Key result
Bivalirudin use in pediatric VAD recipients achieved a mean percent time in therapeutic range of 68.7% in the first 2 weeks, improving to 79.6% over the entire duration of support.
Why the study?
Given adverse bleeding and thrombotic events among pediatric VAD recipients, the potential advantages of direct thrombin inhibitors like bivalirudin had not been fully explored.
Observational (n=11)
Bivalirudin achieves a high percent time in therapeutic range in pediatric VAD recipients, suggesting it may be a promising and manageable anticoagulant agent in this population.
Bivalirudin %TTR data in pediatric VADs are hypothesis-generating; prospective trials needed to assess impact on bleeding or thrombosis.
Given the adverse event rates involving bleeding and thrombosis among children on ventricular assist devices (VADs), anticoagulant management has become a focal point for quality improvement and innovation. There may be advantages to using direct thrombin inhibitors, such as bivalirudin, though this has not been fully explored. As the percent time in therapeutic range (%TTR) for anticoagulants is classically associated with improved clinical outcomes, we evaluated the %TTR for bivalirudin among pediatric VAD recipients. Using a modification of the Rosendaal method, %TTR was calculated using activated partial thromboplastin time measurements for 11 VAD recipients in the early postoperative period (postoperative days 0-14) and for the duration of VAD support. In the initial 2 weeks after VAD implant, mean %TTR was 68.7 (±13.0). During the entire support course, the mean %TTR improved to 79.6 (±11.0). There was an era effect with improving %TTR in the latter half of the study period. We report very good %TTR for bivalirudin both in the first 2 weeks post implant and this improved over the duration of support. Because %TTR reflects the degree of safety and efficacy in chronic anticoagulation, this relatively high %TTR among a diverse, often critically ill cohort suggests that bivalirudin may be a promising agent. Although this study was underpowered to comprehensively evaluate adverse events on bivalirudin, this represents an important next step for larger scale study.
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Daugherty et al. (2020) conducted an observational in Pediatric ventricular assist device (VAD) recipients (n=11). Bivalirudin was evaluated on Percent time in therapeutic range (%TTR). Bivalirudin use in pediatric VAD recipients achieved a mean percent time in therapeutic range of 68.7% in the first 2 weeks, improving to 79.6% over the entire duration of support.
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