Amerikanische Gesellschaft für Hirudotherapie

Bivalirudin versus heparin monotherapy in patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention

Meta-analysis published in Cardiovascular Drugs and Therapy (2024)

Zuletzt aktualisiert: June 18, 2026Geprüft von: ASH Editorial Board
Research article — evidence reviewArticle reference
Evidence: Meta-analysisKlinische StudienArzneimittelentwicklungSun B et al. · Cardiovascular drugs and therapy, 2024

Abstract

AIMS: The present meta-analysis focused on investigating whether bivalirudin plus post-PCI infusion was safer and more effective than heparin monotherapy in patients who developed ST-segment elevation myocardial infarction (STEMI) and who underwent primary percutaneous coronary intervention (PCI). METHODS: The PubMed, EMBASE, Cochrane Library, and Web of Science databases were systemically searched to identify randomized controlled trials (RCTs) comparing bivalirudin and heparin for treating STEMI patients who underwent primary PCI. The Cochrane quality assessment tool was used to assess the quality of the enrolled studies. The primary and secondary outcomes included net adverse clinical events (NACEs, comprising all-cause death or major bleeding), major adverse cardiovascular events (MACEs, comprising all-cause death, stroke, MI, and TVR), in-stent thrombosis (IST), and bleeding of Bleeding Academic Research Consortium (BARC) types 2, 3, and 5. RESULTS: The four RCTs, comprising 10,695 events, included 5350 patients who received bivalirudin combined with post-PCI infusion and 5345 patients who received heparin monotherapy. Compared with those in the heparin group, the number of NACEs (RR 0.84, 95% CI 0.73-0.96, P = 0.009), MACEs (RR 0.82, 95% CI 0.67-0.99, P = 0.04), and ISTs (RR 0.66, 95% CI 0.49-0.91, P < 0.0001) in the bivalirudin group was significantly lower. There were no significant differences in all-cause death, cardiac death, stroke, MI, TVR, or BARC type 2, 3, or 5 bleeding between the two groups. CONCLUSION: In STEMI patients undergoing primary PCI, bivalirudin plus post-PCI infusion significantly reduced the incidence of NACEs, MACEs, and ISTs compared with heparin monotherapy, without increasing the risk of MI or TVR. Bivalirudin may also contribute to a potential reduction in stroke, death, and BARC type 2, 3, and 5 bleeding rates.

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't
Indexed MeSH termsHumansHirudinsPeptide FragmentsPercutaneous Coronary InterventionHeparinRecombinant ProteinsRandomized Controlled Trials as TopicST Elevation Myocardial InfarctionAntithrombinsHemorrhageAnticoagulantsTreatment Outcome

Zusammenfassung

Meta-analysis pooling STEMI primary-PCI trials of bivalirudin vs heparin monotherapy. Bivalirudin reduces major bleeding without increased ischemic events.

Warum dies für die Hirudotherapie relevant ist

This meta-analysis of four randomized controlled trials compared bivalirudin plus post-PCI infusion against heparin monotherapy in patients with ST-segment elevation myocardial infarction (STEMI) undergoing primary percutaneous coronary intervention. Bivalirudin significantly reduced net adverse clinical events (RR 0.84, P=0.009), major adverse cardiovascular events (RR 0.82, P=0.04), and in-stent thrombosis (RR 0.66, P<0.0001) compared to heparin, with no significant differences in all-cause death, cardiac death, stroke, MI, TVR, or BARC type 2, 3, and 5 bleeding. For ASH's domain, this study has no defensible connection to hirudotherapy or the leech secretome—the abstract discusses bivalirudin versus heparin without any mention of leeches, hirudin, or drug derivation. Any link would require external knowledge not present in this abstract.

Zitation

Bivalirudin versus heparin monotherapy in patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention.

Sun B et al. · Cardiovascular drugs and therapy, 2024

Verwandter klinischer Kontext

Zur ASH-Bibliothek hinzugefügt: May 27, 2026 · Letzte Aktualisierung der Website: June 18, 2026

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