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

The Battle with Insurance Companies to Obtain Prescriptions

Philip Seo, MD, MHS  |  Issue: March 2018  |  March 17, 2018

If you are a news junkie, then you know that a tick-tock is a story that relies heavily on chronology, counting down the events of the day, in order, as inexorably as the ticking clock. These types of timeline stories have become very popular in the fast-paced world of modern politics, in which readers eat up the blow-by-blow accounts of the latest scandal.

On occasion, I have been known to keep a tick-tock of my own, largely to figure out why it seems to take me so much time to accomplish so little. On one particular day, my tick-tock would have looked like this:

ad goes here:advert-1
ADVERTISEMENT
SCROLL TO CONTINUE

8:00 a.m.: Called toll-free number to initiate a peer-to-peer review;

10:37 a.m.: Paged to a number with a large phone tree. I could not figure out which option to select to speak to someone;

ad goes here:advert-2
ADVERTISEMENT
SCROLL TO CONTINUE

12:30 p.m.: Called same number again and spoke to Kelly, the pharmacy claims coordinator, who informed me that the drug would be approved if I sent in a note indicating that the patient had received clinical benefit from the drug in the past;

2:05 p.m.: Called the same number. This time, spoke to Jennifer. I reviewed the language of my documentation with her, which stated that the patient had responded to treatment and that continued therapy was appropriate. She agreed that this documentation was adequate.

3:30 p.m.: My office received a call from Carrie, a nurse, who informed me that she needed additional documentation to initiate the appeal. I called back three times to discuss, but reached voicemail all three times;

4:25 p.m.: Spoke to Carrie. She recommended that I list all of the medications the patient had failed in the past, even though the drug had been previously approved. She noted that she was just one of three people who would be reviewing the appeal, and she could not predict what they might be looking for.

I will not bore you with the rest of the chronology, because you may not know the lyrics, but you certainly know the tune. The peer-to-peer review is an interesting concept; it implies that your insurance company is ready to serve as the guardian of sensible prescribing practices, defending the patient from the wanton prescribing practices of the rheumatologist. I have not yet met the Evil Rheumatologist who lives for the sadistic pleasure of starting patients on nonsensical drug regimens, but perhaps he or she lurks among us. For most of us, however, the risks associated with these medications are enough to keep our prescribing practices in check.

Physicians Respond

Stmool / SHUTTERSTOCK.COM

Stmool / SHUTTERSTOCK.COM

Page: 1 2 3 4 5 6 7 | Single Page
Share: 

Filed under:Legal UpdatesLegislation & AdvocacyOpinionRheuminationsSpeak Out Rheum Tagged with:drug benefitspharmacy benefit managersprescription

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.

    Possible Impact of Biosimilar Infliximab on U.S. Market in Prescriptions, Pricing

    September 8, 2016

    The use of biosimilars for rheuma­tology in the U.S. became a reality when the U.S. Food and Drug Administration (FDA) approved Inflectra (infliximab-dyyb), a biosimilar to Remicade (infliximab), in April. What this may mean is increased competition among drug companies with regard to pricing and, therefore, potentially lower costs for U.S. patients, according to Seoyoung…

    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),…

    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…

  • 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