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    cost effectiveness

    Explore " cost effectiveness" with insightful episodes like "S5 - E5.5 - More on GLP-1s and a Broader MASH Wrap-up", "S5 - E5.3 - Strategies to Improve NIT reliability in Diagnosing and Staging MASH Fibrosis", "Long-Acting Lipoglycopeptides for Skin and Soft Tissue Infections : Implementation Into Practice", "S3-E16 - The Prospective Role of Data Modeling in Diagnostic and Drug Development" and "The Lancet Global Health: May 22, 2014" from podcasts like ""Surfing the NASH Tsunami", "Surfing the NASH Tsunami", "CCO Infectious Disease Podcast", "Surfing the NASH Tsunami" and "The Lancet Global Health in conversation with"" and more!

    Episodes (5)

    S5 - E5.5 - More on GLP-1s and a Broader MASH Wrap-up

    S5 - E5.5 - More on GLP-1s and a Broader MASH Wrap-up

    After some final discussion about GLP-1s, this conversation entails Roger Green summarizing what he has heard in the episode so far and testing for confirmation or correction. It goes fast and covers significant ground. 

    Naim Alkhouri starts this conversation by discussing patients for whom he would prescribe resmetirom vs. GLP-1s. Lean MASH patients are likely to receive resmetirom. Earlier fibrosis patients are more likely to receive semaglutide. A multimorbid F3 patient might receive both. 

    Roger asks how things might change with tirzepatide, since it is a dual agonist with strong MASH-lowering effects. Naim expresses doubt that tirzepatide will be antifibrotic, since neither GLP-1 nor GIP have direct liver effects. He has more faith in the glucagon dual- and triple-incretin agonists. 

    The rest of the conversation involves Roger stating themes he has heard earlier and asking for confirmation or amendment. It moves pretty fast, covers a lot of territory, and receives some agreement and some correction.


    S5 - E5.3 - Strategies to Improve NIT reliability in Diagnosing and Staging MASH Fibrosis

    S5 - E5.3 - Strategies to Improve NIT reliability in Diagnosing and Staging MASH Fibrosis

    This conversation focuses more tightly on the specific challenges with the current approaches that use NITs to diagnose and stage advanced MASH fibrosis and explores several newer options and ways of thinking about the challenge.

    Roger Green notes that recent papers discuss the failure to predict accurately with FIB-4. He asks how we can improve predictive performance. Louise Campbell notes some specific challenges, after which Jörn Schattenberg praises John Dillon's work in automating lab detection algorithms. He also reiterates his view that repeat testing will be pivotal in good test protocols. Ian Rowe rejoins the conversation (from a faulty Internet connection) to comment that our inability to stage patients reliably will lead to government payers like NHS believing that they will need biopsy to stage patients accurately and treat them cost-effectively. Jörn says Germany will work differently and if EMA approves it, it will launch in Germany.

    Roger asks about new tests on the horizon and specifically whether there is sufficient improvement in diagnosis, staging or treatment. He refers specifically to MASEF and Naim Alkhouri's earlier comments about four scan vendors at his conference. Ian says there are tests that can rise to this task, but they are not produced in sufficient quantity and cost too much to become a first-line option. Naim notes that the most exciting tests are a couple of years away. Ian returns to Jörn's earlier point about the value of sequential testing vs an individual test. Louise suggests that device size will be pivotal for primary care.

    Long-Acting Lipoglycopeptides for Skin and Soft Tissue Infections : Implementation Into Practice

    Long-Acting Lipoglycopeptides for Skin and Soft Tissue Infections : Implementation Into Practice

    In this episode, Kyle Molina, PharmD, BCIDP, discusses key considerations for successful implementation of long-acting lipoglycopeptides into clinical practice. Listen as he gives perspectives on:

    • Reasons to consider use of long-acting lipoglycopeptides (eg, poor adherence to oral antibiotics, PICC-related costs and complications)
    • Data supporting and challenging cost effectiveness of long-acting lipoglycopeptides 
    • Identifying the target patient population
    • Selecting the right location to provide long-acting lipoglycopeptides 
    • Strategies to maximize institutional impact with key stakeholders (eg, hospital avoidance, reduced ED and hospital length of stay) 
    • Key characteristics of available long-acting lipoglycopeptides 
    • Addressing logistical challenges, including navigating the reimbursement process

     

    Faculty:

    Kyle Molina, PharmD, BCIDP
    Infectious Diseases Clinical Pharmacist
    Scripps Green Hospital
    La Jolla, California

    Link to full program: 

    S3-E16 - The Prospective Role of Data Modeling in Diagnostic and Drug Development

    S3-E16 - The Prospective Role of Data Modeling in Diagnostic and Drug Development

    In Episode 13, we explored ways that data modeling can inform a deeper understanding of the value of community and primary care VCTE screening for NAFLD and NASH. This week, we ask Chris Estes, lead modeler at the Center for Disease Analysis Foundation, what guidance data modeling can provide about diagnostic and drug development.

    The episode is a cross between a discussion and an interview-type program. It starts with Chris explaining how he derives models, which variables he selects as proxy measures, why he chooses those, and where shortcomings exist in the data that is available for him to use in populating models. For much of the rest, the other panelists -- Alina Allen, Louise Campbell, Jörn Schattenberg and Roger Green -- either ask questions about how Chris's models work or what we can learn from them, and Chris answers. Beyond that, panelists share their own observations based on research and patient treatment experiences and Chris responds. The group covers a virtual shopping list of topics, including: underreported and misreported diseases; which proxies are more reliable when modeling disease (and which are less so); gaps in current data; positives, negatives and challenges in using obesity as the proxy variable for NAFLD instead of diabetes; the case for treating F2 agents with drugs when they become available; countries most at risk in the coming global NASH pandemic; the need to forecast pediatric NAFLD and NASH better; impact of alcohol consumption on NAFLD or NASH patients; and the situations where regressing fibrosis is pivotal vs. others where simply stopping progression might be a sufficient goal. In the end, this conversation offers a better understanding of how complex modeling is and how remarkable that people like Chris produce results that bear up so well over time.

    After the episode, keep listening for an "extra-sode," originally recorded on January 27, 2022, focusing on the practical value and uses of MRE in day-to-day practice. In addition to Louise Campbell and Roger Green, the panel for this extra-sode includes Stephen Harrison, Mazen Noureddin, Kay Pepin from Mayo Clinic and Resoundant, and Scott Reeder from the University of Wisconsin. This discussion, which appears as stand-alone conversation S3 E16.4, addresses the uses of MRE in community settings and the unique benefits MRE can bring as a standalone test and combined with MRI-PDFF in a test/reporting structure known as an hepatogram.

    This episode is sponsored by Resoundant, a Mayo Clinic company and the developers of Magnetic Resonance Elastography. MRE is widely available with over 2000 locations worldwide, and can be done as a low-cost, rapid exam in just 5 minutes. Together with PDFF, this quantitative exam is called an Hepatogram – a powerful non-invasive alternative to liver biopsy in many cases. For more information, visit www.resoundant.com on the web.

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