Abstract
PurposeThis study aimed to evaluate the attributable mortality of new-onset acute kidney injury (AKI).MethodsThe data in the present study were derived from a multi-center, prospective cohort study in China that was performed at 18 Chinese ICUs. A propensity-matched analysis was performed between matched patients with and without AKI selected from all eligible patients to estimate the attributable mortality of new-onset AKI.ResultsA total of 2872 critically ill adult patients were eligible. The incidence of new-onset AKI was 29.1% (n = 837). After propensity score matching, 788 patients with AKI were matched 1:1 with 788 controls (patients without AKI). Thirty-day mortality was significantly higher among the patients with AKI than among their matched controls (25.5% versus 17.4%, p < 0.001). Subgroup analysis in terms of AKI classification showed that there was no significant difference (p = 0.509) in 30-day mortality between patients with stage 1 AKI and their matched controls. The attributable mortality values of stage 2 and stage 3 AKI were 12.4% [95% confidence interval (CI) 2.6–21.8%, p = 0.013] and 16.1% (95% CI 8.2–23.8%, p < 0.001), respectively. The attributable mortality of persistent AKI was 15.7% (95% CI 8.8–22.4%, p = 0.001), while no observable difference in 30-day mortality was identified between transient AKI patients and their matched non-AKI controls (p = 0.229).ConclusionThe absolute excess 30-day mortality that is statistically attributable to new-onset AKI is substantial (8.1%) among general ICU patients. However, neither stage 1 AKI nor transient AKI increases 30-day mortality.
Highlights
Acute kidney injury (AKI) is a common complication among critically ill patients and has been increasingly recognized as a risk factor for long-term chronic kidney disease (CKD) development and progression, infection and malignancy [1,2,3]
The additional mortality attributed to AKI has been researched in previous studies [4,5,6], but the attributable mortality of new-onset AKI is still unclear among general ICU patients
The newonset AKI estimate for 30-day mortality is robust to hidden bias from unmeasured covariates up to a gamma coefficient of 3. In this propensity-matched analysis, we found that the estimated absolute excess 30-day mortality statistically attributable to new-onset AKI was 8.1%
Summary
Acute kidney injury (AKI) is a common complication among critically ill patients and has been increasingly recognized as a risk factor for long-term chronic kidney disease (CKD) development and progression, infection and malignancy [1,2,3]. It is difficult to evaluate the impact of this disease on mortality because the development of AKI is a multifactorial process and patients with AKI tend to be in worse condition than those without [7]. We performed a propensity-matched analysis based on the database of a prospective multi-center cohort study to balance the impact of non-renal variables on. International Urology and Nephrology outcomes and precisely estimate the mortality attributed to new-onset AKI. Transient AKI, defined as kidney injury of a duration less than 48 h from AKI onset [8], is usually considered to be “pre-renal dysfunction”, while persistent AKI (kidney injury beyond 48 h) is more closely related to “acute tubular necrosis” [9]. According to the duration of renal injury, we conducted a subgroup analysis of matched new-onset AKI patients and non-AKI controls to explore the influence of AKI duration on mortality
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