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镇痛剂肾病的临床与病理特征

Clinical and pathological aspects of analgesic nephropathy.

作者信息

Nanra R S

出版信息

Br J Clin Pharmacol. 1980 Oct;10 Suppl 2(Suppl 2):359S-368S. doi: 10.1111/j.1365-2125.1980.tb01824.x.

Abstract

1 Analgesic nephropathy is part of the analgesic syndrome which has gastrointestinal, haematological, cardiovascular, psychological and psychiatric, and pregnancy and gonadal manifestations; premature ageing may also be a feature. 2 Analgesic nephropathy is a form of renal disease characterized by renal papillary necrosis, secondary chronic interstitial nephritis and renal failure with features of predominant tubulointerstitial dysfunction. 3 The percentage of patients with analgesic nephropathy who present with terminal renal failure is 12%. With appropriate management, 17% of analgesic nephropathy patients improve, 50% remain stable and 23% deteriorate. The 6 year cumulative survival is 70%. The major factors influencing deterioration are malignant hypertension, persistent proteinuria and small initial renal size. 4 The risk of renal papillary carcinoma in patients who regularly take analgesics is 8 per 100,000 patients per year. 5 Renal papillary necrosis is a consequence of the chronic toxicity of all non-steroidal anti-inflammatory drugs and results from medullary ischaemia secondary to suppression of prostaglandin E2 synthesis and from direct cellular toxicity. 6 Analgesic nephropathy is a preventable form of renal disease and renal failure. It can be prevented by limiting the abuse potential of analgesics rather than by making minor modifications in the composition of analgesic mixtures.

摘要
  1. 镇痛剂肾病是镇痛剂综合征的一部分,该综合征有胃肠道、血液学、心血管、心理和精神方面以及妊娠和性腺方面的表现;早衰也可能是其特征之一。2. 镇痛剂肾病是一种肾脏疾病,其特征为肾乳头坏死、继发性慢性间质性肾炎以及以肾小管间质功能障碍为主的肾衰竭。3. 出现终末期肾衰竭的镇痛剂肾病患者比例为12%。经过适当治疗,17%的镇痛剂肾病患者病情改善,50%保持稳定,23%病情恶化。6年累积生存率为70%。影响病情恶化的主要因素是恶性高血压、持续性蛋白尿和初始肾脏体积小。4. 经常服用镇痛药的患者发生肾乳头癌的风险为每年每10万名患者中有8例。5. 肾乳头坏死是所有非甾体类抗炎药慢性毒性的结果,是由于前列腺素E2合成受抑制继发的髓质缺血以及直接细胞毒性所致。6. 镇痛剂肾病是一种可预防的肾脏疾病和肾衰竭形式。可通过限制镇痛药的滥用可能性来预防,而不是通过对镇痛剂混合物成分进行微小改变来预防。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e22d/1430193/3c60f2ef0236/brjclinpharm00214-0145-a.jpg

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