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急性肾损伤后慢性肾脏病的进展:急性肾损伤试验中肾脏替代治疗标准启动与加速启动的二次分析

CKD Progression after Acute Kidney Injury: A Secondary Analysis of the Standard versus Accelerated Initiation of Renal Replacement Therapy in Acute Kidney Injury Trial.

作者信息

Wing Sara, Neto Ary Serpa, Bellomo Rinaldo, Clark Edward G, Gallagher Martin, Liangos Orfeas, Prasad Bhanu, Silver Samuel A, Tolwani Ashita, Bagshaw Sean, Wald Ron

机构信息

Division of Nephrology, St. Michael's Hospital and University of Toronto, Toronto, Ontario, Canada.

Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), School of Public Health and Preventive Medicine, Monash University, Melbourne, Victoria, Australia.

出版信息

Kidney360. 2025 Apr 1;6(4):636-644. doi: 10.34067/KID.0000000663. Epub 2024 Dec 3.

Abstract

KEY POINTS

Development or progression of CKD occurred in almost 40% of patients after an episode of severe AKI. Receipt of KRT, regardless of allocation to an accelerated or standard initiation strategy, was associated with development or progression of CKD. This study helps identify a subset of patients at risk of CKD after severe AKI who would benefit from dedicated kidney follow-up after discharge.

BACKGROUND

CKD is a common complication after AKI. We aimed to evaluate whether a KRT initiation strategy had an effect on CKD progression. Secondarily, we aimed to identify factors that influenced the development or progression of CKD after severe AKI.

METHODS

This secondary analysis of the Standard versus Accelerated Initiation of Renal Replacement Therapy in AKI trial included patients with outpatient serum creatinine values available in the year before hospitalization and who were alive at 90 days after randomization. Our main analysis focused on patients who had definitive assessment of kidney function at 90 days after randomization. Predictor markers included patient demographics, comorbidities, markers of acute illness, laboratory values, receipt of KRT, and KRT treatment strategy (accelerated versus standard). The primary outcome was CKD progression, a composite of CKD, defined as new eGFR <60 ml/min per 1.73 m if baseline eGFR was ≥60 ml/min; a decline in eGFR ≥25% if baseline eGFR was <60 ml/min; or KRT dependence at day 90. The association of KRT treatment strategy with CKD progression was assessed in an unadjusted mixed-effect logistic regression model.

RESULTS

Of the 401 surviving patients with a baseline serum creatinine, 39% experienced CKD progression. KRT initiation strategy had no effect on CKD progression (accelerated arm [41%], versus the standard arm [38%], odds ratio, 1.13 [95% confidence interval, 0.75 to 1.72]). Receipt of KRT and aortic surgery were the most potent risks of CKD progression.

CONCLUSIONS

These findings suggest that CKD progression is common after severe AKI. Risk factors of CKD progression included receipt of KRT and aortic surgery, suggesting that these patients should be prioritized for dedicated kidney follow-up after hospital discharge.

CLINICAL TRIAL REGISTRY NAME AND REGISTRATION NUMBER

: NCT01557361.

摘要

要点

在严重急性肾损伤发作后,近40%的患者出现慢性肾脏病的发展或进展。接受肾脏替代治疗(KRT),无论采用加速启动策略还是标准启动策略,均与慢性肾脏病的发展或进展相关。本研究有助于识别严重急性肾损伤后有慢性肾脏病风险的患者亚组,这些患者在出院后将受益于专门的肾脏随访。

背景

慢性肾脏病是急性肾损伤后的常见并发症。我们旨在评估肾脏替代治疗启动策略是否对慢性肾脏病进展有影响。其次,我们旨在确定影响严重急性肾损伤后慢性肾脏病发展或进展的因素。

方法

对急性肾损伤中肾脏替代治疗标准启动与加速启动试验的二次分析纳入了在住院前一年有门诊血清肌酐值且随机分组后90天存活的患者。我们的主要分析集中在随机分组后90天对肾功能进行明确评估的患者。预测指标包括患者人口统计学特征、合并症、急性疾病指标、实验室值、接受肾脏替代治疗情况以及肾脏替代治疗策略(加速与标准)。主要结局是慢性肾脏病进展,这是慢性肾脏病的综合指标,定义为:若基线估算肾小球滤过率(eGFR)≥60 ml/min/1.73 m²,则新的eGFR<60 ml/min/1.73 m²;若基线eGFR<60 ml/min/1.73 m²,则eGFR下降≥25%;或在第90天依赖肾脏替代治疗。在未调整的混合效应逻辑回归模型中评估肾脏替代治疗策略与慢性肾脏病进展的关联。

结果

在401例有基线血清肌酐的存活患者中,39%经历了慢性肾脏病进展。肾脏替代治疗启动策略对慢性肾脏病进展无影响(加速组[41%],标准组[38%],比值比为1.13[95%置信区间为0.75至1.72])。接受肾脏替代治疗和主动脉手术是慢性肾脏病进展的最主要风险因素。

结论

这些发现表明严重急性肾损伤后慢性肾脏病进展很常见。慢性肾脏病进展的风险因素包括接受肾脏替代治疗和主动脉手术,这表明这些患者在出院后应优先接受专门的肾脏随访。

临床试验注册名称和注册号

NCT01557361

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f8d/12045516/ea786ea6ba24/kidney360-6-636-g001.jpg

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