Literature DB >> 14564315

Combining enoxaparin and glycoprotein IIb/IIIa antagonists for the treatment of acute coronary syndromes: final results of the National Investigators Collaborating on Enoxaparin-3 (NICE-3) study.

James J Ferguson1, Elliott M Antman, Eric R Bates, Marc Cohen, Nathan R Every, Robert A Harrington, Carl J Pepine, Pierre Theroux.   

Abstract

BACKGROUND: In high-risk patients with acute coronary syndromes (ACS), there have been concerns relating to the safety of using low molecular weight heparins (LMWH) in combination with a glycoprotein (GP) IIb/IIIa antagonist, and the continued use of LMWH in patients brought to the cardiac catheterization laboratory for percutaneous coronary intervention (PCI).
METHODS: The National Investigators Collaborating on Enoxaparin-3 (NICE-3) study was an open-label observational study of enoxaparin in combination with any 1 of 3 available GP IIb/IIIa antagonists in patients presenting with non-ST-elevation ACS. The primary end point was the incidence of major bleeding not related to coronary artery bypass graft (CABG) surgery. Data were also recorded on the incidence of death, myocardial infarction (MI), and urgent revascularization for repeat ischemia.
RESULTS: A total of 671 patients with validated data were treated with enoxaparin; 628 of these patients also received a GP IIb/IIIa antagonist (tirofiban, n = 229; eptifibatide, n = 272; abciximab, n = 127); 283 of 628 underwent percutaneous coronary intervention (PCI). The 30-day incidence of non-CABG major bleeding was 1.9%, and was not significantly higher than a prespecified historical control rate of 2.0%. Outcome events included death (1.0% at hospital discharge and 1.6% at 30 days), MI (3.5% and 5.1%, respectively), and urgent revascularization (2.7% and 6.8%, respectively).
CONCLUSIONS: The safety of enoxaparin plus a GP IIb/IIIa antagonist was comparable to that of unfractionated heparin plus a GP IIb/IIIa antagonist, as reported in other recent major trials. Patients undergoing PCI can be safely managed with enoxaparin and a GP IIb/IIIa antagonist, without supplemental use of unfractionated heparin.

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Year:  2003        PMID: 14564315     DOI: 10.1016/S0002-8703(03)00165-0

Source DB:  PubMed          Journal:  Am Heart J        ISSN: 0002-8703            Impact factor:   4.749


  12 in total

Review 1.  Low-molecular-weight heparins in the cardiac catheterization laboratory.

Authors:  Rajan A Kadakia; Shravantika R Baimeedi; James J Ferguson
Journal:  Tex Heart Inst J       Date:  2004

Review 2.  Optimal use of platelet glycoprotein IIb/IIIa receptor antagonists in patients undergoing percutaneous coronary interventions.

Authors:  H Benjamin Starnes; Ankit A Patel; George A Stouffer
Journal:  Drugs       Date:  2011-10-22       Impact factor: 9.546

Review 3.  Changing roles of anticoagulant and antiplatelet treatment during percutaneous coronary intervention.

Authors:  R V Kelly; S Steinhubl
Journal:  Heart       Date:  2005-06       Impact factor: 5.994

4.  Percutaneous coronary intervention: recommendations for good practice and training.

Authors:  K D Dawkins; T Gershlick; M de Belder; A Chauhan; G Venn; P Schofield; D Smith; J Watkins; H H Gray
Journal:  Heart       Date:  2005-12       Impact factor: 5.994

5.  The use of a HEMOCHRON JR. HEMONOX point of care test in monitoring the anticoagulant effects of enoxaparin during interventional coronary procedures.

Authors:  Soumaya El Rouby; Marc Cohen; Andrea Gonzales; Debra Hoppensteadt; Ted Lee; Marcia L Zucker; Khaula Khalid; Frank M Laduca; Jawed Fareed
Journal:  J Thromb Thrombolysis       Date:  2006-04       Impact factor: 2.300

6.  Efficacy of enoxaparin, certoparin and dalteparin in preventing cardiac catheter thrombosis: an in vitro approach.

Authors:  Uwe Raaz; Michael Buerke; Marese Busshardt; Lars Maegdefessel; Alexander Plehn; Baerbel Hauroeder; Karl Werdan; Axel Schlitt
Journal:  J Thromb Thrombolysis       Date:  2010-04       Impact factor: 2.300

7.  Catheter thrombosis during primary percutaneous coronary intervention for acute ST elevation myocardial infarction despite subcutaneous low-molecular-weight heparin, acetylsalicylic acid, clopidogrel and abciximab pretreatment.

Authors:  Christopher E Buller; Gordon E Pate; Paul W Armstrong; Blair J O'Neill; John G Webb; Richard Gallo; Robert C Welsh
Journal:  Can J Cardiol       Date:  2006-05-01       Impact factor: 5.223

8.  Low-molecular-weight heparin compared with unfractionated heparin for patients with non-ST-segment elevation acute coronary syndromes treated with glycoprotein IIb/IIIa inhibitors: results from the CRUSADE initiative.

Authors:  Kanwar P Singh; Matthew T Roe; Eric D Peterson; Anita Y Chen; Kenneth W Mahaffey; Shaun G Goodman; Robert A Harrington; Sidney C Smith; W Brian Gibler; E Magnus Ohman; Charles V Pollack
Journal:  J Thromb Thrombolysis       Date:  2006-06       Impact factor: 2.300

9.  Tolerability and feasibility of eptifibatide in acute coronary syndrome in patients at high risk for cardiovascular disease: A retrospective analysis.

Authors:  Zaher S Azzam; Elias Sa'ad; Amal Jabareen; Oron Eilam; Petru Bartha; Salim Hadad; Norberto Krivoy
Journal:  Curr Ther Res Clin Exp       Date:  2005-11

10.  Degree of anticoagulation after one subcutaneous and one subsequent intravenous booster dose of enoxaparin: implications for patients with acute coronary syndromes undergoing early percutaneous coronary intervention.

Authors:  Glenn N Levine; Tracy Ferrando
Journal:  J Thromb Thrombolysis       Date:  2004-06       Impact factor: 2.300

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