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. 2020 May-Jun;96(3):333-340.
doi: 10.1016/j.jped.2018.11.008. Epub 2019 Feb 5.

Association between dietary pattern and metabolic disorders in children and adolescents with urolithiasis

Affiliations

Association between dietary pattern and metabolic disorders in children and adolescents with urolithiasis

Mariana S Vieira et al. J Pediatr (Rio J). 2020 May-Jun.

Abstract

Objective: To describe the dietary patterns and occurrence of metabolic disorders in children and adolescents with urolithiasis treatment at a referral hospital in southern Brazil in order to learn the features of urolithiasis in this population to better develop preventive actions.

Methods: Descriptive study conducted between 2016 and 2017 in a tertiary care referral hospital. Fourty patients aged 2-19 years old with urolithiasis proven by imaging were included. Clinical and dietary data were obtained through interviews and medical records. For statistical analyses, the chi-squared test was performed.

Results: 40 individuals were analyzed. Mean age at diagnosis was 7.2±4 years. 25% were overweight or obese. 95% had metabolic disorders, hypocitraturia being the predominant type. Protein intake was adequate in all participants and carbohydrate intake, in 70% of them; 37.5% had lipid intake above recommended and 65% had low fiber intake. The mean daily sodium intake was 2.64g (±1.74), with 55% of participants ingesting more than the recommended amount. A total of 52.5% had low potassium intake, with a mean of 4.79g/day (±2.49). Calcium intake was adequate in 27.5%. No significant differences were identified in relation to mean daily consumption among participants with or without the various metabolic disorders.

Conclusion: Pediatric urolithiasis is often accompanied by metabolic disorders; therefore, metabolic evaluation should be part of the diagnostic process and subsequent analysis of these patients' dietary patterns, helping to optimize treatment and prevent recurrences and complications.

Objetivo: Descrever o padrão alimentar e ocorrência de distúrbios metabólicos em crianças e adolescentes portadoras de urolitíase acompanhadas em hospital de referências no sul do Brasil a fim de conhecer as particularidades da urolitíase nessa população para melhor desenvolver ações de prevenção.

Métodos: Estudo observacional descritivo realizado entre 2016 e 2017 em centro de referência em atenção terciária. Foram selecionados 40 pacientes de 2 a 19 anos com urolitíase comprovada por exame de imagem. Dados clínicos e alimentares foram obtidos através de prontuário e entrevista. Para análise estatística, utilizou-se o teste qui-quadrado.

Resultados: Foram analisados 40 indivíduos, 55% masculinos. Idade média ao diagnóstico 7,2±4 anos. 25% tinham sobrepeso ou obesidade. 95% tinham distúrbios metabólicos, predominando a hipocitratúria. O consumo proteico e de carboidratos foi adequado em 100% e 70% dos participantes, respectivamente. 37,5% apresentaram ingestão de lipídeos acima do recomendado e 65% apresentaram ingestão de fibras alimentares abaixo do recomendado. O consumo diário médio de sódio foi de 2,64 g (±1,74), com 55% acima do recomendado. 52,5% apresentaram baixa ingestão de potássio com média de 4,79 g/dia (±2,49). O consumo de cálcio foi adequado em 27,5%. Não foram identificadas diferenças significativas em relação ao consumo médio diário dos nutrientes entre os participantes com ou sem os diversos distúrbios metabólicos.

Conclusões: A urolitíase pediátrica é frequentemente acompanhada de distúrbios metabólicos, o que confirma a necessidade de avaliação metabólica adequada ao diagnóstico e análise do padrão alimentar a fim de identificar erros alimentares e otimizar o tratamento destes distúrbios, prevenindo recorrências e complicações.

Keywords: Cálculo renal; Diet; Dieta; Hipercalciúria; Hypercalciuria; Kidney calculi; Pediatrics; Pediátrica; Urolithiasis; Urolitíase.

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Figures

Figure 1
Figure 1
Dietary adjustment of macro- and micronutrients for children and adolescents with urolithiasis with or without the three most frequent metabolic disorders in the population studied: hypocitraturia (A and B), hypercalciuria (C and D), and hypernatriuria (E and F).

Comment in

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