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早期肾衰竭中使用氨氯吡咪的限制。

Limitation on the use of amiloride in early renal failure.

作者信息

Knauf H, Reuter K, Mutschler E

出版信息

Eur J Clin Pharmacol. 1985;28(1):61-6. doi: 10.1007/BF00635709.

Abstract

The effect of a single oral dose of 10 mg amiloride was studied on urinary excretion of Na+, K+, Ca++ and Mg++ in healthy subjects and in patients with varying degrees of renal impairment. Amiloride produced a moderate diuresis and sodium excretion, and a slight calciuresis. Urinary excretion of potassium was significantly reduced as compared to the controls. Despite its diuretic and natriuretic effects, amiloride did not change the excretion of Mg++ as compared to the pretreatment period. When the creatinine clearance was below 50 ml/min, the net excretion of Na+ and Ca++ was drastically reduced. However, K+ retention and neutrality of Mg++ excretion were maintained down to end-stage renal disease. In the healthy volunteers the mean elimination half-life of amiloride was 20 h, and it rose to about 100 h in end-stage renal disease. This was because about 3/4 of native amiloride was eliminated through the kidney. Nonrenal elimination of amiloride was calculated to amount to only 1/4 of the total elimination. Therefore, the anticaliuretic amiloride is a valuable comedication in subjects with normal kidney function to prevent K+ and Mg++ loss. However, its use is hazardous if plasma creatinine is raised.

摘要

研究了单次口服10毫克氨氯吡咪对健康受试者及不同程度肾功能损害患者尿中Na+、K+、Ca++和Mg++排泄的影响。氨氯吡咪产生适度利尿和钠排泄,以及轻微的钙利尿作用。与对照组相比,尿钾排泄显著减少。尽管氨氯吡咪有利尿和利钠作用,但与治疗前期相比,其并未改变Mg++的排泄。当肌酐清除率低于50毫升/分钟时,Na+和Ca++的净排泄量急剧减少。然而,直至终末期肾病,钾潴留和Mg++排泄的中性状态仍得以维持。在健康志愿者中,氨氯吡咪的平均消除半衰期为20小时,而在终末期肾病中则升至约100小时。这是因为约3/4的天然氨氯吡咪通过肾脏消除。经计算,氨氯吡咪的非肾性消除仅占总消除量的1/4。因此,对肾功能正常的受试者而言可预防K+和Mg++丢失的抗钙利尿药氨氯吡咪是一种有价值的联合用药。然而,如果血浆肌酐升高,使用该药则有风险。

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