In-Office Procedures, Over-the-Counter Options, Treatment Delays, and Costs
May 15th 2024Selina McGee, OD, FAAO, evaluates the cost and efficacy of in-office procedures like microblepharoexfoliation, the potential clinical and economic costs associated with delaying access to the FDA-approved treatment through prior authorization or mandating prior use of traditional over-the-counter therapies like tea tree oil and lid wipes, and considers impact on patient adherence.
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Traditional Treatment of Demodex Blepharitis, FDA approval, and Lotilaner Ophthalmic Solution, 0.25%
May 8th 2024A key opinion leader examines the historical context of Demodex blepharitis treatment, discussing the efficacy and limitations of previous therapies, and emphasizes a recently FDA-approved therapy that directly targets Demodex mites, leading to improved efficacy compared to treatments that only address symptoms.
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Prevalence and Impact of Hydroxyurea Intolerance or Resistance in Polycythemia Vera
May 1st 2024Timothy Mok, PharmD, BCPS, BCOP, and Gabriela Hobbs, MD, introduce themselves and provide insights on the prevalence of hydroxyurea resistance or intolerance in patients with polycythemia vera (PV) and how it impacts treatment decisions and costs.
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Prescribing Prescription Drug Therapeutics: Factors for Providers and Payers to Consider
April 30th 2024Mahsa Salsabili, PharmD, PhD, offers a comprehensive list of factors for healthcare providers and payers to consider in order to streamline the process of prescription digital therapeutics to patients.
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Navigating Insurance Coverage for Prescription Digital Therapeutics
April 23rd 2024Mahsa Salsabili, PharmD, PhD, addresses the challenges surrounding insurance approval and the limited announcements regarding coverage for prescription digital therapeutics, while exploring various reimbursement models, such as value-based contracts and outcome-based rebates.
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FDA Approval Pathway for Prescription Digital Therapeutics
April 23rd 2024Mahsa Salsabili, PharmD, PhD, delves into the FDA approval process for prescription digital therapeutics , which requires market approval, clinical studies and real-world evidence, to establish their efficacy in treating the targeted disease or condition.
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Diana Isaacs, PharmD, BCPS, BCACP, BC-ADM, CDCES, FADCES, FCCP, discusses socioeconomic barriers, such as financial constraints, unstable housing, stressful living situations, and demanding work schedules, can hinder diabetes self-care, requiring healthcare providers to approach patients with empathy when addressing these challenges.
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Melissa Andel Gives Insights on Potential Changes to Part D Formularies | AMCP 2024
April 17th 2024Andel, principal of CommonHealth Solutions LLC, weighed in on potential strategies and challenges for Part D plans in navigating medication formulary limitations during catastrophic coverage phases in this second part of a two-part video series.
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PBM Legislation and the PBM-affiliated GPOs | AMCP 2024
April 17th 2024Ross Margulies, J.D., M.P.H., a partner at the Foley Hoag law firm, discusses whether proposed transparency rules in the pharmacy benefit manager (PBM) legislation that Congress is considering might apply to the PBM-affiliated group purchasing organizations.
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