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危重症成年患者静脉晶体液的选择与死亡率

Choice of Intravenous Crystalloid Fluid and Mortality in Critically Ill Adult Patients.

作者信息

Jackson Christopher D, Patel Shawn B, Haltom Matthew B, Iyer Praneet S, Odeesh Marwan A, Bradsher Robert W, Kamal Sehrish, Seth Ankur

机构信息

From the Department of Internal Medicine and the Division of Pulmonary Critical Care Medicine, University of Tennessee Health Science Center, Memphis.

出版信息

South Med J. 2019 Jul;112(7):401-405. doi: 10.14423/SMJ.0000000000000993.

Abstract

OBJECTIVES

Intravenous balanced crystalloid fluid therapy may improve mortality and other outcomes in critically ill adult patients, but data are conflicting. We conducted a meta-analysis and literature review to evaluate the impact of intravenous balanced crystalloid, as compared with normal saline, fluid therapy on outcomes in critically ill adult patients.

METHODS

We searched PubMed, Scopus, MEDLINE, and the Cochrane Register of Clinical Trials for relevant studies. Randomized controlled trials comparing the effects of balanced intravenous crystalloids with normal saline on intensive care unit (ICU) or hospital mortality were included. Pooled risk ratios (RRs) were calculated using a fixed effects model. Heterogeneity was calculated using the statistic. The risk of bias was assessed using the Cochrane tool.

RESULTS

Seven randomized controlled trials with 20,171 patients (10,179 participants received balanced crystalloids and 9992 participants received normal saline) were included. For hospital mortality, the pooled RR (95% confidence interval [CI]) was 0.92 (0.85-1.00). For ICU mortality, the pooled RR (95% CI) was 0.91 (0.82-1.00). For major adverse kidney events at 30 days, pooled RR (95% CI) was 0.95 (0.88-1.01). For stage ≥2 acute kidney injury, the pooled RR (95% CI) was 0.94 (0.86-1.02). For receipt of new renal replacement therapy, the pooled RR (95% CI) was 0.91 (0.77-1.07). None of these findings reached statistical significance.

CONCLUSIONS

Intravenous balanced crystalloid use, compared with normal saline, does not result in a statistically significant reduction in hospital or ICU mortality, major adverse kidney events at 30 days, stage ≥2 acute kidney injury, or receipt of new renal replacement therapy in critically ill adult patients.

摘要

目的

静脉输注平衡晶体液治疗可能改善危重症成年患者的死亡率及其他预后,但数据存在冲突。我们进行了一项荟萃分析和文献综述,以评估与生理盐水相比,静脉输注平衡晶体液治疗对危重症成年患者预后的影响。

方法

我们检索了PubMed、Scopus、MEDLINE和Cochrane临床试验注册库以查找相关研究。纳入比较静脉输注平衡晶体液与生理盐水对重症监护病房(ICU)或医院死亡率影响的随机对照试验。使用固定效应模型计算合并风险比(RR)。使用 统计量计算异质性。使用Cochrane工具评估偏倚风险。

结果

纳入了7项随机对照试验,共20171例患者(10179例接受平衡晶体液,9992例接受生理盐水)。对于医院死亡率,合并RR(95%置信区间[CI])为0.92(0.85 - 1.00)。对于ICU死亡率,合并RR(95%CI)为0.91(0.82 - 1.00)。对于30天时的主要不良肾脏事件,合并RR(95%CI)为0.95(0.88 - 1.01)。对于≥2期急性肾损伤,合并RR(95%CI)为0.94(0.86 - 1.02)。对于接受新的肾脏替代治疗,合并RR(95%CI)为0.91(0.77 - 1.07)。这些结果均未达到统计学显著性。

结论

与生理盐水相比,在危重症成年患者中,静脉输注平衡晶体液并不能使医院或ICU死亡率、30天时的主要不良肾脏事件、≥2期急性肾损伤或接受新的肾脏替代治疗出现具有统计学显著性的降低。

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