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    May 19, 2023 — Abiomed, part of Johnson & Johnson MedTech[1], announces results of a third-party analysis showing that utilizing Impella during high-risk percutaneous coronary intervention (PCI) procedures may help physicians achieve a more complete revascularization compared to high-risk PCIs supported using an intra-aortic balloon pump (IABP). Previous studies have shown that a more complete…

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    • @DAICeditor @Abiomed Abiomed announced results of a third-party analysis showing that utilizing #Impella during high-risk #PCI procedures may help physicians achieve a more complete #revascularization compared to high-risk PCIs supported using an #IABP: https://t.co/Mhsm5XZ4sK

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    JoVE | Peer Reviewed Scientific Video Journal | Methods And Protocols – Video. JoVE publishes peer-reviewed scientific video protocols to accelerate biological, medical, chemical and physical research. Watch our scientific video articles. JoVE is the world-leading producer and provider of science videos with the mission to improve scientific research, scientific journals, and education. Millions…

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    • Steps for #IABP insertion @JoVEJournal led by @CvUnmc #IC fellow, Dr. Ganesh Gajanan!! @esbrilakis @JSillerMatula #RonZolty #MCS #ACCEarlyCareer #ACCFIT #ACCIC #UNMCIM @UNMC_IM https://t.co/XLnHZu4ps5 https://t.co/i8pvnjlPgA

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    The U.S. Food and Drug Administration (FDA) has issued a Class I recall on the Arrow AutoCAT 2 and AC3 Intra-Aortic Balloon Pumps. Arrow International, LLC, a subsidiary of Teleflex, Inc, is recalling the pumps after receiving complaints that battery power is not lasting as long as expected. A fully charged battery should last 90 minutes, however, multiple users report the devices are…

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    • @DAICeditor @teleflex Arrow International, LLC, a Subsidiary of Teleflex, Inc, #recalls #Arrow #AutoCAT2, #AC3 #intra_aortic_balloon_pumps #IABP for unexpectedly short battery run times: https://t.co/2QDauwaf69

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    December 5, 2022 —  The U.S. Food and Drug Administration (FDA) is alerting health care facilities and providers of a shortage of Getinge Maquet/Datascope Intra-Aortic Balloon Pump (IABP) devices, including limited supplies of IAB catheters, new Cardiosave IABPs, and Cardiosave IABP parts.  Recommendations  The FDA recommends that health care facilities and providers who use Getinge…

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    • @DAICeditor @GetingeGlobal The #FDA is alerting healthcare facilities of a shortage of Getinge Maquet/Datascope Intra-Aortic Balloon Pump (#IABP) devices, including limited supplies of #IAB_catheters, new #Cardiosave IABPs, and Cardiosave IABP parts: https://t.co/dpI1nPtMhp

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    Impella was approved by the Food and Drug Administration in 2015 for use during high-risk percutaneous coronary interventions (PCIs); however, its safety and efficacy compared with intra-aortic balloon pump (IABP) has not been evaluated in contemporary practice and remains debated. We aimed to compare postapproval outcomes and costs of Impella versus IABP support for high-risk PCI in real-world…

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    • This study from the @Yale demonstrates significant survival benefit in high-risk PCI with #Impella support In-🏥 survival was significantly ⤴️ with Impella compared to #IABP (unadjusted 95.3% vs. 91.0%, p=0.0002; adjusted OR 1.55, 95% CI 1.02, 2.36) https://t.co/hwoejkdijO https://t.co/wNldFylqaH