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首页> 外文期刊>Annals of Intensive Care >Effects of chloride content of intravenous crystalloid solutions in critically ill adult patients: a meta-analysis with trial sequential analysis of randomized trials
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Effects of chloride content of intravenous crystalloid solutions in critically ill adult patients: a meta-analysis with trial sequential analysis of randomized trials

机译:重症成年患者静脉内晶体溶液中氯化物含量的影响:荟萃分析及随机试验的试验顺序分析

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Abstract BackgroundIntravenous crystalloid solutions are administered commonly for critically ill patients. We performed this meta-analysis of randomized trials with trial sequential analysis (TSA) to evaluate effects of chloride content of intravenous crystalloid solutions on clinical outcomes among critically ill adult patients.MethodsElectronic databases were searched up to June 1, 2018, for randomized trials of use of balanced crystalloids versus 0.9% saline solutions in critically ill adult patients. The outcome variables included mortality, renal outcomes, serum content alterations and organ function. Subgroup analysis was conducted according to patient settings, types or volume of crystalloid fluid, or among sepsis versus non-sepsis, TBI versus non-TBI or subpopulations by the categories of baseline kidney function. Random errors were evaluated by trial sequential analysis.ResultsEight studies with 19,301 patients were analyzed. A trend of in-hospital survival benefit with no statistical difference could be observed with balanced crystalloids compared with 0.9% saline (RR 0.92, 95% CI 0.85–1.0, p =?0.06). The use of balanced crystalloid solutions was associated with longer RRT-free days (SMD 0.09, 95% CI 0.06–0.12, p ?0.001), less risk of increase in serum concentrations of chloride (SMD ??1.23, 95% CI ??1.59 to ??0.87, p ?0.001) and sodium (SMD ??1.28, 95% CI ??1.65 to ??0.92, p ?0.001), less risk of decline in serum base deficit (SMD ??0.58, 95% CI ??0.98 to ??0.18, p =?0.004), longer ventilator-free days (SMD 0.08, 95% CI 0.05–0.11, p ?0.001) and vasopressor-free days (SMD 0.04, 95% CI 0.00–0.07, p =?0.02). Subgroup analysis showed that balanced crystalloid solutions were associated with a reduced in-hospital mortality rate among septic patients (RR 0.86, 95% CI 0.75–0.98; p =?0.02) and non-traumatic brain injury patients (RR 0.90, 95% CI 0.82–0.99, p =?0.02), while the TSA results indicated a larger sample size is still in need.ConclusionsLimited evidence supported statistical survival benefit with balanced crystalloid solutions, while it benefited in reducing organ support duration and fluctuations in serum electrolyte and base excess and was associated with decreased in-hospital mortality in subpopulation with sepsis and non-TBI. Large-scale rigorous randomized trials with better designs are needed to provide robust evidence for clinical management.
机译:摘要背景静脉内晶体溶液通常用于重症患者。我们使用试验序贯分析(TSA)进行了这项随机试验的荟萃分析,以评估重症成年患者静脉内晶体溶液的氯化物含量对临床结局的影响。方法检索截至2018年6月1日的电子数据库,以评估在重症成年患者中使用平衡的晶体与0.9%的盐溶液。结果变量包括死亡率,肾脏结局,血清含量改变和器官功能。根据患者设置,晶体液的类型或体积,或在败血症与非败血症,TBI与非TBI或亚人群之间按基线肾功能类别进行亚组分析。通过试验序贯分析评估随机误差。结果分析了18,301例患者的八项研究。与0.9%的生理盐水相比,平衡的晶体可以观察到院内生存获益的趋势,但无统计学差异(RR 0.92,95%CI 0.85–1.0,p =?0.06)。使用平衡的晶体溶液可延长无RRT天数(SMD 0.09,95%CI 0.06-0.12,p <0.001),降低血清氯离子浓度升高的风险(SMD ≤1.23,95%CI≤0.05)。 1.59至0.87,p <0.001)和钠(SMD 1.28,95%CI为1.65至0.92,p <0.001),血清碱缺乏症下降的风险较小(SMD 0.58 ,95%CI为0.98至0.18,p = 0.004,更长的无呼吸机天数(SMD 0.08,95%CI 0.05-0.11,p <0.001)和无升压药的天数(SMD 0.04,95%) CI 0.00-0.07,p =?0.02)。亚组分析表明,平衡的晶体溶液与败血症患者(RR 0.86,95%CI 0.75-0.98; p =?0.02)和非创伤性脑损伤患者(RR 0.90,95%CI)的院内死亡率降低相关0.82–0.99,p =?0.02),而TSA结果表明仍需要更大的样本量。结论有限的证据支持平衡的晶体溶液对统计学生存有帮助,同时也有利于减少器官支持持续时间以及血清电解质和碱基的波动脓毒症和非TBI的亚群会增加患者的住院率,降低院内死亡率。需要具有更好设计的大规模严格随机试验,以为临床管理提供可靠的证据。

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