Non-steroidal anti-inflammatory drugs and the classical arthritides: focus on five-years of piroxicam experience.

A Calin
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Abstract

In recent years, we have seen immense progress in our understanding of rheumatic diseases. As we learn more about the pathogenetic mechanisms of disease, we can begin to classify the disorders more rationally. However, treatment lags behind understanding; we still direct our attention toward inflammation in a non-specific manner. At the beginning of the century, aspirin became a widely used treatment for all forms of arthritis. By the early 1960s, phenylbutazone and then indomethacin were introduced, and later, ibuprofen, naproxen, sulindac, and a variety of other agents had become available. Within the last five years two new agents were introduced that were characterised by a once-a-day regimen. One piroxicam - worked by attacking the cyclooxygenase pathway. The other--benoxaprofen--inhibited both the cyclooxygenase and lipoxygenase pathways, but had to be withdrawn because it was toxic. Since piroxicam was introduced in 1980, eight nonsteroidal anti-inflammatory drugs (NSAIDs) have been withdrawn from the market in the United Kingdom. By contrast, piroxicam is now available in over 90 countries and has been used safely and successfully in millions of people of different ages and in different clinical settings. Short-term open studies, controlled studies, and more recent long-term studies lasting over periods of more than three years give further evidence of effectiveness and tolerance.

非甾体抗炎药和经典关节炎:关注吡罗昔康5年的经验。
近年来,我们对风湿病的认识取得了巨大进展。随着我们对疾病的发病机制了解的越来越多,我们可以开始更合理地对疾病进行分类。然而,治疗滞后于理解;我们仍然以一种非特异性的方式关注炎症。在本世纪初,阿司匹林被广泛用于治疗各种形式的关节炎。到20世纪60年代初,苯丁酮和吲哚美辛相继问世,随后,布洛芬、萘普生、舒林酸和其他各种药物也相继问世。在过去的五年中,两种新的药物被引入,其特点是每天服用一次。一种吡罗西康通过攻击环氧化酶途径起作用。另一种是苯那沙洛芬,它能抑制环加氧酶和脂加氧酶的途径,但由于它有毒,必须停药。自1980年吡罗昔康问世以来,英国已有8种非甾体类抗炎药(NSAIDs)退出市场。相比之下,吡罗昔康现已在90多个国家上市,并已在不同年龄和不同临床环境中安全、成功地用于数百万人。短期开放研究、对照研究和最近持续三年以上的长期研究进一步证明了其有效性和耐受性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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