Temporal Changes and Clinical Implications of Delayed Peridevice Leak Following Left Atrial Appendage Closure.

coil occlusion device-related thrombus left atrial appendage closure peridevice leak transesophageal echocardiography

Journal

JACC. Clinical electrophysiology
ISSN: 2405-5018
Titre abrégé: JACC Clin Electrophysiol
Pays: United States
ID NLM: 101656995

Informations de publication

Date de publication:
01 2022
Historique:
received: 16 02 2021
revised: 21 06 2021
accepted: 21 06 2021
pubmed: 30 8 2021
medline: 3 2 2022
entrez: 29 8 2021
Statut: ppublish

Résumé

The aim of this study was to assess temporal changes and clinical implications of peridevice leak (PDL) after left atrial appendage closure. Endocardial left atrial appendage closure devices are alternatives to long-term oral anticoagulation (OAC) for patients with atrial fibrillation. PDL >5 mm may prohibit discontinuation of OAC. Patients included in the study had: 1) successful Watchman device implantation without immediate PDL; 2) new PDL identified at 45 to 90 days using transesophageal echocardiography; 3) eligibility for OAC; and 4) 1 follow-up transesophageal echocardiographic study for PDL surveillance. Relevant clinical and imaging data were collected by chart review. The combined primary outcome included failure to stop OAC after 45 to 90 days, transient ischemic attack or stroke, device-related thrombi, and need for PDL closure. Relevant data were reviewed for 1,039 successful Watchman device implantations. One hundred eight patients (10.5%) met the inclusion criteria. The average PDL at 45 to 90 days was 3.2 ± 1.6 mm. On the basis of a median PDL of 3 mm, patients were separated into ≤3 mm (n = 73) and >3 mm (n = 35) groups. In the ≤3 mm group, PDL regressed significantly (2.2 ± 0.8 mm vs 1.6 ± 1.4 mm; P = 0.002) after 275 ± 125 days. In the >3 mm group, there was no significant change in PDL (4.9 ± 1.4 mm vs 4.0 ± 3.0 mm; P = 0.12) after 208 ± 137 days. The primary outcome occurred more frequently (69% vs 34%; P = 0.002) in the >3 mm group. The incidence of transient ischemic attack or stroke in patients with PDL was significantly higher compared with patients without PDL, irrespective of PDL size. New PDL detected by transesophageal echocardiography at 45 to 90 days occurred in a significant percentage of patients and was associated with worse clinical outcomes. PDL ≤3 mm tended to regress over time.

Sections du résumé

OBJECTIVES
The aim of this study was to assess temporal changes and clinical implications of peridevice leak (PDL) after left atrial appendage closure.
BACKGROUND
Endocardial left atrial appendage closure devices are alternatives to long-term oral anticoagulation (OAC) for patients with atrial fibrillation. PDL >5 mm may prohibit discontinuation of OAC.
METHODS
Patients included in the study had: 1) successful Watchman device implantation without immediate PDL; 2) new PDL identified at 45 to 90 days using transesophageal echocardiography; 3) eligibility for OAC; and 4) 1 follow-up transesophageal echocardiographic study for PDL surveillance. Relevant clinical and imaging data were collected by chart review. The combined primary outcome included failure to stop OAC after 45 to 90 days, transient ischemic attack or stroke, device-related thrombi, and need for PDL closure.
RESULTS
Relevant data were reviewed for 1,039 successful Watchman device implantations. One hundred eight patients (10.5%) met the inclusion criteria. The average PDL at 45 to 90 days was 3.2 ± 1.6 mm. On the basis of a median PDL of 3 mm, patients were separated into ≤3 mm (n = 73) and >3 mm (n = 35) groups. In the ≤3 mm group, PDL regressed significantly (2.2 ± 0.8 mm vs 1.6 ± 1.4 mm; P = 0.002) after 275 ± 125 days. In the >3 mm group, there was no significant change in PDL (4.9 ± 1.4 mm vs 4.0 ± 3.0 mm; P = 0.12) after 208 ± 137 days. The primary outcome occurred more frequently (69% vs 34%; P = 0.002) in the >3 mm group. The incidence of transient ischemic attack or stroke in patients with PDL was significantly higher compared with patients without PDL, irrespective of PDL size.
CONCLUSIONS
New PDL detected by transesophageal echocardiography at 45 to 90 days occurred in a significant percentage of patients and was associated with worse clinical outcomes. PDL ≤3 mm tended to regress over time.

Identifiants

pubmed: 34454881
pii: S2405-500X(21)00601-0
doi: 10.1016/j.jacep.2021.06.018
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

15-25

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2022 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures Dr Ellis has received research grants (to Vanderbilt University) from Boehringer-Ingelheim, Medtronic, and Boston Scientific; is a consultant or adviser to Medtronic, Abbott Medical, Boston Scientific, and Atricure. All other authors reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Muhammad R Afzal (MR)

The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.

James K Gabriels (JK)

Department of Medicine, Division of Cardiology, Weill Cornell Medicine, New York, New York, USA.

Gregory G Jackson (GG)

Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Lu Chen (L)

Northwell Health, Long Island Jewish Hospital, Division of Electrophysiology, Manhasset, New York, USA.

Benjamin Buck (B)

The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.

Sandra Campbell (S)

The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.

Dawn F Sabin (DF)

Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Bruce Goldner (B)

Northwell Health, Long Island Jewish Hospital, Division of Electrophysiology, Manhasset, New York, USA.

Haisam Ismail (H)

Northwell Health, Long Island Jewish Hospital, Division of Electrophysiology, Manhasset, New York, USA.

Christopher F Liu (CF)

Department of Medicine, Division of Cardiology, Weill Cornell Medicine, New York, New York, USA.

Apoor Patel (A)

Division of Electrophysiology, Northwell Health, North Shore University Hospital, Manhasset, New York, USA.

Stuart Beldner (S)

Division of Electrophysiology, Northwell Health, North Shore University Hospital, Manhasset, New York, USA.

Emile G Daoud (EG)

The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.

John D Hummel (JD)

The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.

Christopher R Ellis (CR)

Vanderbilt University Medical Center, Nashville, Tennessee, USA. Electronic address: christopher.ellis@vumc.org.

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