Rheopheresis for Digital Ulcers and Raynaud's Phenomenon in Systemic Sclerosis Refractory to Conventional Treatments

被引:6
|
作者
Korsten, Peter [1 ]
Muller, Gerhard A. [1 ]
Rademacher, Jan-Gerd [1 ]
Zeisberg, Michael [1 ]
Tampe, Bjoern [1 ]
机构
[1] Univ Med Ctr Gottingen, Dept Nephrol & Rheumatol, Gottingen, Germany
关键词
systemic sclerosis; extracorporeal circulation; raynaud phenomenon; skin ulcers; plasmapheresis; THERAPEUTIC PLASMA-EXCHANGE; ANGIOTENSIN; ANTIBODIES; DISEASE;
D O I
10.3389/fmed.2019.00208
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Raynaud's phenomenon (RP) is almost universally present in patients with Systemic Sclerosis (SSc). RP represents a generalized vasculopathy and potentially lead to digital ulcers (DU), which may be complicated by superinfection, tissue necrosis, and limb loss. We report the analysis of an extracorporeal procedure in a 36-year-old female patient with diffuse SSc with refractory RP and DU despite treatment with diltiazem, candesartan, sildenafil, and intravenous iloprost. We performed rheopheresis (RheoP), a variant of double-filtration plasmapheresis, as a potential new treatment option for refractory patients despite optimal medical therapy. We performed two RheoP per week every 4 weeks for a total of 3 months. Clinical improvement in DU healing occurred with no adverse events directly related to the treatment. While there was no reduction in the number of Raynaud attacks with RheoP, a significant reduction of the duration of attacks from a median of 15 (5-45, 95% CI 10-15) to 7 (3-30, 95% CI 6-10) minutes with an improvement of the Raynaud Condition Score (RCS) improved from 4 to 2. In conclusion, RheoP is a feasible and potentially beneficial treatment modality in patients with refractory RP and DU. We propose that RheoP should be investigated in a larger number of patients in a clinical trial setting.
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页数:5
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