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. 2021 Sep 1;29(10):525–535. doi: 10.1007/s12471-021-01606-2

Table 3.

Bleeding events and ischaemic events during follow-up

Bleeding endpoint Cumulative (n = 524) T1 visit (n = 524) T2 visit b (n = 456) T3 visit b (n = 420)
Any bleeding 254 (48.5) 147 (28.1) 135 (29.6) 82 (19.5)
Most severe bleeding
– BARC type 1 162 (30.9) 102 (19.5) 105 (23.0) 54 (12.9)
– BARC type 2  63 (12.0)  34 (6.5)  19 (4.2) 19 (4.5)
– BARC type 3  29 (5.5)  11 (2.1)  11 (2.4)  9 (2.1)
Total number of bleeding events a 442 188 159 95
– BARC type 1 332 (75.1) 139 (73.9) 126 (79.2) 67 (70.5)
– BARC type 2  75 (16.9)  36 (19.1)  20 (12.6) 19 (20.0)
– BARC type 3  35 (7.9)  13 (6.9)  13 (8.2)  9 (9.5)
Ischaemic event

Cohort

(n=524)

No ischaemic events 416 (79.2)
Major adverse cardiovascular event (myocardial infarction, stroke or all-cause death)  69 (13.2)
Myocardial infarction  36 (6.9)
Stent thrombosis   8 (1.5)
Stroke  13 (2.5)
Death, all-cause  23 (4.4)
– Confirmed cardiovascular death c   6 (1.1)
– Death (non-cardiovascular, unknown)  17 (3.2)
Coronary revascularisation  37 (7.1)
PAD with revascularisation  17 (3.2)
Venous thromboembolism   3 (0.6)

BARC Bleeding Academic Research Consortium, PAD peripheral artery disease

a In patients reporting any bleeding symptoms (one patient can report more than one bleeding event at the same visit)

b Bleeding events since last study visit

c Confirmed cardiovascular death is defined as death due to acute myocardial infarction, death due to stroke, or in-hospital cardiac arrest