Performance of the systemic lupus erythematosus risk probability index (SLERPI) in the Egyptian college of rheumatology (ECR) study cohort.

IF 2.9 3区 医学 Q2 RHEUMATOLOGY Clinical Rheumatology Pub Date : 2024-11-04 DOI:10.1007/s10067-024-07210-0
Nevin Hammam, Ahmed Elsaman, Esam Abualfadl, Soha Senara, Nada M Gamal, Mona H Abd-Elsamea, Abdelhfeez Moshrif, Osman Hammam, Tamer A Gheita, Samar Tharwat
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Abstract

Objectives: This study aimed to evaluate the performance of systemic lupus erythematosus Risk Probability Index (SLERPI) in Egyptian patients with SLE using a national rheumatology database.

Methods: The Egyptian College of Rheumatology (ECR) database comprised of 1,162 patients with SLE and 4,327 with miscellaneous rheumatological diseases who were recruited from the Rheumatology Departments across the country. The diagnosis of SLE was established by expert rheumatologists. Variables of the SLERPI were extracted and recorded as present or absent for each patient. The absolute value for the SLERPI score was calculated for each patient, and the diagnosis of SLE was accounted for if the score was greater than 7 points.

Results: Of 1,162 SLE patients evaluated, 1,031 (88.7%) patients were diagnosed with SLE according to the SLERPI, with an average score of 13.1 (3.8). Differences in the 14 SLERPI variables were significant between the SLE-SLERPI groups, except for the presence of leukopenia and positive ANA. As a score reduction item, the SLE-SLERPI > 7 group had lower interstitial lung diseases. Patients diagnosed with SLE according to SLERPI had significantly higher disease activity (p < 0.001), and this group more commonly received corticosteroids and mycophenolate mofetil. Compared to other miscellaneous rheumatological groups, all 14 SLERPI items are indeed more common in the SLE group. In terms of the overall performance of SLERPI in the diagnosis of SLE, the accuracy of SLERPI was 91.9% (95% CI 90.9%-92.9%), with a specificity of 96.95% and sensitivity of 86.9%. SLERPI showed that accuracy went up to 93.3% (95%CI 92.4%-94.2%), with a specificity of 94.9% and a sensitivity of 91.6% when patients with connective tissue diseases were taken out of the study.

Conclusion: Using a large cohort of SLE, the SLERPI revealed excellent diagnostic efficacy and specificity. The use of SLERPI in clinical practice may contribute to improved patient diagnosis and prognosis. Key Points • SLERPI's performance has high diagnostic efficiency in Egyptian SLE patients. • SLERPI score can efficiently distinguish patients with SLE from other CTDs. • Within the SLERPI score, interstitial lung disease is the lowest predictor of SLE.

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系统性红斑狼疮风险概率指数(SLERPI)在埃及风湿病学院(ECR)研究队列中的表现。
研究目的本研究旨在利用全国风湿病学数据库评估系统性红斑狼疮风险概率指数(SLERPI)在埃及系统性红斑狼疮患者中的表现:埃及风湿病学会(ECR)数据库包括 1,162 名系统性红斑狼疮患者和 4,327 名其他风湿病患者,这些患者来自全国各地的风湿病科。系统性红斑狼疮的诊断由风湿病专家确定。每个患者的 SLERPI 变量均被提取并记录为存在或不存在。计算每位患者 SLERPI 评分的绝对值,如果评分大于 7 分,则可诊断为系统性红斑狼疮:结果:在接受评估的 1162 名系统性红斑狼疮患者中,有 1031 人(88.7%)根据 SLERPI 诊断为系统性红斑狼疮,平均得分为 13.1 分(3.8)。除白细胞减少症和 ANA 阳性外,SLE-SLERPI 两组患者在 14 个 SLERPI 变量上差异显著。作为减分项目,SLE-SLERPI > 7 组的间质性肺病发病率较低。根据 SLERPI 诊断出的系统性红斑狼疮患者的疾病活动度明显较高(p 结论:SLE-SLERPI>7 组患者的肺间质疾病较少:通过对一大批系统性红斑狼疮患者的研究,SLERPI显示出卓越的诊断效果和特异性。在临床实践中使用 SLERPI 可能有助于改善患者的诊断和预后。要点 - SLERPI在埃及系统性红斑狼疮患者中具有很高的诊断效率。- SLERPI 评分能有效区分系统性红斑狼疮患者和其他 CTD 患者。- 在 SLERPI 评分中,间质性肺病是预测系统性红斑狼疮的最低指标。
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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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