Sociedad Americana de Hirudoterapia

Use of bivalirudin for anticoagulation in pediatric extracorporeal membrane oxygenation (ECMO)

Research article published in Perfusion (2021)

Última actualización: June 18, 2026Revisado por: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Research reportDesarrollo de fármacosKaushik S et al. · Perfusion, 2021

Abstract

This study describes the use of bivalirudin in children on extracorporeal membrane oxygenation (ECMO). Pediatric patients receiving bivalirudin were compared to patients receiving heparin as the anticoagulant on ECMO. Data was collected for children under 18 years of age supported by ECMO from January 2016 to December 2019. Data collected included demographics, diagnosis, ECMO indication, type, and duration, indication for bivalirudin use, dose range, activated partial thromboplastin time (aPTT) levels, minor and major bleeding, hemolysis, and mortality. Forty pediatric patients received ECMO; eight received bivalirudin primarily for anticoagulation. The median age was 4 months (IQR 0.5, 92) in the heparin cohort, 0.6 months (IQR 0.0, 80.0) in the primary bivalirudin cohort. The indication for ECMO was respiratory in 5 patients (18%) in the heparin group versus 6 (75%) in the primary bivalirudin group, cardiac in 18 (67%) in heparin versus 1 (12.5%) in primary bivalirudin, and extracorporeal-cardiopulmonary resuscitation (E-CPR) in 4 (15%) in heparin versus 1 (12.5%) in primary bivalirudin. Bivalirudin was the initial anticoagulant for eight patients (66.6%) while three (25%) were switched due to concern for heparin-induced thrombocytopenia (HIT) and one (8%) for heparin resistance. The median time to achieve therapeutic aPTT was 14.5 hours compared to 12 hours in the heparin group. Sixty-five percent of aPTT values in the bivalirudin and 44% of values in the heparin group were in the therapeutic range in the first 7 days. Patients with primary bivalirudin use had significantly lower dose requirement at 12 (p = 0.003), 36 (p = 0.007), and 48 (p = 0.0002) hours compared to patients with secondary use of bivalirudin. One patient (12.5%) had major bleeding, and two patients (25%) required circuit change in the primary bivalirudin cohort. Bivalirudin may provide stable and successful anticoagulation in children. Further large, multicenter studies are needed to confirm these findings.

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

Publication typeJournal Article
Indexed MeSH termsChildHumansAnticoagulantsExtracorporeal Membrane OxygenationHemorrhageHeparinHirudinsPeptide FragmentsRecombinant ProteinsRetrospective StudiesInfantChild, Preschool

Resumen

Use of bivalirudin for anticoagulation in pediatric extracorporeal membrane oxygenation (ECMO).

Por qué esto importa para la hirudoterapia

This study describes the use of bivalirudin compared to heparin for anticoagulation in pediatric patients on extracorporeal membrane oxygenation (ECMO), reporting outcomes including bleeding, circuit changes, time to therapeutic aPTT, and dose requirements. Eight of forty patients received bivalirudin as primary anticoagulant; three were switched from heparin due to concern for heparin-induced thrombocytopenia and one for heparin resistance. The abstract makes no mention of hirudin, leeches, or any relationship to hirudotherapy, so no defensible ASH connection exists. The main limitations are the small sample size in the primary bivalirudin cohort, and the authors note that further large, multicenter studies are needed to confirm these findings.

Citación

Use of bivalirudin for anticoagulation in pediatric extracorporeal membrane oxygenation (ECMO)

Kaushik S et al. · Perfusion, 2021

Contexto clínico relacionado

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

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