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

Standard

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; RICH Investigators and the Sepnet Trial Group.

in: JAMA-J AM MED ASSOC, Jahrgang 324, Nr. 16, 27.10.2020, S. 1629-1639.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Zarbock, A, Küllmar, M, Kindgen-Milles, D, Wempe, C, Gerss, J, Brandenburger, T, Dimski, T, Tyczynski, B, Jahn, M, Mülling, N, Mehrländer, M, Rosenberger, P, Marx, G, Simon, TP, Jaschinski, U, Deetjen, P, Putensen, C, Schewe, J-C, Kluge, S, Jarczak, D, Slowinski, T, Bodenstein, M, Meybohm, P, Wirtz, S, Moerer, O, Kortgen, A, Simon, P, Bagshaw, SM, Kellum, JA, Meersch, M & RICH Investigators and the Sepnet Trial Group 2020, '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', JAMA-J AM MED ASSOC, Jg. 324, Nr. 16, S. 1629-1639. https://doi.org/10.1001/jama.2020.18618

APA

Zarbock, A., Küllmar, M., Kindgen-Milles, D., Wempe, C., Gerss, J., Brandenburger, T., Dimski, T., Tyczynski, B., Jahn, M., Mülling, N., Mehrländer, M., Rosenberger, P., Marx, G., Simon, T. P., Jaschinski, U., Deetjen, P., Putensen, C., Schewe, J-C., Kluge, S., ... RICH Investigators and the Sepnet Trial Group (2020). 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. JAMA-J AM MED ASSOC, 324(16), 1629-1639. https://doi.org/10.1001/jama.2020.18618

Vancouver

Bibtex

@article{816c73af7ae345969bfc13341d218850,
title = "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",
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.",
author = "Alexander Zarbock and Mira K{\"u}llmar and Detlef Kindgen-Milles and Carola Wempe and Joachim Gerss and Timo Brandenburger and Thomas Dimski and Bartosz Tyczynski and Michael Jahn and Nils M{\"u}lling and Martin Mehrl{\"a}nder and Peter Rosenberger and Gernot Marx and Simon, {Tim Philipp} and Ulrich Jaschinski and Philipp Deetjen and Christian Putensen and Jens-Christian Schewe and Stefan Kluge and Dominik Jarczak and Torsten Slowinski and Marc Bodenstein and Patrick Meybohm and Stefan Wirtz and Onnen Moerer and Andreas Kortgen and Philipp Simon and Bagshaw, {Sean M} and Kellum, {John A} and Melanie Meersch and {RICH Investigators and the Sepnet Trial Group}",
year = "2020",
month = oct,
day = "27",
doi = "10.1001/jama.2020.18618",
language = "English",
volume = "324",
pages = "1629--1639",
journal = "JAMA-J AM MED ASSOC",
issn = "0098-7484",
publisher = "American Medical Association",
number = "16",

}

RIS

TY - JOUR

T1 - 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

AU - Zarbock, Alexander

AU - Küllmar, Mira

AU - Kindgen-Milles, Detlef

AU - Wempe, Carola

AU - Gerss, Joachim

AU - Brandenburger, Timo

AU - Dimski, Thomas

AU - Tyczynski, Bartosz

AU - Jahn, Michael

AU - Mülling, Nils

AU - Mehrländer, Martin

AU - Rosenberger, Peter

AU - Marx, Gernot

AU - Simon, Tim Philipp

AU - Jaschinski, Ulrich

AU - Deetjen, Philipp

AU - Putensen, Christian

AU - Schewe, Jens-Christian

AU - Kluge, Stefan

AU - Jarczak, Dominik

AU - Slowinski, Torsten

AU - Bodenstein, Marc

AU - Meybohm, Patrick

AU - Wirtz, Stefan

AU - Moerer, Onnen

AU - Kortgen, Andreas

AU - Simon, Philipp

AU - Bagshaw, Sean M

AU - Kellum, John A

AU - Meersch, Melanie

AU - RICH Investigators and the Sepnet Trial Group

PY - 2020/10/27

Y1 - 2020/10/27

N2 - 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.

AB - 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.

U2 - 10.1001/jama.2020.18618

DO - 10.1001/jama.2020.18618

M3 - SCORING: Journal article

C2 - 33095849

VL - 324

SP - 1629

EP - 1639

JO - JAMA-J AM MED ASSOC

JF - JAMA-J AM MED ASSOC

SN - 0098-7484

IS - 16

ER -