Edoxaban for Thromboembolism Prevention in Pediatric Patients With Cardiac Disease Journal Articles uri icon

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abstract

  • BACKGROUND: Standard of care (SOC) anticoagulation for thromboembolism (TE) prevention in children with cardiac disease includes low molecular weight heparins or vitamin K antagonists. Limited data exists for alternate use of direct oral anticoagulants in children. OBJECTIVES: The investigators aimed to obtain safety and efficacy data for edoxaban in children. METHODS: We performed a phase 3, multinational, prospective, randomized, open-label, blinded-endpoint trial in patients <18 years of age with cardiac disease (ENNOBLE-ATE [Edoxaban for Prevention of Blood Vessels Being Blocked by Clots (Thrombotic Events) in Children at Risk Because of Cardiac Disease] trial). Patients were randomized 2:1 to age- and weight-based oral edoxaban once daily vs SOC for 3 months (main study period), stratified by cardiac diagnosis. Both groups could continue in an open-label edoxaban extension arm through 1 year. The primary endpoint was adjudicated clinically relevant bleeding (CRB). The main secondary endpoint was symptomatic TE or asymptomatic intracardiac thrombosis. RESULTS: The modified intention-to-treat cohort included 167 children. One patient per group experienced a nonmajor CRB in the main period. Treatment-emergent adverse events occurred in 46.8% (51 of 109) with edoxaban and 41.4% (24 of 58) with SOC. One SOC patient experienced 2 TE events (DVT with PE). Among 147 children in the extension, 1 CRB event (0.7%) and 4 TEs occurred (2.8%; 2 strokes and 2 of 33 Kawasaki disease patients with coronary artery thromboses and/or myocardial infarctions). CONCLUSIONS: Edoxaban is a potential alternative mode of thromboprophylaxis in children with cardiac disease showing low rates of CRB and TEs with advantages of once daily dosing and infrequent monitoring requirement. (ENNOBLE-ATE [Edoxaban for Prevention of Blood Vessels Being Blocked by Clots] (Thrombotic Events) in Children at Risk Because of Cardiac Disease trial; NCT03395639).

authors

  • Portman, Michael A
  • Jacobs, Jeffrey P
  • Newburger, Jane W
  • Berger, Felix
  • Grosso, Michael A
  • Duggal, Anil
  • Tao, Ben
  • Goldenberg, Neil A
  • Brothers, Matthew
  • Marino, Bradley
  • Canter, Charles
  • Law, Mark
  • Nguyen, Nguyenvu
  • Sang, Charlie
  • Shimano, Kristin
  • Gupta, Dipankar
  • Portman, Michael
  • Williams, Derek
  • Glass, Lauren
  • Sperrazza, Charles
  • Herold, Steven
  • Garg, Ruchira
  • Vranicar, Mark
  • Awad, Sawsan
  • Asante-Korang, Alfred
  • Druzgal, Colleen
  • Ozment, Caroline
  • Del Toro, Kamill
  • Roses, Ferran
  • Jux, Christian
  • Gravenhorst, Verena
  • Schweigmann, Ulrich
  • Bhatt, Mihir
  • Sabapathy, Christine
  • Dahdah, Nagib
  • Bartonicek, Dototea
  • Tulzer, Gerald
  • Basargina, Elena
  • Zvereva, Tatiana
  • Pertels, Tatiana
  • Plotnikova, Irina
  • Pierre-Emmanuel, SEGUELA
  • Amedro, Pascal
  • Yves, Dulac
  • BONNET, Damien
  • Saraco, Paola
  • Rimini, Alessandro
  • Digtiar, Valerii
  • Gonchar, Margaryta
  • Kryuchko, Tetyana
  • Yablon, Olga
  • Bedi, Varinder Singh
  • Patel, Jashvant
  • Mitra, Monjori
  • Kusa, Jacek
  • Domagala, Kowalczyk
  • KÖRNYEI, László
  • BERECZKI, Csaba
  • ABLONCZY, László
  • Levitas, Vivianne Aviva
  • Mishali, David
  • Revel-Vilk, Shoshana
  • Harlev, Dan
  • Sasmaz, Hatice Ilgen
  • Ozbek, Namik Yasar
  • Unal, Sule
  • Patıroglu, Türkan
  • Malbora, Baris
  • Agin, Hasan
  • Karakas, Zeynep
  • Kavakli, Ramazan Kaan
  • Chalmers, Elizabeth
  • Bu'Lock, Frances
  • Daubeney, Piers
  • Hamza, Hala
  • Badr, Mohamed
  • Elalfy, Mohsen
  • Mansour, Ahmed
  • Hassab, Hoda
  • Sabry, Ayman
  • Daou, Linda
  • Bitar, Fadi

publication date

  • December 2022