7. Medicare's Failure to Cover CGM at Odds With Other Health, Research Agencies. This commentary from US Senator Susan M. Collins, R-Maine, was the most significant of several pieces that The American Journal of Managed Care franchise published to highlight a coverage inequity: CMS does not pay for continuous glucose monitoring technology, despite the evidence that improved control keeps patients out of the emergency room. July 2015.
6. Study Suggests Method of Reducing Blood Clots Without Risking Bleeding. Coverage from the American Society of Hematology meeting in December 2014 featured one of the “Best of ASH” presentations that was also published in the New England Journal of Medicine. Factor XI, an important enzyme in the coagulation pathway, is naturally reduced in some people, and this group is at a lower risk of venous thromboembolism, or VTE. If Factor XI was reduced by other means in patients undergoing a surgical knee replacement—a procedure with high risk for blood clots—would the patients have reduced VTE? Researchers using injectable nucleic acid engineered to reduce Factor XI expression presented their results at a press conference and at a late-breaking session. January 2015.
5. Can mHealth Revolutionize Evidence-Based Practice in Diabetes Care? This original article by Betsy J. Lahue, MPH; Kathleen Hughes, MBA; Bethany J. Hills JD, MPH: Sophia S. Li, MPH; Jo Carol Hiatt, MD, MBA, FACS, explores the emergence of mobile health and the potential to revolutionize the delivery of care because of its “real time” potential. This paper grew out of a presentation at the International Society of Pharmacoeconomics and Outcomes Research (ISPOR) Congress. July 2015.
4. On Lessons Learned: Express Scripts' Steve Miller, MD, Discusses HCV Experience, PCSK9 Inhibitors, and More. Through much of 2015, the pharmacy world waited for the arrival of the PCSK9 inhibitors, which had the potential to upend the balance sheets for health plans if patients who’d been taking statins discarded them for drugs that cost five-figures a year. As the approvals neared, EBDM’s Andrew Smith spoke with an expert who’s been surveying the drug pricing scene closely in recent years. July 2015.
3. How Digital Therapeutics Can Help Payers Comply With Upcoming Government Guidance-and Deliver Outcomes. Sean Duffy, CEO of Omada Health, explained how a forthcoming USPSTF requirement for health plans to provide evidence-based diabetes prevention programs could be met through a digital solution. July 2015.
2. Sanofi Addresses Need for Spirometry Before Physicians Can Prescribe Afrezza. FDA’s approval of the inhaled insulin Afrezza came with a requirement: all patients must be screened for lung problems through a process called spirometry. Sanofi, the marketing partner for drug maker MannKind, used the American Diabetes Association Scientific Sessions in June to educate physicians on how to address this requirement, and EBDM was on hand to cover it. July 2015.
1. Toujeo and Afrezza: New and Improved Insulins, Limited by FDA Labeling Constraints. Andrew Smith writes about the advantages of Sanofi’s successor to Lantus and the fast-acting inhaled insulin that’s been all the rage on social media—including the positives that showed up in clinical trials that the FDA kept off the approved labels. May 2015.