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    LAAO Registry - 2 year(s) ago

    Get the support you need to ensure quality patient care for your atrial fibrillation patients with the American College of Cardiology’s LAAO Registry™.Join the first national registry capturing data on left atrial appendage occlusion procedures to assess real-world procedural outcomes, short and long-term safety, comparative effectiveness and cost effectiveness.The LAAO Registry is approved by…

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    • Join the first national registry capturing data on left atrial appendage occlusion procedures to assess real-world procedural outcomes, short & long-term safety, comparative effectiveness & cost effectiveness. More about the #NCDR #LAAORegistry ➡️ https://t.co/4lFPzNBHrn #NYCVS https://t.co/Ac7BFVhRxj

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    Increased thromboembolic risk, history of a major bleed, and high fall risk were the most common procedural indications for implantation with a Watchman device, according to a paper published Aug. 12 in Circulation: Cardiovascular Quality and Outcomes. In addition, high fall risk resulted in a “modestly increased risk” of in-hospital adverse events. Usama A. Daimee, MD, et al., used data from…

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    • #NCDR 📄 Explores Indications For LAAO in the US: Experts used data from ACC's #LAAORegistry to look at 38,314 Watchman procedures (2016-2018), identifying 🗝️ indications of Watchman device use as well as risk of in-🏥 adverse events. More: https://t.co/h8KBzJ9SsL #ACCQuality22

  • Mashup Score: 6

    Increased thromboembolic risk, history of a major bleed, and high fall risk were the most common procedural indications for implantation with a Watchman device, according to a paper published Aug. 12 in Circulation: Cardiovascular Quality and Outcomes. In addition, high fall risk resulted in a “modestly increased risk” of in-hospital adverse events. Usama A. Daimee, MD, et al., used data from…

    Tweet Tweets with this article
    • Increased thromboembolic risk, history of a major bleed, and high fall risk were the most common procedural indications for implantation with a Watchman device, according to a paper using #NCDR #LAAORegistry data. Read on ➡️ https://t.co/8pGjhdrvHP

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    Quick Takes Peri-device leak is not uncommon after percutaneous left atrial appendage occlusion. This analysis from the NCDR LAAO suggest that small leaks (3mm were present in 13.3% patients at 45 days and in 11.8% at 1-year.1 In the Amulet IDE trial, any PDL at 45 days was present in 37% and 54% in patients randomized to the Amulet versus Watchman device, respectively. Leaks >3mm were detected…

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    • Analysis from the #NCDR #LAAORegistry suggest small leaks may be clinically relevant as they were associated with a small but statistically significant increase in ischemic events. Read more here: https://t.co/5DdYOsLqj5