Optimized Or Maximized Dose Of Mineralocorticoid Receptor Antagonists Among Patients Initiating Outpatient Sodium Zirconium Cyclosilicate Therapy

IF 8.2 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of Cardiac Failure Pub Date : 2025-01-01 Epub Date: 2025-01-14 DOI:10.1016/j.cardfail.2024.10.066
Abiy Agiro , Connie Rhee , Erin Cook , Manasvi Sundar , Alexandra Greatsinger , Fan Mu , Jingyi Chen , Ellen Colman , Arun Malhotra
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Abstract

Introduction

Renin-angiotensin-aldosterone system inhibitor (RAASi) use can exacerbate hyperkalemia, especially in patients with cardiorenal conditions. Sodium zirconium cyclosilicate (SZC) has been previously shown to enable patients with hyperkalemia to continue RAASi; however, the level of dose optimization or maximization of RAASi after the initiation of outpatient SZC therapy is not well described, particularly among patients receiving mineralocorticoid receptor antagonists (MRA).

Methods

Using data from a large US insurance claims database from 7/2018-12/2022, adults who initiated SZC in the outpatient setting with a ≥7 day overlap with a RAASi (index) and ≥1 MRA fill in the 6-month follow-up period were selected. MRA optimization (≥50% of target dose) or maximization (≥100% of target dose) per guidelines were described during follow-up. The target dose for both spironolactone and eplerenone was 50 mg daily. Predictors of MRA optimization and maximization were assessed using separate multivariable logistic regression models.

Results

A total of 395 patients with MRA use after SZC initiation met the inclusion criteria, of whom 341 (86%) had an optimized MRA dose and 129 (33%) had a maximized MRA dose during follow-up. Patients had a mean age of 66 years and 63% of the sample was male. Common comorbidities included hypertension (91%), stage 1-4 or unspecified stage chronic kidney disease (CKD; 81%), diabetes (72%), and heart failure (53%). Predictors of MRA optimization included any vasodilator use (Figure 1). Predictors of MRA maximization included liver disease, stage 3 or stage 4 CKD vs. no CKD, and the absence of heart failure (Figure 2).

Conclusions

Among this real-world sample of patients taking a RAASi, most patients with hyperkalemia optimized their MRA dose and one-third maximized their MRA dose after initiating SZC in the outpatient setting. Certain clinical characteristics are significant predictors of the optimization and maximization of MRA dose.

Funding

AstraZeneca
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在门诊开始环硅酸锆钠治疗的患者中,矿皮质激素受体拮抗剂的优化或最大剂量
肾素-血管紧张素-醛固酮系统抑制剂(RAASi)的使用可加重高钾血症,特别是在有心肾疾病的患者中。先前已证明环硅酸锆钠(SZC)可使高钾血症患者继续RAASi;然而,在门诊SZC治疗开始后,RAASi的剂量优化或最大化水平并没有很好的描述,特别是在接受矿皮质激素受体拮抗剂(MRA)的患者中。方法使用2018年7月至2022年12月美国大型保险索赔数据库的数据,选择在6个月随访期间RAASi(指数)重叠≥7天且MRA填写≥1的门诊开始SZC的成年人。随访期间描述了每个指南的MRA优化(≥50%的目标剂量)或最大化(≥100%的目标剂量)。螺内酯和依普利酮的靶剂量均为每日50毫克。使用独立的多变量logistic回归模型评估MRA优化和最大化的预测因子。结果395例SZC启动后使用MRA的患者符合纳入标准,其中341例(86%)达到最佳MRA剂量,129例(33%)达到最大MRA剂量。患者的平均年龄为66岁,63%的样本为男性。常见的合并症包括高血压(91%)、1-4期或未明确分期的慢性肾脏疾病(CKD;81%),糖尿病(72%)和心力衰竭(53%)。MRA优化的预测因子包括任何血管扩张剂的使用(图1)。MRA最大化的预测因子包括肝脏疾病,3期或4期CKD vs.无CKD,以及无心力衰竭(图2)。结论在接受RAASi的现实世界患者样本中,大多数高钾血症患者优化了MRA剂量,三分之一的患者在门诊开始SZC后最大化了MRA剂量。某些临床特征是MRA剂量优化和最大化的重要预测因素。FundingAstraZeneca
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来源期刊
Journal of Cardiac Failure
Journal of Cardiac Failure 医学-心血管系统
CiteScore
7.80
自引率
8.30%
发文量
653
审稿时长
21 days
期刊介绍: Journal of Cardiac Failure publishes original, peer-reviewed communications of scientific excellence and review articles on clinical research, basic human studies, animal studies, and bench research with potential clinical applications to heart failure - pathogenesis, etiology, epidemiology, pathophysiological mechanisms, assessment, prevention, and treatment.
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