Department of Clinical Pharmacology, Bispebjerg University Hospital, Copenhagen University, Copenhagen, Denmark.
Department of Neonatology, Rigshospitalet, Copenhagen University, Copenhagen, Denmark.
Basic Clin Pharmacol Toxicol. 2018 May;122(5):523-530. doi: 10.1111/bcpt.12950. Epub 2018 Jan 17.
Polymedicated neonates and young infants may be at risk of harmful cumulative exposure to toxic excipients like ethanol, propylene glycol and benzyl alcohol during routine clinical care. The aim of this study was to calculate the cumulative daily alcohol exposure (mg/kg/day) in polymedicated neonates and infants and compare these levels to the tolerance limits found in guidelines published by European Medicines Agency (EMA). As part of the SEEN study, all medicinal products administered to neonates and infants were recorded. All included neonates received ≥2 medicinal products/day and infants ≥3 medicinal products/day. Daily excipient levels were calculated based on quantities obtained from manufacturers or databases. Excipient levels were compared to tolerance limits proposed by the EMA. Altogether, 470 neonates and 160 infants were included, recording 4207 prescriptions and 316 products. In total, 45% (n = 288) of patients were exposed to an alcohol of interest; 2% (n = 14) were exposed to benzyl alcohol (BA), 38% (n = 237) to ethanol and 23% (n = 146) to propylene glycol (PG). Of the total number of prescriptions involving ethanol-containing medicinal products (n = 334), 51% would alone exceed tolerance limit of 6 mg/kg/day. Of the total number of prescriptions involving PG-containing medicinal products (n = 174), 70% would alone exceed a maximum tolerance limit of 50 mg/kg/day. Maximal daily exposure to ethanol (1563 mg/kg/day) or PG (954 mg/kg/day) exceeded the tolerance limits recommended by EMA 260.5 and 19.1 times, respectively. Tolerance limits for ethanol and PG as proposed by the EMA are frequently exceeded in polymedicated neonates and infants due to the cumulative effect of these alcohols. Alternative formulations may minimize excipient exposure.
在常规临床护理中,接受多种药物治疗的新生儿和婴幼儿可能面临有害的、累积性的有毒辅料暴露风险,如乙醇、丙二醇和苯甲醇。本研究旨在计算接受多种药物治疗的新生儿和婴幼儿的每日酒精总暴露量(mg/kg/天),并将这些水平与欧洲药品管理局(EMA)发布的指南中的耐受限度进行比较。作为 SEEN 研究的一部分,记录了给予新生儿和婴幼儿的所有药物。所有纳入的新生儿每天接受≥2 种药物,婴儿每天接受≥3 种药物。根据从制造商或数据库获得的数量计算每日辅料水平。将辅料水平与 EMA 提出的耐受限度进行比较。共纳入 470 名新生儿和 160 名婴儿,记录了 4207 张处方和 316 种药物。共有 45%(n=288)的患者暴露于感兴趣的酒精;2%(n=14)暴露于苯甲醇(BA),38%(n=237)暴露于乙醇,23%(n=146)暴露于丙二醇(PG)。涉及含乙醇药物的总处方数(n=334)中,51%单独超过 6mg/kg/天的耐受限度。涉及含 PG 药物的总处方数(n=174)中,70%单独超过 50mg/kg/天的最大耐受限度。乙醇(1563mg/kg/天)或 PG(954mg/kg/天)的最大日暴露量分别超过 EMA 推荐的 260.5 倍和 19.1 倍。由于这些醇类的累积效应,EMA 提出的乙醇和 PG 的耐受限度在接受多种药物治疗的新生儿和婴幼儿中经常被超过。替代配方可最大程度减少辅料暴露。