Abstract | AIMS: METHODS AND RESULTS: The current analysis of a prospective registry included consecutive patients treated with EES or E-ZES for STEMI. Adjustment for measured confounders was done using Cox regression. In total, 931 patients met the inclusion criteria (412 EES and 519 E-ZES). Baseline characteristics were balanced, apart from a lower rate of renal insufficiency in EES. Median follow-up duration was 2.4 years (IQR 1.6-3.1). Mortality outcomes were similar. Up to three-year follow-up, the composite endpoint of cardiac death, target vessel-related myocardial infarction and target lesion revascularisation (TLR) was lower in EES; 9.7% vs. 13.7% in E-ZES (HR 0.64, 95% CI: 0.42-0.99), primarily driven by reduced TLR rates; 3.4% in EES vs. 7.3% in E-ZES (HR 0.46, 95% CI: 0.23-0.92). Definite stent thrombosis rates were low and similar between groups (1.1% in EES vs. 1.9% in E-ZES, p=0.190). CONCLUSIONS: Use of EES led to lower rates of the composite endpoint, driven by reduced TLR. This suggests that EES are more efficacious than Endeavor ZES in STEMI. Definite ST rates were low, and the strategy of second-generation DES implantation and the administration of upfront GP IIb/IIIa inhibitors appear to be safe in STEMI.
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Authors | Matthijs A Velders, Helèn Boden, Bas L van der Hoeven, Su-San Liem, Jaël Z Atary, Ernst E van der Wall, J Wouter Jukema, Martin J Schalij |
Journal | EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology
(EuroIntervention)
Vol. 8
Issue 10
Pg. 1199-206
(Feb 22 2013)
ISSN: 1969-6213 [Electronic] France |
PMID | 23425544
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Platelet Glycoprotein GPIIb-IIIa Complex
- Everolimus
- zotarolimus
- Sirolimus
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Topics |
- Adult
- Aged
- Drug-Eluting Stents
- Electrocardiography
- Everolimus
- Female
- Humans
- Male
- Middle Aged
- Myocardial Infarction
(therapy)
- Platelet Glycoprotein GPIIb-IIIa Complex
(antagonists & inhibitors)
- Proportional Hazards Models
- Registries
- Sirolimus
(administration & dosage, analogs & derivatives)
- Treatment Outcome
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