Medical Industry Feature

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Medical Industry Feature highlights topics brought to you by makers of products and services in the medical industry.

  1. 5d ago

    The Patient You Might Be Missing: Severe Hypertriglyceridemia in Clinical Practice

    Host: Charles Turck, PharmD, BCPS, BCCCP Guest: Erin D. Michos, MD, MHS Severe hypertriglyceridemia (sHTG) affects more than 3 million people, but it often flies under the clinical radar.1-3 When triglycerides are at or above a 500 mg/dL threshold, it’s no longer just an isolated lab value—it’s a level of hypertriglyceridemia where the clinical implications change, and where a more careful evaluation for underlying causes and risk becomes important.4 That’s why Dr. Charles Turck sits down with Dr. Erin Michos to discuss what sHTG is, why it’s so important to identify, and how we can effectively manage this condition to improve patients’ overall health and reduce complication risk. Dr. Erin Michos is a Professor of Medicine, Director of Women’s Cardiovascular Health, and Associate Director of Preventive Cardiology at Johns Hopkins University School of Medicine. References: Saadatagah S, Larouche M, Naderian M, et al. Recognition and management of persistent chylomicronemia: a joint expert clinical consensus by the National Lipid Association and the American Society for Preventive Cardiology. Am J Prev Cardiol. 2025;22:100978. doi:10.1016/j.ajpc.2025.100978 Sanchez RJ, Ge W, Wei W, Ponda MP, Rosenson RS. The association of triglyceride levels with the incidence of initial and recurrent acute pancreatitis. Lipids Health Dis. 2021;20(1):72. doi:10.1186/s12944-021-01488-8 Sikora Kessler A, Baum SJ, Kutrieb E, et al. Rates …

  2. Aug 5

    Pediatric Influenza: Risks, Realities, and Prevention

    Host: Jennifer Caudle, DO, FACOFP Guest: Laura Sass, MD Pediatric influenza carries a significant clinical burden, with children under four experiencing one of the highest rates of influenza-related illness, healthcare visits, and hospitalization.1,2 Seasonal influenza vaccination remains an evidence-based strategy to reduce illness and severe outcomes, with a well-established safety profile and continued support from leading U.S. health authorities.3,4 Joining Dr. Jennifer Caudle to share her perspective on the importance of influenza vaccination in children is Dr. Laura Sass. Dr. Laura Sass is an Associate Professor of Pediatrics at Eastern Virginia Medical School and a board-certified Pediatric Infectious Diseases specialist at Children's Hospital of The King's Daughters. References: US Centers for Disease Control and Prevention (CDC). Laboratory-confirmed influenza hospitalizations. Accessed March 31, 2026. https://gis.cdc.gov/grasp/fluview/FluHospChars.html#virusTypeDiv. US Centers for Disease Control and Prevention (CDC). Influenza Activity in the United States during the 2024–25 Season and Composition of the 2025–26 Influenza Vaccine. Accessed March 31, 2026. https://www.cdc.gov/flu/whats-new/2025-2026-influenza-activity.html. US Centers for Disease Control and Prevention (CDC). Flu Vaccine Effectiveness for Children and Older Adults. Updated August 14. 2024. Accessed March 31, 2026. https://www.cdc.gov/flu-vaccines-work/risk-groups/index.html. Committee on Infectious Diseases. Recommendations for Prevention and Control of Influenza in Children, 2025-2026: Policy Statement. Pediatrics. 2025;156(6)doi:10.1542/peds.2025-073620

  3. Jun 17

    Redefining Durability in Wet AMD: Insights from the SOL‑1 Superiority Trial

    Host: Priya Vakharia, MD Guest: Andrew Moshfeghi, MD The SOL-1 Phase 3 superiority trial compared the efficacy and safety of the investigational product OTX-TKI (axitinib intravitreal hydrogel) with aflibercept 2 mg. The primary endpoint was proportion of subjects who maintained visual acuity, defined as 15 Early Treatment Diabetic Retinopathy Study letters of best-corrected visual acuity loss from baseline at Week 36. Based on the findings, SOL-1 met its primary endpoint and demonstrated a statistically significant high proportion of subjects maintained visual acuity with OTX-TKI vs. aflibercept 2 mg at Week 36. OTX-TKI demonstrated stability in vision and anatomic outcomes through 36 weeks, with evidence of extended durability and delayed need for rescue therapy. This could contribute to the goal of maintaining disease control in wet AMD. OTX-TKI was generally well tolerated through Week 52. Ocular adverse events were reported in 52.9% of OTX-TKI-treated subjects vs. 33.7% of aflibercept-treated subjects. There were no treatment-related serious adverse events (SAEs) and no cases of retinal vasculitis. The most common AEs reported in OTX-TKI subjects were vitreous floaters (12.4%), cataract (7.1%) and conjunctival hemorrhage (6.5%). To learn more about the SOL-1 trial design, findings, and implications for care, tune in to hear Dr. Priya Vakharia speak with Dr. Andrew Moshfeghi. Reference: Heier …

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Medical Industry Feature highlights topics brought to you by makers of products and services in the medical industry.

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