975 resultados para Vanhanen, Tatu: IQ
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Coordenao de Aperfeioamento de Pessoal de Nvel Superior (CAPES)
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Coordenao de Aperfeioamento de Pessoal de Nvel Superior (CAPES)
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Objectives - Review available guidance for quality assurance (QA) in mammography and discuss its contribution to harmonise practices worldwide. Methods - Literature search was performed on different sources to identify guidance documents for QA in mammography available worldwide in international bodies, healthcare providers, professional/scientific associations. The guidance documents identified were reviewed and a selection was compared for type of guidance (clinical/technical), technology and proposed QA methodologies focusing on dose and image quality (IQ) performance assessment. Results - Fourteen protocols (targeted at conventional and digital mammography) were reviewed. All included recommendations for testing acquisition, processing and display systems associated with mammographic equipment. All guidance reviewed highlighted the importance of dose assessment and testing the Automatic Exposure Control (AEC) system. Recommended tests for assessment of IQ showed variations in the proposed methodologies. Recommended testing focused on assessment of low-contrast detection, spatial resolution and noise. QC of image display is recommended following the American Association of Physicists in Medicine guidelines. Conclusions - The existing QA guidance for mammography is derived from key documents (American College of Radiology and European Union guidelines) and proposes similar tests despite the variations in detail and methodologies. Studies reported on QA data should provide detail on experimental technique to allow robust data comparison. Countries aiming to implement a mammography/QA program may select/prioritise the tests depending on available technology and resources.
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Mestrado em Radiaes Aplicadas s Tecnologias da Sade - Ramo de especializao: Imagem Digital com Radiao X
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The discovery of X-rays was undoubtedly one of the greatest stimulus for improving the efficiency in the provision of healthcare services. The ability to view, non-invasively, inside the human body has greatly facilitated the work of professionals in diagnosis of diseases. The exclusive focus on image quality (IQ), without understanding how they are obtained, affect negatively the efficiency in diagnostic radiology. The equilibrium between the benefits and the risks are often forgotten. It is necessary to adopt optimization strategies to maximize the benefits (image quality) and minimize risk (dose to the patient) in radiological facilities. In radiology, the implementation of optimization strategies involves an understanding of images acquisition process. When a radiographer adopts a certain value of a parameter (tube potential [kVp], tube current-exposure time product [mAs] or additional filtration), it is essential to know its meaning and impact of their variation in dose and image quality. Without this, any optimization strategy will be a failure. Worldwide, data show that use of x-rays has been increasingly frequent. In Cabo Verde, we note an effort by healthcare institutions (e.g. Ministry of Health) in equipping radiological facilities and the recent installation of a telemedicine system requires purchase of new radiological equipment. In addition, the transition from screen-films to digital systems is characterized by a raise in patient exposure. Given that this transition is slower in less developed countries, as is the case of Cabo Verde, the need to adopt optimization strategies becomes increasingly necessary. This study was conducted as an attempt to answer that need. Although this work is about objective evaluation of image quality, and in medical practice the evaluation is usually subjective (visual evaluation of images by radiographer / radiologist), studies reported a correlation between these two types of evaluation (objective and subjective) [5-7] which accredits for conducting such studies. The purpose of this study is to evaluate the effect of exposure parameters (kVp and mAs) when using additional Cooper (Cu) filtration in dose and image quality in a Computed Radiography system.
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Mestrado em Segurana e Higiene no Trabalho
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Dissertao apresentada na Faculdade de Cincias e Tecnologia da Universidade Nova de Lisboa para obteno do grau de Mestre em Engenharia de Materiais
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Aim: Optimise a set of exposure factors, with the lowest effective dose, to delineate spinal curvature with the modified Cobb method in a full spine using computed radiography (CR) for a 5-year-old paediatric anthropomorphic phantom. Methods: Images were acquired by varying a set of parameters: positions (antero-posterior (AP), posteroanterior (PA) and lateral), kilo-voltage peak (kVp) (66-90), source-to-image distance (SID) (150 to 200cm), broad focus and the use of a grid (grid in/out) to analyse the impact on E and image quality (IQ). IQ was analysed applying two approaches: objective [contrast-to-noise-ratio/(CNR] and perceptual, using 5 observers. Monte-Carlo modelling was used for dose estimation. Cohens Kappa coefficient was used to calculate inter-observer-variability. The angle was measured using Cobbs method on lateral projections under different imaging conditions. Results: PA promoted the lowest effective dose (0.013 mSv) compared to AP (0.048 mSv) and lateral (0.025 mSv). The exposure parameters that allowed lower dose were 200cm SID, 90 kVp, broad focus and grid out for paediatrics using an Agfa CR system. Thirty-seven images were assessed for IQ and thirty-two were classified adequate. Cobb angle measurements varied between 162.9 and 19.90.9. Conclusion: Cobb angle measurements can be performed using the lowest dose with a low contrast-tonoise ratio. The variation on measurements for this was 2.9 and this is within the range of acceptable clinical error without impact on clinical diagnosis. Further work is recommended on improvement to the sample size and a more robust perceptual IQ assessment protocol for observers.
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Paracoccidioides brasiliensis foi encontrado, por inoculao de triturado de fgado e bao em hamsters, em 4 de 20 tatus (Dasypus novemcinctus) examinados na regio de Tucuru, Par. Hamsters inoculados por via intradrmica e peritoneal com o parasito desenvolveram infeces generalizadas e morreram em 1 a 13 meses. A diagnose do fungo foi confirmada por histopatologia e cultura. No se observaram sinais macroscpios de doenas nos tatus. A distribuio geogrfica de D. novemcinctus abrange a rea endmica de paracoccidioidomicose humana, sugerindo-se que o tatu tenha algum papel na ecologia do fungo.
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Dissertao apresentada Faculdade de Cincias e Tecnologia da Universidade Nova de Lisboa para obteno do grau de Mestre em Engenharia Geolgica (Geotecnia)
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RESMO: Introduo: A anemia de clulas falciformes doena hereditria, com repercusso multi-orgnica, tem grande variabilidade na sua expresso clnica. Da o interesse do estudo de indicadores de prognstico. A investigao realizada foi precedida de um resumo histrico incidindo sobre a compreenso de aspectos fundamentais da doena ao longo dos tempos. Na primeira parte do estudo e aps reviso bibliogrfica, foram referidos dados da fisiopatologia como base para os estudos que integram a presente dissertao. Abordou-se o estado da arte relativamente s complicaes, aos indicadores de prognstico e teraputica utilizada. Objectivos: Constituram objectivos deste estudo realizado numa amostra populacional representativa: identificar as leses a nvel dos sistemas cardio-respiratrio e nervoso central, avaliando-se as respectivas repercusses; avaliar a presena de indicadores de prognstico entre as variveis seleccionadas; estudar a eficcia e toxicidade da HU nos doentes com as formas graves da ACF. Para a prossecuo destes objectivos foram delineados para alm do estudo global trs estudos especficos: Estudo 1- repercusso no sistema cardio-respiratrio; Estudo 2- repercusso no sistema nervoso central; Estudo 3- teraputica com hidroxiureia. Doentes e mtodos: Procedeu-se a um estudo prospectivo e multi-institucional durante um perodo de trs anos tendo-se seleccionado para a amostra, e de acordo com critrios pr-definidos, 30 doentes com ACF na fase estvel da doena, com idades compreendidas entre os sete e os 18 anos, todos de origem africana excepo de um caucasiano. O diagnstico baseou-se em tcnicas de electroforese e estudo molecular que definiu o genotipo da doena e a presena da deleco da -talassmia assim como os haplotipos da amostra populacional. Foram utilizadas diferentes metodologias para avaliar a existncia de leso pulmonar e cerebral. Atravs do estudo estatstico foram seleccionadas diversas variveis como hipotticos indicadores de prognstico. Estudo 1. Para determinar a existncia de leso a nvel pulmonar usaram-se duas metodologias diferentes, a avaliao da funo pulmonar com estudo da saturao da Hb em O2 no sangue arterial e a tomografia computadorizada de alta resoluo. Estudou-se tambm a possvel disfuno cardaca como repercusso da leso pulmonar, atravs do ecocardiograma, e os indicadores de prognstico com significado estatstico para a leso encontrada. Estudo 2. O desenho deste estudo foi sobreponvel ao anterior, mas com metodologia adequada para o SNC. Procedeu-se ao estudo das leses cerebrais por meio de exames imagiolgicos, (RMN-CE e DTC) e de testes psicolgicos. Correlacionaram-se as trs metodologias utilizadas e a importncia de cada uma para a deciso de atitudes teraputicas preventivas. Estudo 3. Consistiu num estudo aberto prospectivo no controlado com nove crianas e adolescentes com formas graves de ACF, com o objectivo de avaliar a eficcia da teraputica com hidroxiureia, durante um perodo de 24 meses. Todos os doentes completaram no mnimo 15 meses de teraputica, com uma dose final mdia de 194 mg/K/dia. Resultados globais: Durante o perodo anterior investigao caracterizou-se a amostra populacional estudada quanto ao fenotipo gentico, clnico e hematolgico de acordo com os critrios utilizados por outros investigadores. Verificou-se: predomnio do haplotipo Bantu na forma homozigtica em 53% dos doentes; nmero total de EVO 3/ano em 87,5% dos doentes; crises de sequestrao em 18,75%; dactilites no primeiro ano de vida em 31,2%; quadro de spsis grave apenas num doente; crises de hiper-hemlise em 50%; e STA em 59,38% dos doentes. Quanto ao fenotipo hematolgico evidenciaram-se como factores de risco reticulocitose (13,1x103/l) e hiperbilirrubinmia (2,5 mg/dl) e como factores de bom prognstico a presena de deleco de um gene da -talassmia em 46,9% dos doentes e valor mdio de Hb 8,1 g/dl. Resultados dos estudos parcelares: Estudo 1. Deste estudo infere-se que a DPR ligeira foi diagnosticada em 70% dos doentes, uma vez que as alteraes da difuso no foram estatisticamente significativas, o estudo dos gases no sangue no evidenciaram resultados anormais e a TCAR evidenciou alteraes em 43,3% dos doentes. Apenas num doente se verificou doena pulmonar obstrutiva relacionada com maior nmero da STA.O estudo da disfuno cardaca encontrada em 86,7% dos doentes no reflecte a repercusso da DPR a nvel cardaco, podendo estar associada s alteraes fisiopatolgicas da prpria anemia crnica. Encontraram-se indicadores de prognstico hematolgicos e clnicos. Entre os primeiros, valores de Hb 8,5 g/dl e de HbF 13% foram considerados indicadores de bom prognstico para a leso pulmonar. Em relao aos parmetros clnicos, as STA no foram consideradas indicadoras de prognstico para a DPR ao contrrio do que se verificou com o nmero de EVO. Pela anlise dos parmetros genticos e socio-econmicos provou-se a ausncia de relao estatisticamente significativa com leso pulmonar. Estudo 2. Pela RMN-CE foram diagnosticados ES em 33,3% com uma localizao preferencial na substncia branca profunda em 26,6% dos doentes. Relativamente aos parmetros hematolgicos seleccionados, o valor mdio da HbF 8,6% constituu um indicador de bom prognstico para o aparecimento de ES, enquanto o valor mdio de leuccitos 12.39x103/l foi considerado um indicador de mau prognstico. No estudo do DTC apenas um doente apresentou aumento da velocidade do fluxo cerebral na ACM igual a 196 cm/segundos, associado a vasculopatia grave. Os testes psicolgicos alterados em 80% dos doentes mostraram ser o mtodo mais sensvel para detectar alteraes do neurodesenvolvimento, mas sem correlao com os ES em 10% dos doentes. Reala-se a baixa percentagem de DTC patolgicos encontrados neste estudo em relao ao nmero elevado de ES e de testes psicolgicos alterados, no se verificando concordncia entre os trs exames. Dos indicadores de prognstico estudados a -talassmia foi considerada um factor de proteco para o coeficiente de inteligncia da escala de Wechsler. Em relao a parmetros clnicos estudados os doentes com maior nmero de EVO, tem em mdia valores inferiores nos testes psicolgicos. Estudo 3. Neste estudo verificou-se que o valor mdio da HbF aumentou significativamente de 7,04% para 13,75,3% (p=0,028) ao fim de 15 meses de teraputica com hidroxiureia. Clinicamente todos os doentes responderam significativamente com uma reduo de 80% no nmero de EVO, 69% no nmero de internamentos, 76% no nmero de dias de hospitalizao e 67% no nmero de transfuses. Deste modo comprovou-se no s a eficcia desta teraputica neste grupo peditrico como tambm a falta de efeitos secundrios significativos. Considera-se a necessidade de estudos mais prolongados e em grande sries, para com segurana se usar a HU antes que a leso orgnica se estabelea, portanto logo nos primeiros anos de vida. Concluso: Na amostra populacional estudada foram evidenciadas leses pulmonares e cerebrais na grande maioria dos doentes que condicionaram a sua qualidade de vida. Foram identificados indicadores de prognstico que podero eventualmente ditar medidas teraputicas precoces com o objectivo de diminuir a morbilidade e a mortalidade neste grupo etrio. Demonstrou-se que a teraputica com a HU foi eficaz e bem tolerada----------ABSTRACT: Background: Sickle cell anemia (SCA), a hereditary disease characterized by pain and lifetime multi-organic lesion, is a challenge for all that work with carriers of this disease. The clinical expression variability of SCA is a constant reality and a problem to be solved in the current world of investigation, for which the knowledge of prognostic indicators responsible for the different aspects of clinical evolution diversity wiil be an added value. The study is preceded by a historical summary of the most important factors in the evolution of SCA, which are in themselves, an incentive for future research. In the first part of the study, after an extensive bibliographical revision, physiopathology data is referred to in general and specifically regarding the target organs, that constituted the base for the studies presented in the dissertation. The state of the art for the complications to be studied, the choice of prognostic indicators and the therapeutics application, were approached for the renewed interest in the theme. Aims: In regard to the investigation, the objective was to study the lesions in the most affected organs of a chosen pediatric group, to investigate prognostic indicators for lung and cerebral lesions and to evaluate the protective effect of hydroxyurea in children with severe outcomes. Patients and methods: A prospective and multi-institutional study was carried out during a three-year period, February 1998 to March 2001, with children and adolescents followed up at a Immunohematology Outpatient Clinic of Dona Estefnia's Hospital, Lisbon. Based in predefined criteria, 30 children with SCA were selected in a stable phase of the disease, aged from seven to 18 years old, all of whom were of African origin with exception of one who was Caucasian. The diagnosis was based on electrophoresis techniques and molecular study that allowed to define the genotype, the presence of deletional alpha-thalassemia as well as haplotypes in the population. Different methodologies were used to evaluate the existence of lung and cerebral lesion. Statistical study of the different variables selected the prognostic indicators. In Study 1, to determine the existence of lung lesion two different methodologies were used: pulmonar function study with arterial blood gases determination; and high resolution computerized tomography. Heart dysfunction as a repercussion of lung lesion was also studied through echocardiography, and prognostic indicators were statistically significant for lesions found. The design of Study 2 was similar to Study 1, but with the appropriate methodology for CNS. After neurological examination, which was normal in all patients (control group), cerebral lesions were studied with imagiologic exams (MRN-CE and TCD) and psychological tests. These three methodologies were correlated and the importance of each one in the decision of the therapeutic profilactic attitudes. Study 3 consisted of a controlled prospective open study in children with severe forms of SCA, with the aim of the evaluating therapeutic effectiveness of hydroxyurea, during a period of 24 months. Results: In the global overall study preceding the Studies 1,2 and 3, there were a prevalence of haplotype Bantu (53%) and other risk factors, namely the number of VOC (87,5%), sequestration crisis (18,75%), dactilytis in first year of life(31,2%), hyperhemolysis crisis (50%) and ATC in more than half of the patients (59,38%). This group of bad prognostic indicators, associated with the population of the lower class according to the Graffar scale, demonstrates the importance of primary health care services, information provided to the children and their relatives, as well as the interest in prophylactic therapeutics, specific screening and prenatal diagnosis. Study 1. It was evident from this study that slight RPD was diagnosed in 70% of the patients, because alterations of the diffusion had no statistical significance and arterial blood gases determinations were normal. Only one patient had restrictive lung disease related with numerous ACS. However ACS was not considered a prognostic indicator for RPD, contrary to the number of EVO. HRTC revealed discreet fibrotic lines that could be related with slight RPD, but the lack of correlation of these two exams (33%) supports the value of lung function tests for precocious diagnosis of RPD. Heart dysfunction was found in 86,7% of patients, does not reflect the repercussion of RPD, but with the physiopathology of chronic anemia. Hematologic and clinical prognostic indicators were found. Good prognostic indicators for the non-evolution of RPD with average Hb values of 8,5 g/dl and average HbF values of 13%, respectively. The genetic and social-economic factors had no statistical significance; nevertheless, they were more prevalent among Bantu haplotype (53,3%) in patients with RPD. Study 2. RMN-CE detected SI in 33,3% of the patients, with preferential location in deep white substance in 26,6% and in front lobe in 20%. This distribution can be related to structural aspects of the brain and with the high sensibility of this organ to hypoxia. From the hematological parameters selected, average HbF value 8,6% and average leucocyte count 12.39x103/l were prognostic indicators with different meaning to SI. The increase in the total bilirubin related to hyperhemolysis clinically explains the genesis of SI In the TCD study, only one patient had increased cerebral flow speed >196 cm/sec in CMA, which corresponded to serious vasculopathy in AngioMR. This patient never present previously neurological symptoms and had several hyperhemolysis crisis and VOC as risk factors. Low percentage of pathological TCD in this study, in relation to the high number of SI and altered tests, although without correlation among the three exams, is probably attributed to factors related to the methodology, aspects of cerebral physiopathology or perhaps a sign of good prognostic if the duration of study had not been so short. TCD should be used as a screening method in the age groups with higher risk of AVC and should never be considered separately in prophylactic therapeutics indication. Psychological tests were the most sensitive method to detect neurodevelopment impairment; in 80% of patients the neuropsychologics tests were altered, but without correlation with SI (10%). Since SI can become evident during the first two years of life and develop with time, the first psychological tests should be carried out between 3 and 5 years of age to timely be referred to special education and stimulation programs. Prognostic indicators to psychological tests were also found: alpha-thalassemia was found to be a protection factor of the IQ, just as other hematologic factors (hematocrit, MGCV and erythrocytes count). In relation to clinical parameters, although without statistical significance, patients with larger number of VOC had average lower scores versus the average in tests, except in TP. Results from different studies were conclusive as to the type of lesion found and the importance of prognostic indicators. Study 3. All the patients completed a minimum of 15 months therapeutic treatment with the final average daily dose of 194 mg/kg/day. The average value of the fetal hemoglobin increased significantly from 7,03,9% to 13,75,3% (p=0.028). The HbF average values increased from 6% to 15% after 15 months of therapeutic treatment. Clinically there was a reduction of 80% in the number of VOE , 69% in the number of hospitalization, 76% in the number of days of hospitalization and 67% in the number of transfusions. Once again the effectiveness of this treatment in this pediatric group, as well as the lack of any significant secondary effects, was evident. The study confirms the need for further detailed research in order to safely effect the appropriate treatment prior to the development of organic lesions, which ideally should be in the first year of life. Conclusions: These results allow us to clarify the importance of either pulmonary lesions or either nervous central system impairment among patients, children and adolescents, with sickle cell anemia. These lesions were demonstrated in most of the patients studied compromising their quality of life and the mortality. The treatment with HU is proved to be effective and having low toxicity.
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RESUMO - A Paralisia Cerebral (PC) deve ser olhada como uma patologia do neurodesenvolvimento: a infncia um perodo de actividade exploratria por essncia, a restrio motora condiciona as vrias reas do desenvolvimento. Contextos, apoios, oportunidades e experincias de vida sero determinantes no desenvolvimento de todo o seu potencial. Objectivos/finalidade: Identificar, descrever, comparar e analisar factores de risco associados PC, sua caracterizao multidimensional e integrao escolar aos 5 e 10 anos. Procurouse contribuir para a sua preveno primria e secundria, e obter dados para planeamento e implementao dos programas de apoio. Mtodos: Adoptouse a abordagem do Programa Nacional de Vigilncia da Paralisia Cerebral (PNVPC) e da Surveillance of Cerebral Palsy in Europe (SCPE). Analisaramse factores de risco, competncias funcionais, dfices associados, severidade e integrao escolar de duas populaes de Lisboa e Vale do Tejo, (nascimento 1996/19972001/2002 e prevalncia aos 5 e 10 anos). Descreveramse os dados, efectuaramse correlaes, aplicaramse testes de independncia e compararamse com dados dos nadovivos, dados nacionais e europeus. Analisaramse os factores que influenciaram a integrao escolar atravs de mtodos de regresso logstica. Resultados/Concluses/Recomendaes: 1,65 e 1,57 dos nadovivos desenvolveram PC; a prevalncia aos 5 anos foi de 1,7 e de 1,48; 5,9% e 7,9% faleceram antes dos 5 anos. Em 2001/2002 verificouse aumento de: PC espstica bilateral2/3membros, prematuridade, causa posneonatal, nveis funcionais ligeiros e graves; percentil estaturoponderal <3 (5anos). Diminuio de: disquinsia, anxia e alguns dfices associados. Destacaramse as associao: prematuridade e PC espstica bilateral 2/3membros; nascer de termo e anxia, disquinsia, primparas, dfices associados e severidade; infeco prnatal e QI<50, epilepsia e severidade; causa posneonatal e PC espstica bilateral4membros e mltiplos dfices. Aos 5 anos, as variveis explicativas para a no incluso escolar foram: QI<50 e epilepsia; uma elevada percentagem de crianas com PC moderada/grave encontravase integrada; 75% das que se encontravam desintegradas mantiveramse nesta situao aos 10. Nesta idade, as variveis explicativas para a no incluso escolar foram: QI<50 e motricidade fina; 35,1% encontravase fora do ensino regular; 4,5%, embora em idade de escolaridade obrigatria, no frequentavam qualquer estabelecimento escolar. Informao sistematizada, abrangente, objectiva, simples e acessvel, sobre novos casos de PC, factores de risco, prevalncia em idadeschave e caracterizao multidimensional constitui uma ferramenta clnica e epidemiolgica, que deve sustentar as polticas de sade, educacionais e sociais, contribuindo para a permanncia destas crianas no ensino regular, trazendo s crianas e famlias o suporte que as encorajem e sustentem nestes processos. ABSTRACT ------- Cerebral Palsy (CP) must be recognized as a neurodevelopmental disorder: childhood is, on its nature, a period for exploring the environment and therefore motor deficit interferes with all developmental areas. The context, support, opportunities and life experiences are determinants for the development of his full potential. Objective/Aim: To identify, describe, compare and analyze CP risk factors the multidimensional characterization and school integration levels at the age of 5 and 10 years. We aim to contribute to CP primary and secondary prevention and provide information for service planning and implementation of support programs. Methods: The approach of National Cerebral Palsy Surveillance Programme (NCPSP) and Surveillance of Cerebral Palsy in Europe (SCPE) were used. For two groups of children from Lisboa e Vale do Tejo region, birth data 1996/19972001/2002 and prevalence at 5 and 10 years, were analyzed: CP risk factors, functional ability, associated impairments, severity and school integration settings. Data collected was described, analyzed using correlations, applied tests of independence and compared with new born data, national data and european data. To analyze the factors related to school inclusive settings, logistic regression was appealed. Results/Conclusions/Recommendations: 1,65% and 1,57 of the newborn alive developed CP. The prevalence at 5 years was 1,7 and 1,48 5,9% and 7,9% died before their 5th birthday. Bilateral spastic CP 2/3limb, preterm birth, cases of postneonatal origin, mild and sever functional impairment; weight and height percentile <3 at 5 years old Increased in 2001. Decreased dyskinetic CP, anoxia and some additional imparments. Were identified among other the association between prematurity and spastic bilateral CP2/3 members; born at term and anoxia, dyskinetic CP, first child, associated impairments and severity; prenatal infection and IQ<50, epilepsy and severity; postneonatal cause and spastic bilateral CP4 members and associated impairments. At 5yearsold the more explanatory variables for not be in a school inclusive settings were IQ<50 and epilepsy, a high percentage of children with moderate/severe CP was attending regular school, but most children who were out of inclusive settings at 5 years continue on this situations at 10yearsold. At this age the more explanatory variables for not be in a school inclusive settings were: IQ<50 and upper limb function; 35,1% were out of regular school; 4,5%, even in compulsory school age, are out of school. Standardized comprehensive, objective, simple and accessible information about CP new cases, risk factors, prevalence in the keyage and children multidimensional characterization constitutes a clinical and epidemiological tool that should sustain health, educational and social policy. This would support the continuity of these children in regular schools, encouraging g them and their families in these processes.
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Relatrio de estgio
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Panayiotopoulos syndrome (PS) is a common epilepsy syndrome associated with rare clinical seizures and unknown localization of the epileptogenic area. Despite findings of normal development in patientswith PS, recent neuropsychological studies point to subtle and diverse cognitive impairments. No well-outlined hypothesis about the localization of the brain dysfunction responsible for these impairments has been proposed.We further explored the cognitive dysfunctions in PS andmade inferences on the most likely anatomical localization of brain impairment. A group of 19 patients (aged 612) with PS was rated according to spike activity and lateralization. The patients were submitted to a neuropsychological evaluation to assess general intelligence, memory, language, visualperceptual abilities, attention, and executive functions. Using 35-channel scalp EEG recordings, the N170 face-evoked event-related potential (ERP)was obtained to assess the functional integrity of the ventral pathway. All patientswith PS showed normal IQ but subtle and consistent neurocognitive impairments. Namely, we found abnormalities in the copy task of the ReyOsterrieth Complex Figure and in theNarrative Memory Test. There was no correlation between neuropsychological impairments with spike activity and hemispheric spike lateralization. The N170 ERP was normal in all patients except for one. Our neuropsychological findings demonstrate impairments in visualperceptual abilities and in semantic processing. These findings, paired with the absence of occipital lobe dysfunction in all neuropsychological studies of PS performed to this date, support the existence of parietal lobe dysfunction.
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We examined the longitudinal changes of VEGF levels after percutaneous coronary intervention for predicting major adverse cardiac events (MACE) in coronary artery disease (CAD) patients. VEGF was measured in 94 CAD patients' serum before revascularization, 1-month and 1-year after. Independently of clinical presentation, patients had lower VEGF concentration than a cohort of healthy subjects (median, IQ: 15.9, 9.0-264pg/mL versus 419, 212-758pg/mL; P < 0.001) at baseline. VEGF increased to 1-month (median, IQ: 276, 167-498pg/mL; P < 0.001) and remained steady to 1-year (median, IQ: 320, 173-497pg/mL; P < 0.001) approaching control levels. Drug eluting stent apposition and previous medication intake produced a less steep VEGF evolution after intervention (P < 0.05). Baseline VEGF concentration <40.8pg/mL conveyed increased risk for MACE in a 5-year follow-up. Results reflect a positive role of VEGF in recovery and support its importance in CAD prognosis.