Adherence to combination DMARD therapy and treatment outcomes in rheumatoid arthritis: a longitudinal study of new and existing DMARD users

被引:25
|
作者
Wabe, Nasir [1 ,2 ]
Lee, Anita [3 ]
Wechalekar, Mihir [4 ]
McWilliams, Leah [3 ]
Proudman, Susanna [3 ]
Wiese, Michael [1 ,2 ]
机构
[1] Univ South Australia, Sch Pharm & Med Sci, GPO Box 2471, Adelaide, SA 5001, Australia
[2] Univ South Australia, Sansom Inst Hlth Res, GPO Box 2471, Adelaide, SA 5001, Australia
[3] Royal Adelaide Hosp, Rheumatol Unit, Adelaide, SA 5000, Australia
[4] Repatriat Gen Hosp, Rheumatol Unit, Daw Pk, Adelaide, SA 5041, Australia
关键词
Medication adherence; Treatment outcomes; Rheumatoid arthritis; Propensity scores; Clinical outcomes; MODIFYING ANTIRHEUMATIC DRUGS; TO-TARGET STRATEGY; DISEASE-ACTIVITY; RESPONSE CRITERIA; CLINICAL-PRACTICE; EUROPEAN-LEAGUE; 1ST YEAR; VALIDATION; BIOLOGICS; MODELS;
D O I
10.1007/s00296-017-3655-z
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Medication adherence is believed to be a major contributor to treatment outcomes yet studies quantifying this relationship as rare in rheumatoid arthritis (RA). To determine the association of adherence to DMARD therapy with treatment outcomes among new and existing DMARD users over 2 years. Relevant clinical parameters were obtained from a longitudinal cohort of RA patients, most of who were treated with combination therapy. Patients were classified as adherent if the proportion of days covered for each DMARD was ae<yen>80%. Outcome measures were the change in the disease activity score in 28 joints (DAS28), simplified disease activity index (SDAI), modified health assessment questionnaires (mHAQ) and proportion of patients who achieved response criteria. An inverse propensity-score weighting method was used to estimate the association of adherence with each outcome. Of 194 patients invited, a total of 111 patients (new = 45 and existing = 66 DMARD users) met study eligibility. DMARD-naive patients demonstrated relatively higher rates of adherence compared to existing users. After controlling for confounding variables, adherence was significantly associated with reduction in DAS28 (beta = -1.5, 95% CI of beta = - 2.17 to -0.83, p < 0.0001), SDAI (beta = -9.44, 95% CI of beta = -15.53 to -3.35, p = 0.002) and mHAQ (beta = -0.269, 95% CI of beta, -0.462 to -0.077, p = 0.017) over 2 years among new patients and adherent patients were more likely to achieve most response criteria compared to non-adherent patients. Such associations were not replicated among existing DMARD users. Adherence to combination DMARD therapy was associated with improvements in disease activity and functional outcomes in the first 2 years of therapy.
引用
收藏
页码:897 / 904
页数:8
相关论文
共 50 条
  • [1] Adherence to combination DMARD therapy and treatment outcomes in rheumatoid arthritis: a longitudinal study of new and existing DMARD users
    Nasir Wabe
    Anita Lee
    Mihir Wechalekar
    Leah McWilliams
    Susanna Proudman
    Michael Wiese
    [J]. Rheumatology International, 2017, 37 : 897 - 904
  • [2] Combination DMARD therapy for rheumatoid arthritis. Full or low DMARD doses?
    Ferraccioli, GF
    Casatta, L
    DiPoi, E
    Damato, R
    Bartoli, E
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 1997, 56 (05) : 336 - 337
  • [4] Clinical pharmacology of combination DMARD therapy in rheumatoid arthritis
    Furst, DE
    [J]. JOURNAL OF RHEUMATOLOGY, 1996, 23 : 86 - 90
  • [5] COMBINATION DMARD THERAPY FOR RHEUMATOID-ARTHRITIS - TOLERABILITY
    ODELL, J
    HAIRE, C
    ERIKSON, N
    DRYMALSKI, W
    PALMER, W
    ECKHOFF, J
    GARWOOD, V
    MALOLEY, P
    ILLERA, V
    KLASSEN, L
    MOORE, G
    [J]. ARTHRITIS AND RHEUMATISM, 1993, 36 (09): : S53 - S53
  • [6] Combination DMARD therapy including corticosteroids in early rheumatoid arthritis
    Möttönen, TT
    Hannonen, PJ
    Boers, M
    [J]. CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, 1999, 17 (06) : S59 - S65
  • [8] Adherence to biologic DMARD therapies in rheumatoid arthritis
    Koncz, Tamas
    Pentek, Marta
    Brodszky, Valentin
    Ersek, Katalin
    Orlewska, Ewa
    Gulacsi, Laszlo
    [J]. EXPERT OPINION ON BIOLOGICAL THERAPY, 2010, 10 (09) : 1367 - 1378
  • [9] Safety of DMARD combination therapy to single drug treatment in early rheumatoid arthritis.
    LeirisaloRepo, M
    Kautiainen, H
    [J]. ARTHRITIS AND RHEUMATISM, 1997, 40 (09): : 122 - 122
  • [10] Leflunomide: a new DMARD for rheumatoid arthritis
    Emery, P
    [J]. HOSPITAL MEDICINE, 2000, 61 (05): : 344 - 347