Restrictive versus standard IV fluid therapy in adult ICU patients with septic shock—Bayesian analyses of the CLASSIC trial

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Background
The CLASSIC trial assessed the effects of restrictive versus standard intravenous (IV) fluid therapy in adult intensive care unit (ICU) patients with septic shock. This pre-planned study provides a probabilistic interpretation and evaluates heterogeneity in treatment effects (HTE).

Methods
We analysed mortality, serious adverse events (SAEs), serious adverse reactions (SARs) and days alive without life-support within 90 days using Bayesian models with weakly informative priors. HTE on mortality was assessed according to five baseline variables: disease severity, vasopressor dose, lactate levels, creatinine values and IV fluid volumes given before randomisation.

Results
The absolute difference in mortality was 0.2%-points (95% credible interval: −5.0 to 5.4; 47% posterior probability of benefit [risk difference <0.0%-points]) with restrictive IV fluid. The posterior probabilities of benefits with restrictive IV fluid were 72% for SAEs, 52% for SARs and 61% for days alive without life-support. The posterior probabilities of no clinically important differences (absolute risk difference ≤2%-points) between the groups were 56% for mortality, 49% for SAEs, 90% for SARs and 38% for days alive without life-support. There was 97% probability of HTE for previous IV fluid volumes analysed continuously, that is, potentially relatively lower mortality of restrictive IV fluids with higher previous IV fluids. No substantial evidence of HTE was found in the other analyses.

Conclusion
We could not rule out clinically important effects of restrictive IV fluid therapy on mortality, SAEs or days alive without life-support, but substantial effects on SARs were unlikely. IV fluids given before randomisation might interact with IV fluid strategy.
OriginalsprogEngelsk
TidsskriftActa Anaesthesiologica Scandinavica
Vol/bind68
Udgave nummer2
Sider (fra-til) 236-246
Antal sider11
ISSN0001-5172
DOI
StatusUdgivet - 2024

Bibliografisk note

Funding Information:
The CLASSIC trial was funded by the Novo Nordisk Foundation (NNF17OC0028608) and Sofus Friis’ foundation. PS received funding from the research council of Rigshospitalet. The funders had no influence on the trial design, conduct, and interpretation of the results or the decision to publish the results of this secondary study.

Funding Information:
The Department of Intensive Care, Rigshospitalet receives support for research projects from the Novo Nordisk Foundation, Sygeforsikringen “danmark,” and has conducted contract research for AM‐Pharma. AP has received honorarium for advisory board work from Novartis. MLNGM is a member of the medical advisory Board of Pulsion Medical Systems (fully part of Getinge group), Serenno Medical, Potrero Medical, Sentinel Medical and Baxter. He consults for BBraun, Becton Dickinson, ConvaTec, Spiegelberg, Medtronic, MedCaptain, and Holtech Medical, and received speaker's fees from PeerVoice. He holds stock options for Serenno and Potrero. He is a co‐founder and the President of the International Fluid Academy (IFA). The IFA (http://www.fluidacademy.org) is integrated within the not‐for‐profit charitable organization iMERiT, International Medical Education and Research Initiative, under Belgian law.

Publisher Copyright:
© 2023 The Authors. Acta Anaesthesiologica Scandinavica published by John Wiley & Sons Ltd on behalf of Acta Anaesthesiologica Scandinavica Foundation.

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