General Internal Medicine and Thrombotic and Haemorrhagic Diseases Unit, Department of Medicine, Padova University School of Medicine, Padova, Italy.
Semin Thromb Hemost. 2024 Sep;50(6):866-872. doi: 10.1055/s-0043-1778106. Epub 2024 Jan 5.
The incidence of venous thromboembolism (VTE) in the pediatric population has increased more than 10-fold in the last 20 years, as a consequence of the advancement of resuscitation and surgical techniques and the global increase in life expectancy of children suffering from chronic pathologies. Monitoring anticoagulant therapy to achieve outcomes within the target range in childhood VTE, parenteral administration of medications, and frequent blood tests in children are often cumbersome. Availability of safe and effective oral agents with pediatric data to support use would be of clear benefit. A physiologically based pharmacokinetic model was developed to estimate the appropriate dosing schedule for rivaroxaban in children. This incorporated growth/maturation and variability in anthropometrics (e.g., body height, weight, and body mass index), anatomy (e.g., organ weight), physiology (e.g., blood flow rates), metabolism and excretion. Rivaroxaban use in pediatric population underwent a complete investigational program, consisting mainly of one phase I pharmacokinetics/pharmacodynamics trial, three phase II trials, one phase III trial. The phase III trial enrolled 500 patients from birth to <18 years and documented the efficacy and safety of rivaroxaban regimens at dose equivalent to the adult 20 mg dose for the prevention of fatal or symptomatic nonfatal recurrent VTE and major bleeding versus heparin or vitamin K antagonists. Results were similar to those in rivaroxaban studies in adults. The efficacy and safety of rivaroxaban in children reported in the EINSTEIN JUNIOR trial provide further support to previous trials in adults (EINSTEIN Program), which demonstrate a favorable profile for the use of rivaroxaban for the management of VTE in challenging patient populations. Other clinical evidence contributing to the use of rivaroxaban among different risk groups in pediatric VTE population confirms the consistency with principal trial. Our review aims to describe the rationale for using rivaroxaban oral suspension in clinical practice and to summarize its multiple indications in each vascular bed (e.g., cerebral venous thrombosis, symptomatic or asymptomatic central venous catheter-associated thrombosis), etiology, and patients setting.
静脉血栓栓塞症(VTE)在儿科人群中的发病率在过去 20 年中增加了 10 多倍,这是由于复苏和手术技术的进步以及患有慢性疾病的儿童全球预期寿命的增加。监测抗凝治疗以实现儿科 VTE 目标范围内的结果、药物的肠胃外给药以及儿童频繁的血液检查往往很麻烦。如果有安全有效的口服药物,并具有支持使用的儿科数据,将是明显有益的。开发了一种基于生理学的药代动力学模型来估计儿童利伐沙班的适当剂量方案。该模型纳入了生长/成熟和人体测量学(例如身高、体重和体重指数)、解剖学(例如器官重量)、生理学(例如血流速度)、代谢和排泄的变异性。利伐沙班在儿科人群中的使用经历了一个完整的研究计划,主要包括一项 I 期药代动力学/药效学试验、三项 II 期试验和一项 III 期试验。III 期试验招募了 500 名从出生到<18 岁的患者,记录了利伐沙班方案的疗效和安全性,等效于成人 20mg 剂量,用于预防致命或有症状的非致命复发性 VTE 和大出血与肝素或维生素 K 拮抗剂相比。结果与利伐沙班在成人研究中的结果相似。EINSTEIN JUNIOR 试验中报告的利伐沙班在儿童中的疗效和安全性为之前在成人中的试验(EINSTEIN 计划)提供了进一步支持,该试验表明利伐沙班在治疗具有挑战性的患者人群中的 VTE 方面具有良好的应用前景。儿科 VTE 人群中不同风险组使用利伐沙班的其他临床证据证实了与主要试验的一致性。我们的综述旨在描述在临床实践中使用利伐沙班口服混悬液的基本原理,并总结其在每个血管床(例如,脑静脉血栓形成、有症状或无症状中心静脉导管相关血栓形成)、病因和患者情况下的多种适应证。