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- W1566561830 abstract "Background Drug-eluting stents (DES) may be associated with an increased risk of late stent thrombosis (ST) compared with bare metal stents (BMS). We compared major adverse cardiac events (MACE) and long term all cause mortality in patients with isolated proximal LAD disease treated with DES or BMS. Method and Results This study of 1653 patients with isolated proximal LAD disease, includes 643 treated with BMS and 1010 treated with DES. All patients received standard dual antiplatelet treatment. MACE after 5 years were less frequent in DES compared with BMS (12.1% 95% CI 9.3–14.2 versus 21.3% 95% CI: 16.9–25.1, P < 0.0001), driven largely by a decreased rate of both target vessel and lesion revascularization (TVR: 6.3%, 95% CI 4.0–7.5% versus 14.7%, 95% CI 11.0–17.3%, P < 0.0001, TLR: (5.3%, 95% CI 3.2–7.1% versus 13.2%, 95% CI 9.8.0–15.4%, P < 0.0001). There was no difference in the rate of death, myocardial infarction, or CVA. Incidence of stent thrombosis was also comparable (1.2% 95% CI: 0.6–2.6% versus 1.1% 95% CI: 0.6–2.5%, P = 0.8). Adjusted Cox analysis confirmed a decreased risk of MACE for DES compared with BMS 0.55 (95% confidence intervals 0.41–0.73) with no difference in the hazard of all cause mortality (HR: 1.04 95% CI: 0.67–1.61). Conclusion When treating proximal LAD disease, use of DES was associated with a lower MACE rate than BMS, with no differences in the incidence of stent thrombosis, myocardial infarction or 5 year all cause mortality. Our data suggests that despite the adverse prognostic correlates of proximal LAD disease, DES deployment in this location is both safe and clinically more effective than BMS. © 2012 Wiley Periodicals, Inc." @default.
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- W1566561830 date "2012-11-14" @default.
- W1566561830 modified "2023-09-30" @default.
- W1566561830 title "Deployment of drug-eluting stents for isolated proximal lad disease is associated with lower major adverse cardiac events and no increase in stent thrombosis when compared with bare metal stents: A 5-year observational cohort study" @default.
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- W1566561830 doi "https://doi.org/10.1002/ccd.24513" @default.
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