Timing of Initiation of Renal-Replacement Therapy in Acute Kidney Injury Journal Articles uri icon

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abstract

  • BACKGROUND: Acute kidney injury is common in critically ill patients, many of whom receive renal-replacement therapy. However, the most effective timing for the initiation of such therapy remains uncertain. METHODS: We conducted a multinational, randomized, controlled trial involving critically ill patients with severe acute kidney injury. Patients were randomly assigned to receive an accelerated strategy of renal-replacement therapy (in which therapy was initiated within 12 hours after the patient had met eligibility criteria) or a standard strategy (in which renal-replacement therapy was discouraged unless conventional indications developed or acute kidney injury persisted for >72 hours). The primary outcome was death from any cause at 90 days. RESULTS: Of the 3019 patients who had undergone randomization, 2927 (97.0%) were included in the modified intention-to-treat analysis (1465 in the accelerated-strategy group and 1462 in the standard-strategy group). Of these patients, renal-replacement therapy was performed in 1418 (96.8%) in the accelerated-strategy group and in 903 (61.8%) in the standard-strategy group. At 90 days, death had occurred in 643 patients (43.9%) in the accelerated-strategy group and in 639 (43.7%) in the standard-strategy group (relative risk, 1.00; 95% confidence interval [CI], 0.93 to 1.09; P = 0.92). Among survivors at 90 days, continued dependence on renal-replacement therapy was confirmed in 85 of 814 patients (10.4%) in the accelerated-strategy group and in 49 of 815 patients (6.0%) in the standard-strategy group (relative risk, 1.74; 95% CI, 1.24 to 2.43). Adverse events occurred in 346 of 1503 patients (23.0%) in the accelerated-strategy group and in 245 of 1489 patients (16.5%) in the standard-strategy group (P<0.001). CONCLUSIONS: Among critically ill patients with acute kidney injury, an accelerated renal-replacement strategy was not associated with a lower risk of death at 90 days than a standard strategy. (Funded by the Canadian Institutes of Health Research and others; STARRT-AKI ClinicalTrials.gov number, NCT02568722.).

authors

  • STARRT-AKI Investigators
  • Canadian Critical Care Trials Group
  • Australian and New Zealand Intensive Care Society Clinical Trials Group
  • United Kingdom Critical Care Research Group
  • Canadian Nephrology Trials Network
  • Irish Critical Care Trials Group
  • Bagshaw, Sean M
  • Wald, Ron
  • Adhikari, Neill KJ
  • Bellomo, Rinaldo
  • da Costa, Bruno R
  • Dreyfuss, Didier
  • Du, Bin
  • Gallagher, Martin P
  • Gaudry, Stéphane
  • Hoste, Eric A
  • Lamontagne, François
  • Joannidis, Michael
  • Landoni, Giovanni
  • Liu, Kathleen D
  • McAuley, Daniel F
  • McGuinness, Shay P
  • Neyra, Javier A
  • Nichol, Alistair D
  • Ostermann, Marlies
  • Palevsky, Paul M
  • Pettilä, Ville
  • Quenot, Jean-Pierre
  • Qiu, Haibo
  • Rochwerg, Bram
  • Schneider, Antoine G
  • Smith, Orla M
  • Thomé, Fernando
  • Thorpe, Kevin E
  • Vaara, Suvi
  • Weir, Matthew
  • Wang, Amanda Y
  • Young, Paul
  • Zarbock, Alexander

publication date

  • July 16, 2020