Outcome and Trends in Treatment of Systemic Juvenile Idiopathic Arthritis in the German National Pediatric Rheumatologic Database, 2000-2013

被引:37
作者
Klotsche, Jens [1 ,2 ]
Raab, Anna [1 ,2 ]
Niewerth, Martina [3 ]
Sengler, Claudia [3 ]
Ganser, Gerd [4 ]
Kallinich, Tilmann [2 ]
Niehues, Tim [5 ]
Hufnagel, Markus [6 ]
Thon, Angelika [7 ]
Hospach, Toni [8 ]
Horneff, Gerd [9 ]
Minden, Kirsten [1 ,2 ]
机构
[1] German Rheumatism Res Ctr Berlin, Berlin, Germany
[2] Charite, Berlin, Germany
[3] German Rheumatism Res Ctr Berlin, Berlin, Germany
[4] St Josef Stift Sendenhorst Hosp, Sendenhorst, Germany
[5] HELIOS Klinikum Krefeld, Krefeld, Germany
[6] Univ Med Ctr Freiburg, Freiburg, Germany
[7] Hannover Med Sch, Hannover, Germany
[8] Olga Hosp, Clin Ctr Stuttgart, Stuttgart, Germany
[9] Asklepios Clin Sankt Augustin, St Augustin, Germany
关键词
MACROPHAGE ACTIVATION SYNDROME; DISEASE-ACTIVITY; FOLLOW-UP; ONSET; GROWTH; METHOTREXATE; CHILDREN; TRIAL; PROGNOSIS; MODELS;
D O I
10.1002/art.39796
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To investigate the clinical presentation and medical treatment of patients with systemic juvenile idiopathic arthritis (JIA) during the first year of illness. Our study focused on 3-year outcomes in a subsample of patients who were followed up longitudinally. Methods. From 2000 to 2013, 597 patients with systemic JIA and a disease duration of <= 12 months were recorded in the National Pediatric Rheumatologic Database. Among those patients, 3-year outcome data were available for 133. These data included the clinical Juvenile Arthritis Disease Activity Score in 10 joints (JADAS-10) and the physician's global assessment score (on a numerical rating scale), as well as assessment of joint involvement, growth retardation, and patient-reported outcomes. Results. The median clinical JADAS-10 declined significantly, from 7 in 2000 to 2 in 2013, while the proportion of patients with inactive disease increased from 19% in 2000 to 41% in 2013. The rate of treatment with systemic glucocorticoids and disease-modifying antirheumatic drugs (DMARDs) remained stable from 2000 to 2013. By 2013, the proportion of patients with systemic JIA who were treated with biologic DMARDs had increased to 20%. At 3-year follow-up, 72% of patients with systemic JIA had inactive disease, and 77% had no functional limitations. Growth retardation was associated with persistently high disease activity and continuing treatment with systemic glucocorticoids. At the 3-year follow-up, one-third of patients were still being treated with systemic glucocorticoids. Conclusion. The proportion of patients with inactive disease has increased over the past decade. Possible explanations may include improved access to specialized care, additional treatment options, and earlier or faster step-up treatment. However, challenges in the management of systemic JIA remain, as similar to 30% of patients continue to present with ongoing active disease.
引用
收藏
页码:3023 / 3034
页数:12
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