3 resultados para weight at 12 months

em Bioline International


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Objetivo: Traçar o perfil dos frequentadores das academias de ginástica do município de Canguçu-RS. Métodos: Estudo transversal, de caráter descritivo, com 177 frequentadores de academias de diversas modalidades. Utilizou-se um questionário estruturado, contendo 76 questões para mensurar variáveis sociodemograficas, antropométricas, nutricionais e comportamentais, além de informações relacionadas às praticas nas academias. Realizouse análise descritiva dos dados, com cálculo de médias ± desvios-padrão para as variáveis contínuas e cálculo de proporções para as variáveis categóricas. Resultados: Participaram 177 frequentadores das academias na cidade de Canguçu-RS (30±12,5 anos; 70,0±12,8 kg; 1,69±0,1m). Com relação às variáveis comportamentais, a maioria nunca fumou (71,8%), não bebia exageradamente (89,9%) e era ativa no lazer (87%). No tocante às variáveis nutricionais, 66,7% tinham índice de massa corporal normal e a maioria não alcançava as recomendações de consumo diário de frutas, verduras e legumes, e não usava suplementos (69,5%). No que diz respeito às variáveis relacionadas à academia, a maioria dos respondentes frequentava há mais de 12 meses (56,5%), quatro ou mais vezes por semana (52%), à noite (52,5%), relatando que o principal motivo para ir à academia foi permanecer saudável (78%). Os praticantes afirmaram satisfação com os objetivos alcançados (60%) e praticavam a modalidade de musculação (97,2%). Conclusão: A maioria dos frequentadores das academias era do sexo masculino, jovem, ativa no lazer, praticava a modalidade de musculação e estava satisfeita com os resultados buscados nas academias. Apesar disso, são necessárias estratégias de mudança de comportamento em relação ao consumo de frutas, verduras e legumes.

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Background: Perimembranous Ventricular Septal Defect (PMVSD) is the most common subtype of ventricular septal defects. Transcatheter closure of PMVSD is a challenging procedure in management of moderate or large defects. Objectives: The purpose of this study was to show that transcatheter closure of perimembranous ventricular septal defect with Amplatzer Ductal Occluder (ADO) is an effective and safe method. Patients and Methods: Between April 2012 and April 2013, 28 patients underwent percutaneous closure of PMVSD using ADO. After obtaining the size of VSD from the ventriculogram a device at least 2 mm larger than the narrowest diameter of VSD at right ventricular side was chosen. The device deployed after confirmation of its good position by echocardiography and left ventriculography. Follow up evaluations were done 1 month, 6 months, 12 months and yearly after discharge with transthoracic echocardiography and 12 lead electrocardiography. Results: The mean age of patients at procedure was 4.7 ± 6.3 (range 2 to 14) years, mean weight 14.7 ± 10.5 (range 10 to 40) kg. The mean defect size of the right ventricular side was 4.5 ± 1.6 mm. The average device size used was 7.3 ± 3.2mm (range 4 to 12 mm). The ADOs were successfully implanted in all patients. The VSD occlusion rate was 65.7% at completion of the procedure, rising up to 79.5% at discharge and 96.4% during follow-up. Small residual shunts were seen at completion of the procedure, but they disappeared during follow-up in all but one patient. The mean follow-up period was 8.3 ± 3.6 months (range 1 to 18 months). Complete atrioventricular block (CAVB), major complication or death was not observed in our study. Conclusions: Transcatheter closure of PMVSD with ADO in children is a safe and effective treatment associated with excellent success and closure rates, but long-term follow-up in a large number of patients would be warranted.

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Background: H19 is a strong candidate gene for influencing birth weight variation and is exclusively imprinted maternally. In an attempt to understand the relationship of this gene polymorphism with low birth weight children, we investigated association of H19/RsaI polymorphism with low birth weight and normal birth weight in children and their mothers. Objectives: The aim of our study was to establish the association between H19 gene polymorphism and LW in children born in Pernambuco, state of Brazil. Patients and Methods: It were selected 89 children, 40 low birth weight (LW) and 49 normal birth weight (NW) and 71 mothers (40 mothers of newborns NW and 31 mothers of newborns LW) attended at Dom Malan Hospital, Petrolina, Pernambuco - Brazil. Peripheral blood samples were collected from patients and genomic DNA was extracted and detected by electrophoresis agarose gel, stained by Blue Green Loading Dye. DNA PCR amplification was done using the primers H1 (sense) and H3 (antisense). PCR products were digested with RsaI and electrophoresed on agarose gel stained by ethidium bromide. Statistical analyses were performed using the program BioEstat version 5.0. Results: The RsaI polymorphism in the H19 gene showed that genotype frequencies did not differ statistically between low birth weight (AA = 12.5%, AB = 45%, BB = 42.5%) and control (AA = 8.6% AB = 36.73%, BB= 55.10% groups) and the allele frequencies were not significantly different (P = 0.2897). We also did not observe any association between maternal H19 allele polymorphism and low birth weight newborns (P =0.7799) or normal birth weight children (P = 0.8976). Conclusions: The small size of sample may be the explanation for these results; future studies with more patients are needed to confirm the effect of H19/RsaI polymorphism on birth weight of LW newborns.