American Society of Hirudotherapy

A systematic review and meta-analysis of bivalirudin application in peripheral endovascular procedures

Meta-analysis published in Journal of vascular surgery (2019)

Last Updated: June 18, 2026Reviewed by: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Meta-analysisDrug DevelopmentHu Y et al. · Journal of vascular surgery, 2019

Abstract

OBJECTIVE: The direct thrombin inhibitor bivalirudin (BIV) was shown to be superior to unfractionated heparin (UFH) in percutaneous coronary interventions for reducing procedural blood loss. The aim of this study was to compare outcome profiles of BIV and UFH in peripheral endovascular procedures (PEPs) by synthesizing the currently available data. METHODS: Following the PRISMA statement, we conducted a comprehensive literature search using Medline, Cochrane CENTRAL, PubMed, EMBASE, CINAHL Google scholar, and clinicaltrials.gov. We recruited randomized, controlled trials and well-conducted observational studies that compared UFH and BIV in PEPs requiring anticoagulation, excluding endovascular cardiac procedures and coronary interventions. Random-effects meta-analyses were conducted to compare the outcome profiles of these two agents. RESULTS: Thirteen articles containing 14 studies involving a total of 21,057 patients were enrolled. Of these, 2 were randomized controlled trials, 2 were prospective cohort studies, and 10 were retrospective studies. There were no significant differences between BIV and UFH in terms of procedural success rates, major and minor perioperative bleeding, transfusion, perioperative transient ischemic attack, or hemorrhagic strokes. However, compared with UFH, BIV had significantly lower odds ratios (OR) of perioperative mortality (OR, 0.58; 95% confidence interval [CI], 0.40-0.86), major adverse cardiovascular events (OR, 0.65; 95% CI, 0.51-0.83), net adverse clinical events (OR, 0.75; 95% CI, 0.63-0.88), perioperative myocardial infarction (OR, 0.73; 95% CI, 0.55-0.98), major vascular complications (OR, 0.59; 95% CI, 0.39-0.91), and minor vascular complications (OR, 0.58; 95% CI, 0.40-0.84). CONCLUSIONS: Compared with UFH, PEPs using BIV had comparable procedural success rates and odds of perioperative transient ischemic attack and hemorrhagic stroke. However, procedures with BIV had a lower but nonsignificant odds of perioperative bleeding and transfusion. Depending on the procedures conducted, the patients who received BIV will have reduced or comparable odds of perioperative mortality, myocardial infarction, major adverse cardiovascular events, net adverse clinical events, and major and minor vascular complications. Therefore, BIV may be chosen solely as an alternative procedural anticoagulant to UFH for PEPs.

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

Publication typeJournal ArticleMeta-AnalysisResearch Support, Non-U.S. Gov'tSystematic Review
Indexed MeSH termsAnticoagulantsAntithrombinsEndovascular ProceduresHemorrhageHeparinHirudinsHumansIschemic Attack, TransientMyocardial InfarctionObservational Studies as TopicPatient SafetyPeptide FragmentsPeripheral Vascular DiseasesRandomized Controlled Trials as TopicRecombinant ProteinsRisk AssessmentRisk FactorsStrokeTreatment Outcome

Summary

This meta-analysis of 14 studies (21,057 patients) found bivalirudin and unfractionated heparin comparable for procedural success and bleeding in peripheral endovascular procedures, with bivalirudin showing lower odds of mortality and major adverse cardiovascular events.

Why This Matters for Hirudotherapy

This systematic review and meta-analysis compared bivalirudin with unfractionated heparin in peripheral endovascular procedures across 14 studies and 21,057 patients, finding comparable procedural success, bleeding, transfusion, transient ischemic attack, and hemorrhagic stroke outcomes, but lower odds of perioperative mortality, myocardial infarction, major adverse cardiovascular events, net adverse clinical events, and major and minor vascular complications with bivalirudin. The abstract does not mention hirudin, leeches, or any connection to hirudotherapy or leech-derived pharmacology. Bivalirudin (formerly Hirulog) is a synthetic peptide anticoagulant designed partly on the C-terminal sequence of hirudin, the anticoagulant of the medicinal leech (Maraganore et al., 1990); this paper studies the drug, not leech therapy.

Citation

Reference (Vancouver style)

Hu Y, Liu AY, Zhang L, Wu X, Shi S, Elmore JR, et al. A systematic review and meta-analysis of bivalirudin application in peripheral endovascular procedures. J Vasc Surg. 2019;70(1):274-284.e5. doi:10.1016/j.jvs.2018.12.037. PMID: 31230646

Bibliographic details (authors, volume, pages, DOI) are taken from the PubMed record.

Added to ASH library: May 27, 2026 · Site last updated: June 18, 2026

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