Everolimus-Eluting Stents in Patients With Bare-Metal and Drug-Eluting In-Stent Restenosis Results From a Patient-Level Pooled Analysis of the RIBS IV and V Trials


Por: Alfonso, F, Perez-Vizcayno, MJ, del Blanco, BG, Garcia-Touchard, A, Lopez-Minguez, JR, Masotti, M, Zueco, J, Melgares, R, Mainar, V, Moreno, R, Dominguez, A, Sanchis, J, Bethencourt, A, Moreu, J, Cequier, A, Marti, V, Otaegui, I, Bastante, T, Gonzalo, N, Jimenez-Quevedo, P, Cardenas, A, Fernandez, C

Publicada: 1 jul 2016
Resumen:
Background-Treatment of patients with drug-eluting stent (DES) in-stent restenosis (ISR) is more challenging than that of patients with bare-metal stent ISR. However, the results of everolimus-eluting stents (EES) in these distinct scenarios remain unsettled. Methods and Results-A pooled analysis of the RIBS IV (Restenosis Intra-Stent of Drug-Eluting Stents: Paclitaxel-Eluting Balloon vs Everolimus-Eluting Stent) and RIBS V (Restenosis Intra-Stent of Bare Metal Stents: Paclitaxel-Eluting Balloon vs Everolimus-Eluting Stent) randomized trials was performed using patient-level data to compare the efficacy of EES in bare-metal stent ISR and DES-ISR. Inclusion and exclusion criteria were identical in both trials. Results of 94 patients treated with EES for bare-metal stent ISR were compared with those of 155 patients treated with EES for DES-ISR. Baseline characteristics were more adverse in patients with DES-ISR, although they presented later and more frequently with a focal pattern. After intervention, minimal lumen diameter (2.22 +/- 0.5 versus 2.38 +/- 0.5 mm, P=0.01) was smaller in the DES-ISR group. Late angiographic findings (89.3% of eligible patients), including minimal lumen diameter (2.03 +/- 0.7 versus 2.36 +/- 0.6 mm, P<0.001) and diameter stenosis (23 +/- 22 versus 13 +/- 17%, P<0.001) were poorer in patients with DES-ISR. Results were consistent in the in-segment and in-lesion analyses. On multiple linear regression analysis, minimal lumen diameter at followup remained significantly smaller in patients with DES-ISR. Finally, at 1-year clinical follow-up (100% of patients), mortality (2.6 versus 0%, P<0.01) and need for target vessel revascularization (8 versus 2%, P=0.03) were higher in the DES-ISR group. Conclusions-This patient-level pooled analysis of the RIBS IV and RIBS V randomized clinical trials suggests that EES provide favorable outcomes in patients with ISR. However, the results of EES are less satisfactory in patients with DESISR than in those with bare-metal stent ISR.

Filiaciones:
Alfonso, F:
 Hosp Univ La Princesa, Madrid, Spain

Perez-Vizcayno, MJ:
 Hosp Univ Clin San Carlos, Madrid, Spain

 Fdn Interhosp Invest Cardiovasc, Madrid, Spain

del Blanco, BG:
 Hosp Univ Vall dHebron, Barcelona, Spain

Garcia-Touchard, A:
 Hosp Univ Puerta de Hierro Majadahonda, Madrid, Spain

Lopez-Minguez, JR:
 Hosp Univ Infanta Cristina, Badajoz, Spain

Masotti, M:
 Hosp Univ Clin Barcelona, Barcelona, Spain

Zueco, J:
 Hosp Univ Marques de Valdecilla, Santander, Spain

Melgares, R:
 Hosp Univ Virgen de las Nieves, Granada, Spain

Mainar, V:
 Hosp Univ Alicante, Javea, Spain

Moreno, R:
 Hosp Univ La Paz, Madrid, Spain

Dominguez, A:
 Hosp Univ Virgen de la Victoria, Malaga, Spain

Sanchis, J:
 Hosp Univ Clin Valencia, Valencia, Spain

Bethencourt, A:
 Hosp Univ Son Espases, Palma De Mallorca, Spain

Moreu, J:
 Hosp Univ Virgen de la Salud Toledo, Toledo, OH USA

Cequier, A:
 Hosp Univ Bellvitge, Barcelona, Spain

Marti, V:
 Hosp Univ San Pau, Barcelona, Spain

Otaegui, I:
 Hosp Univ Vall dHebron, Barcelona, Spain

Bastante, T:
 Hosp Univ La Princesa, Madrid, Spain

Gonzalo, N:
 Hosp Univ Clin San Carlos, Madrid, Spain

Jimenez-Quevedo, P:
 Hosp Univ Clin San Carlos, Madrid, Spain

Cardenas, A:
 Hosp Univ Clin San Carlos, Madrid, Spain

 USFQ, Sch Med, Quito, Ecuador

Fernandez, C:
 Hosp Univ Clin San Carlos, Madrid, Spain
ISSN: 19417640





Circulation-Cardiovascular Interventions
Editorial
LIPPINCOTT WILLIAMS & WILKINS, TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 9 Número: 7
Páginas:
WOS Id: 000380607800006
ID de PubMed: 27412868
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