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在大多数患有经典失盐型先天性肾上腺皮质增生症的德奥婴儿中,并未常规进行氯化钠补充,且其对线性生长和氢化可的松或氟氢可的松剂量无影响。

Sodium Chloride Supplementation Is Not Routinely Performed in the Majority of German and Austrian Infants with Classic Salt-Wasting Congenital Adrenal Hyperplasia and Has No Effect on Linear Growth and Hydrocortisone or Fludrocortisone Dose.

机构信息

Department of Pediatrics, Klinikum Wels-Grieskirchen, Wels-Grieskirchen, Austria.

Pediatric Endocrinology, Department of Pediatrics, Technische Universität München, München, Germany.

出版信息

Horm Res Paediatr. 2018;89(1):7-12. doi: 10.1159/000481775. Epub 2017 Oct 26.

Abstract

INTRODUCTION

Sodium chloride supplementation in salt-wasting congenital adrenal hyperplasia (CAH) is generally recommended in infants, but its implementation in routine care is very heterogeneous.

OBJECTIVE

To evaluate oral sodium chloride supplementation, growth, and hydrocortisone and fludrocortisone dose in infants with salt-wasting CAH due to 21-hydroxylase in 311 infants from the AQUAPE CAH database.

RESULTS

Of 358 patients with classic CAH born between 1999 and 2015, 311 patients had salt-wasting CAH (133 females, 178 males). Of these, 86 patients (27.7%) received oral sodium chloride supplementation in a mean dose of 0.9 ± 1.4 mmol/kg/day (excluding nutritional sodium content) during the first year of life. 225 patients (72.3%) were not treated with sodium chloride. The percentage of sodium chloride-supplemented patients rose from 15.2% in children born 1999-2004 to 37.5% in children born 2011-2015. Sodium chloride-supplemented and -unsupplemented infants did not significantly differ in hydrocortisone and fludrocortisone dose, target height-corrected height-SDS, and BMI-SDS during the first 2 years of life.

CONCLUSION

In the AQUAPE CAH database, approximately one-third of infants with salt-wasting CAH receive sodium chloride supplementation. Sodium chloride supplementation is performed more frequently in recent years. However, salt supplementation had no influence on growth, daily fludrocortisone and hydrocortisone dose, and frequency of adrenal crisis.

摘要

简介

在盐耗竭型先天性肾上腺皮质增生症(CAH)中,一般建议在婴儿期补充氯化钠,但在常规护理中的实施非常不一致。

目的

评估 311 例 21-羟化酶缺陷导致的盐耗竭型 CAH 婴儿的口服氯化钠补充、生长情况以及氢化可的松和氟氢可的松剂量,这些婴儿来自 AQUAPE CAH 数据库。

结果

在 1999 年至 2015 年期间出生的 358 例经典 CAH 患者中,有 311 例为盐耗竭型 CAH(女性 133 例,男性 178 例)。其中,86 例(27.7%)在生命的第一年接受了口服氯化钠补充治疗,平均剂量为 0.9±1.4mmol/kg/天(不包括营养钠含量)。225 例(72.3%)未接受氯化钠治疗。接受氯化钠治疗的患者比例从 1999-2004 年出生的儿童的 15.2%上升到 2011-2015 年出生的儿童的 37.5%。在生命的前 2 年,接受和未接受氯化钠治疗的婴儿在氢化可的松和氟氢可的松剂量、靶身高校正身高-SDS 和 BMI-SDS 方面没有显著差异。

结论

在 AQUAPE CAH 数据库中,约三分之一的盐耗竭型 CAH 婴儿接受氯化钠补充。近年来,氯化钠补充的应用更为频繁。然而,盐补充对生长、每日氟氢可的松和氢化可的松剂量以及肾上腺危象的频率没有影响。

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