Long-term clinical outcomes from real-world experience of left atrial appendage exclusion with LARIAT device.


Journal

Journal of cardiovascular electrophysiology
ISSN: 1540-8167
Titre abrégé: J Cardiovasc Electrophysiol
Pays: United States
ID NLM: 9010756

Informations de publication

Date de publication:
12 2019
Historique:
received: 02 05 2019
revised: 05 09 2019
accepted: 06 10 2019
pubmed: 10 10 2019
medline: 21 10 2020
entrez: 10 10 2019
Statut: ppublish

Résumé

Left atrial appendage closure (LAAC) with LARIAT has emerged as one of the alternatives to oral anticoagulation (OAC) in patients with nonvalvular atrial fibrillation (AF). Our aim was to study long-term outcomes in patients undergoing LARIAT procedure. We analyzed patients screened for LARIAT device in four centers between December 2009 and June 2012. Out of these, patients who didn't undergo LAAC with the LARIAT device due to unfavorable LAA morphology and other preprocedural contraindications were included in control group. We analyzed thromboembolism, bleeding events, and mortality between LAA and control group. About 153 patients were screened. Out of these, 108 (70.6%) patients underwent LARIAT placement (LAA arm) and 45 (29.4%) excluded patients were included in control arm. There were no differences in CHADS Long-term data from routine clinical practice from our study suggests that LAA exclusion with LARIAT device is an effective treatment in management of nonvalvular AF patients with high risk of stroke, bleeding, and mortality. Further randomized trials, such as aMAZE, will provide more insight in this expanding field.

Sections du résumé

BACKGROUND
Left atrial appendage closure (LAAC) with LARIAT has emerged as one of the alternatives to oral anticoagulation (OAC) in patients with nonvalvular atrial fibrillation (AF). Our aim was to study long-term outcomes in patients undergoing LARIAT procedure.
METHODS
We analyzed patients screened for LARIAT device in four centers between December 2009 and June 2012. Out of these, patients who didn't undergo LAAC with the LARIAT device due to unfavorable LAA morphology and other preprocedural contraindications were included in control group. We analyzed thromboembolism, bleeding events, and mortality between LAA and control group.
RESULTS
About 153 patients were screened. Out of these, 108 (70.6%) patients underwent LARIAT placement (LAA arm) and 45 (29.4%) excluded patients were included in control arm. There were no differences in CHADS
CONCLUSIONS
Long-term data from routine clinical practice from our study suggests that LAA exclusion with LARIAT device is an effective treatment in management of nonvalvular AF patients with high risk of stroke, bleeding, and mortality. Further randomized trials, such as aMAZE, will provide more insight in this expanding field.

Identifiants

pubmed: 31596044
doi: 10.1111/jce.14229
doi:

Substances chimiques

Fibrinolytic Agents 0

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2849-2857

Subventions

Organisme : National Polish Science Centre
ID : UMO 2014/13/D/NZ5/01351
Pays : International
Organisme : National Polish Science Centre
ID : UMO 2015/17/B/NZ5/00125
Pays : International

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Références

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Auteurs

Valay Parikh (V)

Department of Electrophysiology, Baptist Health System, San Antonio, Texas.

Krzysztof Bartus (K)

Department of Cardiovascular Surgery and Transplantology, John Paul II Hospital, Jagiellonian University, Krakow, Poland.

Radoslaw Litwinowicz (R)

Department of Cardiovascular Surgery and Transplantology, John Paul II Hospital, Jagiellonian University, Krakow, Poland.

Mohit K Turagam (MK)

Section of Electrophysiology, Icahn School of Medicine at Mount Sinai, New York.

Jerzy Sadowski (J)

Department of Cardiovascular Surgery and Transplantology, John Paul II Hospital, Jagiellonian University, Krakow, Poland.

Boguslaw Kapelak (B)

Department of Cardiovascular Surgery and Transplantology, John Paul II Hospital, Jagiellonian University, Krakow, Poland.

Magdalena Bartus (M)

Department of Pharmacology, Jagiellonian University, Krakow, Poland.

Jakub Podolec (J)

Department of Cardiovascular Surgery and Transplantology, John Paul II Hospital, Jagiellonian University, Krakow, Poland.

Maciej Brzezinski (M)

Department of Physiology, Medical University of Gdansk, Gdansk, Poland.

Dan Musat (D)

Section of Electrophysiology, Valley Health System, Ridgewood, New Jersey.

Abdi Rasekh (A)

Section of Electrophysiology, Texas Heart Institute, Houston, Texas.

Suneet Mittal (S)

Section of Electrophysiology, Valley Health System, Ridgewood, New Jersey.

Jie Cheng (J)

Section of Electrophysiology, Baylor Medical Center, University of Texas, Houston, Texas.

Nitish Badhwar (N)

Department of Medicine, Division of Cardiac Electrophysiology, University of California San Francisco, San Francisco, California.

Randall Lee (R)

Department of Medicine, Division of Cardiac Electrophysiology, University of California San Francisco, San Francisco, California.
Cardiovascular Research Institute, Institute for Regeneration Medicine, University of California San Francisco, San Francisco, California.

Dhanunjaya Lakkireddy (D)

The Kansas City Heart Rhythm Institute & Research Foundation, Overland Park, Kansas.

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