Literature DB >> 19343162

Anti-Xa activity of enoxaparin and nadroparin in patients with acute coronary syndrome.

Petr Ostadal1, David Alan, Jiri Vejvoda, Jitka Segethova, Andreas Kruger.   

Abstract

BACKGROUND: Clinical studies have clearly revealed that low-molecular-weight heparins (LMWHs) are an effective alternative to unfractionated heparin in the therapy of acute coronary syndrome (ACS); however, data on the comparison of different LMWHs are sparse. AIM: To compare the inhibition of coagulation factor Xa by enoxaparin and nadroparin in the therapy of ACS.
METHODS: Thirty-eight consecutive patients with ACS were randomly assigned to enoxaparin (group E, n=18) or nadroparin (group N, n=20) in the recommended dose. Anti-Xa activity was measured 3 h after administering the first dose of LMWH.
RESULTS: Baseline demographics (age, sex) and clinical (type of ACS, pain-to-door time, elevation of troponin, percutaneous coronary intervention performed, smoking status, and history of diabetes, hypertension and hyperlipoproteinemia) characteristics were similar in both groups. Anti-Xa activity was significantly higher in group E than in group N (0.65+/-0.05 U/mL versus 0.30+/-0.03 U/mL; P<0.001). Moreover, the therapeutic target (0.5 U/mL to 0.8 U/mL) was achieved in 66.7% of patients in group E; on the other hand, effective therapy was observed in 10.0% of patients in group N (P<0.001).
CONCLUSIONS: The results of the present study demonstrate a highly significant difference in anti-Xa activity of enoxaparin and nadroparin in their recommended dosing regimens, in the therapy of ACS 3 h after subcutaneous administration; the anticoagulant effect of enoxaparin was markedly stronger than that of nadroparin.

Entities:  

Keywords:  Acute coronary syndrome; Enoxaparin; Factor Xa; Heparin; Nadroparin

Year:  2008        PMID: 19343162      PMCID: PMC2663480     

Source DB:  PubMed          Journal:  Exp Clin Cardiol        ISSN: 1205-6626


  19 in total

1.  A randomized, placebo-controlled trial of enoxaparin after high-risk coronary stenting: the ATLAST trial.

Authors:  W B Batchelor; K W Mahaffey; P B Berger; E Deutsch; S Meier; V Hasselblad; E T Fry; P S Teirstein; A M Ross; C A Binanay; J P Zidar
Journal:  J Am Coll Cardiol       Date:  2001-11-15       Impact factor: 24.094

2.  Randomized comparison of enoxaparin with unfractionated heparin following fibrinolytic therapy for acute myocardial infarction.

Authors:  S H Baird; I B A Menown; S J Mcbride; T G Trouton; C Wilson
Journal:  Eur Heart J       Date:  2002-04       Impact factor: 29.983

3.  A randomized controlled clinical trial to evaluate the efficacy, safety, cost-effectiveness and effect on PAI-1 levels of the three low-molecular-weight heparins--enoxaparin, nadroparin and dalteparin. The ESCAPe-END study.

Authors:  N Shafiq; S Malhotra; P Pandhi; N Sharma; A Bhalla; A Grover
Journal:  Pharmacology       Date:  2006-10-20       Impact factor: 2.547

4.  Randomized comparison of enoxaparin, a low-molecular-weight heparin, with unfractionated heparin adjunctive to recombinant tissue plasminogen activator thrombolysis and aspirin: second trial of Heparin and Aspirin Reperfusion Therapy (HART II).

Authors:  A M Ross; P Molhoek; C Lundergan; M Knudtson; Y Draoui; L Regalado; V Le Louer; F Bigonzi; W Schwartz; E de Jong; K Coyne
Journal:  Circulation       Date:  2001-08-07       Impact factor: 29.690

5.  Comparison of two treatment durations (6 days and 14 days) of a low molecular weight heparin with a 6-day treatment of unfractionated heparin in the initial management of unstable angina or non-Q wave myocardial infarction: FRAX.I.S. (FRAxiparine in Ischaemic Syndrome).

Authors: 
Journal:  Eur Heart J       Date:  1999-11       Impact factor: 29.983

6.  Postprocedural low molecular weight heparin in patients at high risk of subacute stent thrombosis.

Authors:  Amin Daoulah; Amit Segev; Kori Leblanc; Robert J Chisholm; Bradley H Strauss
Journal:  Cardiovasc Radiat Med       Date:  2003 Oct-Dec

Review 7.  Efficacy and bleeding complications among patients randomized to enoxaparin or unfractionated heparin for antithrombin therapy in non-ST-Segment elevation acute coronary syndromes: a systematic overview.

Authors:  John L Petersen; Kenneth W Mahaffey; Vic Hasselblad; Elliott M Antman; Marc Cohen; Shaun G Goodman; Anatoly Langer; Michael A Blazing; Anne Le-Moigne-Amrani; James A de Lemos; Christopher C Nessel; Robert A Harrington; James J Ferguson; Eugene Braunwald; Robert M Califf
Journal:  JAMA       Date:  2004-07-07       Impact factor: 56.272

8.  Enoxaparin vs unfractionated heparin in high-risk patients with non-ST-segment elevation acute coronary syndromes managed with an intended early invasive strategy: primary results of the SYNERGY randomized trial.

Authors:  James J Ferguson; Robert M Califf; Elliott M Antman; Marc Cohen; Cindy L Grines; Shaun Goodman; Dean J Kereiakes; Anatoly Langer; Kenneth W Mahaffey; Christopher C Nessel; Paul W Armstrong; Alvaro Avezum; Phil Aylward; Richard C Becker; Luigi Biasucci; Steven Borzak; Jacques Col; Marty J Frey; Ed Fry; Dietrich C Gulba; Sema Guneri; Enrique Gurfinkel; Robert Harrington; Judith S Hochman; Neal S Kleiman; Martin B Leon; Jose Luis Lopez-Sendon; Carl J Pepine; Witold Ruzyllo; Steven R Steinhubl; Paul S Teirstein; Luis Toro-Figueroa; Harvey White
Journal:  JAMA       Date:  2004-07-07       Impact factor: 56.272

9.  Guidelines for percutaneous coronary interventions. The Task Force for Percutaneous Coronary Interventions of the European Society of Cardiology.

Authors:  Sigmund Silber; Per Albertsson; Francisco F Avilés; Paolo G Camici; Antonio Colombo; Christian Hamm; Erik Jørgensen; Jean Marco; Jan-Erik Nordrehaug; Witold Ruzyllo; Philip Urban; Gregg W Stone; William Wijns
Journal:  Eur Heart J       Date:  2005-03-15       Impact factor: 29.983

10.  Nadroparine calcium or enoxaparine in acute coronary syndrome patients suffering renal insufficiency: The nadroparin versus enoxaparin (NaVe) study design.

Authors:  Enrique P Gurfinkel; Cecilia Perel; Gonzalo Pombo
Journal:  Thromb J       Date:  2004-06-08
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