E0409 - Prior Authorization of Inflammatory Bowel Disease Prescriptions: A Single System Review of Current Practices and Adverse Events Associated With Delays
Lauren Loeb, MD1, Ayan Nasir, MD1, Michael F. Picco, MD, PhD1, Jami Kinnucan, MD, FACG1, Jana G. Hashash, MD, MSc1, Francis A. Farraye, MD, MSc2 1Mayo Clinic Florida, Jacksonville, FL; 2Mayo Clinic, Jacksonville, FL
Introduction: Since the introduction of the prior authorization (PA) process by health insurances and pharmacy benefit managers (PBM) for a growing number of medications, it has become increasingly challenging for healthcare providers (HCPs) to ensure their patients receive appropriate treatment in a timely manner. Insurers and PBMs justify PA out of concern for unregulated prescription of medications that can have dangerous side effects, interact with other medications, abuse potential, or the availability of less expensive alternatives. HCPs often sacrifice time and resources appealing denials or redesigning management plans. More concerning is potential harm to the patient related to delays in care. While prior studies have looked at subjective HCP viewpoints on PA in Inflammatory Bowel Disease (IBD), there is limited literature in quantification of delays and direct adverse outcomes. This study aims to evaluate practices in PA, potential delays, and adverse effects related to delays in approval for specialty therapy for IBD.
Methods: A retrospective review was performed at a single tertiary academic medical center for adult patients with IBD prescribed new IBD medication(s) requiring PA. Data collected from each medical record included time from prescription to PA approval. Negative outcomes were assessed including hospital admission, steroid bridge to the new prescription, or surgery.
Results: Of 485 PAs submitted, a review was performed on 42 randomly selected IBD patients with IBD prescription requiring a PA between 9/2021- 3/2022. Mean length of time from prescription to PA approval was 5.8 days (Range: 1-34 days). Of 42 patients, 11 (26%) patients waited longer than 2 business weeks for PA approval, 1 patient (3%) required hospitalization and 3 (7%) patients required steroids during windows of delay. Average time to PA approval for non-commercial vs commercial insurers was 22 vs 6 days. All PAs were ultimately approved.
Discussion: In this descriptive study, the average length of PA approval for a new IBD prescription was 5.8 days, with over 25% with greater than 2 business weeks for PA approval. These results show that the PA process for patients with IBD can benefit from closer, data driven investigation. Further analysis is planned for continuation and dosage changes in therapy requiring PA with the goal of identifying the best practices that can be widely adopted to minimize delays and improve patient care.
Disclosures:
Lauren Loeb indicated no relevant financial relationships.
Ayan Nasir indicated no relevant financial relationships.
Michael Picco indicated no relevant financial relationships.
Jami Kinnucan: Abbvie – Advisor or Review Panel Member. BMS – Advisor or Review Panel Member. GiH Foundation – Advisor or Review Panel Member. janssen – Advisor or Review Panel Member. Pfizer – Advisor or Review Panel Member, Consultant.
Jana Hashash indicated no relevant financial relationships.
Lauren Loeb, MD1, Ayan Nasir, MD1, Michael F. Picco, MD, PhD1, Jami Kinnucan, MD, FACG1, Jana G. Hashash, MD, MSc1, Francis A. Farraye, MD, MSc2. E0409 - Prior Authorization of Inflammatory Bowel Disease Prescriptions: A Single System Review of Current Practices and Adverse Events Associated With Delays, ACG 2022 Annual Scientific Meeting Abstracts. Charlotte, NC: American College of Gastroenterology.