A Comparison of Balloon-Expandable-Stent Implantation with Balloon Angioplasty in Patients with Coronary Artery Disease

Patrick W. Serruys(Rotterdam University of Applied Sciences), Peter de Jaegere(Rotterdam University of Applied Sciences), Ferdinand Kiemeneij(OLVG), Carlos Macaya(Hospital Clínico San Carlos), Wolfgang Rutsch(Freie Universität Berlin), Guy R. Heyndrickx(Onze Lieve Vrouwziekenhuis Hospital), Håkan Emanuelsson(Sahlgrenska University Hospital), Jean Marco(Clinique Pasteur), Victor Legrand(Centre Hospitalier Universitaire de Liège), Pierre Materne(Centre hospitalier régional de la Citadelle), Jorge Belardi(Instituto Cardiovascular de Buenos Aires), Ulrich Sigwart(Lung Institute), Antonio Colombo(EMO GVM Centro Cuore Columbus), J J Goy(University Hospital of Lausanne), Paul van den Heuvel(ZNA Middelheim Hospital), Juan L. Delcán(Hospital General Universitario Gregorio Marañón), Marie‐Angèle Morel
New England Journal of Medicine
August 25, 1994
Cited by 4,547Open Access
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Abstract

BACKGROUND: Balloon-expandable coronary-artery stents were developed to prevent coronary restenosis after coronary angioplasty. These devices hold coronary vessels open at sites that have been dilated. However, it is unknown whether stenting improves long-term angiographic and clinical outcomes as compared with standard balloon angioplasty. METHODS: A total of 520 patients with stable angina and a single coronary-artery lesion were randomly assigned to either stent implantation (262 patients) or standard balloon angioplasty (258 patients). The primary clinical end points were death, the occurrence of a cerebrovascular accident, myocardial infarction, the need for coronary-artery bypass surgery, or a second percutaneous intervention involving the previously treated lesion, either at the time of the initial procedure or during the subsequent seven months. The primary angiographic end point was the minimal luminal diameter at follow-up, as determined by quantitative coronary angiography. RESULTS: After exclusions, 52 patients in the stent group (20 percent) and 76 patients in the angioplasty group (30 percent) reached a primary clinical end point (relative risk, 0.68; 95 percent confidence interval, 0.50 to 0.92; P = 0.02). The difference in clinical-event rates was explained mainly by a reduced need for a second coronary angioplasty in the stent group (relative risk, 0.58; 95 percent confidence interval, 0.40 to 0.85; P = 0.005). The mean (+/- SD) minimal luminal diameters immediately after the procedure were 2.48 +/- 0.39 mm in the stent group and 2.05 +/- 0.33 mm in the angioplasty group; at follow-up, the diameters were 1.82 +/- 0.64 mm in the stent group and 1.73 +/- 0.55 mm in the angioplasty group (P = 0.09), which correspond to rates of restenosis (diameter of stenosis, > or = 50 percent) of 22 and 32 percent, respectively (P = 0.02). Peripheral vascular complications necessitating surgery, blood transfusion, or both were more frequent after stenting than after balloon angioplasty (13.5 vs. 3.1 percent, P < 0.001). The mean hospital stay was significantly longer in the stent group than in the angioplasty group (8.5 vs. 3.1 days, P < 0.001). CONCLUSIONS: Over seven months of follow-up, the clinical and angiographic outcomes were better in patients who received a stent than in those who received standard coronary angioplasty. However, this benefit was achieved at the cost of a significantly higher risk of vascular complications at the access site and a longer hospital stay.


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