Sociedad Americana de Hirudoterapia

Bivalirudin or heparin for systemic anticoagulation during pediatric extracorporeal membrane oxygenation: Multicenter retrospective study

Research article published in Thrombosis research (2023)

Última actualización: 18 de junio de 2026Revisado por: ASH Editorial Board
Artículo de investigación — revisión de evidenciaReferencia del artículo
Evidence: Observational studyDesarrollo de fármacosHamzah M et al. · Thrombosis research, 2023

Abstract

BACKGROUND: The objective of this study is to evaluate the outcomes of unfractionated heparin (UFH) compared to bivalirudin anticoagulation in pediatric ExtraCorporeal Membrane Oxygenation (ECMO). METHODS: A multicenter retrospective study, that included pediatric patients <18 years of age, who were supported on ECMO between June 2017 and May 2020. Patients treated with UFH were matched 2:1 by age and type of ECMO support to the bivalirudin group. RESULTS: The bivalirudin group (75 patients) were matched to 150 patients treated with UFH. Baseline characteristics and comorbidities of the two groups were similar. Veno-Arterial ECMO was the most common mode (141/225 [63 %]) followed by extracorporeal cardiopulmonary resuscitation (48/225 [21 %]). Bivalirudin treatment was associated with lower odds of bleeding events (aOR 0.23, 95%CI 0.12-0.45, p < 0.001) and lower odds of thrombotic events (aOR 0.48, 95%CI 0.23-0.98, p = 0.045). Patients who received bivalirudin had lesser odds for transfusion with fresh frozen plasma, and platelets (aOR 0.26, CI 0.12-0.57, p ≤0.001 and aOR 0.28, CI 0.15-0.53, p < 0.001, respectively). After adjusting for the type of ECMO support and adjusting for age, bivalirudin was associated with a decrease in hospital mortality by 50 % compared to the UFH group (aOR 0.50, 95%CI 0.27-0.93, p = 0.028). Similarly, for neurological disability at time of discharge, bivalirudin was associated with higher odds of intact neurological outcomes compared to UFH (OR 1.99 [95%CI 1.13-3.51], p = 0.017). CONCLUSIONS: This study demonstrated that effective anticoagulation can be achieved with bivalirudin, which was associated with lesser odds of bleeding events and utilization of blood products. Bivalirudin, in comparison with UFH, was associated with greater odds of hospital survival and intact neurological function at the time of discharge. A prospective randomized trial is required to validate the results of this study.

Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.

Publication typeJournal ArticleMulticenter Study
Indexed MeSH termsHumansExtracorporeal Membrane OxygenationHirudinsRetrospective StudiesPeptide FragmentsMaleFemaleHeparinRecombinant ProteinsAnticoagulantsChildChild, Preschool

Resumen

Bivalirudin or heparin for systemic anticoagulation during pediatric extracorporeal membrane oxygenation: Multicenter retrospective study.

Por qué esto importa para la hirudoterapia

Este estudio retrospectivo multicéntrico comparó la bivalirudina con la heparina no fraccionada (HNF) para la anticoagulación sistémica en pacientes pediátricos en ECMO (75 con bivalirudina emparejados 2:1 con 150 con HNF). La bivalirudina se asoció con menores probabilidades de eventos hemorrágicos (ORa 0,23), eventos trombóticos (ORa 0,48), transfusiones de hemoderivados, mortalidad hospitalaria (ORa 0,50) y mejores desenlaces neurológicos al alta. El resumen no menciona la hirudina, las sanguijuelas medicinales ni ningún producto derivado de sanguijuela, por lo que no puede establecerse una conexión defendible con el ámbito de la hirudoterapia de la ASH a partir de esta fuente. El estudio es retrospectivo y no aleatorizado, y los autores solicitan un ensayo prospectivo aleatorizado que valide los resultados.

Citación

Bivalirudin or heparin for systemic anticoagulation during pediatric extracorporeal membrane oxygenation: Multicenter retrospective study

Hamzah M et al. · Thrombosis research, 2023

Contexto clínico relacionado

Añadido a la biblioteca ASH: May 27, 2026 · Última actualización del sitio: June 18, 2026

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