Retrograde Chronic Total Occlusion Percutaneous Coronary Interventions: Predictors of Procedural Success From the ERCTO Registry.


Journal

JACC. Cardiovascular interventions
ISSN: 1876-7605
Titre abrégé: JACC Cardiovasc Interv
Pays: United States
ID NLM: 101467004

Informations de publication

Date de publication:
25 04 2022
Historique:
received: 22 09 2021
revised: 31 01 2022
accepted: 08 02 2022
entrez: 22 4 2022
pubmed: 23 4 2022
medline: 26 4 2022
Statut: ppublish

Résumé

The aim of this study was to identify independent predictors of procedural success after retrograde chronic total occlusion (CTO) percutaneous coronary intervention (PCI). Retrograde CTO PCI is an established technique, but predictors of success remain poorly understood. A multivariable logistic regression model was used to analyze potentially important demographic, clinical, anatomical, and technical aspects of retrograde CTO PCI cases uploaded to the multicenter European CTO (ERCTO) Club Registry. In calendar years 2018 and 2019, 2,364 retrograde CTO PCI cases constituted the primary analysis cohort. A primary retrograde strategy was used in 1,953 cases (82.6%), and an initial antegrade approach was converted to retrograde in 411 cases (17.4%). Procedural success was achieved in 1,820 cases (77.0%) and was more likely to occur after a primary retrograde attempt versus conversion from an initial antegrade approach (80.9% vs 58.4%; P < 0.0001). After multivariable analysis, an absence of lesion calcification (OR: 1.86; 95% CI: 1.37-2.51; P < 0.0001), a higher degree of distal vessel opacification (OR: 2.47; 95% CI: 1.72-3.55; P < 0.0001), little or no proximal target vessel tortuosity (OR: 1.84; 95% CI: 1.28-2.64; P = 0.001), Werner collateral connection CC1 (OR: 4.87; 95% CI: 2.90-8.19; P < 0.0001) or CC2 (OR: 5.33; 95% CI: 3.02-9.42; P < 0.0001), and the top tertile of operator volume (>120 cases over 2 years) (OR: 1.88; 95% CI: 1.26-2.79; P = 0.002) were associated with the greatest chance of achieving angiographic success. Less calcification with good distal vessel opacification, little or absent proximal vessel tortuosity, and visible collateral connections, along with high-volume operator status, were all independently predictive of angiographically successful retrograde CTO PCI.

Sections du résumé

OBJECTIVES
The aim of this study was to identify independent predictors of procedural success after retrograde chronic total occlusion (CTO) percutaneous coronary intervention (PCI).
BACKGROUND
Retrograde CTO PCI is an established technique, but predictors of success remain poorly understood.
METHODS
A multivariable logistic regression model was used to analyze potentially important demographic, clinical, anatomical, and technical aspects of retrograde CTO PCI cases uploaded to the multicenter European CTO (ERCTO) Club Registry.
RESULTS
In calendar years 2018 and 2019, 2,364 retrograde CTO PCI cases constituted the primary analysis cohort. A primary retrograde strategy was used in 1,953 cases (82.6%), and an initial antegrade approach was converted to retrograde in 411 cases (17.4%). Procedural success was achieved in 1,820 cases (77.0%) and was more likely to occur after a primary retrograde attempt versus conversion from an initial antegrade approach (80.9% vs 58.4%; P < 0.0001). After multivariable analysis, an absence of lesion calcification (OR: 1.86; 95% CI: 1.37-2.51; P < 0.0001), a higher degree of distal vessel opacification (OR: 2.47; 95% CI: 1.72-3.55; P < 0.0001), little or no proximal target vessel tortuosity (OR: 1.84; 95% CI: 1.28-2.64; P = 0.001), Werner collateral connection CC1 (OR: 4.87; 95% CI: 2.90-8.19; P < 0.0001) or CC2 (OR: 5.33; 95% CI: 3.02-9.42; P < 0.0001), and the top tertile of operator volume (>120 cases over 2 years) (OR: 1.88; 95% CI: 1.26-2.79; P = 0.002) were associated with the greatest chance of achieving angiographic success.
CONCLUSIONS
Less calcification with good distal vessel opacification, little or absent proximal vessel tortuosity, and visible collateral connections, along with high-volume operator status, were all independently predictive of angiographically successful retrograde CTO PCI.

Identifiants

pubmed: 35450685
pii: S1936-8798(22)00498-8
doi: 10.1016/j.jcin.2022.02.013
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

834-842

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Dr Mashayekhi has received consulting, speaker, and proctoring honoraria from Abbott Vascular, Asahi Intecc, AstraZeneca, Biotronik, Boston Scientific, Cardinal Health, Daiichi-Sankyo, Medtronic, Teleflex, and Terumo. Dr Avran has received consulting, speaker, and proctoring honoraria from Asahi Intecc, Biotronik, Boston Scientific, Terumo, Alvimedica, and OrbusNeich. Dr Boudou is a proctor and consultant for Asahi Intecc, Terumo, and Boston Scientific. Dr Garbo is a proctor and consultant for Philips Volcano, Boston Europe, Terumo Italy, and Europe Teleflex. Dr Bryniarski has received speaker and proctoring honoraria from Procardia Medical, Boston Scientific, and Terumo. Prof Spratt has received consulting, speaker, and proctoring honoraria from Abbott Vascular, Asahi Intecc, Boston Scientific, Cardinal Health, and Shockwave Medical. Dr Lesiak has received speaker and proctoring honoraria from Abbott Vascular, Boston Scientific, Biotronik, Medtronic, and Terumo Medical. Prof Di Mario has received research or educational grants from Abbott, Amgen, Asahi Intecc, AstraZeneca, Boston Scientific, Cardinal Health, Behring, Chiesi, Daiichi-Sankyo, Edwards Lifesciences, Medtronic, Menarini, Pfizer, Sanofi, Shockwave, Teleflex, and Volcano-Philips. Dr Hildick-Smith has served on the advisory boards for Abbott, Terumo, Boston Scientific, and Medtronic. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Aung Myat (A)

Sussex Cardiac Center, Brighton, United Kingdom.

Alfredo R Galassi (AR)

Cardiovascular Medicine Department of ProMISE University of Palermo, Palermo, Italy.

Gerald S Werner (GS)

Medizinische Klinik I, Klinikum Darmstadt, Darmstadt, Germany.

Kambis Mashayekhi (K)

Department of Cardiology and Angiology, II University Heartcenter Freiburg, Bad Krozingen, Germany.

Alexandre Avran (A)

Department of Interventional Cardiology, Clinique Pasteur, Essey-les-Nancy, France.

Nicolas Boudou (N)

Interventional Cardiology, Clinique Saint Augustin, Bordeaux, France.

Markus Meyer-Gessner (M)

Klinik Kardiologie Augusta Krankenhaus, Düsseldorf, Germany.

Nicolaus Reifart (N)

Department of Cardiology, Main Taunus Heart Institute, Bad Soden, Germany.

Maciej Lesiak (M)

I Department of Cardiology, Poznan University of Medical Sciences, Poznan, Poland.

Roberto Garbo (R)

Interventional Cardiology Department, Maria Pia Hospital, GVM Care and Research, Turin, Italy.

Alexander Bufe (A)

Heartcenter Krefeld, University Witten/Herdecke, Witten, Germany.

James Spratt (J)

St. George's University of London, London, United Kingdom.

Leszek Bryniarski (L)

II Department of Cardiology and Cardiovascular Interventions, Institute of Cardiology, Jagiellonian University Medical College, Kraków, Poland.

Evald H Christiansen (EH)

Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark.

Georgios Sianos (G)

1st Cardiology Department, AHEPA University Hospital, Thessaloniki, Greece.

Javier Escaned (J)

Hospital Clinico San Carlos IDISSC, Complutense University of Madrid, Madrid, Spain.

Carlo di Mario (C)

Department of Clinical & Experimental Medicine, University Hospital Careggi, Florence, Italy.

David Hildick-Smith (D)

Sussex Cardiac Center, Brighton, United Kingdom. Electronic address: david.hildick-smith@nhs.net.

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