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