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Platelet glycoprotein IIb/IIIa receptor inhibition in non-ST-elevation acute coronary syndromes: early benefit during medical treatment only, with additional protection during percutaneous coronary intervention.

AbstractBACKGROUND:
Glycoprotein (GP) IIb/IIIa receptor blockers prevent life-threatening cardiac complications in patients with acute coronary syndromes without ST-segment elevation and protect against thrombotic complications associated with percutaneous coronary interventions (PCIs). The question arises as to whether these 2 beneficial effects are independent and additive.
METHODS AND RESULTS:
We analyzed data from the CAPTURE, PURSUIT, and PRISM-PLUS randomized trials, which studied the effects of the GP IIb/IIIa inhibitors abciximab, eptifibatide, and tirofiban, respectively, in acute coronary syndrome patients without persistent ST-segment elevation, with a period of study drug infusion before a possible PCI. During the period of pharmacological treatment, each trial demonstrated a significant reduction in the rate of death or nonfatal myocardial infarction in patients randomized to the GP IIb/IIIa inhibitor compared with placebo. The 3 trials combined showed a 2.5% event rate in this period in the GP IIb/IIIa inhibitor group (N=6125) versus 3.8% in placebo (N=6171), which implies a 34% relative reduction (P<0.001). During study medication, a PCI was performed in 1358 patients assigned GP IIb/IIIa inhibition and 1396 placebo patients. The event rate during the first 48 hours after PCI was also significantly lower in the GP IIb/IIIa inhibitor group (4. 9% versus 8.0%; 41% reduction; P<0.001). No further benefit or rebound effect was observed beyond 48 hours after the PCI.
CONCLUSIONS:
There is conclusive evidence of an early benefit of GP IIb/IIIa inhibitors during medical treatment in patients with acute coronary syndromes without persistent ST-segment elevation. In addition, in patients subsequently undergoing PCI, GP IIb/IIIa inhibition protects against myocardial damage associated with the intervention.
AuthorsE Boersma, K M Akkerhuis, P Théroux, R M Califf, E J Topol, M L Simoons
JournalCirculation (Circulation) Vol. 100 Issue 20 Pg. 2045-8 (Nov 16 1999) ISSN: 1524-4539 [Electronic] United States
PMID10562258 (Publication Type: Journal Article, Review)
Chemical References
  • Antibodies, Monoclonal
  • Immunoglobulin Fab Fragments
  • Peptides
  • Platelet Aggregation Inhibitors
  • Platelet Glycoprotein GPIIb-IIIa Complex
  • Tyrosine
  • Tirofiban
  • Eptifibatide
  • Abciximab
Topics
  • Abciximab
  • Angina, Unstable (drug therapy)
  • Angioplasty, Balloon, Coronary
  • Antibodies, Monoclonal (therapeutic use)
  • Electrocardiography
  • Eptifibatide
  • Female
  • Humans
  • Immunoglobulin Fab Fragments (therapeutic use)
  • Male
  • Middle Aged
  • Peptides (therapeutic use)
  • Platelet Aggregation Inhibitors (therapeutic use)
  • Platelet Glycoprotein GPIIb-IIIa Complex (antagonists & inhibitors)
  • Randomized Controlled Trials as Topic
  • Tirofiban
  • Tyrosine (analogs & derivatives, therapeutic use)

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