Digital ulcers: overt vascular disease in systemic sclerosis

被引:184
作者
Steen, V. [1 ]
Denton, C. P. [2 ,3 ]
Pope, J. E. [4 ]
Matucci-Cerinic, M. [5 ]
机构
[1] Georgetown Univ, Med Ctr, Dept Med, Washington, DC 20007 USA
[2] Univ London Royal Free Hosp, Ctr Rheumatol, London NW3 2QG, England
[3] UCL, Sch Med, London W1N 8AA, England
[4] St Josephs Hlth Ctr, Dept Med, London, ON, Canada
[5] AOUC Univ Florence, Div Rheumatol, Ctr DenoThe, Dept Biomed, Florence, Italy
关键词
RP; Endothelin receptor antagonist; Digital ulcers; Systemic sclerosis; RAYNAUDS-PHENOMENON; SCLERODERMA; BOSENTAN; ILOPROST; NUMBER;
D O I
10.1093/rheumatology/kep105
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
RP is an almost universal manifestation of SSc, with 95% of all patients being affected, and resulting in digital ulcers (DUs) in similar to 30% of the patients each year. DUs are a major clinical problem, being associated with substantial morbidity (reduced quality of life, pain, disability and disfigurement) that can escalate to gangrene and amputation. Ideally, the treatment of DUs would improve tissue integrity and viability, promote ulcer healing and reduce the formation of new ulcers. Treatments that have shown potential include calcium channel blockers, prostacyclin analogues and endothelin receptor antagonists. However, until recently, management was based on empirical experience. The recent approval (in Europe) of the dual endothelin receptor antagonist, bosentan, to reduce the number of new DUs in patients with SSc and ongoing DU disease, means that there is now an approved therapy-and new hope-for the treatment of DUs in these severely afflicted patients.
引用
收藏
页码:19 / 24
页数:6
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