Initial experience of a MitraClip valve repair program in Spain.

MitraClip Spain program valve repair

Journal

Annals of translational medicine
ISSN: 2305-5839
Titre abrégé: Ann Transl Med
Pays: China
ID NLM: 101617978

Informations de publication

Date de publication:
Aug 2020
Historique:
entrez: 21 9 2020
pubmed: 22 9 2020
medline: 22 9 2020
Statut: ppublish

Résumé

The main objective of this study was to evaluate one-year clinical outcome of patients with symptomatic mitral regurgitation (MR) treated with transcatheter mitral valve repair (TMVR) according to the etiology of MR. Data from a single high-volume center of all consecutive cases with symptomatic MR undergoing TMVR where prospectively included and followed. Between October 2015 and October 2019, 81 consecutive patients underwent TMVR and were included in the investigation. The mean age was 75.73±7.81 years, 55 (67.9%) were male. The most frequent mechanism was functional MR (FMR) (59%). The mean EuroSCORE II was 5.7±4.94 [FMR 5.38±3.9, degenerative MR (DMR) 5.72±4.7 and mixed MR (MMR) 6.6±7.5; P=0.7776] and STS score mean was 5.21±3.31 (FMR 4.6±2.3, DMR 6.43±5.2 and MMR 5.7±3.2; P=0.126). Patients with FMR had higher rates of dilated (36 patients, 75.5%) and ischemic (15 patients, 31.3%) cardiomyopathy, as well as worse left ventricular ejection fraction (LVEF). Procedural success was achieved in 72 (88.9%) patients, with a similar distribution between groups. The median of follow-up was 16.3 months. The primary combined endpoint occurred in 19 (23.5%) cases. The number of the combined event regarding the different etiologies were 15 (31.2%) in FMR, 2 (11.8%) in DMR and 5 (31.3%) in MMR (P=0.276). Sixteen patients (20.0%) died during the first year of follow-up and 19 (23.5%) had unplanned heart failure (HF) hospitalization. Previous surgical revascularization (HR =4.94, P=0.004) and a redo TMVR (HR =11.3, P=0.006) predicted the main event. TMVR with the Mitraclip device is safe, with a low incidence of complications and a high rate of procedural success. One-year outcomes show reduction of all cause death and HF admissions. Moreover, most of the patients have sustained MR reduction and an improvement in the functional class at the end of follow-up.

Sections du résumé

BACKGROUND BACKGROUND
The main objective of this study was to evaluate one-year clinical outcome of patients with symptomatic mitral regurgitation (MR) treated with transcatheter mitral valve repair (TMVR) according to the etiology of MR.
METHODS METHODS
Data from a single high-volume center of all consecutive cases with symptomatic MR undergoing TMVR where prospectively included and followed.
RESULTS RESULTS
Between October 2015 and October 2019, 81 consecutive patients underwent TMVR and were included in the investigation. The mean age was 75.73±7.81 years, 55 (67.9%) were male. The most frequent mechanism was functional MR (FMR) (59%). The mean EuroSCORE II was 5.7±4.94 [FMR 5.38±3.9, degenerative MR (DMR) 5.72±4.7 and mixed MR (MMR) 6.6±7.5; P=0.7776] and STS score mean was 5.21±3.31 (FMR 4.6±2.3, DMR 6.43±5.2 and MMR 5.7±3.2; P=0.126). Patients with FMR had higher rates of dilated (36 patients, 75.5%) and ischemic (15 patients, 31.3%) cardiomyopathy, as well as worse left ventricular ejection fraction (LVEF). Procedural success was achieved in 72 (88.9%) patients, with a similar distribution between groups. The median of follow-up was 16.3 months. The primary combined endpoint occurred in 19 (23.5%) cases. The number of the combined event regarding the different etiologies were 15 (31.2%) in FMR, 2 (11.8%) in DMR and 5 (31.3%) in MMR (P=0.276). Sixteen patients (20.0%) died during the first year of follow-up and 19 (23.5%) had unplanned heart failure (HF) hospitalization. Previous surgical revascularization (HR =4.94, P=0.004) and a redo TMVR (HR =11.3, P=0.006) predicted the main event.
CONCLUSIONS CONCLUSIONS
TMVR with the Mitraclip device is safe, with a low incidence of complications and a high rate of procedural success. One-year outcomes show reduction of all cause death and HF admissions. Moreover, most of the patients have sustained MR reduction and an improvement in the functional class at the end of follow-up.

Identifiants

pubmed: 32953757
doi: 10.21037/atm.2020.02.121
pii: atm-08-15-957
pmc: PMC7475434
doi:

Types de publication

Journal Article

Langues

eng

Pagination

957

Informations de copyright

2020 Annals of Translational Medicine. All rights reserved.

Déclaration de conflit d'intérêts

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/atm.2020.02.121). The series “Structural Heart Disease: The Revolution” was commissioned by the editorial office without any funding or sponsorship. DHV served as the unpaid Guest Editor of the series and serves as an unpaid editorial board member of Annals of Translational Medicine from Aug 2019 to Jul 2021. The authors have no other conflicts of interest to declare.

Références

Rev Esp Cardiol (Engl Ed). 2020 Aug;73(8):643-651
pubmed: 31732437
J Am Coll Cardiol. 2015 Mar 31;65(12):1231-1248
pubmed: 25814231
JAMA Cardiol. 2017 Oct 1;2(10):1130-1139
pubmed: 28877291
J Am Coll Cardiol. 2014 Sep 2;64(9):875-84
pubmed: 25169171
N Engl J Med. 2018 Dec 13;379(24):2297-2306
pubmed: 30145927
Eur Heart J. 2012 Oct;33(19):2403-18
pubmed: 23026477
N Engl J Med. 2018 Dec 13;379(24):2307-2318
pubmed: 30280640
Rev Esp Cardiol (Engl Ed). 2018 Feb;71(2):110
pubmed: 29425605
Am Heart J. 2015 Jul;170(1):187-95
pubmed: 26093881
Eur Heart J. 2016 Feb 21;37(8):703-12
pubmed: 26614824
J Am Coll Cardiol. 2013 Sep 17;62(12):1052-1061
pubmed: 23747789
N Engl J Med. 2011 Apr 14;364(15):1395-406
pubmed: 21463154
J Am Coll Cardiol. 2015 Jul 21;66(3):278-307
pubmed: 26184622
J Am Coll Cardiol. 2015 Dec 29;66(25):2844-2854
pubmed: 26718672
Eur J Heart Fail. 2012 Sep;14(9):1050-5
pubmed: 22685268
J Am Soc Echocardiogr. 2017 Apr;30(4):303-371
pubmed: 28314623
J Am Coll Cardiol. 2014 Jul 15;64(2):172-81
pubmed: 25011722
Am J Cardiol. 2017 Aug 15;120(4):708-715
pubmed: 28645469
Am J Cardiol. 2016 Jan 15;117(2):271-7
pubmed: 26651454
Can J Cardiol. 2014 Sep;30(9):962-70
pubmed: 24986049
Eur Heart J. 2018 Jan 1;39(1):39-46
pubmed: 29020337

Auteurs

Daniel Henández-Vaquero (D)

Heart Area, Hospital Universitario Central de Asturias, Oviedo, Spain.
Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain.
Functional Biology Department, University of Oviedo, Oviedo, Spain.

Isaac Pascual (I)

Heart Area, Hospital Universitario Central de Asturias, Oviedo, Spain.
Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain.
Functional Biology Department, University of Oviedo, Oviedo, Spain.

Marcel Almendarez (M)

Heart Area, Hospital Universitario Central de Asturias, Oviedo, Spain.
Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain.

Antonio Adeba (A)

Heart Area, Hospital Universitario Central de Asturias, Oviedo, Spain.
Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain.

Alberto Alperi (A)

Heart Area, Hospital Universitario Central de Asturias, Oviedo, Spain.

Rebeca Lorca (R)

Heart Area, Hospital Universitario Central de Asturias, Oviedo, Spain.
Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain.

Héctor Cubero-Gallego (H)

Heart Area, Hospital Universitario Central de Asturias, Oviedo, Spain.
Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain.

Víctor León (V)

Heart Area, Hospital Universitario Central de Asturias, Oviedo, Spain.
Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain.

Félix E Fernández Suárez (FE)

Heart Area, Hospital Universitario Central de Asturias, Oviedo, Spain.

David Fernández Del Valle (D)

Heart Area, Hospital Universitario Central de Asturias, Oviedo, Spain.

César Morís (C)

Heart Area, Hospital Universitario Central de Asturias, Oviedo, Spain.
Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain.
Medicine Department, University of Oviedo, Oviedo, Spain.

Pablo Avanzas (P)

Heart Area, Hospital Universitario Central de Asturias, Oviedo, Spain.
Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), Oviedo, Spain.
Medicine Department, University of Oviedo, Oviedo, Spain.

Classifications MeSH