Bivalirudin Monitoring Using Dilute Thrombin Time in Pediatric Extracorporeal Membrane Oxygenation: Single-Center, Retrospective Cost Analysis, 2018-2023
Retrospective cost analysis published in Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies (2026)
Resumen
OBJECTIVES: The parenteral anticoagulant bivalirudin has favorable safety and efficacy outcomes compared with unfractionated heparin (UFH) in pediatric patients requiring extracorporeal membrane oxygenation (ECMO), and is frequently monitored using the activated partial thromboplastin time (aPTT). Our group has demonstrated that the dilute thrombin time (dTT) provides superior reliability compared with the aPTT for bivalirudin monitoring, but there is a concern about access to using dTT and its cost. We report a comparative cost analysis of monitoring ECMO patients anticoagulated with bivalirudin or UFH. DESIGN: Retrospective analysis of total number of laboratory tests ordered at various time points during ECMO (5, 7, 10, 14, and 21 d) using 2024 institutional list prices for each test. SETTING: Single-center quaternary-care ICUs at Cincinnati Children's Hospital and Medical Center (CCHMC). PATIENTS: Children younger than 18 years supported on ECMO in our ICUs, anticoagulated with UFH (n = 46) or bivalirudin (n = 30) between January 2018 and August 2023. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: The total number of tests (complete blood count, prothrombin time, aPTT, fibrinogen, and antithrombin 3) ordered were lower in patients receiving bivalirudin compared with UFH across multiple time points of ECMO. In comparison with UFH, use of bivalirudin was associated with fewer total tests ordered and lower costs at both early and late time points. At CCHMC, dTT can be run at equivalent cost to aPTT. CONCLUSIONS: From 2018 to 2023, use of dTT monitoring for bivalirudin, rather than aPTT monitoring for UFH, during ECMO was associated with decreased laboratory testing and costs and is available on an automated or semi-automated platform. Overall, our data support the use of dTT-monitored bivalirudin during ECMO support, which is cost-efficient and may lead to reduction in total laboratory testing and blood volume sampling.
Resumen tomado de PubMed (NCBI) para el registro citado, en el idioma original. La versión de referencia es la de la publicación original.
El resumen se deja sin traducir para conservar la redacción original de los autores.
Síntesis
A retrospective single-center cost analysis found that dilute thrombin time monitoring of bivalirudin in pediatric ECMO patients required fewer laboratory tests and lower costs than aPTT-based unfractionated heparin monitoring across ECMO days 5 through 21.
Por qué esto importa para la hirudoterapia
Este análisis de costos retrospectivo unicéntrico en el Cincinnati Children's Hospital comparó las pruebas de laboratorio para niños (menores de 18 años) en oxigenación por membrana extracorpórea (ECMO) anticoagulados con el inhibidor directo de la trombina bivalirudin monitoreado mediante tiempo de trombina diluida (dTT) frente a heparin no fraccionada (UFH) monitoreada mediante aPTT (bivalirudin n=30, UFH n=46, enero de 2018 a agosto de 2023), reportando menos pruebas de laboratorio totales y menores costos con bivalirudin en múltiples puntos temporales de ECMO, con dTT ejecutable a un costo equivalente al de aPTT. Para la historia del descubrimiento de fármacos a partir del secretoma de sanguijuela es relevante porque bivalirudin es un péptido semisintético derivado de hirudin, el anticoagulante de la sanguijuela medicinal, por lo que el estudio muestra un inhibidor directo de la trombina derivado de sanguijuela siendo utilizado en un entorno clínico exigente con un perfil favorable de costos de monitoreo. Advertencia: esta es una comparación de costos retrospectiva, de una sola institución, que utiliza los precios de lista de 2024 de un centro, no un ensayo de resultados aleatorizado; aborda la carga de monitoreo, las pruebas de laboratorio y el costo en lugar de establecer directamente la eficacia o seguridad clínica, y bivalirudin es un fármaco derivado de hirudin, no la terapia con sanguijuelas en sí.
Compuestos relacionados del registro de la ASH
Moléculas de la sanguijuela y fármacos derivados de la hirudina relacionados con el tema de este artículo, cada uno con un perfil completo en el registro de compuestos de la ASH:
Citación
Bivalirudin Monitoring Using Dilute Thrombin Time in Pediatric Extracorporeal Membrane Oxygenation: Single-Center, Retrospective Cost Analysis, 2018-2023.
Dorn LE et al. · Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies, 2026
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Añadido a la biblioteca ASH: 28 de mayo de 2026 · Última actualización del sitio: 18 de junio de 2026