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首页> 外文期刊>Annals of Surgery >Intraoperative Goal-directed Fluid Therapy in Elective Major Abdominal Surgery A Meta-analysis of Randomized Controlled Trials
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Intraoperative Goal-directed Fluid Therapy in Elective Major Abdominal Surgery A Meta-analysis of Randomized Controlled Trials

机译:择期主要腹部手术的术中目标导向输液治疗随机对照试验的荟萃分析

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Objectives:To compare the effects of intraoperative goal-directed fluid therapy (GDFT) with conventional fluid therapy, and determine whether there was a difference in outcome between studies that did and did not use Enhanced Recovery After Surgery (ERAS) protocols.Methods:Meta-analysis of randomized controlled trials of adult patients undergoing elective major abdominal surgery comparing intraoperative GDFT versus conventional fluid therapy. The outcome measures were postoperative morbidity, length of stay, gastrointestinal function and 30-day mortality.Results:A total of 23 studies were included with 2099 patients: 1040 who underwent GDFT and 1059 who received conventional fluid therapy. GDFT was associated with a significant reduction in morbidity (risk ratio [RR] 0.76, 95% confidence interval [CI] 0.66-0.89, P=0.0007), hospital length of stay (LOS; mean difference -1.55 days, 95% CI -2.73 to -0.36, P=0.01), intensive care LOS (mean difference -0.63 days, 95% CI -1.18 to -0.09, P=0.02), and time to passage of feces (mean difference -0.90 days, 95% CI -1.48 to -0.32 days, P=0.002). However, no difference was seen in mortality, return of flatus, or risk of paralytic ileus. If patients were managed in an ERAS pathway, the only significant reductions were in intensive care LOS (mean difference -0.63 days, 95% CI -0.94 to -0.32, P<0.0001) and time to passage of feces (mean difference -1.09 days, 95% CI -2.03 to -0.15, P=0.02). If managed in a traditional care setting, a significant reduction was seen in both overall morbidity (RR 0.69, 95% CI 0.57 to -0.84, P=0.0002) and total hospital LOS (mean difference -2.14, 95% CI -4.15 to -0.13, P=0.04).Conclusions:GDFT may not be of benefit to all elective patients undergoing major abdominal surgery, particularly those managed in an ERAS setting.
机译:目的:比较术中目标导向液体疗法(GDFT)与常规液体疗法的效果,并确定在使用和未使用手术后增强恢复(ERAS)方案的研究之间结果是否存在差异。接受选择性大腹部手术的成年患者的随机对照试验分析,比较了术中GDFT与常规输液治疗。结果指标包括术后发病率,住院时间,胃肠功能和30天死亡率。结果:共纳入23项研究,涉及2099例患者:1040例行GDFT,1059例行常规输液治疗。 GDFT与发病率显着降低(风险比[RR] 0.76,95%置信区间[CI] 0.66-0.89,P = 0.0007),住院时间(LOS;平均差-1.55天,95%CI- 2.73至-0.36,P = 0.01),重症监护室(平均差异-0.63天,95%CI -1.18至-0.09,P = 0.02)和排便时间(平均差异-0.90天,95%CI -1.48至-0.32天,P = 0.002)。但是,死亡率,肠胃气胀或麻痹性肠梗阻的风险均无差异。如果患者采用ERAS途径进行治疗,唯一的显着减少是重症监护室(平均差异-0.63天,95%CI -0.94至-0.32,P <0.0001)和排便时间(平均差异-1.09天) ,95%CI -2.03至-0.15,P = 0.02)。如果在传统护理环境中进行治疗,则总体发病率(RR 0.69,95%CI 0.57至-0.84,P = 0.0002)和总医院LOS(均差-2.14,95%CI -4.15至-)均显着降低。 0.13,P = 0.04)。结论:GDFT可能不适用于所有接受大腹部手术的选择性患者,特别是在ERAS环境中进行治疗的患者。

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