Bivalirudin anticoagulation in neonates and infants undergoing cardiac surgery
Pilot study published in J Cardiothorac Vasc Anesth (2022)
Abstract
OBJECTIVES: To determine the dosage of bivalirudin as the anticoagulant for cardiac surgery in neonates and infants. DESIGN: Pilot study. SETTING: Tertiary-care hospital. PARTICIPANTS: Twenty-five neonates and infants with congenital heart disease (CHD) undergoing cardiac surgery. INTERVENTIONS: The children received a 1 mg/kg bivalirudin bolus followed by a 2.5 mg/kg/h infusion as the anticoagulant for cardiac surgery. The dose was adjusted subsequently to maintain an activated clotting time (ACT) >480 s. MEASUREMENTS AND MAIN RESULTS: The mean age and weight were 5.3 months and 5.2 kg, respectively. Out of the 25 children, 16 were cyanotic. Baseline rotational thromboelastometry (ROTEM) (Tem Innovations GmbH, Munich, Germany) analysis revealed an underlying coagulation defect across EXTEM, INTEM, FIBTEM, and ADPTEM parameters. The dose of anticoagulant required was 1 mg/kg, followed by a 2.2 ± 0.4 mg/kg/h infusion. Only 1 child required an additional bolus dose. The ACT remained elevated for 4 hours after discontinuation of infusion. The mean 24-h postoperative chest tube drainage was 92 ± 36 mL. Excessive bleeding occurred in 4 children, 1 of whom required re-exploration. The platelet count remained low for 5 days, and, postoperatively, the prothrombin time and activated partial thromboplastin time remained low for 2 days. CONCLUSIONS: Effective anticoagulation was achieved with bivalirudin in the neonates and infants undergoing cardiac surgery. The dose required to maintain an ACT >480 s was 1.0 mg/kg, followed by 2.2 ± 0.4 mg/kg/h. The ACT remained elevated for 4 h after the discontinuation of bivalirudin infusion, resulting in an increased chest-tube output in some patients. Randomized, controlled trials are needed to further evaluate the safety of bivalirudin in the neonates and infants with complex congenital heart disease undergoing cardiac surgery with cardiopulmonary bypass.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Resumen
Pilot study of bivalirudin (1 mg/kg bolus, 2.2 mg/kg/h infusion) in 25 neonates/infants undergoing cardiac surgery; effective anticoagulation with ACT >480 s but elevated ACT post-infusion contributed to bleeding.
Por qué esto importa para la hirudoterapia
Este estudio piloto determinó la dosificación de bivalirudina para anticoagulación sistémica durante cirugía cardíaca en 25 neonatos y lactantes con cardiopatía congénita, utilizando un bolo de 1 mg/kg seguido de una infusión ajustada para mantener un tiempo de coagulación activado (TCA) por encima de 480 segundos. Los autores reportan anticoagulación eficaz con una dosis de mantenimiento de 2,2 ± 0,4 mg/kg/h, aunque el TCA permaneció elevado durante cuatro horas tras la suspensión, lo que contribuyó a un mayor débito por tubos torácicos en algunos pacientes, con sangrado excesivo en 4 niños y reintervención en 1. El resumen no menciona la hirudina, las sanguijuelas ni ningún compuesto derivado de sanguijuela, por lo que no existe un vínculo defensible con la hirudoterapia. Los autores describen este trabajo como un estudio piloto y solicitan ensayos controlados aleatorizados para continuar evaluando la seguridad.
Citación
Bivalirudin anticoagulation in neonates and infants undergoing cardiac surgery.
Hasija S et al. · Journal of cardiothoracic and vascular anesthesia, 2022
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Añadido a la biblioteca ASH: May 27, 2026 · Última actualización del sitio: 18 de junio de 2026