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Effect of Regional Citrate Anticoagulation vs Systemic Heparin Anticoagulation During Continuous Kidney Replacement Therapy on Dialysis Filter Life Span and Mortality Among Critically Ill Patients With Acute Kidney Injury: A Randomized Clinical Trial.
Zarbock, Alexander; Küllmar, Mira; Kindgen-Milles, Detlef; Wempe, Carola; Gerss, Joachim; Brandenburger, Timo; Dimski, Thomas; Tyczynski, Bartosz; Jahn, Michael; Mülling, Nils; Mehrländer, Martin; Rosenberger, Peter; Marx, Gernot; Simon, Tim Philipp; Jaschinski, Ulrich; Deetjen, Philipp; Putensen, Christian; Schewe, Jens-Christian; Kluge, Stefan; Jarczak, Dominik; Slowinski, Torsten; Bodenstein, Marc; Meybohm, Patrick; Wirtz, Stefan; Moerer, Onnen; Kortgen, Andreas; Simon, Philipp; Bagshaw, Sean M; Kellum, John A; Meersch, Melanie.
Afiliação
  • Zarbock A; Department of Anesthesiology, Intensive Care and Pain Medicine, University of Münster, Münster, Germany.
  • Küllmar M; Department of Anesthesiology, Intensive Care and Pain Medicine, University of Münster, Münster, Germany.
  • Kindgen-Milles D; Department of Anesthesiology and Critical Care Medicine, Heinrich-Heine University of Düsseldorf, Düsseldorf, Germany.
  • Wempe C; Department of Anesthesiology, Intensive Care and Pain Medicine, University of Münster, Münster, Germany.
  • Gerss J; Institute of Biostatistics and Clinical Research, University of Münster, Münster, Germany.
  • Brandenburger T; Department of Anesthesiology and Critical Care Medicine, Heinrich-Heine University of Düsseldorf, Düsseldorf, Germany.
  • Dimski T; Department of Anesthesiology and Critical Care Medicine, Heinrich-Heine University of Düsseldorf, Düsseldorf, Germany.
  • Tyczynski B; Department of Nephrology, University Hospital Essen, Essen, Germany.
  • Jahn M; Department of Nephrology, University Hospital Essen, Essen, Germany.
  • Mülling N; Department of Nephrology, University Hospital Essen, Essen, Germany.
  • Mehrländer M; Department of Anesthesiology and Intensive Care Medicine, University Hospital Tübingen, Eberhard Karls University Tübingen, Tübingen, Germany.
  • Rosenberger P; Department of Anesthesiology and Intensive Care Medicine, University Hospital Tübingen, Eberhard Karls University Tübingen, Tübingen, Germany.
  • Marx G; Department of Intensive Care Medicine, University of Aachen, Aachen, Germany.
  • Simon TP; Department of Intensive Care Medicine, University of Aachen, Aachen, Germany.
  • Jaschinski U; Department of Anesthesiology and Intensive Care Medicine, University Hospital Augsburg, Augsburg, Germany.
  • Deetjen P; Department of Anesthesiology and Intensive Care Medicine, University Hospital Augsburg, Augsburg, Germany.
  • Putensen C; University Hospital Bonn, Department of Anesthesiology and Intensive Care Medicine, Bonn, Germany.
  • Schewe JC; University Hospital Bonn, Department of Anesthesiology and Intensive Care Medicine, Bonn, Germany.
  • Kluge S; University Medical Center Hamburg-Eppendorf, Department of Intensive Care, Hamburg, Germany.
  • Jarczak D; University Medical Center Hamburg-Eppendorf, Department of Intensive Care, Hamburg, Germany.
  • Slowinski T; Department of Nephrology and Medical Intensive Care, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Bodenstein M; Universitätsmedizin Mainz, Department of Anesthesiology, Mainz, Germany.
  • Meybohm P; Department of Anesthesiology, Intensive Care and Pain Medicine, University Hospital Frankfurt, Frankfurt, Germany.
  • Wirtz S; Department of Anesthesiology, University Hospital Würzburg, Würzburg, Germany.
  • Moerer O; Department of Anesthesiology, Intensive Care and Pain Medicine, Helios Klinikum Bad Saarow, Bad Saarow, Germany.
  • Kortgen A; Department of Anesthesiology, University Medical Center Göttingen, Göttingen, Germany.
  • Simon P; Department of Anesthesiology and Intensive Care Medicine, University Hospital Jena, Jena, Germany.
  • Bagshaw SM; Department of Anesthesiology and Intensive Care Medicine, University Hospital Leipzig, Leipzig, Germany.
  • Kellum JA; Department of Critical Care Medicine, Faculty of Medicine and Dentistry, University of Alberta and Alberta Health Services, Edmonton, Alberta, Canada.
  • Meersch M; Center for Critical Care Nephrology, Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania.
JAMA ; 324(16): 1629-1639, 2020 10 27.
Article em En | MEDLINE | ID: mdl-33095849
ABSTRACT
Importance Although current guidelines suggest the use of regional citrate anticoagulation (which involves the addition of a citrate solution to the blood before the filter of the extracorporeal dialysis circuit) as first-line treatment for continuous kidney replacement therapy in critically ill patients, the evidence for this recommendation is based on few clinical trials and meta-analyses.

Objective:

To determine the effect of regional citrate anticoagulation, compared with systemic heparin anticoagulation, on filter life span and mortality. Design, Setting, and

Participants:

A parallel-group, randomized multicenter clinical trial in 26 centers across Germany was conducted between March 2016 and December 2018 (final date of follow-up, January 21, 2020). The trial was terminated early after 596 critically ill patients with severe acute kidney injury or clinical indications for initiation of kidney replacement therapy had been enrolled.

Interventions:

Patients were randomized to receive either regional citrate anticoagulation (n = 300), which consisted of a target ionized calcium level of 1.0 to 1.40 mg/dL, or systemic heparin anticoagulation (n = 296), which consisted of a target activated partial thromboplastin time of 45 to 60 seconds, for continuous kidney replacement therapy. Main Outcomes and

Measures:

Coprimary outcomes were filter life span and 90-day mortality. Secondary end points included bleeding complications and new infections.

Results:

Among 638 patients randomized, 596 (93.4%) (mean age, 67.5 years; 183 [30.7%] women) completed the trial. In the regional citrate group vs systemic heparin group, median filter life span was 47 hours (interquartile range [IQR], 19-70 hours) vs 26 hours (IQR, 12-51 hours) (difference, 15 hours [95% CI, 11 to 20 hours]; P < .001). Ninety-day all-cause mortality occurred in 150 of 300 patients vs 156 of 296 patients (Kaplan-Meier estimator percentages, 51.2% vs 53.6%; unadjusted difference, -2.4% [95% CI, -10.5% to 5.8%]; unadjusted hazard ratio, 0.91 [95% CI, 0.72 to 1.13]; unadjusted P = .38; adjusted difference, -6.1% [95% CI, -12.6% to 0.4%]; primary adjusted hazard ratio, 0.79 [95% CI, 0.63 to 1.004]; primary adjusted P = .054). Of 38 prespecified secondary end points, 34 showed no significant difference. Compared with the systemic heparin group, the regional citrate group had significantly fewer bleeding complications (15/300 [5.1%] vs 49/296 [16.9%]; difference, -11.8% [95% CI, -16.8% to -6.8%]; P < .001) and significantly more new infections (204/300 [68.0%] vs 164/296 [55.4%]; difference, 12.6% [95% CI, 4.9% to 20.3%]; P = .002). Conclusions and Relevance Among critically ill patients with acute kidney injury receiving continuous kidney replacement therapy, anticoagulation with regional citrate, compared with systemic heparin anticoagulation, resulted in significantly longer filter life span. The trial was terminated early and was therefore underpowered to reach conclusions about the effect of anticoagulation strategy on mortality. Trial Registration ClinicalTrials.gov Identifier NCT02669589.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Heparina / Ácido Cítrico / Injúria Renal Aguda / Terapia de Substituição Renal Contínua / Anticoagulantes Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Heparina / Ácido Cítrico / Injúria Renal Aguda / Terapia de Substituição Renal Contínua / Anticoagulantes Idioma: En Ano de publicação: 2020 Tipo de documento: Article