Clinical Pharmacology of Intravenous Paracetamol in Neonates

K. Allegaert, M. Velde, G. Naulaers
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引用次数: 1

Abstract

Effective analgesia in neonates is still hampered due to the lack of data on pharmacokinetics and -dynamics of analgesics in this specific population. To a certain extent, this is even true for paracetamol. An intravenous formulation might improve prediction of concentration and consequent effect compared to enteral administration. In this review, we summarize the consecutive steps reported in literature to document the pharmacokinetics, metabolism and hepatic toler- ance of intravenous paracetamol in neonates. Based on a single intravenous dose study, pharmacokinetics estimates were calculated and a repeated dose regimen was developed. This dose regimen was subsequently evaluated in a repeated dose study, and paracetamol metabolism was de- scribed during repeated dose administration. Finally, hepatic tolerance in neonates was documented. Based on the available pharmacokinetic estimates, it seems that intravenous paracetamol is an attractive analgesic to be used in neonates, as an alternative or add-on therapy for opioid administration. After the documentation of the pharma- cokinetics of paracetamol in neonates and in the absence of any data on pharmacodynamics of intravenous paracetamol in this population, prospective, well designed and appropriated powered pharmacodynamic studies in neonates are urgently needed.
新生儿静脉注射扑热息痛的临床药理学研究
由于缺乏药物在新生儿中的药代动力学和动力学数据,有效的镇痛仍然受到阻碍。在某种程度上,扑热息痛也是如此。与肠内给药相比,静脉制剂可能改善浓度预测和后续效果。在这篇综述中,我们总结了文献报道的连续步骤,以记录新生儿静脉注射扑热息痛的药代动力学,代谢和肝脏耐受。基于单次静脉给药研究,计算了药代动力学估计,并制定了重复给药方案。该给药方案随后在重复给药研究中进行了评估,并在重复给药期间描述了扑热息痛的代谢。最后,对新生儿肝脏耐受进行了记录。根据现有的药代动力学估计,静脉注射扑热息痛似乎是一种有吸引力的镇痛药,可用于新生儿,作为阿片类药物给药的替代或附加治疗。在记录了新生儿扑热息痛的药物动力学之后,在缺乏静脉注射扑热息痛在这一人群中的药效学数据的情况下,迫切需要前瞻性、精心设计和适当的新生儿药效学研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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