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镇痛剂肾病

Analgesic nephropathy.

作者信息

Gault M H, Barrett B J

机构信息

Faculty of Medicine, Memorial University, St John's Newfoundland.

出版信息

Am J Kidney Dis. 1998 Sep;32(3):351-60. doi: 10.1053/ajkd.1998.v32.pm9740150.

Abstract

Many questions about analgesic nephropathy (AN) lack clear-cut answers. We present available evidence for and against proposed answers to many of these questions. These include: (1) Is acetaminophen (AC) nephrotoxic when taken as the sole analgesic? (2) Is the combination of acetylsalicylic acid (ASA) and AC more nephrotoxic than AC taken alone, and if so, why? (3) What are the minimum doses and durations of ingestion required to produce analgesic nephrotoxicity? (4) Is the combination of ASA and AC (a major metabolite of phenacetin) less nephrotoxic than that of phenacetin and ASA combined? (5) Does caffeine in combination with analgesics contribute to nephrotoxicity? (6) What is the incidence of end-stage renal disease (ESRD) due to AN? (7) What uniform diagnostic criteria should be established for AN? (8) What are the earliest anatomic and biochemical abnormalities? (9) What are the mechanisms of renal injury? (10) Does AC cause uroepithelial neoplasia? (11) What research might be most beneficial? Based mainly on associations, some strong, we suggest that AN still exists as a cause of ESRD in the United States, where AC/ASA combinations are available over the counter, and in Canada, where they are not. We also suggest that the evidence needed to recommend that the AC/ASA combination be excluded from over-the-counter analgesic preparations still has limitations. A prospective multicenter study comparing incidence related to AC/ASA in the United States and to AC in Canada and the United States may be needed to answer this question. For such a study to be worthwhile, an adequate incidence in both countries is required.

摘要

关于镇痛剂肾病(AN)的许多问题都缺乏明确答案。我们针对其中许多问题所提出的答案,给出了支持和反对的现有证据。这些问题包括:(1)对乙酰氨基酚(AC)作为单一镇痛药服用时是否具有肾毒性?(2)乙酰水杨酸(ASA)与AC联用是否比单独服用AC更具肾毒性?如果是,原因是什么?(3)产生镇痛剂肾毒性所需的最低摄入剂量和持续时间是多少?(4)ASA与AC(非那西丁的主要代谢产物)联用是否比非那西丁与ASA联用的肾毒性小?(5)咖啡因与镇痛药联用是否会导致肾毒性?(6)由AN导致的终末期肾病(ESRD)的发病率是多少?(7)应该为AN制定哪些统一的诊断标准?(8)最早出现的解剖学和生化异常是什么?(9)肾损伤的机制是什么?(10)AC是否会导致尿路上皮肿瘤?(11)哪些研究可能最有帮助?主要基于一些有力的关联,我们认为在美国和加拿大,AN仍然是ESRD的一个病因,在美国,AC/ASA组合可在柜台购买,而在加拿大则不可。我们还认为,建议将AC/ASA组合从非处方镇痛药制剂中排除所需的证据仍有局限性。可能需要进行一项前瞻性多中心研究,比较美国AC/ASA以及加拿大和美国AC的发病率,以回答这个问题。为使这样的研究有价值,两个国家都需要有足够的发病率。

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