Cranefield David J, Odd David E, Harding Jane E, Teele Rita L
Department of Radiology, National Women's Hospital, Private Bag 92189, Auckland, New Zealand.
Pediatr Radiol. 2004 Feb;34(2):138-42. doi: 10.1007/s00247-003-1090-7. Epub 2003 Nov 18.
The use of postnatal corticosteroids to treat or prevent chronic lung disease is common in very preterm infants. Medullary nephrocalcinosis has been noted as a possible side effect.
This prospective study was designed to assess the incidence of nephrocalcinosis in extremely preterm infants exposed to dexamethasone.
A prospective study of extremely preterm infants, recruited to a randomized trial of dexamethasone treatment for chronic lung disease, was initiated. Infants had US of the renal tract scheduled on entry into the study, at day 28 and at discharge or at the corrected gestational age of 36 weeks.
Thirty-three infants were enrolled in the study. Birth weight ranged between 440 and 990 g and gestation between 24 and 28 weeks. Nine infants died and six had incomplete data. Because there was no difference in incidence of calcification between those on the short course and those on the long course of dexamethasone, analysis was made on the entire cohort. One infant had nephrocalcinosis at the time of the initial US examination on day 26 of life. By day 28, nephrocalcinosis was present in 31% of those with complete data. By discharge, or corrected gestational age of 36 weeks, US evidence of nephrocalcinosis was present in 15 (83%) of 18 infants. All infants had at least one course of an aminoglycoside antibiotic during the study. All infants had parenteral nutrition. Only four infants received furosemide more regularly than single doses. The longest course was 10 days, received by an infant who did not develop nephrocalcinosis.
The incidence of nephrocalcinosis is high in this group of sick, extremely preterm infants. Dexamethasone may be a factor in the development of nephrocalcinosis. Future research should focus on the natural history of nephrocalcinosis in extremely preterm infants.
产后使用皮质类固醇治疗或预防慢性肺病在极早产儿中很常见。髓质性肾钙质沉着症被认为是一种可能的副作用。
本前瞻性研究旨在评估暴露于地塞米松的极早产儿中肾钙质沉着症的发生率。
启动了一项对极早产儿的前瞻性研究,这些婴儿被纳入地塞米松治疗慢性肺病的随机试验。婴儿在进入研究时、第28天、出院时或矫正胎龄36周时接受肾脏超声检查。
33名婴儿被纳入研究。出生体重在440至990克之间,孕周在24至28周之间。9名婴儿死亡,6名婴儿数据不完整。由于接受短疗程和长疗程地塞米松治疗的婴儿钙化发生率没有差异,因此对整个队列进行了分析。1名婴儿在出生后第26天首次超声检查时出现肾钙质沉着症。到第28天,有完整数据的婴儿中31%出现肾钙质沉着症。到出院时或矫正胎龄36周时,18名婴儿中有15名(83%)有肾钙质沉着症的超声证据。所有婴儿在研究期间至少接受过一个疗程的氨基糖苷类抗生素治疗。所有婴儿均接受肠外营养。只有4名婴儿比单次剂量更频繁地接受呋塞米治疗。最长疗程为10天,接受该疗程的婴儿未发生肾钙质沉着症。
在这群患病的极早产儿中,肾钙质沉着症的发生率很高。地塞米松可能是肾钙质沉着症发生的一个因素。未来的研究应关注极早产儿肾钙质沉着症的自然病程。