Benefits are confined to
patients with elevated troponin levels.
Percutaneous coronary intervention (PCI) is an
established therapy for patients with non–ST segment elevation acute
coronary syndromes (NSTE
The primary endpoint was a
composite of death, myocardial infarction, or urgent target vessel
revascularization within 30 days. Overall, the endpoint occurred in
significantly fewer abciximab recipients than
placebo recipients (8.9% vs. 11.9%), yielding a 25% reduction in
relative risk. In the subset of patients with elevated troponin
levels, the relative risk for the primary endpoint was reduced by
29% in the abciximab group, whereas in patients
without elevated troponin, risk did not
differ significantly between the two groups. There were no
significant differences between the abciximab and
placebo groups in the risk for major bleeding (1.4% and 1.4%), the
risk for minor bleeding (4.2% and 3.3%), and the need for transfusion
(2.5% and 2.0%).
Comment: Platelet activation and aggregability are greatly increased in patients
with NSTE
— John A. Marx, MD,
FAAEM, FACEP
Published in Journal Watch Emergency Medicine May
23, 2006
Source
Kastrati
A et al. Abciximab in patients with acute coronary
syndromes undergoing percutaneous coronary
intervention after clopidogrel pretreatment: The
ISAR-REACT 2 randomized trial. JAMA 2006 Apr 5; 295:1531-8.
Steinhubl
SR and Charnigo R. Clopidogrel
treatment prior to percutaneous coronary
intervention: When enough isn’t enough. JAMA 2006 Apr 5; 295:1581-2.