Literature DB >> 11156724

Low-molecular-weight heparin therapy in percutaneous coronary intervention: the NICE 1 and NICE 4 trials. National Investigators Collaborating on Enoxaparin Investigators.

J J Young1, D J Kereiakes, C L Grines.   

Abstract

Early coronary intervention in patients with non-ST segment elevation acute coronary syndromes (ACS) may be facilitated by adjunctive pharmacotherapies. Concomitant therapies such as low-molecular-weight heparins and platelet glycoprotein (GP) IIb/IIIa receptor blockade offer advantages in safety and efficacy during coronary intervention. Data from randomized clinical trials support the administration of both enoxaparin and platelet GP IIb/IIIa blockade to patients who present with non-ST segment elevation ACS. Enoxaparin, with its proven efficacy, predictability of action, and ease of administration, has been shown to be superior to unfractionated heparin in preventing major coronary events. Abciximab administration during percutaneous coronary intervention (PCI) reduces the incidence of ischemic adverse outcomes and appears to improve survival in long-term follow-up. The preliminary experience with combining these two therapies during PCI in the NICE 4 trial demonstrates a low incidence of minor/major bleeding and transfusion, and infrequent major cardiac events to 30 days follow-up. Algorithms for the use of these newer adjunctive pharmacotherapies in the care of patients presenting to the cardiac catheterization laboratory are presented.

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Year:  2000        PMID: 11156724

Source DB:  PubMed          Journal:  J Invasive Cardiol        ISSN: 1042-3931            Impact factor:   2.022


  9 in total

Review 1.  Unstable angina and non-ST-segment elevation myocardial infarction: perspectives on combination therapy.

Authors:  R P Villareal; P Kim; J J Ferguson; J M Wilson
Journal:  Tex Heart Inst J       Date:  2001

Review 2.  Choice of agents to limit the coagulation cascade in acute coronary syndromes.

Authors:  Richard C Becker
Journal:  Curr Cardiol Rep       Date:  2002-07       Impact factor: 2.931

3.  Identification of the heparin-binding domains of the interferon-induced protein kinase, PKR.

Authors:  Stephen Fasciano; Brian Hutchins; Indhira Handy; Rekha C Patel
Journal:  FEBS J       Date:  2005-03       Impact factor: 5.542

4.  Between-subject variability: should high be the new normal?

Authors:  Hesham S Al-Sallami; Song Lim Cheah; Shiou Yii Han; Joel Liew; Jin Lim; Mary Anne Ng; Hayneil Solanki; Run Jie Soo; Victoria Tan; Stephen B Duffull
Journal:  Eur J Clin Pharmacol       Date:  2014-09-05       Impact factor: 2.953

5.  Regulation of vascular smooth muscle proliferation by heparin: inhibition of cyclin-dependent kinase 2 activity by p27(kip1).

Authors:  Stephen Fasciano; Rekha C Patel; Indhira Handy; Chandrashekhar V Patel
Journal:  J Biol Chem       Date:  2005-02-24       Impact factor: 5.157

Review 6.  Modulating thrombotic potential in catheter-based percutaneous coronary and peripheral vascular interventions.

Authors:  James L Orford; Peter B Berger
Journal:  J Thromb Thrombolysis       Date:  2004-02       Impact factor: 2.300

7.  Recommendations on percutaneous coronary intervention for the reperfusion of acute ST elevation myocardial infarction.

Authors:  G Montalescot; H R Andersen; D Antoniucci; A Betriu; M J de Boer; L Grip; F J Neumann; M T Rothman
Journal:  Heart       Date:  2004-06       Impact factor: 5.994

8.  Safety of enoxaparin versus unfractionated heparin during percutaneous coronary intervention.

Authors:  José G Díez; Hector M Medina; Benjamin Y C Cheong; Lawrence O'Meallie; James J Ferguson
Journal:  Tex Heart Inst J       Date:  2009

Review 9.  Pharmacodynamic and pharmacokinetic properties of enoxaparin : implications for clinical practice.

Authors:  Jawed Fareed; Debra Hoppensteadt; Jeanine Walenga; Omer Iqbal; Qing Ma; Walter Jeske; Taqdees Sheikh
Journal:  Clin Pharmacokinet       Date:  2003       Impact factor: 6.447

  9 in total

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