TY - JOUR
T1 - Randomized comparison between 3-month Cre8 des vs. 1-month Vision/Multilink8 BMS neointimal coverage assessed by OCT evaluation
T2 - The DEMONSTRATE study
AU - Prati, Francesco
AU - Romagnoli, Enrico
AU - Valgimigli, Marco
AU - Burzotta, Francesco
AU - De Benedictis, Mauro
AU - Ramondo, Angelo
AU - Mehran, Roxana
AU - Stella, Pieter R.
N1 - Publisher Copyright:
© 2014 Elsevier Ireland Ltd. All rights reserved.
PY - 2014/10/20
Y1 - 2014/10/20
N2 - Background It has been hypothesized that incomplete endothelialization and delayed vascular healing may trigger stent thrombosis events after drug-eluting stent (DES) implantation. We aimed to demonstrate non-inferiority in terms of neointimal coverage of novel Cre8 DES at 3 months, compared to Vision/Multilink8 Bare Metal Stent (BMS) at 1 month.Methods The ranDomizEd coMparisOn betweeN novel Cre8 DES and BMS to assess neoinTimal coveRAge by OCT Evaluation (DEMONSTRATE) was a multicenter, randomized, parallel group study. Thirty-eight patients undergoing angioplasty of de-novo coronary lesion were randomized to Cre8 (19) or Vision/Multilink8 (19) stent placement at 6 OCT-experienced centers. Primary end-point was the Ratio of Uncovered to Total Stent Struts Per Cross Section (RUTTS) score of < 30%, determined by OCT at 3 and 1 months for Cre8 and Vision/Multilink8, respectively. Percentage of uncovered/malapposed stent struts, neointimal growth and thickness were the main secondary end-points.Results The primary end-point of RUTTS score < 30% occurred in 99.8% (899/901) of Cre8 struts and in 99.6% (1116/1121) of Vision/Multilink8 struts (difference 0.2, CI 95% - 0.2 to 0.6, p for noninferiority < 0.001). The percentage of uncovered/malapposed struts was comparable (0.36 ± 0.64 vs. 0.12 ± 0.24, p = 0.145) in the two study groups, while both neointimal percentage area (8.46 ± 5.29 vs. 19.84 ± 15.93, p < 0.001) and thickness (0.07 ± 0.04 vs. 0.16 ± 0.12, p < 0.001) were significantly reduced by Cre8 stent.Conclusions The Cre8 DES at 3 months has comparable strut coverage to Vision/Multilink8 BMS at 1 month while preserving a greater efficacy in neo-intima formation reduction. Further studies to assess clinical implication of these Cre8 characteristics are warranted.
AB - Background It has been hypothesized that incomplete endothelialization and delayed vascular healing may trigger stent thrombosis events after drug-eluting stent (DES) implantation. We aimed to demonstrate non-inferiority in terms of neointimal coverage of novel Cre8 DES at 3 months, compared to Vision/Multilink8 Bare Metal Stent (BMS) at 1 month.Methods The ranDomizEd coMparisOn betweeN novel Cre8 DES and BMS to assess neoinTimal coveRAge by OCT Evaluation (DEMONSTRATE) was a multicenter, randomized, parallel group study. Thirty-eight patients undergoing angioplasty of de-novo coronary lesion were randomized to Cre8 (19) or Vision/Multilink8 (19) stent placement at 6 OCT-experienced centers. Primary end-point was the Ratio of Uncovered to Total Stent Struts Per Cross Section (RUTTS) score of < 30%, determined by OCT at 3 and 1 months for Cre8 and Vision/Multilink8, respectively. Percentage of uncovered/malapposed stent struts, neointimal growth and thickness were the main secondary end-points.Results The primary end-point of RUTTS score < 30% occurred in 99.8% (899/901) of Cre8 struts and in 99.6% (1116/1121) of Vision/Multilink8 struts (difference 0.2, CI 95% - 0.2 to 0.6, p for noninferiority < 0.001). The percentage of uncovered/malapposed struts was comparable (0.36 ± 0.64 vs. 0.12 ± 0.24, p = 0.145) in the two study groups, while both neointimal percentage area (8.46 ± 5.29 vs. 19.84 ± 15.93, p < 0.001) and thickness (0.07 ± 0.04 vs. 0.16 ± 0.12, p < 0.001) were significantly reduced by Cre8 stent.Conclusions The Cre8 DES at 3 months has comparable strut coverage to Vision/Multilink8 BMS at 1 month while preserving a greater efficacy in neo-intima formation reduction. Further studies to assess clinical implication of these Cre8 characteristics are warranted.
KW - Drug-eluting stent
KW - Optical coherence tomography
KW - Randomized controlled trial
UR - https://www.scopus.com/pages/publications/84908206965
U2 - 10.1016/j.ijcard.2014.08.031
DO - 10.1016/j.ijcard.2014.08.031
M3 - Article
C2 - 25171966
AN - SCOPUS:84908206965
SN - 0167-5273
VL - 176
SP - 904
EP - 909
JO - International Journal of Cardiology
JF - International Journal of Cardiology
IS - 3
ER -