Tálosi Gyula, Katona Márta, Túri Sándor
Department of Paediatrics, University of Szeged, Szeged, Hungary.
Pediatr Int. 2007 Jun;49(3):335-40. doi: 10.1111/j.1442-200X.2007.02380.x.
In some neonates suffering from ductus arteriosus dependent congenital heart defect, a Prostaglandin E(1) (PGE1) therapy longer than 2 weeks may be needed. However, PGE1 analogue compounds may produce several adverse effects.
The authors retrospectively analyzed the data of nine patients who underwent a PGE1 treatment lasting longer than 14 days.
The leukocyte count of the patients remained high throughout the treatment period, and the proportion of neutrophils was over 50%. Transient feeding difficulty and abdominal distension, and possible signs of gastric-outlet obstruction, were observed in two cases. In the case of three patients, cortical hyperostosis developed after different cumulative doses (1584, 3384 and 4320 microg). Significant correlations were found between the doses of PGE1 and serum K(+) levels (r=-0.770, P < 0.05) and between the blood standard bicarbonate levels and PGE1 doses (r= 0.889, P < 0.01). Bartter syndrome-like condition developed in those three patients who received the largest cumulative doses.
Fluid-electrolyte parameters must be controlled frequently in the case of each patient treated with PGE1 for longer than 2 weeks. Although the dose, the length of the therapy and individual susceptibility may be equally important, fluid-electrolyte disturbances and the development of pseudo-Bartter syndrome seem to be more dose-dependent than cortical hyperostosis.
在一些患有动脉导管依赖性先天性心脏病的新生儿中,可能需要进行超过2周的前列腺素E(1)(PGE1)治疗。然而,PGE1类似物可能会产生多种不良反应。
作者回顾性分析了9例接受PGE1治疗超过14天的患者的数据。
患者在整个治疗期间白细胞计数一直较高,中性粒细胞比例超过50%。观察到2例患者出现短暂的喂养困难和腹胀,以及可能的胃出口梗阻迹象。3例患者在接受不同累积剂量(1584、3384和4320微克)后出现皮质骨增生。发现PGE1剂量与血清钾(K+)水平之间存在显著相关性(r=-0.770,P<0.05),血液标准碳酸氢盐水平与PGE1剂量之间也存在显著相关性(r=0.889,P<0.01)。接受最大累积剂量的3例患者出现了类似巴特综合征的情况。
对于接受PGE1治疗超过2周的每位患者,必须频繁控制其水电解质参数。尽管剂量、治疗时长和个体易感性可能同样重要,但水电解质紊乱和假性巴特综合征的发生似乎比皮质骨增生更依赖于剂量。