Randomised comparison of implantation of heparin-coated stents with balloon angioplasty in selected patients with coronary artery disease (Benestent II)

被引:479
|
作者
Serruys, PW
van Hout, B
Bonnier, H
Legrand, V
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, MA
机构
[1] Univ Rotterdam Hosp, Ctr Thorax, Rotterdam, Netherlands
[2] Erasmus Univ, Inst Med Technol, NL-3015 GD Rotterdam, Netherlands
[3] Catharina Hosp, Eindhoven, Netherlands
[4] CHU, Liege, Belgium
[5] Gregorio Maranon, Madrid, Spain
[6] Univ Hosp San Carlos, Madrid, Spain
[7] Inst Dante Pazzanese, Sao Paulo, Brazil
[8] Ctr Cuore Columbus, Milan, Italy
[9] Hosp Santa Cruz, Linda A Velha, Portugal
[10] Onze Lieve Vrouw Hosp, Amsterdam, Netherlands
[11] Green Lane Hosp, Auckland 3, New Zealand
[12] Sahlgrenska Hosp, Gothenburg, Sweden
[13] Clin Pasteur, Toulouse, France
[14] Univ Essen Gesamthsch, Essen, Germany
[15] Osped Maggiore Trieste, Trieste, Italy
来源
LANCET | 1998年 / 352卷 / 9129期
关键词
D O I
10.1016/S0140-6736(97)11128-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 greater than or equal to 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.
引用
收藏
页码:673 / 681
页数:9
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