Radial vs Femoral Access in ACS Patients Undergoing Complex PCI Is Associated With Consistent Bleeding Benefit and No Excess of Risks.


Journal

The Canadian journal of cardiology
ISSN: 1916-7075
Titre abrégé: Can J Cardiol
Pays: England
ID NLM: 8510280

Informations de publication

Date de publication:
10 2022
Historique:
received: 20 01 2022
revised: 15 06 2022
accepted: 17 06 2022
pubmed: 27 6 2022
medline: 12 10 2022
entrez: 26 6 2022
Statut: ppublish

Résumé

The comparative effectiveness of transradial (TRA) compared with transfemoral (TFA) access in acute coronary syndrome (ACS) patients undergoing complex percutaneous coronary intervention (PCI) remains unclear. Among 8404 ACS patients in the Minimising Adverse Haemorrhagic Events by Transradial Access Site and Systemic Implementation of AngioX (MATRIX)-Access trial, 5233 underwent noncomplex (TRA: n = 2590; TFA: n = 2643) and 1491 complex (TRA: n = 777; TFA: n = 714) PCI. Co-primary outcomes were major adverse cardiovascular events (MACE, the composite of all-cause mortality, myocardial infarction, or stroke) and the composite of MACE and Bleeding Academic Research Consortium (BARC) type 3 or 5 bleeding (net adverse cardiovascular events [NACE]) at 30 days. Rates of 30-day MACE (HR 0.94, 95% CI 0.72-1.22) or NACE (HR 0.89, 95% CI 0.69-1.14) did not significantly differ between groups in the complex PCI group, whereas both primary end points were lower (HR 0.84, 95% CI 0.70-1.00; HR 0.83, 95% CI 0.70-0.98; respectively) with TRA among noncomplex PCI patients, with negative interaction testing (P Among ACS patients, PCI complexity did not affect the comparative efficacy and safety of TRA vs TFA, whereas the absolute risk reduction of access-site major bleeding was greater with TRA compared with TFA in complex as opposed to noncomplex PCI.

Sections du résumé

BACKGROUND
The comparative effectiveness of transradial (TRA) compared with transfemoral (TFA) access in acute coronary syndrome (ACS) patients undergoing complex percutaneous coronary intervention (PCI) remains unclear.
METHODS
Among 8404 ACS patients in the Minimising Adverse Haemorrhagic Events by Transradial Access Site and Systemic Implementation of AngioX (MATRIX)-Access trial, 5233 underwent noncomplex (TRA: n = 2590; TFA: n = 2643) and 1491 complex (TRA: n = 777; TFA: n = 714) PCI. Co-primary outcomes were major adverse cardiovascular events (MACE, the composite of all-cause mortality, myocardial infarction, or stroke) and the composite of MACE and Bleeding Academic Research Consortium (BARC) type 3 or 5 bleeding (net adverse cardiovascular events [NACE]) at 30 days.
RESULTS
Rates of 30-day MACE (HR 0.94, 95% CI 0.72-1.22) or NACE (HR 0.89, 95% CI 0.69-1.14) did not significantly differ between groups in the complex PCI group, whereas both primary end points were lower (HR 0.84, 95% CI 0.70-1.00; HR 0.83, 95% CI 0.70-0.98; respectively) with TRA among noncomplex PCI patients, with negative interaction testing (P
CONCLUSIONS
Among ACS patients, PCI complexity did not affect the comparative efficacy and safety of TRA vs TFA, whereas the absolute risk reduction of access-site major bleeding was greater with TRA compared with TFA in complex as opposed to noncomplex PCI.

Identifiants

pubmed: 35753631
pii: S0828-282X(22)00394-4
doi: 10.1016/j.cjca.2022.06.014
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1488-1500

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 Canadian Cardiovascular Society. Published by Elsevier Inc. All rights reserved.

Auteurs

Antonio Landi (A)

Division of Cardiology, Cardiocentro Ticino Institute, Ente Ospedaliero Cantonale, Lugano, Switzerland.

Mattia Branca (M)

Clinical Trials Unit, Faculty of Medicine, University of Bern, Bern, Switzerland.

Pascal Vranckx (P)

Department of Cardiology and Critical Care Medicine, Hartcentrum Hasselt, Jessa Ziekenhuis, Hasselt, Belgium; Faculty of Medicine and Life Sciences, University of Hasselt, Hasselt, Belgium.

Sergio Leonardi (S)

University of Pavia and Fondazione IRCCS Policlinico San Matteo, Pavia, Italy; University of Pavia and Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.

Enrico Frigoli (E)

Clinical Trials Unit, Faculty of Medicine, University of Bern, Bern, Switzerland.

Dik Heg (D)

Clinical Trials Unit, Faculty of Medicine, University of Bern, Bern, Switzerland.

Paolo Calabro (P)

Division of Cardiology, "Sant'Anna e San Sebastiano" Hospital, Department of Translational Medicine, University of Campania "Luigi Vanvitelli," Caserta, Italy; Division of Cardiology, "Sant'Anna e San Sebastiano" Hospital, Department of Translational Medicine, University of Campania "Luigi Vanvitelli," Caserta, Italy.

Giovanni Esposito (G)

Department of Advanced Biomedical Sciences, Federico II University of Naples, Naples, Italy.

Gennaro Sardella (G)

Department of Cardiovascular Sciences, Policlinico Umberto I, Sapienza University of Rome, Rome, Italy.

Carlo Tumscitz (C)

Cardiology Unit, Azienda Ospedaliero Universitaria di Ferrara, Cona, Italy.

Stefano Garducci (S)

Unità Operativa Complessa di Cardiologia, Azienda Socio-Sanitaria Territoriale della Brianza (MB), Vimercate Hospital, Vimercate, Italy.

Giuseppe Andò (G)

Azienda Ospedaliera Universitaria Policlinico "Gaetano Martino," University of Messina, Messina, Italy.

Ugo Limbruno (U)

Cardiology Department, Misericordia Hospital, Grosseto, Italy.

Paolo Sganzerla (P)

IRCCS Istituto Auxologico Italiano, Ospedale San Luca, Milan, Italy.

Andrea Santarelli (A)

Cardiovascular Department, Infermi Hospital, Rimini, Italy.

Carlo Briguori (C)

Interventional Cardiology Unit, Mediterranea Cardiocentro, Naples, Italy.

Jose M de la Torre Hernandez (JM)

Hospital Universitario Marqués de Valdecilla, Instituto de Investigación Sanitaria Valdecilla, Santander, Spain.

Giovanni Pedrazzini (G)

Division of Cardiology, Cardiocentro Ticino Institute, Ente Ospedaliero Cantonale, Lugano, Switzerland; Department of Biomedical Sciences, University of Italian Switzerland, Lugano, Switzerland.

Stephan Windecker (S)

Department of Cardiology, University of Bern, Bern, Switzerland.

Marco Valgimigli (M)

Division of Cardiology, Cardiocentro Ticino Institute, Ente Ospedaliero Cantonale, Lugano, Switzerland; Department of Biomedical Sciences, University of Italian Switzerland, Lugano, Switzerland. Electronic address: marco.valgimigli@eoc.ch.

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