Real-world clinical outcomes with a next-generation left atrial appendage closure device: the FLXibility Post-Approval Study.
Humans
Male
Aged
Aged, 80 and over
Female
Platelet Aggregation Inhibitors
/ therapeutic use
Atrial Appendage
/ diagnostic imaging
Treatment Outcome
Atrial Fibrillation
/ diagnosis
Stroke
/ etiology
Anticoagulants
/ adverse effects
Cardiac Catheterization
/ adverse effects
Echocardiography, Transesophageal
Atrial fibrillation
Left atrial appendage closure
Left atrial appendage obstruction
Stroke prevention (limit 6)
WATCHMAN FLX
Journal
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
ISSN: 1532-2092
Titre abrégé: Europace
Pays: England
ID NLM: 100883649
Informations de publication
Date de publication:
30 03 2023
30 03 2023
Historique:
received:
02
08
2022
accepted:
23
11
2022
medline:
3
4
2023
pubmed:
4
2
2023
entrez:
3
2
2023
Statut:
ppublish
Résumé
The FLXibility Post-Approval Study collected data on unselected patients implanted with a WATCHMAN FLX in a commercial clinical setting. Patients were implanted with a WATCHMAN FLX per local standard of care, with a subsequent first follow-up visit from 45 to 120 days post-implant and a final follow-up at 1-year post-procedure. A Clinical Event Committee adjudicated all major adverse events and TEE/CT imaging results were adjudicated by a core laboratory. Among 300 patients enrolled at 17 centres in Europe, the mean age was 74.6 ± 8.0 years, mean CHA2DS2-VASc score was 4.3 ± 1.6, and 62.1% were male. The device was successfully implanted in 99.0% (297/300) of patients. The post-implant medication regimen was DAPT for 87.3% (262/300). At first follow-up, core-lab adjudicated complete seal was 88.2% (149/169), 9.5% (16/169) had leak <3 mm, 2.4 (4/169) had leak ≥3 mm to ≤5 mm, and 0% had >5 mm leak. At 1 year, 93.3% (280/300) had final follow-up; 60.5% of patients were on a single antiplatelet medication, 21.4% were on DAPT, 5.6% were on direct oral anticoagulation, and 12.1% were not taking any antiplatelet/anticoagulation medication. Adverse event rates through 1 year were: all-cause death 10.8% (32/295); CV/unexplained death 5.1% (15/295); disabling and non-disabling stroke each 1.0% (3/295, all non-fatal); pericardial effusion requiring surgery or pericardiocentesis 1.0% (3/295); and device-related thrombus 2.4% (7/295). The WATCHMAN FLX device had excellent procedural success rates, high LAA seal rates, and low rates of thromboembolic events in everyday clinical practice.
Identifiants
pubmed: 36734247
pii: 7025406
doi: 10.1093/europace/euac270
pmc: PMC10062328
doi:
Substances chimiques
Platelet Aggregation Inhibitors
0
Anticoagulants
0
Types de publication
Journal Article
Comment
Langues
eng
Sous-ensembles de citation
IM
Pagination
914-921Subventions
Organisme : Boston Scientific Corporation
Commentaires et corrections
Type : CommentOn
Informations de copyright
© The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology.
Déclaration de conflit d'intérêts
Conflict of interest. T.R.B.: proctoring/consultancy honoraria (Boston Scientific). M.G.: proctoring/consultancy honoraria (Abbott, Boston Scientific), research grants (Boston Scientific). J.E.N.K.: procotoring/consultancy honoraria (Abbott, Boston Scientific), research grants (Abbott, Boston Scientific). T.S.: proctoring/consultancy honoraria (Boston Scientific). M.S.: nothing to disclose. G.C.: proctoring/consultancy honoraria (Abbott, Boston Scientific, Lifetech). M.B.: Speaker honoraria and study support (Abbott, Boston Scientific, Daiichi, Medtronic, MSD/Pfizer). D.H.-S.: proctoring/advisory board honoraria (Abbott, Boston Scientific, Eclipse Medical). T.C.: salary and equity (Boston Scientific Corporation). D.J.A.: salary and equity (Boston Scientific Corporation).
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