Unidade de ensino estruturado para alunos com perturbações do espectro do Autismo no 2º Ciclo do E.B.: expectativas e realidades

A educação de crianças com necessidades educativas especiais (NEE) coloca nos nossos dias grandes desafios às escolas e famílias. A Inclusão apresenta-se neste contexto como a expressão chave, reveladora de um novo olhar e decidir, expressa na legislação, no discurso político e nas actuais disposições académicas e pedagógicas. Não obstante, nem todos os alunos com NEE dispõem de respostas integralmente inclusivas. Os alunos com espectro de Autismo, por exemplo, colocam às escolas e aos pais sérios problemas, os quais, devido à sua intensidade e variabilidade, questionam sem dúvida o sentido das respostas educativas adequadas a alunos portadores desta problemática. O objectivo geral deste estudo é, neste contexto, procurar aceder a um conhecimento mais actualizado sobre uma Unidade de Ensino Estruturado no atendimento a alunos com espectro de Autismo (UEEA). Pretende-se de modo mais específico aceder ao que pensam os professores sobre o atendimento educativo a alunos com espectro de Autismo e caracterizar uma unidade de ensino estruturado no que respeita aos recursos humanos, físicos e materiais, bem como as estratégias de trabalho privilegiadas no atendimento a este tipo de alunos e formas de colaboração entre técnicos e famílias. No sentido de melhor compreender e aprofundar esta problemática foram realizadas entrevistas semi-directivas a 3 professores do ensino especial com experiência em UEEA e a 3 professores do ensino regular. A escolha dos professores baseou-se em critérios relacionados com a sua experiência no atendimento a alunos com problemas de Autismo. A natureza do objecto de estudo induziu a um desenho de investigação de natureza interpretativa de carácter descritivo - Estudo de caso. O corpus do trabalho foi constituído pelas entrevistas semi-directivas, sujeitas a uma análise qualitativa de acordo com os procedimentos previsto para a análise de conteúdo. Com base na análise dos dados recolhidos, foi possível identificar e caracterizar aspectos relevantes sobre o que pensam os professores sobre a intervenção educativa de alunos com espectro de Autismo e sobre as respostas educativas existentes na UEEA.

Anthropometric evaluation and micronutrients intake in patients submitted to laparoscopic Roux-en-Y gastric bypass with a postoperative period of ≥1 year

Backgroung - Bariatric surgery is indicated as the most effective treatment for morbid obesity; the Roux-en-Y gastric bypass (RYGB) is considered the procedure of choice. However, nutritional deficiency may occur in the postoperative period as a result of reduced gastric capacity and change in nutrients absorption in the gastrointestinal tract. The prescription of vitamin and mineral supplementation is a common practice after RYGB; however, it may not be sufficient to prevent micronutrient deficiencies. The aim of this study was to quantify the micronutrient intake in patients undergoing RYGB and verify if the intake of supplementation would be enough to prevent nutritional deficiencies. Methods - The study was conducted on 60 patients submitted to RYGB. Anthropometric, analytical, and nutritional intake data were assessed preoperatively and 1 and 2 years postoperatively. The dietary intake was assessed using 24-h food recall; the values of micronutrients evaluated (vitamin B12, folic acid, iron, and calcium) were compared to the dietary reference intakes (DRI). Results - There were significant differences (p < 0.05) between excess weight loss at the first and second year (69.9 ± 15.3 vs 9.6 ± 62.9 %). In the first and second year after surgery, 93.3 and 94.1 % of the patients, respectively, took the supplements as prescribed. Micronutrient deficiencies were detected in the three evaluation periods. At the first year, there was a significant reduction (p < 0.05) of B12, folic acid, and iron intake. Conclusions - Despite taking vitamin and mineral supplementation, micronutrient deficiencies are common after RYGB. In the second year after surgery, micronutrient intake remains below the DRI.

A gestão dos custos da qualidade: Modelo A.B.Q.C. aplicado à Mercauto

Mestrado em Controlo e Gestão dos Negócios

Glucose-6-Phosphate dehydrogenase deficiency in children from 0 to 14 years hospitalized at the Pediatric Hospital David Bernardino, Luanda, Angola

The Glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common enzymatic defect in the world. The most common clinical manifestations are acute hemolytic anemia associated with drugs, infections, neonatal jaundice and hemolytic non-spherocytic chronic anemia. The main aim of this study was to determine the frequency of major genetic variants of G6PD leading to enzyme deficiency in children from 0 to 14 years at a Pediatric Hospital in Luanda, Angola. A cross-sectional and descriptive analytical study covered a total of 194 children aged from 0 to 14 years, of both genders and hospitalized at the Pediatric Hospital David Bernardino, Luanda between November and December, 2011. The G202A, A376G and C563T mutations of the G6PD gene were determined by real-time PCR with Taqman probes. The disabled A-/A- genotype was detected in 10 girls (10.9%). Among the boys, 21 (20.6%) presented the genotype A-. Considering all the samples, the A- variant was observed in 22.4% of cases. The Mediterranean mutation was not detected in the Angolan sample. Furthermore, no association was found between genotype and anemia, nutritional state and mucosa color. A significant association, however, was observed with jaundice. Based on the results obtained, there is a clear need to identify those with the disabled genotype in the Angolan population in order to avoid cases of drug-induced anemia, particularly in the treatment of malaria, so prevalent in Angola.