Astorga Paulsen G, Baigun S, Galvao de Figueiredo J, Gomes de Freitas G
Departmento de Reumatologia, Hospital Clinico de la Universidad de Chile, Santiago.
Curr Med Res Opin. 1991;12(6):401-12. doi: 10.1185/03007999109111511.
The efficacy and tolerability of etodolac and piroxicam were compared in patients with osteoarthritis of the knee. Two hundred and twenty patients entered a double-blind, parallel group trial and were randomly assigned to receive 300 mg etodolac twice daily (n = 112) or 20 mg piroxicam once daily (n = 108) for 8 weeks. The etodolac group showed significant improvement (p less than 0.05) from baseline in all efficacy assessments at all evaluations. The piroxicam group showed improvement from baseline in all efficacy assessments at all evaluations except for erythema at Week 2. While mean change from baseline was similar for both groups, the patients' and physicians' final overall evaluations showed that the etodolac-treated patients improved slightly more from baseline than the piroxicam-treated patients. Twenty (18%) patients in the etodolac group reported at least one drug-related study event. In the piroxicam group, 16 (15%) patients reported at least one drug-related study event. Twelve (11%) etodolac-treated patients prematurely withdrew from the study. Of these, 7 had at least one adverse reaction. Two of the 12 patients withdrew because of lack of efficacy. Withdrawals from the piroxicam group were comparable. Thirteen (12%) patients withdrew, 6 of whom had at least one adverse reaction. One of these patients suffered a cardiovascular accident and died. Three patients withdrew because of lack of efficacy. The results of this study indicate that etodolac and piroxicam are comparable in efficacy and tolerability for the treatment of patients with osteoarthritis.
在膝骨关节炎患者中比较了依托度酸和吡罗昔康的疗效及耐受性。220例患者进入一项双盲、平行组试验,随机分配接受每日2次300mg依托度酸(n = 112)或每日1次20mg吡罗昔康(n = 108),疗程8周。依托度酸组在所有评估的疗效指标上较基线均有显著改善(p < 0.05)。吡罗昔康组在所有评估的疗效指标上较基线均有改善,但在第2周时红斑情况除外。虽然两组从基线的平均变化相似,但患者和医生的最终总体评估显示,依托度酸治疗的患者较基线的改善略多于吡罗昔康治疗的患者。依托度酸组有20例(18%)患者报告了至少一项与药物相关的研究事件。在吡罗昔康组,16例(15%)患者报告了至少一项与药物相关的研究事件。12例(11%)接受依托度酸治疗的患者提前退出研究。其中,7例有至少一项不良反应。12例患者中有2例因缺乏疗效而退出。吡罗昔康组的退出情况与之相当。13例(12%)患者退出,其中6例有至少一项不良反应。这些患者中有1例发生心血管意外并死亡。3例患者因缺乏疗效而退出。本研究结果表明,依托度酸和吡罗昔康在治疗骨关节炎患者的疗效和耐受性方面相当。