Efficacy of Coronary Sinus Reducer in Patients With Non-revascularized Chronic Total Occlusions.


Journal

The American journal of cardiology
ISSN: 1879-1913
Titre abrégé: Am J Cardiol
Pays: United States
ID NLM: 0207277

Informations de publication

Date de publication:
01 07 2020
Historique:
received: 24 12 2019
revised: 27 03 2020
accepted: 27 03 2020
pubmed: 30 4 2020
medline: 1 9 2020
entrez: 30 4 2020
Statut: ppublish

Résumé

The coronary sinus reducer (CSR) has been introduced as therapy for patients with refractory angina with no other treatment options. Aim of this study is to investigate the efficacy of the CSR in patients with refractory angina and presence of coronary chronic total occlusions (CTO). In this multicentre, international retrospective study, patients undergoing CSR implantation were screened and divided in 2 groups according to the presence/absence of CTO lesions. Baseline and clinical characteristics were analyzed in the 2 groups. Primary-outcome consisted of the variation in Canadian Cardiovascular Society (CCS) class at 6-month follow-up. Between January 2014 and December 2018, 205 patients with refractory angina were consecutively treated with the study device in the participating centers, 103 (50.2%) of which had a CTO lesion at coronary angiogram and formed the CTO-group. Baseline characteristics of the study population were well balanced between the 2 groups. CSR was successfully implanted in all cases. Baseline CCS class was 3  ±  0.5 in the CTO-group versus 3.1  ±  0.6 in the non-CTO group (p = 0.45), and improved at follow-up to 1.6  ±  0.9 versus 2  ±  1.1 respectively (p <0.01), with a significantly higher improvement in CCS class in the CTO-group (1.4  ±  0.9 vs 1.1  ±  1 respectively, p = 0.01). Any improvement in CCS class was registered in 79 (80.6%) CTO-patients, while a significantly lower percentage (65 patients, 66.3%) of the non-CTO patients reported benefits in CCS class (p = 0.03). In conclusions, patients suffering from refractory angina with non-revascularized CTO lesions have a better response to CSR implantation than patients without CTOs. CSR implantation should be considered a valid complementary therapy to CTO-PCI in these patients.

Identifiants

pubmed: 32345474
pii: S0002-9149(20)30331-3
doi: 10.1016/j.amjcard.2020.03.042
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-7

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of Interests The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Carlo Zivelonghi (C)

HartCentrum, Ziekenhuis Netwerk Antwerpen (ZNA) Middelheim, Antwerp, Belgium; Department of Cardiology, Sint Antonius Ziekenhuis, Nieuwegein, The Netherlands.

Stefan Verheye (S)

HartCentrum, Ziekenhuis Netwerk Antwerpen (ZNA) Middelheim, Antwerp, Belgium.

Leo Timmers (L)

Department of Cardiology, Sint Antonius Ziekenhuis, Nieuwegein, The Netherlands; Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.

Jan Peter van Kuijk (JP)

Department of Cardiology, Sint Antonius Ziekenhuis, Nieuwegein, The Netherlands.

Francesco Giannini (F)

Interventional Cardiology Unit, GVM Care & Research Maria Cecilia Hospital, Ravenna, Italy.

Mirthe Dekker (M)

Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.

Max Silvis (M)

Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.

Masieh Abawi (M)

Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.

Geert Leenders (G)

Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.

Friso Kortland (F)

Department of Cardiology, Sint Antonius Ziekenhuis, Nieuwegein, The Netherlands.

Giorgos Tzanis (G)

Unit of Cardiovascular Interventions, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Alessandro Beneduce (A)

Unit of Cardiovascular Interventions, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Giovanni Benfari (G)

Department of Cardiology, University of Verona, Verona, Italy.

Pieter Stella (P)

Department of Cardiology, University Medical Center Utrecht, Utrecht, The Netherlands.

Josè Paulo Simao Henriques (JPS)

Department of Cardiology, University Medical Center, Amsterdam, The Netherlands.

Shmuel Banai (S)

Tel Aviv Medical Center, Tel Aviv University Sackler School of Medicine, Tel Aviv, Israel.

Pierfrancesco Agostoni (P)

HartCentrum, Ziekenhuis Netwerk Antwerpen (ZNA) Middelheim, Antwerp, Belgium; Department of Cardiology, Sint Antonius Ziekenhuis, Nieuwegein, The Netherlands. Electronic address: agostonipf@gmail.com.

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