Sociedad Americana de Hirudoterapia

Bivalirudin Experience in a Heterogeneous Ventricular Assist Device Population

Retrospective review published in ASAIO J (2020)

Última actualización: 18 de junio de 2026Revisado por: ASH Editorial Board
Artículo de investigación — revisión de evidenciaReferencia del artículo
Evidence: Research reportDesarrollo de fármacosEnsayos clínicosBates A et al. · ASAIO journal, 2020

Abstract

Ventricular assist devices (VADs) are an increasingly common therapy for end-stage heart failure across all ages as a bridge to recovery or transplant and more recently as destination therapy. With increasing experience and difficulties with establishing therapeutic heparin levels, we have begun to explore the effectiveness of direct thrombin inhibitors in this patient population. This is a retrospective review of all long-term VAD patients, both adult and pediatric, who were anticoagulated with bivalirudin between January 2009 and January 2016. The starting dose was 0.3 mg/kg/hr, and dose was titrated for a goal partial thromboplastin time (PTT) of 70-100. There were 14 patients (13 males, 5 ≤18 years) with 17 episodes of bivalirudin therapy. The median age on initiation was 45 years (range, 15 days-67 years) with 10 episodes associated with a HeartWare HVAD, five a HeartMate II, and two with a Berlin Heart EXCOR. The predominant indication of bivalirudin therapy was suspected pump thrombosis (13/17). The median time from VAD insertion to initiation of bivalirudin was 116 days (range, 3-1,870) with the median duration of therapy being 21 days (range, 3-113). In patients with pump thrombosis, the mean baseline lactate dehydrogenase (LDH) was 229 ± 64 U/L, peak 690 ± 380 U/L, and decreased to 330 ± 243 U/L when bivalirudin was stopped. The outcomes following suspected pump thrombosis included: transitioned to warfarin (n = 7), death in two destination therapy patients who did not undergo pump exchange, transplantation (n = 2), and pump exchange (n = 2). A major bleeding complication occurred in only one patient. Our experience highlights the potential use of bivalirudin in a heterogenous VAD population. Although these initial results suggest some potential role for direct thrombin inhibitors for use in long-term VADs, larger prospective studies are required to support these preliminary observations and to determine who may benefit from direct thrombin inhibitors (DTIs) and the side effect profile in this patient population.

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

Publication typeJournal Article
Indexed MeSH termsAdultAgedAntithrombinsBlood CoagulationChildChild, PreschoolFemaleHeart FailureHeart-Assist DevicesHirudinsHumansInfant, Newborn

Resumen

Retrospective review of 14 VAD patients (adult and pediatric) treated with bivalirudin starting at 0.3 mg/kg/h for suspected pump thrombosis; LDH declined from peak 690 to 330 U/L on therapy.

Por qué esto importa para la hirudoterapia

Esta revisión retrospectiva examinó el uso de bivalirudina en 14 pacientes con DAV a largo plazo (adultos y pediátricos; 13 varones) a lo largo de 17 episodios entre enero de 2009 y enero de 2016, con una dosis inicial de 0,3 mg/kg/h ajustada para alcanzar un TTPa de 70–100. El resumen reporta que la indicación predominante fue sospecha de trombosis de la bomba (13/17), con descenso de la LDH desde su pico tras la terapia con bivalirudina y solo una complicación de sangrado mayor. No existe un vínculo defendible con la hirudoterapia, la terapia con sanguijuelas ni el secretoma de la sanguijuela basándose en este resumen, que no menciona la hirudina, las sanguijuelas ni ninguna derivación de ellas. Los autores indican explícitamente que se requieren estudios prospectivos de mayor tamaño para respaldar estas observaciones preliminares y determinar quiénes pueden beneficiarse de los inhibidores directos de la trombina.

Citación

Bivalirudin Experience in a Heterogeneous Ventricular Assist Device Population.

Bates A et al. · ASAIO journal, 2020

Contexto clínico relacionado

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

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