Key result
Sirolimus-eluting stents for bare-metal in-stent restenosis showed a progressive decline in freedom from major adverse cardiovascular events, reaching 75.4% at 24 months and 65.8% at 30 months.
Why the study?
Does sirolimus-eluting stent implantation prevent major adverse cardiovascular events in patients with bare-metal in-stent restenosis?
Cohort (n=271)
Yes
Does sirolimus-eluting stent implantation prevent major adverse cardiovascular events in patients with bare-metal in-stent restenosis?
While sirolimus-eluting stents are effective for bare-metal in-stent restenosis in the mid-term, there is a late catch-up phenomenon with freedom from MACE decreasing to 65.8% at 30 months.
Progressive MACE rise after sirolimus-eluting stents for bare-metal in-stent restenosis warrants long-term caution; leaves open optimal strategies in randomized trials.
OBJECTIVES: In-stent restenosis occurs not infrequently after intracoronary implantation of bare-metal stents. Many techniques have been proposed for the treatment of in-stent restenosis, but drug-eluting stents seem to provide the best early and mid-term results. We aimed to appraise whether the effectiveness of drug-eluting stents for in-stent restenosis is maintained even in the long term. METHODS: Participants in this prospective multicenter study were patients with in-stent restenosis treated with sirolimus-eluting stents. The primary endpoint was freedom from major adverse cardiovascular events (i.e. death, nonfatal myocardial infarction, target vessel revascularization, or stent thrombosis) in the long term (> or =24 months), with 6-month angiography planned for all patients. RESULTS: A total of 271 consecutive patients were enrolled (332 sirolimus-eluting stents). Procedural success was obtained in all patients, with no case of in-hospital death, acute/subacute stent thrombosis, stroke, or urgent coronary bypass. Survival free from major cardiovascular events decreased progressively from 98.8% at 1 month, to 95.7, 83.7, 75.4, and 65.8% at 6, 12, 24, and 30 months, respectively. A similar attrition in freedom from repeat target vessel was found from 97.6% at 6 months to 76.7% at 30 months. A total of four possible and one definite stent thromboses (2.6%) were noted, all occurring several months after clopidogrel discontinuation and in patients on life-long aspirin. CONCLUSION: The present study supports the mid-term safety and effectiveness of sirolimus-eluting stents for the treatment of in-stent restenosis in comparison with the other available treatments. Whether the late catch-up phenomenon observed in repeat target revascularization and stent thrombosis is an incidental finding deserves further rigorous scrutiny.
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Sheiban et al. (2008) conducted a cohort in in-stent restenosis (n=271). Sirolimus-eluting stents was evaluated on freedom from major adverse cardiovascular events (death, nonfatal myocardial infarction, target vessel revascularization, or stent thrombosis) in the long term (≥24 months). Sirolimus-eluting stents for bare-metal in-stent restenosis showed a progressive decline in freedom from major adverse cardiovascular events, reaching 75.4% at 24 months and 65.8% at 30 months.
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