Avaliação Do Perfil Nutricional Em Pacientes Portadores De Fibrose Cística De Acordo Com Faixa Etária

Neri, Lenycia de Cassya Lopes; Bergamaschi, Denise Pimentel; Filho, Luiz Vicente Ribeiro Ferreira da Silva

doi:10.1590/1984-0462/;2019;37;1;00007

Cited by 4 publications

(3 citation statements)

References 26 publications

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“…In the evaluation of the z score according to weight of the participants, the mean z score for children aged 2-10 was 0.1500 ± 1.18621, while the mean z score for children aged 11-18 was -1.4431 ± 1.33970 and there is no statistically significant difference between the two age groups (p=0.107).In a cross-sectional study of 101 children and adolescents with cystic fibrosis in Brazil, Neri et al reported adequate calorie and macronutrient consumption and adequate nutritional status in most patients. However, lower BMI z scores were observed in schoolchildren (5 to <10 years) and adolescents (≥10 years) (20). In another study, 76 children with CF in Greece, 9% of boys and 5% of girls were underweight (BMI Z score for age <-2.0) despite patients meeting or exceeding the recommended total energy intake (19).…”

Section: Discussionmentioning

confidence: 95%

Determination of Nutritional Status in Children with Cystic Fibrosis

Arkin¹,

Basturk

2023

Haliç Üniversitesi Sağlık Bilimleri Dergisi

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Cystic fibrosis is a disease that affects quality of life and life span as a result of mutation in the transmembrane conductivity regulator gene. The aim of this study is to determine the nutritional status of 2–18-year-old children with cystic fibrosis.75 children with cystic fibrosis between the ages of 2-18 were included in the study. The data were obtained online with the "Sociodemographic Form", "Nutrition Evaluation Form" and "24-Hour Food Consumption Record". Dietary quality, energy intake, macro and micronutrient intakes of the participants were determined by taking a 24-hour food consumption record. IBM Statistical Package for Social Sciences Version 24 statistical program and BEBIS 8.2 program were used to analyze the data obtained through the questionnaire. In this study 32 girls and 43 boys were included. It was determined that the daily energy intake of the girls was 1368 ± 394 kcal, and the boys were 1496 ± 494 kcal. When the z-score values of the participants are examined, the z-score value according to the height is minimum -4.16, maximum 3.05; It has been determined that the z-score value for weight is minimum -3.79 and maximum 2.60. The mean z-score of the participants for height was -0.25; The mean z score according to weight was determined as -0.40. The average weight of the boys is 30 kg, and the girls are 28.4 kg. More studies are needed to determine nutritional status, new nutritional therapies, and supplemental doses in children with cystic fibrosis.

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Section: Discussionmentioning

confidence: 95%

Determination of Nutritional Status in Children with Cystic Fibrosis

Arkin¹,

Basturk

2023

Haliç Üniversitesi Sağlık Bilimleri Dergisi

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“…As demonstrated in a recent study, while infants were not underweight, in the preschool age group, around 10% had a nutritional profile below expectations, a proportion that increased significantly among students (35.3%) and adolescents (33.3%). 30 However, regarding BMI percentile and BMI-Z, the higher interquartile range observed in 2020 compared with 2018 deserves attention. The analysis of the absolute and relative frequencies of patients' distribution among each categorization of BMI percentile and BMI-Z showed more people with large gains but also with large losses in 2020 than in 2018, which eventually might have contributed to no significant change in the median.…”

Section: Discussionmentioning

confidence: 96%

“…It is crucial to recognize the early signs of abnormal glucose metabolism to diagnose CFRD. Early diagnosis and treatment correlate with slower rates of pulmonary decline and improved growth 38 …”

Section: Discussionmentioning

confidence: 99%

Clinical and anthropometric evolution of individuals with cystic fibrosis during COVID‐19 pandemic: A 24‐month cohort study

de Oliveira,

Altoé,

Arpini

et al. 2024

Pediatric Pulmonology

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ObjectivesTo analyze the evolution of clinical and anthropometric characteristics of children and adolescents with cystic fibrosis (CF) over 24 months, including the period of the COVID‐19 pandemic.MethodsA longitudinal study with data collection from May 2018 to November 2020 in physical and electronic records from a pediatric reference center, including individuals with CF aged up to 18 years.ResultsThe sample encompassed 72 individuals. Weight (p < 0.01), height (p < 0.01), and body mass index (BMI) (p = 0.043) were higher in 2020 than in 2018. There were no significant changes in BMI‐Z (p = 0.977) and in percentiles of weight (p = 0.540), height (p = 0.458), and BMI percentile (p = 0.454) between both periods. Pancreatic insufficiency was observed in 91.7% of patients in 2020, and there were twice as many confirmed cases of diabetes compared to 2018. There was a 9.7% increase in individuals colonized by the oxacillin‐sensitive Staphylococcus aureus (OSSA) (p = 0.039) and an 11.1% reduction in non‐colonized individuals (p = 0.008).ConclusionAlthough there was an increase in weight, height, and BMI from 2018 to 2020, there were no significant changes in BMI‐Z and in percentiles of weight, height, and BMI percentile, suggesting that the anthropometric aspects of nutritional status did not change in this period of 2 years. Moreover, there was an increase in the prevalence of individuals colonized by OSSA and a reduction in the prevalence of individuals non‐colonized with any bacteria.

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