Sociedad Americana de Hirudoterapia

Impact of anemia on short-term outcomes after TAVR: A subgroup analysis from the BRAVO-3 randomized trial

Randomized controlled trial published in Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions (2021)

Última actualización: 18 de junio de 2026Revisado por: ASH Editorial Board
Artículo de investigación — revisión de evidenciaReferencia del artículo
Evidence: Randomized controlled trialEnsayos clínicosSeguridad y control de infeccionesFarmacología salivalRazuk V et al. · Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions, 2021

Abstract

OBJECTIVES: To determine the prognostic impact of anemia in patients randomized to bivalirudin or unfractionated heparin (UFH) during transcatheter aortic valve replacement (TAVR). BACKGROUND: Whether the periprocedural use of bivalirudin as compared with UFH in anemic patients undergoing TAVR has an impact on outcomes remains unknown. METHODS: The BRAVO-3 trial compared the use of bivalirudin versus UFH in 802 high risk patients undergoing transfemoral TAVR for severe symptomatic aortic stenosis. Patients were stratified according to the presence (defined as hemoglobin levels <13 g/dl in men and <12 g/dl in women) or absence of anemia. The primary outcomes were net adverse cardiac events (NACE; a composite of all-cause mortality, myocardial infarction, stroke, or bleeding) and major bleeding (Bleeding Academic Research Consortium ≥3b) at 30 days. RESULTS: Among 798 patients with available baseline hemoglobin levels, 427 (54%) were anemic of whom 221 (52%) received bivalirudin. There were no significant differences in NACE and major bleeding at 30 days between patients with and without anemia, irrespective of the type of anticoagulant used (pinteraction  = 0.71 for NACE, pinteraction  = 1.0 for major bleeding). However, anemic patients had a higher risk of major vascular complications (adjusted OR 2.43, 95% CI 1.42-4.16, p = 0.001), and acute kidney injury (adjusted OR 1.74, 95% CI 1.16-2.59, p = 0.007) compared to non-anemic patients at 30 days. CONCLUSIONS: Anemia was not associated with a higher risk of NACE or major bleeding at 30 days after TAVR without modification of the treatment effects of periprocedural anticoagulation with bivalirudin versus UFH.

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

Publication typeJournal ArticleRandomized Controlled Trial
Indexed MeSH termsAnemiaAntithrombinsAortic Valve StenosisFemaleHeparinHumansMaleNitrilesTranscatheter Aortic Valve ReplacementTreatment Outcome

Resumen

To determine the prognostic impact of anemia in patients randomized to bivalirudin or unfractionated heparin (UFH) during transcatheter aortic valve replacement (TAVR).

Por qué esto importa para la hirudoterapia

Este análisis de subgrupo del ensayo aleatorizado BRAVO-3 (802 pacientes) examinó si la anemia influía en los desenlaces a 30 días en pacientes que recibieron bivalirudina frente a heparina no fraccionada durante el reemplazo transcatéter de válvula aórtica (TAVR), hallando que la anemia no modificó los efectos comparativos de los dos anticoagulantes sobre los eventos cardíacos adversos netos ni sobre el sangrado mayor, aunque los pacientes anémicos presentaron mayores riesgos de complicaciones vasculares y lesión renal aguda. El resumen no menciona sanguijuelas, hirudina ni el origen de la bivalirudina; en este resumen no se establece ninguna conexión defendible con la hirudoterapia o con el secretoma de la sanguijuela, y su relevancia se limita a los desenlaces de cardiología intervencionista.

Citación

Impact of anemia on short-term outcomes after TAVR: A subgroup analysis from the BRAVO-3 randomized trial

Razuk V et al. · Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions, 2021

Contexto clínico relacionado

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

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