Sarzi-Puttini P, Santandrea S, Boccassini L, Panni B, Caruso I
University Hospital L. Sacco, Rheumatology Unit, Department of Internal Medicine, Via G.B. Grassi 74, 20157 Milan, Italy.
Clin Exp Rheumatol. 2001;19(1 Suppl 22):S17-20.
To define the optimal dose of nimesulide (NIM) for treating psoriatic arthritis.
Eighty patients entered a 4-week, double-dummy, randomised, controlled study. Each patient was allocated to one of the following treatment groups: NIM 100 mg/day, NIM 200 mg/day, NIM 400 mg/day, or placebo. Primary end points for arthritis assessment were the scores for tender and swollen joints, and the physician's and patient's global assessment of efficacy.
76/80 patients completed the study. NIM decreased the score for tender and swollen joints from baseline to the end swollen joints from baseline to the end of therapy (p < 0.05). Pain severity on a visual analogue scale (VAS) was reduced by NIM 200 mg (p = 0.03) or NIM 400 mg (p = 0.019) compared to placebo, as was morning stiffness (p = 0.038 and p = 0.008, respectively), but the trends with 100 mg were not statistically significant. The investigators and patients assessed the global efficacy of the NIM 200 and 400 mg/day groups as better than placebo or NIM 100 mg. Side effects were observed in 12 patients (15%) during treatment. They were mostly mild, only one patient withdrew from the study as a result, and the trend for a higher incidence with NIM was not statistically significant. The Psoriasis Area Severity Index (PASI) and the ESR did not show any significant changes. Patients in the placebo group took more paracetamol per day compared with those in the NIM groups (p = 0.007).
Nimesulide 200 and 400 mg/day are effective and safe in psoriatic arthritis.
确定尼美舒利(NIM)治疗银屑病关节炎的最佳剂量。
80例患者进入一项为期4周的双盲、随机、对照研究。每位患者被分配到以下治疗组之一:尼美舒利100毫克/天、尼美舒利200毫克/天、尼美舒利400毫克/天或安慰剂。关节炎评估的主要终点是压痛和肿胀关节的评分,以及医生和患者对疗效的整体评估。
80例患者中有76例完成了研究。尼美舒利使压痛和肿胀关节的评分从基线降至治疗结束时(p < 0.05)。与安慰剂相比,200毫克尼美舒利(p = 0.03)或400毫克尼美舒利(p = 0.019)可降低视觉模拟量表(VAS)上的疼痛严重程度,晨僵情况也是如此(分别为p = 0.038和p = 0.008),但100毫克组的趋势无统计学意义。研究者和患者评估尼美舒利200毫克/天和400毫克/天组的整体疗效优于安慰剂或尼美舒利100毫克组。治疗期间12例患者(15%)出现副作用。副作用大多轻微,仅1例患者因此退出研究,尼美舒利组副作用发生率较高的趋势无统计学意义。银屑病面积和严重程度指数(PASI)及红细胞沉降率(ESR)无显著变化。与尼美舒利组患者相比,安慰剂组患者每天服用对乙酰氨基酚更多(p = 0.007)。
尼美舒利200毫克/天和400毫克/天治疗银屑病关节炎有效且安全。