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地塞米松治疗极低出生体重儿的肾上腺反应性。

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

作者信息

Strauss A, Brakin M, Norris K, Modanlou H D

机构信息

Department of Pediatrics, Miller Children's Hospital, Long Beach Memorial Medical Center, University of California, Irvine.

出版信息

Dev Pharmacol Ther. 1992;19(2-3):147-54. doi: 10.1159/000457476.

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.

摘要

本研究旨在调查给予患病早产儿类固醇的效果。20名高危极低出生体重(VLBW)婴儿[出生体重(BW)≤1300g],平均BW为948±220g,胎龄(GA)27±1.7周,因支气管肺发育不良(BPD)/气道阻塞接受类固醇治疗,在类固醇治疗后23.6±15.9天进行了1小时促肾上腺皮质激素(考的松)刺激试验,并测定了17-羟孕酮(17OHP)/硫酸脱氢表雄酮(DHEAS)。18名婴儿还进行了甲吡酮试验。5名婴儿获得了促肾上腺皮质激素前后皮质醇、17OHP、DHEAS以及甲吡酮前后化合物S值的基线(未接触类固醇)值。18名婴儿中有8名(44%)基于异常的甲吡酮试验有继发性(下丘脑-垂体)肾上腺抑制的证据。在受抑制组和未受抑制组之间,BW、GA、吸氧或使用人工通气的时间、每千克体重的类固醇剂量或新生儿/新生儿后期死亡率均未发现差异。4名促肾上腺皮质激素试验临界的婴儿中有2名在甲吡酮试验后化合物S水平低于正常。每千克体重的类固醇剂量与促肾上腺皮质激素后皮质醇反应之间未发现相关性。此外,矫正胎龄与促肾上腺皮质激素前后皮质醇、17OHP和DHEAS的变化无关。两名婴儿在类固醇治疗后63天和186天通过重复甲吡酮试验记录到肾上腺抑制恢复。总之,本研究证明了接受地塞米松治疗的VLBW婴儿中继发性肾上腺抑制的明显高发生率。这些发现的临床意义值得进一步研究。

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