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肾钙化:支气管肺发育不良早产儿地塞米松治疗的一种并发症。

Renal calcification: a complication of dexamethasone therapy in preterm infants with bronchopulmonary dysplasia.

作者信息

Kamitsuka M D, Williams M A, Nyberg D A, Fox K A, Lee D L, Hickok D

机构信息

Division of Neonatology, Swedish Medical Center, Seattle, Wash, USA.

出版信息

J Perinatol. 1995 Sep-Oct;15(5):359-63.

PMID:8576746
Abstract

We have previously reported a case study in which renal calcification formation may have been a complication of dexamethasone exposure in an infant with bronchopulmonary dsyplasia. To determine whether dexamethasone is associated with renal calcification formation, we conducted a prospective, nonrandomized study of 36 infants < 30 weeks' gestation and weighing < 1250 gm treated with dexamethasone because of bronchopulmonary dysplasia and compared them with a group not receiving dexamethasone. We identified seven infants in the dexamethasone group (n = 19) but no infant in the comparison group (n = 17) with renal calcifications at 2 months of age (p = 0.008). The urinary calcium excretion tended to be increased (15.5 +/- 16.6 vs 6.9 +/- 6.7 mg/kg/day ¿p = 0.05¿) and the calcium/creatinine ratio was significantly greater in the dexamethasone group (1.2 +/- 1.0 vs 0.6 +/- 0.4 ¿p = 0.02¿). Infants who received dexamethasone were significantly smaller 819.1 +/- 141.1 vs 954.6 +/- 141 gm ¿p = 0.008¿), were younger (26.2 +/- 1.7 vs 27.7 +/- 1.2 weeks ¿p = 0.004¿), received ventilator support longer (33.3 +/- 14.7 vs 12.1 +/- 14.7 days ¿p = 0.0001¿), and required more days of supplemental oxygen (54.3 +/- 9.7 vs 36.4 +/- 23.8 days ¿p = 0.009¿). We conclude that smaller, younger, and sicker infants are at the highest risk for the development of renal calcifications and that dexamethasone may be associated with increased urinary calcium excretion, which contributes to renal calcification formation.

摘要

我们之前曾报道过一项病例研究,其中一名患有支气管肺发育不良的婴儿出现肾钙化形成可能是地塞米松暴露的并发症。为了确定地塞米松是否与肾钙化形成有关,我们对36名孕周小于30周、体重小于1250克且因支气管肺发育不良接受地塞米松治疗的婴儿进行了一项前瞻性、非随机研究,并将他们与未接受地塞米松治疗的一组婴儿进行比较。我们发现地塞米松组(n = 19)中有7名婴儿在2个月大时出现肾钙化,而对照组(n = 17)中没有婴儿出现肾钙化(p = 0.008)。地塞米松组的尿钙排泄量有增加趋势(15.5±16.6 vs 6.9±6.7毫克/千克/天,p = 0.05),钙/肌酐比值显著更高(1.2±1.0 vs 0.6±0.4,p = 0.02)。接受地塞米松治疗的婴儿明显更小(819.1±141.1 vs 954.6±141克,p = 0.008),更年幼(26.2±1.7 vs 27.7±1.2周,p = 0.004),接受呼吸机支持的时间更长(33.3±14.7 vs 12.1±14.7天,p = 0.0001),且需要更多天数的补充氧气(54.3±9.7 vs 36.4±23.8天,p = 0.009)。我们得出结论,更小、更年幼且病情更重的婴儿发生肾钙化的风险最高,并且地塞米松可能与尿钙排泄增加有关,这促成了肾钙化的形成。

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