Lesion characteristics | No of lesions (n=118) |
Vessels treated (%) | |
Left anterior descending | 31 (26) |
Left circumflex | 27 (23) |
Right coronary artery | 60 (51) |
Type of in-stent restenosis (%) | |
(1)Focal | 32 (27) |
(2) Diffuse | 39 (33) |
(3) Proliferative | 28 (24) |
(4) Occlusive | 19 (16) |
More than one scaffold per lesion (%) | 27 (30) |
Aorto-ostial lesions (%) | 2 (1.7) |
Chronic total occlusions (%) | 21 (18) |
Moderate to severe calcification (%) | 61 (52) |
Type of restenosed stent (%) | |
BMS | 7 (6) |
First generation DES | 24 (20) |
Second generation DES | 87 (74) |
Layers of stent (%) | |
One | 86 (73) |
Two or more | 32 (27) |
History of DCB treatment (%) | 10 (8.5) |
OCT guidance (%) | 32 (27) |
Lesion preparation (mm, mean) | |
Pre-dilatation balloon diameter | 3.0±0.07 |
Pre-dilatation pressure | 26.8±1.3 |
Regular NC balloon (%) | 31 (26) |
Ultra-high pressure NC balloon (%) | 89 (75) |
Total scaffolds implanted | 131 |
Absorb BRS characteristics (mm, mean) | |
Scaffold diameter | 3.1±0.07 |
Scaffold length | 24±1 |
Scaffold deployment pressure (atm, mean) | 14.7±0.4 |
Post-dilatation (%) | 56 (47) |
Post-dilatation pressure (atm) | 27.7±1.9 |
Data are mean (SD) or number (percentage), as appropriate.
BMS, bare metal stents; BRS, bioresorbable scaffold; DCB, drug coated balloon; DES, drug eluting stents; NC, non-compliant; OCT, optical coherence tomography.