Article (Scientific journals)
Two-year clinical, angiographic, and intravascular ultrasound follow-up of the XIENCE V everolimus-eluting stent in the treatment of patients with de novo native coronary artery lesions: the SPIRIT II trial.
Claessen, Bimmer E.; Beijk, Marcel A.; Legrand, Victor et al.
2009In Circulation. Cardiovascular Interventions, 2 (4), p. 339-47
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Keywords :
Aged; Angioplasty, Balloon, Coronary/adverse effects/instrumentation/mortality; Cardiovascular Agents/administration & dosage; Coronary Angiography; Coronary Artery Disease/mortality/radiography/therapy/ultrasonography; Drug-Eluting Stents; Europe; Female; Humans; India; Kaplan-Meier Estimate; Male; Middle Aged; Myocardial Infarction/etiology/radiography/ultrasonography; Myocardial Ischemia/etiology/radiography/ultrasonography; New Zealand; Paclitaxel/administration & dosage; Prospective Studies; Single-Blind Method; Sirolimus/administration & dosage/analogs & derivatives; Thrombosis/etiology/radiography/ultrasonography; Time Factors; Treatment Outcome; Ultrasonography, Interventional
Abstract :
[en] BACKGROUND: This article reports the 2-year clinical, angiographic, and intravascular ultrasound outcomes of the everolimus-eluting stent (EES) compared with the paclitaxel-eluting stent (PES) in the randomized SPIRIT II trial. METHODS AND RESULTS: This was a prospective, single-blind clinical trial in which a total of 300 patients with de novo native coronary artery lesions were randomized to either EES or PES in a 3:1 fashion. Clinical follow-up was planned at 2 years in all patients. A subset of 152 patients underwent serial angiographic and intravascular ultrasound analyses at 6 months and 2 years. After 2 years, target lesion failure (cardiac death, myocardial infarction, and ischemia-driven target lesion revascularization) rates were 6.6% and 11% in EES and PES, respectively (P=0.31). At 6 months, a significant reduction in angiographic in-stent late loss and percentage volume obstruction measured by intravascular ultrasound was observed in the EES group. However, at 2-year follow-up, a late increased intimal hyperplasia growth after implantation of an EES was observed. There were no significant differences between EES and PES for in-stent late loss (EES, 0.33+/-0.37 mm versus PES, 0.34+/-0.34 mm; P=0.84) and percentage volume obstruction (EES, 5.18+/-6.22% versus PES, 5.80+/-6.31%; P=0.65) at 2 years. The incidence of stent thrombosis was low and comparable in both groups (EES, 0.9%; PES, 1.4%). CONCLUSIONS: Although the previously reported angiographic and clinical superiority of the EES has vanished over time, this report confirms and extends the previously demonstrated noninferiority in terms of in-stent late loss of the EES when compared with the PES up to 2-year follow-up. There were no significant differences between EES and PES in clinical, angiographic and intravascular ultrasound outcomes at 2 years.
Disciplines :
Cardiovascular & respiratory systems
Author, co-author :
Claessen, Bimmer E.
Beijk, Marcel A.
Legrand, Victor ;  Université de Liège - ULiège > Département des sciences cliniques > Cardiologie
Ruzyllo, Witold
Manari, Antonio
Varenne, Olivier
Suttorp, Maarten J.
Tijssen, Jan G. P.
Miquel-Hebert, Karine
Veldhof, Susan
Henriques, Jose P. S.
Serruys, Patrick W.
Piek, Jan J.
More authors (3 more) Less
Language :
English
Title :
Two-year clinical, angiographic, and intravascular ultrasound follow-up of the XIENCE V everolimus-eluting stent in the treatment of patients with de novo native coronary artery lesions: the SPIRIT II trial.
Publication date :
2009
Journal title :
Circulation. Cardiovascular Interventions
ISSN :
1941-7640
eISSN :
1941-7632
Publisher :
Lippincott Williams & Wilkins, United States - Texas
Volume :
2
Issue :
4
Pages :
339-47
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBi :
since 26 May 2014

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