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1 intervention for secondary prevention after percutaneous coronary revascularization.
2 icantly reduces the risk of restenosis after percutaneous coronary revascularization.
3 ban administered for at least 12 hours after percutaneous coronary revascularization.
4 mong patients undergoing successful elective percutaneous coronary revascularization.
5 elevations (one to five times normal) after percutaneous coronary revascularization.
6 ssel diameter) who were scheduled to undergo percutaneous coronary revascularization.
7 mong a broad spectrum of patients undergoing percutaneous coronary revascularization.
8 tery syndromes and ischemic complications of percutaneous coronary revascularization.
9 protein IIb/IIIa receptors in the setting of percutaneous coronary revascularization.
10 assessing the operator-specific results for percutaneous coronary revascularization.
11 Restenosis remains the major limitation of percutaneous coronary revascularization.
12 stent significantly reduces restenosis after percutaneous coronary revascularization.
13 stenting has emerged as the dominant form of percutaneous coronary revascularization.
14 I and HF were less likely to receive primary percutaneous coronary revascularization (84% versus 79%
16 including 4603 patients undergoing elective percutaneous coronary revascularization and 1071 patient
18 otein IIb/IIIa antagonist xemilofiban before percutaneous coronary revascularization and for up to si
19 Duke University Medical Center who underwent percutaneous coronary revascularization and received the
20 ients with acute ischemic syndromes or after percutaneous coronary revascularization and that persist
21 used for the majority of patients undergoing percutaneous coronary revascularization, and the body of
23 igned patients undergoing urgent or elective percutaneous coronary revascularization at 69 centers to
28 en administered intravenously at the time of percutaneous coronary revascularization, glycoprotein II
29 es clinical outcomes in the months following percutaneous coronary revascularization in a wide variet
30 dialysis patients undergoing surgical versus percutaneous coronary revascularization in the era of dr
32 rocedural myocardial infarction complicating percutaneous coronary revascularization is associated wi
36 ion with a 600-mg dose of clopidogrel before percutaneous coronary revascularization on early outcome
41 tries and prospective trials of surgical and percutaneous coronary revascularization procedures in di
43 c evaluation among 1,314 patients undergoing percutaneous coronary revascularization randomized to ei
44 and low-dose, weight-adjusted heparin during percutaneous coronary revascularization reduces ischemic
46 hin a single-center registry of contemporary percutaneous coronary revascularization strategies with
47 cal outcomes of closure device use following percutaneous coronary revascularization using current st
49 ents who continued to smoke after successful percutaneous coronary revascularization were at greater
51 acute ischemic complications associated with percutaneous coronary revascularization, whereas coronar
52 al outcomes in high risk patients undergoing percutaneous coronary revascularization who received eit
53 e, or repeat revascularization compared with percutaneous coronary revascularization with drug-elutin
54 rolled in the SIRIUS trial and randomized to percutaneous coronary revascularization with either a SE
56 her tirofiban or abciximab before undergoing percutaneous coronary revascularization with the intent
57 r placebo 30 to 90 minutes before undergoing percutaneous coronary revascularization, with maintenanc
58 hin 30 days by 56% among patients undergoing percutaneous coronary revascularization, without increas
59 schemic complications in patients undergoing percutaneous coronary revascularization, without increas
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