Department of Nephrology, Ajou University School of Medicine, Suwon, Korea.
J Clin Pharm Ther. 2014 Feb;39(1):61-8. doi: 10.1111/jcpt.12109. Epub 2013 Nov 22.
Angiotensin receptor blockers (ARBs) frequently induce hyperkalaemia in high-risk patients. Early detection of hyperkalaemia can reduce the subsequent harmful effects. This study was performed to examine the onset time of hyperkalaemia after ARB therapy.
We carried out a retrospective analysis to determine the onset time of hyperkalaemia (serum potassium >5·5 mm) among hospitalized patients newly starting ARB therapy between 2004 and 2012, in a tertiary teaching hospital. Predefined possible risk factors and concomitant medications were evaluated.
During the 97-month study period, a total of 4267 hospitalized patients started ARBs as new drugs and 225 patients showed hyperkalaemia. A significantly increased risk of hyperkalaemia was detected among patients with a high baseline potassium [odds ratio (OR) 6·0] and those who took non-potassium-sparing diuretics (OR 2·2) or potassium supplements (OR 1·6). A high glomerular filtration rate (GFR) was associated with a lower risk of hyperkalaemia (OR 0·992). Fifty-two percentage of hyperkalaemic events occurred within the first week after initiation of ARB therapy. The highest frequency of hyperkalaemia occurred on the first day after initiation of ARBs. Hyperkalaemia occurred earlier in patients with a high baseline serum potassium level, reduced GFR, diabetes and in those without heart failure.
Hyperkalaemia occurs most frequently at the beginning of ARB therapy in hospitalized patients. Monitoring of serum potassium and estimated GFR after initiation of ARBs should be started within a few days or not later than 1 week, especially in patients with risk factors.
血管紧张素受体阻滞剂(ARBs)常导致高危患者发生高钾血症。早期发现高钾血症可以减少随后的有害影响。本研究旨在检查 ARB 治疗后高钾血症的发病时间。
我们对 2004 年至 2012 年期间在一家三级教学医院新开始 ARB 治疗的住院患者进行了回顾性分析,以确定高钾血症(血清钾>5.5mmol/L)的发病时间。评估了预先定义的可能危险因素和伴随药物。
在 97 个月的研究期间,共有 4267 名住院患者开始使用 ARB 作为新药,其中 225 名患者出现高钾血症。高基线血钾(比值比 [OR] 6.0)和使用非保钾利尿剂(OR 2.2)或钾补充剂(OR 1.6)的患者发生高钾血症的风险显著增加。肾小球滤过率(GFR)较高与高钾血症的风险较低相关(OR 0.992)。52%的高钾血症事件发生在 ARB 治疗开始后的第一周内。ARB 治疗开始后的第一天发生高钾血症的频率最高。基线血清钾水平高、GFR 降低、糖尿病和无心力衰竭的患者高钾血症发生较早。
住院患者的 ARB 治疗开始时最常发生高钾血症。应在开始 ARBs 后几天内或不迟于 1 周内开始监测血清钾和估计的 GFR,特别是在有危险因素的患者中。