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https://intl.sentreheart.com/physician/
The LARIAT procedure is a percutaneous approach to immediate and complete left atrial appendage (LAA) closure without the need to leave an implant inside of the heart. Using an innovative approach to remote suture delivery, the LARIAT is precisely placed around the base of the LAA through a 13F SofTIP guide cannula using standard imaging ...
https://www.reviewjournal.com/contact-us/
• Was there a problem with the delivery of your paper? • Do you want to put a hold on your delivery? Las Vegas Review-Journal 1111 W. Bonanza Road Las Vegas, NV 89106. P.O. Box 70 Las Vegas ...
http://www.onlinejacc.org/content/72/4/448
LAA Exclusion for Stroke Prevention. The earliest documented work in humans, by John Madden in 1948, showed that the LAA was a source of thrombus in patients with AF and that its removal could prevent systemic thromboembolism .Over the next few decades after Madden’s work, surgeons routinely excluded the LAA during mitral valve operations.
https://www.cardiovascular.abbott/int/en/hcp/products/structural-heart/amplatzer-laa.html
Left atrial appendage (LAA) anatomies come in all shapes and sizes, and so should the stroke-prevention devices you use for your patients. And the reasons for LAA closure are persuasive, since atrial fibrillation is a key risk factor for ischemic stroke.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4547684/
The LARIAT® Suture Delivery Device (SentreHEART, Inc., Redwood City, CA) is designed to ligate the LAA through the delivery of a surgical suture via a combined trans-septal and subxiphoid approach (Figure 3).34,35 The system has FDA approval (510K) for “suture placement and knot-tying for use in surgical applications where soft tissue are ...
https://www.businesswire.com/news/home/20151008005420/en/SentreHEART-Receives-CE-Mark-Approval-LARIAT-Surgical
SentreHEART, Inc. announced that it has received CE Mark approval for the LARIAT Surgical Left Atrial Appendage (LAA) Suture Delivery Device. The LARI
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