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

Citation
Ml. Simmons et al., 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, LANCET, 357(9272), 2001, pp. 1915-1924
Citations number
35
Categorie Soggetti
General & Internal Medicine","Medical Research General Topics
Journal title
LANCET
ISSN journal
01406736 → ACNP
Volume
357
Issue
9272
Year of publication
2001
Pages
1915 - 1924
Database
ISI
SICI code
0140-6736(20010616)357:9272<1915:EOGIRB>2.0.ZU;2-Q
Abstract
Background Glycoprotein IIb/IIIa blockers reduce procedure-related thrombot ic complications of percutaneous coronary intervention, and the risk of dea th 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 n ot 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 concentrati ons. 2598 were randomly assigned placebo, 2590 an abciximab bolus and 24 h infusion, and 2612 an abciximab bolus and 48 h infusion; all patients recei ved aspirin and either unfractionated or low-molecular-weight heparin. The primary endpoint was death or myocardial infarction at 30 days after random isation. Analysis was by intention to treat. Findings There were no dropouts. 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 myocardi al infarction before day 30 (odds ratio 1.0 [95% CI 0.83-1.24], for differe nce between placebo and 24 h abciximab, and 1.1[0.94-1.39] for difference b etween 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 concentrati ons at enrolment, although these patients did have a strongly increased ris k of subsequent events. Bleeding rates were low, but increased with abcixim ab, particularly when continued for 48 h. Additionally, thrombocytopenia wa s more frequent with abciximab than with placebo. Interpretations Although the explanations for our findings are unclear, thi s study indicates that abciximab is not beneficial as first-line medical tr eatment in patients admitted with acute coronary syndromes.