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Long-term low-dose spironolactone therapy is safe in oligoanuric hemodialysis patients.

机译:长期低剂量螺内酯治疗对少尿性血液透析患者是安全的。

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摘要

The Randomized Aldactone Evaluation Study showed that low-dose spironolactone treatment dramatically reduced mortality in patients with heart failure. However, the clinical use of this drug may be limited due to its tendency to cause life-threatening hyperkalemia in hemodialysis (HD) patients. We assessed whether low-dose spironolactone could be safely administered to HD patients for a long period. The study design comprised 2-month baseline and 6-month treatment periods. Sixty-one oligoanuric HD patients were administered a spironolactone dose of 25 mg/day. Serum potassium levels at baseline were compared with those during the treatment. Eleven patients discontinued the treatment because of adverse events other than hyperkalemia or for other reasons. The remaining 50 patients completed the trial, and none of them showed a potassium level of >6.8 mEq/l or required additional ion exchange resin therapy throughout the study period. The mean potassium levels during the treatment were higher than those at baseline; the differences were statistically significant, but only marginally. The safety of spironolactone should be examined in larger trials. However, from this study, we conclude that long-term low-dose spironolactone treatment is clinically safe for many HD patients. A more extensive treatment may help in determining whether spironolactone can reduce cardiovascular mortality in HD patients.
机译:Aldactone随机评估研究表明,低剂量螺内酯治疗可显着降低心力衰竭患者的死亡率。但是,由于这种药物有可能在血液透析(HD)患者中引起威胁生命的高钾血症,因此其临床应用可能受到限制。我们评估了低剂量螺内酯是否可以长期安全地用于HD患者。研究设计包括2个月的基线和6个月的治疗期。向61名少尿尿性HD患者施用了25 mg /天的螺内酯剂量。将基线时的血清钾水平与治疗期间的血清钾水平进行比较。由于高钾血症以外的不良事件或其他原因,有11名患者中止了治疗。其余50名患者完成了试验,并且在整个研究期间,他们均未显示钾水平> 6.8 mEq / l或需要其他离子交换树脂治疗。治疗期间的平均钾水平高于基线时;差异在统计上是显着的,但只是很小的一部分。螺内酯的安全性应在较大的试验中进行检查。然而,从这项研究中,我们得出结论,长期低剂量螺内酯治疗对许多HD患者而言是临床安全的。更广泛的治疗可能有助于确定螺内酯是否可以降低HD患者的心血管死亡率。

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