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Heparin Versus Bivalirudin Monotherapy in the Setting of Primary Percutaneous Coronary Intervention for Patients With
Kathleen D Faulkenberg1, Janna C Beavers2, Shannon W Finks3
1Cleveland Clinic, Cleveland, OH, USA faulkek@ccf.org.
Insights
Bivalirudin reduces bleeding in ST-segment elevation myocardial infarction (STEMI) patients undergoing primary percutaneous coronary intervention (PPCI) compared to unfractionated heparin (UFH). However, it may increase stent thrombosis risk, necessitating further research.
Area of Science:
- Cardiology
- Pharmacology
- Interventional Cardiology
Background:
- Unfractionated heparin (UFH) is the standard anticoagulant for primary percutaneous coronary intervention (PPCI) in ST-segment elevation myocardial infarction (STEMI).
- Bivalirudin offers predictable pharmacokinetics and favorable bleeding profiles.
- Direct comparisons between bivalirudin and UFH in STEMI patients undergoing PPCI are emerging.
Purpose of the Study:
- To evaluate direct comparative evidence of bivalirudin versus UFH in STEMI patients undergoing PPCI.
- To synthesize current data on anticoagulant strategies in this patient population.
Main Methods:
- Systematic literature search of MEDLINE, International Pharmaceutical Abstracts, and Cochrane Databases (up to September 2015).
- Inclusion of English-language randomized controlled trials and meta-analyses of STEMI patients undergoing PPCI.
- Data extraction focused on outcomes related to bivalirudin and UFH use.
Main Results:
- Bivalirudin use is associated with reduced bleeding events compared to UFH when glycoprotein IIb/IIIa inhibitors are used sparingly.
- Evidence suggests an increased risk of acute stent thrombosis with bivalirudin compared to UFH.
- Variances in adjunctive therapies (GPIs, P2Y12 inhibitors), access sites, and dosing strategies complicate direct comparisons.
Conclusions:
- Bivalirudin reduces bleeding but may increase acute stent thrombosis risk in STEMI patients undergoing PPCI compared to UFH with limited GPI use.
- Further randomized trials are needed to investigate post-PCI bivalirudin infusions.
- Long-term follow-up and mortality data are required to fully elucidate the comparative benefits and risks.
Objective:
To evaluate direct comparisons of bivalirudin versus unfractionated heparin (UFH) as anticoagulants during ST-segment elevation myocardial infarction (STEMI) in patients undergoing primary percutaneous coronary intervention (PPCI).
Data Sources:
Relevant information was identified through a search of MEDLINE (1966-September 2015), International Pharmaceutical Abstracts (1960-September 2015), and Cochrane Databases (publications archived until September 2015) using the terms bivalirudin, unfractionated heparin, ST-segment elevation myocardial infarction, and primary percutaneous coronary intervention.
Study Selection And Data Extraction:
English-language randomized controlled trials and meta-analyses were eligible for inclusion for data review of STEMI where PPCI was performed.
Data Synthesis:
Either bivalirudin or UFH is recommended in the setting of STEMI where PPCI is to be performed. Bivalirudin is touted for its predictable pharmacokinetics, effects on thrombin-mediated platelet inhibition, and favorable outcomes with regard to adverse bleeding profiles, whereas UFH, the gold standard anticoagulant during PPCI, remains a viable treatment strategy. Only recently have direct comparisons of UFH and bivalirudin during PPCI become available. The evidence available is complicated by variances in use of glycoprotein IIb/IIIa inhibitors (GPIs), P2Y12 inhibitors, access sites, and anticoagulant dosing strategies. We provide a review of contemporary trials and advancements in this area.
Conclusions:
When compared to UFH with limited use of GPI, available evidence demonstrates that bivalirudin reduces bleeding at the expense of increasing risk for acute stent thrombosis. Further randomized studies are needed to determine the potential benefits of a post-PCI infusion of bivalirudin to reduce the risk for acute stent thrombosis, long-term follow-up beyond 30 days, and mortality.
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