摘要
目的 评价美洛昔康 /萘丁美酮治疗类风湿关节炎的疗效和安全性。方法 随机对照、双盲的比较研究。共完成病例12 0例 (美洛昔康 5 9例 ;萘丁美酮 6 1例 )。po美洛昔康 15mg每天一次或萘丁美酮 10 0 0mg每天一次 ,疗程 4周 ,其中 41例患者连用 8周。结果 4,8周时美洛昔康总有效率为 6 9.5 % ,95 .0 % ;萘丁美酮为 6 7.2 % ,90 .5 % ,两药均能显著改善患者的症状和体征 ,降低血沉。 8周时美洛昔康改善患者的休息痛和关节压痛指数两项优于萘丁美酮 (P <0 .0 5 )。安全性评价 :美洛昔康不良反应发生率 :10 .2 % ;萘丁美酮 18.0 % ,统计分析两药的耐受性无明显差异。不良反应以消化道症状为主 ,无因不良反应停药病例。
OBJECTIVE To evaluate the efficacy and safety of meloxicam and nabumetone in the treatment of patients with rheumatoid arthritis.METHODS Double-blind,randomized,controlled clinical trial of meloxicam versus nabumetone was performed.120 patients (59 versus 61) were given meloxicam po 15 mg·day -1 or nabumeone 1 000 mg·day -1 for 4 weeks,41 patients (20 versus 21) for 8 weeks.RESULTS Meloxicam and nabumetone improved the symptoms and signs of rheumatoid arthritis,decreased ESR.The total efficacy rates of meloxicam were 69.5% and 95.0%;and the nabumetone were 67.2% and 90.5%,after 4 weeks and 8 weeks treatment,respectively.The incidence of adverse effects was 10.2% for meloxicam and 18.0% for nabumetone.Main adverse effects were symptoms of gastrointestinal tract.All adverse effects of both drugs were mild and none ceased treatment.CONCLUSION Meloxicam appeared to be effective and safe in the treatment of rheumatoid arthritis,compared with nabumetone without significant difference.
出处
《中国药学杂志》
EI
CAS
CSCD
北大核心
2002年第4期310-312,共3页
Chinese Pharmaceutical Journal
关键词
美洛昔康
萘丁美酮
类风湿关节炎
双盲法
随机对照
meloxicam
nabumetone
rheumatoid
arthritis
double-blind
randomized controlled clinical trial