Transcatheter Aortic Valve Implantation Access Sites: Same Goals, Distinct Aspects, Various Merits and Demerits

Author:

Katsaros Odysseas1ORCID,Apostolos Anastasios1ORCID,Ktenopoulos Nikolaos1ORCID,Koliastasis Leonidas12ORCID,Kachrimanidis Ioannis1,Drakopoulou Maria1,Korovesis Theofanis1,Karanasos Antonios1,Tsalamandris Sotirios3,Latsios George1,Synetos Andreas1,Tsioufis Konstantinos1,Toutouzas Konstantinos1

Affiliation:

1. First Department of Cardiology, National and Kapodistrian University of Athens, Hippokration General Hospital of Athens, 11527 Athens, Greece

2. Department of Cardiology, University of Brussels, CHU Saint-Pierre, 1000 Brussels, Belgium

3. Department of Cardiology, Hippokration General Hospital of Athens, 11527 Athens, Greece

Abstract

Transcatheter aortic valve implantation (TAVI) has been established as a safe and efficacious treatment for patients with severe symptomatic aortic stenosis (AS). Despite being initially developed and indicated for high-surgical-risk patients, it is now offered to low-risk populations based on the results of large randomized controlled trials. The most common access sites in the vast majority of patients undergoing TAVI are the common femoral arteries; however, 10–20% of the patients treated with TAVI require an alternative access route, mainly due to peripheral atherosclerotic disease or complex anatomy. Hence, to achieve successful delivery and implantation of the valve, several arterial approaches have been studied, including transcarotid (TCr), axillary/subclavian (A/Sc), transapical (TAp), transaortic (TAo), suprasternal-brachiocephalic (S-B), and transcaval (TCv). This review aims to concisely summarize the most recent literature data and current guidelines as well as evaluate the various access routes for TAVI, focusing on the indications, the various special patient groups, and the advantages and disadvantages of each technique, as well as their adverse events.

Publisher

MDPI AG

Subject

Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics

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