Vanhaesebrouck Sofie, Allegaert Karel, Vanhole Christine, Devlieger Hugo, Gewillig Marc, Proesmans Willem
Neonatal Intensive Care Unit, Department of Paediatrics, University Hospitals Gasthuisberg, Herestraat 49, 3000 Leuven, Belgium.
Eur J Pediatr. 2003 Sep;162(9):569-71. doi: 10.1007/s00431-003-1201-3. Epub 2003 Jun 17.
We describe a case of iatrogenic pseudo-Bartter syndrome caused by administration of prostaglandin E1 (PGE1 alprostadil). Although the use of i.v. PGE1 is a well-established pharmacological therapy in neonates with a ductus-dependent congenital cardiopathy to ensure ductus-dependent flow, we could only find one other report on pseudo-Bartter syndrome related to PGE1 infusion.
Primary Bartter syndrome is associated with endogenous increased levels of prostaglandins. Therefore, we postulate that the dose of prostaglandin E1 administered, immaturity and the genetic background are all relevant factors involved in the phenotypic presentation of iatrogenic pseudo-Bartter syndrome in this preterm infant.
我们描述了一例因使用前列腺素E1(前列地尔)导致的医源性假性巴特综合征病例。尽管静脉注射前列腺素E1在患有动脉导管依赖性先天性心脏病的新生儿中是一种成熟的药物治疗方法,以确保动脉导管依赖性血流,但我们仅发现另一例与前列腺素E1输注相关的假性巴特综合征报告。
原发性巴特综合征与内源性前列腺素水平升高有关。因此,我们推测,所给予的前列腺素E1剂量、不成熟状态以及遗传背景都是该早产儿医源性假性巴特综合征表型表现的相关因素。