Division of Intensive Care Medicine, Department of Anesthesiology, Intensive Care and Pain Medicine, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.
Department of Intensive Care, Austin Hospital, Melbourne, Australia.
Acta Anaesthesiol Scand. 2020 Jul;64(6):831-838. doi: 10.1111/aas.13557. Epub 2020 Feb 26.
Fluid accumulation frequently coexists with acute kidney injury (AKI) and is associated with increased risk for AKI progression and mortality. Among septic shock patients, restricted use of resuscitation fluid has been reported to reduce the risk of worsening of AKI. Restrictive fluid therapy, however, has not been studied in the setting of established AKI. Here, we present the protocol and statistical analysis plan of the REstricted fluid therapy VERsus Standard trEatment in Acute Kidney Injury-the REVERSE-AKI trial that compares a restrictive fluid therapy regimen to standard therapy in critically ill patients with AKI.
REVERSE-AKI is an investigator-initiated, multinational, open-label, randomized, controlled, feasibility pilot trial conducted in seven ICUs in five countries. We aim to randomize 100 critically ill patients with AKI to a restrictive fluid treatment regimen vs standard management. In the restrictive fluid therapy regimen, the daily fluid balance target is neutral or negative. The primary outcome is the cumulative fluid balance assessed after 72 hours from randomization. Secondary outcomes include safety, feasibility, duration, and severity of AKI, and outcome at 90 days (mortality and dialysis dependence).
This is the first multinational trial investigating the feasibility and safety of a restrictive fluid therapy regimen in critically ill patients with AKI.
clinical.trials.gov NCT03251131.
液体蓄积常与急性肾损伤(AKI)并存,并与 AKI 进展和死亡风险增加相关。在脓毒性休克患者中,限制复苏液的使用已被报道可降低 AKI 恶化的风险。然而,在已经存在 AKI 的情况下,尚未对限制性液体疗法进行研究。在这里,我们提出了 REstricted fluid therapy VERsus Standard trEatment in Acute Kidney Injury-the REVERSE-AKI 试验的方案和统计分析计划,该试验比较了限制性液体治疗方案与 AKI 危重症患者的标准治疗。
REVERSE-AKI 是一项由研究者发起的、多中心、开放性标签、随机、对照、可行性先导试验,在五个国家的七个 ICU 中进行。我们旨在将 100 名 AKI 危重症患者随机分为限制性液体治疗组与标准治疗组。在限制性液体治疗方案中,每日液体平衡目标为中性或负平衡。主要结局是从随机分组后 72 小时评估的累积液体平衡。次要结局包括安全性、可行性、持续时间和 AKI 的严重程度以及 90 天(死亡率和透析依赖)的结局。
这是第一项在 AKI 危重症患者中研究限制性液体治疗方案可行性和安全性的多中心试验。
clinical.trials.gov NCT03251131。