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Published on: May 26, 2023
Pediatric Mechanical Circulatory Support: Pathophysiology of Pediatric Hemostasis and Available Options
Chiara Giorni1, Alessandra Rizza1, Isabella Favia1
1Pediatric Cardiac Intensive Care Unit, Department of Cardiology and Cardiac Surgery, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico, Rome, Italy.
Insights
Pediatric mechanical circulatory support (MCS) requires careful anticoagulation. Bivalirudin, a direct thrombin inhibitor, shows promise in reducing thromboembolic complications in children on VADs and ECMO, offering a potential alternative to unfractionated heparin.
Area of Science:
- Pediatric Cardiology
- Hematology
- Critical Care Medicine
Background:
- Mechanical circulatory support (MCS) is vital for pediatric heart failure, but complications like bleeding and thrombosis are significant risks.
- Current anticoagulation with unfractionated heparin (UFH) in pediatric MCS presents challenges, including dose variability and adverse events such as cerebrovascular accidents and thrombocytopenia.
- Direct thrombin inhibitors (DTIs) have emerged as alternative anticoagulation strategies in pediatric MCS.
Purpose of the Study:
- To review non-traditional anticoagulation strategies in pediatric mechanical circulatory support (MCS).
- To focus on the pharmacodynamics, indications, dosing, and monitoring of bivalirudin in pediatric MCS.
- To highlight collaborative efforts to minimize complications in this patient population.
Main Methods:
- Literature review of non-traditional anticoagulation strategies in pediatric MCS.
- Analysis of bivalirudin's role as an alternative to UFH.
- Examination of clinical data and protocols regarding bivalirudin use.
Main Results:
- Bivalirudin has become a preferred anticoagulant for long-term therapy in North American pediatric MCS protocols since 2018.
- The use of bivalirudin in pediatric MCS appears to add value in controlling and potentially reducing thromboembolic complications.
- Ongoing research and collaboration among centers aim to further minimize major complications.
Conclusions:
- Bivalirudin represents a promising alternative to UFH in pediatric MCS, potentially improving outcomes.
- Further prospective trials, including randomized controlled trials comparing UFH and bivalirudin, are necessary.
- Continued research is essential to confirm the benefits of bivalirudin in pediatric MCS settings.
Abstract:
Pediatric mechanical circulatory support (MCS) is considered a strategy for heart failure management as a bridge to recovery and transplantation or as a destination therapy. The final outcome is significantly impacted by the number of complications that may occur during MCS. Children on ventricular assist devices (VADs) and extracorporeal membrane oxygenation (ECMO) are at high risk for bleeding and thrombotic complications that are managed through anticoagulation. The first detailed guideline in pediatric VADs (Edmonton Anticoagulation and Platelet Inhibition Protocol) was based on conventional antithrombotic drugs, such as unfractionated heparin (UFH) and warfarin. UFH is the first-line anticoagulant in pediatric MCS, although its profile is not considered optimal in pediatric setting. The broad variation in heparin doses among children is associated with frequent occurrence of cerebrovascular accidents, bleeding, and thrombocytopenia. Direct thrombin inhibitors (DTIs) have been utilized as alternative strategies to heparin. Since 2018, bivalirudin has become the chosen anticoagulant in the long-term therapy of patients undergoing MCS implantation, according to the most recent protocols shared in North America. This article provides a review of the non-traditional anticoagulation strategies utilized in pediatric MCS, focusing on pharmacodynamics, indications, doses, and monitoring aspects of bivalirudin. Moreover, it exposes the efforts and the collaborations among different specialized centers, which are committed to an ongoing learning in order to minimize major complications in this special pediatric population. Further prospective trials regarding DTIs in a pediatric MCS setting are necessary and in specific well-designed randomized control trials between UFH and bivalirudin. To conclude, based on the reported literature, the clinical use of the bivalirudin in pediatric MCS seems to be a value added in controlling and maybe reducing thromboembolic complications. Further research is necessary to confirm all the results provided by this literature review.
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