Department of Gastroenterology, Infectiology and Rheumatology, Charité - Universitätsmedizin Berlin.
Epidemiology Unit, German Rheumatism Research Centre, Berlin.
Rheumatology (Oxford). 2019 Sep 1;58(9):1634-1638. doi: 10.1093/rheumatology/kez090.
The objective of this study was to assess the current diagnostic delay in axial SpA (axSpA) and to analyse factors associated with it.
A stratified sample of subjects with a diagnosis of axSpA (International Classification of Diseases, 10th Revision code M45) was drawn from health insurance data in Germany and was questioned on disease-related, lifestyle and socio-economic characteristics. The diagnostic delay was calculated as the time from back pain onset until a diagnosis of axSpA. A multivariable linear regression analysis was performed to explore factors associated with the diagnostic delay.
Among 1677 patients with axSpA included in the analysis, the mean diagnostic delay was 5.7 years (median 2.3). Of those, 407 patients were diagnosed in 1996-2005 and 484 patients in 2006-2015. The mean diagnostic delay was not substantially different in both periods: 6.3 years (median 2.6) and 7.4 (2.7), respectively. Multivariable linear regression revealed that female sex [β = 1.85 (95% CI 1.06, 2.65)], negative HLA-B27 status [β = 3.61 (95% CI 2.07, 5.14)], presence of psoriasis [β = 1.40 (95% CI 0.08, 2.73)] and younger age at symptom onset [β = 1.91 (95% CI 1.53, 2.29)] were factors associated with a longer diagnostic delay.
The diagnostic delay in axSpA is still unacceptably long. Patients who are female, young at symptom onset, HLA-B27 negative or have psoriasis have a longer diagnostic delay. Specific referral strategies might be necessary in order to decrease the diagnostic delay in patients presenting with these characteristics.
本研究旨在评估中轴型脊柱关节炎(axSpA)的当前诊断延迟,并分析与之相关的因素。
从德国健康保险数据中抽取了一组 axSpA(国际疾病分类,第 10 版编码 M45)诊断患者的分层样本,并对其疾病相关、生活方式和社会经济特征进行了调查。将诊断延迟定义为从背痛发作到 axSpA 诊断的时间。采用多变量线性回归分析来探讨与诊断延迟相关的因素。
在纳入分析的 1677 例 axSpA 患者中,平均诊断延迟为 5.7 年(中位数 2.3)。其中,407 例患者在 1996-2005 年诊断,484 例患者在 2006-2015 年诊断。两个时期的平均诊断延迟差异不大:分别为 6.3 年(中位数 2.6)和 7.4 年(中位数 2.7)。多变量线性回归显示,女性(β=1.85(95%置信区间 1.06,2.65))、HLA-B27 阴性(β=3.61(95%置信区间 2.07,5.14))、银屑病(β=1.40(95%置信区间 0.08,2.73))和发病年龄较小(β=1.91(95%置信区间 1.53,2.29))是与较长诊断延迟相关的因素。
axSpA 的诊断延迟仍然过长。女性、发病年龄较小、HLA-B27 阴性或患有银屑病的患者诊断延迟较长。为了减少具有这些特征的患者的诊断延迟,可能需要采取特定的转诊策略。