Futier Emmanuel, Constantin Jean-Michel, Petit Antoine, Chanques Gerald, Kwiatkowski Fabrice, Flamein Renaud, Slim Karem, Sapin Vincent, Jaber Samir, Bazin Jean-Etienne
Department of Anesthesiology and Critical Care, University Hospital of Clermont-Ferrand, France.
Arch Surg. 2010 Dec;145(12):1193-200. doi: 10.1001/archsurg.2010.275.
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.
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.
Overall incidence of postoperative complications, especially anastomotic leak and sepsis.
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.
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.
clinicaltrials.gov Identifier: NCT00852449.
比较2种液体量结合目标导向液体治疗对低血容量(组织灌注不足的关键触发因素)和中心静脉血氧饱和度(Scvo₂)的影响,并评估它们与术后发病率的关系。
设计、地点和患者:一项对70例连续接受腹部大手术患者的前瞻性随机试验。
患者被随机分配接受6 mL/kg/h的晶体液(限制性液体策略)或12 mL/kg/h的晶体液(更宽松的液体策略)。两组中,当主动脉峰值流速呼吸变异率(ΔPV)大于13%时给予液体冲击量。记录所有患者的低血容量(ΔPV>13%)、Scvo₂和术后并发症数据。
术后并发症的总体发生率,尤其是吻合口漏和脓毒症。
限制性液体组术后并发症(包括吻合口漏和脓毒症)的总体发生率高于宽松液体组(所有P<.05)。与宽松液体组相比,限制性液体组低血容量患者数量显著增加(P<.001)。限制性液体组围手术期平均Scvo₂(P=.02)和平均最低Scvo₂(P=.04)显著低于宽松液体组。多因素分析显示,低血容量和平均最低Scvo₂均与吻合口漏和脓毒症独立相关。
过度液体限制会增加低血容量水平,导致Scvo₂降低,从而增加术后并发症的发生率。手术患者应谨慎应用过度液体限制。
clinicaltrials.gov标识符:NCT00852449。