Rollins Katie E, Lobo Dileep N
Gastrointestinal Surgery, National Institute for Health Research Nottingham Digestive Diseases Biomedical Research Unit, Nottingham University Hospitals and University of Nottingham, Queen's Medical Centre, Nottingham, UK.
Ann Surg. 2016 Mar;263(3):465-76. doi: 10.1097/SLA.0000000000001366.
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.
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.
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).
GDFT may not be of benefit to all elective patients undergoing major abdominal surgery, particularly those managed in an ERAS setting.
比较术中目标导向液体治疗(GDFT)与传统液体治疗的效果,并确定采用和未采用术后加速康复(ERAS)方案的研究在结局上是否存在差异。
对接受择期腹部大手术的成年患者进行术中GDFT与传统液体治疗比较的随机对照试验的荟萃分析。结局指标为术后发病率、住院时间、胃肠功能和30天死亡率。
共纳入23项研究,2099例患者:1040例接受GDFT,1059例接受传统液体治疗。GDFT与发病率显著降低相关(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)、重症监护病房住院时间(平均差 - 0.63天,95%CI - 1.18至 - 0.09,P = 0.02)以及排便时间(平均差 - 0.90天,95%CI - 1.48至 - 0.32天,P = 0.002)。然而,在死亡率、胃肠排气恢复或麻痹性肠梗阻风险方面未发现差异。如果患者按照ERAS路径管理,唯一显著降低的是重症监护病房住院时间(平均差 - 0.63天,95%CI - 0.94至 - 0.32,P < 0.0001)和排便时间(平均差 - 1.09天,95%CI - 2.03至 - 0.15,P = 0.02)。如果在传统护理环境中管理,总体发病率(RR 0.69,95%CI 0.57至 - 0.84,P = 0.0002)和总住院时间(平均差 - 2.14,95%CI - 4.15至 - 0.13,P = 0.04)均显著降低。
GDFT可能并非对所有接受腹部大手术的择期患者有益,尤其是那些按照ERAS模式管理的患者。