Suppr超能文献

吡咯他尼(一种钾稳定利尿剂)对血清镁无影响。

Lack of effect of piretanide (a potassium-stable diuretic) on serum magnesium.

作者信息

Verho M, Irmisch R, de Looze S, Rangoonwala B

机构信息

Clinical Research Department, Hoechst A.G., Frankfurt, Federal Republic of Germany.

出版信息

Int J Clin Pharmacol Res. 1987;7(6):433-42.

PMID:3440634
Abstract

Serum magnesium and potassium concentrations were determined in 188 patients undergoing diuretic treatment for mild to moderate hypertension in four controlled clinical trials (eleven treatment groups). Measurements were made before and after 12 weeks of treatment with piretanide monosubstance (including the retarded form) in the range 3 to 12 mg daily, with triamterene as monosubstance and in fixed dose combination with piretanide, and with amiloride in combination with hydrochlorothiazide. Eumagnesaemia and eupotassaemia were preserved at all dosage of the piretanide monosubstance. Mean serum potassium concentrations were significantly increased following treatment with the potassium-sparing agents triamterene (with and without piretanide) and amiloride in combination with hydrochlorothiazide. These changes were not accompanied by changes in mean serum magnesium levels, that is, a magnesium-sparing effect was not demonstrated. Individual values of changes in serum magnesium levels before and after diuretic therapy did not correlate with the corresponding changes in serum potassium levels in any of the eleven groups of patients. This result is in contrast to the findings of other authors, which suggested that serum magnesium and potassium levels were correlated. Long-term treatment with diuretics can lead to hypomagnesaemia and hypokalaemia, and, if in combination with a potassium-sparer, to hyperkalaemia. The results of this analysis show that piretanide, in addition to its smooth and effective antihypertensive action, is also able to preserve serum magnesium and potassium homeostasis when administered in the range of 3 to 12 mg for 12 weeks.

摘要

在四项对照临床试验(11个治疗组)中,对188例接受利尿剂治疗轻度至中度高血压的患者测定了血清镁和钾浓度。在用每日剂量范围为3至12毫克的匹可他尼单一物质(包括缓释剂型)、氨苯蝶啶单一物质以及与匹可他尼的固定剂量组合、阿米洛利与氢氯噻嗪组合治疗12周前后进行了测量。在匹可他尼单一物质的所有剂量下均维持了正常镁血症和正常钾血症。在用保钾利尿剂氨苯蝶啶(有或无匹可他尼)以及阿米洛利与氢氯噻嗪组合治疗后,平均血清钾浓度显著升高。这些变化并未伴随平均血清镁水平的变化,即未显示出保镁作用。在11组患者中的任何一组中,利尿剂治疗前后血清镁水平变化的个体值与血清钾水平的相应变化均无相关性。这一结果与其他作者的发现相反,其他作者的研究表明血清镁和钾水平是相关的。利尿剂的长期治疗可导致低镁血症和低钾血症,若与保钾剂联合使用,则可导致高钾血症。该分析结果表明,匹可他尼除具有平稳有效的降压作用外,在3至12毫克的剂量范围内给药12周时,还能够维持血清镁和钾的稳态。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验