Adrenal responsiveness in very-low-birth-weight infants treated with dexamethasone.

A Strauss, M Brakin, K Norris, H D Modanlou
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引用次数: 6

Abstract

This study was designed to investigate the effect of steroid administration in ill premature neonates. Twenty high-risk very-low-birth-weight (VLBW) infants [birth weight (BW) < or = 1,300 g] with a mean BW 948 +/- 220 g, gestational age (GA) 27 +/- 1.7 weeks underwent 1-hour ACTH (Cortrosyn) stimulation tests and determination of 17-hydroxyprogesterone (17OHP)/dehydroepiandrosterone sulfate (DHEAS) at 23.6 +/- 15.9 days poststeroid treatment for bronchopulmonary dysplasia (BPD)/airway obstruction. Metyrapone tests were also obtained in 18 infants. Baseline (nonsteroid-exposed) values for pre-/post-ACTH cortisol, 17OHP, DHEAS, and pre-/post-metyrapone compound S values were obtained in 5 infants. Eight of 18 (44%) infants had evidence of secondary (hypothalamic-pituitary) adrenal suppression based on abnormal metyrapone tests. No difference was found in BW, GA, time on O2 or AV, steroid dose/kg, or neonatal/postneonatal mortality between the suppressed and nonsuppressed groups. Two of 4 infants with borderline ACTH tests had subnormal compound S levels postmetyrapone. No relationship was found between steroid dose/kg and cortisol response post-ACTH. Additionally, corrected GA was not related to change in cortisol, 17OHP, and DHEAS pre-/post-ACTH. Two infants exhibited recovery of adrenal suppression documented by repeated metyrapone testing at 63 and 186 days poststeroid treatment. In conclusion, this study documents the apparent high incidence of secondary adrenal suppression in VLBW infants treated with dexamethasone. Clinical significance of these findings deserves further investigation.

地塞米松治疗极低出生体重儿的肾上腺反应性。
本研究旨在探讨类固醇给药对患病早产儿的影响。20例高危极低出生体重(VLBW)婴儿[出生体重(BW) <或= 1,300 g],平均体重948 +/- 220 g,胎龄(GA) 27 +/- 1.7周]接受1小时ACTH (Cortrosyn)刺激试验,并在类固醇治疗后23.6 +/- 15.9天检测17-羟基孕酮(17OHP)/硫酸脱氢表雄酮(DHEAS),以治疗支气管肺发育不良(BPD)/气道阻塞。对18名婴儿也进行了Metyrapone试验。获得5名婴儿acth前/后皮质醇、17OHP、DHEAS和metyrapone前/后化合物S值的基线(非类固醇暴露)值。18名婴儿中有8名(44%)有证据表明,基于异常的甲屈酮试验,继发性(下丘脑-垂体)肾上腺抑制。在抑制组和非抑制组之间,体重、GA、O2或AV时间、类固醇剂量/kg或新生儿/新生儿后死亡率均无差异。4例ACTH边缘性患儿中有2例服用甲替拉酮后化合物S水平低于正常水平。类固醇剂量/kg与促肾上腺皮质激素后皮质醇反应无关系。此外,校正后的GA与皮质醇、17OHP和DHEAS在acth前/后的变化无关。两名婴儿在类固醇治疗后63天和186天通过重复的美替拉酮测试显示肾上腺抑制恢复。总之,本研究记录了地塞米松治疗的VLBW婴儿继发性肾上腺抑制的明显高发。这些发现的临床意义值得进一步探讨。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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