The study was to retrospectively analyse the efficacy and safety of LAA closure using the LAmbre in our center from April 2014 to November 2015.
The study was to retrospectively analyse the efficacy and safety of percutaneous left atrial appendage (LAA) closure using the LAmbre (Lifetech Scientific Co., Ltd., Shenzhen, China) in our center from April 2014 to November 2015. 89.4% has finished the 12-month esophageal ecllocardiogrhy (TEE) examination. The average followup was 2-years.
Study Type
OBSERVATIONAL
Enrollment
66
Percutaneous Left Atrial Appendage Closure Using the LAmbre Device in Patients With Atrial Fibrillation
Ischemic stroke
Ischemic stroke
Time frame: up to 5 years
The composite safety and efficacy end-points
all-cause death, stroke, major bleeding, thromboembolism, device related severe complications
Time frame: up to 5 years
Successful sealing of the LAA
successful sealing around the device at the LAA orifice (residual jet flow of \< 5 mm) as measured by transesophageal echocardiogram (TEE) at 6 months after device implantation
Time frame: up to 5 years
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