Bivalirudin vs heparin anticoagulation in STEMI: confirmation of the BRIGHT-4 results
Editorial review published in Journal of the American College of Cardiology (2024)
Abstract
BACKGROUND: In the BRIGHT-4 (Bivalirudin With Prolonged Full-Dose Infusion During Primary PCI Versus Heparin Trial-4), anticoagulation with bivalirudin plus a 2- to 4-hour high-dose infusion after percutaneous coronary intervention (PCI) reduced all-cause mortality and bleeding without increasing reinfarction or stent thrombosis compared with heparin alone in patients with ST-segment elevation myocardial infarction (STEMI). These findings require external validation. OBJECTIVES: This study sought to determine outcomes of bivalirudin vs heparin anticoagulation during PCI in STEMI. METHODS: We performed an individual-patient-data meta-analysis of all large randomized trials of bivalirudin vs heparin in STEMI patients undergoing primary PCI performed before BRIGHT-4. The primary endpoint was all-cause mortality. RESULTS: Six trials randomizing 15,254 patients were included. Pooled across all regimens of bivalirudin and glycoprotein IIb/IIIa inhibitor (GPI) use, bivalirudin reduced 30-day all-cause mortality (2.5% vs 2.9%; adjusted OR: 0.78; 95% CI: 0.62-0.99), cardiac mortality (adjusted OR: 0.69; 95% CI: 0.54-0.88), and major bleeding (adjusted OR: 0.53; 95% CI: 0.44-0.64) but increased reinfarction (adjusted OR: 1.30; 95% CI: 1.02-1.65) and stent thrombosis (adjusted OR: 1.43; 95% CI: 1.05-1.93) compared with heparin. In 4 trials in which 6,244 patients were randomized to bivalirudin plus a high-dose post-PCI infusion vs heparin without planned GPI use (the BRIGHT-4 regimens), 30-day all-cause mortality occurred in 1.8% vs 2.9% of patients, respectively (adjusted OR: 0.74; 95% CI: 0.48-1.12), and bivalirudin reduced cardiac mortality (adjusted OR: 0.62; 95% CI: 0.39-0.97) and major bleeding (adjusted OR: 0.49; 95% CI: 0.35-0.70), with similar rates of reinfarction (adjusted OR: 0.89; 95% CI: 0.58-1.38) and stent thrombosis (adjusted OR: 0.80; 95% CI: 0.41-1.57). CONCLUSIONS: In STEMI patients undergoing primary PCI, bivalirudin with a 2- to 4-hour post-PCI high-dose infusion reduced cardiac mortality and major bleeding without an increase in ischemic events compared with heparin monotherapy with provisional GPI use, confirming the BRIGHT-4 results.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Resumen
Editorial confirming BRIGHT-4 conclusions: bivalirudin (with prolonged post-PCI infusion) reduces composite of mortality and major bleeding vs UFH in STEMI patients undergoing primary PCI.
Por qué esto importa para la hirudoterapia
Este metanálisis de datos de pacientes individuales de seis ensayos aleatorizados de gran tamaño compara bivalirudina con heparina para la anticoagulación durante la intervención coronaria percutánea primaria en pacientes con infarto de miocardio con elevación del segmento ST, encontrando una reducción de la mortalidad cardiaca y de la hemorragia mayor con bivalirudina más una infusión de dosis alta post-ICP. El resumen no menciona sanguijuelas, hirudina, saliva de sanguijuela ni ninguna relación entre bivalirudina y el secretoma de la sanguijuela, por lo que no puede establecerse una conexión directa con la hirudoterapia a partir del propio texto fuente. Si bien la bivalirudina figura bajo el término MeSH 'Hirudinas', el resumen no aporta ninguna discusión que respalde esta clasificación. Por tanto, la relevancia para el dominio de ASH es como máximo indirecta y no queda fundamentada por el propio texto del artículo.
Citación
Bivalirudin vs heparin anticoagulation in STEMI: confirmation of the BRIGHT-4 results.
Stone GW · Journal of the American College of Cardiology, 2024
Contexto clínico relacionado
Explore cómo esta investigación se conecta con la práctica clínica
Añadido a la biblioteca ASH: May 27, 2026 · Última actualización del sitio: 18 de junio de 2026