Thomas S L, Edwards C J, Smeeth L, Cooper C, Hall A J
Department of Epidemiology & Population Health, London School of Hygiene & Tropical Medicine, Keppel Street, London WC1E 7HT, UK.
Arthritis Rheum. 2008 Sep 15;59(9):1314-21. doi: 10.1002/art.24015.
To identify characteristics that predict a valid rheumatoid arthritis (RA) or juvenile idiopathic arthritis (JIA) diagnosis among RA- and JIA-coded individuals in the General Practice Research Database (GPRD), and to assess limitations of this type of diagnostic validation.
Four RA and 2 JIA diagnostic groups were created with differing strengths of evidence of RA/JIA (Group 1 = strongest evidence), based on RA/JIA medical codes. Individuals were sampled from each group and clinical and prescription data were extracted from anonymized hospital/practice correspondence and electronic records. American College of Rheumatology and International League of Associations for Rheumatology diagnostic criteria were used to validate diagnoses. A data-derived diagnostic algorithm that maximized sensitivity and specificity was identified using logistic regression.
Among 223 RA-coded individuals, the diagnostic algorithm classified individuals as having RA if they had an appropriate GPRD disease-modifying antirheumatic drug prescription or 3 other GPRD characteristics: >1 RA code during followup, RA diagnostic Group 1 or 2, and no later alternative diagnostic code. This algorithm had >80% sensitivity and specificity when applied to a test data set. Among 101 JIA-coded individuals, the strongest predictor of a valid diagnosis was a Group 1 diagnostic code (>90% sensitivity and specificity).
Validity of an RA diagnosis among RA-coded GPRD individuals appears high for patients with specific characteristics. The findings are important for both interpreting results of published GPRD studies and identifying RA/JIA patients for future GPRD-based research. However, several limitations were identified, and further debate is needed on how best to validate chronic disease diagnoses in the GPRD.
在全科医疗研究数据库(GPRD)中,确定能预测类风湿性关节炎(RA)或幼年特发性关节炎(JIA)编码个体中RA或JIA有效诊断的特征,并评估此类诊断验证的局限性。
基于RA/JIA医学编码,创建了四个具有不同RA/JIA证据强度的RA和2个JIA诊断组(第1组 = 最强证据)。从每组中抽取个体,并从匿名的医院/诊所通信和电子记录中提取临床和处方数据。使用美国风湿病学会和国际风湿病联盟的诊断标准来验证诊断。使用逻辑回归确定了一种能使敏感性和特异性最大化的数据衍生诊断算法。
在223例编码为RA的个体中,如果个体有适当的GPRD改善病情抗风湿药物处方或其他3个GPRD特征:随访期间>1个RA编码、RA诊断第1组或第2组、且无后续替代诊断编码,则诊断算法将其分类为患有RA。当应用于测试数据集时,该算法的敏感性和特异性>80%。在101例编码为JIA的个体中,有效诊断的最强预测因素是第1组诊断编码(敏感性和特异性>90%)。
对于具有特定特征的患者,GPRD中编码为RA的个体中RA诊断的有效性似乎很高。这些发现对于解释已发表的GPRD研究结果以及识别未来基于GPRD的研究中的RA/JIA患者都很重要。然而,确定了几个局限性,并且需要就是否能最好地验证GPRD中的慢性病诊断展开进一步辩论。