Implantation of one, two or multiple MitraClip™ for transcatheter mitral valve repair: insights from a 1824-patient multicenter study.


Journal

Panminerva medica
ISSN: 1827-1898
Titre abrégé: Panminerva Med
Pays: Italy
ID NLM: 0421110

Informations de publication

Date de publication:
Mar 2022
Historique:
pubmed: 27 7 2021
medline: 7 4 2022
entrez: 26 7 2021
Statut: ppublish

Résumé

Transcatheter mitral valve repair (TMVR) with MitraClip™ (Abbott Laboratories; Abbott Park, IL, USA) is an established treatment for mitral regurgitation (MR). More than one MitraClip™ may be implanted if a single one does not reduce MR adequately. We aimed to appraise the outlook of patients undergoing implantation of one, two or multiple MitraClip™ for TMVR. Exploiting the ongoing prospective GISE Registry of Transcatheter Treatment of Mitral Valve Regurgitation (GIOTTO) Study dataset, we compared patients, procedural details and outcomes distinguishing those receiving one, two or multiple MitraClip™. The primary endpoint was the composite of 1-year cardiac death or rehospitalization for heart failure. Additional endpoints included all cause death, surgical mitral repair, and functional class. Multivariable adjusted Cox proportional hazard analysis was used for confirmatory purposes. As many as 1824 patients were included: 718 (39.4%) treated with a single MitraClip™, and 940 (51.5%) receiving two MitraClip™, and 166 (9.1%) receiving three or more. Significant differences were found for baseline features, including age, female gender, diabetes mellitus, hypertension, chronic obstructive pulmonary disease, prior myocardial infarction, atrial fibrillation, permanent pacemaker, cardiac resynchronization therapy, implantable cardioverter defibrillator, and prior mitral valve repair (all P<0.05). Several imaging features were also different, including left ventricular dimensions, MR severity and proportionality, mitral valve area, flail leaflet, and pulmonary vein flow (all P<0.05). Among procedural features, significant differences were found for anesthesia type, MitraClip™ type, fluoroscopy, device, and operating room times, postprocedural mitral gradient, residual MR, smoke-like effect, device success partial detachment and surgical conversion (all P<0.05). In-hospital death occurred more frequently in patients receiving multiple MitraClip™, and the same applied severe residual MR (all P<0.05). Mid-term follow-up (15±13 months) showed significant differences in the risk of death, cardiac death, rehospitalization for heart failure, and their composites, mainly, but not solely, associated with multiple MitraClip™ (all P<0.05). Adjusted analysis confirmed the significantly increased risk of composite adverse events when comparing the multiple vs. single MitraClip™ groups (P=0.014 for death and rehospitalization, P=0.013 for cardiac death or rehospitalization). Implantation of one or two MitraClip™ is associated with favorable clinical outcomes. Conversely, bail-out implantation of three or more MitraClip™ may portend a worse long-term prognosis.

Sections du résumé

BACKGROUND BACKGROUND
Transcatheter mitral valve repair (TMVR) with MitraClip™ (Abbott Laboratories; Abbott Park, IL, USA) is an established treatment for mitral regurgitation (MR). More than one MitraClip™ may be implanted if a single one does not reduce MR adequately. We aimed to appraise the outlook of patients undergoing implantation of one, two or multiple MitraClip™ for TMVR.
METHODS METHODS
Exploiting the ongoing prospective GISE Registry of Transcatheter Treatment of Mitral Valve Regurgitation (GIOTTO) Study dataset, we compared patients, procedural details and outcomes distinguishing those receiving one, two or multiple MitraClip™. The primary endpoint was the composite of 1-year cardiac death or rehospitalization for heart failure. Additional endpoints included all cause death, surgical mitral repair, and functional class. Multivariable adjusted Cox proportional hazard analysis was used for confirmatory purposes.
RESULTS RESULTS
As many as 1824 patients were included: 718 (39.4%) treated with a single MitraClip™, and 940 (51.5%) receiving two MitraClip™, and 166 (9.1%) receiving three or more. Significant differences were found for baseline features, including age, female gender, diabetes mellitus, hypertension, chronic obstructive pulmonary disease, prior myocardial infarction, atrial fibrillation, permanent pacemaker, cardiac resynchronization therapy, implantable cardioverter defibrillator, and prior mitral valve repair (all P<0.05). Several imaging features were also different, including left ventricular dimensions, MR severity and proportionality, mitral valve area, flail leaflet, and pulmonary vein flow (all P<0.05). Among procedural features, significant differences were found for anesthesia type, MitraClip™ type, fluoroscopy, device, and operating room times, postprocedural mitral gradient, residual MR, smoke-like effect, device success partial detachment and surgical conversion (all P<0.05). In-hospital death occurred more frequently in patients receiving multiple MitraClip™, and the same applied severe residual MR (all P<0.05). Mid-term follow-up (15±13 months) showed significant differences in the risk of death, cardiac death, rehospitalization for heart failure, and their composites, mainly, but not solely, associated with multiple MitraClip™ (all P<0.05). Adjusted analysis confirmed the significantly increased risk of composite adverse events when comparing the multiple vs. single MitraClip™ groups (P=0.014 for death and rehospitalization, P=0.013 for cardiac death or rehospitalization).
CONCLUSIONS CONCLUSIONS
Implantation of one or two MitraClip™ is associated with favorable clinical outcomes. Conversely, bail-out implantation of three or more MitraClip™ may portend a worse long-term prognosis.

Identifiants

pubmed: 34309332
pii: S0031-0808.21.04497-9
doi: 10.23736/S0031-0808.21.04497-9
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1-8

Auteurs

Arturo Giordano (A)

Operative Unit for Cardiovascular Interventions, Pineta Grande Hospital, Castel Volturno, Caserta, Italy.

Paolo Ferraro (P)

Unit of Hemodynamics, Santa Lucia Hospital, San Giuseppe Vesuviano, Naples, Italy.

Filippo Finizio (F)

Operative Unit for Cardiovascular Interventions, Pineta Grande Hospital, Castel Volturno, Caserta, Italy.

Giuseppe Biondi-Zoccai (G)

Department of Medico-Surgical Sciences and Biotechnologies, Sapienza University, Latina, Italy - giuseppe.biondizoccai@uniroma1.it.
Mediterranea Cardiocentro, Naples, Italy.

Paolo Denti (P)

Department of Cardiac Surgery, IRCCS San Raffaele Hospital, Vita-Salute San Raffaele University, Milan, Italy.

Francesco Bedogni (F)

Department of Cardiology, IRCCS San Donato Polyclinic, San Donato Milanese, Milan, Italy.

Antonio P Rubbio (AP)

Department of Cardiology, IRCCS San Donato Polyclinic, San Donato Milanese, Milan, Italy.

Anna S Petronio (AS)

Cardiothoracic and Vascular Department, University Hospital of Pisa, Pisa, Italy.

Antonio L Bartorelli (AL)

Luigi Sacco Department of Biomedical and Clinical Sciences, Centro Cardiologico Monzino IRCCS, University of Milan, Milan, Italy.

Annalisa Mongiardo (A)

Division of Cardiology, Department of Medical and Surgical Sciences, The Magna Græcia University of Catanzaro, Catanzaro, Italy.

Salvatore Giordano (S)

Division of Cardiology, Department of Medical and Surgical Sciences, The Magna Græcia University of Catanzaro, Catanzaro, Italy.

Francesco DE Felice (F)

Division of Interventional Cardiology, S. Camillo Forlanini Hospital, Rome, Italy.

Marianna Adamo (M)

Cardiothoracic Department, Spedali Civili Brescia, Brescia, Italy.

Matteo Montorfano (M)

Cardio-Thoracic-Vascular Department, IRCCS San Raffaele Hospital, Milan, Italy.

Cesare Baldi (C)

Heart Department, Scuola Medica Salernitana University Hospital, Salerno, Italy.

Giuseppe Tarantini (G)

Unit of Interventional Cardiology, Department of Cardiac, Thoracic and Vascular Science, University of Padua, Padua, Italy.

Francesco Giannini (F)

Unit of Interventional Cardiology, GVM Care &amp; Research, Maria Cecilia Hospital, Cotignola, Ravenna, Italy.

Federico Ronco (F)

Unit of Interventional Cardiology, Department of Cardio-Thoracic and Vascular Sciences, dell'Angelo Hospital, AULSS3 Serenissima, Mestre, Venice, Italy.

Ida Monteforte (I)

Division of Cardiology, AORN dei Colli - Monaldi Hospital, Naples, Italy.

Emmanuel Villa (E)

Department of Cardiac Surgery, Poliambulanza Foundation Hospital, Brescia, Italy.

Maurizio Ferrario (M)

Division of Cardiology, Foundation IRCCS Polyclinic S. Matteo, Pavia, Italy.

Luigi Fiocca (L)

Cardiovascular Department, Papa Giovanni XXIII Hospital, Bergamo, Italy.

Fausto Castriota (F)

Cardiovascular Department, Humanitas Gavazzeni Hospital, Bergamo, Italy.

Corrado Tamburino (C)

Division of Cardiology, Centro Alte Specialità e Trapianti (CAST), Vittorio Emanuele Polyclinic, University of Catania, Catania, Italy.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH