Table 5

Adverse events at 12- and 24-month follow-up in the entire population (Cohort B1 and B2) (intent-to-treat population)

Cohort B1 and B2 12-Month follow-upCohort B1 and B2 24-Month Follow-up
Small vessels (<2.5 mm) (N=41)Large vessels (≥2.5 mm) (N=60)p ValueSmall vessels (<2.5 mm) (N=41)Large vessels (≥2.5 mm) (N=60)p Value
MACE (Cardiac Death, MI, ID-TLR)7.3% (3/41)6.7% (4/60)1.00007.3% (3/41)10.2% (6/59)0.7335
Cardiac death0.0% (0/41)0.0% (0/60)NA0.0% (0/41)0.0% (0/59)NA
Myocardial infarction (MI)4.9% (2/41)1.7% (1/60)0.56454.9% (2/41)1.7% (1/59)0.5662
QMI0.0% (0/41)0.0% (0/60)NA0.0% (0/41)0.0% (0/59)NA
NQMI4.9% (2/41)1.7% (1/60)0.56454.9% (2/41)1.7% (1/59)0.5662
ID-TLR (PCI)2.4% (1/41)5.0% (3/60)0.64452.4% (1/41)8.5% (5/59)0.3962
Scaffold thrombosis0.0% (0/41)0.0% (0/60)NA0.0% (0/41)0.0% (0/60)NA
  • ID-TLR, ischaemia driven target lesion revascularization; MACE, major adverse cardiac events; MI, myocardial infarction; PCI, percutaneous coronary intervention; QMI, Q wave myocardial infarction; NQMI, non-Q wave myocardial infarction.