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Restrictive versus Liberal Fluid Therapy for Major Abdominal Surgery
Paul S Myles1, Rinaldo Bellomo1, Tomas Corcoran1
1From Alfred Hospital (P.S.M., J.S., S.W.), Monash University (P.S.M., R.B., T.C., A.F., K.L., J.S., S.W.), and the University of Melbourne (R.B., P.P., D.S., C.C., K.L.), Melbourne, VIC, Austin Hospital, Heidelberg, VIC (R.B., P.P., D.S., C.C.), Royal Perth Hospital and the University of Western Australia, Perth (T.C.), Royal Melbourne Hospital, Parkville, VIC (K.L.), and Royal Adelaide Hospital and Discipline of Acute Care Medicine, University of Adelaide, Adelaide, SA (T.P.) - all in Australia; Auckland City Hospital, Auckland, and the Medical Research Institute of New Zealand, Wellington - both in New Zealand (S. McGuinness, R.P.); the Chinese University of Hong Kong, Hong Kong (M.T.V.C.); University Health Network, Toronto (S. McCluskey); and Derriford Hospital, Plymouth, United Kingdom (G.M.).
A restrictive intravenous-fluid strategy for major abdominal surgery did not improve disability-free survival. This approach was linked to increased acute kidney injury and surgical-site infections in high-risk patients.
Area of Science:
- Anesthesiology
- Surgical Critical Care
- Nephrology
Background:
- Current guidelines suggest restrictive intravenous-fluid administration for enhanced recovery after major abdominal surgery.
- However, evidence supporting this strategy is limited, raising concerns about potential impairment of organ perfusion.
Purpose of the Study:
- To investigate the efficacy and safety of a restrictive versus a liberal intravenous-fluid regimen in patients undergoing major abdominal surgery.
- To determine the impact on disability-free survival and key secondary outcomes like acute kidney injury and septic complications.
Main Methods:
- A pragmatic, international randomized trial involving 3000 high-risk patients undergoing major abdominal surgery.
- Patients were assigned to either a restrictive or liberal intravenous-fluid regimen during and up to 24 hours post-surgery.
- The primary outcome was disability-free survival at 1 year, with secondary outcomes including acute kidney injury, renal-replacement therapy, and septic complications.
Main Results:
- The restrictive fluid group received a median of 3.7 liters of intravenous fluid, compared to 6.1 liters in the liberal group.
- Disability-free survival at 1 year was similar between groups (81.9% vs. 82.3%).
- The restrictive group showed a higher incidence of acute kidney injury (8.6% vs. 5.0%), surgical-site infections (16.5% vs. 13.6%), and renal-replacement therapy (0.9% vs. 0.3%).
Conclusions:
- A restrictive intravenous-fluid regimen was not associated with improved disability-free survival compared to a liberal regimen in high-risk patients undergoing major abdominal surgery.
- The restrictive strategy was associated with a higher rate of acute kidney injury and showed trends toward increased surgical-site infections and renal-replacement therapy.
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