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失盐型21-羟化酶缺乏症患儿诊断时及婴儿期的氯化钠补充

Sodium chloride supplement at diagnosis and during infancy in children with salt-losing 21-hydroxylase deficiency.

作者信息

Mullis P E, Hindmarsh P C, Brook C G

机构信息

Endocrine Unit, Middlesex Hospital, London, UK.

出版信息

Eur J Pediatr. 1990 Nov;150(1):22-5. doi: 10.1007/BF01959473.

Abstract

Eight infants (6 female, 2 male) with salt-losing congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency were studied to determine the sodium deficit at diagnosis and the level of salt supplement required in addition to subsequent hormone replacement. The median sodium deficit at diagnosis was 34 mmol (range 16-78) or 10.5 mmol/kg (range 4-24). A mean sodium supplement of 2.2 mmol/kg per day (range 0.5-4.9), double the amount provided with feeds, was required to maintain plasma sodium concentration and plasma renin activity (PRA) in the normal range for age. We present an equation based on sodium output (urine), sodium input (feeding plus supplement) and plasma sodium concentration to calculate the sodium supplement needed to maintain sodium balance on hormone replacement in this condition and some practical management suggestions. The necessity for salt supplements is often underestimated and the salt-losing tendency exacerbated by infection remains an unnecessary reason for hospitalization during the first months of life. In patients with salt-losing CAH life-long mineralocorticoid treatment is necessary but additional salt supplements are needed to maintain plasma sodium concentration and PRA in the normal range during infancy.

摘要

对8例因21-羟化酶缺乏导致失盐型先天性肾上腺皮质增生症(CAH)的婴儿(6例女性,2例男性)进行了研究,以确定诊断时的钠缺乏情况以及在后续激素替代治疗之外所需的盐补充量。诊断时钠缺乏的中位数为34 mmol(范围16 - 78)或10.5 mmol/kg(范围4 - 24)。为使血浆钠浓度和血浆肾素活性(PRA)维持在该年龄的正常范围内,平均每天需要补充2.2 mmol/kg的钠(范围0.5 - 4.9),这是通过喂养提供量的两倍。我们提出了一个基于钠输出(尿液)、钠输入(喂养加补充)和血浆钠浓度的公式,用于计算在这种情况下激素替代治疗时维持钠平衡所需的盐补充量,并给出了一些实际管理建议。盐补充的必要性常常被低估,并且感染加剧的失盐倾向仍然是婴儿出生后头几个月不必要的住院原因。在失盐型CAH患者中,终生进行盐皮质激素治疗是必要的,但在婴儿期需要额外补充盐以维持血浆钠浓度和PRA在正常范围内。

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