Sonntag J, Gaude M
Virchow-Klinikum, Humboldt Universität Berlin.
Klin Padiatr. 1998 Sep-Oct;210(5):354-7. doi: 10.1055/s-2008-1043902.
Dexamethasone and spironolactone are widely used in the management of bronchopulmonary dysplasia in premature infants. There are few data available about adverse effects of this drugs on the urinary excretion of calcium and phosphate in this group of patients.
24 h-urine samples could be collected in 85 infants between 8 and 40 days. 31 infants received dexamethasone and 32 spironolactone.
Multivariate variance analysis was performed to study the influence of dexamethasone and spironolactone on the measured excretion of calcium and phosphate. The influence of gestational and postnatal age, calcium and phosphate intake and theophylline treatment were excluded by use as covariates.
Spironolactone showed no significant influence on the urinary excretion of calcium or phosphate. Dexamethasone treatment increased the daily excretion of phosphate in the urine and decreased the phosphate concentration in serum.
None of the examined drugs showed a significant increase of the renal excretion of calcium in preterm infants. Thus a higher risk of nephrocalcinosis development due to these drugs has not been confirmed. Dexamethasone treatment might increase the risk of osteopenia by enhancing phosphate excretion.
地塞米松和螺内酯广泛用于早产儿支气管肺发育不良的治疗。关于这些药物对该组患者钙和磷尿排泄的不良反应的数据很少。
85名8至40天的婴儿收集了24小时尿液样本。31名婴儿接受了地塞米松治疗,32名接受了螺内酯治疗。
进行多变量方差分析以研究地塞米松和螺内酯对钙和磷测量排泄的影响。通过用作协变量排除了胎龄和出生后年龄、钙和磷摄入量以及茶碱治疗的影响。
螺内酯对钙或磷的尿排泄无显著影响。地塞米松治疗增加了尿中磷的每日排泄量,并降低了血清中磷的浓度。
所检查的药物均未显示早产儿肾钙排泄显著增加。因此,尚未证实这些药物导致肾钙质沉着症发生的风险更高。地塞米松治疗可能通过增加磷排泄而增加骨质减少的风险。