Safety of dabigatran etexilate for the secondary prevention of venous thromboembolism in children.
Publication Title
Blood
Document Type
Article
Publication Date
2-13-2020
Keywords
Adolescent; Child; Child, Preschool; Dabigatran; Endpoint Determination; Female; Follow-Up Studies; Humans; Infant; Kaplan-Meier Estimate; Male; Risk Factors; Secondary Prevention; Time Factors; Venous Thromboembolism
Abstract
This open-label, single-arm, prospective cohort trial is the first phase 3 safety study to describe outcomes in children treated with dabigatran etexilate for secondary venous thromboembolism (VTE) prevention. Eligible children aged 12 to(age stratum 1), 2 to(stratum 2), and >3 months to(stratum 3) had an objectively confirmed diagnosis of VTE treated with standard of care (SOC) for ≥3 months, or had completed dabigatran or SOC treatment in the DIVERSITY trial (NCT01895777) and had an unresolved clinical thrombosis risk factor requiring further anticoagulation. Children received dabigatran for up to 12 months, or less if the identified VTE clinical risk factor resolved. Primary end points included VTE recurrence, bleeding events, and mortality at 6 and 12 months. Overall, 203 children received dabigatran, with median exposure being 36.3 weeks (range, 0-57 weeks); 171 of 203 (84.2%) and 32 of 203 (15.8%) took capsules and pellets, respectively. Overall, 2 of 203 children (1.0%) experienced on-treatment VTE recurrence, and 3 of 203 (1.5%) experienced major bleeding events, with 2 (1.0%) reporting clinically relevant nonmajor bleeding events, and 37 (18.2%) minor bleeding events. There were no on-treatment deaths. On-treatment postthrombotic syndrome was reported for 2 of 162 children (1.2%) who had deep vein thrombosis or central-line thrombosis as their most recent VTE. Pharmacokinetic/pharmacodynamic relationships of dabigatran were similar to those in adult VTE patients. In summary, dabigatran showed a favorable safety profile for secondary VTE prevention in children aged from >3 months tofactor(s). This trial was registered at www.clinicaltrials.gov as #NCT02197416.
Area of Special Interest
Women & Children
Area of Special Interest
Cardiovascular (Heart)
Specialty/Research Institute
Pediatrics
Specialty/Research Institute
Hematology
