Table 1. Clinical events at 5-year follow-up [5].

	EES group (n = 751)	BMS group (n = 747)	Hazard ratio (95% CI)	p value
Patient-oriented endpoint*	159 (21%)	192 (26%)	0.80 (0.65–0.98)	0.033
Device-oriented endpoint†	88 (12%)	113 (15%)	0.75 (0.57–0.99)	0.043
Death§	65 (9%)	88 (12%)	0.72 (0.52–1.00)	0.047
Cardiac	47 (6%)	55 (7%)	0.84 (0.57–1.24)	0.370
Vascular	4 (1%)	5 (1%)	0.79 (0.21–2.92)	0.720
Non-cardiovascular	14 (2%)	28 (4%)	0.49 (0.26–0.92)	0.027
Myocardial infarction	35 (5%)	27 (4%)	1.27 (0.77–2.10)	0.350
Target vessel related	21 (3%)	23 (3%)	0.90 (0.50–1.62)	0.710
Non-target vessel related	15 (2%)	6 (1%)	2.44 (0.95–6.29)	0.070
Revascularization	93 (12%)	116 (16%)	0.77 (0.59–1.01)	0.060
Target lesion	32 (4%)	54 (7%)	0.57 (0.37–0.89)	0.012
Target vessel	49 (7%)	76 (10%)	0.62 (0.43–0.89)	0.009
Non-target vessel	62 (8%)	62 (8%)	0.98 (0.69–1.39)	0.910
Definite or probable stent thrombosis	15 (2%)	23 (3%)	0.64 (0.33–1.23)	0.180

EES = everolimus-eluting stent. BMS = bare metal stent.

*Combined (hierarchical) endpoint of all-cause death, any recurrent myocardial infarction, and any revascularisation.

†Combined (hierarchical) endpoint of cardiac death, target vessel myocardial infarction, and target lesion revascularisation.

§In accordance with the Academic Research Consortium (ARC) recommendations [6].