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非甾体抗炎药的药理学。临床医生实用综述。

Pharmacology of nonsteroidal anti-inflammatory drugs. Practical review for clinicians.

作者信息

O'Brien W M

出版信息

Am J Med. 1983 Oct 31;75(4B):32-9. doi: 10.1016/0002-9343(83)90326-1.

Abstract

Aspirin and the newer nonsteroidal anti-inflammatory drugs are the mainstay of basic therapy in rheumatoid arthritis and the other rheumatic diseases. Despite its many years of clinical use, the pharmacologic actions of aspirin are still not fully understood; those of many of the newer nonsteroidals may offer significant advantages in terms of long-term safety. Studies in animals and normal human volunteers, as well as clinical trials, provide useful information about the absorption, metabolism, excretion, efficacy, appropriate dosage, and safety of a given nonsteroidal agent. Because all of the newer agents have been developed using the same basic animal tests of efficacy, they all closely resemble indomethacin. Differences in half-life, however, may be important in determining the relative safety of a nonsteroidal, especially in older patients. Most of the nonsteroidals bind only to albumin, and therefore have a kind of built-in safety mechanism: once the albumin binding sites are saturated, free drug is rapidly excreted by the kidney and drug accumulation is prevented. Despite this fact, the clinician must be concerned about two frequent sorts of problems that may arise from the prostaglandin-inhibiting effects of the nonsteroidals. Gastrointestinal side effects may include minor symptoms; diffuse gastritis; small erosions of the gastric mucosa, visible only by endoscope; and frank ulceration, which may rarely be life-threatening. Animal studies, various tests in normal volunteers, and pre-marketing clinical studies may all shed light on the relative ulcerogenicity of a given nonsteroidal agent. Long-term clinical experience especially helps indicate which agents appear to be more ulcerogenic than average and which appear to be less than average. Renal effects of the nonsteroidals are also related to their inhibition of prostaglandin synthesis. The most serious of these--a characteristic kind of interstitial nephritis, renal papillary necrosis, and hyperkalemia--are fortunately rare, but some classes of patients--the elderly, those with impaired renal function, and those receiving diuretics--are at increased risk. For these patients, any nonsteroidal anti-inflammatory drug should be prescribed with caution and appropriate monitoring of renal function.

摘要

阿司匹林和新型非甾体抗炎药是类风湿关节炎及其他风湿性疾病基础治疗的主要药物。尽管阿司匹林已临床应用多年,但其药理作用仍未完全明确;许多新型非甾体抗炎药在长期安全性方面可能具有显著优势。对动物和正常人类志愿者的研究以及临床试验,为特定非甾体药物的吸收、代谢、排泄、疗效、合适剂量及安全性提供了有用信息。由于所有新型药物都是基于相同的基本动物药效试验研发的,它们都与吲哚美辛极为相似。然而,半衰期的差异在确定非甾体药物的相对安全性时可能很重要,尤其是在老年患者中。大多数非甾体药物仅与白蛋白结合,因此有一种内在的安全机制:一旦白蛋白结合位点饱和,游离药物会迅速被肾脏排泄,从而防止药物蓄积。尽管如此,临床医生必须关注非甾体药物抑制前列腺素作用可能引发的两类常见问题。胃肠道副作用可能包括轻微症状、弥漫性胃炎、仅通过内窥镜可见的胃黏膜小糜烂以及严重溃疡,严重溃疡很少会危及生命。动物研究、对正常志愿者的各种测试以及上市前临床研究都可能有助于了解特定非甾体药物的相对致溃疡可能性。长期临床经验尤其有助于指出哪些药物似乎比平均水平更易致溃疡,哪些则低于平均水平。非甾体药物对肾脏的影响也与其对前列腺素合成的抑制有关。其中最严重的——一种典型的间质性肾炎、肾乳头坏死和高钾血症——幸运的是较为罕见,但某些类别的患者——老年人、肾功能受损者以及正在接受利尿剂治疗的患者——风险增加。对于这些患者,任何非甾体抗炎药都应谨慎使用并适当监测肾功能。

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