Long-Term Results of Everolimus-Eluting Stents Versus Drug-Eluting Balloons in Patients With Bare-Metal In-Stent Restenosis 3-Year Follow-Up of the RIBS V Clinical Trial

被引:53
作者
Alfonso, Fernando [1 ]
Jose Perez-Vizcayno, Maria [2 ,3 ]
Garcia del Blanco, Bruno [4 ]
Otaegui, Imanol [4 ]
Masotti, Monica [5 ]
Zueco, Javier [6 ]
Velaquez, Maite [7 ]
Sanchis, Juan [8 ]
Garcia-Touchard, Arturo [9 ]
Lazaro-Garcia, Rosa [10 ]
Moreu, Jose [11 ]
Bethencourt, Armando [12 ]
Cuesta, Javier [1 ]
Rivero, Fernando [1 ]
Cardenas, Alberto [3 ,13 ]
Gonzalo, Nieves [3 ]
Jimenez-Quevedo, Pilar [3 ]
Fernandez, Cristina [3 ]
机构
[1] Hosp Univ La Princesa, Madrid, Spain
[2] Fdn Interhosp Invest Cardiovasc, Madrid, Spain
[3] Hosp Univ Clin San Carlos, Madrid, Spain
[4] Hosp Univ Vall Hebron, Barcelona, Spain
[5] Hosp Univ Clin Barcelona, Barcelona, Spain
[6] Hosp Univ Marques de Valdecilla, Santander, Spain
[7] Hosp Univ 12 Octubre, Madrid, Spain
[8] Hosp Univ Clin Valencia, Valencia, Spain
[9] Hosp Univ Puerta de Hierro Majadahonda, Madrid, Spain
[10] Hosp Univ Torrecardenas, Almeria, Spain
[11] Hosp Univ Virgen Salud, Toledo, Spain
[12] Hosp Univ Son Espases, Palma de Mallorca, Spain
[13] USFQ, Sch Med, Quito, Ecuador
关键词
drug-eluting balloon(s); drug-eluting stent(s); everolimus-eluting stent(s); in-stent restenosis; PACLITAXEL-COATED BALLOON; RANDOMIZED-TRIAL; ANGIOPLASTY; MULTICENTER; CATHETER; IMPLANTATION; EFFICACY; DES;
D O I
10.1016/j.jcin.2016.03.037
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVES The aim of this study was to compare the long-term efficacy of everolimus-eluting stents (EES) and drug-eluting balloons (DEB) in patients with bare-metal stent in-stent restenosis (ISR). BACKGROUND The relative long-term clinical efficacy of current therapeutic modalities in patients with ISR remains unknown. METHODS The 3-year clinical follow-up (pre-specified endpoint) of patients included in the RIBS V (Restenosis IntraStent of Bare-Metal Stents: Drug-Eluting Balloon vs Everolimus-Eluting Stent Implantation) randomized clinical trial was analyzed. All patients were followed yearly using a pre-defined structured questionnaire. RESULTS A total of 189 patients with bare-metal stent ISR were allocated to either EES (n = 94) or DEB (n = 95). Clinical follow-up at 1, 2, and 3 years was obtained in all patients (100%). Compared with patients treated with DEB, those treated with EES obtained better angiographic results, including larger minimal luminal diameter at follow-up (primary study endpoint; 2.36 +/- 0.6 mm vs. 2.01 +/- 0.6 mm; p < 0.001). At 3 years, the rates of cardiac death (2% vs. 1%), myocardial infarction (4% vs. 5%) and target vessel revascularization (9% vs. 5%) were similar in the DEB and EES arms. Importantly, however, at 3 years, the rate of target lesion revascularization was significantly lower in the EES arm (2% vs. 8%; p = 0.04; hazard ratio: 0.23; 95% confidence interval: 0.06 to 0.93). The need for "late" (> 1 year) target vessel (3 [3.2%] vs. 3 [3.2%]; p = 0.95) and target lesion (1 [1%] vs. 2 [2.1%]; p = 0.54) revascularization was low and similar in the 2 arms. Rates of definite or probable stent thrombosis (1% vs. 0%) were also similar in the 2 arms. CONCLUSIONS The 3-year clinical follow-up of the RIBS V clinical trial confirms the sustained safety and efficacy of EES and DEB in patients treated for bare-metal stent ISR. In this setting, EES reduce the need for target lesion revascularization at very long-term follow-up. (RIBS V [Restenosis Intra-Stent of Bare Metal Stents: PaclitaxelEluting Balloon vs Everolimus-Eluting Stent] [RIBS V]; NCT01239953) (C) 2016 by the American College of Cardiology Foundation.
引用
收藏
页码:1246 / 1255
页数:10
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