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SHR Neuro Cancer Cardio Lipid Metab Microb

Gurbel, PA; Bliden, KP; Saucedo, JF; Suarez, TA; DiChiara, J; Antonino, MJ; Mahla, E; Singla, A; Herzog, WR; Bassi, AK; Hennebry, TA; Gesheff, TB; Tantry, US.
Bivalirudin and clopidogrel with and without eptifibatide for elective stenting: effects on platelet function, thrombelastographic indexes, and their relation to periprocedural infarction results of the CLEAR PLATELETS-2 (Clopidogrel with Eptifibatide to Arrest the Reactivity of Platelets) study.
J Am Coll Cardiol. 2009; 53(8): 648-657. Doi: 10.1016/j.jacc.2008.10.045 [OPEN ACCESS]
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Co-authors Med Uni Graz
Mahla Elisabeth
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Abstract:
OBJECTIVES: The primary objective of this study was to compare the effect of therapy with bivalirudin alone versus bivalirudin plus eptifibatide on platelet reactivity measured by turbidometric aggregometry and thrombin-induced platelet-fibrin clot strength (TIP-FCS) measured by thrombelastography in percutaneous coronary intervention (PCI) patients. The secondary aim was to study the relation of platelet aggregation and TIP-FCS to the occurrence of periprocedural infarction. BACKGROUND: Bivalirudin is commonly administered alone to clopidogrel naïve (CN) patients and to patients on maintenance clopidogrel therapy (MT) undergoing elective stenting. The effect of adding eptifibatide to bivalirudin on platelet reactivity (PR) and TIP-FCS, and their relation to periprocedural infarction in these patients are unknown. METHODS: Patients (n = 200) stratified to clopidogrel treatment status were randomly treated with bivalirudin (n = 102) or bivalirudin plus eptifibatide (n = 98). One hundred twenty-eight CN patients were loaded with 600 mg clopidogrel immediately after stenting, and 72 MT patients were not loaded. The PR, TIP-FCS, and myonecrosis markers were serially determined. RESULTS: In CN and MT patients, bivalirudin plus eptifibatide was associated with markedly lower PR at all times (5- and 20-microM adenosine diphosphate-induced, and 15- and 25-microM thrombin receptor activator peptide-induced aggregation; p < 0.001 for all) and reduced mean TIP-FCS (p < 0.05). Patients who had a periprocedural infarction had higher mean 18-h PR (p < 0.0001) and TIP-FCS (p = 0.002). CONCLUSIONS: For elective stenting, the addition of eptifibatide to bivalirudin lowered PR to multiple agonists and the tensile strength of the TIP-FCS, 2 measurements strongly associated with periprocedural myonecrosis. Future studies of PR and TIP-FCS for elective stenting may facilitate personalized antiplatelet therapy and enhance the selection of patients for glycoprotein IIb/IIIa blockade. (Peri-Procedural Myocardial Infarction, Platelet Reactivity, Thrombin Generation, and Clot Strength: Differential Effects of Eptifibatide + Bivalirudin Versus Bivalirudin [CLEAR PLATELETS-2]; NCT00370045.
Find related publications in this database (using NLM MeSH Indexing)
Adenosine Diphosphate - pharmacology
Aged - pharmacology
Angioplasty, Transluminal, Percutaneous Coronary - adverse effects
Anticoagulants - administration and dosage
Blood Coagulation - drug effects
Blood Platelets - drug effects
Collagen - pharmacology
Drug Therapy, Combination - pharmacology
Female - pharmacology
Hemorheology - pharmacology
Hirudins - administration and dosage
Humans - administration and dosage
Male - administration and dosage
Middle Aged - administration and dosage
Myocardial Infarction - prevention and control
Peptide Fragments - administration and dosage
Peptides - administration and dosage
Platelet Aggregation - drug effects
Platelet Aggregation Inhibitors - administration and dosage
Receptors, Thrombin - physiology
Recombinant Proteins - administration and dosage
Stents - administration and dosage
Thrombelastography - administration and dosage
Ticlopidine - administration and dosage

Find related publications in this database (Keywords)
eptifibatide
clopidogrel
bivalirudin
platelets
myonecrosis
stents
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