Literature DB >> 20578166

Heparin or enoxaparin anticoagulation for primary percutaneous coronary intervention.

David Brieger1, Jean-Philippe Collet, Johanne Silvain, Antoine Landivier, Olivier Barthélémy, Farzin Beygui, Anne Bellemain-Appaix, Anne Mercadier, Remi Choussat, Nicolas Vignolles, Dominique Costagliola, Gilles Montalescot.   

Abstract

OBJECTIVES: The aim of this study was to compare efficacy and safety outcomes among patients receiving enoxaparin or unfractionated heparin (UFH) while undergoing percutaneous coronary intervention (PCI) for ST-segment elevation myocardial infarction (STEMI).
BACKGROUND: Primary PCI (pPCI) for ST elevation has traditionally been supported by UFH. The low molecular weight heparin enoxaparin may provide better outcomes when used for pPCI.
METHODS: Consecutive eligible patients (580) undergoing pPCI enrolled in the prospective electronic Pitié-Salpêtrière registry of ischemic coronary syndromes (e-PARIS) registry were grouped according to whether they received UFH or enoxaparin as the sole anticoagulant. Logistic regression modeling, propensity-weighted adjustment, and sensitivity analyses were used to evaluate efficacy and safety endpoints for enoxaparin vs. UFH.
RESULTS: Enoxaparin was administered to 346 patients and UFH to 234 without ACT or anti-Xa guided dose adjustment. PCI was performed through the radial artery in 90%, with frequent (75%) use of GPIIb/IIIa antagonists. Patients receiving enoxaparin were more likely to be therapeutically anticoagulated during the procedure (68% vs. 50%, P < 0.0001) and were less likely to experience death or recurrent myocardial infarction (MI) in hospital (adjusted OR 0.28 95% CI (0.12-0.68) or by 30 days (adjusted OR 0.35 95% CI 0.16-0.81). All cause mortality was also reduced in hospital (adjusted OR 0.32, 95% CI (0.12-0.85) and to 30 days (adjusted OR 0.40 95% CI 0.17-0.99). Other ischemic endpoints were similarly reduced with enoxaparin. Thrombolysis in myocardial infarction (TIMI) major bleeding events were numerically fewer among patients receiving enoxaparin (1.2% vs. 2.6%, P = 0.2).
CONCLUSIONS: In patients with STEMI presenting for PCI, enoxaparin was associated with a reduction in all ischemic complications, more frequent therapeutic anticoagulation, and no increase in major bleeding when compared against unfractionated heparin. © 2010 Wiley-Liss, Inc.
Copyright © 2010 Wiley-Liss, Inc.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 20578166     DOI: 10.1002/ccd.22674

Source DB:  PubMed          Journal:  Catheter Cardiovasc Interv        ISSN: 1522-1946            Impact factor:   2.692


  4 in total

1.  Influence of Body Mass Index on the Activated Clotting Time Under Weight-Based Heparin Dose.

Authors:  Xia Hong; Pei-Ren Shan; Wei-Jian Huang; Qian-Li Zhu; Fang-Yi Xiao; Sheng Li; Hao Zhou
Journal:  J Clin Lab Anal       Date:  2014-11-25       Impact factor: 2.352

Review 2.  Administration of low molecular weight and unfractionated heparin during percutaneous coronary intervention.

Authors:  Sadegh Ali-Hassan-Sayegh; Seyed Jalil Mirhosseini; Azadeh Shahidzadeh; Parisa Mahdavi; Mahbube Tahernejad; Fatemeh Haddad; Mohammad Reza Lotfaliani; Anton Sabashnikov; Aron-Frederik Popov
Journal:  Indian Heart J       Date:  2016-01-26

Review 3.  Efficacy and safety of enoxaparin versus unfractionated heparin during percutaneous coronary intervention: systematic review and meta-analysis.

Authors:  Johanne Silvain; Farzin Beygui; Olivier Barthélémy; Charles Pollack; Marc Cohen; Uwe Zeymer; Kurt Huber; Patrick Goldstein; Guillaume Cayla; Jean-Philippe Collet; Eric Vicaut; Gilles Montalescot
Journal:  BMJ       Date:  2012-02-03

4.  Low-Dose Unfractionated Heparin with Sequential Enoxaparin in Patients with Diabetes Mellitus and Complex Coronary Artery Disease during Elective Percutaneous Coronary Intervention.

Authors:  Ji Huang; Nan Li; Zhao Li; Xue-Jian Hou; Zhi-Zhong Li
Journal:  Chin Med J (Engl)       Date:  2018-04-05       Impact factor: 2.628

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.