Sulodexide efficacy in the treatment of patients with chronic lower limb vein diseases of C1-C3 clinical classes according to CEAP

S. Katorkin, M. A. Melnikov, P. F. Kravtsov
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引用次数: 1

Abstract

Aim of the study. To evaluate the clinical efficacy of sulodexide in the daily dosage of 500 LSU in patients with chronic lower limb vein diseases of clinical classes C1-C3 according to CEAP. Patients and methods. This study included 35 patients with chronic C1-C3 CEAP lower limb vein disease who took 500 LSU of Sulodexide for 90 days. In order to evaluate the effectiveness of the treatment we used: a questionnaire to assess the quality of patient’s life with chronic venous insufficiency CIVIQ 20; visually – analogue scale of pain assessment VAS; clinical scale of venous diseases VCSS severity assessment; measuring the circumference of the limbs on the hip and shin. Results of the study. The study was completed by 32 patients. As a result of the performed treatment the convulsive syndrome in calf muscles completely regressed, though on the first visit it was registered in 22,4 % of patients (p = 0,0481), the frequency of complaints about severity and fatigue in the lower limbs at static loads decreased significantly from 28,1 % to 9,6 % (p = 0,2414). The circumference of the femur in the middle third of the limb decreased from 53.7 cm to 51.1 cm (p<0.05), in the middle third of the tibia from 36.8 cm to 33.8 cm (p<0.05) and in the lower third of the tibia from 23.4 cm to 21.5 cm (p<0.05). VAS pain syndrome decreased from 35.36 ± 24.71 mm to 16.44 ± 17.07 mm (p = 0.0005). The global CIVIQ 20 quality of life index increased by 25.3 % compared to the initial parameters (p = 0.0001), the VCSS index decreased from 5.93 ± 1.79 points to 4.79 ± 2.01 points (p = 0.0002). Conclusion. Sulodexide, causing a pronounced clinical effect, is an effective and pathogenetically justified drug for the treatment of initial forms of chronic lower limb vein disease.
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舒洛地特治疗慢性下肢静脉疾病C1-C3临床分型的疗效观察
研究的目的。目的:评价舒洛地特每日剂量500 LSU治疗临床分类C1-C3的慢性下肢静脉疾病患者的临床疗效。患者和方法。本研究纳入35例慢性C1-C3 CEAP下肢静脉疾病患者,他们服用500 LSU的舒洛地特90天。为了评价治疗的有效性,我们采用问卷调查的方式评估慢性静脉功能不全患者的生活质量(civiq20);视觉模拟疼痛评估量表;静脉疾病VCSS严重程度评定临床量表测量臀部和小腿的四肢周长。研究结果。该研究由32名患者完成。由于进行了治疗,小腿肌肉痉挛综合征完全消退,尽管在第一次就诊时有22.4%的患者登记(p = 0,0481),但在静态负荷下下肢严重和疲劳的主诉频率从28.1%显著下降到9.6% (p = 0,2414)。下肢中1 / 3股骨周长由53.7 cm减小至51.1 cm (p<0.05),胫骨中1 / 3股骨周长由36.8 cm减小至33.8 cm (p<0.05),胫骨下1 / 3股骨周长由23.4 cm减小至21.5 cm (p<0.05)。VAS疼痛综合征由35.36±24.71 mm降至16.44±17.07 mm (p = 0.0005)。与初始参数相比,全球CIVIQ 20生活质量指数提高了25.3% (p = 0.0001), VCSS指数从5.93±1.79降至4.79±2.01 (p = 0.0002)。结论。舒洛地特临床疗效显著,是治疗慢性下肢静脉疾病的一种有效且病理合理的药物。
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