Fluid Responsiveness Assessment Using Passive Leg Raising Test to Reduce Fluid Administration and Weight Gain in Patients with Septic Shock

C. Maria, Bergman Magnus, Joelsson-Alm Eva, Divander Mona-Britt, J. Emma, Balintescu Anca, M. Johan, Svensen Christer
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引用次数: 5

Abstract

Background: Several observational studies have demonstrated an association between fluid accumulation and mortality in sepsis. Our aim was to determine if assessment of fluid responsiveness by a passive leg raising (PLR) algorithm could reduce fluid accumulation after 3 days in the intensive care unit (ICU) in patients with septic shock. Methods: This was an open-label single-centre randomised clinical trial performed in a surgical ICU in a tertiary centre in Stockholm, Sweden. We randomised adult (>18 years) patients with septic shock admitted to the ICU to a PLR group or a standard of care group. An increase in stroke volume index of at least 10% on the PLR test was required for the clinician to administer a fluid bolus to patients in the PLR group.  Results: We randomised 34 patients. The mean (SD) weight gain after three full ICU-days was 0.6 ± 3.2 kg in the PLR group and 1.3 ± 3.9 kg in the control group (P = 0.59). The median (IQR) amount of administered resuscitation fluid during the study period was 2103 (1283-2645) ml in the PLR group and 2408 (954-5045) ml in the control group (P = 0.38). We could implement a protocol that required a positive PLR-test before administration of resuscitation fluids, but recruitment rate was low. The trial was terminated early for futility.  Conclusion: The PLR protocol was not meaningful in our clinical setting, as weight gain was already low in the control group. To increase feasibility of a trial which implements a PLR-test we recommend using a non-invasive hemodynamic measurement, to include restriction of maintenance fluids in the protocol and to investigate the level of weight gain in the setting where the trial is to be performed before the start of the trial. (Funded by Stockholm County Council; ClinicalTrials.gov number, NCT02301585.)    Citation:  Maria Cronhjort, Magnus Bergman, Eva Joelsson-Alm, Mona-Britt Divander, Emma Jerkegren, Anca Balintescu, et al. Fluid Responsiveness Assessment Using Passive Leg Raising Test to Reduce Fluid Administration and Weight Gain in Patients with Septic Shock. J Anesth Perioper Med 2017; 4 : 169-78. doi: 10.24015/ JAPM.2017.0049 This is an open-access article, published by Evidence Based Communications (EBC). This work is licensed under the Creative Commons Attribution 4.0 International License, which permits unrestricted use, distribution, and reproduction in any medium or format for any lawful purpose. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
用被动抬腿试验评估脓毒性休克患者的液体反应性以减少液体给药和体重增加
背景:几项观察性研究已经证明了脓毒症中液体积聚与死亡率之间的关联。我们的目的是确定通过被动抬腿(PLR)算法评估液体反应性是否可以减少脓毒性休克患者在重症监护病房(ICU) 3天后的液体积聚。方法:这是一项开放标签单中心随机临床试验,在瑞典斯德哥尔摩一家三级中心的外科ICU进行。我们将入住ICU的成人(>18岁)感染性休克患者随机分为PLR组或标准护理组。在PLR试验中,脑卒中容量指数至少增加10%,临床医生才需要给PLR组患者输液。结果:我们随机选取了34例患者。3个满icu d后,PLR组平均增重(SD)为0.6±3.2 kg,对照组为1.3±3.9 kg (P = 0.59)。研究期间,PLR组复苏液的中位数(IQR)为2103 (1283-2645)ml,对照组为2408 (954-5045)ml (P = 0.38)。我们可以实施一项方案,要求在给予复苏液体之前进行阳性plr测试,但招募率很低。试验因无效而提前终止。结论:PLR方案在我们的临床环境中没有意义,因为对照组的体重增加已经很低了。为了提高实施plr测试的试验的可行性,我们建议使用非侵入性血液动力学测量,在方案中包括维持液体的限制,并在试验开始前调查试验环境中体重增加的水平。(由斯德哥尔摩县议会资助;ClinicalTrials.gov号码:NCT02301585。)出处:Maria cronhort, Magnus Bergman, Eva Joelsson-Alm, Mona-Britt Divander, Emma Jerkegren, Anca Balintescu等。用被动抬腿试验评估脓毒性休克患者的液体反应性以减少液体给药和体重增加。中华外科杂志2017;[4]: 169-78。doi: 10.24015/ JAPM.2017.0049这是一篇开放获取的文章,由Evidence Based Communications (EBC)发表。本作品遵循知识共享署名4.0国际许可协议,允许以任何媒介或格式出于任何合法目的不受限制地使用、分发和复制。要查看此许可证的副本,请访问http://creativecommons.org/licenses/by/4.0/。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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