Why the study?
Does the efficacy of thienopyridine therapy (measured by platelet aggregation) influence the composite endpoint of cardiovascular death, myocardial infarction, and revascularisation in patients after coronary stent implantation?
Cohort (n=134)
Does the efficacy of thienopyridine therapy (measured by platelet aggregation) influence the composite endpoint of cardiovascular death, myocardial infarction, and revascularisation in patients after coronary stent implantation?
Answers are grounded in this paper and cite their sources.
Interindividual variability in response to thienopyridine therapy is significantly associated with late adverse clinical outcomes after coronary stent implantation.
Clinical significance of resistance to aspirin and thienopyridine therapy is poorly defined. The authors aimed to evaluate whether more effective antiplatelet therapy is associated with better outcome in patients on dual-antiplatelet treatment. Using optical aggregometer, maximal platelet aggregation values were measured with induction of adenosine diphosphate, collagen, and adrenaline 30 +/- 5 days after coronary stent implantation in 134 patients. Markers of platelet activation were also analyzed with fluorescent immunoassay in 57 patients. After 10 months of follow-up, 33 patients reached the composite endpoint of cardiovascular death, myocardial infarction, and revascularisation. Adenosine diphosphate-induced maximal aggregation values were in significant relationship with the development of major adverse cardiac events (P < .01). Level of soluble P-selectin proved to be an independent risk factor of adverse outcome (P < .05). As efficacy of thienopyridine therapy showed significant relation with clinical outcome, the authors conclude that interindividual variability in response to adenosine diphosphate-receptor antagonists may be of substantial clinical importance.
No takes yet. Share an insight, caveat, or question.
Aradi et al. (2008) conducted a cohort in Coronary stent implantation (n=134). Adenosine diphosphate-induced maximal platelet aggregation was evaluated on Composite endpoint of cardiovascular death, myocardial infarction, and revascularisation (p=< .01).
Synapse has enriched 10 related papers. Consider them for comparative context: