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Heparin monotherapy or bivalirudin during percutaneous coronary intervention in patients with non-ST-segment-elevation acute coronary syndromes or stable ischemic heart disease: results from the Evaluation of Drug-Eluting Stents and Ischemic Events registry.

Publication ,  Journal Article
Bangalore, S; Pencina, MJ; Kleiman, NS; Cohen, DJ
Published in: Circ Cardiovasc Interv
June 2014

BACKGROUND: The use of bivalirudin versus unfractionated heparin monotherapy in patients without ST-segment-elevation myocardial infarction is not well defined. METHODS AND RESULTS: The study population consisted of patients enrolled in the Evaluation of Drug-Eluting Stents and Ischemic Events (EVENT) registry with either non-ST-segment-elevation acute coronary syndromes or stable ischemic heart disease, who underwent percutaneous coronary intervention with either unfractionated heparin or bivalirudin monotherapy. Propensity score matching was used to adjust for baseline characteristics. The primary bleeding (in-hospital composite bleeding-access site bleeding, thrombolysis in myocardial infarction major/minor bleeding, or transfusion) and primary (in-hospital death/myocardial infarction) and secondary ischemic outcomes (death/myocardial infarction/unplanned repeat revascularization at 12 months) were evaluated. Propensity score matching yielded 1036 patients with non-ST-segment-elevation acute coronary syndromes and 2062 patients with stable ischemic heart disease. For the non-ST-segment-elevation acute coronary syndrome cohort, bivalirudin use was associated with lower bleeding (difference, -3.3% [-0.8% to -5.8%]; P=0.01; number need to treat=30) without increase in either primary (difference, 1.2% [4.1% to -1.8%]; P=0.45) or secondary ischemic outcomes, including stent thrombosis (difference, 0.0% [1.3% to -1.3%]; P=1.00). Similarly, in the stable ischemic heart disease cohort, bivalirudin use was associated with lower bleeding (difference, -1.8% [-0.4% to -3.3%]; P=0.01; number need to treat=53) without increase in either primary (difference, 0.4% [2.3% to -1.5%]; P=0.70) or secondary ischemic outcomes, including stent thrombosis (difference, 0.0% [0.7% to -0.7%]; P=1.00) when compared with unfractionated heparin monotherapy. CONCLUSIONS: Among patients with non-ST-segment-elevation acute coronary syndromes or stable ischemic heart disease undergoing percutaneous coronary intervention, bivalirudin use during percutaneous coronary intervention when compared with unfractionated heparin monotherapy was associated with lower bleeding without significant increase in ischemic outcomes or stent thrombosis.

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Published In

Circ Cardiovasc Interv

DOI

EISSN

1941-7632

Publication Date

June 2014

Volume

7

Issue

3

Start / End Page

365 / 373

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Thrombosis
  • Risk Factors
  • Registries
  • Recombinant Proteins
  • Prospective Studies
  • Percutaneous Coronary Intervention
  • Peptide Fragments
  • Myocardial Ischemia
  • Middle Aged
 

Citation

APA
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ICMJE
MLA
NLM
Bangalore, Sripal, Michael J. Pencina, Neal S. Kleiman, and David J. Cohen. “Heparin monotherapy or bivalirudin during percutaneous coronary intervention in patients with non-ST-segment-elevation acute coronary syndromes or stable ischemic heart disease: results from the Evaluation of Drug-Eluting Stents and Ischemic Events registry.Circ Cardiovasc Interv 7, no. 3 (June 2014): 365–73. https://doi.org/10.1161/CIRCINTERVENTIONS.113.001126.

Published In

Circ Cardiovasc Interv

DOI

EISSN

1941-7632

Publication Date

June 2014

Volume

7

Issue

3

Start / End Page

365 / 373

Location

United States

Related Subject Headings

  • Treatment Outcome
  • Thrombosis
  • Risk Factors
  • Registries
  • Recombinant Proteins
  • Prospective Studies
  • Percutaneous Coronary Intervention
  • Peptide Fragments
  • Myocardial Ischemia
  • Middle Aged