Introdução: Pneumotórax é uma complicação comum em pacientes sob ventilação mecânica. Se não reconhecido, tende a aumentar de volume e pode levar ao colapso cardiovascular. Os métodos utilizados para seu diagnóstico caracterizam-se por baixa sensibilidade (radiografia) ou envolvem transporte potencialmente arriscado à tomografia de raios X. A tomografia de impedância elétrica (TIE) é um método não invasivo que permite monitorização da ventilação em tempo real. O método é baseado na construção da imagem de uma seção transversal das condutividades torácicas através de eletrodos dispostos ao redor do tórax. A TIE correlaciona-se muito bem com as alterações regionais do conteúdo de ar dentro do tórax. Por ter baixo custo, não ser invasiva e ter alta sensibilidade às alterações da ventilação e aeração pulmonar, a TIE é um método promissor para a detecção de pneumotóraces em situações de alto risco. Os objetivos deste estudo foram: 1) caracterizar as alterações na TIE relacionadas ao aparecimento de pneumotórax; 2) desenvolver um algoritmo para detecção automática de pneumotóraces e 3) avaliar prospectivamente a sensibilidade e especificidade deste algoritmo. Métodos: Foram realizados experimentos em 39 porcos (peso médio 31,0 Kg ± 3,2 desvios-padrão). Os animais foram sedados e submetidos à ventilação mecânica. Os dados de TIE foram adquiridos através de um tomógrafo de impedância desenvolvido por nosso grupo (Laboratório de Pneumologia Experimental, Escola Politécnica da Universidade de São Paulo e Dixtal Biomédica Ltda., São Paulo, Brasil), capaz de produzir 50 imagens relativas por segundo. Um primeiro grupo de dez animais foi submetido à drenagem torácica com indução progressiva de pneumotórax através do dreno (de 0 a 500 mL). No grupo seguinte, induzimos lesão pulmonar através de lavagem com salina em oito animais e os submetemos a mudanças progressivas de PEEP. Essas duas primeiras etapas foram utilizadas para a construção de um detector automático de pneumotórax baseado na TIE que foi testado prospectivamente em outros 21 animais. Resultados: A TIE apresenta alterações bem definidas relacionadas ao surgimento de pneumotórax, caracterizadas por aumento da impedância média e diminuição da amplitude da impedância concentrados no quadrante de interesse. Por outro lado, os achados na TIE durante mudanças bruscas de PEEP se distribuíram homogeneamente nos quatro quadrantes. A TIE apresentou alterações significativas mesmo com os menores volumes de ar injetados (20 mL), enquanto as demais variáveis monitorizadas foram pouco sensíveis ao surgimento do pneumotórax. A pressão arterial teve uma pequena queda com volumes superiores a 500 mL, e a pressão parcial de oxigênio arterial diminuiu somente com volumes maiores que 100 mL. Na fase prospectiva do protocolo, a TIE mostrou sensibilidade de 100% e especificidade de 95% para a detecção de pneumotóraces. A localização do pneumotórax foi identificada corretamente em todos os casos. Conclusão: A TIE apresenta alterações reprodutíveis relacionadas ao aparecimento de ar no espaço pleural caracterizadas por aumento da impedância média e diminuição da amplitude de impedância. Foi possível criar um algoritmo baseado nessas alterações capaz de detectar precoce e precisamente pneumotóraces em situações de risco. O processo de detecção é automático e em tempo real. / Introduction: Pneumothorax is a frequent complication during mechanical ventilation. Electrical impedance tomography (EIT) is a noninvasive tool that allows real-time imaging of regional ventilation. The purpose of this study was to: 1) identify characteristic changes in the EIT signals associated with pneumothoraces; 2) develop and fine-tune an algorithm for their automatic detection; and 3) prospectively evaluate this algorithm for its sensitivity and specificity in detecting pneumothoraces in real time. Methods: prospective controlled laboratory animal investigation. Setting: Experimental Pulmonology Laboratory of the University of Sao Paulo. Subjects: 39 anesthetized mechanically ventilated supine pigs (31.0 ± 3.2Kg, mean ± standard deviation). Interventions: In a first group of 18 animals monitored by EIT, we either injected progressive amounts of air (from 20 up to 500 mL) through chest tubes, or we applied large PEEP increments to simulate extreme lung overdistension. This first data set was used to calibrate an EIT-based pneumothorax detection algorithm. Subsequently, we evaluated the real-time performance of the detection algorithm in 21 additional animals (with normal or pre-injured lungs), submitted to multiple ventilatory interventions or traumatic punctures of the lung. Results: primary EIT relative images were acquired on-line (50 images/second) and processed according to a few imaging-analysis routines running automatically and in parallel. Pneumothoraces as small as 20mL could be detected with a sensitivity of 100% and specificity 95% and easily distinguished from parenchymal overdistension induced by PEEP or recruiting maneuvers. Their location was correctly identified in all cases, with a total delay of only 3 respiratory cycles. Conclusion: We created an EIT-based algorithm capable of detecting early signs of pneumothoraces in high-risk situations, which also identifies its location. It requires that the pneumothorax occurs or enlarges at least minimally during the monitoring period. Such detection was operator-free and in quasi real-time, opening opportunities for improving patient safety during mechanical ventilation.

INTRODUÇÃO: O transplante de pâncreas é a opção definitiva para a manutenção do estado normoglicêmico permanente nos portadores de diabetes mellitus tipo 1. O meio de contraste de ultra-som é uma metodologia capaz de avaliar a perfusão tecidual, mas não há um estudo para a avaliação do padrão de perfusão do pâncreas transplantado normal e patológico. A importância da avaliação da perfusão do enxerto e a aplicação do meio de contraste por microbolhas foram os motivos para a realização desta pesquisa. Este estudo, desenvolvido no Instituto de Radiologia do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo no período de novembro de 2004 a setembro de 2006 objetivou: A) estabelecer os padrões de vascularização do enxerto nos pacientes normais e naqueles com suspeita de complicações; B) comparar os achados de exames laboratoriais, uso ou não de insulina exógena e situação clínica dos pacientes com os achados da ultra-sonografia modo-B e com meio de contraste por microbolhas; C) Estabelecer o valor da ultra-sonografia com meio de contraste de microbolhas (USMCM) na avaliação do pâncreas transplantado. CASUÍSTICA e MÉTODOS: Vinte e seis pacientes foram submetidos ao exame de ultra-sonografia com contraste em um total de trinta estudos, 20 (66,7%) em homens e 10 (33,3%) em mulheres. A idade dos pacientes variou de 25 a 51 anos, com média de idade de 40 anos (+ 7,3 anos). O tempo médio da realização do transplante até a realização do estudo variou de um dia a 63 meses (mediana de 24 meses). Ao modo-B, o pâncreas foi analisado quanto a ecogenicidade, dimensões (avaliação qualitativa e quantitativa) e contornos. Após a administração do meio de contraste, observou-se o tempo de chegada do meio de contraste no pâncreas, o padrão e a intensidade de realce. Após esta avaliação foi realizada uma classificação baseada nos achados do modo-B e contraste nas seguintes possibilidades: padrão de perfusão normal, alterações agudas (rejeição, pancreatite ou trombose) ou alterações crônicas (rejeição crônica). RESULTADOS: Observou-se associação estatisticamente significante entre a ecogenicidade e a situação clínica (p=0,010); ecogenicidade e uso de insulina (p= 0,021); dimensões (avaliação qualitativa) e situação clinica (p=0,011); dimensões (avaliação qualitativa) e uso de insulina (p=0,028); padrão de realce (p=0,024) e intensidade do realce com a situação clínica (p=0,039). Houve associação estatisticamente significante também entre o uso ou não de insulina exógena com a perfusão do enxerto (p=0,014) e a hipótese diagnóstica (ultra-som) (p=0,001). CONCLUSÃO: Os padrões de vascularização do pâncreas transplantado normais e naqueles com suspeita de complicações foram estabelecidos. Os critérios de ecogenicidade e a avaliação qualitativa das dimensões do pâncreas ao ultra-som modo-B se mostraram adequados na diferenciação entre estudos normais e alterados. A ultra-sonografia com meio de contraste de microbolhas foi útil na diferenciação entre estudos normais e alterados do pâncreas transplantado, utilizando os critérios de padrão do realce, intensidade do realce e perfusão do enxerto na fase arterial. / INTRODUCTION: Pancreatic transplantation is the long-term therapeutic option for maintaining normoglycemic status in patients with type 1 diabetes mellitus. Sonographic contrast medium allows to evaluate tissue perfusion but there are no studies comparing this parameter in normal and pathologic pancreatic grafts in the literature at the time of this writing. The importance of assessment of graft perfusion and the potential role of contrast-enhanced sonography with microbubbles in this regard were the reasons for this research. The study conducted at the Instituto de Radiologia do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo between November, 2004 and September, 2006 had the following objectives: A) to establish patterns of graft vascularization in normal patients and in those with suspected abnormalities; B) to compare grayscale mode and contrastenhanced sonographic findings with clinical status, laboratory results, and need for exogenous insulin; C) to define the role of contrast-enhanced sonography with microbubbles in the evaluation of pancreatic transplantation.MATERIALS AND METHODS: Twenty-six patients underwent a total of 30 sonographic examinations with microbubbles, 20 (66.7%) men and 10 (33.3%) women. Age range was 25 to 51 years, with a mean of 40 years (+ 7.3 years). Time elapsed between transplantation and imaging ranged from 1 day to 63 months (median, 24 months). Using grayscale mode, pancreas was assessed for echogenicity, dimensions (both quantitatively and qualitatively) and contours. Following intravenous contrast medium administration, time for enhancement of the pancreatic graft, pattern and intensity of enhancement were documented. A classification system based on grayscale and contrast-enhanced sonographic findings was designed, with the following categories: normal perfusion pattern, acute changes (rejection, pancreatitis or thrombosis) and chronic changes (chronic rejection). RESULTS: There was a statistically significant association between echogenicity and clinical status (p=0.010); echogenicity and need for exogenous insulin (p=0.021); dimensions (qualitative criteria) and clinical status (p=0.011); dimensions (qualitative criteria) and need for exogenous insulin (p=0.028); pattern (p=0.024) and intensity of enhancement versus clinical status (p=0.039). There was also statistically significant association between need for exogenous insulin and graft perfusion (p=0.014), and sonography-based diagnosis (p=0.001). CONCLUSION: The study provided patterns of vascularization in normal pancreatic grafts and in patients with suspected abnormalities. Distinction of normal and abnormal pancreatic grafts was possible using echogenicity and qualitative analysis of graft size on grayscale mode. Contrast-enhanced sonography with microbubbles also contributed to differentiation between normal and abnormal pancreatic grafts, using pattern and intensity of enhancement and perfusion of the graft during the arterial phase.

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.

INTRODUÇÃO: O transplante de pâncreas é a opção definitiva para a manutenção do estado normoglicêmico permanente nos portadores de diabetes mellitus tipo 1. O meio de contraste de ultra-som é uma metodologia capaz de avaliar a perfusão tecidual, mas não há um estudo para a avaliação do padrão de perfusão do pâncreas transplantado normal e patológico. A importância da avaliação da perfusão do enxerto e a aplicação do meio de contraste por microbolhas foram os motivos para a realização desta pesquisa. Este estudo, desenvolvido no Instituto de Radiologia do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo no período de novembro de 2004 a setembro de 2006 objetivou: A) estabelecer os padrões de vascularização do enxerto nos pacientes normais e naqueles com suspeita de complicações; B) comparar os achados de exames laboratoriais, uso ou não de insulina exógena e situação clínica dos pacientes com os achados da ultra-sonografia modo-B e com meio de contraste por microbolhas; C) Estabelecer o valor da ultra-sonografia com meio de contraste de microbolhas (USMCM) na avaliação do pâncreas transplantado. CASUÍSTICA e MÉTODOS: Vinte e seis pacientes foram submetidos ao exame de ultra-sonografia com contraste em um total de trinta estudos, 20 (66,7%) em homens e 10 (33,3%) em mulheres. A idade dos pacientes variou de 25 a 51 anos, com média de idade de 40 anos (+ 7,3 anos). O tempo médio da realização do transplante até a realização do estudo variou de um dia a 63 meses (mediana de 24 meses). Ao modo-B, o pâncreas foi analisado quanto a ecogenicidade, dimensões (avaliação qualitativa e quantitativa) e contornos. Após a administração do meio de contraste, observou-se o tempo de chegada do meio de contraste no pâncreas, o padrão e a intensidade de realce. Após esta avaliação foi realizada uma classificação baseada nos achados do modo-B e contraste nas seguintes possibilidades: padrão de perfusão normal, alterações agudas (rejeição, pancreatite ou trombose) ou alterações crônicas (rejeição crônica). RESULTADOS: Observou-se associação estatisticamente significante entre a ecogenicidade e a situação clínica (p=0,010); ecogenicidade e uso de insulina (p= 0,021); dimensões (avaliação qualitativa) e situação clinica (p=0,011); dimensões (avaliação qualitativa) e uso de insulina (p=0,028); padrão de realce (p=0,024) e intensidade do realce com a situação clínica (p=0,039). Houve associação estatisticamente significante também entre o uso ou não de insulina exógena com a perfusão do enxerto (p=0,014) e a hipótese diagnóstica (ultra-som) (p=0,001). CONCLUSÃO: Os padrões de vascularização do pâncreas transplantado normais e naqueles com suspeita de complicações foram estabelecidos. Os critérios de ecogenicidade e a avaliação qualitativa das dimensões do pâncreas ao ultra-som modo-B se mostraram adequados na diferenciação entre estudos normais e alterados. A ultra-sonografia com meio de contraste de microbolhas foi útil na diferenciação entre estudos normais e alterados do pâncreas transplantado, utilizando os critérios de padrão do realce, intensidade do realce e perfusão do enxerto na fase arterial. / INTRODUCTION: Pancreatic transplantation is the long-term therapeutic option for maintaining normoglycemic status in patients with type 1 diabetes mellitus. Sonographic contrast medium allows to evaluate tissue perfusion but there are no studies comparing this parameter in normal and pathologic pancreatic grafts in the literature at the time of this writing. The importance of assessment of graft perfusion and the potential role of contrast-enhanced sonography with microbubbles in this regard were the reasons for this research. The study conducted at the Instituto de Radiologia do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo between November, 2004 and September, 2006 had the following objectives: A) to establish patterns of graft vascularization in normal patients and in those with suspected abnormalities; B) to compare grayscale mode and contrastenhanced sonographic findings with clinical status, laboratory results, and need for exogenous insulin; C) to define the role of contrast-enhanced sonography with microbubbles in the evaluation of pancreatic transplantation.MATERIALS AND METHODS: Twenty-six patients underwent a total of 30 sonographic examinations with microbubbles, 20 (66.7%) men and 10 (33.3%) women. Age range was 25 to 51 years, with a mean of 40 years (+ 7.3 years). Time elapsed between transplantation and imaging ranged from 1 day to 63 months (median, 24 months). Using grayscale mode, pancreas was assessed for echogenicity, dimensions (both quantitatively and qualitatively) and contours. Following intravenous contrast medium administration, time for enhancement of the pancreatic graft, pattern and intensity of enhancement were documented. A classification system based on grayscale and contrast-enhanced sonographic findings was designed, with the following categories: normal perfusion pattern, acute changes (rejection, pancreatitis or thrombosis) and chronic changes (chronic rejection). RESULTS: There was a statistically significant association between echogenicity and clinical status (p=0.010); echogenicity and need for exogenous insulin (p=0.021); dimensions (qualitative criteria) and clinical status (p=0.011); dimensions (qualitative criteria) and need for exogenous insulin (p=0.028); pattern (p=0.024) and intensity of enhancement versus clinical status (p=0.039). There was also statistically significant association between need for exogenous insulin and graft perfusion (p=0.014), and sonography-based diagnosis (p=0.001). CONCLUSION: The study provided patterns of vascularization in normal pancreatic grafts and in patients with suspected abnormalities. Distinction of normal and abnormal pancreatic grafts was possible using echogenicity and qualitative analysis of graft size on grayscale mode. Contrast-enhanced sonography with microbubbles also contributed to differentiation between normal and abnormal pancreatic grafts, using pattern and intensity of enhancement and perfusion of the graft during the arterial phase.

Implanted tissue engineered substitutes constitute dynamic systems, with remodeling mediated by both the implanted cells and the host. Thus, there exists a significant need for methods to monitor the function and morphology of tissue engineered constructs. Noninvasive monitoring using 1H Nuclear Magnetic Resonance (NMR) spectroscopy and imaging can prove to be the solution to this problem. Spectroscopy allows for assessment of cellular function through the monitoring of inherent metabolic markers, such as total-choline, while high resolution imaging enables the evaluation of construct morphology and interfacial remodeling. We applied these 1H NMR methods to monitor betaTC3 mouse insulinoma cells within hydrogel-based materials as a model pancreatic tissue substitute. In vitro research established a strong correlation between total-choline, measured by 1H NMR spectroscopy, and viable betaTC3 cell number, measured by MTT. Extending these methods to in vivo monitoring, however, was met with additional challenges. First, the implanted cells needed to be contained within a planar construct above a threshold density to allow for adequate quantification of the total-choline peak. Secondly, cell-free buffer zones between the implanted cells and the host tissue needed to be incorporated to prevent host tissue signal contamination. Finally, quantitative techniques needed to be developed to accurately account for contaminating signal from diffusing molecules. To overcome these challenges, a disk-shaped agarose construct, initially containing a minimum of 4 million betaTC3 cells and coated with an outer layer of pure agarose, was fabricated. Mathematical simulations aided the implant design by characterizing diffusive transport of nutrients and metabolites into and out of the construct. In vivo 1H NMR studies of these constructs implanted in mice established a strong correlation between total-choline, measured noninvasively using 1H NMR spectroscopy, and viable cell number, measured invasively using MTT. This study establishes total-choline as a reliable marker for noninvasively quantifying dynamic changes in viable betaTC3 cell number in vivo. 1H NMR imaging was used to monitor the implants structural integrity over time, while also assessing the hosts fibrotic response. We expect these studies to establish quantitative criteria for the capabilities and limitations of NMR methodologies for monitoring encapsulated insulinomas, as well as other tissue implants.

This dissertation presents a fully automatic segmentation algorithm for cardiac MR data. Some of the currently published methods are automatic, but they only work well in 2D and sometimes in 3D and do not perform well near the extremities (apex and base) of the heart. Additionally, they require substantial user input to make them feasible for use in a clinical environment. This dissertation introduces novel approaches to improve the accuracy, robustness, and consistency of existing methods. Segmentation accuracy can be improved by knowing as much about the data as possible. Accordingly, we compute a single 4D active surface that performs segmentation in space and time simultaneously. The segmentation routine can now take advantage of information from neighboring pixels that can be adjacent either spatially or temporally. Robustness is improved further by using confidence labels on shape priors. Shape priors are deduced from manual segmentation of training data. This data may contain imperfections that may impede proper manual segmentation. Confidence labels indicate the level of fidelity of the manual segmentation to the actual data. The contribution of regions with low confidence levels can be attenuated or excluded from the final result. The specific advantages of using the 4D segmentation along with shape priors and regions of confidence are highlighted throughout the thesis dissertation. Performance of the new method is measured by comparing the results to traditional 3D segmentation and to manual segmentation performed by a trained clinician.

Atherosclerosis is a systemic disease of the vessel wall that occurs in the aorta, carotid, coronary and peripheral arteries. Atherosclerotic plaques in coronary arteries may cause the narrowing (stenosis) or complete occlusion of the arteries and lead to serious results such as heart attacks and strokes. Medical imaging techniques such as X-ray angiography and computed tomography angiography (CTA) have greatly assisted the diagnosis of atherosclerosis in living patients. Analyzing and quantifying vessels in these images, however, is an extremely laborious and time consuming task if done manually. A novel image segmentation approach and a quantitative shape analysis approach are proposed to automatically isolate the coronary arteries and measure important parameters along the vessels. The segmentation method is based on the active contour model using the level set formulation. Regional statistical information is incorporated in the framework through Bayesian pixel classification. A new conformal factor and an adaptive speed term are proposed to counter the problems of contour leakage and narrowed vessels resulting from the conventional geometric active contours. The proposed segmentation framework is tested and evaluated on a large amount of 2D and 3D, including synthetic and real 2D vessels, 2D non-vessel objects, and eighteen 3D clinical CTA datasets of coronary arteries. The centerlines of the vessels are proposed to be extracted using harmonic skeletonization technique based on the level contour sets of the harmonic function, which is the solution of the Laplace equation on the triangulated surface of the segmented vessels. The cross-sectional areas along the vessels can be measured while the centerline is being extracted. Local cross-sectional areas can be used as a direct indicator of stenosis for diagnosis. A comprehensive validation is performed by using digital phantoms and real CTA datasets. This study provides the possibility of fully automatic analysis of coronary atherosclerosis from CTA images, and has the potential to be used in a real clinical setting along with a friendly user interface. Comparing to the manual segmentation which takes approximately an hour for a single dataset, the automatic approach on average takes less than five minutes to complete, and gives more consistent results across datasets.

The Fontan repair is a three-stage palliative surgical procedure for single ventricle congenital heart diseases, ultimately resulting in the right heart bypass. This is accomplished by routing the systemic venous return directly to the lungs. Although this procedure reduces the mortality rate, its long-term outcome is still considered far from optimal. Over the years several modifications have been suggested, ultimately leading to the total cavopulmonary connection (TCPC), which is the current procedure of choice. A better understanding of the hemodynamics in the TCPC is critical for further optimization of the TCPC design and surgical planning, which may lead to improved surgical outcome. Recent experimental and numerical studies have focused on characterizing the fluid dynamics of the TCPC but to date no study has attempted to relate the geometry of the TCPC anatomies with their hemodynamic parameters. The present study therefore proposes to quantify the complex geometrical characteristics of patient-specific TCPC anatomies and correlate these characteristics with their hemodynamic efficiency. A technique using skeletonization approach is thus developed to achieve this goal. The centerline approximation of the TCPC geometry is used to extract main geometric parameters such as vessel area, curvature and offset. The developed methodology is then applied to characterize the shape of various TCPC templates including extra-cardiac (EC) and intra-atrial (IA) TCPCs, TCPCs with bilateral Superior Vena Cavae and geometries before the third stage. The obtained geometric parameters are then related to the TCPC hemodynamics, particularly to the power loss.

Despite significant developments in imaging modalities and therapeutics, cancer mortality rates remain unchanged. Detecting cancer before it has spread to other organs improves patient outcome dramatically. Therefore, greater emphasis must be placed on developing novel technology for early cancer detection and disease monitoring. Nanometer-sized materials have unique optoelectronic and magnetic properties. In particular, semiconductor quantum dots (QD) are a new class of fluorophores that are bright, photostable, and can be simultaneously excited to emit different wavelengths of light. Magnetic iron oxide nanoparticles are another class of unique nanomaterials that exhibit superparamagnetism and are strongly magnetized only in the presence of a magnetic field. In this dissertation, we describe the integration of semiconductor QDs and magnetic iron oxide nanoparticles and potential applications for (i) early detection of cancer biomarkers through routine screening, and (ii) disease monitoring through the capture and analysis of rare circulating tumor cells. First, we describe the development of integrated magneto-optical beads that can be optically encoded and magnetically separable for isolating low amounts of biomolecules from solution. Second, we demonstrate improved detection sensitivity by combining immunomagnetic beads and highly luminescent nanoparticles in a sandwich assay. Next, we describe integration of magnetic and QD nanotechnology for the selective capture and molecular profiling of rare cells. We demonstrate the ability to spectroscopically determine relative molecular levels of markers to identify invasive cells. As disease monitoring requires the analysis of patient blood samples, we have also studied nanoparticle-cell interactions using QDs to determine nanoparticle behavior in whole blood as a function of surface coatings. We observed that anionic nanoparticles with carboxylic acid groups (-COOH) were strongly associated with leukocytes, but interestingly this association was cell specific. Hydroxyl-modified QDs (QD-OH) suppressed binding and uptake by leukocytes as efficiently as PEG-modified QDs. The integration of nanotechnologies represents a new and exciting approach that has the potential to push the limits of detection sensitivity and permit isolation and profiling of multiple biomarkers from large sample volumes.

Nanoparticles possess unique characteristics that make them well suited for molecular imaging. Particles can be synthesized in a systematic fashion with tight control over diameter and surface chemistry. Contrary to existing gadolinium-based MRI contrast agents, nanoparticle MRI contrast agents circulate in the blood for long periods of time, offer higher sensitivity, and exhibit little known toxicity. The qualities of nanoparticles are also well suited to the design of PET probes. Because of their large surface area nanoparticles can be radiolabeled at high specific activity, increasing the sensitivity of detection as well as the payload of therapeutic isotopes. The work presented here focuses on the development and biological application of novel radiolabeled magnetic nanoparticles for multimodal PET/MRI imaging. The nanoparticle probes contained crystalline iron oxide cores capable of producing strong MRI contrast. Cores were coated with either a micelle composed of functionalized PEGylated lipids, or a cross-linked dextran shell modified with heterobifuntional PEG polymers. For PET imaging, magnetic nanoparticles were labeled with the radionuclide 64Cu. Copper‐64 is a cyclotron produced positron emitter used for PET imaging. With a 12.7 hour half-life, 64Cu can be used to image particles in vivo for up to 48 hr and can be used to evaluate ex vivo biodistribution for 72 hours. 64Cu nuclides also undergo β‐ decay, making it a useful isotope for radiotherapy. Nanoparticles were labeled with 64Cu and PET and MRI contrast and evaluated using phantoms. Pharmacokinetic information was measured using in vivo small animal PET/CT and ex vivo biodistribution at multiple time points. Particles were targeted to the angiogenesis marker αvβ3 integrin using a cyclized arginine-glycine-aspartic acid (RGD) peptide with high affinity for αvβ3 and tested in two tumor models. A unilateral tumor model was constructed using the αvβ3-positive U87MG glioblastoma line, and a bilateral model was constructed using the M21 (αvβ3 positive) and M21L (αvβ3 negative) melanoma lines. In vivo PET/CT and MRI showed that targeted nanoparticles produced both PET and MRI contrast in tumors. In conclusion, we report the development of magnetic nanoparticles for dual‐PET/MR imaging. These findings provide insight into the design and development of future multimodality PET/MRI probes.