Fiszman P, Perpétuo J B, Franco J S, Pernambuco J C, Rubinstein J, Sidi A
Eur J Rheumatol Inflamm. 1985;8(1):9-14.
Seventy-nine patients with arthrosis (40) or rheumatoid arthritis (39) were included in an open, non-comparative multicentric study. All the patients were treated by rectal route with a suppository form of tenoxicam (20 mg/day) during 6 weeks (in the first 3 days the dose was increased to 40 mg). The drug was administered once daily at evening. Clinical evaluation was performed before treatment and thereafter every 2 weeks. In the patients with arthrosis the parameters evaluated for efficacy were: pain on movement, pain at rest, tenderness, spontaneous pain, pain after 1 day of normal activity, flexion, functional status, and time to walk 10 metres. For patients with rheumatoid arthritis the parameters were: articular index, duration of morning stiffness, functional status, spontaneous pain and pain when moving. Efficacy was considered excellent or good in 22 patients with rheumatoid arthritis and moderate or poor in 17. In the group of patients with arthrosis the results were excellent or good in 28 and moderate or poor in 12. Side effects occurred in five cases.
79例骨关节炎患者(40例)或类风湿关节炎患者(39例)纳入一项开放、非对照的多中心研究。所有患者均采用直肠给药方式,使用替诺昔康栓剂(20毫克/天)治疗6周(前3天剂量增至40毫克)。药物于每晚给药1次。治疗前及之后每2周进行一次临床评估。在骨关节炎患者中,评估疗效的参数包括:活动时疼痛、静息时疼痛、压痛、自发痛、正常活动1天后的疼痛、关节屈曲度、功能状态以及步行10米所需时间。对于类风湿关节炎患者,参数包括:关节指数、晨僵持续时间、功能状态、自发痛和活动时疼痛。22例类风湿关节炎患者的疗效被评为优或良,17例为中或差。在骨关节炎患者组中,28例结果为优或良,12例为中或差。5例出现副作用。