Lactated Ringer's or Normal Saline for Initial Fluid Resuscitation in Sepsis-Induced Hypotension.

IF 6 1区 医学 Q1 CRITICAL CARE MEDICINE Critical Care Medicine Pub Date : 2025-05-01 Epub Date: 2025-02-19 DOI:10.1097/CCM.0000000000006601
Georg Gelbenegger, Nathan I Shapiro, Markus Zeitlinger, Bernd Jilma, Ivor S Douglas, Anselm Jorda
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Abstract

Objectives: To assess whether initial fluid resuscitation with lactated Ringer's solution compared with 0.9% saline is associated with improved clinical outcomes in patients with sepsis-induced hypotension.

Design: Secondary analysis of the randomized controlled Crystalloid Liberal or Vasopressors Early Resuscitation in Sepsis (CLOVERS) trial.

Setting: ICUs and emergency departments in 60 U.S. centers from March 2018 to January 2022.

Patients: Participants from the CLOVERS trial. Adult patients with a suspected or confirmed infection and hypotension caused by sepsis.

Interventions: Participants received 1-3 L of crystalloid fluid for initial fluid resuscitation before randomization. In this analysis, participants were categorized into a lactated Ringer's group and a 0.9% saline group based on the fluid type predominantly used for the initial fluid resuscitation (i.e., ≥ 95% of pre-randomization fluid).

Measurements and main results: Of 1563 participants with sepsis-induced hypotension included in the CLOVERS trial, 622 (39.8%) received lactated Ringer's solution and 690 (44.1%) received 0.9% saline as solution for the initial fluid bolus. Death before discharge home by day 90 occurred in 76 of 622 participants (12.2%) in the lactated Ringer's group and in 110 of 690 participants (15.9%) in the 0.9% saline group, resulting in an adjusted hazard ratio of 0.71 (95% CI, 0.51-0.99; p = 0.043). Patients receiving lactated Ringer's solution had more hospital-free days at 28 days than those receiving 0.9% saline (16.6 ± 10.8 vs. 15.4 ± 11.4, respectively; adjusted mean difference, 1.6 d [95% CI, 0.4-2.8 d; p = 0.009]). Treatment with 0.9% saline was associated with higher levels of serum chloride and decreased levels of serum bicarbonate.

Conclusions: Initial fluid resuscitation with lactated Ringer's solution, compared with 0.9% saline, might be associated with improved survival in patients with sepsis-induced hypotension.

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乳酸林格氏盐水或生理盐水用于败血症性低血压的初始液体复苏。
目的:评估与0.9%生理盐水相比,乳酸林格氏液初始液体复苏是否能改善败血症性低血压患者的临床结果。设计:对随机对照Crystalloid Liberal或血管加压素早期复苏败血症(CLOVERS)试验进行二次分析。环境:2018年3月至2022年1月,美国60个中心的icu和急诊科。患者:CLOVERS试验的参与者。怀疑或确诊脓毒症引起的感染和低血压的成年患者。干预措施:随机分组前,参与者接受1-3升晶体液体进行初始液体复苏。在本分析中,根据初始液体复苏主要使用的液体类型(即≥95%的随机化前液体),将参与者分为乳酸林格氏组和0.9%生理盐水组。测量和主要结果:CLOVERS试验中1563例败血症性低血压患者中,622例(39.8%)接受乳酸林格氏液治疗,690例(44.1%)接受0.9%生理盐水作为初始液体丸。622名受试者中有76人(12.2%)在泌乳林格氏组中死亡,690名受试者中有110人(15.9%)在0.9%生理盐水组中死亡,调整后的风险比为0.71 (95% CI, 0.51-0.99;P = 0.043)。在28天时,接受乳酸林格氏液治疗的患者比接受0.9%生理盐水治疗的患者无住院天数(分别为16.6±10.8 vs 15.4±11.4);校正平均差,1.6 d [95% CI, 0.4-2.8 d;P = 0.009])。0.9%生理盐水治疗与血清氯化物水平升高和血清碳酸氢盐水平降低相关。结论:与0.9%生理盐水相比,乳酸林格氏液的初始液体复苏可能与败血症性低血压患者的生存率提高有关。
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来源期刊
Critical Care Medicine
Critical Care Medicine 医学-危重病医学
CiteScore
16.30
自引率
5.70%
发文量
728
审稿时长
2 months
期刊介绍: Critical Care Medicine is the premier peer-reviewed, scientific publication in critical care medicine. Directed to those specialists who treat patients in the ICU and CCU, including chest physicians, surgeons, pediatricians, pharmacists/pharmacologists, anesthesiologists, critical care nurses, and other healthcare professionals, Critical Care Medicine covers all aspects of acute and emergency care for the critically ill or injured patient. Each issue presents critical care practitioners with clinical breakthroughs that lead to better patient care, the latest news on promising research, and advances in equipment and techniques.
期刊最新文献
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