Scheer Tristan, Klotsche Jens, Len Claudio A, Foeldvari Ivan
Faculty of Medicine, Semmelweis University Campus Hamburg, Hamburg, Germany.
Institute for Social Medicine, Epidemiology and Health Economics, Charité Universitätsmedizin Berlin, Berlin, Germany.
Rheumatol Int. 2020 Apr;40(4):643-650. doi: 10.1007/s00296-019-04465-8. Epub 2019 Oct 30.
The primary objective was twofold: (1) to determine whether the German version of a screening instrument for clinical practice for juvenile idiopathic arthritis (SICJIA) is reliable in identifying patients at risk for juvenile idiopathic arthritis (JIA), and (2) secondly whether a weighting scheme of individual questions improves its sensitivity. Data were collected and retrospectively analyzed based upon completed SICJIA questionnaires from patients and their guardians at their first clinical visit at the Hamburg Centre for Pediatric and Adolescence Rheumatology. All patients visited the center between August 2015 and July 2017. The survey included 12 disease-orientated questions. For evaluation, only questionnaires of patients diagnosed with JIA or with a non-inflammatory joint pain (NJP) were selected. Standard statistical techniques were used for evaluation. In total, 165 of 800 questionnaires could be used for evaluation. Of the 800 patients who completed questionnaires, 133 were diagnosed with JIA and 32 with NJP. The analysis of the individual questions was performed by comparing the rate of a positive response to the questions between the two groups. Four questions showed a significant difference by comparing the groups, using JIA patients with at least one active joint. The diagnostic accuracy of the weighted sum score increased from 64 to 68% to discriminate between the groups in comparison to the ordinary sum score. An optimal cutoff of 6.0 for referral to a pediatric rheumatologist was calculated. The validation of the SICJIA showed a discriminative difference in patients with clinical diagnosed JIA and a control group diagnosed with NJP. The weighted sum score performed better to differentiate between JIA and NJP patients. The modified SICJIA can be useful to identify patients at risk of JIA.
(1)确定青少年特发性关节炎临床实践筛查工具的德语版本(SICJIA)在识别青少年特发性关节炎(JIA)风险患者方面是否可靠,以及(2)其次,单个问题的加权方案是否能提高其敏感性。基于患者及其监护人在汉堡儿科和青少年风湿病中心首次临床就诊时填写的完整SICJIA问卷收集数据并进行回顾性分析。所有患者均在2015年8月至2017年7月期间就诊于该中心。该调查包括12个以疾病为导向的问题。为进行评估,仅选择了被诊断为JIA或非炎性关节疼痛(NJP)患者的问卷。采用标准统计技术进行评估。总共800份问卷中的165份可用于评估。在完成问卷的800名患者中,133人被诊断为JIA,32人被诊断为NJP。通过比较两组对问题的肯定回答率来对单个问题进行分析。使用至少有一个活动关节的JIA患者进行组间比较时,有四个问题显示出显著差异。与普通总分相比,加权总分的诊断准确性从64%提高到68%,以区分两组。计算出转诊至儿科风湿病学家的最佳临界值为6.0。SICJIA的验证显示,临床诊断为JIA的患者与诊断为NJP的对照组之间存在判别差异。加权总分在区分JIA和NJP患者方面表现更好。改良后的SICJIA有助于识别有JIA风险的患者。