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紧急钾离子正常化治疗包括硅酸锆钠:一项 II 期、随机、双盲、安慰剂对照研究(ENERGIZE)。

Emergency Potassium Normalization Treatment Including Sodium Zirconium Cyclosilicate: A Phase II, Randomized, Double-blind, Placebo-controlled Study (ENERGIZE).

机构信息

From the, Baylor College of Medicine, Ben Taub General Hospital, Houston, TX.

the, First Pavlov State, Medical University of St. Petersburg, St. Petersburg, Russia.

出版信息

Acad Emerg Med. 2020 Jun;27(6):475-486. doi: 10.1111/acem.13954. Epub 2020 Mar 28.

Abstract

OBJECTIVES

Sodium zirconium cyclosilicate (SZC) is a novel, highly selective potassium binder currently approved in the United States and European Union for treatment of hyperkalemia. This pilot evaluation explored the efficacy of SZC with insulin and glucose as hyperkalemia treatment in the emergency department (ED).

METHODS

This exploratory, phase II, multicenter, randomized, double-blind, placebo-controlled study (NCT03337477) enrolled adult ED patients with blood potassium ≥ 5.8 mmol/L. Patients were randomized 1:1 to receive SZC 10 g or placebo, up to three times during a 10-hour period, with insulin and glucose. The primary efficacy outcome was the mean change in serum potassium (sK ) from baseline until 4 hours after start of dosing.

RESULTS

Overall, 70 patients were randomized (SZC n = 33, placebo n = 37), of whom 50.0% were male. Their mean (± standard deviation [±SD]) age was 59.0 (±13.8) years and mean initial sK was similar between groups (SZC 6.4 mmol/L, placebo 6.5 mmol/L). The least squares mean (±SD) sK change from baseline to 4 hours was -0.41 (±0.11) mmol/L and -0.27 (±0.10) mmol/L with SZC and placebo, respectively (difference = -0.13 mmol/L, 95% confidence interval [CI] = -0.44 to 0.17). A greater reduction in mean (±SD) sK from baseline occurred with SZC compared with placebo at 2 hours: -0.72 (±0.12) versus -0.36 (±0.11) mmol/L (LSM difference = -0.35 mmol/L, 95% CI = -0.68 to -0.02), respectively. A numerically lower proportion of patients in the SZC group required additional potassium-lowering therapy due to hyperkalemia at 0 to 4 hours versus placebo (15.6% vs. 30.6%, respectively; odds ratio = 0.40, 95% CI = 0.09 to 1.77). Comparable proportions of patients experienced adverse events in both treatment groups at 0 to 24 hours.

CONCLUSIONS

This pilot study suggested that SZC with insulin and glucose may provide an incremental benefit in the emergency treatment of hyperkalemia over insulin and glucose alone.

摘要

目的

硅酸锆酸钠(SZC)是一种新型、高度选择性的钾结合剂,目前已获美国和欧盟批准用于治疗高钾血症。本初步评估研究探索了 SZC 联合胰岛素和葡萄糖在急诊科(ED)治疗高钾血症的疗效。

方法

这项探索性、Ⅱ期、多中心、随机、双盲、安慰剂对照研究(NCT03337477)纳入了血钾≥5.8mmol/L 的成年 ED 患者。患者按 1:1 随机分为 SZC 10g 或安慰剂组,在 10 小时内最多接受 3 次治疗,同时给予胰岛素和葡萄糖。主要疗效结局为从基线到给药后 4 小时血清钾(sK)的平均变化。

结果

总体而言,共 70 例患者被随机分组(SZC 组 n=33,安慰剂组 n=37),其中 50.0%为男性。他们的平均(±标准差[±SD])年龄为 59.0(±13.8)岁,两组的初始 sK 均值相似(SZC 组 6.4mmol/L,安慰剂组 6.5mmol/L)。SZC 和安慰剂组从基线到 4 小时 sK 的最小二乘均值(±SD)变化分别为-0.41(±0.11)mmol/L 和-0.27(±0.10)mmol/L(差值=-0.13mmol/L,95%置信区间[CI]为-0.44 至 0.17)。与安慰剂相比,SZC 组在 2 小时时 sK 均值的降幅更大:-0.72(±0.12)mmol/L 与-0.36(±0.11)mmol/L(LSM 差值=-0.35mmol/L,95%CI 为-0.68 至 -0.02)。SZC 组在 0 至 4 小时因高钾血症需要额外降钾治疗的患者比例低于安慰剂组(分别为 15.6%和 30.6%;比值比=0.40,95%CI 为 0.09 至 1.77)。两组患者在 0 至 24 小时均报告了相似比例的不良事件。

结论

这项初步研究表明,与单独使用胰岛素和葡萄糖相比,SZC 联合胰岛素和葡萄糖可能为急诊科高钾血症的紧急治疗提供额外获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f0d/7318712/d808ff658091/ACEM-27-475-g001.jpg

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