Division of Critical Care Medicine, McMaster University, Hamilton, ON L8N 3Z5, Canada ; Critical Care Medicine Residency Program, Room 2U c/o Anesthesia Department, McMaster University, 1200 Main St. W., Hamilton, ON L8N 3Z5, Canada.
J Intensive Care. 2014 Jun 10;2:37. doi: 10.1186/2052-0492-2-37. eCollection 2014.
The background of this study is to determine whether the addition of intravenous colloid to diuretic therapy, in comparison to diuretic therapy alone, improves diuresis and oxygenation and prevents intravascular volume depletion in intensive care unit (ICU) patients without shock.
We searched MEDLINE, Embase, Cochrane Register of Controlled Trials, Google Scholar, conference abstracts of ACCP, SCCM, ATS, and references of relevant articles. Randomized controlled trials (RCTs) of adult ICU patients, not in shock (defined as patients on low dose or no vasopressors, without need for IV fluid bolus or blood transfusion within 24 h), comparing intravenous colloid therapy (human albumin, plasma, synthetic starches, or gels) plus diuretic to control (diuretic alone, or diuretic plus placebo). Two reviewers independently applied eligibility criteria, assessed quality, and extracted data.
Seven hundred fifty five studies were found in the initial search; 14 were deemed relevant; 2 were found to be eligible. There was good agreement between reviewers for study relevance (k = 0.869) and eligibility (k = 0.811). One study of heart failure patients showed no evidence of improved mean or hourly urine output in the group receiving albumin. The second studied patients hypoproteinemic with ARDS and demonstrated an improved fluid balance in 3 days, improved oxygenation status, and improved serum albumin level in patients treated with albumin. No significant differences were found for other outcomes. No studies evaluating colloids other than albumin were found.
Our review is limited by the small number of high-quality RCTs available to study this clinical question, both of which only studied albumin. High-quality RCTs are required to evaluate the effect of albumin as well as other colloids as an adjunct to diuresis in a general ICU population.
本研究旨在确定与单独使用利尿剂治疗相比,在无休克的重症监护病房(ICU)患者中,利尿剂治疗联合静脉胶体是否能改善利尿和氧合作用,并防止血管内容量不足。
我们检索了 MEDLINE、Embase、 Cochrane 对照试验注册库、Google Scholar、ACCP、SCCM、ATS 会议摘要以及相关文章的参考文献。纳入了成人 ICU 患者(无休克,定义为使用低剂量或不使用血管加压药,24 小时内无需静脉补液或输血)的随机对照试验(RCT),比较了静脉胶体治疗(人白蛋白、血浆、合成淀粉或凝胶)联合利尿剂与对照组(单独使用利尿剂或利尿剂联合安慰剂)。两名评审员独立应用纳入标准、评估质量并提取数据。
初步检索发现 755 项研究,其中 14 项被认为是相关的,2 项符合纳入标准。两名评审员在研究相关性(k=0.869)和纳入标准(k=0.811)方面具有很好的一致性。一项心力衰竭患者的研究表明,接受白蛋白治疗的患者平均或每小时尿量没有增加。第二项研究了低蛋白血症合并 ARDS 的患者,结果显示白蛋白治疗组在 3 天内液体平衡得到改善,氧合状态得到改善,血清白蛋白水平升高。其他结局未发现显著差异。没有评估除白蛋白以外胶体的研究。
我们的综述受到可用研究该临床问题的高质量 RCT 数量较少的限制,这两项研究都只研究了白蛋白。需要高质量的 RCT 来评估白蛋白以及其他胶体作为一般 ICU 人群利尿治疗辅助的效果。