Video: Every Case Tells a Story| Webinar: ACR/CHEST ILD Guidelines in Practice

An official publication of the ACR and the ARP serving rheumatologists and rheumatology professionals

  • Conditions
    • Axial Spondyloarthritis
    • Gout and Crystalline Arthritis
    • Myositis
    • Osteoarthritis and Bone Disorders
    • Pain Syndromes
    • Pediatric Conditions
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Sjögren’s Disease
    • Systemic Lupus Erythematosus
    • Systemic Sclerosis
    • Vasculitis
    • Other Rheumatic Conditions
  • FocusRheum
    • ANCA-Associated Vasculitis
    • Axial Spondyloarthritis
    • Gout
    • Psoriatic Arthritis
    • Rheumatoid Arthritis
    • Systemic Lupus Erythematosus
  • Guidance
    • Clinical Criteria/Guidelines
    • Ethics
    • Legal Updates
    • Legislation & Advocacy
    • Meeting Reports
      • ACR Convergence
      • Other ACR meetings
      • EULAR/Other
    • Research Rheum
  • Drug Updates
    • Analgesics
    • Biologics/DMARDs
  • Practice Support
    • Billing/Coding
    • EMRs
    • Facility
    • Insurance
    • QA/QI
    • Technology
    • Workforce
  • Opinion
    • Patient Perspective
    • Profiles
    • Rheuminations
      • Video
    • Speak Out Rheum
  • Career
    • ACR ExamRheum
    • Awards
    • Career Development
  • ACR
    • ACR Home
    • ACR Convergence
    • ACR Guidelines
    • Journals
      • ACR Open Rheumatology
      • Arthritis & Rheumatology
      • Arthritis Care & Research
    • From the College
    • Events/CME
    • President’s Perspective
  • Search

ACR Convergence 2024 Preview: Key Business Takeaways

Carina Stanton  |  October 8, 2024

Rheumatology practices have faced unique challenges this year, from navigating underwater biosimilars and new twists and turns with reimbursements to taking a closer look at complex treatments and enhancing data-driven patient care. With so much to discuss, the business of rheumatology will be a lively track at ACR Convergence 2024.

The ACR’s annual meeting is taking place Nov. 14–19 at the Walter E. Washington Convention Center in Washington, D.C. The conference will be hosted in-person and on-demand with select livestreamed sessions.

Dr. Shepherd

One major business focus will be to address payer challenges to which the ACR is currently responding, and which rheumatology practices are having to endure. These include insurance requirements for therapies with biosimilars, according to Rebecca Shepherd, MD, MBA, a session moderator and chair of the ACR’s Insurance Subcommittee of the Committee on Rheumatologic Care (CORC). “The more rheumatologists know, the more we can influence decision making and educate other stakeholders including patients, employers and government officials who create policy.”

Mark Niemer

Dr. Niemer

Rheumatology practices are also “keen to learn how colleagues are finding success caring for rheumatoid arthritis (RA) patients with complicated treatment regimens, including combination therapies and biologic response modifiers,” notes Mark Niemer, MD, who is moderating a session that will highlight best practices for coding and tools to improve patient workflows.

ad goes here:advert-2
ADVERTISEMENT
SCROLL TO CONTINUE

What to Expect from the Business Track

The business of rheumatology track will cover a wide range of topics targeted toward improving business operations for any rheumatology practice. Sessions will cover coding, payer changes, clinical workflows, conducting research, advocacy, staffing, and technologies in practice such as using artificial intelligence (AI) for documentation.

Two sessions on Saturday, Nov. 16, will help attendees understand payer challenges and learn strategies to handle these and other workflow issues:

  • Facing Payer Challenges: Biosimilars, Closed Formularies, and Telehealth (Nov. 16, 9–10 a.m. EST)
  • RA Toolkit: A Turnkey Workflow for RA Patients in Your Clinic (Nov. 16, 1–2 p.m. EST)

Two sessions on Sunday, Nov. 17, will help you make your rheumatology practice more efficient, from using AI to working with advanced practice providers. Also, be sure to check the networking lounge program for opportunities to talk with peers and ACR staff about topics including work-life balance, handling practice challenges and more.

Facing Payer Challenges

“Rheumatology professionals are critical advocates for their patients, and access to medications is equally critical in treating rheumatologic diseases,” says Dr. Shepherd. In a session she is co-moderating with Louisa Ziglar, MD, attendees will learn more about the evolving access to and reimbursement for biosimilars, as well as the reasons behind formulary restrictions that often limit access to medications essential for disease management.

Page: 1 2 3 | Single Page
Share: 

Filed under:ACR ConvergencePractice ManagementPractice Support Tagged with:ACR Convergence 2024

Related Articles

    Marching to the Biosimilar Beat: Questions on Rollout Remain

    September 7, 2023

    The availability of biosimilars for the treatment of patients with rheumatic diseases exploded in 2023. Here’s where we stand and what to expect going forward.

    The 2018 ACR/ARHP Annual Meeting Program Preview

    September 20, 2018

    Save the date for the 2018 ACR/ARHP Annual Meeting, Oct. 19–24 in Chicago. Connect with your colleagues for an unmatched educational experience featuring exceptional sessions by leading rheumatology experts. The ACR/ARHP Annual Meeting is your gateway to global rheumatology education. With more than 450 sessions—including The Great Debate—the meeting provides boundless opportunities for professional development,…

    Report on EU’s Experience with Biosimilar Drugs Released: Will U.S. Experience Be Similar?

    October 17, 2017

    As questions about biosimilar medications swirl among U.S. rheumatologists, a recently released report sheds some light on the European experience with biosimilars—and may offer some important insights for the U.S. market. The report, Biosimilars in the EU: Information Guide for Healthcare Professionals, was released in late April by the European Medicines Agency (EMA) and the…

    Biosimilars Debate Heats up over Cost Savings, Safety Concerns

    Biosimilars Debate Heats up over Cost Savings, Safety Concerns

    April 15, 2016

    After years of speculation about potential cost savings and debates on safety, biosimilars are about to step onto the stage of rheumatic disease treatment. On Feb. 9, the Arthritis Advisory Committee of the U.S. Food and Drug Administration (FDA) met in Washington, D.C., and recommended the approval of CT-P13, a proposed biosimilar to infliximab (Remicade),…

  • About Us
  • Meet the Editors
  • Issue Archives
  • Contribute
  • Advertise
  • Contact Us
  • Copyright © 2025 by John Wiley & Sons, Inc. All rights reserved, including rights for text and data mining and training of artificial technologies or similar technologies. ISSN 1931-3268 (print). ISSN 1931-3209 (online).
  • DEI Statement
  • Privacy Policy
  • Terms of Use
  • Cookie Preferences