Avoiding and Managing Bleeding Complications in Patients with Non-ST-Segment Elevation Acute Coronary Syndromes

Angiology ◽  
2008 ◽  
Vol 60 (2) ◽  
pp. 148-158 ◽  
Author(s):  
Thomas Z. Potsis ◽  
Christos Katsouras ◽  
John A. Goudevenos

Antithrombotic therapy coupled with early use of cardiac catheterization and revascularization have decreased morbidity and mortality rates in patients who have acute ischemic heart disease but who carry a risk for bleeding. Bleeding complications in patients with acute coronary syndromes are associated with worse clinical outcomes, including recurrent ischemic events and death. Determining the appropriate balance between preventing ischemic events and causing bleeding in patients with acute coronary syndromes present a challenging problem for clinicians. Antithrombotics studied in recent clinical trials that have focused on bleeding reduction include bivalirudin and fondaparinux. In this review, the incidence, predictors, and clinical outcomes associated with bleeding are discussed. Furthermore, the association between antithrombotic agents and bleeding and propose strategies to prevent bleeding complications are also discussed.

2016 ◽  
Vol 9 (22) ◽  
pp. 2267-2276 ◽  
Author(s):  
Laurent Bonello ◽  
Marc Laine ◽  
Etienne Puymirat ◽  
Gilles Lemesle ◽  
Franck Thuny ◽  
...  

Circulation ◽  
2008 ◽  
Vol 118 (suppl_18) ◽  
Author(s):  
Somjot S Brar ◽  
Brent T McLaurin ◽  
David A Cox ◽  
Michel E Bertrand ◽  
A. Michael Lincoff ◽  
...  

Background : Among patients with non ST-segment elevation acute coronary syndromes (ACS), those with biomarker elevation represent a high-risk cohort. The optimal anticoagulation strategy during PCI in this group remains controversial. We therefore examined the clinical outcomes among biomarker positive patients in the ACUITY trial who underwent PCI. Methods : In ACUITY 13,819 patients with ACS were randomized to bivalirudin alone vs. bivalirudin plus glycoprotein IIb/IIIa inhibitor (GPI) vs. heparin plus GPI among; 7,789 patients underwent PCI, of whom 4,687 were biomarker (troponin and/or CKMB) positive. The primary endpoints at 30 days were composite ischemia (death, MI, or unplanned TVR for ischemia), major bleeding not related to CABG, and net adverse clinical events (NACE; composite ischemia or major bleeding). Results : Of the biomarker positive patients undergoing PCI, 1,611 were randomized to bivalirudin alone, 1,532 to heparin plus GPI, and 1,544 to bivalirudin plus GPI. The groups were well balanced for age, gender, and major co-morbidities such as diabetes, hypertension, hyperlipidemia, prior MI, renal insufficiency and TIMI risk score (p ≥ 0.1 for all). 30-day and 1 year outcomes are shown. Among the patients pre-treated with a thienopyridine, bivalirudin compared to heparin plus GPI resulted in reduced major bleeding (3.9% vs. 6.8%, p=0.003) and comparable rates of composite ischemia (8.4% vs. 8.1%, p=0.73) and NACE (11.5% vs. 13.1%, p=0.17). Conclusions : In biomarker positive ACS patients undergoing PCI, bivalirudin alone suppresses adverse ischemic events to a similar extent as does heparin plus GPI while decreasing major bleeding complications.


2007 ◽  
Vol 71 (2) ◽  
pp. 186-190 ◽  
Author(s):  
Masami Kosuge ◽  
Toshiaki Ebina ◽  
Toshiyuki Ishikawa ◽  
Kiyoshi Hibi ◽  
Kengo Tsukahara ◽  
...  

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