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Article (Scientific journals)
Randomised comparison of implantation of heparin-coated stents with balloon angioplasty in selected patients with coronary artery disease (Benestent II)
Serruys, P. W.; van Hout, B.; Bonnier, H. et al.
1998In The Lancet, 352 (9129), p. 673-81
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Keywords :
Adult; Aged; Angina Pectoris/mortality/therapy; Angina, Unstable/mortality/therapy; Angioplasty, Balloon, Coronary; Anticoagulants/therapeutic use; Aspirin/therapeutic use; Coronary Angiography; Equipment Design; Female; Heparin/therapeutic use; Humans; Male; Middle Aged; Platelet Aggregation Inhibitors/therapeutic use; Stents; Survival Analysis; Ticlopidine/therapeutic use; Treatment Outcome
Abstract :
[en] BACKGROUND: The multicentre, randomised Benestent-II study investigated a strategy of implantation of a heparin-coated Palmar-Schatz stent plus antiplatelet drugs compared with the use of balloon angioplasty in selected patients with stable or stabilised unstable angina, with one or more de-novo lesions, less than 18 mm long, in vessels of diameter 3 mm or more. METHODS: 827 patients were randomly assigned stent implantation (414 patients) or standard balloon angioplasty (413 patients). The primary clinical endpoint was event-free survival at 6 months, including death, myocardial infarction, and the need for revascularisation. The secondary endpoints were the restenosis rate at 6 months and the cost-effectiveness at 12 months. There was also one-to-one subrandomisation to either clinical and angiographic follow-up or clinical follow-up alone. Analyses were by intention to treat. FINDINGS: Four patients (one stent group, three angioplasty group) were excluded from analysis since no lesion was found. At 6 months, a primary clinical endpoint had occurred in 53 (12.8%) of 413 patients in the stent group and 79 (19.3%) of 410 in the angioplasty group (p=0.013). This significant difference in clinical outcome was maintained at 12 months. In the subgroup assigned angiographic follow-up, the mean minimum lumen diameter was greater in the stent group than in the balloon-angioplasty group, (1.89 [SD 0.65] vs 1.66 [0.57] mm, p=0.0002), which corresponds to restenosis rates (diameter stenosis > or =50%) of 16% and 31% (p=0.0008). In the group assigned clinical follow-up alone, event-free survival rate at 12 months was higher in the stent group than the balloon-angioplasty group (0.89 vs 0.79, p=0.004) at a cost of an additional 2085 Dutch guilders (US$1020) per patient. INTERPRETATION: Over 12-month follow-up, a strategy of elective stenting with heparin-coated stents is more effective but also more costly than balloon angioplasty.
Disciplines :
Cardiovascular & respiratory systems
Author, co-author :
Serruys, P. W.
van Hout, B.
Bonnier, H.
Legrand, Victor ;  Université de Liège - ULiège > Département des sciences cliniques > Cardiologie
Garcia, E.
Macaya, C.
Sousa, E.
van der Giessen, W.
Colombo, A.
Seabra-Gomes, R.
Kiemeneij, F.
Ruygrok, P.
Ormiston, J.
Emanuelsson, H.
Fajadet, J.
Haude, M.
Klugmann, S.
Morel, M. A.
More authors (8 more) Less
Language :
English
Title :
Randomised comparison of implantation of heparin-coated stents with balloon angioplasty in selected patients with coronary artery disease (Benestent II)
Publication date :
1998
Journal title :
The Lancet
ISSN :
0140-6736
eISSN :
1474-547X
Publisher :
Elsevier
Volume :
352
Issue :
9129
Pages :
673-81
Peer reviewed :
Peer Reviewed verified by ORBi
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since 01 June 2014

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