Bird H A
University of Leeds, General Infirmary, UK.
Scand J Rheumatol Suppl. 1987;65:102-6. doi: 10.3109/03009748709102186.
Tenoxicam, a new non-steroidal anti-inflammatory agent (NSAID) with a long half-life, has been evaluated in a series of nine clinical studies over the last five years. Early studies against naproxen in osteoarthrosis (OA) and against ibuprofen in rheumatoid arthritis (RA) suggested the drug was efficacious in both of these conditions. A series of faecal blood loss studies showed that the drug produced less gastrointestinal blood loss than aspirin and comparable blood loss to piroxicam. Comparisons of tenoxicam and piroxicam in OA and ankylosing spondylitis (AS) showed both drugs to be approximately equally efficacious. A pharmacokinetic study showed a half-life for tenoxicam of 45 h in synovial fluid when the half-life was 42 h in plasma. A single and multiple oral dose pharmacokinetic study of tenoxicam in the elderly showed no progressive accumulation with peak plasma levels of 2.6 micrograms/ml after the single dose and 12.4 micrograms/ml at steady state.
替诺昔康是一种新型非甾体抗炎药(NSAID),半衰期长。在过去五年中,已通过一系列九项临床研究对其进行了评估。早期针对骨关节炎(OA)中的萘普生以及类风湿性关节炎(RA)中的布洛芬开展的研究表明,该药物在这两种病症中均有效。一系列粪便失血研究表明,该药物导致的胃肠道失血量比阿司匹林少,与吡罗昔康的失血量相当。在OA和强直性脊柱炎(AS)中对替诺昔康和吡罗昔康进行的比较表明,两种药物的疗效大致相同。一项药代动力学研究表明,替诺昔康在滑液中的半衰期为45小时,而在血浆中的半衰期为42小时。一项针对老年人的替诺昔康单剂量和多剂量口服药代动力学研究表明,没有出现渐进性蓄积,单剂量后血浆峰值水平为2.6微克/毫升,稳态时为12.4微克/毫升。