Raffayová H, Rovenský J, Mális F
Research Institute for Rheumatic Diseases Pieśt'any, Slovak Republic.
Int J Clin Pharmacol Res. 2000;20(1-2):1-11.
An open 18-week study with a preparation of cyclosporin administered to patients with psoriatic arthritis confirmed the therapeutic efficacy of the preparation. Given the low frequency of adverse effects (at the initial and maintenance daily dose), the preparation could also be considered relatively safe. A pronounced improvement in psoriatic symptoms was observed during the study. As early as 2 weeks after administration of an average daily dose of cyclosporin A of 4.8 mg/kg, skin symptoms improved by 65.5%. The most intense effect on the activity of arthritis was observed after 18 weeks. The lowest optimal effective maintenance dose was 3.26 mg/kg/day. Improvement was achieved after an average of 10 weeks' cyclosporin administration.
一项针对银屑病关节炎患者进行的为期18周的环孢素制剂开放研究证实了该制剂的治疗效果。鉴于不良反应发生率较低(在初始和维持日剂量下),该制剂也可被认为相对安全。研究期间观察到银屑病症状有显著改善。早在平均每日剂量为4.8mg/kg的环孢素A给药2周后,皮肤症状改善了65.5%。对关节炎活动的最强烈影响在18周后观察到。最低最佳有效维持剂量为3.26mg/kg/天。平均给予环孢素10周后病情得到改善。