BMI differences on anticoagulation with bivalirudin vs. heparin during primary PCI: a BRIGHT-4 subanalysis
RCT subanalysis published in BMC Medicine (2025)
Abstract
BACKGROUND: Body mass index (BMI) is associated with ischemic and bleeding events in patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI). Procedural anticoagulation with bivalirudin followed by a prolonged high-dose post-PCI infusion was shown in the BRIGHT-4 trial to reduce mortality and major bleeding compared with heparin monotherapy. We aimed to assess the outcomes of bivalirudin compared with heparin in relation to BMI in STEMI patients undergoing primary PCI. METHODS: This prespecified subgroup analysis from the BRIGHT-4 trial evaluated the treatment effects of bivalirudin with a high-dose infusion for 2-4 h after primary PCI compared with heparin monotherapy in 6,016 randomized STEMI patients undergoing primary PCI predominantly via radial artery access stratified according to baseline BMI. A total of 3284 (54.6%) patients had a BMI < 25 kg/m2, the pre-specified stratification threshold. RESULTS: The primary endpoint of all-cause death or Bleeding Academic Research Consortium (BARC) types 3-5 bleeding events at 30 days in all enrolled patients occurred less often in patients with BMI ≥ 25 kg/m2 compared with those with BMI < 25 kg/m2 [2.9% vs. 4.4%; unadjusted hazard ratio (HR) 0.66, 95% confidence interval (CI) 0.50-0.87; P = 0.003], which was no longer significant after adjusting for confounders (adjusted HR 0.99, 95% CI 0.74-1.31; P = 0.92). Bivalirudin reduced the rate of the primary endpoint compared with heparin in patients with BMI < 25 kg/m2 (3.2% vs. 5.7%; adjusted HR 0.56, 95% CI 0.40-0.79) but not in those with BMI ≥ 25 kg/m2 (2.9% vs. 2.9%; adjusted HR 0.97, 95% CI 0.62-1.52; Pinteraction = 0.04). A similar pattern was observed for the individual components of the primary endpoint, as well as for the composite of all-cause death or BARC types 2-5 bleeding. CONCLUSIONS: Anticoagulation with bivalirudin followed by a prolonged high-dose infusion reduced the composite endpoint of all-cause death or BARC types 3-5 bleeding in STEMI patients undergoing primary PCI with lower BMI but not in those with higher BMI compared with heparin monotherapy. TRIAL REGISTRATION: The BRIGHT-4 trial is registered with ClinicalTrials.gov (NCT03822975).
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Resumen
BRIGHT-4 subanalysis showing bivalirudin's benefit over heparin extends across BMI strata, with greater reduction in major bleeding among obese and overweight STEMI patients.
Por qué esto importa para la hirudoterapia
Este análisis de subgrupo preespecificado del ensayo aleatorizado BRIGHT-4 (6,016 pacientes con STEMI sometidos a ICP primaria) examinó si el índice de masa corporal modifica el beneficio de bivalirudin más una infusión prolongada a dosis alta post-ICP frente a la monoterapia con heparin; bivalirudin redujo el desenlace compuesto de muerte por cualquier causa o hemorragia BARC 3-5 en pacientes con IMC <25 kg/m2 (HR ajustado 0.56, IC del 95% 0.40-0.79) pero no en aquellos con IMC >=25 kg/m2 (HR ajustado 0.97; P de interacción 0.04). La conexión con la hirudoterapia es indirecta pero real: bivalirudin es un péptido sintético modelado a partir de hirudin, el inhibidor de la trombina de la sanguijuela medicinal, por lo que esto constituye una evidencia clínica posterior para el linaje de inhibidores directos de la trombina derivados de la sanguijuela. La advertencia es que se trata de un hallazgo de subgrupo generador de hipótesis de un único ensayo, sobre un análogo sintético de hirudin en cateterismo cardíaco, no sobre la terapia con sanguijuelas o el secretoma completo de la sanguijuela.
Citación
BMI differences on anticoagulation with bivalirudin vs. heparin during primary PCI: a BRIGHT-4 subanalysis.
Zhang D et al. · BMC medicine, 2025
Contexto clínico relacionado
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Añadido a la biblioteca ASH: May 27, 2026 · Última actualización del sitio: June 18, 2026