ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstract Number: 80

Impact of a Patient Support Program on Abandonment of Adalimumab Treatment Initiation in Patients with Rheumatoid Arthritis, Ankylosing Spondylitis, and Psoriatic Arthritis

Philip Mease1, Manish Mittal2, Martha Skup2, Matthew Davis3, Arijit Ganguli2, Scott Johnson3 and Michael Schiff4, 1Swedish Medical Center and University of Washington, Seattle, WA, 2AbbVie Inc., North Chicago, IL, 3Medicus Economics, LLC, Milton, MA, 4University of Colorado, Greenwood Village, CO

Meeting: 2016 ACR/ARHP Annual Meeting

Date of first publication: September 28, 2016

Keywords: Adalimumab, Ankylosing spondylitis (AS), anti-TNF therapy, psoriatic arthritis and rheumatoid arthritis (RA)

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Date: Sunday, November 13, 2016

Title: Health Services Research - Poster I

Session Type: ACR Poster Session A

Session Time: 9:00AM-11:00AM

Background/Purpose: Treatment abandonment (failure to start therapy after prescription) is common among patients (pts) prescribed specialty pharmaceuticals. AbbVie offers a pt support program (PSP) for adalimumab (ADA)-treated pts, which includes assistance with medication costs, nurse support, injection training, pen disposal and medication reminders.1 PSP may reduce abandonment in RA, ankylosing spondylitis (AS) and psoriatic arthritis (PsA). We investigated associations between PSP and rate of ADA treatment abandonment in US pts with RA, AS and PsA.

Methods: A longitudinal study was conducted using pt-level data from AbbVie’s PSP database linked with Source Healthcare Analytics US claims data. Pts aged ≥18 years with a RA, AS or PsA diagnosis, ≥1 pharmacy claim (paid or reversed) for ADA and no ADA claim before 2012 were included; the index date was the first ADA claim from 1/2012–1/2015. Pts required medical coverage ≥3 months pre-index date and pharmacy coverage ≥3 months pre-/post-index date. Abandonment was defined as reversal of first ADA claim (eg, pt did not take possession of medication) with no paid claim during 3 months of follow-up. Abandonment rate was compared between pts who enrolled in any component of the PSP (PSP cohort) vs those who did not (non-PSP cohort) within 30 days of treatment initiation using 2-sample z-test of proportions. The likelihood of abandonment was assessed using logistic regression, controlling for baseline characteristics.

Results: A total of 16780 pts (RA: 6200 PSP, 6155 non-PSP; AS: 451 PSP, 525 non-PSP; PsA: 1785 PSP, 1664 non-PSP) were included. At baseline in RA and PsA, PSP pts were younger (50.5 vs 52.0 yr; P<.0001 and 48.5 vs 49.3 yr; P=.042, respectively) and less likely to be male (20.4% vs 22.5%; P=.005 and 41.2% vs 47.8%; P=.0001, respectively) than non-PSP pts. No significant difference was observed regarding age in AS, but PSP pts were less likely to be male vs non-PSP pts (50.1% vs 57.7%; P=.018). The PSP cohort had lower expected per-patient out of pocket contribution for ADA across diseases (RA [$222 vs $312; P<.0001], AS [$136 vs $240; P<.0001] and PsA [$179 vs $261; P<.0001]) and greater frequency of specialty pharmacy use for first ADA fill (RA: 55.7% vs 47.3%; P<.0001, AS: 65.4% vs 49.5%; P<.0001, PsA: 58.8% vs 54.8%; P=.0173). After controlling for baseline characteristics among PSP vs non-PSP pts, abandonment risk was 78% lower in RA (6.0% vs 26.4%; odds ratio [OR]=0.22; P<.0001), 85% lower in AS (3.8% vs 20.2%; OR=0.15; P<.0001) and 77% lower in PsA (4.8% vs 21.9%; OR=0.23; P<.0001) (Figure).

Conclusion: Enrollment in AbbVie’s free-to-patient PSP was associated with 77–85% reduced abandonment of ADA treatment among US pts with RA, AS and PsA.   References: 1. https://www.humira.com/humira-complete

 

 


Disclosure: P. Mease, AbbVie, Amgen, BMS, Celgene, Genentech, Janssen, Lilly, Merck, Novartis, Pfizer, Roche, UCB, 2,AbbVie, Amgen, BMS, Celgene, Genentech, Janssen, Lilly, Merck, Novartis, Pfizer, Roche, UCB, 5,AbbVie, Amgen, BMS, Celgene, Genentech, Janssen, Lilly, Merck, Novartis, Pfizer, Roche, UCB, 8; M. Mittal, AbbVie, 3,AbbVie, 1; M. Skup, AbbVie, 3,AbbVie, 1; M. Davis, Medicus Economics, which received payment from AbbVie to participate in this research, 3; A. Ganguli, AbbVie, 3,AbbVie, 1; S. Johnson, Medicus Economics, which received payment from AbbVie to participate in this research, 3; M. Schiff, AbbVie, Amgen, BMS, Eli Lilly, JNJ, Novartis, Roche, UCB, 5,AbbVie, 8.

To cite this abstract in AMA style:

Mease P, Mittal M, Skup M, Davis M, Ganguli A, Johnson S, Schiff M. Impact of a Patient Support Program on Abandonment of Adalimumab Treatment Initiation in Patients with Rheumatoid Arthritis, Ankylosing Spondylitis, and Psoriatic Arthritis [abstract]. Arthritis Rheumatol. 2016; 68 (suppl 10). https://acrabstracts.org/abstract/impact-of-a-patient-support-program-on-abandonment-of-adalimumab-treatment-initiation-in-patients-with-rheumatoid-arthritis-ankylosing-spondylitis-and-psoriatic-arthritis/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2016 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/impact-of-a-patient-support-program-on-abandonment-of-adalimumab-treatment-initiation-in-patients-with-rheumatoid-arthritis-ankylosing-spondylitis-and-psoriatic-arthritis/

Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology