Abstract

BackgroundAdherence is a key factor for therapeutic success in patients with rheumatoid arthritis (RA). The aim of this study was to determine whether results from the 5-item Compliance Questionnaire for Rheumatology (CQR5) can predict future poor adherence to biological disease-modifying anti-rheumatic drugs (bDMARDs) in patients with RA, using medication possession ratio (MPR) as the gold standard comparator.MethodsRA patients starting a bDMARD were prospectively followed for 12 months. At baseline, CQR5 was collected in relation to the prescribed bDMARD. Patients were dichotomised into good adherers and poor adherers, categories that were then used as the variable in a predictive function analysis of the CQR5 in order to determine the accuracy of the classification at the end of the study period in comparison with the MPR. The sensitivity, specificity, and likelihood ratio of detecting poor adherers were also determined because this is the clinically important purpose of the questionnaire. Satisfactory adherence was defined as > 80% compliance with the prescribed dose regimen.ResultsOf the 210 RA patients enrolled (147 women and 63 men; mean age 58.6 ± 12.8 years; mean disease duration 7.4 ± 2.5 years), at the end of the 12-month follow-up, 152 patients (72.4%) were good adherers and 58 (27.6%) were poor adherers according to MPR. Predictive analyses showed that the sensitivity and specificity of the CQR5 in detecting poor adherence were respectively 89.9% (95% CI 84.07–94.10%) and 80.8% (95% CI 67.46–90.37%). The accuracy of the CQR5 was 83.04% (95% CI 77.27–87.85%), the positive likelihood ratio (i.e. detecting ≤ 80% adherence) 4.67 (95% CI 2.58–8.18), and the area under curve 0.85 (95% CI 0.79–0.89).ConclusionHigher baseline CQR5 scores significantly predict the treatment adherence of RA patients. This suggests that this instrument could be used for screening purposes in order to identify patients who are poorly adherent to bDMARDs.

Highlights

  • Higher baseline CQR5 scores significantly predict the treatment adherence of rheumatoid arthritis (RA) patients. This suggests that this instrument could be used for screening purposes in order to identify patients who are poorly adherent to biological disease-modifying anti-rheumatic drugs (bDMARDs)

  • Treatment adherence is the extent to which patient behaviour coincided with healthcare [1] and, unlike compliance, indicates a patient’s active and voluntary role in accepting the prescribed therapy and therapeutic schedule, and respecting correct daily dosing over time, whereas treatment persistence describes the continuation of treatment for the prescribed period [2, 3]

  • In this study, we clearly demonstrated the validity of CQR5 as a predictor of poor adherence to bDMARD treatment in patients with RA

Read more

Summary

Introduction

Treatment adherence is the extent to which patient behaviour coincided with healthcare [1] and, unlike compliance (which refers to a physician’s treatment plan), indicates a patient’s active and voluntary role in accepting the prescribed therapy and therapeutic schedule, and respecting correct daily dosing over time, whereas treatment persistence describes the continuation of treatment for the prescribed period [2, 3]. Non-adherence to treatment often explains a failure to achieve therapeutic goals in rheumatoid arthritis (RA) patients [4]. Adherence to disease-modifying anti-rheumatic drug (DMARD) prescriptions has been highly variable in clinical trials [5], and retrospective studies of treatment persistence in RA patients taking tumour necrosis factor alpha (TNFα) antagonists have shown that is 82–89% after 6 months, 48–78% after months, 70% after months, 71% after 18 months, and 62–67% after 24 months [6,7,8]. The aim of this study was to determine whether results from the 5-item Compliance Questionnaire for Rheumatology (CQR5) can predict future poor adherence to biological disease-modifying anti-rheumatic drugs (bDMARDs) in patients with RA, using medication possession ratio (MPR) as the gold standard comparator

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call