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依托度酸:选择性 COX-2 抑制剂概述。

Etodolac: an overview of a selective COX-2 inhibitor.

机构信息

Monmouth Pharmaceuticals, Guildford, Surrey.

出版信息

Inflammopharmacology. 1999;7(3):269-75. doi: 10.1007/s10787-999-0010-3.

Abstract

Etodolac is a non-steroidal anti-inflammatory drug (NSAID) which has been shown to be effective in the treatment of rheumatoid arthritis and osteoarthritis and a selective COX-2 inhibitor in a wide range of clinically relevant assays in direct comparisons with other NSAIDs. Studies have shown etodolac to have no overall suppression of gastric or duodenal prostaglandins and endoscopic analysis with etodolac showed placebo level scores in comparison with ibuprofen, which showed inducement of gastro-intestinal (GI) side effects. This high degree of gastric tolerability was further demonstrated by microbleeding studies. The favourable GI tolerability profile of etodolac has been shown in long-term and large-scale trials and by routine clinical observation. In summary, etodolac is a well established selective COX-2 inhibitor that has been shown not to suppress gastric or duodenal prostaglandins, to have minimal hepatic or renal effects and to have favourable GI tolerability in comparison with ibuprofen.

摘要

依托度酸是一种非甾体抗炎药(NSAID),已被证明在治疗类风湿关节炎和骨关节炎方面有效,并且在与其他 NSAIDs 的直接比较中,在广泛的临床相关测定中是一种选择性 COX-2 抑制剂。研究表明依托度酸对胃或十二指肠前列腺素没有总体抑制作用,并且依托度酸的内镜分析与布洛芬相比显示出安慰剂水平的评分,布洛芬显示出诱导胃肠道(GI)副作用。微出血研究进一步证明了这种高度的胃耐受性。依托度酸的良好 GI 耐受性表现在长期和大规模试验以及常规临床观察中。总之,依托度酸是一种已被证实的选择性 COX-2 抑制剂,它不会抑制胃或十二指肠前列腺素,对肝脏或肾脏的影响最小,与布洛芬相比具有良好的 GI 耐受性。

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