Effect of fluid strategy on stroke volume, cardiac output, and fluid responsiveness in adult patients undergoing major abdominal surgery: a sub-study of the Restrictive versus Liberal Fluid Therapy in Major Abdominal Surgery (RELIEF) trial

冲程容积 医学 脉冲压力 心脏指数 血流动力学 心输出量 血管内容积状态 容积描记器 围手术期 冲程(发动机) 麻醉 心脏病学 内科学 血压 心率 工程类 机械工程
作者
Tuong Phan,Yoshiaki Uda,Philip J. Peyton,Roman Kluger,Paul S. Myles
出处
期刊:BJA: British Journal of Anaesthesia [Elsevier]
卷期号:126 (4): 818-825 被引量:8
标识
DOI:10.1016/j.bja.2021.01.011
摘要

BackgroundWe designed a prospective sub-study of the larger Restrictive versus Liberal Fluid Therapy in Major Abdominal Surgery (RELIEF) trial to measure differences in stroke volume and other haemodynamic parameters at the end of the intraoperative fluid protocols. The haemodynamic effects of the two fluid regimens may increase our understanding of the observed perioperative outcomes.MethodsStroke volume and cardiac output were measured with both an oesophageal Doppler ultrasound monitor and arterial pressure waveform analysis. Stroke volume variation, pulse pressure variation, and plethysmographic variability index were also obtained. A passive leg raise manoeuvre was performed to identify fluid responsiveness.ResultsAnalysis of 105 patients showed that the primary outcome, Doppler monitor-derived stroke volume index, was higher in the liberal group: restrictive 38.5 (28.6–48.8) vs liberal 44.0 (34.9–61.9) ml m−2; P=0.043. Similarly, there was a higher cardiac index in the liberal group: 2.96 (2.32–4.05) vs 2.42 (1.94–3.26) L min−1 m−2; P=0.015. Arterial-pressure-based stroke volume and cardiac index did not differ, nor was there a significant difference in stroke volume variation, pulse pressure variation, or plethysmographic variability index. The passive leg raise manoeuvre showed fluid responsiveness in 40% of restrictive and 30% of liberal protocol patients (not significant).ConclusionsThe liberal fluid group from the RELIEF trial had significantly higher Doppler ultrasound monitor-derived stroke volume and cardiac output compared with the restrictive fluid group at the end of the intraoperative period. Measures of fluid responsiveness did not differ significantly between groups.Clinical trial registrationACTRN12615000125527.
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