Bivalirudin versus heparin in patients with or without bail-out GPI use: a pre-specified subgroup analysis
Pre-specified subgroup analysis published in BMC Med (2024)
Abstract
BACKGROUND: Conflicting results comparing bivalirudin versus heparin anticoagulation in patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention (PCI), in part due to the confounding effect of glycoprotein IIb/IIIa inhibitors (GPI). The aim of the study was to compare the safety and effectiveness of bivalirudin plus a post-PCI high-dose infusion vs heparin with or without bail-out GPI use. METHODS: We conducted a pre-specified subgroup analysis from the BRIGHT-4 trial that randomized 6016 STEMI patients who underwent primary PCI to receive either bivalirudin plus a post-PCI high-dose infusion for 2-4 h or heparin monotherapy. GPI use was only reserved as bail-out therapy for procedural thrombotic complications. The primary outcome was a composite of all-cause death or Bleeding Academic Research Consortium (BARC) types 3-5 bleeding at 30 days. RESULTS: A total of 5250 (87.4%) patients received treatment without GPI while 758 (12.6%) received bail-out GPI. Bail-out GPI use was associated with an increased risk of the primary outcome compared to non-GPI use (5.28% vs. 3.41%; adjusted hazard ratio (aHR), 1.62; 95% confidence interval (CI), 1.13-2.33; P = 0.009) and all-cause death (5.01% vs. 3.12%; aHR, 1.74; 95% CI, 1.20-2.52; P = 0.004) but not in the risk of BARC types 3-5 bleeding (0.53% vs. 0.48%; aHR, 0.90; 95% CI, 0.31-2.66; P = 0.85). Among patients without GPI use, bivalirudin was associated with lower rates of the primary outcome (2.63% vs. 4.21%; aHR, 0.55; 95% CI, 0.39-0.77; P = 0.0005), all-cause death (2.52% vs. 3.74%; aHR, 0.58; 95% CI, 0.41-0.83; P = 0.003), and BARC types 3-5 bleeding (0.15% vs. 0.81%; aHR, 0.19; 95% CI, 0.06-0.57; P = 0.003) compared with heparin. However, among patients requiring bail-out GPI, there were no significant differences observed in the rates of the primary outcome (5.76% vs. 4.87%; aHR, 0.77; 95% CI, 0.36-1.66; P = 0.50; Pinteraction = 0.07) or its individual components between bivalirudin and heparin groups. CONCLUSIONS: Bivalirudin plus a post-PCI high-dose infusion was associated with significantly reduced 30-day composite rate of all-cause death or BARC types 3-5 bleeding compared with heparin monotherapy in STEMI patients undergoing primary PCI without GPI use. However, these benefits might be less pronounced in patients requiring bail-out GPI due to thrombotic complications during primary PCI. TRIAL REGISTRATION: ClinicalTrials.gov NCT03822975.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Resumen
Pre-specified subgroup analysis of bivalirudin versus heparin in patients with or without bail-out GPI use.
Por qué esto importa para la hirudoterapia
Este análisis de subgrupo preespecificado del ensayo BRIGHT-4 aleatorizó a 6.016 pacientes con IAMCEST sometidos a ICP primaria a recibir bivalirudina más una infusión pos-ICP a dosis altas frente a monoterapia con heparina, con inhibidores de la glucoproteína IIb/IIIa reservados únicamente como terapia de rescate. La bivalirudina es un inhibidor directo sintético de la trombina modelado a partir de la hirudina, el potente anticoagulante presente en la saliva de la sanguijuela medicinal, lo que convierte a este amplio ensayo de desenlaces cardiovasculares en directamente relevante para la ASH al informar sobre el desempeño de un anticoagulante derivado del secretoma de la sanguijuela en la anticoagulación clínica de alto riesgo. Entre los pacientes que no requirieron GPI de rescate (87,4%), la bivalirudina se asoció con tasas significativamente menores a 30 días del desenlace compuesto primario (muerte por todas las causas o sangrado BARC 3–5), muerte por todas las causas y sangrado mayor frente a la heparina; sin embargo, estas ventajas no se observaron en el subgrupo con GPI de rescate. Una advertencia honesta: se trata de un ensayo de anticoagulación farmacológica, no de un estudio de terapia con sanguijuelas vivas ni del secretoma completo de la sanguijuela, y los hallazgos de entornos de ICP no deben generalizarse en exceso a aplicaciones más amplias de la hirudoterapia.
Citación
Bivalirudin versus heparin in patients with or without bail-out GPI use: a pre-specified subgroup analysis.
Liao et al. · BMC medicine, 2024
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Añadido a la biblioteca ASH: May 27, 2026 · Última actualización del sitio: 18 de junio de 2026