Von Willebrand Factor Activity Association With Outcomes After Transcatheter Edge-to-Edge Mitral Valve Repair.

CT-ADP MitraClip transcatheter mitral valve repair von Willebrand diseases von Willebrand factor

Journal

JACC. Advances
ISSN: 2772-963X
Titre abrégé: JACC Adv
Pays: United States
ID NLM: 9918419284106676

Informations de publication

Date de publication:
Oct 2024
Historique:
received: 27 11 2023
revised: 11 07 2024
accepted: 26 07 2024
medline: 23 9 2024
pubmed: 23 9 2024
entrez: 23 9 2024
Statut: epublish

Résumé

Residual mitral regurgitation (MR) is associated with worse outcomes after transcatheter edge-to-edge mitral valve repair (TEER). Shear stress induced by MR leads to altered von Willebrand factor activity (vWF:Act) and increased closure time with adenosine diphosphate (CT-ADP). The purpose of this study was to investigate the use of CT-ADP to monitor MR during TEER and the association between the vWF, residual MR, and clinical events post-TEER. Sixty-five patients undergoing TEER were enrolled. CT-ADP was measured at baseline, after each clip deployment, 1 hour and 24 hours post-TEER. CT-ADP values were related to vWF:Act/vWF antigen (vWF:Ag) ratio at the same time points, and MR severity was assessed by echocardiography at 1 month. Combined events of all-cause mortality and heart failure hospitalizations were evaluated at 1 year. At 1 month, 32 (49%) patients had residual MR > mild (of those, 14% had MR > moderate). There was no significant change in CT-ADP values during the procedure. However, CT-ADP significantly decreased 1-hour post-TEER ( CT-ADP evolution in time was not quick enough to provide real-time monitoring of MR severity during TEER. However, vWF:Act/vWF:Ag ratio at baseline and its variations following the procedure were associated with clinical outcomes. Those findings will need external validation.

Sections du résumé

Background UNASSIGNED
Residual mitral regurgitation (MR) is associated with worse outcomes after transcatheter edge-to-edge mitral valve repair (TEER). Shear stress induced by MR leads to altered von Willebrand factor activity (vWF:Act) and increased closure time with adenosine diphosphate (CT-ADP).
Objectives UNASSIGNED
The purpose of this study was to investigate the use of CT-ADP to monitor MR during TEER and the association between the vWF, residual MR, and clinical events post-TEER.
Methods UNASSIGNED
Sixty-five patients undergoing TEER were enrolled. CT-ADP was measured at baseline, after each clip deployment, 1 hour and 24 hours post-TEER. CT-ADP values were related to vWF:Act/vWF antigen (vWF:Ag) ratio at the same time points, and MR severity was assessed by echocardiography at 1 month. Combined events of all-cause mortality and heart failure hospitalizations were evaluated at 1 year.
Results UNASSIGNED
At 1 month, 32 (49%) patients had residual MR > mild (of those, 14% had MR > moderate). There was no significant change in CT-ADP values during the procedure. However, CT-ADP significantly decreased 1-hour post-TEER (
Conclusions UNASSIGNED
CT-ADP evolution in time was not quick enough to provide real-time monitoring of MR severity during TEER. However, vWF:Act/vWF:Ag ratio at baseline and its variations following the procedure were associated with clinical outcomes. Those findings will need external validation.

Identifiants

pubmed: 39309664
doi: 10.1016/j.jacadv.2024.101242
pii: S2772-963X(24)00473-3
pmc: PMC11414672
doi:

Types de publication

Journal Article

Langues

eng

Pagination

101242

Informations de copyright

© 2024 The Authors.

Déclaration de conflit d'intérêts

Ms Hadjadj and Dr Beaudoin are funded by Fonds de Recherche du Québec-Santé. This work was supported by Fondation de l’Institut Universitaire de Cardiologie et Pneumologie de Québec. Dr Rodés-Cabau holds the Research Chair “Fondation Famille Jacques Larivière” for the Development of Structural Heart Disease Interventions. Dr Pibarot has received institutional funding from 10.13039/100006520Edwards Lifesciences, 10.13039/100004374Medtronic, Pi-Cardia, and Cardiac Success for echocardiography core laboratory analyses and research studies in the field of interventional and pharmacologic treatment of valvular heart diseases, for which he received no personal compensation. Dr Beaudoin received research support from JAMP-Pharma, not related to the current work. All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Sandra Hadjadj (S)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Philippe Pibarot (P)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Caroline Gravel (C)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Marie-Annick Clavel (MA)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Ons Marsit (O)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Dounia Rouabhia (D)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Benoît M Labbé (BM)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Kim O'Connor (K)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Mathieu Bernier (M)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Erwan Salaun (E)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Julio Farjat (J)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Jorge Nuche Berenguer (J)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Josep Rodés-Cabau (J)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Jean-Michel Paradis (JM)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Jonathan Beaudoin (J)

Quebec Heart and Lung Institute - Laval University, Quebec, Quebec, Canada.

Classifications MeSH