Sociedad Americana de Hirudoterapia

Bivalirudin versus heparin in STEMI after BRIGHT-4 trial: an updated meta-analysis

Updated meta-analysis published in Coronary Artery Disease (2023)

Última actualización: June 18, 2026Revisado por: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Meta-analysisEnsayos clínicosDesarrollo de fármacosOli PR et al. · Coronary artery disease, 2023

Abstract

BACKGROUND: The use of bivalirudin-based anticoagulation over heparin-based anticoagulation for coronary percutaneous intervention has been debated for a long time. Multiple trials have shown promising benefits of bivalirudin over heparin therapy with the most recent addition being the BRIGHT-4 trial. We performed a meta-analysis to assess evidence from these trials, focusing on the coronary intervention of the STEMI population. METHODS: This meta-analysis was performed based on PRISMA guidelines after registering in PROSPERO (CRD42023394701). Databases were searched for relevant articles published before January 2023. Pertinent data from the included studies were extracted and analyzed using RevMan v5.4. RESULTS: Out of 2375 studies evaluated, 13 randomized control trials with 24 360 acute ST-elevation myocardial infarction patients were included for analysis. The bivalirudin-based anticoagulation reduced the net clinical events (OR 0.75, CI 0.61-0.92), major adverse cardiac or cerebral events (OR 0.85, CI 0.74-0.98), any bleeding (OR 0.61, CI 0.45-0.83), major bleeding (OR 0.54, CI 0.39-0.75), all-cause mortality (OR 0.79, CI 0.67-0.92) and cardiac mortality (OR 0.78, CI 0.65-0.93) significantly without increasing the risk of any stent thrombosis (OR 0.92, 95% CI 0.52-1.61), definite stent thrombosis (OR 1.17, 95% CI 0.62-2.22) and acute stent thrombosis (OR 2.06, 95% CI 0.69-6.09) significantly at 30 days. CONCLUSION: Based on this meta-analysis, bivalirudin plus a post-PCI high-dose infusion-based anticoagulation during STEMI PCI has significant benefits over heparin therapy for cardiovascular outcomes without a significant increase in the risk of thrombotic outcomes.

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

Publication typeMeta-AnalysisJournal Article
Indexed MeSH termsHumansHeparinST Elevation Myocardial InfarctionAntithrombinsPercutaneous Coronary InterventionHirudinsAnticoagulantsPeptide FragmentsThrombosisRecombinant ProteinsRandomized Controlled Trials as Topic

Resumen

Updated post-BRIGHT-4 STEMI meta-analysis confirming bivalirudin reduces 30-day all-cause mortality and major bleeding in primary PCI versus heparin.

Por qué esto importa para la hirudoterapia

This meta-analysis of 13 randomized controlled trials (24,360 STEMI patients) assessed bivalirudin-based versus heparin-based anticoagulation during percutaneous coronary intervention, incorporating the BRIGHT-4 trial data. Bivalirudin with post-PCI high-dose infusion significantly reduced net clinical events, major adverse cardiac or cerebral events, all bleeding, major bleeding, all-cause mortality, and cardiac mortality, without significantly increasing stent thrombosis risk. The abstract does not mention leeches, hirudin derivation, or any connection to hirudotherapy, so no defensible link to ASH's domain exists based solely on this article. The findings concern a pharmaceutical anticoagulant in interventional cardiology and cannot be directly related to traditional leech therapy.

Citación

Bivalirudin versus heparin in STEMI after BRIGHT-4 trial: an updated meta-analysis.

Oli PR et al. · Coronary artery disease, 2023

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: June 18, 2026

Este sitio web proporciona información educativa y no constituye consejo médico, diagnóstico ni recomendaciones de tratamiento. La terapia con sanguijuelas medicinales conlleva riesgos clínicamente significativos y debe ser realizada únicamente por profesionales calificados bajo protocolos aprobados institucionalmente. La autorización 510(k) de la FDA para sanguijuelas medicinales se limita a indicaciones específicas; las discusiones sobre uso investigativo y fuera de indicación se señalan correspondientemente. Para orientación médica específica, consulte a un profesional de salud calificado.