Anticoagulants in Children with Renal Impairment: A Narrative Review
- PMID: 40154508
- DOI: 10.1055/a-2546-0126
Anticoagulants in Children with Renal Impairment: A Narrative Review
Abstract
Venous thromboembolism is a common cause of morbidity and mortality in children with renal disease. To properly treat and prevent thromboembolism in this patient population, it is important to be familiar with the multitude of anticoagulant agents currently available. Many anticoagulant drugs undergo some extent of renal elimination. There are important considerations for the selection, dosing, and monitoring of anticoagulant drugs for patients with renal impairment due to various pharmacokinetic alterations that may occur. While there are data to help guide dosing and monitoring in adults, evidence regarding renal dose adjustment of many anticoagulant drugs in children are limited. For the clinician, anticoagulation management in children with renal impairment presents unique challenges. In addition to considering overall bleeding risk, the extent of renal impairment may vary by patient, making a one-size-fits-all approach to managing these patients difficult. These factors, combined with limited data, can make managing anticoagulation in children with renal impairment a challenge. Therefore, the focus of this review will be to describe the pharmacokinetics of the following anticoagulants in children with impaired renal function: unfractionated heparin, enoxaparin, dalteparin, rivaroxaban, apixaban, edoxaban, fondaparinux, bivalirudin, argatroban, dabigatran, and warfarin.
Thieme. All rights reserved.
Conflict of interest statement
N.A.G. receives research support and salary support from the National Institutes of Health and the National Heart Lung and Blood Institute for clinical and translational investigation in venous thromboembolism in patients <21 years old. He receives or has recently received (past 12 months) consultancy fees from Anthos Therapeutics, Bayer, and the University of Colorado-affiliated Academic Research Organization CPC Clinical Research for roles in clinical trial planning or oversight committees (e.g., advisory committee, steering committee, data and safety monitoring committee) in pharmaceutical industry-sponsored pediatric multicenter clinical trials of antithrombotic agents. He also receives consultancy fees from Novartis for data and safety monitoring committee membership in multicenter clinical trials of an immunomodulatory agent. His employer, Johns Hopkins University, receives salary support on his behalf from Boehringer-Ingelheim for data coordinating center leadership for a pediatric antithrombotic multicenter prospective observational study.M.B. receives research support and salary support from the National Institutes of Health and the National Heart Lung and Blood Institute for clinical and translational investigation in venous thromboembolism in patients <21 years old.A.A.S. receives research support and salary support from the National Institutes of Health and the National Heart Lung and Blood Institute for clinical and translational investigation in venous thromboembolism in patients <21 years old.D.M.W. has received research and salary support from the Agency for Healthcare Research and Quality for clinical and translational investigation in warfarin therapy patient self-management in adult patients.All other authors have nothing to disclose.
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