EFFECT
OF GLYCOPROTEIN IIB/IIIA RECEPTOR BLOCKER ABCIXIMAB ON OUTCOME IN PATIENTS WITH
ACUTE CORONARY SYNDROMES WITHOUT EARLY CORONARY REVASCULARISATION: THE GUSTO
IV-ACS RANDOMISED TRIAL
Simoons
ML; GUSTO IV-ACS Investigators. Lancet 2001 Jun 16;357(9272):1915-24.
BACKGROUND:
Glycoprotein IIb/IIIa blockers reduce procedure-related thrombotic
complications of percutaneous coronary intervention, and the risk of death and
myocardial infarction in patients with acute coronary syndromes. The effect on
risk of death and myocardial infarction is particularly apparent in patients
undergoing early percutaneous coronary interventions. We did a randomised,
multicentre trial to study the effect of the glycoprotein IIb/IIIa blocker
abciximab on patients with acute coronary syndromes who were not undergoing
early revascularisation.
METHODS:
We enrolled 7800 patients who were admitted to hospital with chest pain and
either ST-segment depression or raised troponin T or I concentrations. 2598
were randomly assigned placebo, 2590 an abciximab bolus and 24 h infusion, and
2612 an abciximab bolus and 48 h infusion; all patients received aspirin and
either unfractionated or low-molecular-weight heparin. The primary endpoint was
death or myocardial infarction at 30 days after randomisation. Analysis was by
intention to treat.
FINDINGS:
There were no drop-outs. 209 (8.0%) patients on placebo, 212 (8.2%) on 24 h
abciximab, and 238 (9.1%) on 48 h abciximab died or had a myocardial infarction
before day 30 (odds ratio 1.0 [95% CI 0.83-1.24], for difference between
placebo and 24 h abciximab, and 1.1 [0.94-1.39] for difference between placebo
and 48 h abciximab). The lack of benefit from treatment with abciximab was
consistent in most subgroups investigated; in particular, no benefit was seen
in patients with raised cardiac troponin T or I concentrations at enrolment,
although these patients did have a strongly increased risk of subsequent
events. Bleeding rates were low, but increased with abciximab, particularly
when continued for 48 h. Additionally, thrombocytopenia was more frequent with
abciximab than with placebo.
INTERPRETATIONS:
Although the explanations for our findings are unclear, this study indicates
that abciximab is not beneficial as first-line medical treatment in patients
admitted with acute coronary syndromes.