Prevalence and Nutritional Status of Infants With Cystic Fibrosis and Pseudo-Bartter Syndrome During the First Year of Life

I. Ciampo, N. S. Martins, R. Sawamura, I. Facincani, L. Ciampo, M. M. Fernandes
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引用次数: 1

Abstract

Background. Cystic fibrosis (CF) is an autosomal recessive disease more commonly occurring among Caucasians. An electrolyte derangement, pseudo-Bartter syndrome (PBS) is a complication leading to failure to thrive. Objectives. To describe the prevalence of PBS and related nutritional status in infants with CF detected after a newborn screening test who were treated in a Brazilian town with a very warm climate. Methods. This was a retrospective study with data collected from medical records. The diagnosis of PBS was based on hypokalemia (K+ 7.45; bicarbonate >28 mEq/L). The anthropometric data assessed were weight and length at the following: birth, diagnosis of CF, diagnosis of PBS, and discharge from hospital after correction of PBS and at 12 months of age. The nutritional indicators were weight/height, weight/age, length/age, and body mass index/age ratios. The cutoff point was z-score < p ...
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囊性纤维化和伪巴特综合征婴儿出生后第一年的患病率和营养状况
背景。囊性纤维化(CF)是常见于白种人的常染色体隐性遗传病。电解质紊乱,伪巴特综合征(PBS)是一种导致无法茁壮成长的并发症。目标。描述在巴西一个气候非常温暖的城镇接受新生儿筛查试验后发现的CF婴儿中PBS的患病率和相关营养状况。方法。这是一项从医疗记录中收集数据的回顾性研究。PBS的诊断基于低钾血症(K+ 7.45;碳酸氢盐>28 mEq/L)。评估的人体测量数据是出生时的体重和身高,诊断为CF,诊断为PBS, PBS矫正后出院,12个月大。营养指标为体重/身高、体重/年龄、身高/年龄、体质指数/年龄。截止点为z-score < p…
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