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Five-year clinical outcomes of sirolimus-eluting versus paclitaxel-eluting stents in high-risk patients
Catheterization and cardiovascular interventions, 2011-03, Vol.77 (4), p.494-501
Birkmeier, K. Anette
Kastrati, Adnan
Byrne, Robert A.
Holle, Heidrun
Schulz, Stefanie
Tiroch, Klaus
Kufner, Sebastian
Massberg, Steffen
Laugwitz, Karl-Ludwig
Schömig, Albert
Mehilli, Julinda
2011
Volltextzugriff (PDF)
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Autor(en) / Beteiligte
Birkmeier, K. Anette
Kastrati, Adnan
Byrne, Robert A.
Holle, Heidrun
Schulz, Stefanie
Tiroch, Klaus
Kufner, Sebastian
Massberg, Steffen
Laugwitz, Karl-Ludwig
Schömig, Albert
Mehilli, Julinda
Titel
Five-year clinical outcomes of sirolimus-eluting versus paclitaxel-eluting stents in high-risk patients
Ist Teil von
Catheterization and cardiovascular interventions, 2011-03, Vol.77 (4), p.494-501
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
2011
Quelle
Wiley Blackwell Single Titles
Beschreibungen/Notizen
Objectives and Background: First generation drug‐eluting stents have shown differential efficacy in high‐risk patient subsets at one year. It is unclear whether these differences endure over the medium‐ to long‐term. We compared the five‐year clinical efficacy and safety of sirolimus‐eluting stents (SES) and paclitaxel‐eluting stents (PES) in a population of high‐risk patients. Methods: The patient cohorts of the ISAR‐DESIRE, ISAR‐DIABETES, and ISAR‐SMART‐3 randomized trials were followed up for five years and data were pooled. The primary efficacy endpoint of the analysis was the need for target lesion revascularization (TLR) during a five‐year follow‐up period. The primary safety endpoint was the combination of death or myocardial infarction (MI) after five years. Results: A total of 810 patients (405 patients in the SES group and 405 patients in the PES group) was included. Over five years TLR was reduced by 39% with SES compared with PES stent (hazard ratio [HR] 0.61; 95% confidence interval [CI] 0.44–0.85; P = 0.004). No difference was observed according to death or MI rates between the two groups (HR 1.10; 95% CI 0.80–1.50; P = 0.57). Definite stent thrombosis occurred in 0.2% (n = 1) in the SES group and in 1.6% (n = 6) in the PES group (HR 0.16; 95% CI 0.02–1.34; P = 0.12). Conclusions: In high‐risk patient subsets the lower rate of 12‐month TLR observed with SES in comparison PES is maintained out to five years. In terms of safety, although there was no difference in the overall incidence of death or MI, there was a trend towards more frequent stent thromboses with PES. © 2011 Wiley‐Liss, Inc.
Sprache
Englisch
Identifikatoren
ISSN: 1522-1946
eISSN: 1522-726X
DOI: 10.1002/ccd.22757
Titel-ID: cdi_proquest_miscellaneous_853995302
Format
–
Schlagworte
Aged
,
Angioplasty, Balloon, Coronary - adverse effects
,
Angioplasty, Balloon, Coronary - instrumentation
,
Angioplasty, Balloon, Coronary - mortality
,
Cardiovascular Agents - administration & dosage
,
Chi-Square Distribution
,
Coronary Angiography
,
Coronary Restenosis - etiology
,
Coronary Stenosis - diagnostic imaging
,
Coronary Stenosis - mortality
,
Coronary Stenosis - therapy
,
Disease-Free Survival
,
drug-eluting stent
,
Drug-Eluting Stents
,
Female
,
Humans
,
Kaplan-Meier Estimate
,
long-term outcome
,
Male
,
Middle Aged
,
Myocardial Infarction - etiology
,
paclitaxel
,
Paclitaxel - administration & dosage
,
Proportional Hazards Models
,
Randomized Controlled Trials as Topic
,
Risk Assessment
,
Risk Factors
,
sirolimus
,
Sirolimus - administration & dosage
,
stent thrombosis
,
target lesion revascularization
,
Thrombosis - etiology
,
Time Factors
,
Treatment Outcome
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