Long-term clinical follow-up of the multicentre, randomized study to test immunosuppressive therapy with oral prednisone for the prevention of restenosis after percutaneous coronary interventions: Cortisone plus BMS or DES veRsus BMS alone to EliminAte Restenosis (CEREA-DES)

被引:20
作者
Ribichini, Flavio [1 ,2 ]
Tomai, Fabrizio [3 ]
Pesarini, Gabriele [1 ]
Zivelonghi, Carlo [1 ]
Rognoni, Andrea [4 ]
De Luca, Giuseppe [4 ]
Boccuzzi, Giacomo [5 ]
Presbitero, Patrizia [6 ]
Ferrero, Valeria [1 ]
Ghini, Anna S. [3 ]
Marino, Paolo [4 ]
Vassanelli, Corrado [1 ]
机构
[1] Univ Verona, Dept Med, I-37100 Verona, Italy
[2] Univ Verona, Cardiovasc Intervent Unit, I-37126 Verona, Italy
[3] European Hosp, Dept Cardiovasc Sci, Rome, Italy
[4] Univ Piemonte Orientale, Dept Clin & Expt Med, Novara, Italy
[5] Osped San Giovanni Bosco, Div Cardiol, Turin, Italy
[6] Ist Clin Humanitas, Intervent Cardiol Unit, Milan, Italy
关键词
Randomized clinical trial; Long-term follow-up; Coronary artery disease; Stent; Prednisone; DRUG-ELUTING STENTS; C-REACTIVE PROTEIN; BARE-METAL; SIROLIMUS; RAPAMYCIN; OUTCOMES; TRIAL; IMPLANTATION; REVASCULARIZATION; GLUCOCORTICOIDS;
D O I
10.1093/eurheartj/eht079
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims To analyse the clinical outcome at 4 years in patients with coronary artery disease treated with bare metal stents (BMS) vs. BMS and oral prednisone, or drug-eluting stents (DES), all assuming similar adjunctive medical treatment. Methods and results Five Italian hospitals enrolled 375 non-diabetic, ischaemic patients without contraindications to dual anti-platelet treatment or corticosteroid therapy in a randomized controlled study. The primary endpoint was the event-free survival of cardiovascular death, myocardial infarction, and recurrence of ischaemia needing repeated target vessel revascularization at 1 year, and this was significantly lower in the BMS group (80.8%) compared with the prednisone (88.0%) and DES group (88.8%, P = 0.04 and 0.006, respectively). The long-term analysis of the primary endpoint was a pre-specified aim of the trial, and was performed at 1447 days (median, IQ range = 1210-1641). Patients receiving BMS alone had significantly lower event-free survival (75.3%) compared with 84.1% in the prednisone group (HR: 0.447; 95% CI: 0.25-0.80, P = 0.007) and 80.6% in DES patients (HR: 0.519; 95% CI: 0.29-0.93, P = 0.03). Prednisone-treated patients did not develop new treatment-related clinical problems. Drug-eluting stents patients suffered more very late stent thrombosis as a cause of spontaneous myocardial infarction. The need for target vessel revascularization remained lower in the prednisone and DES groups (13.6 and 15.2%, respectively), compared with BMS (23.2%). Conclusions The clinical benefits of prednisone compared with BMS only persisted almost unchanged at 4 years. Drug-eluting stents performed better than BMS at long-term, although the advantages observed at 1 year were in part attenuated because of the occurrence of very late stent thrombosis and late revascularizations.
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收藏
页码:1740 / 1748
页数:9
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