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Introduction: Advances in comprehensive genomic profiling (CGP) of lung adenocarcinomas (LUADs) led to personalized treatment for patients. This study evaluated medical oncologists' attitudes toward CGP in a scenario where sponsored funding for CGP was available. Methods: We designed an online survey assessing CGP use and treating physicians' confidence, composed of three self-confidence domains, which are as follows: confidence in interpreting CGP results, confidence in treating oncogenic-driven LUAD, and confidence in managing tyrosine kinase inhibitor adverse events. The survey was distributed to medical oncologists who treat lung cancer in Brazil. Comparisons between groups were performed using the chi-square or Fisher's exact test. Univariable and multivariable (adjusted OR) analyses were performed. Results: Among 104 respondents who treat patients with lung cancer, 55% were from the Southeast region, 28% had high lung cancer clinical load, and 33% had in-house molecular testing. More than half (51%) of the participants request CGP systematically to stage IV LUAD. As for provider confidence, 67% stated being confident in all three domains: 76% confident in interpreting CGP, 84% confident in treating oncogenic-driven LUAD, and 81% in managing tyrosine kinase inhibitor adverse events. Providers' confidence was associated with systematically requesting CGP to stage IV LUAD (p = 0.013). After controlling for the variables of interest, systematic requesting CGP for stage IV LUAD revealed a significant association with the provider's confidence (adjusted OR = 0.35, p = 0.028, 95% CI: 0.14-0.84). The major challenge for properly requesting CGP was the long turnaround time and the fear of treatment delays. Conclusions: Even though CGP for stage IV LUAD in Brazil is fully sponsored, only half of the oncologists in our survey systematically request it.. Requesting CGP was associated with providers' confidence. Improving access and promoting providers' awareness of CGP utility is necessary to increase CGP use and better inform treatment decisions.

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Objetivo ­ Analisar o desenvolvimento de fungos filamentosos existentes nos brinquedos denominados slime. Métodos ­ Por se tratar de uma pesquisa experimental, a mesma foi realizada no laboratório escola da UNIP ­ Universidade Paulista. Neste local foi empregada a coleta de amostras e seu armazenamento em um recipiente plástico durante o período de 14 dias. O seu processamento foi realizado através da semeadura de colônias em ágar Sabouraud-Dextrose e posteriormente em ágar Batata Dextrose para a obtenção de colônias gigantes. Além disso, foram realizados os métodos de análise e identificação bioquímica, o qual foi dividido em análise macroscópicae microscópica. Resultados ­ Quando examinamos os caracteres fenotípicos no microcultivo, comprovou-se a presença do gênero Aspergillus em todas as amostras (cinco), sendo os isolados classificados em seções, uma classificação infragenérica que agrupa diferentes espécies que possuem morfologia similar. As seções encontradas foram: Aspergillus seção Flavi (3 isolados) e Aspergillus seção Nigri (2 isolados). Conclusão ­ A presença do Aspergillus no slime é um fato que não pode ser ignorado, pois necessita-se de uma atenção maior quanto à eficácia dos componentes químicos existentes no brinquedo, visto que esse tipo de objeto é, na sua maior parte, manuseado pela classe infantil, podendo gerar processos infecciosos, possibilitando, assim, diversos danos à saúde

Objective ­ Analyze the development of filamentous fungi existing in toys called slime. Methods ­ As this is an experimental research, it was carried out in the school laboratory at UNIP ­ Universidade Paulista. In this place, the collection of samples and their storage in a plastic container was used during the period of 14 days. Its processing was carried out by sowing colonies on Sabouraud-Dextrose agar and later on Potato Dextrose agar to obtain giant colonies. In addition, the methods of analysis and biochemical identification were carried out, which was divided into macroscopic and microscopic analysis. Results ­ When the phenotypic characters in the microcultivation were examined, the presence of the genus Aspergillus was verified in all samples (five), and the isolates were classified in sections, an infrageneric classification that groups different species that have similar morphology. The sections found were: Aspergillus section Flavi (3 isolates) and Aspergillus section Nigri (2 isolates). Conclusions ­ The presence of the Aspergillus in the slime is a fact that cannot be ignored, as greater attention is needed as to the effectiveness of the chemical components in the toy, since this type of object is mostly handled by the infant class, it can generate infectious processes, thus making possible several health damages

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Os fungos desempenham vários papéis que impactam a humanidade de diversas maneiras. Suas características metabólicas são importantes na biotecnologia, porém, tais microrganismos podem desencadear alguns problemas de saúde pública e até mesmo serem letais. Objetivo: detectar a presença de fungos no acervo de uma biblioteca no município de São José do Rio Preto. Metodologia: foram coletadas quarenta amostras nas superfícies inanimadas (livros, estantes, documentos, mapas, artigos e revistas) das principais salas da biblioteca com o auxílio de swabs umedecidos em solução salina estéril, posteriormente encaminhados ao laboratório de Biomedicina da Universidade Paulista ­ UNIP. As amostras foram semeadas em meio de cultura ágar Sabouraud Dextrose (SDA), tendo adicionado cloranfenicol e incubadas a 30 °C. Foi realizada a colônia gigante em todas as cepas crescidas em SDA para a realização da técnica de microcultivo para a identificação dos fungos, de acordo com o Manual de Detecção e Identificação dos Fungos de Importância Médica da Agência Nacional de Vigilância Sanitária. Resultados: Houve positividade em trinta e uma amostras (78%) e em quatro delas foi observado mais de um tipo de colônia (13%). Das vinte e duas superfícies de livros analisadas, foram isolados e identificados: Aspergillus flavus, Aspergillus niger, Cunninghamella sp., Cladosporium sp., Curvularia sp., Mucor sp. e Nigrospora sp. Nas oito superfícies de estantes: Aspergillus flavus, Aspergillus niger, Aspergillus versicolor, Penicillium sp. e Scopulariopsis sp. e, nos dez documentos: Aspergillus nidulans, Aspergillus sp., Cladosporium sp., Cunninghamella sp. e Trichoderma sp. Conclusão: Os fungos encontrados estão amplamente distribuídos no ambiente como solo e ar e, por diversos fatores, instalam-se em locais como bibliotecas. Em condições favoráveis, podem infectar o homem e causar perdas patrimoniais para os acervos.

Fungi play many roles that impact humankind in different ways. Their metabolic characteristics are important in biotechnology; however, these microorganisms can trigger some public health problems or may even be lethal. Objective: detect the presence of fungi in the collection of a public library in the city of São José do Rio Preto, Brazil. Methods: a total of forty samples were collected from inanimate surfaces (books, shelves, documents, maps, articles and magazines) located in the main rooms of the library with swabs soaked in sterile saline solution and sent to the Universidade Paulista ­ UNIP laboratories. The samples were plated in Sabouraud Dextrose Agar (SDA) supplemented with chloramphenicol and incubated at 30 °C. The colonies that grew in SDA were isolated in Potato Dextrose Agar for performing the slide culture technique for the identification of the fungi, performed according to the Manual of Detection and Identification of Fungi of Medical Importance from the Brazilian Health Surveillance Agency (ANVISA). Results: Thirty-one samples (78%) were positive, and in four of them more than one fungus genus was observed (13%). From the twenty-two book surfaces analyzed, the following fungi were isolated and identified: Aspergillus flavus, Aspergillus niger, Cunninghamella sp., Cladosporium sp., Curvularia sp., Mucor sp. and Nigrospora sp. On the eight shelves: Aspergillus flavus, Aspergillus niger, Aspergillus versicolor, Penicillium sp. and Scopulariopsis sp. The ten documents analyzed presented the following fungi: Aspergillus nidulans, Aspergillus sp., Cladosporium sp., Cunninghamella sp. and Trichoderma sp.. Conclusion: These fungi are widely distributed in the environment such as in the soil and air, and due to several factors, they colonize public places, such as libraries. In favorable conditions, they may infect humans and cause diseases.

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Objetivo ­ Quantificar a presença de agentes da flora microbiana da pele de usuários da sala de coleta de uma unidade básica de saúde ­ UBS, assim como verificar a eficácia da antissepsia da pele com o uso do álcool etílico 70% prévia à coleta de sangue. Métodos ­ A coleta da região antecubital do braço dos 40 pacientes selecionados aleatoriamente, foi realizada antes e após antissepsia do local com álcool etílico 70%, com auxílio de um swab embebido em solução fisiológica estéril para posterior transporte e processamento o qual foi realizado no laboratório escola da Universidade Paulista UNIP, campus JK, São José do Rio Preto. Resultados ­ Das 80 amostras (40 antes da antissepsia e 40 depois da antissepsia) coletadas, foi observada uma redução de 87,01% do número de colônias de micro-organismos identificados como cocos e bacilos Gram-positivos, catalase positivos. Conclusão ­ Os resultados da pesquisa permitem concluir que o álcool etílico a 70% é eficaz na antissepsia da pele e que a antissepsia com álcool etílico 70% reduz a flora microbiana da pele conferindo maior segurança e liberdade de riscos ao procedimento prévio à coleta de sangue.

Objective ­ To quantify the presence of agents of the microbial flora of the skin of patients in the collection room of a hospital (UBS) as well as to verify the efficacy of skin antisepsis with the use of 70% ethyl alcohol prior to blood collection. Methods ­ The collection of the antecubital region of the arm of the 40 randomly selected patients was performed before and after site antisepsis with 70% ethyl alcohol, with the aid of a swab soaked in sterile solution for subsequent transportation and processing, which was performed in the laboratory University of São Paulo UNIP, JK campus, São José do Rio Preto. Results ­ From the 80 samples (40 before antisepsis and 40 after antisepsis) collected, a reduction of 87.01% in the number of colonies of microorganisms identified as cocci and gram positive bacilli, catalase positive, was observed. Conclusion ­ The results of the research allow us to conclude that 70% ethyl alcohol is effective in antisepsis of the skin and that antisepsis with 70% ethyl alcohol reduces the microbial flora of the skin giving greater safety and reduced risk to the procedure prior to blood collection

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Objetivo ­ Identificar e isolar bactérias em superfícies inanimadas de uma Unidade Básica de Saúde no interior de São Paulo e verificar a suscetibilidade bacteriana frente aos antibióticos testados. Métodos ­ Foram coletadas 60 amostras de superfícies inanimadas de uma Unidade Básica de Saúde realizado um esfregaço da superfície utilizando um swab umidificado em solução salina estéril e inoculado em caldo BHI. Após foram semeadas em meio de cultura não seletivo e identificadas através de coloração de gram, catalase, crescimento no manitol, coagulase, DNAse, fermentação da lactose, EPM, Mili e Citrato. O teste de suscetibilidade antimicrobiana por difusão de disco foi aplicado. Resultados ­ Das 60 superfícies inanimadas analisadas, 59 (98,3%) estavam contaminadas, sendo 29% (17) contaminadas por Staphylococcus aureus, 71,1% (41) por Staphylococcus coagulase negativa e 72,9% por enterobactérias (20,9% Escherichia coli, 16,3% Citrobacter freundii, 13,9% Serratia marcescens, 13,9% Serratia liquefaciens, 7% Salmonella paratyphi, 7% Klebsiella pneumoniae, 4,6% Shigella sp., 4,6% Yersinia enterocolitica, 2,3% Klebsiella oxytoca, 2,3% Serratia odorifera, 2,3% Providencia sp. e 2,3% Enterobacter sp.). Foi observada uma multirresistência dessas bactérias frente aos antibióticos testados. Conclusão ­ A contaminação em superfícies inanimadas, assim como o perfil de resistência microbiana, foram evidentes na UBS analisada, resultados estes que demonstram a necessidade de uma maior vigilância no que diz respeito ao controle de infecções, assim ao que se refere a reavaliação das estratégias de limpeza e desinfecção dessas superfícies inanimadas

Objective ­ Identify and bacteria isolates on inanimate surfaces of a Basic Health Unit in the interior of São Paulo and to verify the bacterial susceptibility against the tested antibiotics. Methods ­ Sixty samples of inanimate surfaces from a Basic Health Unit were collected by swabbing the surface using a swab humidified in sterile saline and inoculated into BHI broth. After sowing in non-selective culture medium and identified by staining of gram, catalase, growth in mannitol, coagulase, DNAse, fermentation of lactose, EPM, Mili, Citrate. The antimicrobial susceptibility test by disk diffusion were applied. Results ­ Of the 60 inanimate surfaces analyzed, 59 (98.3%) were contaminated, with 28.9% (17) being contaminated by Staphylococcus aureus, 71.1% (42) Staphylococcus coagulase negative and 72.9% by enterobacteria (20.9% Escherichia coli, 16.3% Citrobacter freundii, 13.9% Serratia marcescens, 13.9% Serratia liquefaciens, 7% Salmonella paratyphi, 7% Klebsiella pneumoniae, 4.6% Shigella sp., 4.6% Yersinia enterocolitica, 2.3% Klebsiella oxytoca, 2.3% Serratia odorifera, 2.3% Providencia sp. e 2.3% Enterobacter sp.) A multiresistance of these bacteria was observed against the tested antibiotics. Conclusions ­ The contamination on inanimate surfaces, as well as the microbial resistance profile, were evident in the Basic Health Unit analyzed, which results demonstrate the need for greater vigilance with regard to infection control, as well as the reevaluation of strategies for cleaning and disinfecting these inanimate surfaces.

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BACKGROUND: In recent years real­time reverse transcription polymerase chain reaction (real-time RT-PCR) has become a leading technique for nucleic acid detection and quantification of flaviviruses, including Dengue virus (DENV). Trioplex real-time RT-PCR has the advantages of providing the concurrent detection of Zika virus (ZIKV), DENV, and Chikungunya virus (CHIKV) RNA in human serum. OBJECTIVE: This study sought to compare the sensitivity and specificity of the Trioplex real-time RT-PCR assay to those provided by CDC DENV TaqMan® RT-qPCR assay and conventional PCR when used for DENV detection in the context of a dengue epidemic. STUDY DESIGN: We analyzed 1656 serum samples from symptomatic patients with acute febrile disease for 5 days less between December 2018 and May 2019. The samples were tested using the various PCR-based assays. RESULTS: Of the 1656 serum samples analyzed, 713 (43%) were laboratory-confirmed as arboviruses: 99.86% (712/713) were confirmed as DENV and 0.14% (1/713) were confirmed as ZIKV. Next, 590 samples were selected, and of these, 331 samples (56.1%) were determined to be positive (Ct < 38) and 259 samples (43.9%) were determined to be negative (Ct > 38) using the Trioplex real-time RT-PCR assay. The multiplex method found that the test exhibits 95% sensitivity and 100% specificity. CONCLUSION: This evaluation demonstrates the capacity of the Trioplex real-time RT-PCR assay to detect DENV at a high sensitivity and specificity in a geographic area with a current dengue outbreak and a lower co-circulation of other arboviruses - such as ZIKV and CHIKV, and the results prove it´s applicability as clinical screening test that can serve as a confirmatory test.

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Objetivo ­ Esta pesquisa teve o intuito de realizar um estudo microbiológico em estojos de lentes de contato, bem como correlacionar com os hábitos de higiene dos usuários. Métodos ­ Após aprovação do comitê de ética, 50 estojos de lente de contato foram cedidos por acadêmicos voluntários, os quais também responderam a um questionário contendo dados pessoais, assim como sobre a forma de manipulação das lentes. As amostras foram coletadas da superfície interna do estojo, isoladas em meios de cultura e identificadas através de provas bioquímicas específicas. Resultados ­ Dos 50 estojos, 49 (98%) apresentaram crescimento de microrganismos, tais como Staphylococcus sp (27), Staphylococcus aureus (9), Serratia liquefaciens (4), Citrobacter freundii (2), Escherichia coli (1) e Hafnia alvei (1), sendo que em um estojo foi identificado ambas as bactérias Staphylococcus aureus e Serratia liquefaciens. As lentes mais utilizadas (96% dos usuários) foram dos tipos gelatinosas descartáveis, seguida do tipo rígida (4%). O uso terapêutico esteve presente em 76% dos usuários, já o uso estético em 24%. O tempo de uso das mesmas lentes foi de 30 dias até quatro anos. Quando questionados sobre higienização, 34% afirmaram lavar as mãos sempre que manipulavam as lentes, 10% armazenavam os estojos em locais fechados, enquanto os outros 84% armazenavam em gabinetes de banheiros ou expostos sobre as pias. Em relação a incômodos na utilização, 32% relataram prurido, ardência ou vermelhidão. Conclusão ­ A falta de cuidado na higienização e no armazenamento do

Objective ­ This research aimed to carry out a microbiological study in contact lens cases, as well as to correlate with users' hygiene habits. Methods ­ After approval by the ethics committee, 50 contact lens cases were provided by volunteer academics, who also answered a questionnaire containing personal data, as well as how to manipulate the lens. Samples were collected from the inner surface of the kit, isolated in culture media and identified by specific biochemical tests. Results ­ Of the 50 kits, 49 (98%) showed growth of microorganisms such as Staphylococcus sp (27), Staphylococcus aureus (9), Serratia liquefaciens (4), Citrobacter freundii (2), Escherichia coli (1) and Hafnia alvei (1), and in one kit both Staphylococcus aureus and Serratia liquefaciens bacteria were identified. The most used lenses (96% of users) were of the disposable soft types, followed by the rigid type (4%). Therapeutic use was present in 76% of users, while aesthetic use in 24%. The wearing time of the same lenses was from 30 days to four years. When asked about sanitation, 34% said they washed their hands whenever they manipulated the lenses, 10% stored the cases indoors, while the other 84% stored in bathroom cabinets or exposed on the sinks. Regarding discomfort in use, 32% reported itching, burning or redness. Conclusions ­ The lack of care in the hygiene and storage of the cases were extremely important for its microbiological contamination, answering the hypothesis raised at the beginning of the study.

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Objetivo ­ Identificar quais os microrganismos responsáveis por esta infecção e seu perfil de resistência aos antimicrobianos. Metódos ­ A pesquisa foi realizada no Laboratório CDAC-Centro de Diagnósticos de Análises Clínicas, situado no município de Nova Granada - SP. Foram analisadas amostras de uroculturas positivas e seus respectivos antibiogramas, cujos resultados foram obtidos através de laudos laboratoriais digitais no período de janeiro de 2017 a janeiro de 2018 e à partir da realização dessa coleta de dados, foi feito um levantamento dos principais agentes patológicos causadores das infecções do trato urinário que atingem a população do município, assim como foi verificado o perfil de suscetibilidade aos antibioticos testados. Resultados ­ O uropatógeno mais frequente foi Escherichia coli (N = 58/136; 43%), seguido por Enterobacter sp. (N = 30/136; 22%), Klebsiella sp. (N = 15/136; 11%), Shigella sp. (N = 10/136; 7%), Proteus vulgaris. (N = 6/136; 4,5%), Citrobacter sp. (N = 5/136; 3,5%), Providencia sp. (N = 4/136; 3%), Proteus mirabilis. (N = 4/136; 3%), Edwardsiella sp. (N = 2/136; 1,5%) e Proteus sp. (N = 2/136; 1,5%). Oxacilina e ácido nalidixico apresentaram menor poder inibitório contra os uropatógenos encontrados. Conclusão ­ O uropatógeno mais frequente foi Escherichia coli,seguido por Enterobacter sp., Klebsiella sp. e Shigella sp. Os dados aqui relatados demonstram que a etiologia das infecções urinárias é semelhante à encontrada em outros municípios. Porém, o padrão de resistência desses uropatógenos pode possuir características diferenciadas de acordo com o histórico de consumo de antimicrobianos em cada comunidade. Assim, é importante que dados epidemiológicos sejam periodicamente divulgados com a intenção de auxiliar a comunidade médica

Objective ­ To identify the responsible microorganisms for the urine infection and their antimicrobial resistance profile. Methods ­ We carried out the research at the Laboratory-Diagnostic Center for Clinical Analysis (CDAC), located at the Nova Granada city. We analyzed samples of positive urocultures and their respective antibiograms, whose results were taken through laboratory reports from January 2017 to January 2018 and from the data gathering. We performed a data survey of the main pathological agents who causes infections in the urinary tract affecting the city's population, as well as the susceptibility profile of the antibiotics tested. Results ­ Escherichia coli (N = 58/136, 43%) was the most frequent uropathogen identified, followed by Enterobacter sp. (N = 30/136, 22%), Klebsiella sp. (N = 15/136, 11%), Shigella sp. (N = 10/136, 7%), Proteus vulgaris (N = 6/136, 4,5%), Citrobacter sp. (N = 5/136; 3,5%), Providencia sp. (N = 4/136, 3%), Proteus mirabilis (N = 4/136, 3%), Edwardsiella sp. (N = 2/136, 1.5%), and Proteus sp. = 2/136, 1.5%). Oxacillin and nalidixic acid showed lower inhibitory power against the found uropathogens. Conclusion ­ Escherichia coli was the most frequent uropathogen found, followed by Enterobacter sp, Klebsiella sp and Shigella sp. We demonstrate with the data reported here that the etiology of urinary infections of our research is similar to the found in other cities. However, the antimicrobial resistance profile of these uropathogens may have different characteristics according to the history of antibiotics use in each community. It is therefore important that epidemiological data be periodically disclosed with the intention of assisting the medical community

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BACKGROUND: Dengue virus type 4 (DENV-4) was first reported in Brazil in 1982 and since then no more cases were detected again in Brazil until 2010, when the virus was reintroduced. Over the following years, the virus spread to several Brazilian states and resulted in about 1,400,000 dengue cases, in 2013. The largest number of cases were documented in the Southeast macro-region. OBJECTIVES: To determine the phylogeography of DENV-4 Genotype IIB strains isolated during the epidemics in 2012-2013 in São Paulo, Brazil, we aimed to contextualise the contribution of viruses sampled in different localities across the overall movement of DENV-4 in Brazil. METHODS: Based on the envelope gene sequences retrieved from GenBank, we employed a Bayesian phylogeographic approach to assess the spatiotemporal dynamics of DENV-4 Genotype IIB in São Paulo, Brazil. FINDINGS: The dispersal dynamics of DENV-4 Genotype IIB in Brazil indicated Rio de Janeiro and Mato Grosso states as the most likely routes toward São Paulo before the 2012-2013 outbreak. Likewise, Guarujá and São José do Rio Preto facilitated viral spread and transmission to other localities in the South and Southeast macro-regions in Brazil. CONCLUSIONS: The spread pattern of DENV-4 Genotype IIB strains across the country supports two independent introductions of the virus in São Paulo in a short period of time. Furthermore, São Paulo appears to have played a pivotal role in the dissemination of DENV-4 to other locations in Brazil.

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BACKGROUND Dengue virus type 4 (DENV-4) was first reported in Brazil in 1982 and since then no more cases were detected again in Brazil until 2010, when the virus was reintroduced. Over the following years, the virus spread to several Brazilian states and resulted in about 1,400,000 dengue cases, in 2013. The largest number of cases were documented in the Southeast macro-region. OBJECTIVES To determine the phylogeography of DENV-4 Genotype IIB strains isolated during the epidemics in 2012-2013 in São Paulo, Brazil, we aimed to contextualise the contribution of viruses sampled in different localities across the overall movement of DENV-4 in Brazil. METHODS Based on the envelope gene sequences retrieved from GenBank, we employed a Bayesian phylogeographic approach to assess the spatiotemporal dynamics of DENV-4 Genotype IIB in São Paulo, Brazil. FINDINGS The dispersal dynamics of DENV-4 Genotype IIB in Brazil indicated Rio de Janeiro and Mato Grosso states as the most likely routes toward São Paulo before the 2012-2013 outbreak. Likewise, Guarujá and São José do Rio Preto facilitated viral spread and transmission to other localities in the South and Southeast macro-regions in Brazil. CONCLUSIONS The spread pattern of DENV-4 Genotype IIB strains across the country supports two independent introductions of the virus in São Paulo in a short period of time. Furthermore, São Paulo appears to have played a pivotal role in the dissemination of DENV-4 to other locations in Brazil.

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Dengue fever is a viral condition that has become a recurrent issue for public health in tropical countries, common endemic areas. Although viral structure and composition have been widely studied, the infection phenotype in terms of small molecules remains poorly established. This contribution providing a comprehensive overview of the metabolic implications of the virus-host interaction using a lipidomic-based approach through direct-infusion high-resolution mass spectrometry. Our results provide further evidence that lipids are part of both the immune response upon Dengue virus infection and viral infection maintenance mechanism in the organism. Furthermore, the species described herein provide evidence that such lipids may be part of the mechanism that leads to blood-related complications such as hemorrhagic fever, the severe form of the disease.

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Introdução: O estudo da frequência dos alelos detectados nos doadores e pacientes previamente selecionados para o transplante de medula óssea permite estimar as reais chances de um paciente em lista de espera encontrar um doador com antígeno leucocitário humano (Human leucocite antigen; HLA) idêntico não relacionado, além de facilitar e direcionar o planejamento do crescimento do Registro Nacional deDoadores de Medula Óssea. Objetivo: Descrever e analisar afrequência dos alelos do sistema HLA de classe I (HLA-A, -B e -C) e classe II (HLA-DRB1 e -DQB1) de doadores e pacientespré-transplante de medula óssea, do Hospital de Câncer deBarretos. Material e Métodos: Um total de 98 amostras dedoadores e 106 amostras de pacientes foi selecionado comtipificações em alta resolução, no período de outubro de 2014a outubro de 2015. As amostras foram tipificadas para os lociHLA-A, -B, -C, -DR e -DQ. Resultados: O predomínio daraça branca reflete a composição étnica do Brasil. As doençasde base mais comuns que levaram o paciente ao transplanteforam a leucemia aguda linfóide (34%) e mieloide (29,2%).Os grupos alélicos mais frequentes nos registros foramA*02, A*24, A*03, A*01, B*35, B*44, C*07, DQB1*03,DQB1*05, DQB1*06, DRB1*01 e DRB1*13. Conclusão: Osresultados encontrados reforçam a importância de conhecero perfil demográfico e imunogenético das regiões do Brasil,contribuindo desta forma na redução do tempo de espera porum doador histocompatível

Introduction: The study of allele frequencies detected in donors and patients previously selected for bone marrow transplantation allows us to estimate the real chances of a patient in the waiting list to find an Human leucocite antigen (HLA) identical unrelated donor. This also facilitates and drives the growth planning of the Brazilian Registry of planning Bone Marrow Transplantation (REDOME). Objective: Describe and analyze the frequency of HLA class I alleles (HLA-A*, -B* and ­C*) and class II alleles, genotypes, and haplotypes(HLA-DRB1* and -DQB1*) from donors and bone marrowpre-transplant patients. Material and Methods: A total of 98donor samples and 106 patient samples were selected withhigh resolution typing, from October 2014 to October 2015.Samples were typed for HLA-A, -B, -C, -DR and -DQ loci.Results: The predominance of the white race reflects theethnic composition of Brazil. The most common underlyingdiseases that led to transplantation patients were acutelymphoid leukemia (34%) and myeloid (29.2%). The mostfrequent allelic groups were A*02, A*24, A*03, A*01, B*35,B*44, C*07, DQB1*03, DQB1*05, DQB1*06, DRB1*01 andDRB1*13. Conclusion: The results reinforce the importanceof understanding the demographic and immunogenic profilefrom Brazilian Regions. This can contribute to the reduction ofwaiting time for a histocompatible donor.

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Objetivo ­ Verificar a influência da dislipidemia no surgimento e agravamento de cardiopatias em adultos na cidade de Barretos-SP. Métodos ­ Foi efetuado um estudo exploratório, através de pesquisa bibliográfica e levantamento de dados de prontuários do Ambulatório Médico de Especialidades de Barretos (AME) e Hospital São Jorge, ambos situados no município de Barretos, e retrospectivo, referentes ao período entre fevereiro de 2015 a agosto de 2015. Resultados ­ Foram analisados os dados de 86 pacientes, sendo 37 homens (43,02%) e 49 mulheres (56,97%). A faixa etária variou de 31 a 88 anos (média de 59,10 anos de idade). Dentre o total de pacientes, 19 (22,09%) apresentaram dislipidemia, 13 (15,11%) cardiopatia, 45 (52,32%) dislipidemia associada a cardiopatia e nove (10,46%) não apresentaram nenhuma alteração. Conclusões ­ Conforme os resultados obtidos no presente estudo, bem como o que foi descrito na literatura, confirmou-se que a dislipidemia pode ser avaliada como um significativo fator de risco para as cardiopatias, sendo capaz de influenciar o surgimento e o agravamento dessas patologias na população. Descritores: Cardiopatias; Fatores de risco

Objective ­ To investigate the effect of dyslipidemia in the emergence and worsening of heart disease in the population. Methods ­ We performed an exploratory study through literature search and data collection outpatient Barretos Medical Specialties (AME) and St. George Hospital, both located in the city of Barretos, and retrospective, covering the period from February 2015 to August 2015. Results ­ We analyzed data from 86 patients, 37 men (43.02%) and 49 women (56.97%). The age range was 31-88 years (mean 59.10 years old). Among the total patients, 19 (22.09%) had dyslipidemia, 13 (15.11%) disease, 45 (52.32%) dyslipidemia associated with heart disease and nine (10.46%) showed no change. Conclusion ­ According to the results obtained in this study, as well as what was described in the literature, it was confirmed that dyslipidemia can be assessed as a significant risk factor for heart disease, being able to influence the emergence and worsening of these diseases in population. Descriptors: Cardiac disorders; Risk factors

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Many countries in the Americas have detected local transmission of multiple arboviruses that cause febrile illnesses. Therefore, laboratory testing has become an important tool for confirming the etiology of these diseases. The present study aimed to compare the sensitivity and specificity of three different Zika virus detection assays. One hundred serum samples from patients presenting with acute febrile symptoms were tested using a previously reported TaqMan® RT-qPCR assay. We used a SYBR® Green RT-qPCR and a conventional PCR methodologies to compare the results. Of the samples that were determined to be negative by the TaqMan® RT-qPCR assay, 100% (Kappa = 0.670) were also found to be negative by SYBR® Green RT-qPCR based on Tm comparison; however, 14% (Kappa = 0.035) were found to be positive by conventional PCR followed by agarose gel electrophoresis. The differences between the ZIKV strains circulating worldwide and the low viremia period can compromise diagnostic accuracy and thereby the accuracy of outbreak data. Therefore, improved assays are required to improve the diagnosis and surveillance of arbovirus.(AU)

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Objetivo ­ Descrever e analisar a frequência dos alelos, genótipos e haplótipos HLA de classe I (HLA-A, -B e -C) e classe II (HLA-DRB1 e -DQB1) dos pacientes na fase pré-transplante de medula óssea, genotipados no laboratório de Imunogenética-HLA do Hospital de Câncer de Barretos. O estudo da frequência dos alelos detectados nos doadores e pacientes previamente selecionados para o transplante de medula óssea permite estimar as reais chances de um paciente em lista de espera encontrar um doador HLA idêntico não relacionado, além de facilitar e direcionar o planejamento do crescimento do Registro. Métodos ­ Os dados foram obtidos através da técnica de amplificação em cadeia de polimerase e para a genotipagem dos alelos dos genes A, B, C, DRB1 e DQB1 foi empregado o método de sequenciamento de nucleotídeos. Resultados ­ Entre outubro de 2014 a outubro de 2015 foram tratados 106 pacientes e 98 doadores de medula óssea cadastrados. As doenças de base mais comuns que levaram o paciente ao transplante foram as leucemias agudas linfóides (34%) e mielóides (29,2%). A caracterização imunogenética dos pacientes na fase pré-transplante de medula óssea mostrou um total de 19 alelos do loco A, 24 do loco B, 14 do loco C, 5 do loco DQ, 13 do loco DR; já nos dadores de medula óssea, 16 alelos do loco A, 25 do loco B, 13 do loco C, 5 do loco DQ e 12 do loco DR. Conclusão ­ Os grupos alélicos mais frequentes nos registros foram A*02, A*24, A*03, A*01, B*35, B*44, C*07, DQB1*03, DQB1*05, DQB1*06, DRB1*01 e DRB1*13. Apenas o conhecimento da frequência do tipo HLA específico do paciente na população não garante que ele encontre o doador compatível, é necessário também que o portador desse tipo HLA se encontre cadastrado no REDOME como doador voluntário.

Objective ­ Describe and analyze the frequency of the alleles, genotypes, and haplotypes HLA class I (HLA-A*, -B* and ­C*) and class II (HLA-DRB1* and -DQB1*) of patients in the bone marrow before transplantation phase genotyped in laboratory of ImmunogeneticsHLA Barretos Cancer Hospital. The study detected the frequency of alleles in patients and donors selected for bone marrow transplantation allows to estimate the real chances of a patient on the waiting list to find an unrelated HLA-identical donor, and to facilitate and direct the Brazilian Registry of planning Bone Marrow Transplantation (REDOME). Methods ­ The data were obtained by amplification using polymerase chain, and for genotyping the alleles of the genes A, B, C, DRB1 and DQB1 was employed nucleotide sequencing method. Results ­ From October 2014 to October 2015 were treated 106 patients and 98 donors registered bone marrow. The most common underlying diseases that led to transplantation patients were acute lymphoid leukemias (34%) and myeloid (29.2%). Immunogenetics characterization of patients in the bone marrow pre-transplant phase showed a total of 19 alleles at the A loci, 24 in B loci, 14in C loci, 5 in DQB1 loci and 13 in DRB1 loci; already in the bone marrow donors, 16 alleles at the A loci, 25 in B loci, 13 in C loci, 5 in DQB1 loci and 12 in DRB1 loci. Conclusion ­ The most frequent allelic groups were A*02, A*24, A*03, A*01, B*35, B*44, C*07, DQB1*03, DQB1*05, DQB1*06, DRB1*01 and DRB1*13. Knowledge of the frequency of HLA genes patients are not enough to find a compatible donor, it is necessary that the record contains the donor available

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ABSTRACT Many countries in the Americas have detected local transmission of multiple arboviruses that cause febrile illnesses. Therefore, laboratory testing has become an important tool for confirming the etiology of these diseases. The present study aimed to compare the sensitivity and specificity of three different Zika virus detection assays. One hundred serum samples from patients presenting with acute febrile symptoms were tested using a previously reported TaqMan® RT-qPCR assay. We used a SYBR® Green RT-qPCR and a conventional PCR methodologies to compare the results. Of the samples that were determined to be negative by the TaqMan® RT-qPCR assay, 100% (Kappa = 0.670) were also found to be negative by SYBR® Green RT-qPCR based on Tm comparison; however, 14% (Kappa = 0.035) were found to be positive by conventional PCR followed by agarose gel electrophoresis. The differences between the ZIKV strains circulating worldwide and the low viremia period can compromise diagnostic accuracy and thereby the accuracy of outbreak data. Therefore, improved assays are required to improve the diagnosis and surveillance of arbovirus.

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Many countries in the Americas have detected local transmission of multiple arboviruses that cause febrile illnesses. Therefore, laboratory testing has become an important tool for confirming the etiology of these diseases. The present study aimed to compare the sensitivity and specificity of three different Zika virus detection assays. One hundred serum samples from patients presenting with acute febrile symptoms were tested using a previously reported TaqMan® RT-qPCR assay. We used a SYBR® Green RT-qPCR and a conventional PCR methodologies to compare the results. Of the samples that were determined to be negative by the TaqMan® RT-qPCR assay, 100% (Kappa=0.670) were also found to be negative by SYBR® Green RT-qPCR based on Tm comparison; however, 14% (Kappa=0.035) were found to be positive by conventional PCR followed by agarose gel electrophoresis. The differences between the ZIKV strains circulating worldwide and the low viremia period can compromise diagnostic accuracy and thereby the accuracy of outbreak data. Therefore, improved assays are required to improve the diagnosis and surveillance of arbovirus.

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BACKGROUND: The emergence of Zika virus (ZIKV) presents new challenges to both clinicians and public health authorities. Overlapping clinical features between the diseases caused by ZIKV, dengue (DENV) and chikungunya (CHIKV) and the lack of validated serological assays for ZIKV make accurate diagnosis difficult. Brazilian authorities largely rely on clinical and epidemiological data for the epidemiological and clinical classifications of most ZIKV cases. OBJECTIVE: To report the laboratory and clinical profiles of patients diagnosed with Zika fever based only on clinical and epidemiological data. STUDY DESIGN: We analyzed 433 suspected cases of ZIKV identified by the attending physician based on proposed clinical criteria. The samples were also screened for ZIKV, DENV and CHIKV using PCR. RESULTS: Of the 433 patients analyzed, 168 (38.8%) were laboratory-confirmed for arboviruses: 96 were positive for ZIKV, 67 were positive for DENV (56 for DENV-2, 9 for DENV-1, and 2 for DENV-4), four were positive for co-infection with ZIKV/DENV-2, and one was positive for CHIKV. The most common signs or symptoms in the patients with laboratory-confirmed ZIKV were rash (100%), arthralgia (77.1%), fever (74.0%), myalgia (74.0%) and non-purulent conjunctivitis (69.8%). In patients with laboratory-confirmed DENV infections, the most frequently observed symptoms were rash (100%), fever (79.1%), myalgia (74.6%), headache (73.1%) and arthralgia (70.1%). The measure of association between clinical manifestations and laboratory manifestations among patients with ZIKV and DENV detected a statistically significant difference only in abdominal pain (p=0.04), leukopenia (p=0.003), and thrombocytopenia (p=0.01). CONCLUSION: Our data suggests that clinical and epidemiological criteria alone are not a good tool for ZIKV and DENV differentiation, and that laboratory diagnosis should be mandatory.

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Dengue viruses are the most common arbovirus infection worldwide and are caused by four distinct serotypes of the dengue virus (DENV). In the present study, we assessed DENV transmission in São José do Rio Preto (SJRP) from 2010 to 2014. We analyzed blood samples from febrile patients who were attended at health care centers in SJRP. DENV detection was performed using multiplex RT-PCR, using flavivirus generic primers, based on the genes of the non-structural protein (NS5), followed by nested-PCR assay with species-specific primers. We analyzed 1549 samples, of which 1389 were positive for NS1 by rapid test. One thousand and eight-seven samples (78%) were confirmed as positive by multiplex RT-PCR: DENV-4, 48.5% (528/1087); DENV-1, 41.5% (449/1087); DENV-2, 9.5% (104/1087); and co-infection (5 DENV-1/DENV-4, 1 DENV-1/DENV-2), 0.5% (6/1087). Phylogenetic analysis of the DENV-4 grouped the isolates identified in this study with the American genotype and the showed a relationship between isolates from SJRP and isolates from the northern region of South America. Taken together, our data shows the detection and emergence of new dengue genotype in a new region and reiterate the importance of surveillance programs to detect and trace the evolution of DENV.

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