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循证吗啡剂量滴定用于术后新生儿和婴儿。

Evidence-based morphine dosing for postoperative neonates and infants.

机构信息

Division of Pharmacology, Leiden Academic Center for Drug Research, Leiden University, Leiden, The Netherlands.

出版信息

Clin Pharmacokinet. 2014 Jun;53(6):553-63. doi: 10.1007/s40262-014-0135-4.

Abstract

BACKGROUND AND OBJECTIVES

From a previously validated paediatric population pharmacokinetic model, it was derived that non-linear morphine maintenance doses of 5 μg/kg(1.5)/h, with a 50 % dose reduction in neonates with a postnatal age (PNA) <10 days, yield similar morphine and metabolite concentrations across patients younger than 3 years. Compared with traditional dosing, this model-derived dosing regimen yields significantly reduced doses in neonates aged <10 days.

METHODS

Concentration predictions of the population model were prospectively evaluated in postoperative term neonates and infants up to the age of 1 year who received morphine doses according to the model-derived algorithm. The efficacy of this dosing algorithm was evaluated using morphine rescue medication and actual average infusion rates.

RESULTS

Morphine and metabolite concentrations were accurately predicted by the paediatric pharmacokinetic morphine model. With regard to efficacy, 5 out of 18 neonates (27.8 %) with a PNA of <10 days needed rescue medication versus 18 of the 20 older patients (90 %) (p = 0.06). The median (interquartile range [IQR]) total morphine rescue dose was 0 (0-20) μg/kg in younger patients versus 193 (19-362) μg/kg in older patients (p = 0.003). The median (IQR) actual average morphine infusion rate was 4.4 (4.0-4.8) μg/kg/h in younger patients versus 14.4 (11.3-23.4) μg/kg/h in older patients (p < 0.001).

CONCLUSION

Morphine paediatric dosing algorithms corrected for pharmacokinetic differences alone yield effective doses that prevent over-dosing for neonates with a PNA <10 days. The fact that many neonates and infants with a PNA ≥10 days still required rescue medication warrants pharmacodynamic studies to further optimize the dosing algorithm for these patients.

摘要

背景和目的

从之前验证过的儿科群体药代动力学模型中得出,对于出生后年龄(PNA)<10 天的新生儿,5μg/kg(1.5)/h 的非线性吗啡维持剂量,减少 50%,可使 3 岁以下患者的吗啡和代谢物浓度相似。与传统剂量相比,这种基于模型的剂量方案可使<10 天的新生儿的剂量显著减少。

方法

前瞻性评估了基于模型的人群模型对接受吗啡剂量的术后足月新生儿和 1 岁以下婴儿的浓度预测,该模型是根据模型衍生的算法计算的。通过吗啡抢救药物和实际平均输注率来评估这种剂量方案的疗效。

结果

儿科药代动力学吗啡模型准确预测了吗啡和代谢物的浓度。在疗效方面,18 名 PNA<10 天的新生儿中有 5 名(27.8%)需要抢救药物,而 20 名年龄较大的患者中有 18 名(90%)(p=0.06)。较年轻的患者的中位数(四分位距[IQR])总吗啡抢救剂量为 0(0-20)μg/kg,而年龄较大的患者为 193(19-362)μg/kg(p=0.003)。较年轻的患者实际平均吗啡输注率的中位数(IQR)为 4.4(4.0-4.8)μg/kg/h,而年龄较大的患者为 14.4(11.3-23.4)μg/kg/h(p<0.001)。

结论

单独校正药代动力学差异的吗啡儿科剂量方案可产生有效的剂量,防止 PNA<10 天的新生儿用药过量。事实上,许多 PNA≥10 天的新生儿和婴儿仍需要抢救药物,这需要进行药效学研究,以进一步优化这些患者的剂量方案。

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