Sociedad Americana de Hirudoterapia

Efficacy and safety of bivalirudin in coronary artery disease patients with mild to moderate chronic kidney disease: Meta-analysis

Meta-analysis published in J Cardiol (2017)

Última actualización: 18 de junio de 2026Revisado por: ASH Editorial Board
Artículo de investigación — revisión de evidenciaReferencia del artículo
Evidence: Meta-analysisDesarrollo de fármacosEnsayos clínicosZeng X et al. · J Cardiol, 2017

Abstract

BACKGROUND: Patients with chronic kidney disease (CKD) have elevated bleeding and ischemic outcomes. We aim to assess the short- and long-term efficacy and safety of bivalirudin compared to heparin plus glycoprotein IIb/IIIa inhibitors (GPIs) in coronary artery disease (CAD) patients with CKD. METHODS: Randomized trials were searched in PubMed, Cochrane, and Embase databases up to January 2017. Among the trials retrieved, efficacy endpoints were defined as mortality, myocardial infarction (MI), repeat revascularization, stent thrombosis, and major adverse cardiac events (MACEs). Safety endpoints were reported as non-coronary artery bypass grafting (CABG) related major bleeding and thrombolysis in myocardial infarction (TIMI) major bleeding. Risk ratio (RR) and 95% confidence interval (CI) were calculated for each outcome using a fixed effect model. RESULTS: Five studies with a total of 3796 patients were included. In short-term follow up (30 days), bivalirudin significantly reduced non-CABG related major bleeding (p=0.0004) and TIMI major bleeding (p=0.007) compared to heparin plus GPIs. No significant differences were observed in rates of mortality, MI, repeat revascularization, stent thrombosis, and MACEs between the two groups in short- and long-term follow up (6 months to 3 years). In patients with ST elevated myocardial infarction (STEMI) with concurrent CKD, the decreased non-CABG related major bleeding (p=0.04) without increasing ischemic events was also observed after short-term follow up. CONCLUSIONS: (1) Bivalirudin is safer than and as effective as heparin plus GPIs in CAD patients with CKD. (2) Impaired renal function does not affect the safety benefits of bivalirudin. (3) Similar efficacy profiles were identified between the two groups after both short- and long-term follow up in the CAD patients with CKD.

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

Publication typeComparative StudyJournal ArticleMeta-AnalysisResearch Support, Non-U.S. Gov't
Indexed MeSH termsAgedAnticoagulantsCoronary Artery DiseaseFemaleFollow-Up StudiesHemorrhageHeparinHirudinsHumansKidney Function TestsMaleMiddle Aged

Resumen

Meta-analysis of 5 trials (3,796 CKD patients with CAD); bivalirudin reduced non-CABG major bleeding (p=0.0004) vs heparin plus GPIs without affecting ischemic outcomes.

Por qué esto importa para la hirudoterapia

Este metaanálisis de cinco ensayos aleatorizados (3.796 pacientes) evaluó la eficacia y la seguridad de bivalirudina en comparación con heparina más inhibidores de la glucoproteína IIb/IIIa en pacientes con enfermedad arterial coronaria y enfermedad renal crónica. La bivalirudina redujo significativamente las hemorragias mayores no relacionadas con CABG y las hemorragias mayores según la escala TIMI en el seguimiento a corto plazo, sin aumentar los eventos isquémicos, y la función renal alterada no anuló estos beneficios de seguridad, con perfiles de eficacia similares entre los grupos tanto en el seguimiento a corto como a largo plazo. El resumen no menciona sanguijuelas, hirudina ni sustancias derivadas de sanguijuela, y no proporciona ninguna base para establecer una conexión con la hirudoterapia o el secretoma de las sanguijuelas. Este metaanálisis de farmacoterapia clínica no presenta relevancia demostrable para el ámbito de ASH.

Citación

Efficacy and safety of bivalirudin in coronary artery disease patients with mild to moderate chronic kidney disease: Meta-analysis.

Zeng X et al. · J Cardiol, 2017

Contexto clínico relacionado

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

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