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Incidence of acute kidney injury and attributive mortality in acute respiratory distress syndrome randomized trials.
Antonucci, Edoardo; Garcia, Bruno; Chen, David; Matthay, Michael A; Liu, Kathleen D; Legrand, Matthieu.
Affiliation
  • Antonucci E; Department of Anesthesia and Perioperative Care, Division of Critical Care Medicine, University of California, San Francisco (UCSF), San Francisco, CA, USA.
  • Garcia B; Department of Anesthesia and Critical Care Medicine, University of Milan, Milan, Italy.
  • Chen D; Department of Anesthesia and Perioperative Care, Division of Critical Care Medicine, University of California, San Francisco (UCSF), San Francisco, CA, USA.
  • Matthay MA; Department of Intensive Care, Centre Hospitalier Universitaire de Lille, Lille, France.
  • Liu KD; Experimental Laboratory of Intensive Care, Université Libre de Bruxelles, Brussels, Belgium.
  • Legrand M; Department of Anesthesia and Perioperative Care, Division of Critical Care Medicine, University of California, San Francisco (UCSF), San Francisco, CA, USA.
Intensive Care Med ; 50(8): 1240-1250, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38864911
ABSTRACT

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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Distress Syndrome / Randomized Controlled Trials as Topic / Acute Kidney Injury Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Intensive Care Med Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Respiratory Distress Syndrome / Randomized Controlled Trials as Topic / Acute Kidney Injury Limits: Aged / Female / Humans / Male / Middle aged Language: En Journal: Intensive Care Med Year: 2024 Document type: Article Affiliation country: United States Country of publication: United States