Literature DB >> 31898006

The influence of implantation techniques on lesion oriented-outcomes in Absorb BVS and Xience EES lesions treated in routine clinical practice at complete three year follow-up: AIDA trial QCA substudy.

Ruben Y G Tijssen1, Laura S M Kerkmeijer1, Kuniaki Takahashi1, Norihiro Kogame1, Yuki Katagiri1, Robin P Kraak1,2, Ply Chichareon1, Rodrigo Modolo1, Taku Asano1, Martina Nassif1, Deborah N Kalkman1, Yohei Sotomi1, Carlos Collet1, Sjoerd H Hofma3, Rene J van der Schaaf2, E Karin Arkenbout4, Auke P J D Weevers5, Jan J Piek1, Jan G P Tijssen1, Jose P Henriques1, Robbert J de Winter1, Yoshinobu Onuma6, Patrick W Serruys7, Joanna J Wykrzykowska8.   

Abstract

It has been hypothesized that dedicated optimized Absorb BVS implantation techniques might mitigate the risk of adverse events such as target vessel failure and device thrombosis. In this explorative AIDA trial QCA substudy, we sought to investigate the influence of implantation techniques on lesion-oriented outcomes in both the Absorb BVS and Xience EES arm at complete 3-year follow-up. The current analysis includes 2152 study lesions treated with at least one study device, of which the baseline angiogram was suited for offline QCA analysis, including Dmax analysis. The lesion-oriented composite outcome (LOCE) of this analysis was a composite of definite device thrombosis, target lesion revascularization and target-vessel myocardial infarction. In Absorb BVS, the Lesion-oriented composite endpoint (LOCE) occurred numerically less in correctly QCA sized vessels when compared to incorrectly sized vessels 8.5% (58/696) versus 11.1% (39/358), p = 0.151. In Xience EES, LOCE had occurred more frequently in incorrectly sized devices according to device diameter/RVD matching; 2.2% (4/187) in correctly sized devices versus 7.1% (63/911) in incorrectly sized devices (p = 0.014). In this AIDA trial QCA substudy, rates of LOCE were significantly lower in Xience EES treated lesions in which devices were correctly sized according to the definitions of device diameter/RVD matching.

Entities:  

Keywords:  Bioresorbable scaffolds; Drug eluting stents; Quantitative coronary angiography

Mesh:

Year:  2020        PMID: 31898006     DOI: 10.1007/s10554-019-01756-w

Source DB:  PubMed          Journal:  Int J Cardiovasc Imaging        ISSN: 1569-5794            Impact factor:   2.357


  14 in total

1.  From metallic cages to transient bioresorbable scaffolds: change in paradigm of coronary revascularization in the upcoming decade?

Authors:  Patrick W Serruys; Hector M Garcia-Garcia; Yoshinobu Onuma
Journal:  Eur Heart J       Date:  2011-10-31       Impact factor: 29.983

2.  Bioresorbable Scaffolds versus Metallic Stents in Routine PCI.

Authors:  Joanna J Wykrzykowska; Robin P Kraak; Sjoerd H Hofma; Rene J van der Schaaf; E Karin Arkenbout; Alexander J IJsselmuiden; Joëlle Elias; Ivo M van Dongen; Ruben Y G Tijssen; Karel T Koch; Jan Baan; M Marije Vis; Robbert J de Winter; Jan J Piek; Jan G P Tijssen; Jose P S Henriques
Journal:  N Engl J Med       Date:  2017-03-29       Impact factor: 91.245

Review 3.  2-year outcomes with the Absorb bioresorbable scaffold for treatment of coronary artery disease: a systematic review and meta-analysis of seven randomised trials with an individual patient data substudy.

Authors:  Ziad A Ali; Patrick W Serruys; Takeshi Kimura; Runlin Gao; Stephen G Ellis; Dean J Kereiakes; Yoshinobu Onuma; Charles Simonton; Zhen Zhang; Gregg W Stone
Journal:  Lancet       Date:  2017-07-18       Impact factor: 79.321

4.  Anatomical and clinical characteristics to guide decision making between coronary artery bypass surgery and percutaneous coronary intervention for individual patients: development and validation of SYNTAX score II.

Authors:  Vasim Farooq; David van Klaveren; Ewout W Steyerberg; Emanuele Meliga; Yvonne Vergouwe; Alaide Chieffo; Arie Pieter Kappetein; Antonio Colombo; David R Holmes; Michael Mack; Ted Feldman; Marie-Claude Morice; Elisabeth Ståhle; Yoshinobu Onuma; Marie-angèle Morel; Hector M Garcia-Garcia; Gerrit Anne van Es; Keith D Dawkins; Friedrich W Mohr; Patrick W Serruys
Journal:  Lancet       Date:  2013-02-23       Impact factor: 79.321

5.  Complete two-year follow-up with formal non-inferiority testing on primary outcomes of the AIDA trial comparing the Absorb bioresorbable scaffold with the XIENCE drug-eluting metallic stent in routine PCI.

Authors:  Ruben Yannick G Tijssen; Robin P Kraak; Sjoerd H Hofma; Rene J van der Schaaf; E Karin Arkenbout; Auke Weevers; Joelle Elias; Ivo M van Dongen; Karel T Koch; Jan Baan; Marije Vis; Robbert J de Winter; Jan J Piek; Jan G P Tijssen; Jose P S Henriques; Joanna J Wykrzykowska
Journal:  EuroIntervention       Date:  2018-07-20       Impact factor: 6.534

6.  Predilation, sizing and post-dilation scoring in patients undergoing everolimus-eluting bioresorbable scaffold implantation for prediction of cardiac adverse events: development and internal validation of the PSP score.

Authors:  Luis Ortega-Paz; Davide Capodanno; Tommaso Gori; Holger Nef; Azeem Latib; Giuseppe Caramanno; Carlo Di Mario; Christoph Naber; Maciej Lesiak; Piera Capranzano; Jens Wiebe; Julinda Mehilli; Aleksander Araszkiewicz; Stelios Pyxaras; Alessio Mattesini; Salvatore Geraci; Toru Naganuma; Antonio Colombo; Thomas Münzel; Manel Sabaté; Corrado Tamburino; Salvatore Brugaletta
Journal:  EuroIntervention       Date:  2017-04-20       Impact factor: 6.534

7.  Comparison of an everolimus-eluting bioresorbable scaffold with an everolimus-eluting metallic stent for the treatment of coronary artery stenosis (ABSORB II): a 3 year, randomised, controlled, single-blind, multicentre clinical trial.

Authors:  Patrick W Serruys; Bernard Chevalier; Yohei Sotomi; Angel Cequier; Didier Carrié; Jan J Piek; Ad J Van Boven; Marcello Dominici; Dariusz Dudek; Dougal McClean; Steffen Helqvist; Michael Haude; Sebastian Reith; Manuel de Sousa Almeida; Gianluca Campo; Andrés Iñiguez; Manel Sabaté; Stephan Windecker; Yoshinobu Onuma
Journal:  Lancet       Date:  2016-10-30       Impact factor: 79.321

8.  Amsterdam Investigator-initiateD Absorb strategy all-comers trial (AIDA trial): a clinical evaluation comparing the efficacy and performance of ABSORB everolimus-eluting bioresorbable vascular scaffold strategy vs the XIENCE family (XIENCE PRIME or XIENCE Xpedition) everolimus-eluting coronary stent strategy in the treatment of coronary lesions in consecutive all-comers: rationale and study design.

Authors:  Pier Woudstra; Maik J Grundeken; Robin P Kraak; Mariëlla E C J Hassell; E Karin Arkenbout; Jan Baan; Marije M Vis; Karel T Koch; Jan G P Tijssen; Jan J Piek; Robbert J de Winter; José P S Henriques; Joanna J Wykrzykowska
Journal:  Am Heart J       Date:  2013-10-17       Impact factor: 4.749

9.  The Impact of Post-Procedural Asymmetry, Expansion, and Eccentricity of Bioresorbable Everolimus-Eluting Scaffold and Metallic Everolimus-Eluting Stent on Clinical Outcomes in the ABSORB II Trial.

Authors:  Pannipa Suwannasom; Yohei Sotomi; Yuki Ishibashi; Rafael Cavalcante; Felipe N Albuquerque; Carlos Macaya; John A Ormiston; Jonathan Hill; Irene M Lang; Mohaned Egred; Jean Fajadet; Maciej Lesiak; Jan G Tijssen; Joanna J Wykrzykowska; Robbert J de Winter; Bernard Chevalier; Patrick W Serruys; Yoshinobu Onuma
Journal:  JACC Cardiovasc Interv       Date:  2016-06-01       Impact factor: 11.195

10.  Predictive value of SYNTAX score II for clinical outcomes in cardiogenic shock underwent primary percutaneous coronary intervention; a pilot study.

Authors:  Mert İlker Hayıroğlu; Muhammed Keskin; Ahmet Okan Uzun; Emrah Bozbeyoğlu; Özlem Yıldırımtürk; Ömer Kozan; Seçkin Pehlivanoğlu
Journal:  Int J Cardiovasc Imaging       Date:  2017-09-09       Impact factor: 2.357

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