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标准和加速起始肾脏替代治疗在急性肾损伤中的比较。

Comparison of standard and accelerated initiation of renal replacement therapy in acute kidney injury.

机构信息

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

Li Ka Shing Knowledge Institute of St Michael's Hospital, Toronto, Ontario, Canada.

出版信息

Kidney Int. 2015 Oct;88(4):897-904. doi: 10.1038/ki.2015.184. Epub 2015 Jul 8.

Abstract

In patients with severe acute kidney injury (AKI) but no urgent indication for renal replacement therapy (RRT), the optimal time to initiate RRT remains controversial. While starting RRT preemptively may have benefits, this may expose patients to unnecessary RRT. To study this, we conducted a 12-center open-label pilot trial of critically ill adults with volume replete severe AKI. Patients were randomized to accelerated (12 h or less from eligibility) or standard RRT initiation. Outcomes were adherence to protocol-defined time windows for RRT initiation (primary), proportion of eligible patients enrolled, follow-up to 90 days, and safety in 101 fully eligible patients (57 with sepsis) with a mean age of 63 years. Median serum creatinine and urine output at enrollment were 268 micromoles/l and 356 ml per 24 h, respectively. In the accelerated arm, all patients commenced RRT and 45/48 did so within 12 h from eligibility (median 7.4 h). In the standard arm, 33 patients started RRT at a median of 31.6 h from eligibility, of which 19 did not receive RRT (6 died and 13 recovered kidney function). Clinical outcomes were available for all patients at 90 days following enrollment, with mortality 38% in the accelerated and 37% in the standard arm. Two surviving patients, both randomized to standard RRT initiation, were still RRT dependent at day 90. No safety signal was evident in either arm. Our findings can inform the design of a large-scale effectiveness randomized control trial.

摘要

在没有紧急肾脏替代治疗(RRT)指征的严重急性肾损伤(AKI)患者中,开始 RRT 的最佳时机仍存在争议。虽然抢先开始 RRT 可能有好处,但这可能使患者暴露于不必要的 RRT 中。为了研究这一点,我们对有容量过多的严重 AKI 的重症成年人进行了一项 12 中心开放标签的先导试验。患者被随机分为加速(从符合条件到开始 RRT 的时间少于 12 小时)或标准 RRT 开始。主要结局是符合方案定义的 RRT 开始时间窗口的依从性(主要结局)、符合条件的患者比例、90 天随访和 101 名完全符合条件的患者(57 名脓毒症)的安全性,平均年龄为 63 岁。登记时的血清肌酐中位数和尿量中位数分别为 268μmol/L 和 356ml/24h。在加速组中,所有患者均开始 RRT,其中 45/48 例在符合条件后 12 小时内开始(中位数为 7.4 小时)。在标准组中,33 例患者在符合条件后中位数 31.6 小时开始 RRT,其中 19 例未接受 RRT(6 例死亡,13 例恢复肾功能)。所有患者在登记后 90 天均可获得临床结局,加速组的死亡率为 38%,标准组为 37%。两名存活患者均随机分到标准 RRT 开始组,在第 90 天仍依赖 RRT。在两个治疗组中均未出现安全信号。我们的研究结果可为一项大型有效性随机对照试验的设计提供信息。

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