Impact of procedural success on clinical outcome after MitraClip: Results from the MITRA-FR trial.


Journal

Archives of cardiovascular diseases
ISSN: 1875-2128
Titre abrégé: Arch Cardiovasc Dis
Pays: Netherlands
ID NLM: 101465655

Informations de publication

Date de publication:
Nov 2022
Historique:
received: 28 12 2021
revised: 23 05 2022
accepted: 24 05 2022
pubmed: 17 10 2022
medline: 7 12 2022
entrez: 16 10 2022
Statut: ppublish

Résumé

Differences in procedural success rates have been proposed to explain the divergent results between the MITRA-FR trial (Percutaneous Repair with the MitraClip Device for Severe Functional/Secondary Mitral Regurgitation) and the COAPT trial (Cardiovascular Outcomes Assessment of the MitraClip Percutaneous Therapy for Heart Failure Patients with Functional Mitral Regurgitation). To examine whether MITRA-FR patients who had successful clip implantation achieved a better outcome than the control group. Based on the per protocol population of MITRA-FR, we compared the outcome in 71 patients in whom optimal clip implantation was achieved (group 1: mitral regurgitation grade ≤ 1 + at discharge) with that in 23 patients with non-optimal clip implantation (group 2: mitral regurgitation grade ≥ 2 + at discharge) and that in 137 patients in the control group (group 3). The primary endpoint was all-cause death or unplanned hospitalization for heart failure at 24 months. Event-free survival was not different across the groups (42±6% in group 1, 30±10% in group 2 and 31±4% in group 3; log-rank P=0.32). In multivariable analyses, after adjustment for age, sex, rhythm, aetiology, left ventricular ejection fraction and mitral regurgitation severity, group was not associated with variations in outcome: using Group 3 as reference, hazard ratio 0.86, 95% confidence interval 0.58-1.27 (P=0.43) in group 1; and hazard ratio 0.98 95% confidence interval 0.54-1.76 (P=0.94) in group 2. The clinical outcome of patients in whom optimal procedural result was achieved at discharge was not different compared with the control group. Our results do not support the hypothesis that the differences in rates of residual mitral regurgitation at discharge between MITRA-FR and COAPT explain the divergent results between the two trials.

Sections du résumé

BACKGROUND BACKGROUND
Differences in procedural success rates have been proposed to explain the divergent results between the MITRA-FR trial (Percutaneous Repair with the MitraClip Device for Severe Functional/Secondary Mitral Regurgitation) and the COAPT trial (Cardiovascular Outcomes Assessment of the MitraClip Percutaneous Therapy for Heart Failure Patients with Functional Mitral Regurgitation).
AIM OBJECTIVE
To examine whether MITRA-FR patients who had successful clip implantation achieved a better outcome than the control group.
METHODS METHODS
Based on the per protocol population of MITRA-FR, we compared the outcome in 71 patients in whom optimal clip implantation was achieved (group 1: mitral regurgitation grade ≤ 1 + at discharge) with that in 23 patients with non-optimal clip implantation (group 2: mitral regurgitation grade ≥ 2 + at discharge) and that in 137 patients in the control group (group 3). The primary endpoint was all-cause death or unplanned hospitalization for heart failure at 24 months.
RESULTS RESULTS
Event-free survival was not different across the groups (42±6% in group 1, 30±10% in group 2 and 31±4% in group 3; log-rank P=0.32). In multivariable analyses, after adjustment for age, sex, rhythm, aetiology, left ventricular ejection fraction and mitral regurgitation severity, group was not associated with variations in outcome: using Group 3 as reference, hazard ratio 0.86, 95% confidence interval 0.58-1.27 (P=0.43) in group 1; and hazard ratio 0.98 95% confidence interval 0.54-1.76 (P=0.94) in group 2.
CONCLUSIONS CONCLUSIONS
The clinical outcome of patients in whom optimal procedural result was achieved at discharge was not different compared with the control group. Our results do not support the hypothesis that the differences in rates of residual mitral regurgitation at discharge between MITRA-FR and COAPT explain the divergent results between the two trials.

Identifiants

pubmed: 36244966
pii: S1875-2136(22)00172-3
doi: 10.1016/j.acvd.2022.05.013
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

545-551

Informations de copyright

Copyright © 2022 Elsevier Masson SAS. All rights reserved.

Auteurs

David Messika-Zeitoun (D)

Department of Cardiology, University of Ottawa Heart Institute, ON K1Y 4W7 Ottawa, Canada. Electronic address: dmessika-zeitoun@ottawaheart.ca.

David Attias (D)

Centre Cardiologique du Nord, 93200 Saint-Denis, France.

Nicolas Piriou (N)

Inserm, CNRS, Institut du thorax, CHU de Nantes, Université de Nantes, 44007 Nantes, France.

Bernard Iung (B)

Inserm 1148, Université de Paris, 75877 Paris, France; Hôpital Bichat, AP-HP, 75018 Paris, France.

Xavier Armoiry (X)

Pharmacy Department, Hôpital Édouard-Herriot, 69003 Lyon, France; Laboratoire MATEIS, Université Claude-Bernard, 69100 Villeurbanne, France.

Jean-Noël Trochu (JN)

Inserm, CNRS, Institut du thorax, CHU de Nantes, Université de Nantes, 44007 Nantes, France; Hôpital Guillaume- et René-Laennec, 44093 Saint-Herblain, France.

Erwan Donal (E)

CHU de Rennes, Hôpital Pontchaillou, 35000 Rennes, France; Inserm, LTSI UMR 1099, Université de Rennes 1, 35043 Rennes, France.

Gilbert Habib (G)

Cardiology Department, Hôpital de la Timone, AP-HM, 13005 Marseille, France; IRD, APHM, MEPHI, IHU-Méditerranée Infection, Aix-Marseille Université, 13005 Marseille, France.

Bertrand Cormier (B)

Institut Cardiovasculaire Paris Sud, Hôpital Privé Jacques-Cartier, 91300 Massy, France.

Patrice Guerin (P)

Inserm UMR 1229, Interventional Cardiology Unit, Institut du Thorax, CHU de Nantes, Université de Nantes, 44007 Nantes, France.

Thierry Lefèvre (T)

Institut Cardiovasculaire Paris Sud, Hôpital Privé Jacques-Cartier, 91300 Massy, France.

Delphine Maucort-Boulch (D)

Université Lyon 1, 69100 Villeurbanne, France; Équipe Biostatistique-Santé, Pôle Santé Publique, Laboratoire de Biométrie et Biologie Évolutive, CNRS, UMR 5558, Service de Biostatistique-Bioinformatique, Hospices Civils de Lyon, 69622 Villeurbanne, France.

Florent Boutitie (F)

Université Lyon 1, 69100 Villeurbanne, France; Équipe Biostatistique-Santé, Pôle Santé Publique, Laboratoire de Biométrie et Biologie Évolutive, CNRS, UMR 5558, Service de Biostatistique-Bioinformatique, Hospices Civils de Lyon, 69622 Villeurbanne, France.

Alec Vahanian (A)

Inserm 1148, Université de Paris, 75877 Paris, France.

Benjamin Riche (B)

Université Lyon 1, 69100 Villeurbanne, France; Équipe Biostatistique-Santé, Pôle Santé Publique, Laboratoire de Biométrie et Biologie Évolutive, CNRS, UMR 5558, Service de Biostatistique-Bioinformatique, Hospices Civils de Lyon, 69622 Villeurbanne, France.

Jean-Francois Obadia (JF)

Chirurgie Cardiovasculaire et Transplantation Cardiaque, Hôpital Cardiovasculaire Louis Pradel, Université Claude-Bernard, Hospices Civils de Lyon, 69677 Bron, France. Electronic address: jean-francois.obadia@chu-lyon.fr.

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