Study goal: This study will examine whether there is a significant difference in postoperative outcomes between GDFT using a colloid solution versus a crystalloid solution. Hypothesis: Perioperative fluid optimization through the use of a closed-loop assistance with a balanced starch solution (volulyte®) will be associated with a decrease in postoperative complications compared to the same approach using a balanced crystalloid solution (Plasmalyte®). Objective: To establish which kind of intravenous fluid used for goal directed therapy with closed-loop assistance will reduce the number of postoperative complications (evaluation made by the POMS score).
Controversy still persists regarding the type of fluid to use in the operating room to avoid hypovolemia and any circulatory insufficiency. While crystalloids and colloid solutions are frequently used to optimize intravascular volume during surgery, crystalloid solutions require more volume for hemodynamic optimization which may result in higher volumes of fluid administration and potentially side effects. Compared with crystalloids, colloids have the advantages of remaining in the intravascular space longer, achieving faster circulatory stabilization, maintaining colloid osmotic pressure and increasing micro perfusion. However, colloids are more expensive and may have various side effects. In addition to the effect of crystalloids and colloids on the patient, the amount of each fluid administered is also under debate. Goal-directed fluid therapy (GDFT) strategies based on cardiac output (CO) optimization have been shown to benefit moderate- to high-risk surgery patients and have recently been recommended by professional societies in the UK, in France, and in Europe. However, despite the growing evidence, these strategies are often not implemented in current practice. One of the reasons for this lack of implementation is that GDFT strategies, like any other complex clinical protocol, require significant provider attention and vigilance for consistent implementation and it is well known that even under study conditions protocol compliance rates are often not greater than 50% In another hand, one of the chief complicating factors in fluid administration studies is variation in provider administration practices, even when attempting to follow a protocol. Previous studies have used closed-loop (automated) systems to deliver fluid by a standardized protocol, removing variation between providers as one of the confounders of the study. Dr. Cannesson and Rinehart (UC Irvine, California, USA) have recently developed and used a closed-loop system for the provision of GDFT in clinical studies at UC Irvine and La Pitie hospital in France. The closed-loop system is beneficial because it involves the standardization of fluid management and all patients are treated equivalently. This system will thus provide consistent GDFT for all cases in the protocol and remove inter-provider variability as a confounder between groups. Study goal: This study will examine whether there is a significant difference in postoperative outcomes between GDFT using a colloid solution versus a crystalloid solution. Hypothesis: Perioperative fluid optimization through the use of a closed-loop assistance with a balanced starch solution (volulyte®) will be associated with a decrease in postoperative complications compared to the same approach using a balanced crystalloid solution (Plasmalyte®). Objective: To establish which kind of intravenous fluid used for goal directed therapy with closed-loop assistance will reduce the number of postoperative complications (evaluation made by the POMS score).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
160
CHU Brugmann
Brussels, Belgium
Erasme
Brussels, Belgium
POMS score
Difference between the 2 groups in postoperative morbidity identified with the Post-Operative Morbidity Survey (POMS score) on postoperative days 2.
Time frame: 48 hours
Mortality rate
Difference in 30-day post-operative mortality between the 2 groups
Time frame: 30 days
Length of hospitalisation
Difference in duration of hospital length of stay as well as ICU length of stay.
Time frame: every day up to 90 days after hospitalisation
Quantity of fluid administered during surgery
Fluid balance during surgery
Time frame: 24 hours
Transfusion rate
Differences of transfusion rate between the two groups, in ml
Time frame: 8 days
Hypotension incidence
Incidence of hypotension (defined as total case time spent with 20% drop from baseline preoperative blood pressure).
Time frame: 8 days
Need of vasopressors
Difference in the need and quantity of vasopressors between the two groups
Time frame: 24 hours
Mean case cardiac index (L /BSA)
Mean case cardiac index (L /BSA), Mean case cardiac stroke volume index (mL/ BSA).
Time frame: 24 hours
Whodas scale
Enrolled patients will be contacted by phone and their quality of life assessed by the Whodas scale
Time frame: 6 months after surgery
Whodas scale
Enrolled patients will be contacted by phone and their quality of life assessed by the Whodas scale
Time frame: 1 year after surgery
Pruritus apparition
Enrolled patients will be contacted by phone 6 months after surgery and any pruritus apparition will be recorded
Time frame: 6 months after surgery
Pruritus apparition
Enrolled patients will be contacted by phone 1 year after surgery and any pruritus apparition will be recorded
Time frame: 1 year after surgery
Renal function - urea level
Urea levels. Measured in a blood sample taken according to the standard of care outpatient post-operative follow appointments.
Time frame: 6 months after surgery
Renal function - urea level
Urea levels. Measured in a blood sample taken according to the standard of care outpatient post-operative follow appointments.
Time frame: 1 year after surgery
Renal function - creatinine level
Creatinine levels. Measured in a blood sample taken according to the standard of care outpatient post-operative follow appointments.
Time frame: 6 months after surgery
Renal function - creatinine level
Creatinine levels. Measured in a blood sample taken according to the standard of care outpatient post-operative follow appointments.
Time frame: 1 year after surgery
Renal function - Estimated glomerular filtration rate (eGFR)
Creatinine levels. Measured in a blood sample taken according to the standard of care outpatient post-operative follow appointments.
Time frame: 6 months after surgery
Renal function - Estimated glomerular filtration rate (eGFR)
Creatinine levels. Measured in a blood sample taken according to the standard of care outpatient post-operative follow appointments.
Time frame: 1 year after surgery
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