Cox Zachary L, Siddiqi Hasan K, Stevenson Lynne W, Bales Brian, Han Jin H, Hart Kimberly, Imhoff Brant, Ivey-Miranda Juan B, Jenkins Cathy A, Lindenfeld JoAnn, Shotwell Matthew S, Miller Karen F, Ooi Henry, Rao Veena S, Schlendorf Kelly, Self Wesley H, Siew Edward D, Storrow Alan, Walsh Ryan, Wrenn Jesse O, Testani Jeffrey M, Collins Sean P
Department of Pharmacy, Lipscomb University College of Pharmacy, Nashville, TN; Department of Pharmacy, Vanderbilt University Medical Center, Nashville, TN.
Department of Medicine, Vanderbilt University Medical Center, Nashville, TN.
Am Heart J. 2023 Nov;265:121-131. doi: 10.1016/j.ahj.2023.07.014. Epub 2023 Aug 6.
Diuresis to achieve decongestion is a central aim of therapy in patients hospitalized for acute decompensated heart failure (ADHF). While multiple clinical trials have investigated initial diuretic strategies for a designated period of time, there is a paucity of evidence to guide diuretic titration strategies continued until decongestion is achieved. The use of urine chemistries (urine sodium and creatinine) in a natriuretic response prediction equation accurately estimates natriuresis in response to diuretic dosing, but a randomized clinical trial is needed to compare a urine chemistry-guided diuresis strategy with a strategy of usual care. The urinE chemiStry guided aCute heArt faiLure treATmEnt (ESCALATE) trial is designed to test the hypothesis that protocolized diuretic therapy guided by spot urine chemistry through completion of intravenous diuresis will be superior to usual care and improve outcomes over the 14 days following randomization. ESCALATE will randomize and obtain complete data on 450 patients with acute heart failure to a diuretic strategy guided by urine chemistry or a usual care strategy. Key inclusion criteria include an objective measure of hypervolemia with at least 10 pounds of estimated excess volume, and key exclusion criteria include significant valvular stenosis, hypotension, and a chronic need for dialysis. Our primary outcome is days of benefit over the 14 days after randomization. Days of benefit combines patient symptoms captured by global clinical status with clinical state quantifying the need for hospitalization and intravenous diuresis. CLINICAL TRIAL REGISTRATION: NCT04481919.
通过利尿实现充血缓解是急性失代偿性心力衰竭(ADHF)住院患者治疗的核心目标。虽然多项临床试验研究了指定时间段内的初始利尿策略,但缺乏证据来指导持续至充血缓解的利尿滴定策略。在利钠反应预测方程中使用尿液化学指标(尿钠和肌酐)可准确估计利尿剂给药后的利钠情况,但需要进行一项随机临床试验,以比较尿液化学指标指导的利尿策略与常规治疗策略。尿液化学指标指导急性心力衰竭治疗(ESCALATE)试验旨在检验以下假设:通过完成静脉利尿,由即时尿液化学指标指导的标准化利尿治疗将优于常规治疗,并在随机分组后的14天内改善预后。ESCALATE试验将把450例急性心力衰竭患者随机分组,并获取关于尿液化学指标指导的利尿策略或常规治疗策略的完整数据。主要纳入标准包括通过客观测量确定存在血容量过多,估计多余容量至少为10磅,主要排除标准包括严重瓣膜狭窄、低血压以及长期需要透析。我们的主要结局是随机分组后14天内的获益天数。获益天数将患者的整体临床状态所反映的症状与量化住院和静脉利尿需求的临床状态相结合。临床试验注册号:NCT04481919。