Transcatheter valve‐in‐valve interventions after aortic root replacement: A systematic review

Author:

Baudo Massimo12ORCID,Cuko Besart3ORCID,Ternacle Julien3ORCID,Sicouri Serge2ORCID,Torregrossa Gianluca12ORCID,Pernot Mathieu3ORCID,Busuttil Olivier3ORCID,Beurton Antoine4ORCID,Alaux Anouk4,Ouattara Alexandre4ORCID,Lafitte Stephane3ORCID,Bonnet Guillaume35ORCID,Leroux Lionel3ORCID,De Vincentiis Carlo6ORCID,Labrousse Louis3ORCID,Ramlawi Basel12ORCID,Modine Thomas3ORCID

Affiliation:

1. Department of Cardiac Surgery, Lankenau Heart Institute Lankenau Medical Center, Main Line Health Wynnewood Pennsylvania USA

2. Department of Cardiac Surgery Research Lankenau Institute for Medical Research, Main Line Health Wynnewood Pennsylvania USA

3. Department of Cardiology and Cardio‐Vascular Surgery, Hopital Cardiologique de Haut‐Leveque Bordeaux University Hospital Pessac France

4. Department of Cardiovascular Anesthesia and Critical Care, Hopital Cardiologique de Haut‐Leveque Bordeaux University Hospital Pessac France

5. Cardiovascular Research Foundation New York New York USA

6. Department of Cardiac Surgery IRCCS Policlinico San Donato Milan Italy

Abstract

AbstractStructural valve deterioration after aortic root replacement (ARR) surgery may be treated by transcatheter valve‐in‐valve (ViV‐TAVI) intervention. However, several technical challenges and outcomes are not well described. The aim of the present review was to analyze the outcomes of ViV‐TAVI in deteriorated ARR. This review included studies reporting any form of transcatheter valvular intervention in patients with a previous ARR. All forms of ARR were considered, as long as the entire root was replaced. Pubmed, ScienceDirect, SciELO, DOAJ, and Cochrane library databases were searched until September 2023. Overall, 86 patients were included from 31 articles that met our inclusion criteria out of 741 potentially eligible studies. In the entire population, the mean time from ARR to reintervention was 11.0 years (range: 0.33–22). The most frequently performed techniques/grafts for ARR was homograft (67.4%) and the main indication for intervention was aortic regurgitation (69.7%). Twenty‐three articles reported no postoperative complications. Six (7.0%) patients required permanent pacemaker implantation (PPI) after the ViV‐TAVI procedure, and 4 (4.7%) patients had a second ViV‐TAVI implant. There were three device migrations (3.5%) and 1 stroke (1.2%). Patients with previous ARR present a high surgical risk. ViV‐TAVI can be considered in selected patients, despite unique technical challenges that need to be carefully addressed according to the characteristics of the previous surgery and on computed tomography analysis.

Publisher

Wiley

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