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达比加群酯在儿科患者与成人中的抗凝效果比较:三项儿科临床试验的汇总数据。

Anticoagulant Effects of Dabigatran in Paediatric Patients Compared with Adults: Combined Data from Three Paediatric Clinical Trials.

机构信息

Translational Medicine and Clinical Pharmacology, Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach, Germany.

Clinical Development and Medical Affairs, Boehringer Ingelheim International GmbH, Ingelheim, Germany.

出版信息

Thromb Haemost. 2018 Sep;118(9):1625-1636. doi: 10.1055/s-0038-1668132. Epub 2018 Aug 15.

Abstract

BACKGROUND

Physiological age-related changes in the haemostatic and coagulation systems result in differing anticoagulant assay responses to standard anticoagulants. Therefore, we investigated the response of anticoagulant assays to dabigatran etexilate (DE) in children compared with adults.

OBJECTIVE

This article assesses the relationship between plasma dabigatran concentration and coagulation assay results across age groups in children and adults.

PATIENTS AND METHODS

Data from three clinical trials in which children received DE following standard of care for venous thromboembolism were compared with data from adult clinical trials. The effects of dabigatran concentration on diluted thrombin time (dTT), ecarin clotting time (ECT) and activated partial thromboplastin time (aPTT) were analysed graphically and with modelling.

RESULTS

The concentration-dTT relationships were consistent in children across all ages and adults in the graphical analysis. For ECT and aPTT, relationships based on ratios over baseline were similar across all ages; absolute clotting times showed that the same exposure resulted in longer clotting times in some of the children aged < 1 year versus adults. Modelling showed concentration-clotting time relationships for all three assays were largely comparable between adults and children, except in those aged < 2 months, in whom there was a slight upward shift in ECT and aPTT relative to adults.

CONCLUSION

Results suggest that developmental haemostatic changes will have little impact on response to DE. However, further paediatric clinical trials assessing the relationship between coagulation assay responses and clinical outcomes will be needed to confirm this finding.

摘要

背景

止血和凝血系统的生理年龄相关变化导致对抗凝剂检测的反应与标准抗凝剂不同。因此,我们研究了抗凝剂检测在儿童与成人中对达比加群酯(DE)的反应。

目的

本文评估了儿童和成人各年龄段血浆达比加群浓度与凝血检测结果之间的关系。

患者和方法

比较了儿童接受 DE 治疗静脉血栓栓塞症的三项临床试验数据与成人临床试验数据。分析了达比加群浓度对稀释凝血酶时间(dTT)、蝰蛇凝血酶时间(ECT)和活化部分凝血活酶时间(aPTT)的影响,并进行了图形和模型分析。

结果

图形分析显示,儿童各年龄段的浓度-dTT 关系与成人一致。对于 ECT 和 aPTT,基于与基线比值的关系在所有年龄段均相似;绝对凝血时间表明,相同的暴露在一些<1 岁的儿童中导致比成人更长的凝血时间。模型分析表明,除了<2 个月的儿童外,所有三种检测方法的浓度-凝血时间关系在成人和儿童之间基本相似,在这些儿童中,ECT 和 aPTT 相对于成人略有向上偏移。

结论

结果表明,发育性止血变化对 DE 的反应影响不大。然而,需要进一步的儿科临床试验来评估凝血检测反应与临床结果之间的关系,以证实这一发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e3e/6202931/b19bf69c4896/10-1055-s-0038-1668132-i180064-1.jpg

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