The Potential Role of Albumin in Reducing Cardiac Surgery–Associated Acute Kidney Injury: A Randomized Controlled Trial

IF 2.1 4区 医学 Q2 ANESTHESIOLOGY Journal of cardiothoracic and vascular anesthesia Pub Date : 2025-02-01 Epub Date: 2024-10-16 DOI:10.1053/j.jvca.2024.10.012
Jordi Miralles Bagán MD, PhD , Laura Parrilla Quiles MD , Pilar Paniagua Iglesias MD, PhD , Antoni J. Betbesé Roig MD, PhD , Sergi Sabaté Tenas MD, PhD , Sergio Pérez García MD , Mercedes García Álvarez MD, PhD
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Abstract

Objectives

Cardiac surgery–associated acute kidney injury (CSA-AKI) is a common complication with high morbidity and mortality. This study was designed to determine whether adding human albumin to the cardiopulmonary bypass (CPB) priming solution reduces the incidence of CSA-AKI.

Design

A double-blind, randomized controlled trial (RCT) involving 248 patients scheduled for cardiac surgery with CPB.

Setting

A single-center tertiary university hospital.

Participants

Adults with a baseline estimated glomerular filtration rate (eGFR) of ≥60 mL/min/1.73 m2 and left ventricular ejection fraction ≥40%.

Interventions

Patients were randomized to receive either a crystalloid priming solution (Plasma-Lyte) plus 4% albumin (intervention group, n = 126) or a crystalloid solution alone (control group, n = 122) for CPB.

Measurements and Main Results

Data analyses were performed using the Chi-square test and Student's t-test, or their nonparametric equivalent. The primary outcome was the incidence of CSA-AKI, as defined by the Kidney Disease Improving Global Outcomes criteria, within 5 days postoperatively. Both cohorts were comparable in baseline and perioperative characteristics, including preoperative albumin levels. The incidence of CSA-AKI was 29.3% (n = 37) in the intervention group compared with 31.2% (n = 38) in the control group (odds ratio: 0.91, 95% confidence interval: 0.53-1.58). The observed difference in CSA-AKI incidence between the groups was not statistically significant. A post-hoc subgroup analysis of patients with a baseline eGFR of 60 to 70 mL/min/1.73 m² indicated a trend toward a reduced incidence of CSA-AKI in the intervention group compared with the control group (35.7% v 57.6%; odds ratio: 0.41, 95% confidence interval: 0.16-1.03). This trend was not observed in patients with an eGFR greater than 70 mL/min/1.73 m². No significant differences were observed between groups for the need for inotropes or vasoconstrictors, incidence of cardiogenic or distributive shock, bleeding, need for transfusion, or use of nephrotoxic drugs.

Conclusions

Adding albumin to the CPB priming solution did not decrease the incidence of CSA-AKI in patients with normal preoperative renal function. These findings suggest that albumin might benefit patients with impaired renal function, warranting further investigation.
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白蛋白在减少心脏手术相关急性肾损伤中的潜在作用:一项随机对照试验
目的心脏手术相关急性肾损伤(CSA-AKI)是一种常见的并发症,具有较高的发病率和死亡率。本研究旨在确定在体外循环(CPB)启动液中加入人白蛋白是否能降低CSA-AKI的发生率。设计一项双盲、随机对照试验(RCT),纳入248例计划行CPB心脏手术的患者。单中心三级大学附属医院。参与者:基线肾小球滤过率(eGFR)≥60ml /min/1.73 m2,左室射血分数≥40%的成年人。干预:患者被随机分为两组,一组接受晶体溶液(血浆- lyte)加4%白蛋白(干预组,n = 126),另一组接受晶体溶液(对照组,n = 122)治疗CPB。测量和主要结果数据分析使用卡方检验和学生t检验或其非参数等效检验进行。主要终点是术后5天内CSA-AKI的发生率,由肾脏疾病改善总体结局标准定义。两个队列在基线和围手术期特征(包括术前白蛋白水平)方面具有可比性。干预组CSA-AKI发生率为29.3% (n = 37),对照组为31.2% (n = 38)(优势比:0.91,95%可信区间:0.53-1.58)。CSA-AKI发生率组间比较差异无统计学意义。对基线eGFR为60 ~ 70 mL/min/1.73 m²的患者进行的一项事后亚组分析显示,与对照组相比,干预组的CSA-AKI发病率有降低的趋势(35.7% vs 57.6%;优势比:0.41,95%可信区间:0.16-1.03)。在eGFR大于70 mL/min/1.73 m²的患者中没有观察到这种趋势。两组之间对肌力药物或血管收缩剂的需求、心源性或分布性休克的发生率、出血、输血需求或肾毒性药物的使用没有显著差异。结论在CPB启动液中加入白蛋白并不能降低术前肾功能正常患者CSA-AKI的发生率。这些发现表明白蛋白可能对肾功能受损的患者有益,值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.80
自引率
17.90%
发文量
606
审稿时长
37 days
期刊介绍: The Journal of Cardiothoracic and Vascular Anesthesia is primarily aimed at anesthesiologists who deal with patients undergoing cardiac, thoracic or vascular surgical procedures. JCVA features a multidisciplinary approach, with contributions from cardiac, vascular and thoracic surgeons, cardiologists, and other related specialists. Emphasis is placed on rapid publication of clinically relevant material.
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