Table 3

30-day clinical outcome

Total (n=1007)Non-HPR (n=664, 66%)Individualised (n=343, 34%)Adjusted HR (95% CI)
p Value
Crude HR (95% CI)
p Value
MACE (cardiovascular death, myocardial infarction, stent thrombosis)18 (1.8%)9 (1.4%)9 (2.6%)0.67
(0.23 to 2.03)
0.5
0.51
(0.20 to 1.30)
0.16
Cardiovascular death18 (1.8%)9 (1.4%)9 (2.6%)
 Non-shock8 (0.8%)4 (0.6%)4 (1.2%)
 Cardiogenic shock (n=shock patients; % of shock)10 (26; 38%)5 (8; 62%)5 (18; 28%)
Myocardial infarction Stent thrombosis1 (0.09%)1 (0.15%)0 (0%)
  Definite and probable3 (0.29%)3 (0.45%)0 (0%)
  Definite1 (0.09%)1 (0.15%)0 (0%)
  Probable2 (0.19%)2 (0.3%)0 (0%)
Bleeding
 TIMI major and minor26 (2.6%)17 (2.6%)9 (2.6%)0.78
(0.33 to 1.85)
0.574
0.96
(0.42 to 2.20)
0.914
 TIMI major10 (1.0%)6 (0.9%)4 (1.2%)
 TIMI minor16 (1.6%)11 (1.7%)5 (1.5%)
 Type
 Instrumented14 (1.4%)10 (1.5%)4 (1.2%)
 Spontaneous12 (1.2%)7 (1.1%)5 (1.5%)
  • MACE, major adverse cardiac event; TIMI, thrombolysis in myocardial infarction.