Incidence of acute kidney injury and attributive mortality in acute respiratory distress syndrome randomized trials

被引:5
作者
Antonucci, Edoardo [1 ,2 ]
Garcia, Bruno [1 ,3 ,4 ]
Chen, David [1 ]
Matthay, Michael A. [5 ]
Liu, Kathleen D. [6 ]
Legrand, Matthieu [1 ]
机构
[1] Univ Calif San Francisco UCSF, Dept Anesthesia & Perioperat Care, Div Crit Care Med, San Francisco, CA 94115 USA
[2] Univ Milan, Dept Anesthesia & Crit Care Med, Milan, Italy
[3] Ctr Hosp Univ Lille, Dept Intens Care, Lille, France
[4] Univ Libre Bruxelles, Expt Lab Intens Care, Brussels, Belgium
[5] Univ Calif San Francisco Med & Anesthesia, Cardiovasc Res Inst CVRI, San Francisco, CA USA
[6] Univ Calif San Francisco, Dept Med & Anesthesia, Div Nephrol & Crit Care Med, San Francisco, CA USA
关键词
Acute kidney injury; Acute respiratory distress syndrome; Attributable mortality; Predictive enrichment; ACUTE LUNG INJURY; CRITICALLY-ILL PATIENTS; CONSENSUS REPORT; CLINICAL-TRIAL; OUTCOMES; EPIDEMIOLOGY; RECOVERY; DISEASE; CARE; ARDS;
D O I
10.1007/s00134-024-07485-6
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Purpose The development of acute kidney injury (AKI) after the acute respiratory distress syndrome (ARDS) reduces the chance of organ recovery and survival. The purpose of this study was to examine the AKI rate and attributable mortality in ARDS patients. Methods We performed an individual patient-data analysis including 10 multicenter randomized controlled trials conducted over 20 years. We employed a Super Learner ensemble technique, including a time-dependent analysis, to estimate the adjusted risk of AKI. We calculated the mortality attributable to AKI using an inverse probability of treatment weighting estimator integrated with the Super Learner. Results There were 5148 patients included in this study. The overall incidence of AKI was 43.7% (n = 2251). The adjusted risk of AKI ranged from 38.8% (95% confidence interval [CI], 35.7 to 41.9%) in ARMA, to 55.8% in ROSE (95% CI, 51.9 to 59.6%). 37.1% recovered rapidly from AKI, with a significantly lower recovery rate in recent trials (P < 0.001). The 90-day excess in mortality attributable to AKI was 15.4% (95% CI, 12.8 to 17.9%). It decreased from 25.4% in ARMA (95% CI, 18.7 to 32%), to 11.8% in FACTT (95% CI, 5.5 to 18%) and then remained rather stable over time. The 90-day overall excess in mortality attributable to acute kidney disease was 28.4% (95% CI, 25.3 to 31.5%). Conclusions The incidence of AKI appears to be stable over time in patients with ARDS enrolled in randomized trials. The development of AKI remains a significant contributing factor to mortality. These estimates are essential for designing future clinical trials for AKI prevention or treatment.
引用
收藏
页码:1240 / 1250
页数:11
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