The efficacy and safety of bivalirudin and heparin in patients with acute coronary syndrome: a systematic review and meta-analysis
Systematic review with meta-analysis published in Systematic Reviews (2025)
Abstract
BACKGROUND: Patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI) are at high risk of thrombosis. However, bleeding-related complications during antithrombotic therapy remain a major barrier to effective treatment and can often lead to adverse outcomes. This meta-analysis aimed to determine the efficacy and safety of bivalirudin and heparin in patients with ACS after PCI. METHODS: Randomized controlled trials (RCTs) on the efficacy and safety of bivalirudin versus heparin in patients with ACS after PCI were identified from the PubMed, Embase, Cochrane Library, CBM, CNKI, WanFang, and VIP database until August 2024. The outcomes included all-cause mortality, major adverse cardiovascular events (MACEs), incidence of recurrent myocardial infarction, stent thrombosis, short-term bleeding, revascularization, and retransfusion. Meta-analysis was performed using RevMan 5.3 and Stata 12.0 softwares. The included studies were assessed for risk of bias using the Cochrane risk-of-bias assessment tool. RESULTS: A total of 70,199 patients from 27 randomized controlled trials (RCTs) were analyzed in this review. There were no significant differences between the bivalirudin and heparin groups in terms of all-cause mortality, major adverse cardiovascular events (MACEs), recurrent myocardial infarction, stent thrombosis within 30 days, or subacute stent thrombosis. Specifically, the incidence of short-term bleeding (P = 0.001) and retransfusion (P = 0.001) was significantly lower in the bivalirudin group compared to the heparin group. Conversely, the incidence of acute stent thrombosis (P < 0.0001) and revascularization (P = 0.009) was significantly higher in the bivalirudin group. CONCLUSIONS: Compared with heparin, bivalirudin has definite anticoagulant effect in patients with acute myocardial infarction after PCI, and the risk of bleeding and the incidence of retransfusion were lower in the bivalirudin group. This review helps doctors in PCI management choose bivalirudin or heparin more precisely based on patients' conditions for better treatment and fewer adverse events.
Abstract sourced from PubMed (NCBI) for the cited record. See the original publication for the authoritative version.
Resumen
Systematic review and meta-analysis comparing bivalirudin vs heparin across ACS RCTs. Bivalirudin associated with lower major bleeding; non-inferior on ischemic endpoints.
Por qué esto importa para la hirudoterapia
Esta revisión sistemática y metanálisis de 27 ensayos controlados aleatorizados (70.199 pacientes) comparó la eficacia y la seguridad de bivalirudina frente a heparina en pacientes con síndrome coronario agudo sometidos a intervención coronaria percutánea. No se encontraron diferencias significativas en la mortalidad por todas las causas, los MACEs, el infarto de miocardio recurrente ni la trombosis del stent a 30 días, pero la bivalirudina se asoció con tasas significativamente menores de hemorragia a corto plazo (P=0,001) y de retransfusión (P=0,001), junto con mayores tasas de trombosis aguda del stent (P<0,0001) y de revascularización (P=0,009). Los autores concluyen que la bivalirudina tiene un efecto anticoagulante definido en pacientes con infarto de miocardio agudo post-ICP, con menor riesgo de hemorragia y de retransfusión. Para el dominio de ASH, este estudio no tiene una conexión defendible con la hirudoterapia o el secretoma de la sanguijuela — el resumen no menciona sanguijuelas, hirudina ni la derivación del fármaco.
Citación
The efficacy and safety of bivalirudin and heparin in patients with acute coronary syndrome: a systematic review and meta-analysis.
Zhai Y et al. · Systematic reviews, 2025
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