Conservative vs restrictive individualized goal-directed fluid replacement strategy in major abdominal surgery: A prospective randomized trial

Arch Surg. 2010 Dec;145(12):1193-200. doi: 10.1001/archsurg.2010.275.

Abstract

Objectives: To compare the influence of 2 volumes of fluid, integrated with goal-directed fluid therapy, on hypovolemia (a key trigger of tissue hypoperfusion) and central venous oxygen saturation (Scvo₂) and to assess their relationships with postoperative morbidity.

Design, setting, and patients: A prospective, randomized trial of 70 consecutive patients undergoing major abdominal surgery.

Interventions: Patients were randomly assigned to 6 mL/kg/h of crystalloid (a restrictive fluid strategy) or 12 mL/kg/h of crystalloid (a more conservative fluid strategy). In both groups, a fluid bolus was administered when respiratory variation in peak aortic flow velocity (ΔPV) was greater than 13%. Data on hypovolemia (ΔPV > 13%), Scvo₂, and postoperative complications were recorded for all patients.

Main outcome measures: Overall incidence of postoperative complications, especially anastomotic leak and sepsis.

Results: Overall incidence of complications, including postoperative anastomotic leak and sepsis, was higher in the restrictive group than in the conservative group (all P < .05). The number of patients with hypovolemia increased significantly in the restrictive group compared with the conservative group (P < .001). The perioperative mean Scvo₂ (P = .02) and mean minimum Scvo₂ (P = .04) were significantly lower in the restrictive group than in the conservative group. Multivariate analysis showed that both hypovolemia and mean minimum Scvo₂ were independently associated with anastomotic leak and sepsis.

Conclusions: Excessive fluid restriction increased the level of hypovolemia, leading to reduced Scvo₂ and thereby increased incidence of postoperative complications. Excessive fluid restriction should be applied cautiously in surgical patients.

Trial registration: clinicaltrials.gov Identifier: NCT00852449.

Publication types

  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdomen / surgery*
  • Adult
  • Aged
  • Analysis of Variance
  • Central Venous Pressure
  • Confidence Intervals
  • Crystalloid Solutions
  • Digestive System Surgical Procedures / methods
  • Female
  • Fluid Therapy / methods*
  • Fluid Therapy / standards
  • Follow-Up Studies
  • Hospital Mortality / trends*
  • Humans
  • Hypovolemia / prevention & control
  • Intraoperative Care / methods*
  • Isotonic Solutions / therapeutic use*
  • Laparotomy / adverse effects
  • Laparotomy / methods
  • Male
  • Middle Aged
  • Monitoring, Physiologic / methods
  • Multivariate Analysis
  • Odds Ratio
  • Oxygen / blood*
  • Oxygen Consumption / physiology
  • Postoperative Complications / mortality
  • Postoperative Complications / prevention & control
  • Prospective Studies
  • Survival Rate
  • Treatment Outcome

Substances

  • Crystalloid Solutions
  • Isotonic Solutions
  • Oxygen

Associated data

  • ClinicalTrials.gov/NCT00852449