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一项多中心研究评估了静脉用布洛芬在 1-6 个月龄婴儿中的药代动力学和安全性。

A Multi-Center Evaluation of the Pharmacokinetics and Safety of Intravenous Ibuprofen in Infants 1-6 Months of Age.

机构信息

Department of Anesthesiology, Perioperative and Pain Medicine, Texas Children's Hospital, Baylor College of Medicine, 6621 Fannin Street, Houston, TX, 77030-2399, USA.

"Just For Kids" Critical Care Center, Norton Children's Hospital, Louisville, KY, USA.

出版信息

Paediatr Drugs. 2023 Sep;25(5):585-593. doi: 10.1007/s40272-023-00576-9. Epub 2023 Jun 9.

Abstract

BACKGROUND

Enteral ibuprofen was first approved as a prescription drug in 1974 for the US market. An intravenous (IV) ibuprofen formulation is approved for use in children older than 6 months of age, but there are limited studies specifically evaluating the pharmacokinetics and safety in children 1-6 months of age.

AIMS

The primary purpose of this study was to evaluate the pharmacokinetics of IV ibuprofen in infants younger than 6 months of age. The secondary objective was to evaluate the safety of single and repeated doses of IV ibuprofen in infants younger than 6 months of age.

METHODS

This was an industry-sponsored multi-center study. Institutional Review Board approval and informed parental consent were obtained prior to enrollment. Hospitalized neonates and infants younger than 6 months of age with fever or expected postoperative pain were eligible. Enrolled patients received 10 mg/kg of IV ibuprofen every 6 h, with up to four doses per day. Patients were randomized to two sparse sampling technique pharmacokinetic sample time groups. Group 1 samples were drawn at 0, 30 min, and 2 h, while group 2 samples were drawn at 0 min, 1, and 4 h after administration.

RESULTS

A total of 24 children were enrolled in the study, with 15 male patients and 9 female patients. The median age of the cohort was 4.4 months (range 1.1-5.9 months), and the median weight was 5.9 kg (range 2.3-8.8 kg). The arithmetic mean and standard error for peak plasma ibuprofen concentration was 56.28 ± 2.77 µg/mL. Plasma levels declined rapidly with a mean elimination half-life of 1.30 h. Time to peak ibuprofen effect and concentration were similar when compared with older pediatric patients. Clearance and volume of distribution were also similar to those reported in older pediatric patients. No drug-related adverse events were reported.

CONCLUSIONS

The pharmacokinetic and short-term safety profiles of IV ibuprofen in pediatric patients 1-6 months of age are comparable to those in children older than 6 months of age.

TRIAL REGISTRATION

Clinicaltrials.gov Trial Registration number and date: NCT02583399-Registered July 2017.

摘要

背景

1974 年,肠内布洛芬首次被批准为美国市场的处方药。一种静脉(IV)布洛芬制剂被批准用于 6 个月以上的儿童,但针对 1-6 个月大的儿童的药代动力学和安全性的研究有限。

目的

本研究的主要目的是评估 6 个月以下婴儿 IV 布洛芬的药代动力学。次要目的是评估 6 个月以下婴儿单次和重复使用 IV 布洛芬的安全性。

方法

这是一项由行业赞助的多中心研究。在入组前获得了机构审查委员会的批准和家长的知情同意。患有发热或预期术后疼痛的住院新生儿和 6 个月以下的婴儿有资格参加。入组患者接受 10mg/kg IV 布洛芬,每 6 小时一次,每天最多 4 次。患者随机分为两组稀疏采样技术药代动力学样本时间组。第 1 组在 0、30 分钟和 2 小时时采集样本,第 2 组在给药后 0 分钟、1 小时和 4 小时时采集样本。

结果

共有 24 名儿童参加了这项研究,其中 15 名男性患者和 9 名女性患者。队列的中位年龄为 4.4 个月(范围 1.1-5.9 个月),中位体重为 5.9kg(范围 2.3-8.8kg)。峰血浆布洛芬浓度的算术平均值和标准误差为 56.28±2.77μg/ml。血浆水平迅速下降,平均消除半衰期为 1.30 小时。与年龄较大的儿科患者相比,布洛芬作用和浓度达峰时间相似。清除率和分布容积也与年龄较大的儿科患者相似。未报告与药物相关的不良事件。

结论

6 个月以下儿科患者 IV 布洛芬的药代动力学和短期安全性与 6 个月以上儿科患者相似。

试验注册

Clinicaltrials.gov 试验注册号和日期:NCT02583399-2017 年 7 月注册。

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