Dick W C, Franchimont P, Veys E
Department of Rheumatology, Royal Victoria Infirmary, Newcastle Upon Tyne, United Kingdom.
Clin Ther. 1993 Jan-Feb;15(1):148-59.
Etodolac is the first of a new class of nonsteroidal anti-inflammatory drugs--the pyranocarboxylic acids--and has potent analgesic and anti-inflammatory properties. Etodolac and piroxicam were compared in the treatment of patients with active rheumatoid arthritis. A total of 118 patients entered this double-blind parallel study and were randomly assigned to receive 200 mg of etodolac twice a day (60 patients) or 20 mg of piroxicam once a day (58 patients) for 12 weeks. After the baseline evaluation, efficacy and tolerability evaluations were made at 2, 4, 6, 8, and 12 weeks. Significant improvement from baseline was noted in both treatment groups in the patient's and physician's global evaluations, in the number of swollen and tender joints, and in the pain intensity scores. Improvement was noted at the first visit (week 2) and continued through week 12. Based on changes in the patient's global evaluation, 56% of the etodolac-treated patients and 47% of the piroxicam-treated patients showed improvement at the final evaluation. Based on changes in the physician's global evaluation, 47% of the etodolac-treated patients and 42% of the piroxicam-treated patients showed improvement at the final evaluation. Eight (13%) patients in the etodolac group and 7 (12%) patients in the piroxicam group withdrew from the study because of adverse events. Most adverse events were mild to moderate; gastrointestinal complaints were the most prevalent adverse events in both treatment groups. No clinically significant changes were seen in laboratory test results or vital signs. These results demonstrate that etodolac is well tolerated and effective in the treatment of the signs and symptoms of rheumatoid arthritis and compares favorably to piroxicam in safety and efficacy.
依托度酸是新型非甾体抗炎药——吡喃羧酸类药物中的首个药物,具有强效镇痛和抗炎特性。对依托度酸和吡罗昔康治疗活动性类风湿关节炎患者的疗效进行了比较。共有118例患者进入这项双盲平行研究,并被随机分配,接受每日两次200毫克依托度酸治疗(60例患者)或每日一次20毫克吡罗昔康治疗(58例患者),疗程为12周。在基线评估后,于第2、4、6、8和12周进行疗效和耐受性评估。两个治疗组在患者和医生的整体评估、肿胀和压痛关节数量以及疼痛强度评分方面均较基线有显著改善。在首次就诊时(第2周)即有改善,并持续至第12周。根据患者整体评估的变化,在最终评估时,56%接受依托度酸治疗的患者和47%接受吡罗昔康治疗的患者病情有所改善。根据医生整体评估的变化,在最终评估时,47%接受依托度酸治疗的患者和42%接受吡罗昔康治疗的患者病情有所改善。依托度酸组有8例(13%)患者和吡罗昔康组有7例(12%)患者因不良事件退出研究。大多数不良事件为轻度至中度;胃肠道不适是两个治疗组中最常见的不良事件。实验室检查结果或生命体征未见具有临床意义的变化。这些结果表明,依托度酸在治疗类风湿关节炎的体征和症状方面耐受性良好且有效,在安全性和疗效方面与吡罗昔康相比具有优势。