Sociedad Americana de Hirudoterapia

Impact of Bleeding and Bivalirudin Therapy on Mortality Risk in Women Undergoing Percutaneous Coronary Intervention (from the REPLACE-2, ACUITY, and HORIZONS-AMI Trials)

Randomized controlled trial published in Am J Cardiol (2015)

Última actualización: June 18, 2026Revisado por: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Randomized controlled trialDesarrollo de fármacosEnsayos clínicosNg VG et al. · Am J Cardiol, 2015

Abstract

Women have higher bleeding complication and mortality rates after percutaneous coronary interventions (PCI). The contribution of female gender to bleeding and mortality is poorly understood. We evaluated the effect of gender and bleeding on outcomes of patients treated with bivalirudin during PCI by performing a patient-level pooled analysis of 3 randomized controlled trials (the Randomized Evaluation in PCI Linking Angiomax to Reduced Clinical Events, Acute Catheterization and Urgent Intervention Triage strategY, and Harmonizing Outcomes with Revascularization and Stents in Acute Myocardial Infarction) comparing bivalirudin versus heparin plus glycoprotein IIb/IIIa inhibitor (GPI) treatment in patients undergoing PCI. Of 14,784 patients, 7,413 patients received bivalirudin (1,870 women) and 7,371 patients received heparin + GPI (1,910 women). Women had significantly higher 30-day non-coronary artery bypass grafting (CABG)-related major bleeding rates (7.6% vs 3.8%, p <0.0001). After multivariate adjustment, female gender increased the hazard of major bleeding by 80% (hazard ratio 1.80, 95% confidence interval 1.52 to 2.11, p <0.001). Furthermore, women had a higher 1-year mortality rate (3.7% vs 2.7%, p = 0.002) than men; 30-day major bleeding was the strongest independent predictor of 1-year mortality in women (hazard ratio 2.48, 95% confidence interval 1.57 to 3.91, p = 0.001). Bivalirudin therapy in women reduced 30-day non-CABG-related major bleeding (5.6% vs 9.7%, p <0.0001) and 1-year mortality (2.9% vs 4.4%, p = 0.02) compared to standard therapy. In conclusion, in this cohort of patients treated for acute coronary syndrome and ST-segment elevation myocardial infarction, women have a near 2-fold increase in bleeding complications compared to men after PCI. Bleeding complications rather than gender is the strongest independent predictor of 1-year mortality in patients undergoing PCI. Furthermore, we observed a more pronounced clinical benefit in women treated with bivalirudin including a 44% reduction in major bleeding and a significant reduction in mortality rates at 1 year.

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

Publication typeJournal ArticleMulticenter StudyRandomized Controlled TrialResearch Support, Non-U.S. Gov't
Indexed MeSH termsAgedAntithrombinsArgentinaElectrocardiographyFemaleFollow-Up StudiesHemorrhageHirudinsHumansMaleMiddle AgedMyocardial Infarction

Resumen

Women have higher bleeding complication and mortality rates after percutaneous coronary interventions (PCI).

Por qué esto importa para la hirudoterapia

This patient-level pooled analysis of three randomized controlled trials (REPLACE-2, ACUITY, HORIZONS-AMI; 14,784 patients) evaluated the effect of gender and bleeding on outcomes in patients treated with bivalirudin versus heparin plus glycoprotein IIb/IIIa inhibitor during percutaneous coronary intervention. Women had nearly twice the 30-day major bleeding rates and higher one-year mortality; bivalirudin therapy in women reduced major bleeding (5.6% vs 9.7%) and one-year mortality (2.9% vs 4.4%) compared to standard therapy. The abstract does not mention leeches, hirudotherapy, hirudin, or leech-secretome components. CAVEAT: This is a pooled analysis of randomized trials focused on gender differences in PCI outcomes; its connection to ASH's domain cannot be established from the abstract alone.

Citación

Impact of Bleeding and Bivalirudin Therapy on Mortality Risk in Women Undergoing Percutaneous Coronary Intervention (from the REPLACE-2, ACUITY, and HORIZONS-AMI Trials).

Ng VG et al. · Am J Cardiol, 2015

Contexto clínico relacionado

Añadido a la biblioteca ASH: May 27, 2026 · Última actualización del sitio: June 18, 2026

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