Høst A, Halken S, Kamper J, Lillquist K
Department of Paediatrics, Odense University Hospital.
Dan Med Bull. 1988 Feb;35(1):81-4.
Thirty-four sick neonates with major duct dependent cardiac defects were given short term (1 h-408 h) intravenous infusions of prostaglandin E1 (alprostadil) in doses varying between 0.1 micrograms/kg/min (starting dose) and 0.01 micrograms/kg/min. The aim of the study was to establish an effective and safe regiment that could be initiated after clinical diagnosis of a severe duct dependent cardiac defect, whose clinical course would be adversely affected by ductus closure. After an initial dosage of 0.1 micrograms/kg/min, effective clinical improvement was achieved in 28 infants (82%). In all 28 responders, the effect was maintained at a reduced dosage of 0.05 micrograms/kg/min, and in 21 a low dosage of 0.01 micrograms/kg/min was effective. Side effects, which occurred in 21 infants (62%), were reversible and dose related, and no serious side effects were noted at a dosage of less than 0.05 micrograms/kg/min. A starting dose of 0.05 micrograms/kg/min with subsequent reduction is recommended, but in case of institution of treatment before transfer to a pediatric cardiac centre a lower starting dose of 0.01 micrograms/kg/min may be preferred.
34例患有严重依赖动脉导管的心脏缺陷的患病新生儿接受了前列腺素E1(前列地尔)的短期(1小时至408小时)静脉输注,剂量在0.1微克/千克/分钟(起始剂量)至0.01微克/千克/分钟之间变化。该研究的目的是建立一种有效且安全的治疗方案,以便在临床诊断出严重依赖动脉导管的心脏缺陷后启动,这种缺陷的临床病程会因动脉导管闭合而受到不利影响。初始剂量为0.1微克/千克/分钟后,28例婴儿(82%)实现了有效的临床改善。在所有28例有反应者中,以0.05微克/千克/分钟的降低剂量维持了效果,并且在21例中,0.01微克/千克/分钟的低剂量是有效的。21例婴儿(62%)出现了副作用,这些副作用是可逆的且与剂量相关,并且在剂量低于0.05微克/千克/分钟时未观察到严重副作用。建议起始剂量为0.05微克/千克/分钟并随后降低,但如果在转至小儿心脏中心之前开始治疗,较低的起始剂量0.01微克/千克/分钟可能更可取。