Estimation of optimal adherence threshold for tumor necrosis factor inhibitors in rheumatoid arthritis

被引:0
|
作者
Harris, Jennifer Toth [1 ]
Yang, Yi [2 ]
Bentley, John P. [2 ]
Chen, Yixin [2 ]
Ramachandran, Sujith [2 ]
机构
[1] Verana Hlth, 360 3rd St, San Francisco, CA 94107 USA
[2] Univ Mississippi, POB 1848, University, MS 38677 USA
关键词
Adherence threshold; Claims; Medicare; Proportion of days covered; Rheumatoid arthritis; Tumor necrosis factor inhibitors; MODIFYING ANTIRHEUMATIC DRUGS; MEDICATION ADHERENCE; PERSISTENCE; PATTERNS; IMPACT; COSTS;
D O I
10.1007/s10067-024-06971-y
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Optimal adherence thresholds can vary across medications and disease states. The objective of the study was to determine the optimal threshold of the proportion of days covered (PDC) for tumor necrosis factor (TNF) inhibitors in patients with rheumatoid arthritis (RA).Methods Patients with RA initiating self-administered TNF inhibitors were identified using 2012-18 Medicare fee-for-service claims. Time-varying PDC was calculated every day for the preceding 90 days during follow-up. Oral and injected glucocorticoid use, hospitalizations, emergency room (ER) visits, serious infections, and a composite of these were measured as outcomes. Time to first occurrence of each outcome as a function of time-varying PDC for TNF inhibitors was evaluated using Cox regression. Incident/dynamic time-dependent receiver operating characteristic curves and Youden's J index were used to obtain the optimal PDC threshold for outcomes at 365 days.Results Of the 1190 patients who met the study inclusion criteria, almost 75% (865 patients) experienced at least one of the outcomes. Increasing PDC by 10% was significantly associated with decreased risks of the composite outcome (HR 0.98, 95% CI 0.96-1.00), oral glucocorticoid use (HR 0.93, 95% CI 0.91-0.96), and hospitalization (HR 0.96, 95% CI 0.94-0.99) but an increased risk of ER visits (HR 1.04, 95% 1.01-1.07). Optimal PDC thresholds for the composite outcome, oral glucocorticoid use, and hospitalization were 0.64, 0.59, and 0.56, respectively.Conclusions Increased PDC was associated with a decreased risk of adverse outcomes, except ER visits. The optimal PDC for TNF inhibitors in Medicare patients with RA based on clinical outcomes was about 60%. Key Points center dot The optimal proportion of days covered threshold for tumor necrosis factor inhibitors at 365 days based on clinical outcomes was found to be about 60%, which is lower than the traditional 80% used to define adherence. center dot Increased adherence was associated with decreased risks of oral glucocorticoid use, hospitalization, and the composite outcome. However, it was also associated with an increased risk of emergency room visits. center dot The mean time-varying 90-day proportion of days covered decreased throughout the study starting 92% at day 1 of follow-up to 62% at day 365.
引用
收藏
页码:2435 / 2444
页数:10
相关论文
共 50 条
  • [31] Rheumatoid arthritis and tuberculosis in the tumor necrosis factor inhibitors era - Observations from Brazil
    Pinheiro, GDC
    JCR-JOURNAL OF CLINICAL RHEUMATOLOGY, 2005, 11 (06) : 344 - 346
  • [32] Is there a pharmacoeconomic argument supporting the use of tumor necrosis factor inhibitors in early rheumatoid arthritis?
    Kavanaugh, Arthur
    NATURE CLINICAL PRACTICE RHEUMATOLOGY, 2006, 2 (07): : 346 - 347
  • [33] Is there a pharmacoeconomic argument supporting the use of tumor necrosis factor inhibitors in early rheumatoid arthritis?
    Arthur Kavanaugh
    Nature Clinical Practice Rheumatology, 2006, 2 : 346 - 347
  • [34] Predictors of Treatment Initiation with Tumor Necrosis Factor-α Inhibitors in Patients with Rheumatoid Arthritis
    Desai, Rishi J.
    Rao, Jaya K.
    Hansen, Richard A.
    Fang, Gang
    Maciejewski, Matthew L.
    Farley, Joel F.
    JOURNAL OF MANAGED CARE & SPECIALTY PHARMACY, 2014, 20 (11): : 1110 - 1120
  • [35] Ischemic Colitis During Treatment with Tumor Necrosis Factor Alpha Inhibitors in Rheumatoid Arthritis
    Salk, Allison
    Stobaugh, Derrick
    Deepak, Parakkal
    Ehrenpreis, Eli
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2012, 107 : S208 - S208
  • [36] Cardiovascular Safety of Tocilizumab Versus Tumor Necrosis Factor Inhibitors in Patients with Rheumatoid Arthritis
    Kim, Seoyoung C.
    Solomon, Daniel H.
    Rogers, James R.
    Gale, Sara
    Klearman, Micki
    Sarsour, Khaled
    Schneeweiss, Sebastian
    ARTHRITIS & RHEUMATOLOGY, 2016, 68
  • [37] Persistence and Dose Escalation of Tumor Necrosis Factor Inhibitors in US Veterans with Rheumatoid Arthritis
    Cannon, Grant W.
    DuVall, Scott L.
    Haroldsen, Candace L.
    Caplan, Liron
    Curtis, Jeffrey R.
    Michaud, Kaleb
    Mikuls, Ted R.
    Reimold, Andreas
    Collier, David H.
    Harrison, David J.
    Joseph, George J.
    Sauer, Brian C.
    JOURNAL OF RHEUMATOLOGY, 2014, 41 (10) : 1935 - 1943
  • [38] The kynurenine pathway in patients with rheumatoid arthritis during tumor necrosis factor α inhibitors treatment
    Witoszynska-Sobkowiak, Joanna
    Sikorska, Dorota
    Niklas, Karolina
    Zychowska, Iwona
    Rutkowski, Rafal
    Samborski, Wlodzimierz
    REUMATOLOGIA, 2024, 62 (04): : 220 - 225
  • [39] Tumor Necrosis Factor Inhibitors and the Risk of Cancer among Older Americans with Rheumatoid Arthritis
    D'Arcy, Monica E.
    Beachler, Daniel C.
    Pfeiffer, Ruth M.
    Curtis, Jeffrey R.
    Mariette, Xavier
    Seror, Raphaele
    Mahale, Parag
    Rivera, Donna R.
    Yanik, Elizabeth L.
    Engels, Eric A.
    CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION, 2021, 30 (11) : 2059 - 2067
  • [40] LABORATORY SAFETY OF ADALIMUMAB AND OTHER TUMOR NECROSIS FACTOR INHIBITORS IN THE TREATMENT OF RHEUMATOID ARTHRITIS
    Pappas, D. A.
    Shaw, J. W.
    Chang, H.
    Cifaldi, M. A.
    Reed, G. W.
    Garg, V.
    Lacerda, A. P.
    Mozaffarian, N.
    ANNALS OF THE RHEUMATIC DISEASES, 2014, 73 : 931 - 931