Sreekanth V R, Handa R, Wali J P, Aggarwal P, Dwivedi S N
Department of Medicine, All India Institute of Medical Sciences, New Delhi.
J Assoc Physicians India. 2000 Aug;48(8):804-7.
To assess the efficacy and safety of doxycycline as a disease modifying anti-rheumatic drug (DMARD) in rheumatoid arthritis (RA) and compare it with methotrexate, a standard DMARD.
A single (assessor) blind prospective study with 15 patients of RA randomized to doxycycline and 14 to methotrexate. Baseline disease characteristics were similar in both groups.
All disease activity measures studied viz. tender and swollen joint counts, physician and patient global assessment, visual analogue pain scale, health assessment questionnaire and ESR improved in both the treatment groups after six months of treatment. The difference between doxycycline and methotrexate was not statistically significant. No major side effects necessitating drug withdrawal were reported from either group. The side effects were few and mostly gastrointestinal.
Doxycycline is a safe disease modifying drug in RA whose effect is sustained at six months. It compared favourably with methotrexate over a six month follow up.
评估强力霉素作为改善病情抗风湿药(DMARD)治疗类风湿关节炎(RA)的疗效和安全性,并与标准DMARD甲氨蝶呤进行比较。
一项单(评估者)盲前瞻性研究,将15例RA患者随机分为强力霉素组和14例甲氨蝶呤组。两组的基线疾病特征相似。
治疗6个月后,两个治疗组中所有研究的疾病活动指标,即压痛和肿胀关节计数、医生和患者整体评估、视觉模拟疼痛量表、健康评估问卷和血沉均有所改善。强力霉素组和甲氨蝶呤组之间的差异无统计学意义。两组均未报告需要停药的重大副作用。副作用很少,主要是胃肠道反应。
强力霉素是一种治疗RA的安全的病情改善药物,其疗效在6个月时持续存在。在6个月的随访中,它与甲氨蝶呤相比效果良好。