» Articles » PMID: 26642470

What is Better for Predilatation in Bioresorbable Vascular Scaffold Implantation: a Non-compliant or a Compliant Balloon?

Overview
Publisher Kare Publishing
Date 2015 Dec 8
PMID 26642470
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: The bioresorbable vascular scaffold system (BVS) is a fully absorbable vascular treatment system. In this study, we aimed to compare the periprocedural effectiveness and long term results of non-compliant balloon (NCB) and compliant balloon (CB) systems, which are used for predilatation before BVS implantation.

Methods: One hundred forty-six BVS-treated lesions from 119 patients were retrospectively analyzed in the study. Patients with acute coronary syndrome, stable angina and silent ischemia were included in the study. Lesions and patients were categorized into the NCB and CB groups according to the type of balloon used for predilatation. NCB was implemented on 72 lesions (59 patients) and CB was implemented on 74 lesions (60 patients). The two groups were compared on terms of procedural features and both in-hospital and 1-year clinical follow-up results. Chi-square and independent sample t test were performed for statistical analysis.

Results: There was no significant difference between the two groups in terms of patient characteristics and lesion properties. The number of postdilated lesions was significantly higher in the CB group. Procedure time, fluoroscopy time, and contrast volume were significantly lower in the NCB group. At follow-up, one patient had myocardial infarction in the CB group because of scaffold thrombosis and no mortality was observed.

Conclusion: Predilatation with NCB before BVS implantation reduces the need for postdilatation. In addition, use of NCB reduces the procedure time, fluoroscopy time, and contrast volume but had no effect on 1 year clinical follow-up results compared with CB.

Citing Articles

Clinical Outcomes of a Non-Compliant Balloon Dilatation Catheter: MOZEC™ NC Study.

Pradhan A, Vishwakarma P, Bhandari M, Sethi R, Chandra S, Chaudhary G Int J Environ Res Public Health. 2022; 19(23).

PMID: 36498303 PMC: 9738498. DOI: 10.3390/ijerph192316231.


The use of semi-compliant versus non-compliant balloon systems for predilatation during the implantation of self-expandable transcatheter aortic valves: Data from the VIenna CardioThOracic Aortic Valve RegistrY (VICTORY).

Mach M, Szalkiewicz P, Poschner T, Hasan W, Andreas M, Winkler B Eur J Clin Invest. 2021; 51(9):e13570.

PMID: 33954997 PMC: 8459263. DOI: 10.1111/eci.13570.


Author`s Reply.

Ozel E Anatol J Cardiol. 2017; 17(1):75-76.

PMID: 28144009 PMC: 5324869.


Balloon postdilatation is a mandatory step in the deployment of bioresorbable vascular scaffold.

Karabulut A Anatol J Cardiol. 2017; 17(1):75.

PMID: 28144008 PMC: 5324868. DOI: 10.14744/AnatolJCardiol.2017.7551.


Procedural and one-year clinical outcomes of bioresorbable vascular scaffolds for the treatment of chronic total occlusions: a single-centre experience.

Ozel E, Tastan A, Ozturk A, Ozcan E, Kilicaslan B, Ozdogan O Cardiovasc J Afr. 2016; 27(6):345-349.

PMID: 27078224 PMC: 5408394. DOI: 10.5830/CVJA-2016-033.

References
1.
Baim D, Flatley M, Caputo R, OShaughnessy C, Low R, Fanelli C . Comparison of PRE-dilatation vs direct stenting in coronary treatment using the Medtronic AVE S670 Coronary Stent System (the PREDICT trial). Am J Cardiol. 2001; 88(12):1364-9. DOI: 10.1016/s0002-9149(01)02114-2. View

2.
Gomez-Lara J, Diletti R, Brugaletta S, Onuma Y, Farooq V, Thuesen L . Angiographic maximal luminal diameter and appropriate deployment of the everolimus-eluting bioresorbable vascular scaffold as assessed by optical coherence tomography: an ABSORB cohort B trial sub-study. EuroIntervention. 2011; 8(2):214-24. DOI: 10.4244/EIJV8I2A35. View

3.
Gomez-Lara J, Garcia-Garcia H, Onuma Y, Garg S, Regar E, De Bruyne B . A comparison of the conformability of everolimus-eluting bioresorbable vascular scaffolds to metal platform coronary stents. JACC Cardiovasc Interv. 2010; 3(11):1190-8. DOI: 10.1016/j.jcin.2010.07.016. View

4.
Zueco J, Lopez-Minguez J, Moreu J, Calvo I, Ramirez J, Alonso M . Direct coronary stenting versus stenting with balloon pre-dilation: immediate and follow-up results of a multicentre, prospective, randomized study. The DISCO trial. DIrect Stenting of COronary Arteries. Eur Heart J. 2002; 23(8):633-40. DOI: 10.1053/euhj.2001.2893. View

5.
Serruys P, Chevalier B, Dudek D, Cequier A, Carrie D, Iniguez A . A bioresorbable everolimus-eluting scaffold versus a metallic everolimus-eluting stent for ischaemic heart disease caused by de-novo native coronary artery lesions (ABSORB II): an interim 1-year analysis of clinical and procedural secondary outcomes.... Lancet. 2014; 385(9962):43-54. DOI: 10.1016/S0140-6736(14)61455-0. View