Intraoperative fluid optimization using stroke volume variation in high risk surgical patients: results of prospective randomized study
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Open Access
- 16 June 2010
- journal article
- research article
- Published by Springer Nature in Critical Care
- Vol. 14 (3) , R118
- https://doi.org/10.1186/cc9070
Abstract
Introduction: Stroke volume variation (SVV) is a good and easily obtainable predictor of fluid responsiveness, which can be used to guide fluid therapy in mechanically ventilated patients. During major abdominal surgery, inappropriate fluid management may result in occult organ hypoperfusion or fluid overload in patients with compromised cardiovascular reserves and thus increase postoperative morbidity. The aim of our study was to evaluate the influence of SVV guided fluid optimization on organ functions and postoperative morbidity in high risk patients undergoing major abdominal surgery. Methods: Patients undergoing elective intraabdominal surgery were randomly assigned to a Control group (n = 60) with routine intraoperative care and a Vigileo group (n = 60), where fluid management was guided by SVV (Vigileo/FloTrac system). The aim was to maintain the SVV below 10% using colloid boluses of 3 ml/kg. The laboratory parameters of organ hypoperfusion in perioperative period, the number of infectious and organ complications on day 30 after the operation, and the hospital and ICU length of stay and mortality were evaluated. The local ethics committee approved the study. Results: The patients in the Vigileo group received more colloid (1425 ml [1000-1500] vs. 1000 ml [540-1250]; P = 0.0028) intraoperatively and a lower number of hypotensive events were observed (2[1-2] Vigileo vs. 3.5[2-6] in Control; P = 0.0001). Lactate levels at the end of surgery were lower in Vigileo (1.78 ± 0.83 mmol/l vs. 2.25 ± 1.12 mmol/l; P = 0.0252). Fewer Vigileo patients developed complications (18 (30%) vs. 35 (58.3%) patients; P = 0.0033) and the overall number of complications was also reduced (34 vs. 77 complications in Vigileo and Control respectively; P = 0.0066). A difference in hospital length of stay was found only in per protocol analysis of patients receiving optimization (9 [8-12] vs. 10 [8-19] days; P = 0.0421). No difference in mortality (1 (1.7%) vs. 2 (3.3%); P = 1.0) and ICU length of stay (3 [2-5] vs. 3 [0.5-5]; P = 0.789) was found. Conclusions: In this study, fluid optimization guided by SVV during major abdominal surgery is associated with better intraoperative hemodynamic stability, decrease in serum lactate at the end of surgery and lower incidence of postoperative organ complications. Trial registration: Current Controlled Trials ISRCTN95085011.Keywords
This publication has 49 references indexed in Scilit:
- Goal-directed haemodynamic therapy and gastrointestinal complications in major surgery: a meta-analysis of randomized controlled trialsBritish Journal of Anaesthesia, 2009
- Esophageal Doppler-guided fluid management decreases blood lactate levels in multiple-trauma patients: a randomized controlled trialCritical Care, 2007
- Monitoring of peri‐operative fluid administration by individualized goal‐directed therapyActa Anaesthesiologica Scandinavica, 2007
- Performing perioperative optimization of the high-risk surgical patientBritish Journal of Anaesthesia, 2006
- Intraoperative oesophageal Doppler guided fluid management shortens postoperative hospital stay after major bowel surgeryBritish Journal of Anaesthesia, 2005
- Preoperative optimization of the high-risk surgical patientBritish Journal of Anaesthesia, 2004
- Occult hypoperfusion is associated with increased mortality in hemodynamically stable, high-risk, surgical patientsCritical Care, 2004
- Goal-directed Intraoperative Fluid Administration Reduces Length of Hospital Stay after Major SurgeryAnesthesiology, 2002
- Pathophysiology and clinical implications of perioperative fluid excessBritish Journal of Anaesthesia, 2002
- Randomised controlled trial investigating the influence of intravenous fluid titration using oesophageal Doppler monitoring during bowel surgery*Anaesthesia, 2002