急性心力衰竭发作时,利尿对肾功能恶化的影响。

IF 7.2 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Pedro Caravaca Pérez, Ignacio Fernández-Herrero, José Jesús Broseta, Nikein Ibarra-Márquez, Zorba Blázquez-Bermejo, Juan Carlos López-Azor, César Del Castillo Gordillo, Marta Cobo Marcos, Javier de Juan Bagudá, María Dolores García Cosío, Ana García-Álvarez, Marta Farrero, Juan F Delgado
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引用次数: 0

摘要

引言和目的:肾功能恶化(WRF)是急性心力衰竭(AHF)的常见并发症,其预后价值尚存争议。我们旨在研究钠尿症对评估 WRF 的作用:我们对接受呋塞米负荷试验的 AHF 患者进行了一项观察性、前瞻性、多中心研究。根据 WRF 是否存在以及利钠反应的中位数对患者进行分类。主要终点是随访6个月时的死亡率、因心房颤动再次住院和心脏移植的综合情况:共有 156 名患者入选,其中 60 人(38.5%)发生了 WRF。患者分为 4 组:a) 47 例(30.1%)无 WRF/低 UNa(UNa ≤ 109 mEq/L);b) 49 例(31.4%)无 WRF/高 UNa(UNa > 109 mEq/L);c) 31 例(19.9%)WRF/低 UNa;d) 29 例(18.6%)WRF/高 UNa。WRF/ 低 UNa 组的参数显示临床严重程度更高,利尿和减充血反应更差。WRF 的发生与较高的合并事件风险相关(HR,1.88;95%CI,1.01-3.50;P = .046)。按钠尿反应分层时,低钠尿患者发生 WRF 与不良事件的风险增加有关(HR,2.28;95%CI,1.15-4.53;P = .019),而高钠尿患者则无关(HR,1.18;95%CI,0.26-5.29;P = .826):钠尿症可能是解释和预后AHF中WRF的有用生物标志物。只有在低钠血症的情况下,WRF才与较高的不良事件风险相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of natriuresis on worsening renal function during episodes of acute heart failure.

Introduction and objectives: Worsening renal function (WRF) is a frequent complication in acute heart failure (AHF) with a controversial prognostic value. We aimed to study the usefulness of natriuresis to evaluate WRF.

Methods: We conducted an observational, prospective, multicenter study of patients with AHF who underwent a furosemide stress test. The patients were classified according to whether WRF was present or absent and according to the median natriuretic response. The main endpoint was the combination of mortality, rehospitalization due to HF, and heart transplant at 6 months of follow-up.

Results: One hundred and fifty-six patients were enrolled, and WRF occurred in 60 (38.5%). The patients were divided into 4 groups: a) 47 (30.1%) no WRF/low UNa (UNa ≤ 109 mEq/L); b) 49 (31.4%) no WRF/high UNa (UNa >109 mEq/L); c) 31 (19.9%) WRF/low UNa and d) 29 (18.6%) WRF/high UNa. The parameters of the WRF/low UNa group showed higher clinical severity and worse diuretic and decongestive response. The development of WRF was associated with a higher risk of the combined event (HR, 1.88; 95%CI, 1.01-3.50; P=.046). When stratified by natriuretic response, WRF was associated with an increased risk of adverse events in patients with low natriuresis (HR, 2.28; 95%CI, 1.15-4.53; P=.019), but not in those with high natriuresis (HR, 1.18; 95%CI, 0.26-5.29; P=.826).

Conclusions: Natriuresis could be a useful biomarker for interpreting and prognosticating WRF in AHF. WRF is associated with a higher risk of adverse events only in the context of low natriuresis.

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