chamber angle was studied in section 3.7. OCT was demonstrated to be clinically useful for visualization of the different patterns of angle configurations in different forms of angle closure glaucoma. / In section 3.5, RNFL measurement by OCT was cross-validated by another nerve fiber analyzer, scanning laser polarimetry (SLP). While both OCT and SLP demonstrated comparable diagnostic performance for glaucoma detection and high correlation in the respective RNFL measurements, OCT was found to provide a closer estimation of RNFL thickness with reference to the reported histological measurements. In section 3.6, the structural-functional relationship between RNFL thickness and visual sensitivity was evaluated and compared between OCT and SLP. The relationships were found to be dependent on the choice of the perimetry scale, the type of RNFL measuring devices and the characteristics of the studied subjects. It was concluded that regression analysis of the structural-functional profile could provide important information in the assessment of the trend and pattern of glaucoma progression. / In summary, optical coherence tomography was shown to be useful in the diagnosis of glaucoma and in the evaluation of the trend and pattern of disease progression. / Objectives. The research project was designed to investigate the applications of optical coherence tomography in the assessment of glaucoma. The goals are to identify sensitive and specific anatomic markers, and analytical method for detection of glaucomatous changes, to evaluate the intricate structural-functional relationships in glaucoma with regression analysis and to assess the potential application of optical coherence tomography imaging system in visualization of the anterior chamber angle with a view to obtain OCT data to help understanding the pathophysiology of different forms of angle-closure glaucoma. / Sections 3.1 to 3.3 were designed to identify the most sensitive and specific diagnostic marker(s) for glaucoma detection. Peripapillary retinal nerve fiber layer (RNFL), macular thickness, optic nerve head parameters measured with different reference planes, and a novel anatomic marker - macular nerve fiber layer were investigated. The averaged peripapillary RNFL thickness measured with a high resolution scan (512 scan point) was found to have the best discriminating power for detection of glaucoma. It also has the strongest correlation with visual function. To examine if utilization of the complete data profile of peripapillary RNFL could further improve diagnostic sensitivity, a novel approach with the use of neural network trained to recognize RNFL pattern was studied in section 3.4. It was concluded that neural network analysis could enhance the diagnostic performance for glaucoma detection. / Summary. Glaucoma is a progressive optic neuropathy characterized by the loss of retinal ganglion cells resulting in constriction of visual field and loss of vision as the disease progresses. Since structural damage in glaucoma occurs well before any detectable loss in visual function, clinical examination of the optic nerve head and its nerve fiber layer is crucial in establishing the diagnosis, monitoring the progression and initiating treatment before irreversible damage takes place. The present research project is composed of 7 coherent studies (sections 3.1 to 3.7), aiming to investigate the clinical applications of optical coherence tomography (OCT), an advanced imaging device for detailed examination of optic nerve head and nerve fiber layer, in the assessment of glaucoma. / Leung Kai-shun. / "June 2006." / Adviser: Chi Pui Pang. / Source: Dissertation Abstracts International, Volume: 67-11, Section: B, page: 6323. / Thesis (M.D.)--Chinese University of Hong Kong, 2006. / Includes bibliographical references (p. 212-227). / Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web. / School code: 1307.

OBJETIVO: Avaliar a capacidade do eletrorretinograma de padrão reverso (PERG) de campo total de detectar alterações funcionais da retina em olhos com papiledema resolvido de pacientes com a síndrome do pseudotumor cerebral (PTC). Utilizar a tomografia de coerência óptica de domínio Fourier (FD-OCT) para avaliar a espessura total e das camadas internas da retina (após segmentação dos dados) na área macular e a camada de fibras nervosas retinianas (CFNR) peripapilar em pacientes com PTC, e compará-las com aquelas de olhos normais. Estudar a correlação entre as amplitudes do PERG, as medidas da tomografia de coerência óptica (OCT) e a perda de campo visual (CV) avaliada pela perimetria computadorizada. MÉTODOS: Cinquenta e dois olhos com papiledema clinicamente resolvidos de 29 pacientes portadores de PTC foram submetidos a exame oftalmológico completo, CV, PERG e OCT. As seguintes medidas obtidas pelo OCT foram analisadas: a espessura da CFNR peripapilar, a espessura macular total (EMT), avaliada em oito setores, de acordo com o mapa do Early Treatment Diabetes Retinopathy Study, e medidas segmentadas na região da mácula da CFNR, da camada de células ganglionares (CCG) e da camada nuclear interna (CNI). Os resultados do CV foram avaliados, levando em consideração o mean deviation (MD) e os valores de diferentes regiões do CV divididos, de acordo com sua correspondência no nervo óptico, seguindo o mapa de Garway-Heath. Foram, também, calculados os desvios médios de 12 ou de 16 pontos centrais do CV, que estimulam áreas semelhantes àquelas avaliada pelo OCT macular e pelo PERG. Os achados foram comparados utilizando-se as equações de estimativas generalizadas para compensação da interdependência dos dois olhos de um mesmo indivíduo. Foram, também, calculadas e comparadas as áreas sob as curvas ROC (receiver operating characteristics). As correlações entre os achados do PERG, do OCT e do CV foram avaliadas pela correlação de Pearson ou Spearman. RESULTADOS: Comparadas aos controles, as espessuras do OCT, da CFNR peripapilar, CFNR macular, CCG macular e EMT foram significativamente menores em pacientes com PTC. Com relação ao PERG, houve redução da amplitude de N95 e P50+N95, e aumento do tempo de pico de N95, ambos para o estímulo de 48\', em olhos doentes, quando comparados ao grupo controle. Correlações estatisticamente significantes foram encontradas entre os valores de amplitude do PERG e da espessura retiniana do OCT. As reduções de espessura das camadas retinianas do OCT também foram significativamente associadas à perda de sensibilidade do CV. CONCLUSÕES: O PERG e o OCT foram capazes de demonstrar a perda anatômica e funcional dos doentes com papiledema decorrente de PTC, apresentando significativa correlação entre os métodos analisados. Tanto o OCT avaliando as medidas maculares como o PERG podem ser úteis na monitorização da perda neural retiniana de pacientes com papiledema decorrente da síndrome do PTC / PURPOSE: To evaluate the ability of the full field pattern electroretinogram (PERG) to detect functional changes of retina in eyes with resolved papiledema from patients with pseudotumor cerebri (PTC). To analyze full thickness macular measurements, peripapillary retinal nerve fiber layer (RNFL) thickness as well as segmented inner retinal layers in patients with PTC using of Fourier domain optical coherence tomography (FD-OCT) and compare them with normal eyes. To study the correlation between the PERG parameters, the optical coherence tomography (OCT) measurements and the visual field (VF) sensitivity loss, using standard automated perimetry. METHODS: Fifty-two eyes with resolved papilledema of 29 patients with PTC syndrome were submitted to a complete ophthalmic examination including VF, PERG and OCT. The following OCT measurements were analyzed: the peripapillary RNFL thickness, the total macular thickness (TMT), which was sub-divided in 8 sectors according to the Early Treatment Diabetes Retinopathy Study map, and the segmented inner macula layers, RNFL, the ganglion cell layer (GCL) and inner nuclear layer (INL). The VF results were analyzed through the mean deviation (MD) and the different sectors of the VF according to their correspondence to Garway-Heath optic nerve map. Central mean deviation, an average from VF sensitivity for the 12 and 16 central points, an area roughly equivalent to the area tested by macular cube scan protocol and PERG, was evaluated in patients and controls. Generalized estimating equation models accounting for inter-eye correlations were used to compare the results among different groups. Areas under ROC (receiver operating characteristics) curves were also calculated and compared. The correlations between the findings of the PERG, OCT and VF were assessed by Pearson correlation coefficients or Spearman\'s rank correlation coefficients. RESULTS: Compared to controls, the OCT thickness of the peripapillary RNFL, macular RNFL, macular GCL and TMT were significantly thinner in eyes with PTC. When PERG was studied, the amplitude of P50 and N95 + N95 were significantly reduced and N95 peak time increased, both based on 48 min check size, in patients when compared with normal controls. Significant correlations were found between the PERG amplitude and OCT retinal thickness. The decreased thickness of the OCT retinal layers was also significantly associated with VF sensitivity loss. CONCLUSIONS: PERG and OCT were able to demonstrate anatomical and functional loss in patients with resolved papiledema from PTC, showing significant correlation between the methods analyzed. It is known that the main morbidity of this disease is visual impairment. It is therefore of great importance to monitor the visual function during treatment. Whereas papilledema may be reversible at early stages, permanent visual loss may occur. These findings suggest that both measurements can be complementary in assessing axonal loss in patients with PTC

OBJETIVO: Utilizar a tomografia de coerência óptica (TCO) de domínio Fourier para avaliar as camadas internas da retina de olhos de pacientes com esclerose múltipla (EM) ou neuromielite óptica (NMO), com ou sem história de neurite óptica (NO), e compará-los entre si e com os olhos de controles normais. Investigar a correlação entre os achados da TCO e os achados do campo visual nesse grupo de pacientes. MÉTODOS: Cento e oitenta e dois indivíduos foram estudados incluindo 74 com diagnóstico de EM, 33 com NMO, 30 com mielite transversa aguda longitudinal extensa (MTALE) e 45 controles normais. Todos os indivíduos foram submetidos a exame oftalmológico completo incluindo a perimetria computadorizada e a TCO de domínio Fourier. Os olhos estudados foram divididos em 5 grupos: olhos de pacientes com EM e episódio prévio de neurite óptica (EM-NO) olhos de pacientes com EM sem episódio prévio de neurite óptica (EM-sNO), olhos de pacientes com NMO e história de neurite olhos de pacientes com MTALE e olhos de controles normais. Foram analisadas as seguintes medidas obtidas pela TCO: a espessura da camada de fibras nervosas retiniana (CFNR) peri-papilar, a espessura macular total (EMT) avaliada em 8 setores de acordo com o mapa do \"Early Treatment Diabetes Retinopathy Treatment Trial\" e medidas segmentadas da CFNR na mácula, da camada de células ganglionares (CCG), camada nuclear interna (CNI). Os resultados da perimetria foram avaliados levando em consideração o \" mean deviation ( desvio médio)\" (MD) e os valores de diferentes regiões do campo visual divididos de acordo com a sua correspondência no disco óptico seguindo o mapa de Garway-Heath. A comparação dos achados entre os diferentes grupos foi feita usando modelos \"generalized estimated equations\" (GEE) de tal forma a fazer a compensação pela interdependência dos dois olhos de um mesmo indivíduo. Foram também calculadas e comparadas as áreas sob as áreas sob as curvas ROC (\"Receiver operating characteristics\") nos diferentes grupos. Foram calculadas as correlações de Spearman ou Pearson dependendo da distribuição dos valores. RESULTADOS: Não houve diferença significativa em relação à idade média e à distribuição dos pacientes quanto ao sexo nos 5 grupos estudados. Quando comparados ao grupo controle, os 4 grupos de olhos dos doentes apresentaram a espessura da CFNR peri-papilar e a CFNR macular significativamente menor que as medidas dos controles normais. Em relação à CCG e à EMT, os grupos NMO, EM-NO e EM-sNO apresentaram espessura estatisticamente menor que os controles enquanto que no grupo MTALE esta diferença não foi evidenciada. Quando a CNI foi estudada não houve diferença entre os controles e os 2 grupos com EM, enquanto que os grupos NMO e MTALE apresentaram espessura estatisticamente maior que os controles. Os dois grupos com história prévia de NO (NMO e EM-NO) apresentaram a espessura da CFNR peri-papilar e macular, da CCG e da EMT menores do que seus grupos correspondentes sem história prévia de NO (respectivamente MTALE e EM-sNO). Quando os grupos NMO e EM-NO foram comparados entre si não houve diferença de espessura em nenhuma camada exceto na CNI onde o grupo NMO foi estatisticamente mais espesso. Houve correlação entre os achados do TCO e aqueles da campimetria para ambas as doenças e esta correlação foi maior na NMO do que na EM, em especial quando a EMT foi o parâmetro do TCO utilizado na comparação. CONCLUSÕES: A TCO é capaz de demonstrar a perda neural nos doentes com EM ou NMO e evidencia perda neural subclínica tanto em olhos com MTALE como em pacientes com EM, sem história de NO prévia e demonstra aumento da CNI nos olhos de pacientes com NMO ou MTALE. Além do já conhecido mecanismo de lesão do nervo óptico por desmielinização o fato da CNI estar alterada no espectro NMO mostra que outros processos podem estar envolvidos na patogênese destas doenças e que esta camada pode ajudar na diferenciação entre as duas doenças, EM e NMO / PURPOSE: To evaluate, by the using of Fourier domain optical coherence tomography (OCT) the retinal inner layers of eyes with or without previous history of optic neuritis (ON) in multiple sclerosis (MS) or neuromyelitis optica (NMO) patients and compare them with normal controls. To investigate the correlation between the OCT and the visual field fidings. METHODS: One hundred two subjects were studied, 74 diagnosed as MS, 33 as NMO, 30 as longitudinally extensive transverse myelitis (LETM) and 45 nolmal controls. All patients were submitted to a complete ophthalmic evaluation including automated perimetry and Fourier domain OCT. The studied eyes were divided in 5 groups: eyes of MS patients with previous episodes of optic neuritis (MS-ON, group 1), eyes of MS patients without previous episodes of optic neuritis (MS-nON, group 2), eyes of NMO patients (group 3), eyes of LETM patients (group 4) and eyes of normal controls (group 5). The retinal layers measured by OCT were from the optic nerve, peri-papillary retinal nerve fiber layer (RNFL) and from the macula: the total macular thickness (TMT), which was sub-divided in 8 sectors according to \"Early treatment diabetic retinopathy study\", and the segmented inner macula layers, RNFL, ganglion cell layer (CGL) and inner nuclear layer (INL). Regard to automated perimetry we analyzed the \"mean deviation\" (MD) and different sectors of the visual field according to their correspondence to Garway-Heath optic nerve map. Generalized estimation equation (GEE) models accounting for age and within-patient, inter-eye correlations, were used to compare the results among different groups. We also compare the area under ROC (receiver operating charactheristics) curve among the different groups. We also compute either Spearman or Pearson correlation according to values distributions. RESULTS: There was no statistical difference among the groups regard to sex or mean age. All 4 diseased groups presented peri-papillary RNFL and macular RNFL thicknesses statistically thinner than normal controls. Regarding to GCL thickness and TMT, the NMO, MS-ON and MS-nON groups were statistically thinner than controls, on the other hand the LETM group was not statistically different. When the INL thickness was studied, there was no statistical difference between controls and both MS groups, whereas the NMO and LETM groups were statistically thicker than controls. Both groups with previous history of ON (NMO and MS-ON) presented peri-papillary RNFL, macular RNFL, GCL and TMT thinner than theirs corresponding groups without previous history of ON (LETM and MS-nON, respectively). When NMO and MS-ON were compared, there was no statistical difference in any layer, except the INL, which was thicker in NMO group. There was statistical correlation between OCT and automated perimetry findings for both, MS and NMO, diseases and the correlation was bigger in NMO, particularly when TMT was the OCT parameter used. CONCLUSION: The OCT is able to demonstrate the neural loss in MS and NMO patients and it also shows sub-clinical neural loss in LETM and MS-nON patients. Besides the already known mechanism of optic nerve injury caused by demyelination, the presence of a abnormal INL in the NMO and LETM patients suggest that different processes may be involved in the pathogenesis of these diseases and also that the INL may help differentiating between NMO and MS

Bancos de Tecidos de diversas regiões do mundo têm estocado cartilagens humanas obtidas de doadores post mortem para uso em diversos tipos de cirurgias reconstrutivas. Para garantir que tais tecidos não estejam contaminados, estes têm sido esterilizados com radiação ionizante. Entretanto, altas doses de radiação gama podem causar efeitos indesejáveis nos tecidos. No presente trabalho, avaliamos a viabilidade de utilizar duas técnicas, Tomografia por Coerência Óptica (OCT) e Termogravimetria (TGA), para identificar possíveis modificações estruturais causadas na cartilagem costal humana em decorrência dos métodos de preservação e doses de radiação ionizante utilizadas. As cartilagens obtidas de doadores cadavéricos foram congeladas a -70 ºC ou preservadas em glicerol. A seguir, as amostras foram irradiadas por fontes de 60Co com doses de 15, 25 e 50 kGy. Nos resultados de TGA verificamos que as cartilagens preservadas em glicerol e irradiadas com diferentes doses de radiação não apresentaram diferenças estatisticamente significantes quando comparadas ao grupo controle, no que tange a taxa de desidratação do tecido, sendo que o mesmo não ocorre com cartilagens congeladas a -70 ºC e irradiadas com doses de 15 kGy. Em relação ao uso da técnica de OCT, por meio do cálculo do coeficiente de atenuação óptica total, verificamos que doses de 15 kGy promovem a criação de ligações cruzadas entre as fibrilas de colágeno, corroborando os resultados de TGA. Ainda, os valores do coeficiente de atenuação óptica total são diretamente proporcionais à tensão de ruptura das cartilagens, o que nos possibilitará, em um futuro próximo, predizer a qualidade de um enxerto sem a necessidade de perda de material biológico, visto ser o OCT um método não destrutivo. Por meio das imagens de PS-OCT podemos verificar que as doses de radiação utilizadas para esterilizar as amostras não provocam danos à rede de colágeno a ponto de que sua birrefringência seja perdida. Assim, o TGA e OCT são técnicas que podem ser utilizadas por bancos de tecidos de forma a verificar a qualidade dos tecidos antes de serem transplantados em pacientes. / Tissue Banks around the world have stored human cartilages obtained from post mortem donors for use in several kinds of reconstructive surgeries. To ensure that such tissues are not contaminated, they have been sterilized with ionizing radiation. However, high doses of gamma radiation may cause undesirable changes in the tissues. In this work, we evaluated the possibility of use Optical Coherence Tomography (OCT) and Thermogravimetric Analysis (TGA) to identify possible structural modifications caused by both preservation methods of cartilage and gamma irradiation doses. Cartilages were obtained from cadaveric donors and were frozen at -70 ºC or preserved in glycerol. Irradiation was performed by 60Co source with doses of 15, 25 and 50 kGy. Our TGA results showed that glycerolized cartilages irradiated with different doses of radiation does not presented statistical differences when compared to the control group for the dehydration rate. However, the same was not observed for deep-fronzen cartilages irradiated with 15 kGy. The results of OCT associated to total optical attenuation coefficient showed that doses of 15 kGy promote cross-link between collagen fibrils, corroborating the results obtained from TGA. Moreover, total optical attenuation coefficient values are proportionals to stress at break of cartilages, what will be very useful in a near future to predict the quality of the allografts, without unnecessary loss of biological tissue, once OCT is a nondestructive technique. By PS-OCT images, we found that high doses of ionizing radiation does not promote sufficient impairments to promote complete loss of tissue birefringence. Thus, TGA and OCT are techniques that can be used for tissue banks to verify tissue quality before its transplant.

Glaucoma is characterized by progressive optic nerve head (ONH) deformation and retinal nerve fiber layer (RNFL) thinning but the relative sequence of ONH and RNFL changes in glaucoma remains largely uncertain. It has been proposed that structural damage of the optic nerve can often be detected before detectable functional loss. Therefore, investigating structural changes of the ONH and RNFL is of importance and relevance in the monitoring and management of glaucoma progression. Spectral domain optical coherence tomography (OCT), scanning laser polarimetry (SLP) and confocal scanning laser ophthalmoscopy (CSLO) are the three prevailing digital imaging technologies for measurement of RNFL thickness, RNFL retardance and ONH parameters, respectively. Although these instruments have been extensively investigated for detection of glaucomatous damage, less is known about their relative performance for detection of change in glaucoma progression. Although previous studies on non- human primates showed that disruption of the microtubule structure of the retinal ganglion cell axons detected by SLP as reduction of RNFL retardance, as well as ONH surface deformation detected by CSLO, could be detected prior to reduction of RNFL thickness measured with OCT, clinical data corroborating this observation are lacking. The sequence of change of RNFL thickness, RNFL retardance and ONH parameters has not been investigated in human glaucoma. / This research project aimed to investigate the performance of OCT, SLP and CLSO for change detection of RNFL and ONH damages, determine the relative sequence of change of RNFL retardance and RNFL thickness and ONH deformation, and evaluate if ocular biomechanical properties, measured as corneal hysteresis by the ocular response analyzer (ORA, Reichert Inc.), influence the detection of ONH and RNFL progression in glaucoma patients. We hypothesized that ONH deformation and loss of RNFL retardance could be detected before detectable RNFL thinning and that the baseline corneal hysteresis would be a risk factor for ONH and RNFL damage in glaucoma. / In the first study, we analyzed 184 eyes of 116 patients with glaucoma and 43 normal eyes of 23 healthy individuals followed for a mean of 4.6 years. All subjects had RNFL retardance and RNFL thickness measurements obtained with GDx ECC (Carl Zeiss Meditec) and Cirrus HD-OCT (Carl Zeiss Meditec), respectively, at 4-month intervals. Progressive reduction of RNFL retardance and RNFL thickness were evaluated with Guided Progression Analysis (GPA, Carl Zeiss Meditec) with reference to the RNFL retardance change map and RNFL thickness change map, respectively. Twenty seven eyes of 26 patients showed progressive RNFL thinning whereas 8 eyes of 8 patients had RNFL retardance reduction in the latest follow-up visit. Seven eyes of 7 patients had progressive RNFL thinning and reduction of RNFL retardance detected by both instruments; all had progressive RNFL thinning evident before reduction of RNFL retardance and the mean lag time was 13.4 months (range: 4.0-37.6 months). The survival time of eyes detected with RNFL thinning was significantly shorter than the survival time of eyes detected with reduction of RNFL retardance (P=0.001). No eyes in the normal group showed progressive RNFL changes during follow-up. Collectively, we showed that at a comparable specificity (100%, 95% confidence interval: 96.3%-100%), progressive RNFL thinning was detected more often than progressive reduction of RNFL retardance and the former preceded the latter in eyes with both progressive RNFL thinning and reduction of RNFL retardance. / In the second study using a similar study design, we investigated the sequence of change of ONH surface depression detected by CSLO (HRT 3, Heidelberg Engineering) and RNFL thinning detected by OCT (Cirrus HD-OCT, Carl Zeiss Meditec) in 146 eyes of 90 glaucoma patients followed at approximately 4-month intervals for an average of 5.4 years. Significant ONH surface depression and RNFL thinning were defined with reference to Topographic Change Analysis (TCA, Heidelberg Engineering) and Guided Progression Analysis (GPA, Carl Zeiss Meditec), respectively. At a specificity of 94.3% (95% confidence interval: 86.2%-97.8%) for both RNFL thinning and ONH surface depression (determined in a normal group comprising 70 eyes from 35 normal subjects), 57 eyes (39.0%) had ONH surface depression, 46 eyes (31.5%) had RNFL thinning, and 23 eyes (15.8%) had both in the glaucoma group. Among these 23 eyes, 19 (82.6%) had ONH surface depression detected prior to RNFL thinning and the median lag time was 15.8 months (range, 4.0-40.8 months). Although only 7.0% of eyes (4/57) had RNFL thinning at the onset of ONH surface depression, 45.7% (21/46) had ONH surface depression at the onset of RNFL thinning. The survival time of eyes with ONH surface depression was significantly shorter than the survival time of eyes detected with RNFL thinning (P=0.002). With reference to the HRT TCA and OCT GPA, ONH surface depression occurred before RNFL thinning in a significant proportion of patients with glaucoma at a comparable specificity. / Of note, a significant proportion of eyes had ONH surface depression without any detectable progressive RNFL thinning in the second study, and vice versa. Investigating whether the risk factors for ONH surface depression and RNFL progression are different is therefore important. In the final study, we investigated if baseline corneal hysteresis is a risk factor for progressive ONH surface depression and RNFL thinning. Following the same cohort of 146 eyes of 90 glaucoma patients for an average of 6.8 years, we detected that 65 eyes (44.5%) had progressive ONH surface depression, 55 eyes (37.7%) had progressive RNFL thinning and 20 eyes (13.7%) had visual field progression (based on the EMGT criteria). After adjusting for ages, CCT, baseline diastolic IOP, average IOP during follow-up, baseline disc area and baseline MD in the cox proportional hazards model, baseline corneal hysteresis was significantly associated with ONH surface depression (HR=0.70, P=0.008), visual field progression (HR=0.56, P=0.019), but not with progressive RNFL thinning (HR=0.96, P=0.751). For each 1-mmHg decrease of baseline CH, the hazards for ONH surface depression and visual field progression increased by 30% and 44%, respectively. / In summary, at a comparable level of specificity, progressive ONH surface depression detected by CSLO could be observed prior to progressive RNFL thinning detected by OCT, which preceded identified reduction of RNFL retardance detected by SLP. For eyes with concomitant ONH surface depression, RNFL thinning and visual field progression, ONH surface depression always preceded visual field progression. Our finding indicates that a time window for therapeutic intervention may exist upon detection of ONH surface depression before irreversible RNFL and visual field loss and that measurement of CH would be useful to predict ONH surface depression and visual field progression. / Further studies are required to investigate the sequence of optic nerve head change and RNFL progression with the same instrument. Whether IOP lowering treatment initiated at the time of ONH deformation would be effective to prevent or slow down RNFL and visual field loss needs to be further investigated. A more reliable and accurate measure of the ocular biomechanical properties is necessary for evaluation of their contribution to glaucoma progression. / 青光眼是一種進展性視神經病變，其特徵為﹕視神經乳頭變形，神經纖維層（RNFL）的變薄以及相應的視野缺損。然而，青光眼結構性改變和功能性變化發生的相對順序仍不清楚。視神經結構性改變被認為要早於功能性改變的發生。因此，研究視乳頭的結構性改變具有重要意義，有助於早期診斷青光眼的進展及隨訪青光眼患者。目前主要用於RNFL厚度，RNFL阻滯性以及視乳頭參數的影像學掃描儀器為頻域OCT，鐳射偏振光掃描器（SLP）和共聚焦鐳射掃描眼底鏡（CSLO）。儘管這三種儀器已經廣泛用於青光眼損傷的檢測，但在青光眼患者結構性變化的應用並不常見。既往在非人靈長類動物的實驗中，通過破壞神經節細胞軸突中的微小管結構，從而發現RNFL的阻滯性以及視乳頭的變化要先於RNFL厚度變化的發生。然而在臨床研究中並未得到證實。同時，在青光眼患者中，RNFL厚度變化，RNFL阻滯減少以及視神經頭參數改變之間的先後順序並未得到證實。 / 本次實驗研究的目的在於探討OCT，SLP及CSLO在診斷青光眼病人RNFL及視乳頭進展的能力，確定RNFL厚度變化，RNFL阻滯性減少以及視神經頭參數改變之間的相對順序，以及評估眼反應分析儀（ORA）測得的角膜粘滯性（CH）是否影響視乳頭及RNFL厚度的進展。我們假設：視神經乳頭的變形，RNFL阻滯性的減少要先於RNFL厚度的變化，基線角膜粘滯性的測量會影響視乳頭及RNFL進展的檢測。116個青光眼病人的184隻眼以及23個正常對照的43隻眼被納入第一個研究中。所有受試物件均接受每4個月一次的OCT以及SLP RNFL的掃描，平均隨訪時間為4.6年。通過OCT及SLP中Guided Progression Analysis（GPA, Carl Zeiss Meditec）程式，一系列RNFL厚度及粘滯性圖被自動分析從而獲得RNFL厚度及粘滯性的變化結果。26個青光眼患者的27隻眼表現為RNFL厚度的進行性變薄，8個患者的8隻眼表現為RNFL粘滯性的減少。其中7個患者的7隻眼同時表現為RNFL厚度變薄及粘滯性的減少，所有這7隻眼的RNFL變薄的發生要早於RNFL粘滯性的減少，兩者間隔時間平均為13.4月（4.0-37.6月）。RNFL厚度變薄者的生存概率明顯小於RNFL粘滯性減少的青光眼患者（P=0.001）。隨訪中，我們未發現正常對照組中RNFL厚度變薄或者粘滯性改變者。總體說來，在同一特異性水準（100%），RNFL厚度的變化頻率高於粘滯性的改變，RNFL厚度的變薄要早於粘滯性減少的發生。 / 採用相同於第一個研究的研究方法，我們研究CSLO測得的視乳頭表面凹陷以及測得OCT的RNFL厚度變化發生的相對順序。90個青光眼患者的146隻眼以及35個正常對照物件的70隻眼被納入第二個研究中。所有受試物件均接受4個月一次的CSLO及OCT掃描從而獲得一系列的視神經頭表面的拓撲圖像以及RNFL厚度圖。CSLO TCA及OCT GPA程式自動對比基線及隨訪中所獲得的視神經頭表面的拓撲圖像以及RNFL厚度圖，從而獲得視乳頭表面凹陷及RFNL進展報告。平均隨訪5.4年後，CSLO及OCT在診斷視神經頭及RNFL進展的特異性為94.3%，57只青光眼患眼（39.0%）表現為顯著性視乳頭表面凹陷，46隻眼（31.5%）表現為RFNL厚度的進行性變薄，而23隻眼（15.8%）同時表現為視乳頭面凹陷和RFNL的進行性變薄。在這23只眼中，19隻眼（82.6%）變現為視乳頭表面凹陷先於RFNL厚度變薄的發生，間隔時間的中值為15.8個月（4.0-40.8月）。儘管在顯著性視乳頭表面凹陷發生時，僅有7.0%的患眼表現為RNFL厚度的變薄；但是，在RNFL厚度發生顯著性變薄時已有45.7%的患眼表現為視乳頭表面凹陷。視乳頭表面凹陷患眼的生存概率差於RNFL厚度變薄患眼（P=0.002）。在青光眼患者的隨訪中，CLSO TCA測得的視乳頭表面凹陷要早於OCT GPA測得的RNFL厚度的變化。 / 最後的一個研究目在於評估眼反應分析儀（ORA）測得的基線角膜粘滯性（CH）是否為視乳頭表面凹陷及RNFL厚度變薄的危險因素。平均隨訪同一人群即第二個研究中的90個青光眼患者的146眼6.8年，65隻眼（44.5%）被檢測出具有進行性視乳頭表面凹陷，55隻眼（37.7%）表現為進行性RNFL厚度的變薄，20隻眼（13.7%）表現為進行性視野的缺損（基於EMGT標準）。基線CH與視乳頭表面凹陷，視野進展間具有顯著性相關關係（HR=0.70，P=0.008及HR=0.56，P=0.019），但CH與進行性RNFL厚度變薄間並無顯著性相關關係（HR=0.96，P=0.751）。每1毫米汞柱基線CH的降低，發生視乳頭表面凹陷及視野缺損的危險性將增加30%及44%。CH的測量值與青光眼進展的危險性具有顯著相關關係。 / 總之，在具有可比性特異性水準下，CSLO檢測的進展性視乳頭表面凹陷的發生要先於OCT檢測的進行性RNFL厚度的變薄，後者的發生早於SLP測得的RNFL粘滯性的改變。對於同時有視乳頭表面凹陷，RNFL厚度變薄及RNFL粘滯性改變的青光眼患眼，視乳頭表面凹陷的發生要早於視野的進展。我們的實驗研究表明了在青光眼患者發生視乳頭表面凹陷時，治療的時間窗的存在有助於避免不可逆的RNFL缺失及視野的缺損。角膜粘滯性的測量對於預測視乳頭表面凹陷及視野進展具有重要意義。 / 展望未來的研究中，用同一種儀器進行視乳頭及神經纖維層的隨訪，從而得出相對的變化次序很有必要。研究在視乳頭或者神經纖維層發生變化時進行眼壓的干預是否能避免視功能的進一步損傷顯得尤為重要。用於測量角膜生物學特性的更為準確，可信度更高的儀器真正研發中，以及進一步探討角膜生物學特性與青光眼進展之間的關係。 / Xu, Guihua. / Thesis Ph.D. Chinese University of Hong Kong 2015. / Includes bibliographical references (leaves 116-145). / Abstracts also in Chinese. / Title from PDF title page (viewed on 18, October, 2016). / Detailed summary in vernacular field only. / Detailed summary in vernacular field only. / Detailed summary in vernacular field only. / Detailed summary in vernacular field only. / Detailed summary in vernacular field only. / Detailed summary in vernacular field only.

Coronary atherosclerosis is by far the most frequent cause of ischemic heart disease. Intravascular ultrasound (IVUS) along with virtual histology (VH) is a useful tool for quantification of coronary plaque buildup and provides new insights into the diagnosis of coronary disease. Rupture of vulnerable plaque causing acute coronary syndromes, coronary remodeling maintaining lumen size and plaque phenotype revealing pathological severity are among the most important topics related to atherosclerosis. In this thesis, variations of IVUS-VH-derived thin-cap fibroatheroma (TCFA) definitions are proposed to evaluate the plaque rupture, which is further analyzed in a layered manner; statins effects on coronary remodeling are comprehensively assessed with the implementation of automated IVUS segmentation and registration of IVUS pullbacks based on baseline and 1-year followup datasets; plaque phenotypes are determined and analyzed morphologically and compositionally on segmental basis using the same serial datasets. In addition, our research involves another important coronary disease — coronary allograft vasculopathy (CAV) which is a frequent complication of heart transplantation (HTx). Another intra-coronary imaging modality — intravascular optical coherence tomography (IVOCT) for quantifying CAV is involved. We present an optimal and automated 3-D graph search approach for the simultaneous IVOCT multi-layer segmentation by transforming the 3-D segmentation problem into finding a minimum-cost closed set in a weighted graph. Furthermore, a computer-aided just-enough-interaction refinement method is proposed to help achieve fully satisfactory 3-D segmentation of IVOCT images. We believe this is the first work that provides a fast, efficient and accurate solution for IVOCT multi-layer assessment in the context of CAV. The major contributions of this thesis are: (1) Proving that IVUS-VH-derived TCFA prevalence may be overestimated, and elucidating the potential loss of plaque material during rupture, (2) providing a comprehensive understanding of remodeling in the context of both changing the remodeling direction and changing the remodeling extent, and demonstrating the statin therapy effects on remodeling across patients, based on automated segmentation of IVUS images and registration of serial data, (3) showing that the pathological intimal thickening is the most active plaque phenotype in terms of plaque composition changes and plaque vulnerability progression, and (4) developing and validating a method for multi-layer 3-D segmentation of IVOCT images within a novel interactive environment.

In laser materials processing, the direct measurement and characterization of material and process depth is traditionally a diffcult task. This is particularly difficult when such information needs to be obtained in real-time for feedback and dynamic analysis applications. This thesis outlines a novel method and apparatus for real-time depth measurement during laser processes such as welding, drilling, cutting and ablation called inline coherent imaging (ICI). The approach borrows the coherent imaging ideas from the primarily medical field of optical coherence tomography and adapts them to the new application. Without requirements for flawless image quality and limitations on sample exposure the design is free to emphasize speed in acquisition and processing. Furthermore, the imaging optics are specialized for compatibility with off-the-shelf beam delivery systems. Several generations of the imaging technique and relevant design equations are described and shown and realized. Also described is the design and construction of two laser processing stations used for testing ICI in macro- and micro-processing applications. A variety of applications for ICI in the understanding of percussion drilling and welding of metals and other industrial materials are discussed. The imaging technique is further extended to provide manual and fully automatic closed-loop control of drilling and ablation processes in industrial materials. Finally, some important applications of ICI in the processing of bone in both open and closed-loop configurations are demonstrated. / Thesis (Ph.D, Physics, Engineering Physics and Astronomy) -- Queen's University, 2012-11-04 15:34:14.379

<p>Developmental biology is a field in which explorations are made to answer how an organism transforms from a single cell to a complex system made up of trillions of highly organized and highly specified cells. This field, however, is not just for discovery, it is crucial for unlocking factors that lead to diseases, defects, or malformations. The one key ingredient that contributes to the success of studies in developmental biology is the technology that is available for use. Optical coherence tomography (OCT) is one such technology. OCT fills a niche between the high resolution of confocal microscopy and deep imaging penetration of ultrasound. Developmental studies of the chicken embryo heart are of great interest. Studies in mature hearts, zebrafish animal models, and to a more limited degree chicken embryos, indicate a relationship between blood flow and development. It is believed that at the earliest stages, when the heart is still a tube, the purpose of blood flow is not for convective transport of oxygen, nutrients and waster, bur rather to induce shear-related gene expressions to induce further development. Yet, to this date, the simple question of "what makes blood flow?" has not been answered. This is mainly due limited availability to adequate imaging and blood flow measurement tools. Earlier work has demonstrated the potential of OCT for use in studying chicken embryo heart development, however quantitative measurement techniques still needed to be developed. In this dissertation I present technological developments I have made towards building an OCT system to study chick embryo heart development. I will describe: 1) a swept-source OCT with extended imaging depth; 2) a spectral domain OCT system for non-invasive small animal imaging; 3) Doppler flow imaging and techniques for quantitative blood flow measurement in living chicken embryos; and 4) application of the OCT system that was developed in the Specific Aims 2-5 to test hypotheses generated by a finite element model which treats the embryonic chick heart tube as a modified peristaltic pump.</p> / Dissertation

<p>Optical interrogation techniques are particularly well-suited for imaging tissue morphology, biological dynamics, and disease pathogenesis by providing noninvasive access to subcellular-resolution diagnostic information. State-of-the-art spectral domain optical coherence tomography (SDOCT) systems provide real-time optical biopsies of in vivo tissue, and have demonstrated clinical potential, particularly for applications in ophthalmology. </p><p>Recent advances in microscopy and endoscopy have led to improved resolution and compact optical designs, beyond those of conventional imaging systems. Application of encoded and multiplexed illumination and detection schemes may allow for the development of optical tools that surpass classical imaging limitations. Furthermore, complementary technologies can be combined to create multimodal optical imaging tools with advantages over current-generation systems. </p><p>In this dissertation, the development of coherence-gated and resolution-multiplexed technologies, aimed towards applications in human vitreoretinal imaging is described. Technology development in coherence-gated systems included increasing the imaging range of SDOCT by removing the complex conjugate artifact, improving acquisition speed using a scanning spectrometer design and a two-dimensional detector array, and hardware and algorithmic implementations that facilitated imaging of Doppler flow. </p><p>Structured illumination microscopy techniques were applied for resolution enhancement, and a spectrally encoded ophthalmic imaging system was developed for en face confocal fundus imaging through a single-mode fiber. These devices were resolution-multiplexed extensions of existing ophthalmic imaging devices, such as scanning laser ophthalmoscopes (SLO), which demonstrated improved resolution and more compact optical designs as compared to their conventional counterparts.</p><p>Finally, several multimodal ophthalmic diagnostic tools were developed that combined the advantages of OCT with existing imaging devices. These included a combined SLO-OCT system and a vitreoretinal surgical microscope combined with OCT. These devices allowed for concurrent ophthalmic imaging using complementary modalities for improved visualization and clinical utility.</p> / Dissertation

The purpose of this research was to investigate detect and monitor laser-tissue interactions at threshold and potentially sub-threshold levels of injury. High resolution imaging modalities can provide a deeper understanding of candidate biomarkers disease and injury at the molecular, cellular, and tissue-levels which can be used to identify and diagnose early stages disease and damage. In addition, multi-scale and multi-modal imaging have also been used to identify inherent biomarkers of retinal disease and injury. Monitoring tissue changes can be mapped back to biological changes at the cellular and sub-cellular level. Diseases often alter tissue on the ultra-structural level yet retinal clinical diagnosis often monitor changes in tissue at the organ level. If injury and disease is detected and diagnosed during an “early” stage of development, treatments and drug interventions may prevent further spread of the pathology. Non-invasive imaging is expected to be a valuable tool for in vivo medical research as well as for the diagnosis and management of disease. In addition to developing new imaging tools and techniques to image the retina, the identification of inherent biomarkers of disease and health using diagnostic methods are almost equally as important. Using the inherent optical properties of retinal tissue, we can non- invasively quantify differences in the absorption and reflection of light to gauge the risk for visual disability or worse yet irreversible vision loss as a result of retinal disease and chronic light exposure. The research presented with in this dissertation is three separate studies aimed at identifying light injury and potential biomarkers indicating the risk of light mediated development of disease. / text