Critical Care Division, The George Institute for Global Health, University of New South Wales, Sydney.
Malcolm Fisher Department of Intensive Care, Royal North Shore Hospital, Sydney.
NEJM Evid. 2022 Feb;1(2):EVIDoa2100010. doi: 10.1056/EVIDoa2100010. Epub 2022 Jan 18.
The comparative efficacy and safety of balanced crystalloid solutions and saline for fluid therapy in critically ill adults remain uncertain. METHODS: We systematically reviewed randomized clinical trials (RCTs) comparing the use of balanced crystalloids with saline in critically ill adults. The primary outcome was 90-day mortality after pooling data from low-risk-of-bias trials using a random-effects model. We also performed a Bayesian meta-analysis to describe the primary treatment effect in probability terms. Secondary outcomes included the incidence of acute kidney injury (AKI), new treatment with renal replacement therapy (RRT), and ventilator-free and vasopressor-free days to day 28. RESULTS: We identified 13 RCTs, comprising 35,884 participants. From six trials (34,450 participants) with a low risk of bias, the risk ratio (RR) for 90-day mortality with balanced crystalloids versus saline was 0.96 (95% confidence interval [CI], 0.91 to 1.01; I2 = 12.1%); using vague priors, the posterior probability that balanced crystalloids reduce mortality was 89.5%. The RRs of developing AKI and of being treated with RRT with balanced crystalloids versus saline were 0.96 (95% CI, 0.89 to 1.02) and 0.95 (95% CI, 0.81 to 1.11), respectively. Ventilator-free days (mean difference, 0.18 days; 95% CI, −0.45 to 0.81) and vasopressor-free days (mean difference, 0.19 days; 95% CI, −0.14 to 0.51) were similar between groups. CONCLUSIONS: The estimated effect of using balanced crystalloids versus saline in critically ill adults ranges from a 9% relative reduction to a 1% relative increase in the risk of death, with a high probability that the average effect of using balanced crystalloids is to reduce mortality. (PROSPERO number, CRD42021243399.)
在危重症成人患者中,平衡晶体液与生理盐水用于液体治疗的疗效和安全性比较仍不确定。
我们系统性地检索了比较危重症成人患者使用平衡晶体液与生理盐水的随机临床试验(RCT)。使用随机效应模型汇总低偏倚风险试验数据,主要结局为 90 天死亡率。我们还进行了贝叶斯荟萃分析,以概率形式描述主要治疗效果。次要结局包括急性肾损伤(AKI)的发生率、新开始肾脏替代治疗(RRT)以及至第 28 天的无呼吸机天数和无血管加压素天数。
我们确定了 13 项 RCT,共纳入 35884 名患者。在来自 6 项低偏倚风险试验(34450 名患者)的资料中,平衡晶体液与生理盐水相比,90 天死亡率的风险比(RR)为 0.96(95%置信区间[CI],0.91 至 1.01;I2=12.1%);使用模糊先验,平衡晶体液降低死亡率的后验概率为 89.5%。平衡晶体液与生理盐水相比,发生 AKI 的 RR 为 0.96(95%CI,0.89 至 1.02),开始 RRT 的 RR 为 0.95(95%CI,0.81 至 1.11)。两组间无呼吸机天数(平均差值,0.18 天;95%CI,−0.45 至 0.81)和无血管加压素天数(平均差值,0.19 天;95%CI,−0.14 至 0.51)相似。
使用平衡晶体液与生理盐水在危重症成人患者中的估计效果范围为,死亡率的相对风险降低 9%至增加 1%,使用平衡晶体液的平均效果很可能降低死亡率。(PROSPERO 注册号:CRD42021243399。)