z-logo
open-access-imgOpen Access
Safety and efficacy of transcatheter left atrial appendage closure using the Watchman device in Egyptian patients with nonvalvular atrial fibrillation
Author(s) -
Hazem Khamis,
Ahmed Ramzy,
Neama Elmelegy,
Khaled Elrabbat,
Ahmed Taher Masoud
Publication year - 2015
Publication title -
the egyptian heart journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.212
H-Index - 9
eISSN - 2090-911X
pISSN - 1110-2608
DOI - 10.1016/j.ehj.2015.07.002
Subject(s) - medicine , atrial fibrillation , cardiology , stroke (engine) , warfarin , embolism , heart failure , diabetes mellitus , clinical endpoint , randomized controlled trial , mechanical engineering , engineering , endocrinology
BackgroundAtrial fibrillation (AF) is considered the major cause of stroke in the elderly. Alternative therapies to the anticoagulant therapy are warranted, particularly in patients who are ineligible or at high risk of bleeding. The left atrial appendage (LAA) is a prominent source of thrombi in nonvalvular AF, accounting for 90% of thrombi. As a result, surgical and transcatheter techniques have been explored to reduce the risk of stroke in patients with AF by occluding the LAA.ObjectivesTo assess the safety and efficacy of LAA closure in patients with nonvalvular atrial fibrillation (AF) ineligible for warfarin therapy.MethodsA prospective study that evaluated LAA closure with the Watchman device (Boston Scientific, Natick, MA; group A) in fifteen patients with nonvalvular AF and CHADS2 (congestive heart failure, hypertension, age ⩾75years, diabetes mellitus, and prior stroke or transient ischemic attack) score ⩾1, who were considered ineligible for warfarin therapy. The primary efficacy endpoint was the combined events of ischemic/hemorrhagic stroke, systemic embolism and cardiovascular/unexplained death during a period of six months follow-up.ResultsSuccessful closure of the LAA using the Watchman device was achieved in 15 patients (100%). The mean age was found to be 67.9±9years with 40% of them being males. No device or procedure related adverse events were detected. The mean CHADS2 score was 2.4±0.8, while the mean CHA2DS2-VASC score was 4.4±1.0. After a mean period of 8±2months of follow-up, no device dislodgement or device-related thrombi were documented. The all-cause stroke (ischemic and hemorrhagic) and systemic embolism were 0%. The device and procedure related mortality was found to be 0%. Only one patient died after 8months of device implantation from pneumonia.ConclusionLAA closure with the Watchman device can be safely performed, and may be a reasonable alternative to consider for patients at high risk for stroke but with contraindications to systemic oral anticoagulation or with high risk of bleeding

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom