Adolescentes com DM1: conhecimento acerca da doença e dificuldades no autocuidado

Background: type 1 Diabetes Mellitus is a chronic disease increasingly prevalent in children, thus it is essential to encourage adherence to self-care and minimize the difficulties experienced. Objectives: characterize the knowledge of adolescents with type 1 diabetes mellitus about their disease and identify their difficulties in self-care. Methodology: quantitative, simple descriptive study. Application of Knowledge Test of Adolescents with DM1 about the disease and the Inventory of Difficulties in Self-Care Roles by Flora & Gameiro (2016). Data collected between june and november 2021 at Diabetes Consultation of a Hospital in the central region of Portugal. Sample of 34 diabetic adolescents with a mean age of 14.9 (±2.3) years. Results: in overall knowledge, adolescents show a level of knowledge between reasonable and good, and it is in domain 1 (Nature of the disease/physiopathology) where they show the best level of knowledge. In the difficulties in the self-care roles, they show higher percentages of difficulty in maintaining a balanced diet, fighting stress and interventions when facing hypoglycemia. Conclusion: adolescents have difficulties in self-care roles, and the nurses\u27 intervention in the implementation of adjusted therapeutic plans is essential to overcome the knowledge gaps and reduce the identified difficultiesMarco Contextual: la diabetes mellitus tipo 1 es una enfermedad crónica cada vez más prevalente en niños, por lo que es fundamental fomentar la adherencia al autocuidado y minimizar las dificultades que experimentan. Objetivos: caracterizar el conocimiento de los adolescentes con diabetes mellitus tipo 1 sobre su enfermedad e identificar sus dificultades en el autocuidado. Metodologia: estudo quantitativo, descritivo simples. Aplicação de Test de Conocimientos de Adolescentes con DM1 sobre la enfermedad y el Inventario de Dificultades en los Roles de Autocuidado de Flora & Gameiro (2016). Datos recogidos entre junio y noviembre de 2021 en la Consulta de Diabetes de un Hospital de la región central de Portugal. Muestra de 34 adolescentes diabéticos con edad media de 14,9 (±2,3) años. Resultados: en el conocimiento global, los adolescentes muestran un nivel de conocimiento entre razonable y bueno, y es en el dominio 1 (Naturaleza de la enfermedad/fisiopatología) donde muestran el mejor nivel de conocimiento. En cuanto a las dificultades en las funciones de autocuidado, estos pacientes mostraron mayores porcentajes de dificultad para mantener una dieta equilibrada, combatir el estrés e intervenir ante una hipoglucemia. Conclusión: adolescentes tienen una dificultad para los en los roles de autocuidado, siendo fundamental la intervención del enfermero en la implementación de planes terapéuticos ajustados, con el fin de llenar los vacíos de conocimiento y reducir las dificultades identificadas.Enquadramento: a Diabetes Mellitus tipo 1 enquanto doença crónica é, cada vez mais prevalente, em idade pediátrica, sendo fundamental o incentivo de adesão ao autocuidado e a minimização das dificuldades sentidas. Objetivos: caracterizar o conhecimento de adolescentes com diabetes mellitus tipo 1 acerca da sua doença e identificar as suas dificuldades no autocuidado. Metodologia: estudo quantitativo, descritivo simples. Aplicação do Teste de Conhecimento dos Adolescentes com DM1 acerca da doença e o Inventário de Dificuldades nos Papéis de Autocuidado de Flora & Gameiro (2016). Recolha de dados de junho a novembro de 2021, na Consulta de Diabetes de um Hospital da região centro de Portugal. Amostra de 34 adolescentes com média de idades de 14.9 (±2.3) anos. Resultados: no conhecimento global, os adolescentes apresentam um nível de conhecimento entre o razoável e bom, sendo o domínio 1 (Natureza da doença/fisiopatologia) onde estes apresentam melhor nível de conhecimento. Nas dificuldades nos papéis de autocuidado, apresentam maior dificuldade na manutenção de uma alimentação equilibrada, combate ao stress e intervenções numa hipoglicemia. Conclusão: verifica-se dificuldade destes nos papeis de autocuidado, sendo fundamental a intervenção dos enfermeiros na implementação de planos terapêuticos ajustados, no sentido de colmatar falhas de conhecimento e dificuldades identificadas

Satisfacción de los padres con respecto al cuidado de enfermería en los cuidados intensivos neonatales

Introdução: O internamento do recém-nascido implica uma fonte contínua de stress para os pais. Ao adotar medidas de apoio individualizadas e em parceria com os pais, o enfermeiro potencia o desenvolvimento harmonioso e competente do recém-nascido, favorecendo o desenvolvimento das competências parentais. Materiais e métodos: Estudo quantitativo, tipo descritivo simples, com recurso à aplicação da Escala de Apoio dos Enfermeiros aos Pais, cuja validação de conteúdo para a população portuguesa, foi efetuada por Sandra Valadão em 2012. A amostra foi constituída por 100 pais de recém-nascidos internados numa Unidade de Cuidados Intensivos Neonatais de um Hospital do Norte de Portugal. Resultados: A avaliação média dos quatro domínios apresentou um resultado de 4,67. Dos quatro domínios que constituem a Escala, os pais demonstraram maior satisfação relativamente ao domínio instrumental com uma média de 4,75, seguido do domínio apreciativo com 4,73. Os domínios emocional e informativo, obtiveram resultados mais baixos, de 4,59e 4,58 respetivamente. Discussão: Os resultados obtidos vão de encontro aos resultados de Valadão de 2012, em que o domínio instrumental também foi o que obteve um maior resultado, seguido dos domínios cognitivo/apreciativo, emocional e informativo e também estão em concordância com o estudo de Tran et al. de 2009. No entanto, o domínio emocional foi o que obteve menor resultado, não indo ao encontro dos nossos resultados.Conclusão: A satisfação dos pais em relação aos cuidados de enfermagem prestados aos seus filhos é elevada, existindo áreas passíveis de melhoria de que são exemplo a comunicação estabelecida e a informação fornecida.Introducción: el ingreso de un recién nacido implica una fuente continua de estrés para los padres. Al adoptar medidas de apoyo individualizadas y en colaboración con los padres, el enfermero potencia el desarrollo asertivo del recién nacido y simultáneamente, favorece el desarrollo de las habilidades parentales. Materiales y métodos: estudio cuantitativo, tipo descriptivo simple, mediante la aplicación de una Escala de Apoyo de los Enfermeros a los Padres, validado por Sandra Valadão en 2012. La muestra consistió en 100 padres de recién nacidos admitidos en una Unidad Cuidados Intensivos Neonatales de un hospital del norte de Portugal. Resultados: la evaluación media de los cuatro dominios obtuvo una puntuación de 4,67. De los cuatro dominios que componen la Escala, los padres mostraron mayor satisfacción en el dominio instrumental con un promedio de 4,75, seguido del dominio apreciativo con 4,73. Los dominios emocional e informativo obtuvieron puntuaciones más bajas, de 4,59 y 4,58 respectivamente. Discusion: los resultados obtenidos coinciden con los de otro estudio, concretamente el de Valadão de 2012, en el que el dominio instrumental también fue el que obtuvo una mayor puntuación, seguido del cognitivo/apreciativo, emocional e informativo. Los resultados también concuerdan con un estudio de Tran et al. de 2009. Sin embargo, el dominio emocional obtuvo la puntuación más baja, lo que no coincide con nuestros resultados. Conclusión: la satisfacción de los padres con la atención de enfermería prestada a sus hijos es alta, pero todavía hay aspectos que deben mejorarse, como la comunicación establecida y la información proporcionada.Introduction: The hospitalization of the newborn implies a continuous source of stress for the parents. By adopting individualized support measures and in partnership with the parents, the nurse enhances the harmonious and competent development of the newborn, favoring the development of parental skills. Materials and methods: Quantitative study, simple descriptive type, using the Scale of Support from Nurses to Parents, whose content validation for the Portuguese population was carried out by Sandra Valadão in 2012. The sample consisted of 100 parents of newborns born in a Neonatal Intensive Care Unit of a Hospital in Northern Portugal. Discussion: The results obtained are in line with the results of Valadão 2012, in which the instrumental domain was also the one with the highest score, followed by the cognitive / appreciative, emotional and informative domains. They are also in agreement with the study by Tran et al in 2009. However, the emotional domain was the one with the lowest score, not meeting our results. Conclusion: The satisfaction of parents in about nursing care provided to their children is high, with areas that can be improved, such as the established communication and the information provided

Dinâmicas de (investig)ação em contextos de promoção da língua portuguesa: a presença do CIDTFF na rede Camões, I.P.

Sem resumo disponível.publishe

Educomunicação e suas áreas de intervenção: Novos paradigmas para o diálogo intercultural

oai:omp.abpeducom.org.br:publicationFormat/1O material aqui divulgado representa, em essência, a contribuição do VII Encontro Brasileiro de Educomunicação ao V Global MIL Week, da UNESCO, ocorrido na ECA/USP, entre 3 e 5 de novembro de 2016. Estamos diante de um conjunto de 104 papers executivos, com uma média de entre 7 e 10 páginas, cada um. Com este rico e abundante material, chegamos ao sétimo e-book publicado pela ABPEducom, em seus seis primeiros anos de existência. A especificidade desta obra é a de trazer as “Áreas de Intervenção” do campo da Educomunicação, colocando-as a serviço de uma meta essencial ao agir educomunicativo: o diálogo intercultural, trabalhado na linha do tema geral do evento internacional: Media and Information Literacy: New Paradigms for Intercultural Dialogue

Search for dark matter produced in association with bottom or top quarks in √s = 13 TeV pp collisions with the ATLAS detector

A search for weakly interacting massive particle dark matter produced in association with bottom or top quarks is presented. Final states containing third-generation quarks and miss- ing transverse momentum are considered. The analysis uses 36.1 fb−1 of proton–proton collision data recorded by the ATLAS experiment at √s = 13 TeV in 2015 and 2016. No significant excess of events above the estimated backgrounds is observed. The results are in- terpreted in the framework of simplified models of spin-0 dark-matter mediators. For colour- neutral spin-0 mediators produced in association with top quarks and decaying into a pair of dark-matter particles, mediator masses below 50 GeV are excluded assuming a dark-matter candidate mass of 1 GeV and unitary couplings. For scalar and pseudoscalar mediators produced in association with bottom quarks, the search sets limits on the production cross- section of 300 times the predicted rate for mediators with masses between 10 and 50 GeV and assuming a dark-matter mass of 1 GeV and unitary coupling. Constraints on colour- charged scalar simplified models are also presented. Assuming a dark-matter particle mass of 35 GeV, mediator particles with mass below 1.1 TeV are excluded for couplings yielding a dark-matter relic density consistent with measurements

TRY plant trait database – enhanced coverage and open access

Plant traits - the morphological, anatomical, physiological, biochemical and phenological characteristics of plants - determine how plants respond to environmental factors, affect other trophic levels, and influence ecosystem properties and their benefits and detriments to people. Plant trait data thus represent the basis for a vast area of research spanning from evolutionary biology, community and functional ecology, to biodiversity conservation, ecosystem and landscape management, restoration, biogeography and earth system modelling. Since its foundation in 2007, the TRY database of plant traits has grown continuously. It now provides unprecedented data coverage under an open access data policy and is the main plant trait database used by the research community worldwide. Increasingly, the TRY database also supports new frontiers of trait‐based plant research, including the identification of data gaps and the subsequent mobilization or measurement of new data. To support this development, in this article we evaluate the extent of the trait data compiled in TRY and analyse emerging patterns of data coverage and representativeness. Best species coverage is achieved for categorical traits - almost complete coverage for ‘plant growth form’. However, most traits relevant for ecology and vegetation modelling are characterized by continuous intraspecific variation and trait–environmental relationships. These traits have to be measured on individual plants in their respective environment. Despite unprecedented data coverage, we observe a humbling lack of completeness and representativeness of these continuous traits in many aspects. We, therefore, conclude that reducing data gaps and biases in the TRY database remains a key challenge and requires a coordinated approach to data mobilization and trait measurements. This can only be achieved in collaboration with other initiatives

Mortality from gastrointestinal congenital anomalies at 264 hospitals in 74 low-income, middle-income, and high-income countries: a multicentre, international, prospective cohort study

Summary Background Congenital anomalies are the fifth leading cause of mortality in children younger than 5 years globally. Many gastrointestinal congenital anomalies are fatal without timely access to neonatal surgical care, but few studies have been done on these conditions in low-income and middle-income countries (LMICs). We compared outcomes of the seven most common gastrointestinal congenital anomalies in low-income, middle-income, and high-income countries globally, and identified factors associated with mortality. Methods We did a multicentre, international prospective cohort study of patients younger than 16 years, presenting to hospital for the first time with oesophageal atresia, congenital diaphragmatic hernia, intestinal atresia, gastroschisis, exomphalos, anorectal malformation, and Hirschsprung’s disease. Recruitment was of consecutive patients for a minimum of 1 month between October, 2018, and April, 2019. We collected data on patient demographics, clinical status, interventions, and outcomes using the REDCap platform. Patients were followed up for 30 days after primary intervention, or 30 days after admission if they did not receive an intervention. The primary outcome was all-cause, in-hospital mortality for all conditions combined and each condition individually, stratified by country income status. We did a complete case analysis. Findings We included 3849 patients with 3975 study conditions (560 with oesophageal atresia, 448 with congenital diaphragmatic hernia, 681 with intestinal atresia, 453 with gastroschisis, 325 with exomphalos, 991 with anorectal malformation, and 517 with Hirschsprung’s disease) from 264 hospitals (89 in high-income countries, 166 in middleincome countries, and nine in low-income countries) in 74 countries. Of the 3849 patients, 2231 (58·0%) were male. Median gestational age at birth was 38 weeks (IQR 36–39) and median bodyweight at presentation was 2·8 kg (2·3–3·3). Mortality among all patients was 37 (39·8%) of 93 in low-income countries, 583 (20·4%) of 2860 in middle-income countries, and 50 (5·6%) of 896 in high-income countries (p<0·0001 between all country income groups). Gastroschisis had the greatest difference in mortality between country income strata (nine [90·0%] of ten in lowincome countries, 97 [31·9%] of 304 in middle-income countries, and two [1·4%] of 139 in high-income countries; p≤0·0001 between all country income groups). Factors significantly associated with higher mortality for all patients combined included country income status (low-income vs high-income countries, risk ratio 2·78 [95% CI 1·88–4·11], p<0·0001; middle-income vs high-income countries, 2·11 [1·59–2·79], p<0·0001), sepsis at presentation (1·20 [1·04–1·40], p=0·016), higher American Society of Anesthesiologists (ASA) score at primary intervention (ASA 4–5 vs ASA 1–2, 1·82 [1·40–2·35], p<0·0001; ASA 3 vs ASA 1–2, 1·58, [1·30–1·92], p<0·0001]), surgical safety checklist not used (1·39 [1·02–1·90], p=0·035), and ventilation or parenteral nutrition unavailable when needed (ventilation 1·96, [1·41–2·71], p=0·0001; parenteral nutrition 1·35, [1·05–1·74], p=0·018). Administration of parenteral nutrition (0·61, [0·47–0·79], p=0·0002) and use of a peripherally inserted central catheter (0·65 [0·50–0·86], p=0·0024) or percutaneous central line (0·69 [0·48–1·00], p=0·049) were associated with lower mortality. Interpretation Unacceptable differences in mortality exist for gastrointestinal congenital anomalies between lowincome, middle-income, and high-income countries. Improving access to quality neonatal surgical care in LMICs will be vital to achieve Sustainable Development Goal 3.2 of ending preventable deaths in neonates and children younger than 5 years by 2030