Validation of a prediction rule for disease outcome in patients with recent-onset undifferentiated arthritis

被引:120
作者
van der Helm-van Mil, Annette H. [1 ]
Detert, Jacqueline [2 ]
le Cessie, Saskia
Filer, Andrew [3 ]
Bastian, Hans [2 ]
Burmester, Gerd R. [2 ]
Huizinga, Tom W. J.
Raza, Karim [3 ]
机构
[1] Leiden Univ, Med Ctr, Dept Rheumatol, NL-2300 RC Leiden, Netherlands
[2] Charite, D-13353 Berlin, Germany
[3] Univ Birmingham, Sandwell & W Birmingham Hospitals NHS Trust, Birmingham B15 2TT, W Midlands, England
来源
ARTHRITIS AND RHEUMATISM | 2008年 / 58卷 / 08期
基金
英国医学研究理事会;
关键词
D O I
10.1002/art.23681
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. The decision to start disease-modifying antirheumatic drugs in patients with recent-onset undifferentiated arthritis (UA) is complicated by a varied natural disease course in which the disease in one-third of patients progresses to rheumatoid arthritis (RA), whereas 40-50% of patients experience spontaneous remission. Recently, a prediction rule was developed to estimate the chance of progression to RA in individual patients presenting with UA. This study investigates the accuracy of this prediction rule in independent cohorts of patients with UA. Methods. In 3 cohorts of patients with recent-onset UA, from the UK, Germany, and The Netherlands, the prediction score and the corresponding chance of developing RA were calculated. These data were compared with the observed disease outcome after >= 1 year of followup. Positive predictive values (PPVs) and negative predictive values (NPVs) were. calculated and the overall discriminative ability of the prediction rule was assessed using area under the receiver operating characteristic curves (AUCs). Results. Since data on the severity of morning stiffness were not available in all validation cohorts, the prediction rule was rederived with the duration of morning stiffness as a substitute. The AUC for this rule was 0.88 (SEM 0.015). For each validation cohort, the AUC was 0.83 (SEM 0.041), 0.82 (SEM 0.037), and 0.95 (SEM 0.031) in the British, German, and Dutch cohorts, respectively. The NPV (for a prediction score <= 6) in these 3 cohorts was 83%, 83%, and 86%, respectively; the PPV (for a prediction score :8) was 100%, 93%, and 100%, respectively. Conclusion. The recently derived prediction rule, when applied to 3 independent cohorts of patients with UA, has an excellent discriminative ability for assessing the likelihood of progression to RA. Application of this rule will allow individualized treatment decision-making for patients with UA.
引用
收藏
页码:2241 / 2247
页数:7
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