Outcomes of transcatheter aortic valve implantation for native aortic valve regurgitation.


Journal

EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology
ISSN: 1969-6213
Titre abrégé: EuroIntervention
Pays: France
ID NLM: 101251040

Informations de publication

Date de publication:
02 Sep 2024
Historique:
medline: 2 9 2024
pubmed: 2 9 2024
entrez: 2 9 2024
Statut: epublish

Résumé

Large datasets of transcatheter aortic valve implantation (TAVI) for pure aortic valve regurgitation (PAVR) are scarce. We aimed to report procedural safety and long-term clinical events (CE) in a contemporary cohort of PAVR patients treated with new-generation devices (NGD). Patients with grade III/IV PAVR enrolled in the FRANCE-TAVI Registry were selected. The primary safety endpoint was technical success (TS) according to Valve Academic Research Consortium 3 criteria. The co-primary endpoint was defined as a composite of mortality, heart failure hospitalisation and valve reintervention at last follow-up. From 2015 to 2021, 227 individuals (64.3% males, median age 81.0 [interquartile range {IQR} 73.5-85.0] years, with EuroSCORE II 6.0% [IQR 4.0-10.9]) from 41 centres underwent TAVI with NGD, using either self-expanding (55.1%) or balloon-expandable valves (44.9%; p=0.50). TS was 85.5%, with a non-significant trend towards increased TS in high-volume activity centres. A second valve implantation (SVI) was needed in 8.8% of patients, independent of valve type (p=0.82). Device size was ≥29 mm in 73.0% of patients, post-procedure grade ≥III residual aortic regurgitation was rare (1.2%), and the permanent pacemaker implantation (PPI) rate was 36.0%. At 30 days, the incidences of mortality and reintervention were 8.4% and 3.5%, respectively. The co-primary endpoint reached 41.6% (IQR 34.4-49.6) at 1 year, increased up to 61.8% (IQR 52.4-71.2) at 4 years, and was independently predicted by TS, with a hazard ratio of 0.45 (95% confidence interval: 0.27-0.76); p=0.003. TAVI with NGD in PAVR patients is efficient and reasonably safe. Preventing the need for an SVI embodies the major technical challenge. Larger implanted valves may have limited this complication, outweighing the increased risk of PPI. Despite successful TAVI, PAVR patients experience frequent CE at long-term follow-up.

Sections du résumé

BACKGROUND BACKGROUND
Large datasets of transcatheter aortic valve implantation (TAVI) for pure aortic valve regurgitation (PAVR) are scarce.
AIMS OBJECTIVE
We aimed to report procedural safety and long-term clinical events (CE) in a contemporary cohort of PAVR patients treated with new-generation devices (NGD).
METHODS METHODS
Patients with grade III/IV PAVR enrolled in the FRANCE-TAVI Registry were selected. The primary safety endpoint was technical success (TS) according to Valve Academic Research Consortium 3 criteria. The co-primary endpoint was defined as a composite of mortality, heart failure hospitalisation and valve reintervention at last follow-up.
RESULTS RESULTS
From 2015 to 2021, 227 individuals (64.3% males, median age 81.0 [interquartile range {IQR} 73.5-85.0] years, with EuroSCORE II 6.0% [IQR 4.0-10.9]) from 41 centres underwent TAVI with NGD, using either self-expanding (55.1%) or balloon-expandable valves (44.9%; p=0.50). TS was 85.5%, with a non-significant trend towards increased TS in high-volume activity centres. A second valve implantation (SVI) was needed in 8.8% of patients, independent of valve type (p=0.82). Device size was ≥29 mm in 73.0% of patients, post-procedure grade ≥III residual aortic regurgitation was rare (1.2%), and the permanent pacemaker implantation (PPI) rate was 36.0%. At 30 days, the incidences of mortality and reintervention were 8.4% and 3.5%, respectively. The co-primary endpoint reached 41.6% (IQR 34.4-49.6) at 1 year, increased up to 61.8% (IQR 52.4-71.2) at 4 years, and was independently predicted by TS, with a hazard ratio of 0.45 (95% confidence interval: 0.27-0.76); p=0.003.
CONCLUSIONS CONCLUSIONS
TAVI with NGD in PAVR patients is efficient and reasonably safe. Preventing the need for an SVI embodies the major technical challenge. Larger implanted valves may have limited this complication, outweighing the increased risk of PPI. Despite successful TAVI, PAVR patients experience frequent CE at long-term follow-up.

Identifiants

pubmed: 39219361
pii: EIJ-D-24-00339
doi: 10.4244/EIJ-D-24-00339
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1076-e1085

Auteurs

Robin Le Ruz (R)

Interventional Cardiology Department, Nantes Université, CHU Nantes, L'institut du thorax, Nantes, France.
Nantes Université, CHU Nantes, CNRS, INSERM, L'institut du thorax, Nantes, France.

Lionel Leroux (L)

Department of Cardiology and Cardiovascular Surgery, Hôpital Cardiologique de Haut-Lévêque, Pessac, France.

Thibault Lhermusier (T)

Department of Cardiology, Rangueil University Hospital, Toulouse, France.

Thomas Cuisset (T)

Centre for Cardiovascular and Nutrition Research, Aix Marseille Université, Marseille, France.

Eric Van Belle (E)

University of Lille, INSERM, Centre Hospitalier Universitaire Lille, Institut Pasteur de Lille, Lille, France.

Alain Dibie (A)

Institut Mutualiste Montsouris, Paris, France.

Vincenzo Palermo (V)

Hôpital Marie-Lannelongue (groupe hospitalier Paris Saint-Joseph), Le Plessis-Robinson, France.

Didier Champagnac (D)

Médipôle Lyon-Villeurbanne, Villeurbanne, France.

Jean-François Obadia (JF)

Clinical Investigation Center & Heart Failure Department, Hôpital Cardiovasculaire Louis Pradel, INSERM 1407, Hospices Civils de Lyon and Claude Bernard University, Lyon, France.

Emmanuel Teiger (E)

Department of Cardiology, APHP, Henri-Mondor University Hospital, Créteil, France.

Patrick Ohlman (P)

Department of Cardiology, University Hospital of Strasbourg, Strasbourg, France.

Didier Tchétché (D)

Clinique Pasteur, Toulouse, France.

Hervé Le Breton (H)

Department of Cardiology, University of Rennes, CHU Rennes, INSERM, LTSI - UMR 1099, Rennes, France.

Christophe Saint-Etienne (C)

Centre Hospitalier Régional Universitaire Tours, Tours, France.

Pierre-Guillaume Piriou (PG)

Interventional Cardiology Department, Nantes Université, CHU Nantes, L'institut du thorax, Nantes, France.

Julien Plessis (J)

Interventional Cardiology Department, Nantes Université, CHU Nantes, L'institut du thorax, Nantes, France.

Sylvain Beurtheret (S)

Saint-Joseph Hospital, Marseille, France.

Florence Du Chayla (F)

Clinityx, Paris, France.

Manon Leclère (M)

Clinityx, Paris, France.

Thierry Lefèvre (T)

Institut Cardiovasculaire Paris Sud, Hôpital privé Jacques Cartier, Ramsay Santé, Massy, France.

Jean-Philippe Collet (JP)

ACTION Study Group, Sorbonne Université, UMRS 1166, Institut de Cardiologie, Pitié-Salpêtrière Hospital (AP-HP), Paris, France.

Hélène Eltchaninoff (H)

Department of Cardiology, University Rouen Normandie, INSERM U1096, CHU Rouen, Rouen, France.

Martine Gilard (M)

Department of Cardiology, Brest University Hospital, Brest, France.

Bernard Iung (B)

Department of Cardiology, Université Paris-Cité, Paris, France and Assistance Publique-Hôpitaux de Paris (AP-HP), Bichat Hospital, Paris, France.

Thibaut Manigold (T)

Interventional Cardiology Department, Nantes Université, CHU Nantes, L'institut du thorax, Nantes, France.

Vincent Letocart (V)

Interventional Cardiology Department, Nantes Université, CHU Nantes, L'institut du thorax, Nantes, France.

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