Joshi V R, Lele R D, Virani A R, Nagarwala H K, Pispati P K, Desai M M
Curr Med Res Opin. 1977;5(1):43-7. doi: 10.1185/03007997709108975.
A double-blind placebo controlled trial was carried out in 14 steroid-dependent patients with rheumatoid arthritis to assess the effectiveness and steroid-sparing action of flurbiprofen over a 4-week period. During the first week, the patients' steroid dosage was stabilized at the minimum necessary to control symptoms. They were then treated with either 100 mg flurbiprofen or placebo 3-times daily for 3 weeks. Steroid dosage was initially reduced to 50% of the stabilized dose and reduced further if practicable, depending on therapeutic response. Clinical assessments were made, at weekly intervals, of pain, swelling, tenderness, erythema, range of movement, grip strength, walking time, and duration of morning stiffness. Joint scanning of 99mTc uptake was also measured before and after treatment in 11 patients. The results showed that whereas 3 out of 6 patients on placebo has distinct inflammatory flare-up, this did not occur in any of the 8 patients on flurbiprofen. Moreover, 3 of the flurbiprofen group showed improvement and a further reduction in steriod dosage was possible in 3 patients. Improvements in joint scans correlated well with the clinical findings in 6 of 11 patients.
对14例类风湿性关节炎类固醇依赖患者进行了一项双盲安慰剂对照试验,以评估氟比洛芬在4周内的有效性和节省类固醇的作用。在第一周,将患者的类固醇剂量稳定在控制症状所需的最低水平。然后,他们每天接受3次100毫克氟比洛芬或安慰剂治疗,持续3周。类固醇剂量最初减至稳定剂量的50%,并根据治疗反应在可行的情况下进一步减少。每周对疼痛、肿胀、压痛、红斑、活动范围、握力、行走时间和晨僵持续时间进行临床评估。还对11例患者治疗前后的99mTc摄取进行了关节扫描。结果显示,6例服用安慰剂的患者中有3例出现明显的炎症复发,而8例服用氟比洛芬的患者中均未出现这种情况。此外,氟比洛芬组中有3例显示病情改善,3例患者的类固醇剂量可能进一步降低。11例患者中有6例关节扫描的改善与临床结果密切相关。