Pacientes envenenados pela serpente Bothrops jararaca manifestam uma tendência hemorrágica em que a plaquetopenia é um achado consistente. Manifestações clínicas sistêmicas, como sangramento de mucosas e microangiopatia trombótica em alguns pacientes, apresentam similaridades com sinais clínicos de doença de von Willebrand e púrpura trombocitopênica trombótica. Algumas proteínas do veneno - como a botrocetina (uma proteína relacionada às lectinas do tipo C) e as metaloproteinases do veneno (SVMP) - interferem direta ou indiretamente na interação entre plaquetas e o fator de von Willebrand (vWF) in vitro e in vivo. E dessa forma, podem contribuir para os sangramentos induzidos pelo envenenamento devido à importância que o vWF tem para a hemostasia primária. Pensando em compreender a participação do vWF do organismo e a botrocetina e as SVMP do veneno bruto de B. jararaca (BjV) na plaquetopenia induzida pelo envenenamento, utilizamos dois modelos experimentais: ratos Wistar heterogênicos e camundongos nocautes do gene Vwf (Vwf-/-). No modelo em ratos, o BjV foi pré-incubado com salina (controle positivo), um inibidor de metaloproteinases (Na2-EDTA), anticorpos policlonais anti-botrocetina, glicerol (veículo dos anticorpos), ou a combinação do Na2-EDTA e anticorpos anti-botrocetina; o grupo controle negativo foi injetado somente com salina. Após a administração subcutânea (s.c.) dos venenos tratados (1,6 mg/kg), amostras de sangue foram coletadas após 3, 6 ou 24 h, e analisaram-se a contagem de plaquetas, quantificação antigênica (vWF:Ag) e da atividade de ligação do vWF ao colágeno (vWF:CB), a atividade de ADAMTS13, a distribuição multimérica de vWF, e a atividade coagulante de fator VIII (FVIII). Para explorar a participação do vWF na plaquetopenia, camundongos nocautes de vWF (Vwf-/-) e camundongos controles (C57BL/6) foram injetados s.c. com BjV incubado com salina (grupo positivo do envenenamento) ou apenas salina (grupo controle negativo). As injeções dos tratamentos, bem como os períodos analisados foram idênticos aos dos ratos. Em nossos resultados, todos os ratos injetados com algum tratamento de BjV, inclusive nos animais que receberam veneno pré-tratado com anticorpo anti-botrocetina e/ou Na2-EDTA, apresentaram plaquetopenia, com maior intensidade em 6 h. Na avaliação do vWF foi encontrada uma grande variação individual nos grupos de tratamentos, porém ainda assim houve uma tendência a redução nos níveis de vWF:Ag em 3 e 6 h nos ratos que receberam BjV sem inibidores. A administração de BjV tratado somente com anticorpo anti-botrocetina promoveu uma maior redução nos níveis de vWF:Ag em 3 h, com retorno aos níveis semelhantes aos de controle negativo em 6 h e 24 h. A inibição sozinha das metaloproteinases não promoveu efeito importante, porém em 6 h, potencializou a ação do anticorpo anti-botrocetina na inibição conjunta do decréscimo de vWF:Ag e vWF:CB. A análise dos multímeros do vWF mostrou perfis bastante variáveis individualmente, porém os multímeros de alto peso molecular e intermediário tenderam a diminuir e os de baixo peso a aumentar nos animais que receberam algum tratamento com BjV, especialmente em 24 h. Na dosagem de FVIII, houve redução em 3 e 6 h em todos os ratos que receberam qualquer tratamento de BjV, sem grandes variações entre esses grupos. A atividade de ADAMTS13 apresentou uma redução dos valores em 3 e 6 h, que foi revertida pela inibição das metaloproteinases do veneno. Já nos camundongos, a plaquetopenia esteve presente em todos os animais nocautes e controles que receberam BjV, mostrando ser independente da presença de vWF. Nos camundongos controles (C57BL/6), não houve alterações evidentes em vWF:Ag durante o envenenamento, porém em 3 h houve uma tendência a sua diminuição. Em conjunto, nossos resultados mostram que a presença da botrocetina no veneno bruto não afeta a plaquetopenia desencadeada pelo envenenamento, porém influencia o vWF plasmático quantitativa e funcionalmente. As metaloproteinases do veneno têm forte efeito sobre a enzima fisiológica reguladora da atividade biológica do vWF, a ADAMTS13, que indiretamente pode afetar os níveis de vWF. Ademais, a intensidade da plaquetopenia durante o envenenamento de B. jararaca não depende da presença de vWF, e tendo em conta o caráter multifatorial do consumo plaquetário durante o envenenamento, sugerimos que outros mecanismos possam ser responsáveis pela plaquetopenia induzida pelo BjV. Com isso, concluímos que o consumo de vWF no envenenamento por B. jararaca é um fator contribuinte, porém não determinante, para as alterações da contagem plaquetária / Patients bitten by Bothrops snakes manifest a bleeding tendency in which thrombocytopenia is consistently observed. Systemic clinical manifestations, such as mucous bleeding and thrombotic microangiopathy in some patients, share similarities with symptoms of von Willebrand disease and thrombotic thrombocytopenic purpura. Some venom proteins - e.g. botrocetin (a C-type lectin-related protein) and snake venom metalloproteinases (SVMP) - disturbs, direct or indirectly, the interaction between platelets and von Willebrand factor (vWF) in vitro and in vivo, and may contribute thereby to snakebite-induced bleedings, once vWF is required for primary hemostasis. To better understand the relation between plasma vWF, and botrocetin and SVMPs from B. jararaca crude venom (BjV) in the thrombocytopenia induced by envenomation, we used two experimental models: Wistar heterogenic rats and vWF knockout mice (Vwf-/-). In the rat model, BjV was pre-incubated with saline (positive control), metalloproteinase inhibitor (Na2-EDTA), polyclonal anti-botrocetin antibodies, glycerol (antibody vehicle), or the combination of Na2-EDTA and anti-botrocetin antibodies; the negative control group was injected with saline only. After subcutaneous injection (s.c.) of treated venom (1.6 mg/kg), blood samples were collected after 3, 6 or 24 h, and platelet count, vWF antigen (vWF:Ag) and collagenbinding activity (vWF:CB), ADAMTS13 activity, vWF multimer distribution, and factor VIII (FVIII) coagulant activity were analyzed. To investigate the participation of vWF in thrombocytopenia, vWF knockout mice (Vwf-/-) and control mice (C57BL/6) were injected s.c. with saline only (negative control group) or BjV pre-incubated with saline (positive control group). The same protocols used for rats were accomplished in mice. Our results showed that all rats injected with any BjV treatment, including animals which received anti-botrocetin antibodies and/or Na2-EDTA-treated BjV, showed thrombocytopenia, with the nadir at 6h. vWF analysis exhibited a large individual variation among treatment groups, but there was a tendency to reduce vWF:Ag levels at 3 and 6 h in rats that received BjV pre-incubated with saline (without any inhibitor). Administration of BjV pre-incubated only with anti-botrocetin antibodies evoked a large reduction in vWF:Ag levels at 3 h, which returned to levels similar to those of the negative control group at 6 and 24 h. SVMP inhibition alone did not induce an important effect, but potentialized the activity of anti-botrocetin antibodies to inhibit the fall in both vWF:Ag and vWF:CB levels at 6 h. VWF multimer analysis had a large individual profile variation, although animals that received any BjV treatment tended to decrease the high and intermediate molecular weight multimers and to increase the low ones, especially at 24 h. FVIII showed diminished levels in all rats that received any BjV treatment at 3 and 6 h, without important variations among groups. Decreased levels of ADAMTS13 activity were noticed at 3 and 6 h, which were reverted by SVMP inhibition. In mice, thrombocytopenia was present in all control and knockout mice that received BjV, demonstrating independence of vWF presence. In control mice (C57BL/6), there were no relevant alterations in vWF:Ag during envenomation, although at 3 h there was a tendency to decrease it. Al together, our results showed that botrocetin present in crude venom does not affect thrombocytopenia induced by envenomation, but it changes the levels and function of plasma vWF. SVMP had a marked effect in ADAMTS13, the physiological enzyme that regulates vWF biological activity, which may affect vWF levels indirectly. In addition, thrombocytopenia during B. jararaca envenomation is independent of vWF, and considering the multifactorial features of platelet consumption during envenomation, we suggest that other mechanisms might account for BjV-induced thrombocytopenia. Therefore, we conclude that vWF consumption during B. jararaca envenomation is an ancillary mechanism, but not the main one to decrease platelet counts

Fundamentos: O implante de stents coronários constitui-se na técnica mais prevalente de revascularização percutânea, em especial pela prevenção da reestenose, quando comparado às intervenções com o balão. No entanto, a reestenose intra-stent, que ocorre em cerca de 25% dos casos, restringe os seus benefícios clínicos e econômicos tardios. Demonstrou-se que a hiperplasia neo-intimal decorrente da reação da parede vascular causada pelo implante do stent, é responsável pelas recidivas. Interroga-se se um protocolo de medicamentos contemplando doses máximas de manutenção de clopidogrel e atorvastatina poderia reduzir a hiperplasia neo-intimal e a reestenose. Objetivos: O objetivo primário foi aferir se esta associação de medicamentos reduziria o volume de hiperplasia neo-intimal (35% ou mais), expressa pela obstrução volumétrica da luz, mensurada pelo ultrassom intracoronário, 12 meses após a intervenção. Os objetivos secundários foram: os resultados da angiografia quantitativa e os eventos cardíacos adversos maiores (óbito, infarto e revascularização do vaso-alvo). Casuística e métodos: Foram incluídos casos eletivos e com lesões primárias nas artérias naturais. Os pacientes foram tratados com stents não farmacológicos e randomizados em dois grupos: A, com 50 pacientes medicados com doses máximas de clopidogrel e atorvastatina; e grupo B com 50 casos, medicados com 75mg de clopidogrel e doses de sinvastatina rotineiramente prescritas para obtenção das metas recomendadas para controle lipídico. Resultados: Ambos os grupos não apresentaram diferenças significantes em relação às características clínicas, angiográficas e técnicas, com exceção do diabetes, mais comum em A (36% vs 16%; p=0,02). Aos 12 meses de evolução, observaram-se eventos cardíacos maiores (12% versus 18%; p = 0,56) e revascularização do vaso-alvo (4% versus 2%; p>0,99) sem diferença significante. Nova angiografia coronária foi obtida em 98% dos casos dos dois grupos, observando-se taxa de reestenose de 8,1% e 8,2% nos grupos A e B (p>0,99). A perda tardia da luz arterial foi semelhante [0,9 mm (DP 0,5 mm) versus 1,1 mm (DP 0,7 mm); p = 0,22], o mesmo acontecendo com o diâmetro mínimo da luz [2,2 mm (DP 0,6 mm) versus 1,9 mm (DP 0,6 mm); p = 0,12]. Realizou-se ultrassom intracoronário em 98% dos pacientes de ambos os grupos, observando-se obstrução do volume da luz de 36,3% (DP 10,3%) no grupo A e de 40,1% (DP 10,9%) no grupo B (p = 0,14). Conclusões: Os resultados deste estudo demonstram que: 1) a terapêutica adjunta utilizando doses máximas de clopidogrel 150 mg/dia e atorvastatina 80 mg/dia não reduz o volume de hiperplasia neo-intimal, expressa pela obstrução volumétrica da luz; 2) as variáveis da angiografia quantitativa e os eventos cardíacos adversos maiores não mostraram diferenças significativas entre os dois grupos. / Coronary stent implantation is the current technique of choice in patients undergoing percutaneous intervention. They effectively reduce acute occlusion and restenosis even in complex lesions. However, instent restenosis occurs in up to 25% of the treated cases and there are several theories elaborating the possible relation between coronary artery thrombosis and inflammation to neointimal proliferation and the mechanism of obstruction recurrence. There are questions whether an optimized medical treatment based on maximum doses of Clopidogrel and Atorvastatin could limit neointimal hyperplasia and restenosis. Objectives: Primary endpoint was to assess the efficacy of this scheme in reducing neointimal hyperplasia volume (XX% or more), according to intravascular ultrasound measurements, 12 months after the index intervention. Secondary endpoints were quantitative angiography measurements and major adverse cardiac events (death, myocardial infarction and target vessel revascularization). Methods: We included patients with de novo lesions undergoing elective implantation of uncoated stents. Patients were divided according to the drug regimen into Group A - 50 patients receiving maximal atorvastatin and clopidogrel doses; and Group B - 50 cases treated with standard clopidogrel and simvastatin doses. Results: Groups were similar concerning clinical and angiographic characteristics, except for diabetes, more frequent in Group A (36% vs 16%, p = 0.02). At the end of 12 months major cardiac events (12% versus 18%, p = 0.56) and target vessel revascularization (4% versus 2%, p> 0.99) did not show differences between groups. Coronary angiography was obtained in 98% of the cases and the restenosis rate was 8.1% (A group) and 8,2% (B group) (p> 0.99). Late luminal loss was similar [0.9 mm (SD 0.5 mm) versus 1.1 mm (SD 0.7 mm), p = 0.22], as well as the minimum lumen diameter [2.2 mm (SD 0.6 mm) versus 1.9 mm (SD 0.6 mm), p = 0.12]. IVUS was done in 98% of patients in both groups, and the volume of neointimal hyperplasia was not significantly different in both groups [61.8 mm 3 (SD 35.4 mm3) mm3 versus 66.3 (SD 31.6 mm3), p = 0.58]. Luminal volume obstruction was 36.3% (SD 10.3%) in group A and 40.1% (SD 10.9%) in group B (p = 0.14). Conclusions: According to our results we may conclude that: 1) the therapeutic regimen using maximum doses of atorvastatin and clopidogrel did not reduce the volume of neointimal hyperplasia, 2) restenosis rate, quantitative angiography results and the rate of major adverse cardiac events were not affected by the treatment regimen.

Introdução: As modificações evolutivas e o impacto clínico da composição da aterosclerose coronária em pacientes sob prevenção secundária permanecem pouco conhecidos. O ultrassom intravascular com histologia virtual (VH-IVUS) permite caracterizar in vivo tais componentes. Os objetivos desse estudo foram avaliar o papel prognóstico da composição da aterosclerose da árvore coronária proximal, bem como descrever o comportamento dinâmico da placa, explorando a relação entre seus componentes e as alterações geométricas do vaso. Métodos: Conduziu-se um estudo prospectivo, observacional e unicêntrico, que incluiu pacientes encaminhados para intervenção coronária percutânea. Durante essa intervenção, realizou-se VH-IVUS tipo \"artéria inteira\" das três coronárias principais para mensurar os parâmetros geométricos do vaso (luz, membrana elástica externa, placa+média e volume percentual do ateroma) e os componentes das placas (fibrótico, fibrolipídico, núcleo necrótico e cálcio denso). Calculou-se o volume indexado de cada parâmetro por paciente, artéria e subsegmento arterial. Avaliou-se a influência dos volumes indexados da árvore coronária proximal (por paciente), sem considerar a categorização fenotípica das placas, na ocorrência de eventos cardíacos adversos maiores (MACE), definidos como óbito, infarto agudo do miocárdio e revascularização miocárdica não planejada, após 4 anos de seguimento. Em um subgrupo de pacientes, VH-IVUS volumétrico seriado foi realizado para estudar variações do ateroma nas artérias e em seus subsegmentos, testando correlações entre componentes da placa e variações geométricas do vaso. Resultados: Foram incluídos 67 pacientes com idade média de 58,9 ± 9,2 anos, 66% do sexo masculino, 42% diabéticos, 69% multiarteriais e 45% com síndrome coronária aguda recente. Obtiveram-se imagens de VH-IVUS para 255 artérias. As médias dos volumes indexados basais da árvore coronária proximal, em escala de cinza, foram: luz 8,8±2,5mm3/mm, membrana elástica externa 15,4±3,5mm3/mm e placa+média 6,6±2,0mm3/mm, com percentual de volume do ateroma de 42,8±8,9%. Quanto aos componentes do ateroma, predominou o fibrótico 2,1 ± 1,0mm3/mm (61,8 ± 6,6%), seguido por núcleo necrótico 0,6±0,4mm3/mm (16,6±6,7%), fibrolipídico 0,5±0,3mm3/mm (14,1±6,0%) e cálcio denso 0,3±0,2mm3/mm (7,6 ± 4,6%). Após 4,9 anos (intervalo interquartil: 4,5 - 5,1 anos) sob prevenção secundária, ocorreram MACE em 18 pacientes, a maioria por reestenose. Não houve correlação entre os volumes indexados basais da árvore coronária proximal e a ocorrência de MACE. VH-IVUS seriado, após 20,6 meses (intervalo interquartil: 9,1 - 23,8 meses), foi realizado em 52 pacientes. Nas artérias desses pacientes, houve redução no volume indexado de luz, redução no volume indexado de membrana elástica externa, sem alteração no volume indexado de placa+média ou no percentual de volume do ateroma. Modificações na composição da placa foram observadas, com incremento absoluto e relativo dos componentes cálcio denso (0,09±0,21mm3/mm p < 0,01; 2,2±7,1% p < 0,01) e núcleo necrótico (0,13±0,47mm3/mm p < 0,01; 3,0 ± 10,9% p < 0,01), redução relativa do componente fibrolipídico (-0,05 ± 0,81mm3/mm p=0,37; -3,7 ± 10,3% p < 0,01) sem variação do componente fibrótico (-0,04 ± 1,00mm3/mm p=0,62; -1,6 ± 13,3% p=0,12). Nos subsegmentos arteriais, a composição basal da placa correlacionou-se com a resposta de remodelamento do vaso. A quantidade total de volume indexado basal dos componentes não calcificados correlacionou-se positivamente com a resposta de remodelamento constrictiva do vaso, que ocorreu menos frequentemente em diabéticos e associou-se a maior incremento do componente cálcio denso durante a evolução. Conclusão: Em coronarianos sob prevenção secundária, a composição média da aterosclerose na árvore coronariana proximal não se associou a ocorrência de eventos cardíacos adversos maiores. O comportamento dinâmico do ateroma foi compatível com estabilização da doença, ocorrendo variação não significativa na quantidade de placa, redução luminal associada a remodelamento negativo do vaso e modificação nos constituintes da placa com desvio de um \"perfil fibrolipídico para um mais calcificado\". A quantidade basal de componentes não calcificados da placa modulou as alterações geométricas direcionadas para o remodelamento constrictivo do vaso / Background: Clinical impact of coronary atherosclerosis composition and their modifications related to secondary prevention remains not well known. Virtual histology intravascular ultrasound (VH-IVUS) allows in vivo characterization of atherosclerotic plaque components. The aim of this study was to evaluate the prognostic value of atherosclerotic plaque composition of proximal coronary tree and to describe the variations in atherosclerotic plaques, exploring the relations of theirs components with geometric modifications of the vessel. Methods: It was conducted a prospective observational single center study, including patients referred to percutaneous coronary intervention. During the interventional procedure, volumetric three vessel \"whole artery\" VH-IVUS was performed to measure geometric vessel (lumen, elastic external membrane, plaque+media, percent atheroma volume) and atheroma compositional parameters (fibrotic, fibrolipid, necrotic core, and dense calcium). It was computed the volumetric index of each parameter in patient, artery, and arterial subsegment level. It was tested the prediction value of the volumetric indexes of proximal coronary tree (patient level), disregarding the phenotypical categorization of plaques, in the occurrence of major adverse cardiac events (MACE) defined by death, acute myocardial infarction, and unplanned myocardial revascularization, after 4 years of follow-up. In a subgroup of patients, serial volumetric VH-IVUS was performed to evaluate the modifications of the atheroma in arteries and their subsegments, testing the correlations between plaque components and geometric variations of the vessel. Results: It was included 67 patients with mean age of 58.9 ± 9.2 yearsold, 66% male, 42% with diabetes, 69% with multivessel coronary disease, and 45% with recent acute coronary syndrome. VH-IVUS was obtained for 255 arteries. The average of volumetric indexes of proximal coronary tree was: lumen 8.8±2.5mm3/mm; elastic external membrane 15.4 ± 3.5mm3/mm; placa+media 6.6 ± 2.0mm3/mm and percent atheroma volume 42.8±8.9%. In terms of composition, the predominant component was fibrotic 2.1 ± 1,0mm3/mm (61.8 ± 6.6%), followed by necrotic core 0.6 ± 0.4mm3/mm (16.6 ± 6.7%), fibrolipid 0.5 ± 0.3mm3/mm (14.1 ± 6.0%) and dense calcium 0.3 ± 0.2mm3/mm (7.6 ± 4.6%). After a 4.9- year (interquartile interval: 4.5 - 5.1) follow-up, MACE occurred in 18 patients, mainly motivated by stent reestenosis. There was no correlation between baseline volumetric indexes of proximal coronary tree and the occurrence of MACE. Serial VH-IVUS, after 20.6 months (interquartile interval: 9.1 - 23.8 months), was performed in 52 patients. In arterial level, there was decrease in lumen index volume, reduction in elastic external membrane index volume, with no variation in placa+media index volume and percent atheroma volume. Changes in plaque composition were observed, with increase in absolute and relative dense calcium (0.09 ± 0.21mm3/mm p < 0.01; 2.2 ± 7.1% p < 0.01) and necrotic core (0.13 ± 0.47mm3/mm p < 0.01; 3.0 ± 10.9% p < 0.01), relative decrease in fibrolipid (-0.05 ± 0.81mm3/mm p=0.37; - 3.7 ± 10.3% p < 0.01), and no modification in fibrotic component (-0.04 ± 1.00mm3/mm p=0.62; -1.6 ± 13.3% p=0.12). In arterial subsegment level, baseline plaque composition correlated with remodeling response of the vessel. Total index volume of non-calcified plaque components positively correlated with a trend toward constrictive remodeling of the vessel, which occurred less frequently in diabetic patients and was associated with greater increase in dense calcium component. Conclusion: In patients with coronary artery disease treated with secondary prevention strategies, mean atherosclerotic plaque composition of the proximal coronary tree was not able to predict major adverse cardiac events. Dynamic behavior of atheroma in these patients was compatible with disease stabilization, related to quantitative plaque steadiness, lumen reduction associated with constrictive remodeling of the vessel, and modifications of plaque components with shifting from \"fibrolipid to more calcified profile\". Total non-calcified plaque components modulated geometric modifications toward constrictive remodeling of the vessel

Trauma continues to be a major cause of death across the globe. While the exact causes of trauma differ greatly between the military and civilian lifestyles, the ability to stop bleeding after trauma is paramount for survival. Over the past decade coagulation research has transitioned from a classical understanding of plasma based protein coagulation to the current cell focused research. As part of this shift, platelets have become a central player in hemostasis. Unfortunately little is currently understood about how platelet function is affected by trauma. In an effort to better define platelet function during trauma and the resulting shock from exsanguination, a multipronged approach was developed. The hypothesis that the introduction of a state of clinical shock in a controlled environment would allow for an in-depth assessment of trauma-induced coagulopathy led to the development of a swine based model of hemorrhagic shock. In this model a composite injury consisting of soft tissue damage, long bone fracture, and controlled hemorrhage was used to induce a moderate state of hypovolemic shock. As a result of this injury the animals showed both the beginning of a plasma protein consumption coagulopathy as well as kinetic quickening in the clotting process. These surprising results show competing up-regulation and down-regulation of the coagulation system in response to trauma induced shock. To better define the effect of polytrauma on platelet function in a human population a clinical study was conducted. The hypothesis behind the development of this study was that the examination of platelet function during polytrauma would lead to a more complete understanding of the effects of trauma on hemostasis. This study resulted in the identification of two separate but not mutually exclusive coagulopathies in response to trauma. The first was the traditional consumption based coagulopathies recently suggested to be varying degrees of disseminated intravascular coagulopathy. The second was a development a hypercoagulable state that may be attributed to increased platelet function. The identification of these two competing coagulopathies in separate models highlights the inadequacies of the current plasma based clinical testing, and the need for increased whole blood testing in the trauma treatment environment.

Although the drug-eluting stent (DES) has dramatically reduced the rate of coronary restenosis, it still occurs in up to 20% of patients with a DES. Monitoring drug delivery could be one way to decrease restenosis rates. We demonstrate real-time photoacoustic imaging and spectroscopy (PAIS) using a wavelength-tunable visible laser and clinical ultrasound scanner to track cardiac drug delivery. The photoacoustic signal was initially calibrated using porcine myocardial samples soaked with a known concentration of a drug surrogate (Dil). Next, an in situ coronary artery was perfused with DiI for 20 min and imaged to monitor dye transport in the tissue. Finally, a partially DiI-coated stent was inserted into the porcine brachiocephalic trunk for imaging. The photoacoustic signal was proportional to the DiI concentration between 2.4 and 120 mu g/ml, and the dye was detected over 1.5 mm from the targeted coronary vessel. Photoacoustic imaging was also able to differentiate the DiI-coated portion of the stent from the uncoated region. These results suggest that PAIS can track drug delivery to cardiac tissue and detect drugs loaded onto a stent with sub-mm precision. Future work using PAIS may help improve DES design and reduce the probability of restenosis. (C) 2017 Society of Photo-Optical Instrumentation Engineers (SPIE)

Optimal surface finding (OSF), a graph-based optimization approach to image segmentation, represents a powerful framework for medical image segmentation and analysis. In many applications, a pre-segmentation is required to enable OSF graph construction. Also, the cost function design is critical for the success of OSF. In this thesis, two issues in the context of OSF segmentation are addressed. First, a robust model-based segmentation method suitable for OSF initialization is introduced. Second, an OSF-based segmentation refinement approach is presented. For segmenting complex anatomical structures (e.g., lungs), a rough initial segmentation is required to apply an OSF-based approach. For this purpose, a novel robust active shape model (RASM) is presented. The RASM matching in combination with OSF is investigated in the context of segmenting lungs with large lung cancer masses in 3D CT scans. The robustness and effectiveness of this approach is demonstrated on 30 lung scans containing 20 normal lungs and 40 diseased lungs where conventional segmentation methods frequently fail to deliver usable results. The developed RASM approach is generally applicable and suitable for large organs/structures. While providing high levels of performance in most cases, OSF-based approaches may fail in a local region in the presence of pathology or other local challenges. A new (generic) interactive refinement approach for correcting local segmentation errors based on the OSF segmentation framework is proposed. Following the automated segmentation, the user can inspect the result and correct local or regional segmentation inaccuracies by (iteratively) providing clues regarding the location of the correct surface. This expert information is utilized to modify the previously calculated cost function, locally re-optimizing the underlying modified graph without a need to start the new optimization from scratch. For refinement, a hybrid desktop/virtual reality user interface based on stereoscopic visualization technology and advanced interaction techniques is utilized for efficient interaction with the segmentations (surfaces). The proposed generic interactive refinement method is adapted to three applications. First, two refinement tools for 3D lung segmentation are proposed, and the performance is assessed on 30 test cases from 18 CT lung scans. Second, in a feasibility study, the approach is expanded to 4D OSF-based lung segmentation refinement and an assessment of performance is provided. Finally, a dual-surface OSF-based intravascular ultrasound (IVUS) image segmentation framework is introduced, application specific segmentation refinement methods are developed, and an evaluation on 41 test cases is presented. As demonstrated by experiments, OSF-based segmentation refinement is a promising approach to address challenges in medical image segmentation.

Previous data have shown that the most prevalent, indirect plasma volume (PV) measurement technique, which utilises changes in haematocrit (Hct) and haemoglobin concentration ([Hb]), underestimates actual PV changes during immersion, when compared to a direct tracer-dilution method. An increase in the F-cell ratio (whole-body haematocrit (Hctw) to large-vessel haematocrit (Hctv) ratio) has been purported as a possible explanation, probably due to hydrostatic and thermally-mediated changes during water immersion. Previous investigators have not quantified the F-cell ratio during immersion. Therefore, this study sought to determine the effect of the F-cell ratio on the indirect method during both, thermoneutral and cold-water immersions. Seven healthy males were tested three times, seated upright in air (control: 21.2°C SD ±1.1), and during thermoneutral (34.5oC SD ±0.2) and cold-water immersion (18.6oC SD ±0.2), immersed to the third intercostal space for 60 min. Measurements during the immersion tests included PV (Evans blue dye column elution, Evans blue dye computer programme, and Hct [Hb]), red cell volume (RCV; sodium radiochromate), cardiac frequency (fc) and rectal temperature (Tre). Plasma volume during the control trial remained stable, and equivalent across the three tests. There was a hydrostatically-induced increase in PV during thermoneutral immersion, when determined by the Evans blue dye method (16.2%). However, the Hct/[Hb] calculation did not adequately reflect this change, and underestimated the relative PV change by 43%. In contrast, PV decreased during cold immersion when determined using the Evans blue dye method by 17.9% and the Hct/[Hb] calculation by 8.0%, respectively, representing a 52% underestimation by the latter method. There was a non-significant decline in RCV during both immersions. Furthermore, an increase (8.6%) and decrease (-14.4%) in blood volume (BV) was observed during thermoneutral and cold-water immersions, respectively. The decline in RCV during thermoneutral immersion attenuated the BV expansion. Despite the disparity between the PV methods, there was no increase in the F-cell ratio during either immersion. In contrast, there was a significant decline in the F-cell ratio during the control: air and thermoneutral immersion, which may indicate that other, undefined variables may impact on the stability of the red cell compartment. The current study is the first to show that the Hct/[Hb] method clearly underestimates PV changes during both thermoneutral and cold-water immersion. Furthermore, RCV was shown, for the first time, to decline during both immersions. However, the changes in the F-cell ratio during this study, did not account for the underestimation of PV change using the Hct/[Hb] method.

No description available.

Introdução: No momento, pouco se conhece sobre o desempenho diagnóstico da angiotomografia de coronárias com 64 colunas de detectores (Angio-TC 64) frente aos achados do ultrassom intracoronário com técnica de histologia virtual (USIC-HV). Este estudo compara a capacidade diagnóstica de ambos os métodos para a avaliação das dimensões vasculares e para avaliação da composição da placa aterosclerótica através da análise de toda extensão dos três vasos epicárdicos principais. Métodos e Resultados: Um total de 21 pacientes com diagnóstico de doença arterial coronária obstrutiva foi incluído neste estudo. Angio-TC 64 foi realizada em todos os pacientes antes da realização do USIC-HV, com intervalo<72horas entre os dois exames. No total, 70 vasos foram avaliados (3,3 vasos por paciente) e divididos em 641 subsegmentos de 4 mm de extensão cada. Um total de 5.972 cortes seccionais de USIC-HV e 5.233 cortes seccionais da Angio-TC 64 foram analisados. As medidas de área luminar, área do vaso, área da parede arterial e carga de placa à Angio-TC 64 e ao USIC-HV foram significativamente correlacionadas (r-Spearman: 0,81; 0,78; 0,55 e 0,49; respectivamente - p<0,001 para todas as correlações). A Angio-TC 64 subestimou a área luminar ao USIC-HV (em mediana: 0,4mm2 ,variando entre -5,6 mm2 e 10,2 mm2). A Angio-TC 64 superestimou a área do vaso, a área da parede arterial (placa+média) e a carga de placa (em mediana: 3,0 mm2; 3,2 mm2 e 13,9%, respectivamente). O aumento da densidade média da placa à Angio-TC 64 foi significativamente associado com o aumento da contribuição percentual dos componentes cálcio denso e núcleo necrótico ao USIC-HV. O aumento da densidade média da placa à Angio-TC 64 foi significativamente associado com a diminuição da contribuição percentual do componente fibro-lipídico ao USIC-HV. Parâmetros de qualidade da imagem (atenuação luminar, ruído da atenuação luminar e relação sinal ruído) influenciaram significativamente os resultados da Angio-TC 64. Conclusão: Nosso estudo demonstra que as imagens da Angio-TC 64 se correlacionam significativamente com as imagens do USIC-HV. Estes achados indicam que a Angio-TC 64 pode ser uma ferramenta útil para a avaliação quantitativa da luz arterial e da placa aterosclerótica; bem como para a avaliação da composição da placa aterosclerótica in vivo / Background: Currently, little is known about the comparative diagnostic performance for coronary assessment of 64-slice multidetector computed tomography (64-MDCT) versus virtual histology intravascular ultrasound technique (VH-IVUS). The present study compares the diagnostic ability of both methods for the evaluation of coronary lumen and vessel wall dimensions as well as plaque composition in a three-vessel whole-artery analysis protocol. Methods and Results: A total of 21 patients with diagnosed obstructive coronary artery disease was included. 64-MDCT was performed within 72 hours before the VH-IVUS examination. Overall, 70 vessels were imaged (3.3 vessels per patient), and divided into 641 subsegments of 4 mm each. A total of 5,972 VH-IVUS cross-sections and 5,233 64-MDCT cross-sections were analyzed. 64-MDCT and VH-IVUS measurements for luminar area, vessel area, arterial wall area (plaque plus media area) and plaque burden were significantly correlated (r-Spearman: 0.81; 0.78; 0.55 e 0.49; respectively - p<0,001 for all correlations). 64-MDCT underestimated VH-IVUS measurements for luminar area (median: 0.4mm2, range: -5.6 mm2 to 10,2 mm2). 64-MDCT overestimated VH-IVUS measurements for vessel area, arterial wall area, and plaque burden (median: 3.0 mm2; 3.2 mm2 e 13.9%, respectively). Increasing plaque density at 64-MDCT was significantly associated with increasing dense calcium and necrotic core percent composition at VH-IVUS. Increasing plaque density at 64-MDCT was significantly associated with decreasing fibrofatty percent composition, and decreasing necrosis-to-calcium ratio at VH-IVUS. Image quality parameters (i.e. lumen attenuation, image noise, signal-to-noise ratio) significantly influenced the results of 64-MDCT. Conclusion: Our study shows that 64-MDCT imaging significantly correlates with VH-IVUS. These findings indicate that 64-MDCT may be a useful non-invasive tool for quantitative evaluation of lumen and plaque parameters, as well as for the in vivo assessment of atherosclerotic plaque composition

Introdução: No momento, pouco se conhece sobre o desempenho diagnóstico da angiotomografia de coronárias com 64 colunas de detectores (Angio-TC 64) frente aos achados do ultrassom intracoronário com técnica de histologia virtual (USIC-HV). Este estudo compara a capacidade diagnóstica de ambos os métodos para a avaliação das dimensões vasculares e para avaliação da composição da placa aterosclerótica através da análise de toda extensão dos três vasos epicárdicos principais. Métodos e Resultados: Um total de 21 pacientes com diagnóstico de doença arterial coronária obstrutiva foi incluído neste estudo. Angio-TC 64 foi realizada em todos os pacientes antes da realização do USIC-HV, com intervalo<72horas entre os dois exames. No total, 70 vasos foram avaliados (3,3 vasos por paciente) e divididos em 641 subsegmentos de 4 mm de extensão cada. Um total de 5.972 cortes seccionais de USIC-HV e 5.233 cortes seccionais da Angio-TC 64 foram analisados. As medidas de área luminar, área do vaso, área da parede arterial e carga de placa à Angio-TC 64 e ao USIC-HV foram significativamente correlacionadas (r-Spearman: 0,81; 0,78; 0,55 e 0,49; respectivamente - p<0,001 para todas as correlações). A Angio-TC 64 subestimou a área luminar ao USIC-HV (em mediana: 0,4mm2 ,variando entre -5,6 mm2 e 10,2 mm2). A Angio-TC 64 superestimou a área do vaso, a área da parede arterial (placa+média) e a carga de placa (em mediana: 3,0 mm2; 3,2 mm2 e 13,9%, respectivamente). O aumento da densidade média da placa à Angio-TC 64 foi significativamente associado com o aumento da contribuição percentual dos componentes cálcio denso e núcleo necrótico ao USIC-HV. O aumento da densidade média da placa à Angio-TC 64 foi significativamente associado com a diminuição da contribuição percentual do componente fibro-lipídico ao USIC-HV. Parâmetros de qualidade da imagem (atenuação luminar, ruído da atenuação luminar e relação sinal ruído) influenciaram significativamente os resultados da Angio-TC 64. Conclusão: Nosso estudo demonstra que as imagens da Angio-TC 64 se correlacionam significativamente com as imagens do USIC-HV. Estes achados indicam que a Angio-TC 64 pode ser uma ferramenta útil para a avaliação quantitativa da luz arterial e da placa aterosclerótica; bem como para a avaliação da composição da placa aterosclerótica in vivo / Background: Currently, little is known about the comparative diagnostic performance for coronary assessment of 64-slice multidetector computed tomography (64-MDCT) versus virtual histology intravascular ultrasound technique (VH-IVUS). The present study compares the diagnostic ability of both methods for the evaluation of coronary lumen and vessel wall dimensions as well as plaque composition in a three-vessel whole-artery analysis protocol. Methods and Results: A total of 21 patients with diagnosed obstructive coronary artery disease was included. 64-MDCT was performed within 72 hours before the VH-IVUS examination. Overall, 70 vessels were imaged (3.3 vessels per patient), and divided into 641 subsegments of 4 mm each. A total of 5,972 VH-IVUS cross-sections and 5,233 64-MDCT cross-sections were analyzed. 64-MDCT and VH-IVUS measurements for luminar area, vessel area, arterial wall area (plaque plus media area) and plaque burden were significantly correlated (r-Spearman: 0.81; 0.78; 0.55 e 0.49; respectively - p<0,001 for all correlations). 64-MDCT underestimated VH-IVUS measurements for luminar area (median: 0.4mm2, range: -5.6 mm2 to 10,2 mm2). 64-MDCT overestimated VH-IVUS measurements for vessel area, arterial wall area, and plaque burden (median: 3.0 mm2; 3.2 mm2 e 13.9%, respectively). Increasing plaque density at 64-MDCT was significantly associated with increasing dense calcium and necrotic core percent composition at VH-IVUS. Increasing plaque density at 64-MDCT was significantly associated with decreasing fibrofatty percent composition, and decreasing necrosis-to-calcium ratio at VH-IVUS. Image quality parameters (i.e. lumen attenuation, image noise, signal-to-noise ratio) significantly influenced the results of 64-MDCT. Conclusion: Our study shows that 64-MDCT imaging significantly correlates with VH-IVUS. These findings indicate that 64-MDCT may be a useful non-invasive tool for quantitative evaluation of lumen and plaque parameters, as well as for the in vivo assessment of atherosclerotic plaque composition