Impact of abciximab in diabetic patients with acute coronary syndrome who undergo percutaneous coronary intervention: results from a high-volume, single-center registry

Research output: Contribution to journalJournal articleResearchpeer-review

  • Allan Iversen
  • Sune Ammentorp Haahr-Pedersen
  • Christian Joens
  • Rasmus Mogelvang
  • Soren Galatius
  • Anders Galloe
  • Ulrik Abildgaard
  • Hansen, Peter Riis
  • Jan K Madsen
  • Jan S Jensen
BACKGROUND:
The prevalence of diabetes mellitus (DM) and ischemic heart disease is increasing. Moreover, patients with DM experiencing an acute coronary syndrome (ACS) have an increased risk of adverse outcomes after revascularization compared to non-diabetics. Data have suggested that the glycoprotein IIb/IIIa inhibitor abciximab might be more efficient in diabetics than in those without DM.
METHODS AND RESULTS:
We evaluated the effect of abciximab in patients with DM and ACS from our percutaneous coronary intervention (PCI) registry. Among 5,003 patients with ACS who underwent PCI, 629 had DM. Patients were followed for up to 3 years with regard to mortality, myocardial infarction (MI) and target vessel revascularization (TVR). Despite a more severe risk profile, adjusted analyses revealed a marked reduction in TVR (hazard ratio [HR], 0.30; confidence interval [CI], 0.14-0.63; p = 0.002), mortality (HR, 0.53; CI, 0.28-0.97; p = 0.04) and the combined endpoint, also including MI (HR, 0.53; CI, 0.35-0.79; p = 0.002) in the DM patients who received abciximab compared to those who did not, resulting in a risk of reaching the endpoints at levels similar to the risk in patients without DM. The reduction in MI was not significant.
CONCLUSION:
Our findings suggest that abciximab administered to ACS patients with DM during PCI reduces mortality and the need for TVR to rates similar to those seen in patients without DM and far below the risk in DM patients who do not receive abciximab.
Original languageEnglish
JournalJournal of Invasive Cardiology
Volume23
Issue number1
Pages (from-to)21-6
Number of pages6
ISSN1042-3931
Publication statusPublished - 1 Jan 2011

ID: 34049821