Schattenkirchner M
Rheumatology Unit, Ludwig-Maximilians-Universität München, Germany.
Curr Med Res Opin. 1991;12(8):497-506. doi: 10.1185/03007999109111660.
A study was carried out to compare the efficacy and tolerability of etodolac and piroxicam in patients with rheumatoid arthritis. Sixty patients entered this double-blind, parallel study and after a wash-out period of up to 2 weeks were randomly assigned to receive 200 mg etodolac twice daily or 20 mg piroxicam once daily for 12 weeks. Efficacy and tolerability assessments were made after 2, 4, 6, 8 and 12 weeks. Patients in the etodolac group demonstrated statistically significant improvement in the number of tender joints and the duration of morning stiffness after 12 weeks, as did the piroxicam-treated patients. In addition, the etodolac-treated patients had significant improvement according to the patients' and physician's global evaluations, pain intensity, number of swollen joints, and grip strength. There were significant differences between therapies favouring etodolac for the assessments of the number of tender joints and the physician's global evaluation by the end of the study. Forty-seven percent (47%) of 15 etodolac-treated patients compared with 7% of 15 piroxicam-treated patients showed improvement according to the physician's global evaluation at Week 12. Similarly, the patients' global evaluation showed that 40% of etodolac-treated patients and 19% of piroxicam-treated patients had improved by the end of therapy. Both therapies were well tolerated. There were no significant differences between groups in the incidence of any adverse reactions or the frequency of withdrawals.
一项研究旨在比较依托度酸和吡罗昔康对类风湿性关节炎患者的疗效和耐受性。60名患者进入了这项双盲平行研究,在长达2周的洗脱期后,他们被随机分配,分别接受每日两次200毫克依托度酸或每日一次20毫克吡罗昔康的治疗,为期12周。在第2、4、6、8和12周进行疗效和耐受性评估。12周后,依托度酸组患者在压痛关节数量和晨僵持续时间方面显示出统计学上的显著改善,吡罗昔康治疗的患者也是如此。此外,根据患者和医生的整体评估、疼痛强度、肿胀关节数量和握力,依托度酸治疗的患者有显著改善。在研究结束时,对于压痛关节数量评估和医生的整体评估,两种治疗方法之间存在显著差异,更有利于依托度酸。在第12周,15名接受依托度酸治疗的患者中有47%根据医生的整体评估显示有所改善,而15名接受吡罗昔康治疗的患者中这一比例为7%。同样,患者的整体评估显示,到治疗结束时,40%接受依托度酸治疗的患者和19%接受吡罗昔康治疗的患者有所改善。两种治疗方法耐受性都良好。两组在任何不良反应的发生率或退出治疗的频率方面均无显著差异。