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1.
Clin Exp Rheumatol ; 41(11): 2249-2256, 2023 Nov.
Article de Anglais | MEDLINE | ID: mdl-37382462

RÉSUMÉ

OBJECTIVES: We aimed to assess the prevalence and factors affecting the discrepancy between patient global assessment (PtGA) and physician global assessment of disease activity (PhGA) in patients with early rheumatoid arthritis (RA) at enrolment and after one year. METHODS: Patients from the Ontario Best Practices Research Initiative (OBRI) were included. The discrepancy between PtGA and PhGA was calculated by simple subtraction (PtGA-PhGA). An absolute value ≥30 was considered discordant. Linear regression analysis was used to assess factors affecting PtGA, PhGA, and PtGA-PhGA discrepancy at enrolment and 1-year follow-up. RESULTS: A total of 531 patients with mean disease duration of 0.3 years were analysed. The discordance prevalence was 22.4% at enrolment and 20.3% after one year. PtGA was higher in the majority of the discordant cases. Multivariable regression analysis showed higher PtGA was significantly associated with higher pain score, tender joint counts (TJC28), ESR, and fatigue at enrolment and 1-year follow-up while PtGA was associated with higher swollen joint counts (SJC28) only at enrolment. Similar associations were found for PhGA, with the exception of fatigue, which was not a significant factor at one year. Multivariable analysis showed that higher discrepancy between PtGA-PhGA was associated with lower SJC28 and higher pain score at enrolment and lower SJC28 and higher pain and fatigue score at 1-year follow-up. CONCLUSIONS: Significant PtGA-PhGA discrepancy was found in approximately one-quarter of early RA patients. In the majority of these patients, PtGA was higher than PhGA. The main predictors of PtGA and PhGA remained the same after one year.


Sujet(s)
Polyarthrite rhumatoïde , Médecins , Humains , Ontario/épidémiologie , Polyarthrite rhumatoïde/diagnostic , Polyarthrite rhumatoïde/épidémiologie , Polyarthrite rhumatoïde/complications , Douleur , Fatigue , Indice de gravité de la maladie
2.
Arthritis Care Res (Hoboken) ; 69(5): 737-741, 2017 05.
Article de Anglais | MEDLINE | ID: mdl-27564591

RÉSUMÉ

OBJECTIVE: To compare the European League Against Rheumatism (EULAR) and Simplified Disease Activity Index 50% (SDAI50) response measures (RMs) and their impact on future response to treatment in patients with early rheumatoid arthritis (ERA). METHODS: Biologic agent-naive ERA patients from the Canadian Early Arthritis Cohort study with complete data at baseline, 3, and 6 months were evaluated. Kappa statistics were used to evaluate the agreement between the EULAR (moderate or good response) and SDAI50 RMs. The RMs at 3 months were also compared for their ability to predict low disease activity state (LDAS) or remission (REM) at 6 months. RESULTS: A total of 1,124 patients were evaluated. Of those, 215 patients (30%) and 294 patients (45%) failed to achieve a EULAR and SDAI50 response, respectively. There was a good agreement between EULAR and SDAI50 RMs with a kappa of 0.59 (95% confidence interval 0.53-0.66). Throughout the range of disease activity, the SDAI50 response was shown to be more stringent than the EULAR response. Multivariable linear regression analysis demonstrated that both RMs at 3 months were associated with LDAS or REM at 6 months, and SDAI50 had a more significant impact on this outcome compared to the EULAR response. CONCLUSION: There is a good agreement between the EULAR and SDAI50 RMs. Although a minority of patients have discordant RMs at each end of the disease activity spectrum at baseline, the SDAI50 response at 3 months appears to be a more significant predictor of outcomes at 6 months than EULAR response.


Sujet(s)
Polyarthrite rhumatoïde/diagnostic , Indice de gravité de la maladie , Adulte , Sujet âgé , Polyarthrite rhumatoïde/épidémiologie , Polyarthrite rhumatoïde/anatomopathologie , Canada/épidémiologie , Études de cohortes , Évolution de la maladie , Femelle , Humains , Modèles linéaires , Mâle , Adulte d'âge moyen , Analyse multifactorielle , Induction de rémission , Reproductibilité des résultats , Facteurs temps
3.
J Rheumatol ; 40(6): 831-41, 2013 Jun.
Article de Anglais | MEDLINE | ID: mdl-23588942

RÉSUMÉ

OBJECTIVE: To assess whether hydroxychloroquine (HCQ) prevents early damage in patients with systemic lupus erythematosus (SLE). METHODS: We updated an existing systematic review of literature on clinical effects of HCQ in patients with SLE. We conducted a nested case-control study embedded in an inception cohort of patients with SLE. Systemic Lupus International Collaborating Clinics Damage Index (SDI) at 3 years was considered as our primary outcome. Patients with SDI > 0 at 3 years were considered cases and patients with SDI = 0 were controls. Cases and controls were first compared by univariate analysis. Then conditional logistic regression models adjusting for potential confounders were done to study the effect of HCQ on damage accrual. RESULTS: Included in the analysis were 481 patients who had 3 or more years of followup. Out of this cohort, we could match 151 cases with 151 controls. Univariate analysis identified age, the use of any immunosuppressive drugs, HCQ, and cumulative dose of steroids as significant covariates associated with damage accrual. In multivariate analysis, the use of HCQ remained significantly associated with less damage (OR 0.34, 95% CI 0.132-0.867), while age (OR 1.05, 95% CI 1.027-1.078) and a variable combining SLE activity and steroid dose (OR 1.73, 95% CI 1.306-2.295) were associated with damage at 3 years. CONCLUSION: We demonstrated that HCQ use was associated with less damage at 3 years after diagnosis of SLE when attention was given and adjustment done for disease activity and steroid dose, duration of disease, and calendar year of diagnosis.


Sujet(s)
Antirhumatismaux/usage thérapeutique , Hydroxychloroquine/usage thérapeutique , Lupus érythémateux disséminé/traitement médicamenteux , Adulte , Études cas-témoins , Femelle , Humains , Mâle , Adulte d'âge moyen , Indice de gravité de la maladie , Résultat thérapeutique
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