同时使用肾素-血管紧张素系统药物和保钾利尿剂时血清钾的变化:使用电子健康记录数据的美国队列研究

M. Sakil Syeed, Ainhoa Gomez-Lumbreras, Malinda Tan, Daniel C. Malone
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引用次数: 0

摘要

背景:保钾利尿剂(KSDs)和肾素-血管紧张素系统(RAS)药物(包括血管紧张素转换酶抑制剂[ACEIs]和血管紧张素II受体阻滞剂[ARBs])通常用于高血压、心血管疾病和糖尿病肾病的治疗。然而,当这些药物同时使用时,有可能出现高钾血症。本研究探讨RAS药物(ACEI或ARB)和KSD同时使用时血清钾的变化。方法采用Cerner Health Facts数据库进行回顾性观察性研究。使用来自独特患者住院的电子健康记录来比较5个不同队列(ACEI、ARB、KSD、ACEI-KSD和ARB-KSD)和非ras -非KSD暴露组(对乙酰氨基酚[APAP]队列)的血清钾变化。用广义线性回归估计队列的描述性数据和血清钾升高的风险。结果共分析了5816例患者的特殊遭遇。入院后,5.2% (N = 303)患者血清钾大于5.5 mmol/L。结果显示,与APAP对照组相比,同时使用KSD和RAS药物以及仅使用KSD时血清钾显著升高(P <0.05)。血清钾水平升高的其他显著预测因素包括男性(P = 0.002)、黑人(P <0.001),以及估计肾小球滤过率低的个体(P <0.001)。结论:本研究发现,即使在控制其他可能影响血清钾水平的潜在因素的情况下,在机构设置的患者中,当KSD和其他可能增加钾水平的药物联合使用时,没有证据表明高钾血症。当KSD与可能影响钾的药物一起开处方时,有关钾水平过高的警告应仅限于已存在较高钾水平的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in serum potassium with concomitant administration of renin-angiotensin system agents and potassium-sparing diuretics: U.S. cohort study using electronic health record data

Background

Potassium-sparing diuretics (KSDs) and renin-angiotensin system (RAS) agents (including angiotensin-converting enzyme inhibitors [ACEIs] and angiotensin II receptor blockers [ARBs]) are commonly prescribed for the management of hypertension, cardiovascular diseases, and diabetic nephropathy. However, there is a concern of developing hyperkalemia when these drugs are concomitantly used. This study investigates the change in serum potassium during concomitant administration of RAS agents (ACEI or ARB) and KSD.

Methods

This is a retrospective observational study using the Cerner Health Facts database. Electronic health records from unique patient hospitalization encounters were used to compare change in the serum potassium among 5 different cohorts (ACEI, ARB, KSD, ACEI-KSD, and ARB-KSD) and a non-RAS non-KSD exposed one (acetaminophen [APAP] cohort). Descriptive data of the cohorts and the risk of increase in potassium serum were estimated by generalized linear regression.

Results

A total of 5816 patients’ unique encounters were analyzed. After admission, 5.2% (N = 303) had serum potassium greater than 5.5 mmol/L. Results showed a significant increase in serum potassium during concomitant use of KSD and RAS agents and when only using KSD compared with the control APAP group (all P < 0.05). Other significant predictors of increased serum potassium levels included male (P = 0.002), black race (P < 0.001), and individuals with low estimated glomerular filtration rate (P < 0.001).

Conclusions

This study found no evidence of hyperkalemia when combining KSD and other medications that may increase potassium levels, even when controlling for other potential factors that may affect serum potassium levels, for patients within institutional settings. Warnings concerning excessive potassium levels when a KSD is prescribed with a medication that may affect potassium should be limited to patients with pre-existing higher levels of potassium.

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