Role of stent type and of duration of dual antiplatelet therapy in patients with chronic kidney disease undergoing percutaneous coronary interventions. Is bare metal stent implantation still a justifiable choice? A post-hoc analysis of the all comer PRODIGY trial

被引:25
作者
Crimi, Gabriele [1 ]
Leonardi, Sergio [1 ]
Costa, Francesco [2 ]
Adamo, Marianna [2 ]
Ariotti, Sara [3 ]
Valgimigli, Marco [3 ]
机构
[1] Fdn IRCCS Policlin San Matteo, SC Cardiol, Pavia, Italy
[2] Erasmus MC, Thoraxctr, Rotterdam, Netherlands
[3] Swiss Cardiovasc Ctr Bern, Bern, Switzerland
关键词
Chronic kidney disease; Stent thrombosis; Drug eluting stent; 2nd generation drug eluting stent; ELEVATION MYOCARDIAL-INFARCTION; INDUCED INTIMAL HYPERPLASIA; DRUG-ELUTING STENTS; SHORT-TERM; CLOPIDOGREL; THROMBOSIS; EFFICACY; OUTCOMES; POTENCY; IMPACT;
D O I
10.1016/j.ijcard.2016.03.033
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim: Chronic kidney disease (CKD) is a powerful predictor of major cardiovascular events and stent thrombosis (ST) in patients undergoing percutaneous coronary interventions (PCI). No randomized data are available to compare, and guide the selection of type of stent between bare metal (BMS) or drug eluting stent (DES) in this population. Methods and results: We performed a post-hoc analysis of the PROlonging Dual antiplatelet treatment after Grading stent-induced Intimal hyperplasia studY (PRODIGY) trial, in which stable or unstable patients with coronary artery disease undergoing PCI were randomized 1:1:1:1 to receive BMS, paclitaxel-(PES), zotarolimus- (ZES-S), or everolimus- (EES) eluting stent. A total of 2003 patients were randomized, and 22 patients were excluded for missing serum creatinine leading to a final population of 1981 patients. Primary outcome was definite or probable ST. We also assessed MACE (myocardial infarction, stroke, or death), and all-cause death, as secondary outcome. CKD, defined with estimated glomerular filtration rate <60 ml/min/1.73 m(2), was found in 373 patients (18.8%). The incidence of ST at 2 years was 5.1% in CKD and 2.1% in non-CKD patients (HR 2.57, 95% confidence interval (CI) 1.46 to 4.52, p < 0.001). At multivariable regression we found that patients randomized to EES or ZES-S, but not PES, had lower risk of ST at two years as compared with BMS: adjusted HR = 0.288, 95% CI [0.107-0.778, p = 0.014] and HR = 0.394, 95% CI [0.164-0.947, p = 0.037] respectively. The number of patients needed to be treated to prevent 1 ST with an EES vs BMS was 20 in CKD and 50 in patients without CKD. EES patients had the lowest incident MACE events 26.4% as compared to BMS 35.1%, ZES-S 33.0%, or PES 35.7% patients, p = 0.551. All-cause death was lowest in ZES-S group 10.6% as compared to BMS 18.1%, PES 25.5% and EES 14.9%, p = 0.040. We found no significant interaction between DAPT duration (6 vs 24 months) and stent type on primary outcome, P-INT = 0.47 for BMS, P-INT = 0.57 for PES, P-INT = 0.41 for ZES-S and P-INT = 0.28 for EES. Conclusions: In an all-comer population of patients with stable and unstable CAD, CKD at baseline was associated with a double risk of ST and MACE. CKD patients receiving EES had less than half risk of ST 2 years after PCI as compared with BMS and PES. Our analysis suggests that 2nd generation limus-based stent should be favored over paclitaxel-based DES or BMS to reduce ST and MACE in CKD patients. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:110 / 117
页数:8
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