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首页> 外文期刊>Neonatology >Phenobarbital, Midazolam Pharmacokinetics, Effectiveness, and Drug-Drug Interaction in Asphyxiated Neonates Undergoing Therapeutic Hypothermia
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Phenobarbital, Midazolam Pharmacokinetics, Effectiveness, and Drug-Drug Interaction in Asphyxiated Neonates Undergoing Therapeutic Hypothermia

机译:苯巴罗布尔,苦参药代动力学,有效性和窒息新生儿的药物 - 药物相互作用在进行治疗体温过低

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Background: Phenobarbital and midazolam are commonly used drugs in (near-)term neonates treated with therapeutic hypothermia for hypoxic-ischaemic encephalopathy, for sedation, and/or as anti-epileptic drug. Phenobarbital is an inducer of cytochrome P450 (CYP) 3A, while midazolam is a CYP3A substrate. Therefore, co-treatment with phenobarbital might impact midazolam clearance. Objectives: To assess pharmacokinetics and clinical anti-epileptic effectiveness of phenobarbital and midazolam in asphyxiated neonates and to develop dosing guidelines. Methods: Data were collected in the prospective multicentre PharmaCool study. In the present study, neonates treated with therapeutic hypothermia and receiving midazolam and/or phenobarbital were included. Plasma concentrations of phenobarbital and midazolam including its metabolites were determined in blood samples drawn on days 2-5 after birth. Pharmacokinetic analyses were performed using non-linear mixed effects modelling; clinical effectiveness was defined as no use of additional anti-epileptic drugs. Results: Data were available from 113 (phenobarbital) and 118 (midazolam) neonates; 68 were treated with both medications. Only clearance of 1-hydroxy midazolam was influenced by hypothermia. Phenobarbital co-administration increased midazolam clearance by a factor 2.3 (95% CI 1.9-2.9, p < 0.05). Anticonvulsant effectiveness was 65.5% for phenobarbital and 37.1% for add-on midazolam. Conclusions: Therapeutic hypothermia does not influence clearance of phenobarbital or midazolam in (near-)term neonates with hypoxic-ischaemic encephalopathy. A phenobarbital dose of 30 mg/kg is advised to reach therapeutic concentrations. Phenobarbital co-administration significantly increased midazolam clearance. Should phenobarbital be substituted by non-CYP3A inducers as first-line anticonvulsant, a 50% lower midazolam maintenance dose might be appropriate to avoid excessive exposure during the first days after birth. (C) 2019 The Author(s) Published by S. Karger AG, Basel
机译:背景:苯巴比妥和咪达唑仑是常用的(近)术语新生儿用治疗性低温治疗的缺氧缺血性脑病治疗,用于镇静,和/或作为抗癫痫药物。苯巴比妥是细胞色素P450(CYP)3A的诱导剂,而MidazoLam是CYP3A衬底。因此,用苯巴比妥的共同治疗可能会影响咪达唑仑清关。目的:评估苯巴比妥和咪达唑仑在窒息的新生儿中的药代动力学和临床抗癫痫作用,并制定给药指导。方法:在预期多长期药房研究中收集数据。在本研究中,包括用治疗性低温治疗并接受咪达唑仑和/或苯巴比妥的新生儿。在出生后2-5天绘制的血液样本中测定包括其代谢物的苯甲虫和咪达唑仑的血浆浓度。使用非线性混合效应建模进行药代动力学分析;临床效果定义为不使用额外的抗癫痫药物。结果:数据可从113种(苯巴比特)和118(Midazolam)新生儿提供; 68均用两种药物治疗。只有1-羟基咪达唑仑的清除受到体温过低的影响。苯甲虫共同给药咪达唑仑清除率为22.3(95%CI 1.9-2.9,P <0.05)。苯巴比妥的抗惊厥效果为65.5%,占咪达唑蛋白的37.1%。结论:治疗性低温不会影响苯巴比妥或咪达唑仑在缺氧缺血性脑病中的清除症。建议建议苯甲脂肪剂量为30mg / kg以达到治疗浓度。苯巴比妥共同管理显着增加了咪达唑仑清关。苯巴罗布尔巴妥氏菌作为第一线抗癌剂的诱导剂,50%降低的咪达唑仑维持剂量可能适当,以避免出生后的第一天过度暴露。 (c)2019年由巴塞尔的S. Karger AG发布的提交人

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