Macrophage Activation Syndrome in Children With Systemic Lupus Erythematosus and Children With Juvenile Idiopathic Arthritis

被引:51
|
作者
Bennett, Tellen D. [1 ]
Fluchel, Mark
Hersh, Aimee O.
Hayward, Kristen N. [2 ]
Hersh, Adam L.
Brogan, Thomas V. [2 ]
Srivastava, Rajendu
Stone, Bryan L.
Korgenski, E. Kent
Mundorff, Michael B. [3 ]
Casper, T. Charles
Bratton, Susan L.
机构
[1] Univ Utah, Sch Med, Salt Lake City, UT 84158 USA
[2] Univ Washington, Seattle, WA 98195 USA
[3] Intermt Healthcare, Primary Childrens Med Ctr, Salt Lake City, UT USA
来源
ARTHRITIS AND RHEUMATISM | 2012年 / 64卷 / 12期
关键词
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; CORTICOSTEROIDS; COMPLICATION; GUIDELINES; EXPERIENCE; DISORDERS; ANAKINRA;
D O I
10.1002/art.34661
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To describe patient demographics, interventions, and outcomes in hospitalized children with macrophage activation syndrome (MAS) complicating systemic lupus erythematosus (SLE) or juvenile idiopathic arthritis (JIA). Methods. We performed a retrospective cohort study using data recorded in the Pediatric Health Information System (PHIS) database from October 1, 2006 to September 30, 2010. Participants had International Classification of Diseases, Ninth Revision, Clinical Modification diagnosis codes for MAS and either SLE or JIA. The primary outcome was hospital mortality (for the index admission). Secondary outcomes included intensive care unit (ICU) admission, critical care interventions, and medication use. Results. A total of 121 children at 28 children's hospitals met the inclusion criteria, including 19 children with SLE and 102 children with JIA. The index admission mortality rate was 7% (8 of 121 patients). ICU admission (33%), mechanical ventilation (26%), and inotrope/vasopressor therapy (26%) were common. Compared to children with JIA, those with SLE had a similar mortality rate (6% versus 11%, respectively; exact P = 0.6). More patients with SLE than those with JIA received ICU care (63% versus 27%; P = 0.002), received mechanical ventilation (53% versus 21%; P = 0.003), and had cardiovascular dysfunction (47% versus 23% received inotrope/vasopressor therapy; P = 0.02). Children with SLE and those with JIA received cyclosporine at similar rates, but more children with SLE received cyclophosphamide and mycophenolate mofetil, and more children with JIA received interleukin-1 antagonists. Conclusion. Organ system dysfunction is common in children with rheumatic diseases complicated by MAS, and more organ system support is required in children with underlying SLE than in children with JIA. Current treatment of pediatric MAS varies based on the underlying rheumatic disease.
引用
收藏
页码:4135 / 4142
页数:8
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