Deescalation and glucocorticoid-free treatment in SLE

被引:1
|
作者
Fischer-Betz, Rebecca [1 ,2 ]
Schneider, Matthias [1 ,2 ]
机构
[1] Univ Klinikum Dusseldorf, Poliklin Rheumatol, Moorenstr 5, D-40225 Dusseldorf, Germany
[2] Univ Klinikum Dusseldorf, Hiller Forschungszentrum, Moorenstr 5, D-40225 Dusseldorf, Germany
来源
ZEITSCHRIFT FUR RHEUMATOLOGIE | 2021年 / 80卷 / 04期
关键词
Immunosuppression; Long-term adverse effects; Prednisone; Systemic lupus erythematosus; Lupus nephritis; SYSTEMIC-LUPUS-ERYTHEMATOSUS; COATED MYCOPHENOLATE SODIUM; PREDNISONE; DAMAGE; NEPHRITIS; DISEASE; RITUXIMAB; MOFETIL;
D O I
10.1007/s00393-021-00981-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Treatment of systemic lupus erythematosus (SLE) without permanent glucocorticoid therapy is inconceivable for most patients and their physicians. Although we have significantly improved the prognosis of SLE, management remains constrained by a lack of effective, targeted therapies and the lack of evidence-based approaches to the use of existing compounds. For example, for glucocorticoids (GC), which are used continuously in a majority of patients, there are no evidence-based recommendations for initiation, tapering, and cessation in the treatment of SLE. Even today, GC are without alternatives in acute situations, especially organ- or life-threatening ones. However, due to the known long-term adverse effects, the role of GC is viewed increasingly critically. Long-term data from cohorts show that the use of GC actually contributes to morbidity and mortality in SLE. Strategies to reduce the use of GC in SLE are therefore urgently needed and are proposed in this paper.
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页码:332 / 338
页数:7
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