Restriction of Intravenous Fluid in ICU Patients with Septic Shock

Tine Sylvest Meyhoff(Copenhagen University Hospital), Peter Buhl Hjortrup(Copenhagen University Hospital), Jørn Wetterslev(Copenhagen University Hospital), Praleene Sivapalan(Copenhagen University Hospital), Jon Henrik Laake(Copenhagen University Hospital), Maria Cronhjort(Copenhagen University Hospital), Stephan M. Jakob(Copenhagen University Hospital), Maurizio Cecconi(Copenhagen University Hospital), Marek Nalos(Copenhagen University Hospital), Marlies Ostermann(Copenhagen University Hospital), Manu L. N. G. Malbrain(Copenhagen University Hospital), Ville Pettilä(Copenhagen University Hospital), Morten Hylander Møller(Copenhagen University Hospital), Maj-Brit N. Kjær(Copenhagen University Hospital), Theis Lange(Copenhagen University Hospital), Christian Overgaard‐Steensen(Copenhagen University Hospital), Björn Brand(Copenhagen University Hospital), Marie Winther‐Olesen(Copenhagen University Hospital), Jonathan O. White(Copenhagen University Hospital), Lars Quist(Copenhagen University Hospital), Bo Westergaard(Copenhagen University Hospital), Andreas Bender Jonsson(Copenhagen University Hospital), Carl Johan Steensen Hjortsø(Copenhagen University Hospital), Nick Meier(Copenhagen University Hospital), Thomas Steen Jensen(Copenhagen University Hospital), Janus Engstrøm(Copenhagen University Hospital), Lars Nebrich(Copenhagen University Hospital), Nina Christine Andersen‐Ranberg(Copenhagen University Hospital), Jacob V. Jensen(Copenhagen University Hospital), Neeliya Anton Joseph(Copenhagen University Hospital), Lone Musaeus Poulsen(Copenhagen University Hospital), Louise Stenbryggen Herløv(Copenhagen University Hospital), Christoffer Sølling(Copenhagen University Hospital), Susan K Pedersen(Copenhagen University Hospital), Kurt K Knudsen(Copenhagen University Hospital), Therese Simonsen Straarup(Copenhagen University Hospital), Marianne Vang(Copenhagen University Hospital), Helle Bundgaard(Copenhagen University Hospital), Bodil Steen Rasmussen(Copenhagen University Hospital), Søren Rosborg Aagaard(Copenhagen University Hospital), Thomas Hildebrandt(Copenhagen University Hospital), Lene Russell(Copenhagen University Hospital), Morten H. Bestle(Copenhagen University Hospital), Martin Schønemann‐Lund(Copenhagen University Hospital), Anne Craveiro Brøchner(Copenhagen University Hospital), Claes F Elvander(Copenhagen University Hospital), Søren Hoffmann(Copenhagen University Hospital), Michael L. Rasmussen(Copenhagen University Hospital), Yvonne Karin Martin(Copenhagen University Hospital), Fredrik Femtehjell Friberg(Copenhagen University Hospital), Herman Seter(Copenhagen University Hospital), Tayyba Naz Aslam(Copenhagen University Hospital), Sigrid Ådnøy(Copenhagen University Hospital), Philipp Seidel(Copenhagen University Hospital), Kristian Strand(Copenhagen University Hospital), Bror Johnstad(Copenhagen University Hospital), Eva Joelsson‐Alm(Copenhagen University Hospital), Jens Jørgen Christensen(Copenhagen University Hospital), Christian Ahlstedt(Copenhagen University Hospital), Carmen A. Pfortmueller(Copenhagen University Hospital), Martin Siegemund(Copenhagen University Hospital), Massimiliano Greco(Copenhagen University Hospital), Jaroslav Raděj(Copenhagen University Hospital), Miroslav Kříž(Copenhagen University Hospital), Doug W Gould(Copenhagen University Hospital), Kathy Rowan(Copenhagen University Hospital), Paul Mouncey(Copenhagen University Hospital), Anders Perner(Copenhagen University Hospital)
New England Journal of Medicine
June 17, 2022
Cited by 373Open Access
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Abstract

BACKGROUND: Intravenous fluids are recommended for the treatment of patients who are in septic shock, but higher fluid volumes have been associated with harm in patients who are in the intensive care unit (ICU). METHODS: In this international, randomized trial, we assigned patients with septic shock in the ICU who had received at least 1 liter of intravenous fluid to receive restricted intravenous fluid or standard intravenous fluid therapy; patients were included if the onset of shock had been within 12 hours before screening. The primary outcome was death from any cause within 90 days after randomization. RESULTS: We enrolled 1554 patients; 770 were assigned to the restrictive-fluid group and 784 to the standard-fluid group. Primary outcome data were available for 1545 patients (99.4%). In the ICU, the restrictive-fluid group received a median of 1798 ml of intravenous fluid (interquartile range, 500 to 4366); the standard-fluid group received a median of 3811 ml (interquartile range, 1861 to 6762). At 90 days, death had occurred in 323 of 764 patients (42.3%) in the restrictive-fluid group, as compared with 329 of 781 patients (42.1%) in the standard-fluid group (adjusted absolute difference, 0.1 percentage points; 95% confidence interval [CI], -4.7 to 4.9; P = 0.96). In the ICU, serious adverse events occurred at least once in 221 of 751 patients (29.4%) in the restrictive-fluid group and in 238 of 772 patients (30.8%) in the standard-fluid group (adjusted absolute difference, -1.7 percentage points; 99% CI, -7.7 to 4.3). At 90 days after randomization, the numbers of days alive without life support and days alive and out of the hospital were similar in the two groups. CONCLUSIONS: Among adult patients with septic shock in the ICU, intravenous fluid restriction did not result in fewer deaths at 90 days than standard intravenous fluid therapy. (Funded by the Novo Nordisk Foundation and others; CLASSIC ClinicalTrials.gov number, NCT03668236.).


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